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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
September 1999
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1999
Report date:
1999

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Test type:
acute toxic class method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
4-(2,6,6-trimethyl-1-cyclohexen-1-yl)butan-2-one
EC Number:
241-318-1
EC Name:
4-(2,6,6-trimethyl-1-cyclohexen-1-yl)butan-2-one
Cas Number:
17283-81-7
Molecular formula:
C13H22O
IUPAC Name:
4-(2,6,6-trimethyl-1-cyclohexen-1-yl)butan-2-one
impurity 1
Chemical structure
Reference substance name:
rel-4-((1R,6R)-2,2,6-trimethylcyclohexyl)butan-2-one
Cas Number:
60761-23-1
Molecular formula:
C13H24O
IUPAC Name:
rel-4-((1R,6R)-2,2,6-trimethylcyclohexyl)butan-2-one
Test material form:
liquid

Test animals

Species:
rat
Strain:
other: HanIbm: WIST (SPF)
Sex:
male/female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
polyethylene glycol
No. of animals per sex per dose:
3 female or three male rats were used in each of the 2 groups
Control animals:
not specified

Results and discussion

Effect levels
Key result
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
test mat.
Mortality:
No deaths occured during the study
Clinical signs:
other: In two females, ruffled fur, hunched posture and sedation were observed on test day 2. In one female ruffled fur persisted until test day 3.
Gross pathology:
No macroscopic findings were observed at necropsy.

Applicant's summary and conclusion

Interpretation of results:
Category 5 based on GHS criteria
Executive summary:

LD50 in the rat for this study is greated than 2000 mg/kg body weight.