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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2011

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
EU Method B.1 tris (Acute Oral Toxicity - Acute Toxic Class Method)
GLP compliance:
yes (incl. QA statement)
Test type:
acute toxic class method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
methyl 2,2,3,3,4,4-hexafluoro-4-[(1,2,2-trifluoroethenyl)oxy]butanoate
EC Number:
700-677-9
Cas Number:
19190-61-5
Molecular formula:
C7H3F9O3
IUPAC Name:
methyl 2,2,3,3,4,4-hexafluoro-4-[(1,2,2-trifluoroethenyl)oxy]butanoate

Test animals

Species:
rat
Strain:
Wistar
Sex:
female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
maize oil
Remarks:
lowest dose group only
Doses:
2000 mg/kg bw
300 mg/kg bw
50 mg/kg bw
No. of animals per sex per dose:
2000 and 300 mg/kg bw group: 3 females each
50 mg/kg bw groups: 2 x 3 females
Control animals:
yes

Results and discussion

Effect levels
Sex:
female
Dose descriptor:
LD50
Effect level:
> 50 - < 300 mg/kg bw
Based on:
test mat.
Mortality:
2000 mg/kg bw group: 3/3
300 mg/kg bw group: 3/3
50 mg/kg bw group: 0/6
Clinical signs:
other: 2000 mg/kg bw group: Sluggishness (3/3), Blepharospasm (3/3), piloerection (3/3), coldness (3/3), coma 300 mg/kg bw group: Sluggishness (3/3), Blepharospasm (3/3), Ataxia (1/3), encrustation eye (1/3), piloerection (3/3), coldness (2/3), coma (2/3) 50 mg/
Gross pathology:
2000 mg/kg bw group: No treatment related gross alterations.
300 mg/kg bw group: One animal showed pale kidneys and a dark liver. No treatment related gross alterations for the other animals of this group.
50 mg/kg bw groups: No treatment related gross alterations.

Applicant's summary and conclusion

Interpretation of results:
toxic
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The oral LD50 value is considered to be between 50 and 300 mg/kg bw. The test substance is considered to be toxic if swalloed.