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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
not reported
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
documentation insufficient for assessment

Data source

Reference
Reference Type:
publication
Title:
Unnamed
Year:
1962

Materials and methods

Test guideline
Qualifier:
no guideline followed
GLP compliance:
no
Test type:
standard acute method

Test material

Constituent 1
Chemical structure
Reference substance name:
2,2,3,3-tetrafluoropropan-1-ol
EC Number:
200-955-5
EC Name:
2,2,3,3-tetrafluoropropan-1-ol
Cas Number:
76-37-9
Molecular formula:
C3H4F4O
IUPAC Name:
2,2,3,3-tetrafluoropropan-1-ol
Test material form:
not specified

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
no details reported

Administration / exposure

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

Results and discussion

Effect levelsopen allclose all
Sex:
not specified
Dose descriptor:
LDLo
Effect level:
3 400 mg/kg bw
Key result
Sex:
not specified
Dose descriptor:
LD50
Effect level:
> 3 400 mg/kg bw
Remarks on result:
not measured/tested
Remarks:
LD50 > LDlo
Mortality:
not reported
Clinical signs:
other: Respiratory impairment, gastric irritation, narcosis, incoordination, and prostration
Gross pathology:
not reported

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
The acute oral LD50 in the rat is greater than 3400 mg/kg bw, which was reported as "approximate lethal dose".