Registration Dossier
Registration Dossier
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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.
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EC number: 906-125-5 | CAS number: -
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: acceptable, well documented publication
Data source
Referenceopen allclose all
- Reference Type:
- publication
- Title:
- Food Flavourings and Compounds of Related Structure I. Acute Oral Toxicity.
- Author:
- Jenner PM, Hagan EC, Taylor JM, Cook EL, and Fitzhugh OG
- Year:
- 1 964
- Bibliographic source:
- Fd. Cosm. Toxicol. 2: 327-343
- Reference Type:
- secondary source
- Title:
- Fragrance Raw Materials Monographs
- Author:
- Opdyke DLJ
- Year:
- 1 974
- Bibliographic source:
- Food and Cosmetics Toxicology, Vol. 12: 881-882
- Reference Type:
- secondary source
- Title:
- Die Situation in der gesundheitlichen Beurteilung der Aromatisierungsmittel fuer Lebensmittel
- Author:
- Bar VF and Griepentrog F
- Year:
- 1 967
- Bibliographic source:
- Medizin Ernaehr. 8: 244-251
- Reference Type:
- secondary source
- Title:
- No information
- Author:
- Jenner PM, Hagan EC, Taylor JM, Cook EL, and Fitzhugh OG
- Year:
- 2 008
- Bibliographic source:
- RIFM database
- Reference Type:
- secondary source
- Title:
- No information
- Author:
- INCHEM
- Year:
- 2 004
- Bibliographic source:
- WHO FOOD ADDITIVES SERIES: 52
- Reference Type:
- secondary source
- Title:
- Unnamed
- Year:
- 2 001
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- no method specified
- GLP compliance:
- not specified
- Test type:
- standard acute method
- Limit test:
- no
Test material
- Reference substance name:
- Geraniol
- EC Number:
- 203-377-1
- EC Name:
- Geraniol
- Cas Number:
- 106-24-1
- Molecular formula:
- C10H18O
- IUPAC Name:
- (2E)-3,7-dimethylocta-2,6-dien-1-ol
- Details on test material:
- - Name of test material (as cited in study report): Geraniol Extra
- Isomers composition: 3,7-Dimethyl-2,6-octadienol
; 3,7-Dimethyl-1,6-octadienol
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Osborne-Mendel
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALsS
- Fasting period before study: ca. 18 h
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- unchanged (no vehicle)
- Doses:
- no data
- No. of animals per sex per dose:
- 5
- Control animals:
- not specified
- Details on study design:
- - Duration of observation period following administration: 14 days; when no acute toxic signs were seen, the animals were observed for only one week
-The animals were maintained under close observation for recording of toxic signs and time of death.
Such observation was continued until animals appeared normal and showed weight gain. - Statistics:
- LD50 values were computed by the method of Lichfield and Wilcoxon (J. Pharmacol. 96, 99, 1949).
Results and discussion
Effect levels
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- 3 600 mg/kg bw
- 95% CL:
- 2 840 - 4 570
- Mortality:
- Death time was between 4 hours and 18 hours
- Clinical signs:
- other: The described symptoms were depression, coma, and wet fur
Applicant's summary and conclusion
- Interpretation of results:
- practically nontoxic
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
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