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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
acute toxicity: dermal
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Data available as short summary from a secondary source beeing cited in a peer-reviewed publication

Data source

Reference
Reference Type:
secondary source
Title:
Acute oral and dermal toxicity studies
Author:
Russell TJ
Year:
1973
Bibliographic source:
Report to RIFM (Location 2033, Sub-Reference 03/06); cited in: Opdyke DLJ (1975): Monographs on Fragrance Raw Materials. Food Cosmet Toxicol 13: 887

Materials and methods

Principles of method if other than guideline:
No data given.
GLP compliance:
not specified
Test type:
other: no data given

Test material

Constituent 1
Chemical structure
Reference substance name:
3,7,11-trimethyldodeca-1,6,10-trien-3-ol,mixed isomers
EC Number:
230-597-5
EC Name:
3,7,11-trimethyldodeca-1,6,10-trien-3-ol,mixed isomers
Cas Number:
7212-44-4
Molecular formula:
C15H26O
IUPAC Name:
3,7,11-trimethyldodeca-1,6,10-trien-3-ol
Details on test material:
- Name of test material (as cited in study report): Nerolidol
- Analytical purity and isomere specification: no data given

Test animals

Species:
rabbit
Strain:
not specified
Sex:
not specified

Administration / exposure

Type of coverage:
not specified
Vehicle:
not specified
Duration of exposure:
No data given.
Doses:
5000 mg/kg bw
No. of animals per sex per dose:
10
Control animals:
not specified
Details on study design:
Observation period lasted 14 days. The animals were observed for moratlity and clinical signs of toxicity.

Results and discussion

Effect levels
Dose descriptor:
LD50
Effect level:
> 5 000 mg/kg bw
Mortality:
No deaths occured.
Clinical signs:
No effects were seen.

Applicant's summary and conclusion