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Diss Factsheets
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EC number: 201-645-2 | CAS number: 85-98-3
- 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
Endpoint summary
Administrative data
Key value for chemical safety assessment
Genetic toxicity in vitro
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (negative)
Additional information
Ethylcentralite did not demonstrate mutagenic activity in any of the tests conducted. Ethylcentralite was not mutagenic in Salmonella Mutagenicity Test using strains TA97, TA98, TA100 and TA1535 or in Bacterial Reverse Mutation Test (acc. to EU method B.13/14 analogous to the OECD TG 471) both in the presence and absence of S9 metabolic activation and in In vitro Mammalian Chromosome Aberration Test on the human peripheral blood lymphocytes without and with metabolic activation and finally Ethylcentralite was not even mutagenic in the In vitro Mammalian Cell Gene Mutation Assay (Thymidine Kinase Locus/TK+/-) in mouse lymphoma L5178Y cells without and with metabolic activation.
Justification for selection of
genetic toxicity endpoint
No study was selected, all studies were negative.
Short description of key information:
Ethyl centralit was tested for mutagenicity:
- in Salmonella typhimurium, using a
preincubation protocol. Test was performed in the absence of exogenous
metabolic activation, and in the presence of liver S-9 from
Aroclor-induced male Sprague-Dawley rats and Syrian hamsters,
- in Bacterial Reverse Mutation Test
Four indicator Salmonella typhimurium strains TA 98, TA 100, TA 1535, TA 1537 and one indicator Escherichia coli WP2 uvrA strain were used with and without metabolic activation using a supernatant of rat liver S9
- in vitro Mammalian Chromosome Aberration Test on the human peripheral blood lymphocytes without and with metabolic activation,
- in vitro Mammalian Cell Gene Mutation Assay (Thymidine Kinase Locus/TK+/-) in mouse lymphoma L5178Y cells without and with metabolic activation
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
Based on the available data, the substance is not classified for genetic toxicity.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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