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EC number: 295-411-7 | CAS number: 92045-29-9
- 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- migrated information: read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: This study is classified as reliable without restriction because it was conducted similar to OECD Guideline 404.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 996
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- A second untreated skin area was not used as a control in the animals
- GLP compliance:
- yes
Test material
- Reference substance name:
- 64741-59-9
- Cas Number:
- 64741-59-9
- IUPAC Name:
- 64741-59-9
- Reference substance name:
- Light catalytic cracked distillate
- IUPAC Name:
- Light catalytic cracked distillate
- Test material form:
- other: low viscosity liquid hydrocarbon
- Details on test material:
- - Name of test material (as cited in study report): MD-7 or MRD-92-180
- Physical state: amber liquid
- Expiration date of the lot/batch: December 1996
- Storage condition of test material: room temperature
- pH: 6
Constituent 1
Constituent 2
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: HRP Inc., Denver, Pennsylvania
- Age at study initiation: approximately 14 weeks
- Weight at study initiation: 2.09 to 2.37 kg
- Housing: singly housed in suspended stainles steel and wire mesh with absorbent paper below cages
- Diet (e.g. ad libitum): the amount of feed administered to the animals was limited on a daily basis (limits were not reported in the study report)
- Water (e.g. ad libitum): not reported
- Acclimation period: 8 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 18.3 to 21.1°C
- Humidity (%): 40 to 60 percent
- Air changes (per hr): not reported
- Photoperiod (hrs dark / hrs light): 12 hours light/12 hours dark
IN-LIFE DATES: not reported
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- clipped
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 mL
- Concentration (if solution): neat - Duration of treatment / exposure:
- 4 hours
- Observation period:
- 72 hours
- Number of animals:
- 3 male animals
- Details on study design:
- TEST SITE
- Area of exposure: clipped back
- % coverage: not reported
- Type of wrap if used: not reported
REMOVAL OF TEST SUBSTANCE
- Washing (if done): not reported
- Time after start of exposure: not reported
SCORING SYSTEM: mean erythema and oedema scores were calculated by the method of Snedecor and Cochran, 1989
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 2.7
- Max. score:
- 4
- Reversibility:
- fully reversible within: 10 days
- Remarks on result:
- other: MD-7
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 1.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 7 days
- Remarks on result:
- other: MD-7
- Irritant / corrosive response data:
- No corrosivity was observed.
- Other effects:
- None
Any other information on results incl. tables
No clinical signs were observed during the test period.
Applicant's summary and conclusion
- Interpretation of results:
- irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Light catalytic cracked distillate is classified as irritating to skin according to EU criteria.
- Executive summary:
In a primary dermal irritation study, three male New Zealand White rabbits were exposed to 0.5 mL of light catalytic cracked distillate under semi-occlusive conditions for a 4 -hour exposure period. Animals were observed for 10 days following exposure.
No clinical signs were observed during the test period. Well-defined erythema was observed in one animal, and moderate to severe erythema was observed in two animals at the 1, 24, 48, and 72 hour observation timepoints. Moderate to slight oedema was observed in all animals. Erythema and oedma resolved by day 10, and therefore the study was terminated at that time. Light catalytic cracked distillate is classified as irritating to skin according to EU criteria.
This study is classified as reliable without restriction because it was conducted similar to OECD Guideline 404.
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