Registration Dossier
Registration Dossier
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EC number: 947-968-9 | CAS number: -
Genetic toxicity: in vivo
Administrative data
- Endpoint:
- genetic toxicity in vivo, other
- Remarks:
- In vivo Single Cell Gel/Comet Assay
- Type of information:
- experimental study planned
- Justification for type of information:
- TESTING PROPOSAL ON VERTEBRATE ANIMALS
NON-CONFIDENTIAL NAME OF SUBSTANCE:
- Name of the substance on which testing is proposed to be carried out : Base terpenica
- Name of the substance for which the testing proposal will be used [if different from tested substance] : N/A
CONSIDERATIONS THAT THE GENERAL ADAPTATION POSSIBILITIES OF ANNEX XI OF THE REACH REGULATION ARE NOT ADEQUATE TO GENERATE THE NECESSARY INFORMATION:
- Available GLP studies : Not available.
- Available non-GLP studies : Not available.
- Historical human data: Not available.
- (Q)SAR: Not available.
- In vitro methods: In vitro methods are possitive
- Weight of evidence : Not available.
- Grouping and read-across : Not available. Substance UVCB.
CONSIDERATIONS THAT THE SPECIFIC ADAPTATION POSSIBILITIES OF ANNEXES VI TO X (AND COLUMN 2 THEREOF) OF THE REACH REGULATION ARE NOT ADEQUATE TO GENERATE THE NECESSARY INFORMATION:
- One of the in vitro studies of genetic toxicity is positive, so according annex XI of REACH Regulation it is necessary to carry out an in vivo assay.
FURTHER INFORMATION ON TESTING PROPOSAL IN ADDITION TO INFORMATION PROVIDED IN THE MATERIALS AND METHODS SECTION:
- Details on study design / methodology proposed: In vivo Single Cell Gel/Comet Assay – OECD 489
Data source
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 489 (In vivo Mammalian Alkaline Comet Assay)
- GLP compliance:
- yes
- Type of assay:
- other: IN VIVO SINGLE CELL GEL/COMET ASSAY
Test material
- Reference substance name:
- Product obtained by rectification during the manufacturing process of Dihydromyrcenol
- EC Number:
- 947-968-9
- Molecular formula:
- C10H18
- IUPAC Name:
- Product obtained by rectification during the manufacturing process of Dihydromyrcenol
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
Administration / exposure
- Route of administration:
- oral: gavage
- Duration of treatment / exposure:
- 2 treatments at approximately 24 hour intervals
- Post exposure period:
- 2-6 hours after the final administration
Doses / concentrationsopen allclose all
- Dose / conc.:
- 2 000 mg/kg bw/day (nominal)
- Dose / conc.:
- 1 000 mg/kg bw/day (nominal)
- Dose / conc.:
- 500 mg/kg bw/day (nominal)
- No. of animals per sex per dose:
- 5 males* per treated group
3 male animals for positive control group
both sexes should be considered if any existing toxicity, metabolism or exposure data indicate a toxicologically meaningful sex difference.
Examinations
- Tissues and cell types examined:
- Liver (other tissues/organs can be selected depending on the proposed use for exposure to the test substance)
- Details of tissue and slide preparation:
- 150 cells analysed per tissue (50 cells scored per each of three replicate slides)
- Evaluation criteria:
- number of heavily damaged cells (hedgehogs, clouds, ghost cells)
% tail intensity and tail moment
Results and discussion
Applicant's summary and conclusion
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.
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