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EC number: 246-850-8 | CAS number: 25327-89-3
- 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
The test substance was evalueted for its irritant effects on skin and eyes on Albino Rabbits.
The primary skin irritation index was calculated to be 1 and all the effects were completely reversible after 72h.
The primary eye irritation index was calculated to be 1.33 for the rinsed test animals and all the effects were completely reversible after 72h.
Key value for chemical safety assessment
Skin irritation / corrosion
Link to relevant study records
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- November 1981
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study with acceptable restrictions
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- The skin of the tested animals was abraded and epidermal incisions were made prior to the application of the substance and the exposition lasted for 24 hours.
- GLP compliance:
- yes
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- Each rabbit was sexed, weighted and ear tagged. The weight ranged from 2.25kg to 2.55kg. The rabbits were quarantined and acclimated to laboratory conditions for 12 days. The animals were individually housed in steel wire-bottomed cages, suspended above the droppings. Animals were observed twice daily during the quarantine period.
- Type of coverage:
- occlusive
- Preparation of test site:
- other: On each rabbit, two test sites were only clipped, the other two were also abraded.
- Remarks:
- 24 hours prior to the dermal application an Oster small animal electric clipper was used on the backs of the animals.The clipped area was about 10% of the total body surface area.
- Vehicle:
- physiological saline
- Controls:
- no
- Amount / concentration applied:
- 0.5g of the test material was slightly moistened with physiological saline and applied to each of the test sites with a small plastic weight boat
- Duration of treatment / exposure:
- 24h exposure
- Observation period:
- 4 days
- Number of animals:
- 6
- Details on study design:
- Six animals (3 males and 3 females) were selected after the quarantine period and weighted: the weight ranged from 2.25kg to 2.55kg.
- Irritation parameter:
- primary dermal irritation index (PDII)
- Basis:
- mean
- Time point:
- other: 24h/72h
- Score:
- 1
- Max. score:
- 1
- Reversibility:
- fully reversible within: 72h
- Remarks on result:
- no indication of irritation
- Irritant / corrosive response data:
- The primary irritation index was calculated to be 1.
- Other effects:
- No other effects were observed.
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- The substance is not classified as irritant for skin.
- Executive summary:
The primary skin irritation index was calculated to be 1 and all the effects were completely reversible after 72h, therefore the substance is not classified as irritant for skin.
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Eye irritation
Link to relevant study records
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- November 1981
- Reliability:
- 3 (not reliable)
- Rationale for reliability incl. deficiencies:
- significant methodological deficiencies
- Remarks:
- eye rinsed after 30sec instead of 1 hour and not all the required data are given in the test report.
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- EU Method B.5 (Acute Toxicity: Eye Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- The eyes of the tested animals were rinsed after 30 seconds instead of 1 hour.
- GLP compliance:
- yes
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- Each rabbit was sexed, weighted and ear tagged with a unique animal numer (weight range: 1.95 kg to 2.55kg). The rabbts were quarantined and acclimated to laboratory conditions for 12 days prior to initiation of the study. The rabbits were individually housed in stain-less steel wire-bottomed cages suspended above the droppings. Animals were observed twice daily during the quarantine period.
- Vehicle:
- unchanged (no vehicle)
- Controls:
- yes, concurrent no treatment
- Amount / concentration applied:
- 100mg applied to the right eye - 6 not rinsed and 3 rinsed after 30 seconds
- Duration of treatment / exposure:
- Single dose
- Observation period (in vivo):
- 7 days
- Number of animals or in vitro replicates:
- 9 animals (4 males and 5 females)
- Details on study design:
- Grading for irrittation and injury were made at 24, 48 and 72 hours and at 4 and 7 days, using the standard scoring system of Draize. Fluoroscein examinations were used to facilitate evaluation of potential corneal damage.
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 24/48/72 h - 4d - 7d
- Score:
- >= 0 - <= 4
- Max. score:
- 4
- Reversibility:
- fully reversible within: 72h for rinsed animals - 7 days for not rinsed animals
- Irritant / corrosive response data:
- The primary irritation index was calculated to be 4.0 for the not rinsed test animals and 1.33 for the rinsed test animals.
- Other effects:
- no signs of systemic toxicity and no deaths occurred
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- The substance is not classified as irritant for eyes.
- Executive summary:
The primary eye irritation index was calculated to be 1.33 for the rinsed test animals and all the effects were completely reversible after 72h, therefore the substance is not classified as irritant for eyes.
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Additional information
Justification for classification or non-classification
The primary skin irritation index was calculated to be 1 and all the effects were completely reversible after 72h, therefore the substance is not classified as irritant for skin.
The primary eye irritation index was calculated to be 1.33 for the rinsed test animals and all the effects were completely reversible after 72h, therefore the substance is not classified as irritant for eyes.
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