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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: Acceptable study report which meets basic scientific principles

Data source

Referenceopen allclose all

Reference Type:
study report
Title:
Unnamed
Year:
1976
Report date:
1976
Reference Type:
secondary source
Title:
Fragrance raw materials monographs
Author:
Ford RA et al.
Year:
1988
Bibliographic source:
Food Chem. Toxicol. 26 (4), 311-312

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
10 rabbits per dose were used. Observations for mortality and/or systemic effects were made over a 14 day period.
GLP compliance:
no
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
6,10-dimethylundeca-3,5,9-trien-2-one
EC Number:
205-457-1
EC Name:
6,10-dimethylundeca-3,5,9-trien-2-one
Cas Number:
141-10-6
Molecular formula:
C13H20O
IUPAC Name:
6,10-dimethylundeca-3,5,9-trien-2-one

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
Doses:
5000 mg/kg bw
No. of animals per sex per dose:
10
Control animals:
not specified
Details on study design:
- Duration of observation period following administration: 14 days
- Other examinations performed: mortality and/or systemic effects

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
> 5 000 mg/kg bw
Mortality:
1/10; death on day 13
Clinical signs:
other: Slight anorexia in 8/10 on days 4-6

Applicant's summary and conclusion

Interpretation of results:
practically nontoxic
Remarks:
Migrated information Criteria used for interpretation of results: EU