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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
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EC number: 216-374-5 | CAS number: 1569-02-4
- 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
In a GLP bacterial reverse mutation assay (Salmonella strains TA98, TA100, TA1535, TA1537, TA1538) ethoxypropanol tested up to 5000 ug/plate did not produce evidence of mutation with or without exogenous metabolic activation by rat liver S-9. In studies using the read across substance methoxypropyl acetate, negative results were obtained using the bacterial strain E Coli WP2 uvr A.
In a guideline and GLP in vitro cytogenetics assay using human lymphocytes, ethoxypropanol tested at concentrations up to 5000 ug/ml did not induce chromosome aberrations with or without exogenous metabolic activation by rat liver S-9.
In a reliable in vitro gene mutation study using mammalian cells (Chinese hamster lung fibroblasts V79) and the test substance methoxypropanol (the methyl analogue of ethoxypropanol), no increase in gene mutations was observed. No metabolic activation was used but the absence of any molecule structures associated with mutagenic properties can be combined with other data to make a reliable prediction for this end point that gentoxicity is not a significant property of this substance.
Detailed justification for using the read across substances methoxypropanol and its acetate ester methoxypropyl acetate can be found in a document attached to chapter 13 of the IUCLID dossier.
Short description of key information:
Bacterial reverse mutation: negative, with and without metabolic activation
Chromosome abberation/cytogenicity: negative with and without metabolic activation
(analogue - methoxypropanol) in vitro gene mutation using mammalian cells: negative
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
The substance has no significant genotoxic properties and therefore classification is not warranted.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.