Screening Assessment for the Challenge Benzenamine, 4-[(2,6-dichloro-4-nitrophenyl)azo]-N-(4-nitrophenyl)-

Chemical Abstracts Service Registry Number 72927-94-7

Environment Canada
Health Canada

August 2009

Table of Contents

  1. Synopsis
  2. Introduction
  3. Substance Identity
  4. Physical and Chemical Properties
  5. Sources
  6. Uses
  7. Releases to the Environment
  8. Environmental Fate
  9. Persistence and Bioaccumulation Potential
  10. Potential to Cause Ecological Harm
  11. Conclusion
  12. References
  13. Appendix I - Robust Study Summaries for Key Studies

Synopsis

Pursuant to section 74 of the Canadian Environmental Protection Act, 1999 (CEPA 1999), the Ministers of the Environment and of Health have conducted a screening assessment on benzenamine, 4-[(2,6-dichloro-4-nitrophenyl)azo]-N-(4-nitrophenyl)- (DNAN), Chemical Abstracts Service Registry Number 72927-94-7. This substance was identified as a high priority for screening assessment and included in the Challenge because it had been found to meet the ecological categorization criteria for persistence, bioaccumulation potential and inherent toxicity to non-human organisms and is believed to be in commerce in Canada.

The substance DNAN was not considered to be a high priority for assessment of potential risks to human health, based upon application of the simple exposure and hazard tools developed by Health Canada for categorization of substances on the Domestic Substances List. Therefore, this assessment focuses on information relevant to the evaluation of ecological risks.

DNAN is an organic substance that has been previously reported to be used in Canada as a colorant. The substance is not naturally produced in the environment. No manufacturing or importation of this substance in Canada was reported for the years 2005 and 2006 above the section 71 reporting threshold of 100 kg per year. Based on known use patterns of structurally-similar azo dyes, the assumption is made in this assessment that DNAN is used in textiles.

Based on reported use patterns in Canada and certain assumptions, most of the substance ends up in solid waste disposal sites (85.2%) but a significant amount is released to sewer water (14.8%). DNAN is not expected to be soluble in water or volatile, but is expected to partition to particles because of its hydrophobic nature. For these reasons, after release to water, DNAN will likely end up mostly in sediments, and possibly to a much lesser extent, in agricultural soil that has been amended with sewage sludge. It is not expected to be significantly present in other media. It is also not expected to be subject to long-range atmospheric transport.

Based on its physical and chemical properties, DNAN is expected to be persistent in the environment (in water, sediment and soil). However, new experimental data relating to the bioaccumulation potential of a relatively close structural analogue suggests that this dye has a low potential to accumulate in the lipid tissues of organisms. The substance therefore meets the persistence criteria but does not meet the bioaccumulation criteria as set out in the Persistence and Bioaccumulation Regulations. In addition, experimental toxicity data for chemical analogues suggest that DNAN does not harm aquatic organisms exposed at low concentrations.

For this screening assessment, a very conservative exposure scenario was developed in which an industrial operation (i.e. the largest importer of the dye) discharges DNAN into a relatively small receiving water body at one discharge point. The predicted environmental concentration in water was below the predicted no-effect concentrations calculated for sensitive aquatic species. Additionally, since DNAN may be used in consumer products, a conservative consumer release scenario was developed based on an estimate of the quantity of DNAN in Canadian commerce. This scenario indicated that all modelled watercourses would have predicted environmental concentrations below the predicted no-effect concentrations.

This substance will be included in the upcoming Domestic Substances List inventory update initiative. In addition and where relevant, research and monitoring will be undertaken to confirm assumptions used during the screening assessment.

Based on the information available, it is concluded that DNAN does not meet any of the criteria set out in section 64 of CEPA 1999.

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Introduction

The Canadian Environmental Protection Act, 1999 (CEPA 1999) (Canada 1999) requires the Minister of the Environment and the Minister of Health to conduct screening assessments of substances that have met the categorization criteria set out in the Act to determine whether these substances present or may present a risk to the environment or human health. Based on the results of a screening assessment, the Ministers can propose to take no further action with respect to the substance, to add the substance to the Priority Substances List (PSL) for further assessment, or to recommend that the substance be added to the List of Toxic Substances in Schedule 1 of the Act and, where applicable, the implementation of virtual elimination.

Based on the information obtained through the categorization process, the Ministers identified a number of substances as high priorities for action. These include substances that

The Ministers therefore published a notice of intent in the Canada Gazette, Part I, on December 9, 2006 (Canada 2006a), that challenged industry and other interested stakeholders to submit, within specified timelines, specific information that may be used to inform risk assessment, and to develop and benchmark best practices for the risk management and product stewardship of those substances identified as high priorities.

The substance benzenamine, 4-[(2,6-dichloro-4-nitrophenyl)azo]-N-(4-nitrophenyl)- (DNAN) was identified as a high priority for assessment of ecological risk as it had been found to be persistent, bioaccumulative and inherently toxic to aquatic organisms and was believed to be in commerce in Canada. The Challenge for this substance was published in the Canada Gazette on February 16, 2008 (Canada 2008). A substance profile was released at the same time. The substance profile presented the technical information available prior to December 2005 that formed the basis for categorization of this substance. As a result of the Challenge, submissions of information pertaining to the uses of the substance were received.

Although DNAN was determined to be a high priority for assessment with respect to the environment, it did not meet the criteria for GPE or IPE and high hazard to human health based on classifications by other national or international agencies for carcinogenicity, genotoxicity, developmental toxicity or reproductive toxicity. Therefore, this assessment focuses principally on information relevant to the evaluation of ecological risks.

Under CEPA 1999, screening assessments focus on information critical to determining whether a substance meets the criteria for defining a chemical as toxic as set out in section 64 of the Act, where

"64. [...] a substance is toxic if it is entering or may enter the environment in a quantity or concentration or under conditions that

  1. have or may have an immediate or long-term harmful effect on the environment or its biological diversity;
  2. constitute or may constitute a danger to the environment on which life depends; or
  3. constitute or may constitute a danger in Canada to human life or health."

Screening assessments examine scientific information and develop conclusions by incorporating a weight of evidence approach and precaution.

This screening assessment includes consideration of information on chemical properties, hazards, uses and exposure, including the additional information submitted under the Challenge. Data relevant to the screening assessment of this substance were identified in original literature, review and assessment documents, stakeholder research reports and from recent literature searches, up to August 2008 for exposure, effects and ecological sections of the document. Key studies were critically evaluated and generally only results from studies of good quality were used to reach conclusions, although other studies and modelling results may have been considered as part of the weight of evidence. When available and relevant, information presented in hazard assessments from other jurisdictions was considered. The screening assessmentdoes not represent an exhaustive or critical review of all available data. Rather, it presents the most critical studies and lines of evidence pertinent to the conclusion.

This screening assessment was prepared by staff in the Existing Substances Programs at Health Canada and Environment Canada and incorporates input from other programs within these departments. The assessment has undergone external written peer review.
While external comments were taken into consideration, the final content and outcome of the screening risk assessment remain the responsibility of Health Canada and Environment Canada. Additionally, the draft of this screening assessment was subject to a 60-day public comment period. The critical information and considerations upon which the assessment is based are summarized below.

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Substance Identity

For the purposes of this document, the substance benzenamine, 4-[(2,6-dichloro-4-nitrophenyl)azo]-N-(4-nitrophenyl) will be referred to as DNAN. Information on substance identity is included in Table 1.

Table 1. Substance Identity
Chemical Abstracts Service Registry Number (CAS RN) 72927-94-7
Domestic Substances List (DSL) name Benzenamine, 4-[(2,6-dichloro-4-nitrophenyl)azo]-N-(4-nitrophenyl)-
National Chemical Inventories (NCI) namesTable note a Benzenamine, 4-[(2,6-dichloro-4-nitrophenyl)azo]-N-(4-nitrophenyl)- (TSCA, DSL, AICS, PICCS, ASIA-PAC);
4-[(2,6-Dichloro-4-nitrophenyl)azo]-N-(4-nitrophenyl)aniline (English, French) (DSL, EINECS, PICCS);
4-[(2,6-Dichlor-4-nitrophenyl)azo]-N-(4-nitrophenyl)anilin (German) (EINECS);
4-[(2,6-dicloro-4-nitrofenil)azo]-N-(4-nitrofenil)anilina (Spanish) (EINECS);
4-[(2,6-dichloro-4-nitrophenyl)azo]-N-(4-nitrophenyl)azo]aniline (PICCS)
Other names 1-[(2',6'-Dichloro-4'-nitrophenyl)azo]-4-(4''-nitrophenylamino)benzene
Chemical group Azo Compounds
Chemical sub-group Monoazo Compounds
Chemical formula C18H11Cl2N5O4
Chemical structure  Chemical Structure of CAS RN 72927-94-7
Simplified Molecular Line Input Entry System (SMILES) N(=O)(=O)c(cc(c(N=Nc(ccc(Nc(ccc(N(=O)(=O))c1)c1)c2)c2)c3Cl)Cl)c3
Molecular mass 432.22 g/mol

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Physical and Chemical Properties

No experimental data are available for DNAN. At the Environment Canada-sponsored Quantitative Structure-Activity Relationship (QSAR) Workshop in 1999 (Environment Canada 2000), Environment Canada and other invited modelling experts identified many structural classes of pigments and dyes as "difficult to model" using QSARs. The physical and chemical properties of many of the structural classes of dyes and pigments (including acid and disperse dyes) are not amenable to model prediction because they are considered "out of the model domain of applicability" (e.g., structural and/or property parameter domains). Therefore, to determine potential utility, the domains of applicability, Environment Canada reviews the applicability of QSAR models to dyes and pigments on a case-by-case basis. Environment Canada has considered it generally inappropriate to use QSAR models to predict the physical and chemical properties of DNAN. Consequently, a number of analogues were identified and "read-across" data has been used to determine the approximate physical and chemical properties in Table 2. These properties were subsequently used for further modeling and lines of evidence in this assessment.

An analogue is a chemical which is structurally similar to the substance under assessment and is therefore expected to have similar physical-chemical properties, behaviour in the environment and/or toxicity. Where there are experimental data for a given parameter for an analogue substance, these can be used directly or with adjustment as an estimate of that parameter value for the substance under assessment.

