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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: 905-287-4 | CAS number: 1638758-52-7
- 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:
- adverse effect observed (sensitising)
- Additional information:
Of the two studies available on xylenols, 3,5 xylenol returned an equivocal result. Whilst the author of this study concluded that the test material, 3,5 xylenol did not exhibit any skin sensitising potential, due to similar skin reactions being elicited by the solvent and the test preparation, the outcome of the study could not be concluded with confidence. The study conducted on 2,4 xylenol returned a positve result, furthermore, no reactivity with the solvent was observed.
Both the Draize test and the human maximisation test on p-cresol confirmed this cresol isomer to be a non-sensitiser. The GPMT on o-cresol did not provide sufficient information to allow a definitive conclusion to be drawn.
Currently no skin sensitisation data is available for ethyl phenols; based on structural similarities a conservative approach who be to conclude that ethyl phenols will give a similar effect to that observed by 2,4 xylenol, Skin Sensitiser.
The overall conclusion for this endpoint who be that of a potential skin sensitiser.
Migrated from Short description of key information:
Skin Sensitisation:
Key study on 2,4 xylenol (GPMT). Weimann, 1999. KL.1 - Sensitiser
Disregarded study on 3,5 xylenol (GPMT). Weimann, 1999. KL.3 - No conclusion drawn due to cross reaction in vehicle animals
Supporting study on p-cresol (Draize). Sharp, 1978 - Non-sensitiser.
Supporting study on p-cresol (human MT). Opdyke, 1974. KL.2 - Non sensitiser
Disregarded study on o-cresol (GPMT). Bruze, 1986. KL.4 - Insufficient information to draw a conclusion.
Respiratory Sensitisation:
Currently no validated in vivo methods available.
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
Respiratory sensitisation
Currently no validated in vivo methods are available. Neither xylenols, cresols or ethylphenols contain reactive chemical groups which are known respiratory sensitisers. Consequently there is no concern regarding this endpoint.
Migrated from Short description of key information:
N/A
Justification for classification or non-classification
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.