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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2020

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
GLP compliance:
yes
Test type:
acute toxic class method

Test material

Constituent 1
Reference substance name:
Oligomerisation products of 2-(chloromethyl)oxirane and 2-ethyl-2-(hydroxymethyl)propane-1,3-diol
EC Number:
922-223-0
Molecular formula:
not applicable for UVCB
IUPAC Name:
Oligomerisation products of 2-(chloromethyl)oxirane and 2-ethyl-2-(hydroxymethyl)propane-1,3-diol
Test material form:
liquid

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
corn oil

Results and discussion

Effect levels
Key result
Sex:
female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
test mat.
Mortality:
In the 2000 mg/kg B.W. (3nd step) 1 animal dead at Day 1 after administration were observed. No dead animals were observed in the 300 mg/kg B.W. (1st, 2nd step) and 2000 mg/kg B.W. (4th step) test substance administration groups.
Clinical signs:
other: All animal in the 2000 mg/kg (3rd step) test substance group from 2 hours to 4 hours after administration clinical signs were observed soiled perineal region, diarrhea and one animal were dead at Day 2 after administration. Also, one animal was recovered
Gross pathology:
In necropsy of dead animal at 2000 mg/kg B.W. (3rd step) test substance administration group, soiled perineal region was observed in one animal. In survived animals in 300 mg/kg B.W. (1st, 2nd step), 2000 mg/kg B.W. (4th step) and the other two survived animals in 2000 mg/kg B.W. (3th step) were no lesions caused by administration of test substance.

Applicant's summary and conclusion

Interpretation of results:
Category 5 based on GHS criteria