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EC number: 272-341-5 | CAS number: 68814-87-9 A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C9 through C25 and boiling in the range of approximately 150°C to 400°C (320°F to 752°F).
- 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
Genetic toxicity: in vitro
Administrative data
- Endpoint:
- in vitro DNA damage and/or repair study
- Remarks:
- Type of genotoxicity: DNA damage and/or repair
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- 1987-07-29 to 1988-04-12
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: This study is classified as reliable without restrictions because it closely followed OECD Guideline 479 and appears to be GLP compliant
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 988
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 479 (Genetic Toxicology: In Vitro Sister Chromatid Exchange Assay in Mammalian Cells)
- GLP compliance:
- yes
- Remarks:
- Study report states that the study was conducted in compliance with GLP regulations
- Type of assay:
- sister chromatid exchange assay in mammalian cells
Test material
- Reference substance name:
- 64742-80-9
- Cas Number:
- 64742-80-9
- IUPAC Name:
- 64742-80-9
- Reference substance name:
- Hydrodesulfurised middle distillate
- IUPAC Name:
- Hydrodesulfurised middle distillate
- Test material form:
- other: liquid
- Details on test material:
- - Name of test material (as cited in study report): API 81-10
Details of test material from report: API (1986a). Four Week Subchronic Inhalation Toxicity Study in rats. Testing laboratory: International Research and Development Corporation, Mattawan, Michigan. Report no.: 418-027. Owner company: American Petroleum Institute. Study number: 33-32724. Report date: 1986-08-28.
- Substance type: Hydrodesulfurized Middle Distillate
- Physical state: Clear liquid
- CAS number: 64742-80-9
- Gravity API degrees: 34.9
- Sulfur wt %:0.28
- Nitrogen ppm: 97
- Flash Point °F: 160
- Boiling range (ASTM D-86) 10-95%: 421-637 °F
- Initial Boiling Point 342 °F
- End Boiling Point 651 °F
- Composition % by MS:
olefins 0
aromatics 30.9
paraffins 48.9
naphthenes 20.2
Constituent 1
Constituent 2
Method
Species / strain
- Species / strain / cell type:
- Chinese hamster Ovary (CHO)
- Metabolic activation:
- with and without
- Test concentrations with justification for top dose:
- 0.008, 0.016, 0.03 and 0.06 µl/ml
- Vehicle / solvent:
- acetone
Results and discussion
Test resultsopen allclose all
- Species / strain:
- Chinese hamster Ovary (CHO)
- Metabolic activation:
- with
- Genotoxicity:
- positive
- Remarks:
- statistically significant increase in the frequency of SCEs was observed at the lowest two doses
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity
- Vehicle controls validity:
- not examined
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Species / strain:
- Chinese hamster Ovary (CHO)
- Metabolic activation:
- without
- Genotoxicity:
- negative
- Remarks:
- no statistically significant increase in the frequency of SCEs was observed
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity
- Vehicle controls validity:
- not examined
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Remarks on result:
- other: all strains/cell types tested
- Remarks:
- Migrated from field 'Test system'.
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information):
ambiguous with metabolic activation
negative without metabolic activation
The study authors concluded that Hydrodesulfurised middle distillate did not induce an increase in sister chromatid exchange (SCE) in CHO cells in the absence of S-9 activation. In the presence of S-9, since there was statistically significant increase in the frequency of SCEs at the lower doses, Hydrodesulfurised middle distillate was concluded to be equivocal in the SCE assay. - Executive summary:
Justification for Read Across
Compositional and physico-chemical data show that Straight-Run Gas Oils are very similar to Other Gas Oils. It is considered appropriate, therefore, to read across from the Other Gas Oil data to SRGOs.
In a sister chromatid exchange (SCE) assay, Chinese hamster ovary (CHO) cells were initially tested with Hydrodesulfurised middle distillate in acetone at doses ranging from 1.0 to 0.0001 µl/ml in a preliminary toxicity test to determine the dose range to be used for the main SCE assay. Following the results from this preliminary test, Hydrodesulfurised middle distillate dose levels of 0.008, 0.016, 0.03 and 0.06 µl/ml in the absence of S-9 and dose levels of 0.13, 0.25, 0.5, and 1µl/ml in presence of S-9 activation were selected for the SCE assay. A harvest time of 27 hours after study initiation was selected to ensure that enough analysable second division metaphase cells can be collected at the high dose. In addition to treated cells, a solvent control group and positive controls consisting of trimethylenemelamine (TEM) for inactive studies (no S-9) and cyclophosphamide (CP) for active studies (with S-9) were also used to test the efficacy of the SCE assay.
Hydrodesulfurised middle distillate did not induce an increase in SCEs in the CHO cells in the absence of S-9 activation. In contrast, in cells treated with the test material in the presence of S-9 activation, there was a statistically significant increase in the frequency of SCEs at two consecutive low dose levels compared to the solvent control. However, an inverse dose-response trend was observed with no significance at the highest two doses tested. The positive control CP induced SCEs as expected. Based on these results, the study authors concluded that Hydrodesulfurised middle distillate did not induce an increase in SCEs in CHO cells in the absence of S-9. However, due to a statistically significant increase in SCE frequency at two consecutive low dose levels, the study authors concluded that Hydrodesulfurised middle distillate was equivocal for induction of SCEs in the CHO cells in the presence of S-9.
This study received a Klimisch rating of "reliable without restriction" because it closely followed OECD Guideline 479 and appears to be GLP compliant.
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