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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Type of information:
experimental study
Adequacy of study:
key study
Study period:
No data
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Literature data with limited details
Cross-referenceopen allclose all
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to other study

Data source

Reference
Reference Type:
review article or handbook
Title:
Ref. substance: 5233 Isopropylidene Glycerol
Author:
O’Neil M.J. Smith A. Heckelman P.E. Obenchain J.R.Jr. Gallipeau J.A.R. D’Arecca M.A. Budavari S.
Year:
2001
Bibliographic source:
The Merck Index : an encyclopedia of chemicals, drugs, and biological, Thirteenth edition

Materials and methods

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

Test material

Constituent 1
Chemical structure
Reference substance name:
2,2-dimethyl-1,3-dioxolan-4-ylmethanol
EC Number:
202-888-7
EC Name:
2,2-dimethyl-1,3-dioxolan-4-ylmethanol
Cas Number:
100-79-8
Molecular formula:
C6H12O3
IUPAC Name:
(2,2-dimethyl-1,3-dioxolan-4-yl)methanol
Test material form:
liquid

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
No data

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
not specified
Details on oral exposure:
No data
Doses:
No data
No. of animals per sex per dose:
No data
Control animals:
not specified
Details on study design:
No data
Statistics:
No data

Results and discussion

Preliminary study:
No data
Effect levels
Key result
Sex:
not specified
Dose descriptor:
LD50
Effect level:
7 000 mg/kg bw
Based on:
not specified
Mortality:
No data
Clinical signs:
other: other: No data
Gross pathology:
No data
Other findings:
No data

Any other information on results incl. tables

No data

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
The oral LD50 of the submitted substance, 2,2-Dimethyl-1,3-dioxolane-4-methanol, has been reported to be 7000 mg/kg in rats in literature data.
Executive summary:

The only data available for acute oral toxicity of the submitted substance 2,2-Dimethyl-1,3-dioxolane-4-methanol was a literature data with no details on test method and results. The oral LD50 of the submitted substance has been reported to be 7000 mg/kg in rats. Therefore the substance cannot be classified for acute oral toxicity according to the Regulation (EC) N° 1272-2008 (CLP) and to the  GHS.