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EC number: 203-453-4 | CAS number: 107-02-8
- 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

Toxic effects on livestock and pets
Administrative data
Description of key information
“Based on metabolism studies of acrolein in lactating goats and laying hens, the qualitative nature of the residue in ruminants and poultry is adequately understood. Acrolein was not found in any tissue sample in either study. Major metabolites (>3%) in milk and tissue from the goat study included glucose, glycogen, and lactic acid, aspartate, glutamate, alanine, glycine/serine, and glycerol. Major metabolites identified in the hen study included glycine, glutamate, alanine, oleic acid, stearic acid, glycerol, creatine, cholesterol, aspartate, ornithine, and lactic acid. Other amino acids and fatty acids were identified but were present at lower concentrations in both studies.” quotation from United States Environmental Protection Agency HED Risk Assessment for Reregistration Eligibility Decision (RED) (US EPA 2008)
Additional information
Acrolein has been the subject of a risk assessment carried out under Community Regulation (EEC) No 793/93 (EU, 2001. However, Toxic Effects on Livestock and Pets is no specific chapter in the EU Risk Assessment. The key information on toxic effects of acrolein on livestock an pets as stated is a quotations taken from a further assessments carried out under other international and national programmes published after finalisation of the EU Risk Assessment Report 2001 (United States Environmental Protection
HED Risk Assessment for Reregistration Eligibility Decision (RED) Document for Acrolein (US-EPA, 2008):
1. European Union Risk Assessment Report of Acrolein (EU, 2001)
There is no specific chapter on toxic effects on livestock and pets in the EU Risk assessment.
2. Agreement with further International Reports and Studies Published after Finalisation of the EU Risk Assessment Report 2001
Not applicable.
3. Substantial Disagreements in Comparison to further International Reports to European Union Risk Assessment Report 2001
Not applicable.
4. Additional Aspects in further International Reports
Acrolein is used as pesticide (an aquatic herbicide and biocide) in the . In the recently (March 25, 2008) released document: HED Risk Assessment for Reregistration Eligibility Decision (RED) Document for Acrolein (US-EPA, 2008) some information on Metabolism in livestock and poultry is included: “Based on metabolism studies of acrolein in lactating goats and laying hens, the qualitative nature of the residue in ruminants and poultry is adequately understood. Acrolein was not found in any tissue sample in either study. Major metabolites (>3%) in milk and tissue from the goat study included glucose, glycogen, and lactic acid, aspartate, glutamate, alanine, glycine/serine, and glycerol. Major metabolites identified in the hen study included glycine, glutamate, alanine, oleic acid, stearic acid, glycerol, creatine, cholesterol, aspartate, ornithine, and lactic acid. Other amino acids and fatty acids were identified but were present at lower concentrations in both studies.” EPA, 2008, p19
5. Additional Information in Newer Studies, not Included in the European Union Risk Assessment Report 2001 or further Cited International Reports
None.
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.

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