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EC number: 204-558-8 | CAS number: 122-62-3
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data

Genetic toxicity: in vitro
Administrative data
- Endpoint:
- in vitro cytogenicity / chromosome aberration study in mammalian cells
- Remarks:
- Type of genotoxicity: chromosome aberration
- Type of information:
- migrated information: read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- GLP - Guideline study. According to the ECHA guidance document "Practical guide 6: How to report read-across and categories (March 2010)", the reliability was changed from RL1 to RL2 to reflect the fact that this study was conducted on a read-across substance.
Data source
Referenceopen allclose all
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 004
- Report date:
- 2004
- Reference Type:
- publication
- Title:
- In Vitro Chromosomal Aberration Test of Bis(2-ethylhexyl) azelate in Cultured Chinese Hamster Cells
- Author:
- Miwa, Y.
- Year:
- 2 004
- Bibliographic source:
- Toxicity Testing Reports of Environmental Chemicals, 11, 287-320
- Reference Type:
- secondary source
- Title:
- Bis(2-ethylhexyl) azelate
- Author:
- OECD
- Year:
- 2 006
- Bibliographic source:
- SIDS Initial Assessment Report for SIAM 22, Paris, France, 18-21 April, 2006
- Reference Type:
- secondary source
- Title:
- Diesters Category of the Aliphatic Esters Chemicals (Test Plan and Robust Summaries for Substances in the HPV Test Plan)
- Author:
- US-EPA (American Chemistry Council's Aliphatic Esters Panel)
- Year:
- 2 010
- Bibliographic source:
- High Production Volume (HPV) Chemical Challenge Program (201-16837A and 201-16837B)
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 473 (In Vitro Mammalian Chromosome Aberration Test)
- Deviations:
- no
- GLP compliance:
- yes
- Type of assay:
- in vitro mammalian chromosome aberration test
Test material
- Reference substance name:
- 103-24-2 (analytical purity 77.2%)
- IUPAC Name:
- 103-24-2 (analytical purity 77.2%)
- Details on test material:
- - Name of test material (as cited in study report): Bis(2-ethylhexyl)nonanedioate
- Analytical purity: 77.2%
- Impurities (identity and concentrations):
Bis(2-ethylhexyl)glutarate 2.2%,
Bis(2-ethylhexyl)adipate 2.4%,
Bis(2-ethylhexyl)pimelate 2.8%,
Bis(2-ethylhexyl)suberate 3.8%,
Bis(2-ethylhexyl)sebacate 3.3%,
Bis(2-ethylhexyl) 1-,9-nonamethylenedicarboxylate 5.3%,
Bis(2-ethylhexyl)1-,10-decamethylenedicarboxylate 0.6%,
Bis(2-ethylhexyl)1-,11-undecamethylenedicarboxylate 0.3%
- Lot/batch No.: N-31101
Constituent 1
Method
- Target gene:
- Not applicable
Species / strain
- Species / strain / cell type:
- mammalian cell line, other: Chinese hamster lung (CHL/IU) cell
- Details on mammalian cell type (if applicable):
- - Type and identity of media: Eagles's MEM modified with NaHCO3 and HCl (pH 7.0 - 7.1). Fetal calf serum was added up to 10%.
- Properly maintained: yes
- Periodically "cleansed" against high spontaneous background: yes
- Metabolic activation:
- with and without
- Metabolic activation system:
- cofactor supplemented post-mitochondrial fraction (S9 mix), prepared from the livers of rats treated with phenobarbital and 5,6-benzoflavone.
- Test concentrations with justification for top dose:
- 6 h treatment: 150, 300, 600, 1200, 2400 µg/mL with and without metabolic activation.
24 h treatment: 37.5, 75, 150, 300, 600 µg/mL without metabolic activation. - Vehicle / solvent:
- - Vehicle(s)/solvent(s) used: ethanol
Controls
- Untreated negative controls:
- yes
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- other: -S9: Mitomycin C (MMC, 0.1 µg/mL ); +S9: Dimethylnitrosamin (DMN; 500 µg/mL)
- Details on test system and experimental conditions:
- METHOD OF APPLICATION: in medium
DURATION
- Exposure duration: 6 h and 24 h
NUMBER OF REPLICATIONS: duplicates in single experiment
NUMBER OF CELLS EVALUATED: 200
DETERMINATION OF CYTOTOXICITY
- Method: mitotic index
OTHER EXAMINATIONS:
- Determination of polyploidy: yes - Evaluation criteria:
- Evaluation was made on the basis of incidence as; -: negative (less than 5.0%); ±: equivocal (5.0% or higher to less than 10.0%); +: positive (10.0% or higher)
Results and discussion
Test results
- Species / strain:
- mammalian cell line, other: Chinese hamster lung (CHL/IU) cell
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- cytotoxicity
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Additional information on results:
- TEST-SPECIFIC CONFOUNDING FACTORS
- Precipitation: There were colorless clear fine oil drop-like precipitations and oil membrane-like precipitations in the culture fluid in petri plate at the concentrations of 1200 µg/mL or more.
RANGE-FINDING: The maximum concentration was established, based on the growth inhibition test. In this test, 50% growth inhibition was observed at 1859.0 µg/mL with S9 and at 1555.5 µg/mL without S9 for 6 h short treatment and 534.2 µg/mL without S9 for 24 h continuous treatment. - Remarks on result:
- other: all strains/cell types tested
- Remarks:
- Migrated from field 'Test system'.
Any other information on results incl. tables
Table 1. Test results
Test item |
Concentration |
Mitotic Index |
Aberrant cells in % |
|
|
in µg/mL |
in % |
with gaps |
without gaps |
Exposure period 6 h, without S9 mix |
||||
Medium |
|
99 |
0.5 |
0.5 |
Ethanol |
|
100 |
1 |
1 |
MMC |
0.1 |
83 |
55.5 |
55.5 |
Test substance |
150 |
99 |
0 |
0 |
300 |
88 |
0 |
0 |
|
600 |
70 |
0.5 |
0.5 |
|
1200 P |
51 |
1 |
1 |
|
2400 P |
39 |
0.5 |
0.5 |
|
Exposure period 6 h, fixation time 24 h, with S9 mix |
||||
Medium |
|
100 |
0 |
0 |
Ethanol |
|
100 |
0 |
0 |
DMN |
500 |
78 |
65.5 |
65.5 |
Test substance |
150 |
99 |
1 |
1 |
300 |
80 |
0 |
0 |
|
600 |
64 |
0.5 |
0.5 |
|
1200 P |
48 |
0 |
0 |
|
2400 P |
35 |
0 |
0 |
|
Exposure period 24 h, fixation time 24 h, without S9 mix |
||||
Medium |
|
97 |
0.5 |
0.5 |
Ethanol |
|
100 |
1 |
1 |
MMC |
0.05 |
86 |
44.5 |
44.5 |
Test substance |
37.5 |
97 |
1.5 |
1.5 |
75 |
98 |
0 |
0 |
|
150 |
87 |
0 |
0 |
|
300 |
56 |
1 |
1 |
|
600 |
35 |
0 |
0 |
MMC: Mitomycin C
DMN: Dimethylnitrosamine
P: Colorless clear fine oile drop-like precipitations were noted in the culture fluid in petri plate.
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information):
negative
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