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EC number: 214-269-9 | CAS number: 1118-84-9
- 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
Basic toxicokinetics
Administrative data
- Endpoint:
- basic toxicokinetics
- Type of information:
- other: Weight of evidence
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
Data source
Reference
- Reference Type:
- other: Weight of evidence
- Title:
- Toxicokinetics
- Author:
- Sustainability Support Services (Europe) AB
- Year:
- 2 012
- Bibliographic source:
- Based on the weight of evidence of various phys chem and bioaccumulative parameters in the dossier
Materials and methods
- Objective of study:
- toxicokinetics
Test guideline
- Qualifier:
- no guideline available
- Principles of method if other than guideline:
- Based on the weight of evidence of various phys chem and bioaccumulative parameters in the dossier
- GLP compliance:
- no
Test material
- Reference substance name:
- Allyl acetoacetate
- EC Number:
- 214-269-9
- EC Name:
- Allyl acetoacetate
- Cas Number:
- 1118-84-9
- Molecular formula:
- C7H10O3
- IUPAC Name:
- allyl acetoacetate
Constituent 1
Test animals
- Species:
- other: unspecified
- Strain:
- not specified
- Sex:
- not specified
Administration / exposure
- Route of administration:
- other: estimation
- Vehicle:
- unchanged (no vehicle)
Results and discussion
Toxicokinetic / pharmacokinetic studies
- Details on absorption:
- Absorption of allyl acetoacetate via the inhalation route is expected since its vapour pressure is 85-59 Pa. Assuming that the absoprtion via the other route of exposure (oral or intravenous) is significant, but since the bio-concentration factor (BCF) of allyl acetoacetate is very low (3.2) even if the chemical is absorbed within the living system it shall not bio-accumulate and thereby no bio-concentration shall occur within the living system.
- Details on distribution in tissues:
- The water solubility of allyl acetoacetate is poor compred to its solubility in organic solvents. Thus it is expected that the chemical shall not be distribute via blood to the other rgans of the body but it could distribute in those areas of the body where the lipid content is high. However, given the fact that it will not bio-accumulate or bio-concentrate will ensure its elimination from the human body.
- Details on excretion:
- As chemicals are absorbed at different entry portals, they can be excreted via various routes and mechanisms. The relative importance of the excretion processes depends on the physical and chemical properties of the compound and its various metabolites. There are no available reports of allyl acetoacetate metabolites being formed upon absorption. Also given the fact that the chemical has very low bio-concentration factor, it is assumed that allyl acetoacetate shall be excreted mostly unchanged from the body via the faeces (given that the molecular weight is less than 300 and poor water solubility) or through urine .
Metabolite characterisation studies
- Metabolites identified:
- no
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information): other: No bio-accumulation potential deduced on the basis of physico-chemical properties and molecular weight
Based upon the physico-chemical properties and bio-concentration factor of allyl acetoacetate, it has been deduced that the chemical has potentially low bio-accumulative property and hence shall be rapidly eliminated from the body system through the bile/feaces or urine. - Executive summary:
Based upon the physico-chemical properties and bio-concentration factor of allyl acetoacetate, it has been deduced that the chemical has potentially low bio-accumulative property and hence shall be rapidly eliminated from the body system through the bile/feaces or urine.
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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