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EC number: 700-483-4 | 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
Endpoint summary
Administrative data
Description of key information
Skin and eye irritation studies conducted to evaluate the irritation potential of CR-39 were performed prior to the adoption of the OECD guidelines and the GLP regulations. The studies are acceptable, well-documented, which meet basic scientific principles (Klimish et al., 1997). The acute Eye Irritation Study in Albino rabbits with 100% DDC (Endpoint 7.3.2.001) is a GLP study (report date 1981-03-24).
Key value for chemical safety assessment
Skin irritation / corrosion
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Eye irritation
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Additional information
Since RAV 7NG contains as main ingredient 'diallyl 2,2'oxydiethyl dicarbonate' and experimental data are lacking for RAV 7NG, the experimental data from 'diallyl 2,2'oxydiethyl dicarbonate' were used in a read-across approach. Justification for read-across from supporting substance RAV 7AT (diallyl 2,2'-oxydiethyl dicarbonate; CAS 142-22-3; EC 205-528-7): about 70 % of RAV 7NG (EC 700-483-4) consists of components that can be found in the commercial ADC grades known as RAV 7AT, Nouryset 200 and CR39. Merely from comparing the similar production processes of these two substances it is apparent that RAV 7AT and RAV 7NG are closely related to each other. Finally, the physical-chemical, toxicological and ecotoxicological properties of RAV 7NG and RAV 7AT are almost equal and as a result, read across is justified. |
In the "Primary Skin Irritation Test" (Acute Toxicity Studies IBT No. A254, 1971 -09 -10) with 'diallyl 2,2'oxydiethyl dicarbonate the exposure period was 24 hours. In accordance with the OECD Guideline 404 Acute Dermal Irritation-Corrosion the exposure period should be normally 4 hours. After 24 hour exposure period in three of the four rabbits, both abraded and non-abraded sites showed severe erythema and edema at 24 and 72 hour reading. Carbonic acid was found to be highly irritating to rabbit skin. Contradictive results were obtained in the irritation tests on the skin of rabbits (data published M.Lacroix et al., 1976, endpoint 7.3.1.003). Here 'diallyl 2,2'oxydiethyl dicarbonate provoked only minimal changes in the skin after 24 hours (slight erythema in certain animals). The exposure period of 24 hours is not realistic to humans. Therefore, the study "Skin Irritation Studies of CR-39 Monomer" (report dated 1976 -06 -04) was taken forward for risk characterization. In this study undiluted test material (0.5 mL) was applied to one intact and one abraded skin site on rabbits (3/sex) under occluded conditions for 6 hours and assessed for up to 13 days after exposure. At 48 hours, moderate to severe erythema were noted on all sites and by 72 hours, irritation progressed to necrosis with severe erythema and very slight edema. Reddened and blackened skin at all sites was noted. By 13 days, edema, but not erythema, resolved. "...there is no dose relationship between the reaction that occurred in the first treatment and the third treatment and the pattern of reaction inconsistent and not reproducible... The reaction seems not to depend upon the animal that is being tested or the amount of solution or site selection and thus, one can conclude that there certainly is reaction taking place but being not reproducible and one must consider this is a spurious result." (from the conversation letter of Dr. M. Vinegar, Toxicologist and P.T. Breen, Dermatologist, dated 1979- 03 -12). Carbonic acid, oxydiethylene diallyl ester irritating to rabbit skin.
Eye irritation
In the earlier study "Eye Irritation Test"[(Acute Toxicity Studies IBT No. A254, 1971 -09 -10) Endpoint 7.3.2.002] undiluted 'diallyl 2,2'oxydiethyl dicarbonate' (0.1 mL) was instilled in the conjunctival sac of the right eye of five rabbits. Test eyes were not washed. Irritation was scored at 1 minute, 1, 24 and 72 hours and 7 days after administration. Conjunctival redness and slight discharge was seen which resolved after 24 – 72 hours. In this study the test material was slightly irritating to rabbit eyes. In the Acute Eye Irritation Study in Rabbits with 100% DDC (report date 1981 -03 -24) the principle of test design was the same as in the previous one except the number of animals. 6 not rinsed and 3 rinsed animals were tested. The cornea and the iris were not affected, the conjunctiva was affected by one- and six-hour examination and the lesions were fully reversible within 24 hours. The one-hour interval provided the highest mean score (8.0) for 100% DDC (diallyl diglycol carbonate) and was therefore used as the primary irritation index and classified the test compound as minimally irritating using the method of Draize. Instillation of water into the treated eyes of three rabbits did not change the classification but decreased the mean score to 3.0. The test material is considered to be slightly irritating to eyes.
Effects on skin irritation/corrosion: irritating
Effects on eye irritation: slightly irritating
Justification for classification or non-classification
The classification is warranted according to the criteria of EU Directive 67/548/EEC and EU Classification, Labelling and Packaging of Substances and Mixtures (CLP) Regulations No 1272/2008.
DSD:Xi, R38; Irritant; Irritating to skin;
GHS:Skin irritation Cat 2.
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