In order to find acceptable analogues, a review of data for several disperse azo dyes was performed (Anliker et al. 1981, Anliker and Moser 1987, Baughman and Perenich 1988, ETAD 1995, Brown 1992, Yen et al. 1989, Sijm et al. 1999). These compounds have structural similarities to DNAN but also share other important attributes that contribute to their suitability as analogues. This includes properties affecting their fate in the environment such as high molecular weights (generally greater than 300 g/mol), similar cross sectional diameters (1.31 - 2.05 nm) solid particulate structures, decomposition at greater than 74°C (to 236°C), and "dispersibility" in water (i.e. not truly soluble). In addition, they have low to moderate solubility in n-octanol, a negligible vapour pressure and are stable under environmental conditions. 

Table 2 contains analogue as well as read-across experimental and calculated physical and chemical properties of DNAN that are relevant to its environmental fate. No experimental values were found for DNAN.

Table 2. Physical and chemical properties for DNAN and some chemical analogues.
  TypeTable note b Value Temperature (°C) Reference
Melting pointTable note c (°C) Analogue Disperse Blue 79 157   PhysProp 2006
Melting pointTable note c (°C) Analogue Disperse Blue 79:1 132 to 153   Sijm et al. 1999; Yen et al. 1989
Melting pointTable note c (°C) Analogue with CAS RN 68877-63-4 175 to 193   Anliker and Moser 1987; Yen et al. 1989
Melting pointTable note c (°C) Analogue Disperse Blue 165 252   Sijm et al. 1999
Melting pointTable note c (°C) Read-across for azo disperse dyes 117 to 175 74 to 236   Anliker and Moser 1987; Baughman and Perenich 1988
Boiling pointTable note d (°C) Not applicable Not applicable Not applicable Not applicable
Density (kg/m3) Not available Not available Not available Not available
Vapour pressure (Pa) Analogue Disperse Blue 79 4.53 × 10-7   Clariant 1996
Vapour pressure (Pa) Read-across for azo disperse dyes 5.33 × (10-12 to 10-5)
(4 × 10-14 to 4 × 10-7 mm Hg)
25 Baughman and Perenich 1988
Henry's Law constant (Pa·m3/mol) Read-across for azo disperse dyesTable notee 10-8 to 10-1
(10-13 to 10-6atm·m3/mol)
  Baughman and Perenich 1988
Log Kow (octanol-water partition coefficient) (dimensionless) Analogue Disperse Blue 79 4.1; 4.3   Clariant 1996; Brown 1992
Log Kow (dimensionless) Analogue Disperse Blue 79:1 4.4; 4.8   Sijm et al. 1999; Yen et al. 1989
Log Kow (dimensionless) Analogue with CAS RN 68877-63-4 2.5; 5.4   Anliker and Moser 1987; Yen et al. 1989
Log Kow (dimensionless) Analogue Disperse Orange 30 4.2   Brown 1992
Log Kow (dimensionless) Read-across for disperse azo dyes 1.79 to 5.1   Baughman and Perenich 1988
Log Kow (dimensionless) Read-across for disperse azo dyes greater than 2 to 5.1   Anliker et al. 1981; Anliker and Moser 1987
Log Koc (organic carbon-water partition coefficient) (dimensionless) Read-across, calculatedTable note f 3.4 to 4.2   Baughman and Perenich 1988
Water solubility (mg/L) Analogue Disperse Blue 79 0.0054 25 Clariant 1996
Water solubility (mg/L) Analogue Disperse Blue 79 0.02   Brown 1992
Water solubility (mg/L) Analogue Disperse Blue 79:1 0.02   Sijm et al. 1999
Water solubility (mg/L) Analogue Disperse Blue 79:1 0.0052   Yen et al. 1989
Water solubility (mg/L) Analogue Disperse Blue 79:1 0.00063 100-125 Baughman and Perenich 1988
Water solubility (mg/L) Analogue with CAS RN 68877-63-4 0.00069   Yen et al. 1989
Water solubility (mg/L) Analogue Disperse Blue 165 0.0058 to 1.3   Sijm et al. 1999
Water solubility (mg/L) Read-across for azo disperse dyes less than 0.01 20 Anliker and Moser 1987
Water solubility (mg/L) Read-across for azo disperse dyes Substantially water insoluble   ETAD 1995
Water solubility (mg/L) Read-across for azo disperse dyes 1.2 × 10-5 to 35.5
(4 × 10-11 to 1.8 × 10-4 mol/L)
  Baughman and Perenich 1988
n-octanol solubility (mg/L) Analogue Disperse Blue 79:1 14   Sijm et al. 1999
n-octanol solubility (mg/L) Analogue with CAS RN 68877-63-4 81 20 Anliker and Moser 1987
n-octanol solubility (mg/L) Analogue Disperse Blue 165 225   Sijm et al. 1999
n-octanol solubility (mg/L) Read-across for azo disperse dyes 81-2100 20 Anliker and Moser 1987
pKa (acid dissociation constant) (dimensionless) Modelled -4.63 for base form   ACD/pKa DB 2005

Structural disperse azo analogues to DNAN are presented in Table 3a below. Certain empirical physical-chemical properties (Table 2), bioaccumulation data (Table 6) and toxicity data (Table 7) of these analogues were used in support of the weight of evidence and proposed decisions in this screening assessment. Specifically, data were obtained for the structural analogues: Disperse Orange 30, Disperse Blue 79, Disperse Blue 79:1, CAS RN 68877-63-4, Disperse Blue 165, Disperse Red 73, Disperse Orange 25 and Disperse Red 17.

Table 3a. Structural analogues for DNAN.
 CAS RN Common Name DSL name Structure of analogue Available empirical data
3618-72-2 Disperse Blue 79:1 Acetamide, N-[5-[bis[2-(acetyloxy)ethyl] amino]-2-[(2-bromo-4,6-dinitrophenyl)azo]-4-methoxyphenyl ]-  Chemical Structure of CAS RN 3618-72-2 Melting point, log Kow, water solubility, bioaccumulation, aquatic toxicity
12239-34-8 Disperse Blue 79 Acetamide,N-[5-[bis[2-(acetyloxy)ethyl]amino]-2-[(2-bromo-4,6-dinitrophenyl)azo]-4-ethoxyphenyl]-  Chemical Structure of CAS RN 12239-34-8 Melting point, vapour pressure, log Kow, water solubility, aquatic toxicity
68877-63-4 n/a Acetamide, N-(2-(2-(2-bromo-4,6-dinitrophenyl)diazenyl)-5-((2-cyanoethyl)-2-propen-1-ylamino)-4-methoxyphenyl)-  Chemical Structure 68877-63-4 Melting point, log Kow, water solubility, octanol solubility, bioaccumulation
41642-51-7 Disperse Blue 165 Acetamide, N-(2-(2-(2,6-dicyano-4-nitrophenyl) diazenyl)-5-(diethylamino) phenyl)-  Chemical Structure 41642-51-7 Melting point, water solubility, octanol water solubility
5261-31-4 Disperse Orange 30 Propanenitrile, 3-[[2-(acetyloxy)ethyl][4-[(2,6-dichloro-4-nitrophenyl) azo]phenyl]amino]-  Chemical Structure of CAS RN 5261-31-4 Bioaccumulation, aquatic toxicity, log Kow
16889-10-4 Disperse Red 73 2-((4-((2-Cyanoethyl) ethylamino)phenyl)azo)-5-nitro benzonitrile  Chemical Structure of CAS RN 16889-10-4 Aquatic toxicity
31482-56-1 Disperse Orange 25 3-(Ethyl(4-((4-nitro phenyl)azo)phenyl) amino)propanenitrile  Chemical Structure of CAS RN 31482-56-1 Aquatic toxicity
3179-89-3 Disperse Red 17 Ethanol, 2,2'-((3-methyl-4-(2-(4-nitrophenyl) diazenyl)phenyl) imino)bis-  Chemical Structure of CAS RN 3179-89-3 Aquatic toxicity

It should be noted that there are several uncertainties associated with the use of physical-chemical, toxicological and bioaccumulation data available for the substances presented in Table 3a. All these substances belong to the same chemical class (disperse azo dyes with their characteristic azo bond) and are used for similar industrial purposes. However, there are differences between these substances associated with their unique functional groups (see Table 3b below) and for some of their molecular sizes. As a result, these analogues have empirical water solubilities that range over four orders of magnitude from 10-4 to 1 mg/L and empirical log Kow values that vary over two orders of magnitude from 2.5 to 5.4 (Table 2). Due to this variability, caution should be exercised when applying analogue values to DNAN as it would be preferable to use empirical water solubility and log Kow data specific to the substance DNAN (Table 2).

Table 3b. Comparisons of structural analogues with DNAN.
 CAS RN Common Name Molecular mass (g/mol) Structure similarTable note g Minimum-maximum cross-sectional diameter (nm)Table note h
3618-72-2 Disperse Blue 79:1 625.39 N/A 1.43-2.03
12239-34-8 Disperse Blue 79 639.4 N/A 1.69-2.045
68877-63-4 n/a 546.3 N/A 1.48-1.97
41642-51-7 Disperse Blue 165 405.4 N/A 1.35-1.82
5261-31-4 Disperse Orange 30 450.28 66.9 1.75-1.98
16889-10-4 Disperse Red 73 348.36 N/A 1.31-1.93
31482-56-1 Disperse Orange 25 323.35 N/A 1.37-1.95
3179-89-3 Disperse Red 17 344.36 N/A 1.41-1.86

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Sources

Recent information was collected through industry surveys conducted for the years 2005 and 2006 under Canada Gazette Notices issued pursuant to section 71 of CEPA 1999 (Canada 2006b and 2008). These Notices required submission of data on the Canadian manufacture and import of the substance. For 2006, data were also required on use quantities of DNAN.

In 2006, no companies reported importing or manufacturing DNAN above the prescribed reporting threshold of 100 kg/year in Canada. No companies reported using a total quantity greater than 1,000 kg of the substance, whether alone, in a mixture, in a product or in a manufactured item, at any concentration in 2006. In the Declaration of Stakeholder-Interest form associated with the section 71 survey for 2006, one company reported a stakeholder interest in this substance despite not meeting mandatory reporting requirements (Canada 2008).

In 2005, no companies reported manufacturing or importing DNAN in quantities above the prescribed reporting threshold of 100 kg/year. However, one company identified themselves as having a stakeholder interest in the substance (Canada 2006b).

