Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 242-895-2 | CAS number: 19224-29-4
- 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
Water solubility
Administrative data
Link to relevant study record(s)
Description of key information
The water solubility of Z-Acetate at 25°C was determined to be 3.5 µg/L using a modified column elution test method.
Key value for chemical safety assessment
Additional information
The water solubility of Z-Acetate was determined using a modified column elution test similar to OECD guideline 105. Triplicate test systems were prepared and incubated for 0, 1, 2, 5, 6, 7, 8, 9, 12, 13 and 14 day at 25°C ± 1 °C. Triplicate aliquots of water samples were taken on each sampling day, diluted with acetonitrile and analyzed using LC/MS/MS. Additionally, the syringe was rinsed with acetonitrile and the rinseate analyzed for any syringe-bound Z-Acetate. The total Z-Acetate in the water sample and the syringe rinseate was combined as total concentration of Z-Acetate in the water sample. A water saturation equilibrium was reached by day 5. The overall average water solubility concentration for Z-Acetate was 3.50 µg/L, based on results for all three test system from day 5 through day 14 (n = 72).The overall RSD% was 50%.
This is a modified guideline study conducted under GLP. The modification was made to accommodate the liquid state of the test substance whereas a flow through cell containing the liquid substance was used in place of the flow through column design. The modification of test method does not affect the outcome of the test results. The precision value of RSD of 50% was due to the measurement of very low level concentrations, and near the limits of quantitation for the method. However, this does not affect the conclusion that the test substance has very low water solubility. Therefore, this study is considered as a key study, valid with restriction with a Klimisch 2 ranking. A water solubility description of “negligible” was also found. However, due to few details available, the reliability of the description is not assignable.
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.