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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: other routes
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Study well documented, meets generally accepted scientific principles, acceptable for assessment

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1980
Report date:
1980

Materials and methods

Principles of method if other than guideline:
BASF-Test: Mice were injected intraperitoneally with the test substance (three different concentrations used) and then observed for 14 days.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
N-(1-cyanoethyl)formamide
EC Number:
248-440-4
EC Name:
N-(1-cyanoethyl)formamide
Cas Number:
27394-99-6
Molecular formula:
C4H6N2O
IUPAC Name:
N-(1-cyanoethyl)formamide
Details on test material:
N-Formylalaninnitril (purity 98%)

Test animals

Species:
mouse
Strain:
NMRI
Sex:
male/female
Details on test animals or test system and environmental conditions:
no data

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
water
Details on exposure:
no data
Doses:
50, 200, 700 mg/kg bw
No. of animals per sex per dose:
5
Control animals:
not specified
Details on study design:
- Duration of observation period following administration: 14 days
Statistics:
no data

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
200 - 700 mg/kg bw
Mortality:
Dose 700 mg/kg: 1 male animal died within 1 hour, 4 male animals died within 1 day; 4 female animals died within 1 day
Clinical signs:
Dose 200 mg/kg: dyspnoea, apathy, spastic gait, piloerection and a poor general state
Dose 700 mg/kg: dyspnoea, apathy, abnormal position, staggering, tremor, convulsions, exsiccosis, poor general state
Body weight:
no data
Gross pathology:
In dead as well as sacrificed animals, no intraabdominal deposits or
conglutinations were observed.

Any other information on results incl. tables

The LD50 was determined to be > 200 and < 700 mg/kg bw.


Applicant's summary and conclusion