The quantity reported during development of the Domestic Substances List (DSL) to be manufactured, imported or in commerce in Canada during the calendar year 1986 was 10,000 kg. The number of notifiers for the calendar years 1984-86 was fewer than four. 

DNAN is an existing chemical in Europe, but is not on the low or high production volume chemicals lists (ESIS 2008). The production volume of DNAN in the United States was 10,000 - 500,000 pounds/year in 1998 (US EPA 2007). The Substances in Preparation in Nordic Countries (SPIN) database indicates that this substance was in use in Sweden from 1999-2006 and in Norway in 2002, but the quantities in use in those countries were not stated (SPIN 2008).

No manufacturing, importation or use of this substance was reported for 2006. However the s.71 reporting threshold (i.e., 100 kg) was used throughout this screening assessment to capture the maximum potential mass of this substance that could be in use in Canada that would not subject to reporting.

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Uses

During the DSL nomination (1984-1986) DNAN was reported to be used in Canada as a colourant in pigments, stains, dyes and inks (Environment Canada 1988). However, no recent information on the use of this substance in Canada has been identified. No additional information on potential uses of DNAN was identified through searches of the available scientific and technical literature. Based on known use patterns of structurally-similar azo dyes, the assumption made in this assessment is that DNAN is used in textiles.

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Releases to the Environment

Mass Flow Tool

To estimate potential releases of the substance to the environment at different stages of its life cycle, a Mass Flow Tool is usually developed (Environment Canada 2008a). Empirical data concerning releases of specific substances to the environment are seldom available. Therefore, for each identified type of use of the substance, the proportion and quantity of release to the different environmental media are estimated, as is the proportion of the substance chemically transformed or sent for waste disposal. Unless specific information on the rate or potential for release of the substance from landfills and incinerators is available, the Mass Flow Tool does not quantitatively account for releases to the environment from disposal.

Assumptions and input parameters used in making the release estimates are based on information obtained from a variety of sources including responses to regulatory surveys, Statistics Canada, manufacturers' websites and technical databases and documents. Of particular relevance are emission factors, which are generally expressed as the fraction of a substance released to the environment, particularly during its manufacture, processing, and use associated with industrial processes. Sources of such information include emission scenario documents, often developed under the auspices of the Organization for Economic Cooperation and Development (OECD), and default assumptions used by different international chemical regulatory agencies. It is noted that the level of uncertainty in the mass of substance and quantity released to the environment generally increases towards the end of the life-cycle.

The Mass Flow Tool result for other in-commerce disperse azo dyes was used in this document to estimate the fraction of DNAN being released to the environment, since DNAN is structurally similar to other disperse azo dyes and their use patterns are also expected to be similar (textiles).

Based on Statistics Canada information and an analysis by Industry Canada (2008), it is proposed that DNAN may be imported in manufactured articles. A ratio of the amount of textiles manufactured in Canada relative to the amount imported textiles of 30/70 has been used to estimate the amount of dye imported in textiles (Environment Canada 2008b). This import quantity was included in the Mass Flow Tool calculations.

Table 4. Estimated releases and losses of disperse azo dyes to environmental media, chemical transformation and transfer to waste disposal sites, based on the Mass Flow Tool.
Fate Proportion of the mass (%)Table note i Major life cycle stage involvedTable note j
Releases to soil 0.0 Not applicable
Releases to air 0.0 Not applicable
Releases to sewerTable note k 14.8 Formulation, consumer use
Chemically transformed 0.0 Not applicable
Transferred to waste disposal sites (e.g., landfill, incineration) 85.2 Formulation, waste disposal

Results indicate that, like other disperse azo dyes, DNAN can be expected to be found largely in solid waste disposal sites (85.2%), due to the eventual disposal of manufactured items containing it. The calculations assume that there is no release of the substance from these sites, although long-term releases may be possible. A small fraction of solid waste is incinerated which is expected to result in chemical transformation of the substance. Based largely on information contained in OECD emission scenario documents for processing and uses associated with this type of substance, it is estimated that 14.8% of DNAN may be released to sewers (5.4% from industrial processing and 9.4% from consumer uses).

Based on the above, sewer water is the medium potentially receiving the greatest proportion of DNAN emitted during product use. It is anticipated that the majority of the substance bound in the product will be sent to landfills for disposal.

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Environmental Fate

As indicated by the results of the Mass Flow Tool (Table 4), the substance DNAN is expected to be released to waste water effluents during industrial processing and use. The moderate to high read-across log Kow values (2.5 to 5.4) and high log Koc (read-across 3.4 to 4.2) values (see Table 2) indicate that this substance may have affinity for solids. However, the log Koc is a calculated value (see footnote 3 below Table 2) and the adsorption potential of disperse particulate dye structures is generally not well understood, therefore the degree of adsorption of DNAN is uncertain.

DNAN is expected to be mostly found in sediment or soil, and is not expected to be subject to long-range atmospheric transport.

According to aerobic biodegradation models, DNAN is not expected to biodegrade quickly (see Table 5 below). It may inadvertently be applied to agricultural soils and pasture lands in Canada as a component of biosludge which is commonly used for soil enrichment. Moreover, it may also be released from coloured textiles deposited in landfills.

In solution DNAN behaves as a neutral base with an estimated pKa that is very low (-4.63; see Table 2). Consequently dissolved forms of DNAN are not expected to ionize in water at environmentally relevant pHs. Based on the water solubility of various analogues (Table 2), DNAN is however expected to be only sparingly soluble. Thus, when released into water, this substance is expected to be mostly present as a particulate solid or adsorbed to suspended particles and to sink eventually to bed sediments where it is expected to remain in a relatively biologically unavailable form. Razo-Flores et al. (1997) have stated that due to the recalcitrant nature of azo dyes in the aerobic environment, they eventually end up in anaerobic sediments, shallow aquifers and in groundwater. In buried sediment DNAN may undergo anaerobic degradation, as described in the following section on Persistence.

Baughman and Perenich (1988) state that volatilization from aquatic systems will not be an important loss process for disperse dyes which agrees with the low to negligible Henry's Law constant (10-8 to 10-1 Pa·m3/mol, read-across data in Table 2). Transport to air due to the loss of this substance from moist and dry soil surfaces is not likely to be important for this substance as indicated by the very low vapour pressure of DNAN (5.33 × (10-12 to 10-5) Pa; read-across data in Table 2). These data are consistent with the physical state (solid particle) of DNAN which does not make it a likely candidate for volatilization.

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Persistence and Bioaccumulation Potential

Persistence

No experimental degradation data for DNAN have been identified. No environmental monitoring data relating to the presence of DNAN in the Canadian environment (air, water, soil, sediment) have been identified.

According to the Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers, with some exceptions, dyes are considered essentially non-biodegradable under aerobic conditions (ETAD 1995). Repeated evaluation of ready and inherent biodegradability using accepted screening tests (see OECD Guidelines for Testing Chemicals) have confirmed this assumption (Pagga and Brown 1986; ETAD 1992). Based on the chemical structure of DNAN, there is no reason to suspect that biodegradation will be other than that described for dyes generally (ETAD 1995).

Some disperse azo dyes have been shown to undergo relatively rapid anaerobic degradation in sediment at depth where anoxic conditions persist (Yen et al. 1991, Baughman and Weber 1994, Weber and Adams 1995). Disperse dyes enter the aquatic system mostly as a dispersion of fine suspended particles, eventually settling to the aerobic layers of surface sediment where they will persist until sediment burial creates reducing conditions. The rate of sediment deposition and the extent of bioturbation varies from site to site and thus it is very difficult to ascertain the residence time of dyes in aerobic sediment layers. It is likely however, that in many cases this is greater than 365 days. Once under anaerobic or reducing conditions, azo dyes may undergo rapid degradation to substituted aromatic amine constituents as demonstrated by Yen et al. who measured reduction half-life values in compacted sediments at room temperature of 1.9-2.0 days for an azo benzothiazole dye (CAS 68133-69-7). However, in anoxic sediment, these biodegradation transformation products are not expected to present a high degree of exposure potential to most aquatic organisms, and therefore they are not likely to present an ecological concern.

Given the expected release of DNAN into wastewater, persistence was primarily examined using predictive QSAR models for aerobic biodegradation in water. The following analysis applies primarily to the portion of this substance that is present in the environment in the dissolved form, recognizing that a significant proportion would also likely exist in dispersed form as solid particles. DNAN does not contain functional groups expected to undergo hydrolysis in aerobic environments (dyes are designed to be stable in aqueous conditions). Table 5 summarizes the results of available QSAR models for biodegradation in water.

Table 5. Modelled data for degradation of DNAN in water
Fate Process Model and model basis Result Interpretation Extrapolated half-life (days) Extrapolation Reference and/or source
Biodegradation (aerobic) BIOWIN 2000 Sub-model 1: Linear probability -0.44 Does not biodegrade fast in water n/a n/a
Biodegradation (aerobic) BIOWIN 2000 Sub-model 2: Non-linear probability 0.00 Does not biodegrade fast in water n/a n/a
Biodegradation (aerobic) BIOWIN 2000 Sub-model 3: Expert Survey (ultimate biodegradation) 1.05 Recalcitrant 182 US EPA 2002 Aronson et al. 2006
Biodegradation (aerobic) BIOWIN 2000 Sub-model 4: Expert Survey (primary biodegradation) 2.65 Primary biodegradation in weeks-months in water 37.5 US EPA 2002, Aronson et al. 2006
Biodegradation (aerobic) BIOWIN 2000 Sub-model 5: MITI linear probability -0.79  Does not biodegrade fast in water greater than 60 Aronson et al. 2006
Biodegradation (aerobic) BIOWIN 2000 Sub-model 6: MITI non-linear probability 0.00 Does not biodegrade fast in water greater than 60 Aronson et al. 2006
Biodegradation BIOWIN 2000 Overall Conclusion No Not readily biodegradable in water n/a n/a
Biodegradation (aerobic) CATABOL v. 5.10.2 % BOD (OECD 301C) 0 Persistent in water greater than 182 calculated from BOD assuming first order rate kinetics

The results from Table 5 show that the majority of the biodegradation models (BIOWIN1, 2, 3, 5, 6 and 7) suggest this substance does not biodegrade fast. In fact all probability results are less than 0.3, the cut-off suggested by Aronson et al. (2006) to identify substances as having a half-life greater than 60 days (based on the MITI probability models). The half-life result from the primary survey model (BIOWIN 4) of "weeks-months" is suggested to mean approximately 37.5 days (US EPA 2002; Aronson et al. 2006); however, the nature of degradation products is unknown. The ultimate survey model (BIOWIN 3) result of "recalcitrant" is suggested to mean greater than 182 days by the US EPA (2002). The overall conclusion from BIOWIN is not readily biodegradable.

