Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
screening for reproductive / developmental toxicity
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
other:
Justification for type of information:
A screening study for reproductive/developmental toxicity does not need to be conducted because there is no evidence from available information (e.g. (Q)SAR) that the substance may be a developmental toxicant.
The acute oral toxicity of the test item is very low (LD50: > 5 mL/kg). Also in a study with repeated oral dosing over 28 consecutive days no adverse clinical effects or histopathological findings were seen in rats dosed with up to 1000 mg/kg (NOAEL: > 1000 mg/kg). As also reported in the attached (Q)SAR predicted profile, the test item does not suggest a specific alert for a teratogenic potential in humans. Therefore, at present there is no need to perform a screening study for reproductive/developmental toxicity in experimental animals.

Data source

Materials and methods

Test material

Constituent 1
Chemical structure
Reference substance name:
3,7-dimethyloctane-1,7-diol
EC Number:
203-517-1
EC Name:
3,7-dimethyloctane-1,7-diol
Cas Number:
107-74-4
Molecular formula:
C10H22O2
IUPAC Name:
3,7-dimethyloctane-1,7-diol
Test material form:
liquid

Results and discussion

Applicant's summary and conclusion