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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: dermal
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Referenced source in an international report.

Data source

Reference
Reference Type:
secondary source
Title:
Dimethylformamide, SIDS Initial Assessment Report For SIAM 13
Author:
OECD
Year:
2001
Bibliographic source:
UNEP publications

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
No further details
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
N,N-dimethylformamide
EC Number:
200-679-5
EC Name:
N,N-dimethylformamide
Cas Number:
68-12-2
Molecular formula:
C3H7NO
IUPAC Name:
N,N-dimethylformamide
Details on test material:
No further details

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female

Administration / exposure

Type of coverage:
occlusive
Vehicle:
unchanged (no vehicle)
Remarks:
Concentration: undiluted
Duration of exposure:
24 hours
Doses:
3160 mg/kg
No. of animals per sex per dose:
2 animals per sex per dose
Control animals:
not specified
Details on study design:
On days 2, 4, 8, 11 and 15 exposure sites were examined and scored for erythema and edema on a graded scale of 0 to 4. Each animal was observed for mortality and toxic effects 2 and 4 hours post-dosing and daily thereafter.

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
other: Lethal dose
Effect level:
> 3 160 mg/kg bw
Based on:
not specified
Mortality:
In the 14-days post observation period, 1/4 animals died (one male animal) on day 4 of the study.
Gross pathology:
Gross necropsy revealed no substance-related effect.
Other findings:
Among the remaining animals, no signs of systemic toxicity or percutaneous absorption were observed.

Applicant's summary and conclusion

Conclusions:
The lethal dose in an acute dermal toxicity test on rats was found > 3160 mg/kg bw.