Another ultimate degradation model, CATABOL, predicts that DNAN will be persistent in water.

When the results of the probability models, the overall BIOWIN conclusion and ultimate degradation models are considered, there is greater model consensus suggesting the ultimate biodegradation half-life in water is greater than 182 days. This finding is consistent with what would be expected for this chemical structure (i.e., few degradable functional groups, solid sparingly soluble particle).

Using an extrapolation ratio of 1:1:4 for a water: soil: sediment biodegradation half-life (Boethling et al 1995), the ultimate degradation half-life in soil should be greater than 182 days and the half-life in aerobic sediments should be greater than 365 days. This suggests that DNAN is expected to be persistent in soil and sediment.

Based on modelled ultimate degradation data (see Table 5 above) and on expert judgment (ETAD 1995), DNAN meets the persistence criteria in water, soil and sediment (half-lives in soil and water 182 days and half-life in sediment 365 days) as set out in the Persistence and Bioaccumulation Regulations (Canada 2000).

Potential for Bioaccumulation

No experimental bioaccumulation data are available for DNAN. Since azo dyes fall outside the domains of applicability for available bioaccumulation models, predictions from such models are considered unreliable for this group of substances. As a result, in this assessment bioaccumulation modelling has not been used to evaluate the bioaccumulation status of DNAN.

In the absence of experimental and modelled data for DNAN itself, bioconcentration (BCF) and bioaccumulation (BAF) factors for structural analogues were used to estimate DNAN's potential for bioaccumulation. To that end, a bioconcentration study submitted for a relatively close structural analogue, Disperse Orange 30, suggests that it is unlikely to accumulate in fish (Shen and Hu 2008). This test was performed according to OECD Guidelines for Testing of Chemicals, Test No. 305B-1996, Bioconcentration: Semi-Static Fish Test. The bioconcentration of Disperse Orange 30 in zebra fish (Brachydanio rerio) was determined in a 28-day semi-static test with test medium renewal every two days. An exposure test at a nominal concentration of 20 mg/L (mean measured concentration 0.028 - 0.28 mg/L) was performed in accordance with the result of the fish acute toxicity test to check the bioconcentration potential of the test substance. Samples from both test solutions and test organisms were taken daily from the 26th day to the last day during the 28-day exposure test period. Samples were prepared by extracting the lipid component from the test fish. The measured concentration of test substance, fish lipid content and BCF calculation are reported in Table 6.

Table 6. Measured concentrations, fish lipid content and BCF calculation for analogue Disperse Orange 30
Treatments (20 mg/L) Sampling on 26th day Sampling on 27th day Sampling on 28th day
Measured concentration of the test substance in extracted solutions (mg/L) less than 0.028 less than 0.028 less than 0.028
Content of the test substance in the fish lipids (mg) less than 1.68 less than 1.68 less than 1.68
Fish total weight (g) 2.07 2.13 2.53
Concentration of the test substance in the fish Cf (mg/kg) less than 0.81 less than 0.79 less than 0.66
Measured concentration of the test substance in the water Cw (mg/L) 0.028 ~ 0.28 0.028 ~ 0.28 0.028 ~ 0.28
Fish lipid content (%) 0.81 0.57 1.25
BCF less than 100 less than 100 less than 100
Average BCF less than 100 less than 100 less than 100

The Shen and Hu (2008) study has been reviewed and was considered acceptable (see Appendix 1). Lack of detection in fish extracts (less than 0.028 mg/L) suggests a limited solubility in lipids and/or limited potential to partition into fish tissue from aqueous systems. However, there is some uncertainty associated with limit bounded values in any study because the absolute value is not known. But given the structure and likely behavior of disperse dyes in aqueous systems, a low BCF result is expected. Most disperse dyes, as their name suggests, exist as fine dispersible particles with limited truly soluble fractions. Solubility, however, can be increased by adding polar functional groups to the molecule. While DNAN contains some of these solubilizing functional groups (nitro groups), experimental solubility values for analogues containing many of the same groups are quite low.

While the above study serves as primary evidence to support DNAN's lack of bioaccumulation potential, other research corroborates this conclusion. Anliker et al. (1981) reported experimental fish bioaccumulation values for 18 disperse monoazo dyes, performed according to test methods specified by the Japanese Ministry of International Trade and Industry (MITI). Expressed on the basis of wet body weight of the fishes, these log bioaccumulation factors ranged from 0.00 to 1.76 (Anliker et al. 1981). A lack of reporting of chemical registry numbers and chemical structures limited the utility of this study for read-across purposes to DNAN. However, follow-up studies, which provided the chemical structures for the disperse dyes tested, confirmed low bioaccumulation potential for ten nitroazo dyes, with reported log bioaccumulation factors ranging from 0.3 to 1.76 (Anliker and Moser 1987; Anliker et al. 1988). Studies available from MITI also support low bioaccumulation potential for disperse azo dyes. Reported BCFs for three disperse azo dyes (CAS Nos. 40690-89-9, 61968-52-3 and 71767-67-4) tested at a concentration of 0.01 mg/L were in the range of less than 0.3 to 47 (MITI 1992). An accumulation study by Brown (1987) also showed that none of the twelve disperse dyes tested accumulated during an eight week study with carp.

A high, median read-across log Kow value of 4.3 for DNAN (Table 2) is the only line of evidence that suggests DNAN may have a high potential for bioaccumulation. In spite of the high Kow values for DNAN' and other disperse azo dyes, evidence for bioaccumulation of such dyes is lacking (Anliker et al. 1981, Anliker and Moser 1987, Anliker et al. 1988, MITI 1992). Authors who have measured high log Kows and concomitant low bioaccumulation factors for disperse azo dyes suggest the low accumulation factors may be due in some cases to their low absolute fat solubility (Brown 1987) or to their relatively high molecular weight (typically 450-550 g/mol) which may make transport across fish membranes difficult (Anliker et al. 1981, Anliker and Moser 1987). It is also likely that the lack of bioavailability and limited capacity to partition under BCF test conditions limits accumulation in fish lipids.

It has been stated by ETAD (1995) that the molecular characteristics indicating the absence of bioaccumulation are a molecular weight of greater than 450 g/mol and a cross-sectional diameter of greater than 1.05 nm. Recent investigation by Dimitrov et al. (2002), Dimitrov et al. (2005) and the BBM (2008) suggests that the probability of a molecule crossing cell membranes as a result of passive diffusion declines significantly with increasing maximum cross-sectional diameter (Dmax). The probability of passive diffusion lowers appreciably when cross-sectional diameter is greater than ~1.5 nm and more significantly for molecules having a cross-sectional diameter of greater than 1.7 nm. Sakuratani et al. (2008) have also investigated the effect of cross-sectional diameter on passive diffusion from a test set of about 1200 new and existing chemicals, also observing that substances not having a very high bioconcentration potential often have a Dmax greater than 2.0 nm and an effective diameter (Deff) greater than 1.1 nm.

DNAN has a molecular weight of 432.2 g/mol (see Table 1) and its molecular structure is relatively uncomplicated; both these characteristics indicate a bioaccumulation capability of this substance if molecular weight is used as the only parameter. In addition, an Environment Canada (2007) report points out that there is no clear evidence for establishing strict molecular size cut-offs for assessing bioaccumulation potential. However, the report does not dispute the notion that a reduction in uptake rate can be associated with increasing cross-sectional diameter as demonstrated by Dimitrov et al. (2002, 2005). The maximum diameter of DNAN and its conformers ranges from 1.44 to 2.11 nm (BBM 2008) suggesting that a potential for a significantly reduced uptake rate from water and in vivo bioavailability exists with this dye.

Based on a lack of accumulation observed in bioconcentration tests of Disperse Orange 30 and other related disperse azo dyes, and DNAN's large molecular size which likely limits its partitioning behavior, DNAN is expected to have low potential for bioaccumulation. Therefore, considering analogue BCF evidence, and structural and bioavailability considerations, DNAN does not meet the bioaccumulation criteria (BCF or BAF greater than 5000) as set out in the Persistence and Bioaccumulation Regulations (Canada 2000).

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Potential to Cause Ecological Harm

Ecological Effects Assessment

A - In the Aquatic Compartment

No empirical ecotoxicity data were identified for DNAN. A range of aquatic toxicity predictions for DNAN were obtained from various QSAR models. However, as with bioaccumulation, these QSAR ecotoxicity predictions are not considered reliable because of the potential error associated with input parameters and the unique nature of disperse dyes - specifically structural and/or physical-chemical properties which fall outside of the models' domain of applicability.

Ecotoxicological data have however been located for several analogues of DNAN. A study submitted on behalf of ETAD provides acute ecotoxicity data in fish, invertebrates, algae and bacteria for 5 nitroazo disperse dyes (Brown 1992). Acute zebra fish, Daphnia magna and Scenedesmus subspicatus toxicity for the 5 analogues ranged from 17 to 710 mg/L, 4.5 to 110 mg/L and 6.7 to 54 mg/L, respectively (Table 7). In addition, all bacteria tests had an IC50 exceeding 100 mg/L. The experimental details for the dyes tested were not provided, which greatly limited evaluation of this study. However, these data were considered usable and are included in this screening assessment as part of the available weight of evidence.

Another acute fish toxicity study was submitted for Disperse Blue 79 (BASF 1990). According to the study, Disperse Blue 79 has a 96-hour LC50 in golden orfe between 100 and 220 mg/L. However, due to lack of details, this study was considered of uncertain reliability (Appendix 1).

Environment Canada received ecotoxicological data for another structurally similar disperse azo dye through the New Substances Notification Regulations (Environment Canada 1995). An acute fish toxicity study submitted to meet notification requirements revealed this substance has a 96-hour LC50 of 505 mg/L in rainbow trout (Table 7). The test was conducted according to OECD guideline No. 203. The Material Safety Data Sheet also contained information on bacterial toxic effects. The results indicate an activated sludge respiration inhibition EC50 of greater than 100 mg/L. Based on the available ecotoxicity information, the notified substance is expected to be of low concern for toxic effects to aquatic organisms. Reliability of the study was assessed using a robust study summary and considered as satisfactory (Appendix 1).

