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Diss Factsheets
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EC number: 200-879-2 | CAS number: 75-56-9
- 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
Description of key information
Key value for chemical safety assessment
Skin sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
A small number of cases in workers provide some limited evidence that repeated dermal exposure to liquid propylene oxide may cause skin sensitisation(Jensen, 1981; van Ketel, 1986; Steinkraus and Hawsen, 1994), however a study conducted in animals did not find skin sensitisation effects (Dow Chemical Company, 1982).
The skin sensitisation study was performed in guinea pigs according to a modification of the Maguire method (Dow Chemical Company, 1982). The study examined one positive control group and one test group. The test group received 4 applications of a 10% solution of propylene oxide applied on a gauze square and covered by tape. The positive control group received DER 331 epoxy resin as a 10% solution in the same way as the test group. After 2 days, a second application was administered. At the time of the third application 0.2 ml of Freund's Adjuvant was injected intradermally adjacent to the insult site. Every time the patches were removed, observations about primary irritation were made and recorded. After two weeks of rest the animals were challenged and the skin response was scored 24 and 48 hours after the challenge. A positive response indicative of sensitisation (slight/moderate redness) was observed on 8 of l0 guinea pigs treated with DER 331. None of the 10 guinea pigs treated with the propylene oxide solution revealed signs of sensitisation. Therefore as a 10% solution this material is not considered a potential human skin sensitiser.
Migrated from Short description of key information:
Based on the result of the modified Maguire method test with guinea pigs, propylene oixde is not sensitising to skin.
Respiratory sensitisation
Endpoint conclusion
- Additional information:
No data on respiratory sensitisation are available. However, in accordance with Section 1 of REACH Annex XI, the study is scientifically unjustified, as respiratory tract sensitisation is not expected based on the fact that propylene oxide is not skin sensitiser and no human data are available indicating a concern for respiratory sensitisation.
Justification for classification or non-classification
Based on the absence of skin sensitising effect in a modified Maguire method study with guinea pigs and the lack of data indicating the respiratory sensitisation of propylene oxide, classification according to EU Classification, Labeling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 1272/2008 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.
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