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EC number: 239-743-2 | CAS number: 15667-63-7
- 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 irritation (in vivo, similar to OECD 404): irreversible damage, corrosive based on effects observed in acute dermal toxicity study (expert judgement)
Eye irritation (in vivo, OECD 405): irreversible damage
Key value for chemical safety assessment
Skin irritation / corrosion
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (corrosive)
Eye irritation
Link to relevant study records
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Version / remarks:
- 1981
- GLP compliance:
- no
- Species:
- rabbit
- Strain:
- other: White Russian
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: Asta-Werke AG, Bielefeld, Germany
- Housing: only one animal was tested
- Diet (e.g. ad libitum): n.a.
- Water (e.g. ad libitum): n.a.
- Acclimation period: 1 day
ENVIRONMENTAL CONDITIONS
according to guideline - Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- 0.01 mL
- Duration of treatment / exposure:
- no washing
- Observation period (in vivo):
- up to 72 hours
- Number of animals or in vitro replicates:
- 1
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Washing (if done): no
SCORING SYSTEM: DRAIZE score, irritation index
TOOL USED TO ASSESS SCORE: hand-slit lamp - Irritation parameter:
- cornea opacity score
- Basis:
- animal #1
- Time point:
- other: 72h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- other: animal was killed for ethical reasons after 72 h
- Remarks on result:
- other: reading at 72 h only because of severe chemosis;
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- animal #1
- Time point:
- other: 24h -72h
- Score:
- 3
- Max. score:
- 3
- Reversibility:
- other: animal was killed for ethical reasons after 72 h
- Remarks on result:
- other: hemorrhages
- Irritation parameter:
- chemosis score
- Basis:
- animal #1
- Time point:
- other: 24h -72h
- Score:
- 4
- Max. score:
- 4
- Reversibility:
- other: animal was killed for ethical reasons after 72 h
- Remarks on result:
- other: complete closure of eyelids due to severe swelling
- Irritation parameter:
- iris score
- Basis:
- animal #1
- Time point:
- other: 24h -72h
- Max. score:
- 2
- Reversibility:
- not reversible
- Remarks on result:
- not determinable
- Irritant / corrosive response data:
- cornea score: reading was only at 72 h possible because of severe chemosis
iris score: could not be evaluated because of severe chemosis - Other effects:
- The animal was killed for ethical reasons at day 3. Severe damage of the eye.
- Interpretation of results:
- Category 1 (irreversible effects on the eye) based on GHS criteria
Reference
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irreversible damage)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Skin irritation:
A skin irritation study was performed similar to OECD guideline 404 (82-0009 -DKT, non-GLP). An amount of 2x 0.5 mL unchanged test substance (corresponds to 444 mg/kg bw) was applied on the skin of one rabbit for 40 min.
Skin effects could not be determined, because 10 minutes after application strong toxic respones was observed and the animal died after 40 minutes.
Based on the results of the study and the fact that in the dermal acute toxicity study (85 -0005 -DKT) redness, crusts and nose bleeding were observed 3 -40 minutes post-application, the substance is considered as corrosive.
Eye irritation:
The key study was performed in an eye irritation/corrosion study performed similar to OECD guideline 405 (86-0007 -DKT, non-GLP).
A single White Russian rabbit received a single instillation of 0.01 mL test item into the eye. Washing of the treated eye was not done. The local irritation effects on the eye was scored according to Draize criteria 24-72 h post instillation.
Corneal opacity of score 4 was observed 72 h after dosing. Conjunctival redness score 3 was observed 24 -72 hours post-application. Chemosis was scored 4 after 24 -72 hours. Iritis could not be evaluated becuase of severe chemosis. Hence, the animal was killed for ethical reasons on day 3. The experimental findings clearly show that the test item causes irreversible damage to the eye.
Justification for classification or non-classification
The available data on skin irritation/corrosion and acute dermal toxicity meet the criteria for classification as Skin Corrosive Cat. 1B (H314) according to Regulation (EC) No. 1272/2008 (CLP) and according to the criteria of the Globally Harmonized System of Classification and Labelling of Chemicals (GHS) of the United Nations.
The available data on eye irritation/corrosion meet the criteria for classification as Eye Damage Cat. 1 (H318) according to Regulation (EC) No. 1272/2008 (CLP) and according to the criteria of the Globally Harmonized System of Classification and Labelling of Chemicals (GHS) of the United Nations.
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