Lastly, a chronic study submitted for Disperse Blue 79:1, revealed its no effect concentration (NOEC) in rainbow trout to be greater than 0.0048 mg/L (Table 7). Reliability of this study was assessed as high (Appendix 1). However, this value was not used to calculate the predicted no effect concentration because the value is a hypothesis-based unbounded result. When considering all structural analogue toxicity information, these data suggest that DNAN is not highly hazardous to aquatic organisms (i.e., acute LC50 values are greater than 1 mg/L).

Table 7. Empirical data for aquatic toxicity of DNAN analogues
Common Name or CAS RN Test Organism End point Value (mg/L) Reference
Disperse Blue 79 Golden orfe The median concentration of a substance that is estimated to be lethal to 50% of the test organisms (LC50) 100 less than LC50 less than 220 BASF 1990
Disperse Blue 79 Zebra fish LC50 340 Brown 1992
Disperse Blue 79 Daphnia magna The median concentration of a substance that is estimated to cause some toxic sublethal effect on 50% of the test organisms (EC50) 4.5 Brown 1992
Disperse Blue 79 Scenedesmus subspicatus EC50 9.5 Brown 1992
Disperse Blue 79 Bacteria The median concentration of a substance that is estimated to cause inhibition to growth in 50% of the test organisms (IC50) greater than 100 Brown 1992
Disperse Red 73 Zebra fish LC50 17 Brown 1992
Disperse Red 73 Daphnia magna EC50 23 Brown 1992
Disperse Red 73 Scenedesmus subspicatus EC50 greater than 10 Brown 1992
Disperse Red 73 Bacteria IC50 greater than 100 Brown 1992
Disperse Orange 30 Zebra fish LC50 710 Brown 1992
Disperse Orange 30 Daphnia magna EC50 5.8 Brown 1992
Disperse Orange 30 Scenedesmus subspicatus EC50 6.7 Brown 1992
Disperse Orange 30 Bacteria IC50 greater than 100 Brown 1992
Disperse Orange 25 Zebra fish IC50 268 Brown 1992
Disperse Orange 25 Daphnia magna LC50 110 Brown 1992
Disperse Orange 25 Scenedesmus subspicatus EC50 54 Brown 1992
Disperse Orange 25 Bacteria EC50 greater than 100 Brown 1992
Disperse Red 17 Zebra fish LC50 103 Brown 1992
Disperse Red 17 Daphnia magna EC50 98 Brown 1992
Disperse Red 17 Scenedesmus subspicatus EC50 7 Brown 1992
Disperse Red 17 Bacteria IC50 greater than 100 Brown 1992
Analogous azo disperse dye Rainbow trout LC50 505 Environment Canada 1995
Disperse Blue 79:1 Rainbow trout NOEC (122 days) greater than 0.0048 Cohle and Mihalik 1991

In general, due to their low solubility (less than 1 mg/L), disperse dyes are expected to have a low acute ecological impact (Hunger 2003). The results of empirical toxicity studies with several analogues of DNAN are consistent with this expectation, indicating fish LC50s in the 17 to 505 mg/L range, withDaphnia being the most sensitive organisms tested (EC50/LC50s from 4.5 to 110 mg/L). Although interpretation of results from these tests is complicated by the fact that the reported effect values (i.e. EC50 and LC50s) are likely to be much greater than the solubility of the substances tested as well as of DNAN, the analogue data available do indicate that the toxicity of DNAN is likely to be low.

The available empirical ecotoxicity information for analogues of DNAN thus indicates that it is not likely to be highly hazardous to aquatic organisms.

B - In Other Environmental Compartments

Because DNAN could be released to soil from application of biosludge which is commonly used for soil enrichment as well as from the disposal of products that degrade and release DNAN, it would be desirable to obtain toxicity data for soil organisms. Although, no suitable ecological effects studies were found for this compound in soil, considering the toxicity data for aquatic organisms as well as the lack of bioaccumulation potential and its low bioavailability, potential for toxicity to soil- dwelling organisms is likely to be low. For the same reasons, the toxicity potential is also likely to be low for sediment dwelling organisms, although this cannot be substantiated due to lack of whole organism sediment toxicity data for DNAN or suitable analogues.

Ecological Exposure Assessment

No data concerning concentrations of this substance in water in Canada have been identified. Environmental concentrations are, therefore, estimated from available information, including estimated substance quantities, estimated release rates, and characteristics of receiving water bodies. Environment Canada's Industrial Generic Exposure Tool - Aquatic (IGETA) was employed to estimate the substance concentration (worst-case) in a generic water course receiving industrial effluents (Environment Canada 2008c). The generic scenario is designed to provide these estimates based on conservative assumptions regarding the amount of chemical processed and released, the number of processing days, sewage treatment plant (STP) removal rate, and the size of the receiving watercourse. The tool models an industrial-release scenario based on loading data from sources such as industrial surveys and knowledge of the distribution of industrial discharges in the country, and calculates a predicted environmental concentration (PEC). The equation and inputs used to calculate the PEC in the receiving water course are described in Environment Canada (2008d). In spite of the fact that no information was received to confirm DNAN's quantities in Canada, the s. 71 reporting threshold for import/manufacture (i.e. 100 kg) was used in the exposure models as a reasonable worst case scenario. As a conservative estimate, the release to water (sewer) from industrial activities only was set at 16% of the amount used as per previous experience of Environment Canada on assessing other disperse azo dyes. Conservative assumptions were made regarding receiving water body, by assuming the chemical is released to a very small river with no removal from sewage treatment plants. The conservative PEC for water was calculated to be 0.0018 mg/L (Environment Canada 2008d).

Environment Canada's spreadsheet model to estimate down-the-drain releases from consumer uses (Mega Flush) was further employed to estimate the potential substance concentration in multiple water bodies receiving sewage treatment plant effluents to which consumer products containing the substance may have been released (Environment Canada 2008e). The spreadsheet model is designed to provide these estimates based on conservative assumptions regarding the amount of chemical used and released by consumers. By default, primary and secondary STP removal rates are set at 0%, losses from use are set at 100%, the consumer use of the substance is assumed to extend over 365 days/year, and the flow rate used for receiving water bodies at all sites is a low-end (10th percentile) value. These estimates are made for approximately 1000 release sites across Canada, which account for most of the major STPs in Canada. These parameter values are considered to result in a very conservative scenario.

The equation and inputs used in Mega Flush to calculate the predicted environmental concentration (PEC) of DNAN in the receiving water bodies are described in Environment Canada (2008f). The predicted releases to water (sewers) from formulation use and from consumer use of products containing this substance were based on the Mass Flow Tool results for similar disperse azo dyes. A scenario was run assuming a total consumer use quantity of 281 kg/year (Environment Canada 2008f). This consumer use quantity was estimated conservatively using the upper bound mass of substance that could be in commerce in Canada (100 kg) and applying the 30/70 ratio for dyes in textiles manufactured/ imported in Canada. A 10% loss of dye was then assumed for the total amount of the substance being used by consumers (Øllgaard et al. 1998). That is, 28 kg of DNAN were predicted to be released to water as a result of loss to sewers during the laundering of manufactured articles that contain this dye (articles either imported or manufactured in Canada). Primary and secondary STP removal rates of 0% were used. These assumptions result in a very conservative scenario. Using this scenario, the Mega Flush model estimates that the PEC in the receiving water bodies ranges from 0.0000035 to 0.000043 mg/L

Characterization of Ecological Risk

A predicted no-effect concentration (PNEC) was estimated based on the 48-hour EC50 of 4.5 mg/L in Daphnia magna for analogue Disperse Blue 79 (Table 7). A factor of 100 was then applied to account for acute to chronic toxicity and lab to field extrapolations and use of a surrogate substance. The resulting PNEC is 0.045 mg/L.

When compared to the conservative PEC calculated above for industrial releases using IGETA, the resulting risk quotient (PEC/PNEC) is 0.0018/0.045 = 0.04. Therefore, concentrations of DNAN in surface waters from industrial releases in Canada appear unlikely to cause adverse effects to aquatic organisms. Given that IGETA provides a conservative estimate of exposure and risk, the results indicate a low potential for ecological harm to the aquatic environment resulting from local exposure to a point source industrial release. A more realistic evaluation of risk resulting from this type of source is not necessary.

For exposure resulting from down-the-drain releases through consumer uses (conservative scenario), MegaFlush results estimate that the PEC will not exceed the PNEC at any sites (i.e., all risk quotients less than 1). This indicates that down-the-drain consumer releases of DNAN are not expected to harm aquatic organisms.

Based on the available information, DNAN is expected to be persistent in water, soil and sediment and it is expected to have a low bioaccumulation potential. The lack of reports of manufacturing or importation of DNAN into Canada, along with information on its physical and chemical properties and its uses, indicate a low to moderate potential for releases into the Canadian environment. If released into the environment, DNAN is expected to be discharged mainly to surface waters, although it is expected to ultimately be transferred to sediment. Through use of analogue data, DNAN has also been demonstrated to have only a low to moderate potential for acute toxicity to aquatic organisms. Risk quotients for aquatic exposures indicate that DNAN concentrations likely do not exceed concentrations associated with effects, even when using conservative scenarios and assumptions. Therefore, DNAN is unlikely to be causing harm to populations of aquatic organisms in Canada.

Uncertainties in Evaluation of Ecological Risk

An area of uncertainty for DNAN is associated with the use of read-across data for physical and chemical properties, as well as toxicity data from analogues. While the chemicals identified (Disperse Blue 79, Disperse Blue 79:1, Disperse Orange 30, Disperse Orange 25, Disperse Red 17 and Disperse Red 73), share many similarities with DNAN, including being azo dyes with high molecular weights, similar cross sectional diameters, having solid particulate structures that decompose at greater than 74 °C (to 240 °C), and being "dispersible" in water (i.e., not truly soluble), they do have some differences in functional groups. These differences in chemical structure add uncertainty because the properties and toxicity of DNAN may be somewhat different. However, it was reasoned that the similarities were sufficient to include the data from analogues to contribute to the weight of evidence in the assessment of DNAN.

