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EC number: 266-733-5 | CAS number: 67584-55-8
- 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
Endpoint summary
Administrative data
Description of key information
OECD 404: C4 Acrylate was not a skin irritant
OECD 405: C4 Acrylate was not an eye irritant
Key value for chemical safety assessment
Additional information
The primary skin irritation/corrosion potential of C4 acrylate was assessed in the rabbit (4-hour semi-occlusive application). The study was carried out based on the guidelines described in EC Commission Directive 92/69/EEC, B.4 and OECD No. 404. Three male rabbits were exposed to 0.5 grams of the test article, applied onto clipped skin for 4 hours using a semi-occlusive dressing. Observations were made 1, 24, 48 and 72 hours after exposure. No mortality, systemic toxicity, corrosive effects or skin irritation was caused by 4 hours exposure to the test article. Based on the results of this study and according to the EC criteria for classification and labelling requirements (CLP Regulation No 1272/2008), the test substance does not have to be classified and has no obligatory labeling requirement for skin irritation.
The eye irritation potential of C4 Acrylate was evaluated in 3 male rabbits. The study was carried out based on the following guidelines: OECD 405 and EC Commission Directive 92/69/EEC. Single samples of approximately 55 mg of the test article (volume of 0.1 ml) were instilled into one eye of each of three rabbits. Observations were made 1, 24, 48 and 72 hours and 7 days after instillation. The test substance caused irritation of the conjunctivae, shown as redness, chemosis and discharge. The irritation was and completely resolved within 72 hours in one animal and within 7 days in the other animals. Remnants of the test substance were present in the eyes of all animals on day 1. Based on the results of the study, the test article has no obligatory labelling requirement for eye irritation according to EC criteria for classification and labelling requirements (CLP Regulation No 1272/2008).
Justification for classification or non-classification
The test results for in the skin and eye Irritation studies do not meet the criteria for classification as a skin or eye irritant.
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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