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Diss Factsheets
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EC number: 941-379-0 | 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
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: This study is classified as reliable without restrictions because it was carried out in a method equivalent/similar to OECD TG 401.
- Justification for type of information:
- Read across justification included in Section 13
Cross-reference
- Reason / purpose for cross-reference:
- read-across: supporting information
Reference
- Endpoint:
- acute toxicity: oral
- Type of information:
- read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: This study is classified as reliable without restrictions because it was carried out in a method equivalent/similar to OECD TG 401.
- Justification for type of information:
- Read across justification included in Section 13
- Reason / purpose for cross-reference:
- read-across source
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 401 (Acute Oral Toxicity)
- GLP compliance:
- yes
- Test type:
- standard acute method
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Route of administration:
- oral: gavage
- Vehicle:
- other: Undiluted
- Doses:
- Single dose level of 5000 mg/kg
- No. of animals per sex per dose:
- Five
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- > 5 000 mg/kg bw
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- The LD50 was greater than 5000 mg/kg.
- Executive summary:
The acute oral toxicity of hydrodesulfurised kerosine was studied in 5 male and 5 female albino Sprague-Dawley rats. Animals weighing 188-330g received a single dose of 5000 mg/kg by oral gavage and were observed for clinical signs and mortality at hourly intervals during the first 6 hours after administration. Thereafter animals were observed twice daily for 14 days. At termination of the study, all animals were sacrificed and subjected to gross necropsy examination. Clinical signs observed throughout the study include hypoactivity, excess salivation, diarrhoea, urine stained abdomen and hair loss around the anal area. No mortality was observed. The LD50 for hydrodesulfurised kerosine was > 5000 mg/kg.
No deaths resulted. Main clinical signs were hypoactivity, excess salivation, diarrhoea, urine-stained abdomen and hair loss around the anal area. At necropsy, the only visible finding was kidney distension in one male animal.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 982
- Report date:
- 1982
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 401 (Acute Oral Toxicity)
- GLP compliance:
- yes
- Test type:
- standard acute method
Test material
- Reference substance name:
- Kerosine (petroleum), hydrodesulfurized
- EC Number:
- 265-184-9
- EC Name:
- Kerosine (petroleum), hydrodesulfurized
- Cas Number:
- 64742-81-0
- IUPAC Name:
- Kerosine (petroleum), hydrodesulfurized
- Reference substance name:
- Hydrodesulfurised kerosine
- IUPAC Name:
- Hydrodesulfurised kerosine
- Test material form:
- other: low viscosity liquid hydrocarbon
- Details on test material:
- - Name of test material (as cited in study report): Hydrodesulfurised kerosine, CAS No. 64742-81-0
- Lot/batch No.: API 81-07
Constituent 1
Constituent 2
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- other: Undiluted
- Doses:
- Single dose level of 5000 mg/kg
- No. of animals per sex per dose:
- Five
Results and discussion
Effect levels
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- > 5 000 mg/kg bw
Any other information on results incl. tables
No deaths resulted. Main clinical signs were hypoactivity, excess salivation, diarrhoea, urine-stained abdomen and hair loss around the anal area. At necropsy, the only visible finding was kidney distension in one male animal.
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- The LD50 was greater than 5000 mg/kg.
- Executive summary:
The acute oral toxicity of hydrodesulfurised kerosine was studied in 5 male and 5 female albino Sprague-Dawley rats. Animals weighing 188-330g received a single dose of 5000 mg/kg by oral gavage and were observed for clinical signs and mortality at hourly intervals during the first 6 hours after administration. Thereafter animals were observed twice daily for 14 days. At termination of the study, all animals were sacrificed and subjected to gross necropsy examination. Clinical signs observed throughout the study include hypoactivity, excess salivation, diarrhoea, urine stained abdomen and hair loss around the anal area. No mortality was observed. The LD50 for hydrodesulfurised kerosine was > 5000 mg/kg.
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