The persistence assessment is limited by the absence of biodegradation data, which necessitated generation of model predictions. Although all model prediction has some degree of error, the aerobic biodegradation model outputs confirmed the expected persistence of DNAN given its uses and structural characteristics. In addition, the persistence assessment is limited by the uncertainty about the rate and extent to which degradation occurs in anaerobic sediments and whether the degradation products (e.g., amines) would be biologically available. Nevertheless it is clear that anaerobic degradation of the bioavailable portion azo dyes in sediments to constitutive amines is much faster (half-lives in the order of days) than aerobic biodegradation. Although the amine degradation products are not expected to be biologically available because they form only in relatively deep anoxic sediment and can be irreversibly bound to sediment through nucleophilic addition and oxidative radical coupling (Colon et al 2002, Weber et al 2001), this issue is a source of uncertainty in the assessment of DNAN.

The bioaccumulation assessment for this substance was limited by the lack of empirical data and the inability of available models to reliably estimate bioaccumulation for disperse azo dyes. Instead the assessment relied on the use of bioaccumulation data for a structural analogue.

Uncertainties are also present due to the lack of information on environmental concentrations in Canada for DNAN. However, the lack of reports of manufacturing or importation of DNAN into Canada above reporting thresholds, its high fixation rate to textiles and the anticipated high removal rate from sewage treatment plants suggests low to moderate potential for release of this chemical into the Canadian environment, even if it is used in Canada at levels below the reporting thresholds.

The experimental concentrations associated with inherent toxicity for aquatic organisms may have an additional source of uncertainty when these concentrations exceed the solubility of the chemical in water (either experimental or predicted). Despite this, the available data indicate that DNAN is not highly hazardous to aquatic organisms

Uncertainties are also associated with the fraction of the substance that is released, and with the fraction that is removed in sewage treatment plants. These uncertainties were addressed by making conservative assumptions. Best model estimates were thus required to fill these data gaps.

There were also uncertainties with respect to the use of the substance in Canada. Based on known use patterns of structurally-similar azo dyes, the assumption made in this assessment is that DNAN is used in textiles.

Regarding ecotoxicity, based on the predicted partitioning behaviour of this chemical, the significance of soil and sediment as important media of exposure is not well addressed by the effects data available. Indeed, the only effects data identified apply primarily to pelagic aquatic exposures.

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Conclusion

Based on the information presented in this screening assessment, it is proposed that DNAN is not entering the environment in a quantity or concentration or under conditions that have or may have an immediate or long-term harmful effect on the environment or its biological diversity or that constitute or may constitute a danger to the environment on which life depends. 

It is therefore proposed that DNAN does not meet the definition of toxic as set out in section 64 of CEPA 1999. Additionally, DNAN meets the persistence criteria but does not meet the bioaccumulation criteria as set out in the Persistence and Bioaccumulation Regulations.(Canada 2000).

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[ETAD] Ecological and Toxicological Association of Dyes and Organic Pigments Canadian Affiliates, Dayan J, Trebitz H, consultants. 1995. Health and environmental information on dyes used in Canada. Unpublished report submitted to Environment Canada, New Substances Division. On the cover: An overview to assist in the implementation of the New Substances Notification Regulations under the Canadian Environmental Protection Act.

[ETAD] Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers. 1992. Draft Guidelines for the Assessment of Environmental Exposure to Dyestuffs.

Hunger K, editor. 2003. Industrial dyes; chemistry, properties, applications. Weinheim (DE): WILEY-VCH Verlag GmbH & Co. kgaA.

Industry Canada. 2008. Textile and Fabric Finishing [NAICS 31331]: 2004-2007 and Fabrics Coating 2004-2007. [NAICS 31332]: 2004-2007. Prepared by: Apparel and Textiles Directorate, Service Industries and Consumer Products Branch, Industry Canada, Enquiries B John (Jazz) Szabo, 613-957-1242. Email: szabo.john@ic.gc.ca

[MITI] Ministry of International Trade & Industry (Jpn). 1992. Biodegradation and bioaccumulation data of existing chemicals based on the CSCL Japan, Basic Industries Bureau, Chemical Products Safety Division. Japan Chemical Industry Ecology-Toxicology & Information Centre,Tokyo (Jpn).

[NCI] National Chemical Inventories [database on CD-ROM]. 2006. Columbus (OH): American Chemical Society. [cited 2006 Dec 11]. http://www.cas.org/products/cd/nci/index.html

[OECD] Organisation for Economic Co-operation and Development. 2004. Draft emission scenario on textile manufacturing wool mills [Internet]. Paris (FR): OECD, Environment Directorate. Report No.: ENV/JM/EEA(2004)8/1/REV, JT00175156. [cited 2008 July 9]. http://www.oecd.org/dataoecd/2/47/34003719.pdf

[OECD] Organisation for Economic Co-operation and Development. 2007. Emission scenario document on adhesive formulation [Internet]. Final report. Paris (FR): OECD, Environment Directorate. (Series on Emission Scenario Documents). [cited 2008 July 9]. http://ascouncil.org/news/adhesives/docs/EPAFormulation.pdf

Øllgaard H, Frost L, Galster J, Hansen OC. 1998. Survey of azo-colorants in Denmark - Consumption, use, health and environmental aspects. Miljøprojekt nr. 509. Miljøstyrelsen

Pagga U, Brown D. 1986. The degradation of dyestuffs: Part II Behaviour of dyestuffs in aerobic biodegradation tests. Chemosphere 15(4):479-491.

[PhysProp] Interactive PhysProp Database [database on the Internet]. 2006. Syracuse (NY): Syracuse Research Corporation. [cited 2006 Mar] http://www.syrres.com/esc/physdemo.htm

Razo-Flores E. Luijten M Donlon B. Lettinga G, Field J. 1997. Biodegradation of selected azo dyes under methanogenic conditions. Wat. Sci Technol 36(6-7): 65-72.

SafePharm Laboratories Ltd. 1990. Acute toxicity to rainbow trout. Project number 47/918. Challenge submission ID#11347. Submitted to Environment Canada July 30, 2008

Sakuratani Y, Noguchi Y, Kobayashi K, Yamada J, Nishihara T. 2008. Molecular size as a limiting characteristic for bioconcentration in fish. J Environ Biol 29(1):89-92

Shen, Genxiang and Hu, Shuangqing. 2008. Bioconcentration Test of C.I. Disperse Orange 30 in Fish. Prepared by Environmental Testing Laboratory, Shanghai Academy of Environmental Sciences, Shanghai, China for Dystar in the name of Ecological and Toxicological Association of the Dyes and Organic Pigments Manufacturers (ETAD) Basel, Switzerland. Report No. S-070-2007. Submitted to Environment Canada in April 2008. Challenge Submission ID#8351

Sijm DTHM, Schuurmann G, deVries PJ, Opperhuizen A. 1999. Aqueous solubility, octanol solubility, and octanol/water partition coefficient of nine hydrophobic dyes. Environ Toxicol Chem 18(6):1109-1117.

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Weber EJ, Adams RL. 1995. Chemical- and sediment-mediated reduction of the azo dye Disperse Blue 79. Environ Sci Technol 29: 1163-1170.

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Appendix I - Robust Study Summaries for Key Studies

Table A-1. Robust Study Summaries Form: Aquatic B

Reference: Hu, Shuangqing and Shen, Genxiang (Environmental Testing Laboratory, Shanghai Academy of Environmental Sciences, Shanghai, China). 2008. Bioconcentration Test of C.I. Disperse Orange 30 in Fish. Prepared for Dystar in the name of Ecological and Toxicological Association of the Dyes and Organic Pigments Manufacturers (ETAD) Basel, Switzerland. Report No. S-070-2007. Submitted to Environment Canada in April 2008.

Table A-1(a). Robust Study Summaries Form: Aquatic B - Details
No Item Weight Yes/No Specify
2 Substance identity: CAS RN n/a Y 5261-31-4
3 Substance identity: chemical name(s) n/a Y Propanenitrile, 3-[[2-(acetyloxy)ethyl][4-[(2,6-dichloro-4-nitrophenyl)azo]phenyl]amino]-
4 Chemical composition of the substance 2 Y  
5 Chemical purity 1 N  
6 Persistence/stability of test substance in aquatic solution reported? 1 N  
7 If test material is radiolabelled, were precise position(s) of the labelled atom(s) and the percentage of radioactivity associated with impurities reported? 2    
Table A-1(b). Robust Study Summaries Form: Aquatic B - Method
No Item Weight Yes/No Specify
8 Reference 1 Y  
9 OECD, EU, national, or other standard method? 3 Y  
10 Justification of the method/protocol if not a standard method was used 2    
11 GLP (Good Laboratory Practice) 3 N  
Table A-1(c). Robust Study Summaries Form: Aquatic B - Test organism
No Item Weight Yes/No Specify
12 Organism identity: name n/a Y zebra fish, Brachydanio rerio
13 Latin or both Latin & common names reported? 1 Y  
14 Life cycle age / stage of test organism 1 N  
15 Length and/or weight 1 Y  
16 Sex 1 N  
17 Number of organisms per replicate 1 Y 7
18 Organism loading rate 1 Y  
19 Food type and feeding periods during the acclimation period 1 Y  
Table A-1(d). Robust Study Summaries Form: Aquatic B - Test design/conditions
No Item Weight Yes/No Specify
20 Experiment type (laboratory or field) n/a Y Laboratory
21 Exposure pathways (food, water, both) n/a Y Water
22 Exposure duration n/a Y 28 days
23 Number of replicates (including controls) 1 Y  
24 Concentrations 1 Y 20 mg/L
25 Food type/composition and feeding periods during the test 1 Y  
26 If BCF/BAF derived as a ratio of chemical concentration in the organism and in water, was experiment duration equal to or longer than the time required for the chemical concentrations to reach steady state? 3 Y  
27 If BCF/BAF derived as a ratio of chemical concentration in the organism and in water, were measured concentrations in both water and organism reported? 3 Y  
28 Were concentrations in the test water measured periodically? 1 Y  
29 Were the exposure media conditions relevant to the particular chemical reported? (e.g., for the metal toxicity - pH, DOC/TOC, water hardness, temperature) 3 Y  
30 Photoperiod and light intensity 1 Y  
31 Stock and test solution preparation 1 Y  
32 Analytical monitoring intervals 1 Y  
33 Statistical methods used 1 Y  
34 Was solubilizer/emulsifier used, if the chemical was unstable or poorly soluble? n/a N  
Table A-1(e). Robust Study Summaries Form: Aquatic B - Information relevant to the data quality
No Item Weight Yes/No Specify
35 Was the test organism relevant to the Canadian environment? 3 Y  
36 Were the test conditions (pH, temperature, DO, etc.) typical for the test organism? 1 Y  
37 Does system type and design (static, semi-static, flow-through; sealed or open; etc.) correspond to the substance's properties and organism's nature/habits? 2 Y  
38 Was pH of the test water within the range typical for the Canadian environment (6 to 9)? 1 Y  
39 Was temperature of the test water within the range typical for the Canadian environment (5 to 27°C)? 1 Y  
40 Was lipid content (or lipid-normalized BAF/BCF) reported? 2 Y  
41 Were measured concentrations of a chemical in the test water below the chemical's water solubility? 3 N  
42 If radiolabelled test substance was used, was BCF determination based on the parent compound (i.e. not on total radiolabelled residues)? 3    
Table A-1(f). Robust Study Summaries Form: Aquatic B - Results
No Item Weight Yes/No Specify
43 Endpoints (BAF, BCF) and values n/a n/a BCF
44 BAF or BCF determined as: 1) the ratio of chemical concentration in the organism and in water, or 2) the ratio of the chemical uptake and elimination rate constants n/a n/a 1
45 Whether BAF/BCF was derived from a 1) tissue sample or 2) whole organism? n/a n/a 2
46 Whether 1) average or 2) maximum BAF/BCF was used? n/a n/a 1
Table A-1(g). Robust Study Summaries Form: Aquatic B - Score and reliability
No Item Specify
47 Score: ... % 79.2
48 EC Reliability code: 2
49 Reliability category (high, satisfactory, low): Satisfactory Confidence
50 Comments The present procedure is based on semi-static conditions (renewal of test solutions every 2 days). Therefore, test chemical with very low water solubility like Disperse Blue 79, can also be characterized as to their bioconcentration potential without adding solvents or other auxiliary substances which may affect the results.

