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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
Genetic toxicity: in vivo
Administrative data
- Endpoint:
- in vivo mammalian somatic cell study: cytogenicity / bone marrow chromosome aberration
- Remarks:
- Type of genotoxicity: chromosome aberration
- Type of information:
- migrated information: read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: This study is reliable with restrictions because it is an acceptable and well-documented study report.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 986
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 475 (Mammalian Bone Marrow Chromosome Aberration Test)
- GLP compliance:
- yes
- Type of assay:
- chromosome aberration assay
Test material
- Reference substance name:
- 64741-59-9
- Cas Number:
- 64741-59-9
- IUPAC Name:
- 64741-59-9
- Reference substance name:
- Light Catalytically Cracked Distillate
- IUPAC Name:
- Light Catalytically Cracked Distillate
- Test material form:
- other: low viscosity hydrocarbon liquid
- Details on test material:
- Light catalytically cracked distillate
Sample API 83-07
EC number 265-060-4
EC name Distillates (petroleum), light catalytic cracked
Constituent 1
Constituent 2
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
Administration / exposure
- Route of administration:
- intraperitoneal
- Duration of treatment / exposure:
- Single dose
Doses / concentrations
- Remarks:
- Doses / Concentrations:
0.2, 0.67 and 2.0 g/kg
Basis:
Results and discussion
Test results
- Sex:
- male/female
- Genotoxicity:
- negative
- Toxicity:
- yes
Any other information on results incl. tables
Immediately after dosing all animals in the 2 g/kg group were lethargic.
There were some mortalities in the high dose group and where possible they
were replaced. Throughout the study lethargy was observed in the high dose
group animals but no toxic signs were seen in any of the other dose groups.
A summary of the chromosomal results is given in the following table.
Group Time Frequency % cells Mitotic
of 1+ 2+ index
aberrations aberrations
Str* Num**
Male
-ve control
6 0 .024 0 0 4.1
24 .004 .016 .4 0 2.8
48 .01 .02 1 0 3.5
+ve control (TEM @1.0 mg/kg)
24 >1.17
.1 29 18.8 1.3
Test material
0.2 6 .015
.005 1.5 0 2.8
24 0 .016 0
0 4.3
48 0 .02 0
0 3.6
0.67 6 0 .04 0
0 5.9
24 >.02 .03 2
.4 4.1
48 0 .01 0
0 4.5
2.0 6 0 .028 0
0 3.8
24 .01 .01 1
0 4.7
48 0 .02 0
0 3.6
Female
-ve control
6 .01 .01 1 0 4.2
24 .012 .024 1.2 0 2.6
48 0 .036 0 0 4.2
+ve control (TEM @1.0 mg/kg)
24 >4.199
0 59.9 54.5 .2
Test material
0.2 6 0 .012 0 0 3.1
24 .004 .04 .4 0 3.3
48 .004 .012 .4 0 2.9
0.67 6 >.016
.044 1.6 .4 4.6
24 0 .008 0 0 3.6
48 0 .016 0 0 5.5
2.0 6 0 .032 0 0 4.1
24 0 .016 0 0 4.9
48 0 .01 0 0 6.2
For simplicity only standard error values have not been shown in the above
table.
The authors make the following interpretation of the results
The test material did not induce a significant increase in the percentage of
aberrant cells above the controls for either sex at any of the doses or kill
times. No apparent test article effects on the mitotic index were noted in
any of the dose groups. The positive control (TEM) induced significant
increases in the percentage of cells with structural chromosomal aberrations
in the male animals (29%). The positive control also produced a very high
percentage of cells with structural chromosomal aberrations in the female
dose group (59.9%). However, the data from the female positive control group
could not be statistically analyzed since only 32 metaphase cells could be
analyzed. The lack of analyzable metaphase cells can be attributed to bone
marrow toxicity induced by the TEM.
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information): negative
The test material did not induce a significant increase in the percentage of aberrant cells above the controls for either sex at any of the doses or kill times. - Executive summary:
The authors make the following interpretation of the results
The test material did not induce a significant increase in the percentage of aberrant cells above the controls for either sex at any of the doses or kill times. No apparent test article effects on the mitotic index were noted in any of the dose groups. The positive control (TEM) induced significant increases in the percentage of cells with structural chromosomal aberrations in the male animals (29%). The positive control also produced a very high percentage of cells with structural chromosomal aberrations in the female dose group (59.9%). However, the data from the female positive control group could not be statistically analyzed since only 32 metaphase cells could be analyzed. The lack of analyzable metaphase cells can be attributed to bone marrow toxicity induced by the TEM.
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