Registration Dossier
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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: - | CAS number: -
- 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
Hydrolysis
Administrative data
Link to relevant study record(s)
Description of key information
In accordance with column 2 of REACH Annex VIII, this study does not need to be conducted if the substance is highly insoluble in water.
Key value for chemical safety assessment
Additional information
Testing was not carried out using Method C7 Abiotic Degradation, Hydrolysis as a Function of pH of Commission Regulation (EC) No 440/2008 of 30 May 2008.
This was because the water solubility was low, determined to be≤1.4 x 10-4 g/L. The hydrolysis test would have had to be performed at no more than half this value, as stipulated in the guidelines, and would have been below the sensitivity of relevant analytical techniques to quantify the concentration of test item as it decreased due to hydrolysis. Therefore, extraction procedures were attempted to concentrate the test item in solution, namely solid phase extraction cartridges and solvent/solvent extraction using dichloromethane.
However, even though recovery was relatively successful at higher levels (0.5 mg/L gave approximately 75 % recovery) it was noticed that as the sample concentration became lower the recovery efficiency also reduced. At 0.1 mg/L a recovery of approximately 55 % was achieved but at 0.01 mg/L this had dropped to approximately 25 %. Therefore, as the test item concentration reduced due to hydrolysis, the extracted sample concentration would reduce even further due to the decreasing efficiency of the extraction procedure. This would then not produce a straight line hydrolysis plot with time.
Although the test was not performed due to the above reasons, it was known that the test item would hydrolyse and seen to degrade in solution during the study. The functional group present within the test item that is well known to hydrolyse is an ester. Being part of a 5 membered ring may put strain on the structure and increase the rate of hydrolysis which would alleviate the strain by opening the ring. Esters are well known to hydrolyse at all pHs, but significantly in strong basic conditions and to a lesser degree in strong acidic conditions. The other functional groups within the test item structure, an hydroxyl, aryl and ether, would not be expected to hydrolyse in environmental conditions of pH and temperature.
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.