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EC number: 627-034-4 | CAS number: 1213789-63-9
- 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
Endpoint summary
Administrative data
Key value for chemical safety assessment
Additional information
With regard to mutagenicity, only negative results were obtained for primary alkylamines in both, in vitro and in vivo. (Z)-octadec-9 -enylamines have been shown to be not mutagenic in bacterial gene mutation testing. Likewise only negative results from tests on bacterial mutagenicity and data on gene and chromosome mutations in mammalian cells in vitro and on chromosomal aberrations and micronuclei in vivo were revealed for this compound and other primary alkylamines of this category. Alltogether, the negative data are considered as sufficient to exclude a mutagenic potential of (Z)-octadec-9 -enylamines in vivo. This conclusion is in line with the existing EU risk assessment on primary alkylamines in general..
Short description of key information:
(Z)-octadec-9-enylamines were tested in a GLP compliant bacterial gene mutation test (Ames-test) in Salmonella typhimurium TA 100, TA 1535, TA 1537, TA 1538, TA 98 according to OECD TG 471 with and without endogenous metabolic activation (S9-mix from Aroclor-induced rat liver). No increases in the number of revertants were induced in any of the tester strains used.
No data is available for C12-18-(even numbered)-alkylamines in other test systems. However, data from closely related primary alkylamines can be used based on read-across. Data from (Z)-octadec-9-enylamine (CAS No. 112-90-3) indicate absence of mutagenicity at the hprt locus in mammalian CHO cells up to 10 nl/ml with and without S9-mix.
Negative results for mutagenicity of (Z)-octadec-9-enylamine (CAS No. 112-90-3) were also obtained in a valid L5178Y TK+/- mouse lymphoma assay in the presence and absence of metabolic activation. No increases in mutation frequency as compared to solvent controls were found.
Additionally, (Z)-octadec-9-enylamine (CAS No. 112-90-3) did also not induce chromosomal aberrations in a valid cytogenetic study in vitro in CHO cells in the presence and absence of aroclor 1254 induced rat liver S9-mix.
Data from in vivo mutagenicity studies on C12-18-(even numbered)-alkyamines are not available. However, based on read-across no indications of a related potential exist from analogous compounds. A GLP-compliant bone marrow micronucleus test with tallow alkylamines (CAS No. 61790-33-8) in 50 Sprague Dawley rats led to a negative result after a single oral dose of 2000 mg/kg body weight.
Negative results are also reported from an in vivo chromosomal aberration test in mice. Administration of single doses up to 5000 mg/kg body weight in corn oil via gavage revealed no significant increases in aberrant cells although clinical signs of toxicity indicated that the test material was systemically available after oral application.
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
Based on the available database confirming the absence of a mutagenic potential in vitro as well as in vivo, respective classification of (Z)-octadec-9 -enylamines, as well as of the whole category of primary alkylamines, is not warranted.
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