Table A-2. Robust Study Summaries Form: Aquatic B

Reference: Shen, Genxiang and Hu, Shuangqing. 2008. Bioconcentration Test of C.I. Disperse Orange 30 in Fish. Prepared by Environmental Testing Laboratory, Shanghai Academy of Environmental Sciences, Shanghai, China for Dystar in the name of Ecological and Toxicological Association of the Dyes and Organic Pigments Manufacturers (ETAD) Basel, Switzerland. Report No. S-070-2007. Submitted to Environment Canada in April 2008. Challenge Submission ID#8351

Table A-2(a). Robust Study Summaries Form: Aquatic B - Details
No Item Weight Yes/No Specify
2 Substance identity: CAS RN n/a Y 5261-31-4
3 Substance identity: chemical name(s) n/a Y Propanenitrile, 3-[[2-(acetyloxy)ethyl][4-[(2,6-dichloro-4-nitrophenyl)azo]phenyl]amino]-
4 Chemical composition of the substance 2 N  
5 Chemical purity 1 N  
6 Persistence/stability of test substance in aquatic solution reported? 1 N  
7 If test material is radiolabelled, were precise position(s) of the labelled atom(s) and the percentage of radioactivity associated with impurities reported? 2 n/a   
Table A-2(b). Robust Study Summaries Form: Aquatic B - Method
No Item Weight Yes/No Specify
8 Reference 1 Y  OECD guidelines for the testing of chemicals No 305B-1996
9 OECD, EU, national, or other standard method? 3 Y  OECD
10 Justification of the method/protocol if not a standard method was used 2    
11 GLP (Good Laboratory Practice) 3 N  
Table A-2(c). Robust Study Summaries Form: Aquatic B - Test organism
No Item Weight Yes/No Specify
12 Organism identity: name n/a Y zebra fish, Brachydanio rerio
13 Latin or both Latin & common names reported? 1 Y  both
14 Life cycle age / stage of test organism 1 N  
15 Length and/or weight 1 Y  Mean body length 3.91+/-0.18cm and mean body weight 0.32+/-0.06g
16 Sex 1 N  
17 Number of organisms per replicate 1 Y 7
18 Organism loading rate 1 Y  20mg/L
19 Food type and feeding periods during the acclimation period 1 Y  Fed a commercial fish diet until one day before start of test
Table A-2(d). Robust Study Summaries Form: Aquatic B - Test design/conditions
No Item Weight Yes/No Specify
20 Experiment type (laboratory or field) n/a Y Laboratory
21 Exposure pathways (food, water, both) n/a Y Water
22 Exposure duration n/a Y 28 days
23 Number of replicates (including controls) 1 Y  
24 Concentrations 1 Y 20 mg/L
25 Food type/composition and feeding periods during the test 1 Y  Fish were fed two hours before water renewal
26 If BCF/BAF derived as a ratio of chemical concentration in the organism and in water, was experiment duration equal to or longer than the time required for the chemical concentrations to reach steady state? 3 Y  28 days
27 If BCF/BAF derived as a ratio of chemical concentration in the organism and in water, were measured concentrations in both water and organism reported? 3 Y  
28 Were concentrations in the test water measured periodically? 1 Y  On three separate days
29 Were the exposure media conditions relevant to the particular chemical reported? (e.g., for the metal toxicity - pH, DOC/TOC, water hardness, temperature) 3 Y  Yes every second day
30 Photoperiod and light intensity 1 Y  12:12
31 Stock and test solution preparation 1 Y  
32 Analytical monitoring intervals 1 Y  Every second day for dissolved oxygen, pH and temperature
33 Statistical methods used 1 Y  
34 Was solubilizer/emulsifier used, if the chemical was unstable or poorly soluble? n/a N  
Table A-2(e). Robust Study Summaries Form: Aquatic B - Information relevant to the data quality
No Item Weight Yes/No Specify
35 Was the test organism relevant to the Canadian environment? 3 Y  
36 Were the test conditions (pH, temperature, DO, etc.) typical for the test organism? 1 Y  
37 Does system type and design (static, semi-static, flow-through; sealed or open; etc.) correspond to the substance's properties and organism's nature/habits? 2 Y  Semi-static
38 Was pH of the test water within the range typical for the Canadian environment (6 to 9)? 1 Y  7.22-7.84
39 Was temperature of the test water within the range typical for the Canadian environment (5 to 27°C)? 1 Y  22-23
40 Was lipid content (or lipid-normalized BAF/BCF) reported? 2 Y  
41 Were measured concentrations of a chemical in the test water below the chemical's water solubility? 3 N  
42 If radiolabelled test substance was used, was BCF determination based on the parent compound (i.e. not on total radiolabelled residues)? 3 n/a   
Table A-2(f). Robust Study Summaries Form: Aquatic B - Results
No Item Weight Yes/No Specify
43 Endpoints (BAF, BCF) and values n/a n/a BCF
44 BAF or BCF determined as: 1) the ratio of chemical concentration in the organism and in water, or 2) the ratio of the chemical uptake and elimination rate constants n/a n/a 1
45 Whether BAF/BCF was derived from a 1) tissue sample or 2) whole organism? n/a n/a 2
46 Whether 1) average or 2) maximum BAF/BCF was used? n/a n/a 1
Table A-2(g). Robust Study Summaries Form: Aquatic B - Score and reliability
No Item Specify
47 Score: ... % 75.0
48 EC Reliability code: 2
49 Reliability category (high, satisfactory, low): Satisfactory Confidence
50 Comments The present procedure is based on semi-static conditions (renewal of test solutions every 2 days). Therefore, test chemical with very low water solubility like AADM, can also be characterized as to their bioconcentration potential without adding solvents or other auxiliary substances which may affect the results.

Table A-3. Robust Study Summaries Form: Aquatic iT

Reference: BASF 1990. Bericht uber die Prufung der akuten Toxizitit an der Goldorfe (Leuciscus idus L.,. Goldvariante. Submitted by ETAD to Environment Canada, August 2008.

Table A-3(a). Robust Study Summaries Form: Aquatic iT - Details
No Item Weight Yes/No Specify
2 Substance identity: CAS RN n/a    
3 Substance identity: chemical name(s) n/a    
4 Chemical composition of the substance 2 N  
5 Chemical purity 1 N  
6 Persistence/stability of test substance in aquatic solution reported? 1 N  
Table A-3(b). Robust Study Summaries Form: Aquatic iT - Method
No Item Weight Yes/No Specify
7 Reference 1 N  
8 OECD, EU, national, or other standard method? 3 N  
9 Justification of the method/protocol if not a standard method was used 2 N  
10 GLP (Good Laboratory Practice) 3    
Table A-3(c). Robust Study Summaries Form: Aquatic iT - Test organism
No Item Weight Yes/No Specify
11 Organism identity: name n/a Y Golden orfe
12 Latin or both Latin & common names reported? 1 Y  
13 Life cycle age / stage of test organis 1 N  
14 Length and/or weight 1 N  
15 Sex 1 N  
16 Number of organisms per replicate 1 N  
17 Organism loading rate 1 N  
18 Food type and feeding periods during the acclimation period 1 N  
Table A-3(d). Robust Study Summaries Form: Aquatic iT - Test design/conditions
No Item Weight Yes/No Specify
19 Test type (acute or chronic n/a Y Acute
20 Experiment type (laboratory or field n/a N  
21 Exposure pathways (food, water, both) n/a N  
22 Exposure duration n/a Y 96 hrS
23 Negative or positive controls (specify) 1 N  
24 Number of replicates (including controls) 1 N  
25 Nominal concentrations reported? 1 N  
26 Measured concentrations reported? 3 N  
27 Food type and feeding periods during the long-term tests 1   n/a
28 Were concentrations measured periodically (especially in the chronic test)? 1 N  
29 Were the exposure media conditions relevant to the particular chemical reported? (e.g., for the metal toxicity - pH, DOC/TOC, water hardness, temperature) 3 N  
30 Photoperiod and light intensity 1 N  
31 Stock and test solution preparation 1 N  
32 Was solubilizer/emulsifier used, if the chemical was poorly soluble or unstable? 1 N  
33 If solubilizer/emulsifier was used, was its concentration reported? 1 N  
34 If solubilizer/emulsifier was used, was its ecotoxicity reported? 1 N  
35 Analytical monitoring intervals 1 N  
36 Statistical methods used 1 N  
Table A-3(e). Robust Study Summaries Form: Aquatic iT - Information relevant to the data quality
No Item Weight Yes/No Specify
37 Was the endpoint directly caused by the chemical's toxicity, not by organism's health (e.g. when mortality in the control greater than 10%) or physical effects (e.g. 'shading effect')? n/a N  
38 Was the test organism relevant to the Canadian environment? 3 Y  
39 Were the test conditions (pH, temperature, DO, etc.) typical for the test organism? 1 N  
40 Does system type and design (static, semi-static, flow-through; sealed or open; etc.) correspond to the substance's properties and organism's nature/habits? 2 N  
41 Was pH of the test water within the range typical for the Canadian environment (6 to 9)? 1 N  
42 Was temperature of the test water within the range typical for the Canadian environment (5 to 27°C)? 1 N  
43 Was toxicity value below the chemical's water solubility? 3    
Table A-3(f). Robust Study Summaries Form: Aquatic iT - Results
No Item Weight Yes/No Specify
44 Toxicity values (specify endpoint and value) n/a   LC50= greater than 100 less than 220mg/L
45 Other endpoints reported - e.g. BCF/BAF, LOEC/NOEC (specify)? n/a   NOEC=100mg/L
46 Other adverse effects (e.g. carcinogenicity, mutagenicity) reported? n/a    
Table A-3(g). Robust Study Summaries Form: Aquatic iT - Score and reliability
No Item Specify
47 Score: ... % 9.5
48 EC Reliability code: 4
49 Reliability category (high, satisfactory, low): Not Satisfactory
50 Comments  Not enough data submitted to properly assess the reliability of this study.

