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Diss Factsheets
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EC number: 200-816-9 | CAS number: 74-86-2
- 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
Non-human information
In vitro data
The key studies are considered to be a bacterial mutation assay (Harlan Laboratories, 2010a), a mammalian cell gene mutation assay (Harlan Laboratories, 2010b) and a mammalian cell cytogenetic assay (Harlan Laboratories, 2010c). These are three recognised core assay types for investigating mutation in vitro.
Acetylene was tested in an Ames plate assay modified to allow exposure to a gaseous material (Harlan Labortaories, 2010a). S. typhimurium strains TA1535, TA1537, TA98 and TA100, together with E.Coli strain WP2uvrA were used with exposures carried out both with and without auxiliary metabolic activation (S9). A range of doses was used from 0.5 to 50% atmospheres. Acetylene was negative in this assay.
In the mammalian cell gene mutation assay (Harlan Laboratories, 2010b), mouse lymphoma (L5178Y) cells were exposed to acetylene in a contained system in both the absence and presence of S9, again at doses up to 50% atmosphere. Exposure times of 4 hours (+/- S9) and 24 hours (-S9) were used. Acetylene was negative in this assay.
In the mammalian cell cytogenetic assay (Harlan Laboratories, 2010c), CHL cells were exposed to acetylene in a contained system in both the absence and presence of S9, at doses up to 1.25% atmosphere. Exposure times of 6 hours (+/- S9) and 24 hours (-S9) were used. Acetylene was negative in this assay, both for endpoints of chromosomal damage and also numerical changes.
In vivo data
There are no in vivo mutagenicity data for acetylene. Acetylene has been examined for mutagenic activity in vitro in a range of recognised core assay types, examining for endpoints of gene mutation, chromosomal damage and chromosomal numerical changes, and was negative in all assays. There are no data to indicate any likely genotoxic activity for acetylene in vivo.
Human information
There is no information indicating any adverse effects of acetylene.
Short description of key information:
Acetylene has been examined for mutagenicity in vitro in a range of recognised core assay types, examining for endpoints of gene mutation, chromosomal damage and chromosomal numerical changes. It has shown negative results in all assays. It is concluded that the available data indicate that acetylene has no significant genotoxicity.
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
It is concluded that the available data indicate that acetylene does not warrant classification under CLP.
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