Registration Dossier
Registration Dossier
Data platform availability banner - registered substances factsheets
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 308-132-3 | CAS number: 97862-82-3
- 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
Genetic toxicity: in vitro
Administrative data
- Endpoint:
- in vitro gene mutation study in bacteria
- Remarks:
- Type of genotoxicity: gene mutation
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- No data reported
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: This study is classified as reliable without restriction because it was carried out according to OECD TG 471.
Data source
Reference
- Reference Type:
- publication
- Title:
- Estimation of the dermal carcinogenic activity of petroleum fractions using a modified Ames assay
- Author:
- Blackburn GR, Deitch RA, Schreiner CA, Mehlman MA, and Mackerer CR
- Year:
- 1 984
- Bibliographic source:
- Cell Biol Toxicol, Vol 1(1), pp 67-80
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 471 (Bacterial Reverse Mutation Assay)
- GLP compliance:
- not specified
- Type of assay:
- other: modified bacterial reverse mutation assay (modified Ames test)
Test material
- Reference substance name:
- Solvent refined/Hydrotreated heavy naphthenic distillate, (CAS # 64741-96-4/CAS # 64742-52-5)
- IUPAC Name:
- Solvent refined/Hydrotreated heavy naphthenic distillate, (CAS # 64741-96-4/CAS # 64742-52-5)
- Details on test material:
- Read Across to Unrefined/Acid Treated Oils
The following substances were tested:
Number 7, Solvent refined/Hydrotreated heavy naphthenic distillate, CAS # 64741-96-4/CAS # 64742-52-5.
Number 9, 10, and 11, Solvent refined/hydrotreated heavy paraffinic distillate, CAS # 64741-88-4/CAS # 64742-54-7.
Number 13: Solvent refined/dewaxed heavy paraffinic distillate, CAS # 64741-88-4/CAS # 64742-65-0.
Constituent 1
Method
- Target gene:
- Not applicable.
Species / strain
- Species / strain / cell type:
- S. typhimurium TA 98
- Details on mammalian cell type (if applicable):
- Not applicable.
- Additional strain / cell type characteristics:
- not specified
- Metabolic activation:
- with
- Metabolic activation system:
- Aroclor 1254-induced rat or hamster liver S9
- Test concentrations with justification for top dose:
- 50 ul
- Vehicle / solvent:
- dimethyl sulphoxide
Controls
- Untreated negative controls:
- not specified
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- not specified
- Positive controls:
- yes
- Positive control substance:
- other: benzo(a)pyrene at 5 μg/plate and 2-aminoanthracene at 2 μg/plate
- Details on test system and experimental conditions:
- METHOD OF APPLICATION: preincubation
DURATION
- Preincubation period: not reported
- Exposure duration: not reported
- Expression time (cells in growth medium): not reported
- Selection time (if incubation with a selection agent): not reported
- Fixation time (start of exposure up to fixation or harvest of cells): not reported
NUMBER OF REPLICATIONS: not reported
NUMBER OF CELLS EVALUATED: not reported
DETERMINATION OF CYTOTOXICITY
- Method: mitotic index
- Evaluation criteria:
- Mutagenicity Index
- Statistics:
- No data reported.
Results and discussion
Test results
- Species / strain:
- S. typhimurium TA 98
- Metabolic activation:
- with
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity
- Additional information on results:
- No data reported.
- Remarks on result:
- other: other: Modified Ames Test using Salmonella typhimurium strain TA 98 and Aroclor 1254-induced hamster liver S-9
- Remarks:
- Migrated from field 'Test system'.
Any other information on results incl. tables
The modified assay was used to rank the test samples, and a corn oil control, for relative mutagenic activity. The ranking correlated closely (r=0.97) with potency ratings from previously determined carcinogenicity bioassays. Samples subjected to solvent refining were non-carcinogenic.
In the table below, the sample number in the study report along with the study ID and mutagenicity index of each substance is listed.
Sample Number |
Sample ID |
CAS# |
Mutagenicity Index |
7 |
Solvent-Refined/Hydrotreated Heavy Naphthenic Distillate |
64741-96-4/ 64742-52-5 |
0 |
9 |
Solvent-Refined/Hydrotreated Heavy Paraffinic Distillate |
64741-88-4/ 64742-54-0 |
0 |
10 |
Solvent-Refined/Hydrotreated Heavy Paraffinic Distillate |
64741-88-4/ 64742-54-0 |
0 |
11 |
Solvent-Refined/Hydrotreated Heavy Paraffinic Distillate |
64741-88-4/ 64742-54-0 |
0 |
13 |
Solvent-Refined/Dewaxed Heavy Paraffinic Distillate |
64741-88-4/ 64742-65-0 |
0 |
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information):
negative
All five solvent refined samples had mutagenicity indices of 0 and are therefore not considered positive in the AMES test for bacterial mutagenicity. - Executive summary:
- In an in vitro modified Ames assay, five lubricating base oils were tested using S. typhimurium strain TA98 at concentrations of 50 micrlitres per plate. The solvent-refined samples tested were not mutagenic and had mutagenicity indices of 0. This study received a Klimisch score of 1 and is classified as reliable without restriction because it was carried out according to OECD TG 471.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.