Table A-4. Robust Study Summaries Form: Aquatic iT

Reference: Environment Canada. 1995. Acute fish toxicity test submission in fulfillment of new substances notification regulations to New Substances Branch, Environment Canada under New Substance Notification Program.

Table A-4(a). Robust Study Summaries Form: Aquatic iT - Details
No Item Weight Yes/No Specify
2 Substance identity: CAS RN n/a N  
3 Substance identity: chemical name(s) n/a Y  
4 Chemical composition of the substance 2 N  
5 Chemical purity 1 N  
6 Persistence/stability of test substance in aquatic solution reported? 1 N  
Table A-4(b). Robust Study Summaries Form: Aquatic iT - Method
No Item Weight Yes/No Specify
7 Reference 1 Y OECD 203
8 OECD, EU, national, or other standard method? 3 Y  
9 Justification of the method/protocol if not a standard method was used 2   not applicable
10 GLP (Good Laboratory Practice) 3 Y  
Table A-4(c). Robust Study Summaries Form: Aquatic iT - Test organism
No Item Weight Yes/No Specify
11 Organism identity: name n/a Y Rainbow trout
12 Latin or both Latin & common names reported? 1 Y  
13 Life cycle age / stage of test organis 1 Y mean length 51mm and mean weight 1.54
14 Length and/or weight 1 Y see above
15 Sex 1   not applicable
16 Number of organisms per replicate 1 Y 10
17 Organism loading rate 1 Y  
18 Food type and feeding periods during the acclimation period 1 Y  
Table A-4(d). Robust Study Summaries Form: Aquatic iT - Test design/conditions
No Item Weight Yes/No Specify
19 Test type (acute or chronic n/a Y acute
20 Experiment type (laboratory or field n/a y lab
21 Exposure pathways (food, water, both) n/a y water
22 Exposure duration n/a y 96 hrs
23 Negative or positive controls (specify) 1 Y 3
24 Number of replicates (including controls) 1 Y 2
25 Nominal concentrations reported? 1 Y 320 to 3200 mg/L
26 Measured concentrations reported? 3 N  
27 Food type and feeding periods during the long-term tests 1   not applicable
28 Were concentrations measured periodically (especially in the chronic test)? 1 N  
29 Were the exposure media conditions relevant to the particular chemical reported? (e.g., for the metal toxicity - pH, DOC/TOC, water hardness, temperature) 3 Y  
30 Photoperiod and light intensity 1 Y  
31 Stock and test solution preparation 1 Y  
32 Was solubilizer/emulsifier used, if the chemical was poorly soluble or unstable? 1 N  
33 If solubilizer/emulsifier was used, was its concentration reported? 1    
34 If solubilizer/emulsifier was used, was its ecotoxicity reported? 1    
35 Analytical monitoring intervals 1 Y  
36 Statistical methods used 1 Y  
Table A-4(e). Robust Study Summaries Form: Aquatic iT - Information relevant to the data quality
No Item Weight Yes/No Specify
37 Was the endpoint directly caused by the chemical's toxicity, not by organism's health (e.g. when mortality in the control greater than 10%) or physical effects (e.g. 'shading effect')? n/a Y  
38 Was the test organism relevant to the Canadian environment? 3 Y  
39 Were the test conditions (pH, temperature, DO, etc.) typical for the test organism? 1 Y  
40 Does system type and design (static, semi-static, flow-through; sealed or open; etc.) correspond to the substance's properties and organism's nature/habits? 2 Y  
41 Was pH of the test water within the range typical for the Canadian environment (6 to 9)? 1 Y  
42 Was temperature of the test water within the range typical for the Canadian environment (5 to 27°C)? 1 Y  
43 Was toxicity value below the chemical's water solubility? 3   unknown water solubility
Table A-4(f). Robust Study Summaries Form: Aquatic iT - Results
No Item Weight Yes/No Specify
44 Toxicity values (specify endpoint and value) n/a n/a 96 hr LC50
45 Other endpoints reported - e.g. BCF/BAF, LOEC/NOEC (specify)? n/a N  
46 Other adverse effects (e.g. carcinogenicity, mutagenicity) reported? n/a N  
Table A-4(g). Robust Study Summaries Form: Aquatic iT - Score and reliability
No Item Specify
47 Score: ... % 77.5
48 EC Reliability code: 2
49 Reliability category (high, satisfactory, low): Satisfactory Confidence
50 Comments  

Table A-5. Robust Study Summaries Form: Aquatic iT

Reference: Cohle P, R Mihalik R. 1991. Early life stage toxicity of C.I. Disperse Blue 79:1 purified preecake to rainbow trout (Oncorhynchus mykiss) in a flow-through system. Final report. ABC Laboratories Inc. Columbia MO.

Table A-5(a). Robust Study Summaries Form: Aquatic iT - Details
No Item Weight Yes/No Specify
2 Substance identity: CAS RN n/a    
3 Substance identity: chemical name(s) n/a   Disperse Blue 79:1
4 Chemical composition of the substance 2   n/a
5 Chemical purity 1 Y 96.61
6 Persistence/stability of test substance in aquatic solution reported? 1 N  
Table A-5(b). Robust Study Summaries Form: Aquatic iT - Method
No Item Weight Yes/No Specify
7 Reference 1 Y  
8 OECD, EU, national, or other standard method? 3 Y  
9 Justification of the method/protocol if not a standard method was used 2   n/a
10 GLP (Good Laboratory Practice) 3 Y  
Table A-5(c). Robust Study Summaries Form: Aquatic iT - Test organism
No Item Weight Yes/No Specify
11 Organism identity: name n/a   Rainbow trout
12 Latin or both Latin & common names reported? 1 Y  
13 Life cycle age / stage of test organis 1 Y  
14 Length and/or weight 1 Y  
15 Sex 1   n/a
16 Number of organisms per replicate 1 Y 20
17 Organism loading rate 1 Y 0.36 to 4.8ug/L
18 Food type and feeding periods during the acclimation period 1 Y  
Table A-5(d). Robust Study Summaries Form: Aquatic iT - Test design/conditions
No Item Weight Yes/No Specify
19 Test type (acute or chronic n/a Y chronic
20 Experiment type (laboratory or field n/a Y lab
21 Exposure pathways (food, water, both) n/a Y water
22 Exposure duration n/a Y 122 days
23 Negative or positive controls (specify) 1 Y control and carrier blank
24 Number of replicates (including controls) 1 Y 2
25 Nominal concentrations reported? 1 Y 5
26 Measured concentrations reported? 3 Y  
27 Food type and feeding periods during the long-term tests 1 Y  
28 Were concentrations measured periodically (especially in the chronic test)? 1 Y  
29 Were the exposure media conditions relevant to the particular chemical reported? (e.g., for the metal toxicity - pH, DOC/TOC, water hardness, temperature) 3 Y  
30 Photoperiod and light intensity 1 Y  
31 Stock and test solution preparation 1 Y  
32 Was solubilizer/emulsifier used, if the chemical was poorly soluble or unstable? 1 Y  
33 If solubilizer/emulsifier was used, was its concentration reported? 1 Y  
34 If solubilizer/emulsifier was used, was its ecotoxicity reported? 1 Y no tox value but however is was used as a control
35 Analytical monitoring intervals 1 Y  
36 Statistical methods used 1 Y  
Table A-5(e). Robust Study Summaries Form: Aquatic iT - Information relevant to the data quality
No Item Weight Yes/No Specify
37 Was the endpoint directly caused by the chemical's toxicity, not by organism's health (e.g. when mortality in the control greater than 10%) or physical effects (e.g. 'shading effect')? n/a Y  
38 Was the test organism relevant to the Canadian environment? 3 Y  
39 Were the test conditions (pH, temperature, DO, etc.) typical for the test organism? 1 Y  
40 Does system type and design (static, semi-static, flow-through; sealed or open; etc.) correspond to the substance's properties and organism's nature/habits? 2 Y flow through
41 Was pH of the test water within the range typical for the Canadian environment (6 to 9)? 1 Y  
42 Was temperature of the test water within the range typical for the Canadian environment (5 to 27°C)? 1 Y  
43 Was toxicity value below the chemical's water solubility? 3   n/a
Table A-5(f). Robust Study Summaries Form: Aquatic iT - Results
No Item Weight Yes/No Specify
44 Toxicity values (specify endpoint and value) n/a n/a NOEC greater than 0.005mg/L
45 Other endpoints reported - e.g. BCF/BAF, LOEC/NOEC (specify)? n/a    
46 Other adverse effects (e.g. carcinogenicity, mutagenicity) reported? n/a    
Table A-5(g). Robust Study Summaries Form: Aquatic iT - Score and reliability
No Item Specify
47 Score: ... % 97.6
48 EC Reliability code: 1
49 Reliability category (high, satisfactory, low): High Confidence
50 Comments  

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