Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Remarks:
USE OF (ROBUST) STUDY SUMMARIES PROVIDED BY ECHA, the study data of the Robust Study Summaries are older than 12 years.
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
other: USE OF (ROBUST) STUDY SUMMARIES PROVIDED BY ECHA.
Title:
Unnamed
Year:
1991

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
GLP compliance:
not specified
Test type:
other: not specified
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
2-isopropyl-2-(1-methylbutyl)-1,3-dimethoxypropane
EC Number:
406-970-5
EC Name:
2-isopropyl-2-(1-methylbutyl)-1,3-dimethoxypropane
Cas Number:
129228-11-1
Molecular formula:
C13H28O2
IUPAC Name:
1-methoxy-2-(methoxymethyl)-5-methyl-2-(propan-2-yl)hexane
Test material form:
liquid

Test animals

Species:
rat

Administration / exposure

Route of administration:
oral: unspecified
Doses:
2000 mg/kg bw
Control animals:
no

Results and discussion

Effect levels
Key result
Sex:
not specified
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
test mat.
Mortality:
no information provided
Clinical signs:
other: no information provided
Gross pathology:
no information provided

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
the substance should not be classified for acute oral toxicity