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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: The study is comparable to OECD 401 with acceptable restrictions mostly due to reduced reporting in times before GLP.

Data source

Referenceopen allclose all

Reference Type:
study report
Title:
Unnamed
Year:
1975
Report date:
1975
Reference Type:
secondary source
Title:
Unnamed
Year:
1975
Report date:
1975

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
3-dimethylaminopropiononitrile
EC Number:
217-090-4
EC Name:
3-dimethylaminopropiononitrile
Cas Number:
1738-25-6
Molecular formula:
C5H10N2
IUPAC Name:
3-(dimethylamino)propanenitrile
Details on test material:
- Name of test material (as cited in study report): N,N-Dimethyl-amino-propionitril
- Physical state: liquid

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
water
Doses:
4640, 3160, 2150, 1470, 1000 µL/kg bw. (corresponding to ca. 3990 - 860 mg/kg bw; calculated with a density of 0.86 g/mL)
No. of animals per sex per dose:
2 (in the lowest and highest dose) or 5
Control animals:
no

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
ca. 1 290 mg/kg bw
Remarks on result:
other: original value: 1500 µl/kg, calculated with a density of 0.86 g/mL
Mortality:
1000 µL/kg bw: 0/4 animals
1470 µL/kg bw: 4/10 animals
all other animals treated with higher doses died
Clinical signs:
Dyspnoe, stretch/bend convulsions, tremor, tonic-clonic convulsions, apathy, abdominal/ lateral position, unusual noises, reddish salivation, bad general state
Gross pathology:
Animals that died: acute heart dilatation, congestion, hyperemia, stomach dilatated, partly diffuse reddened

Applicant's summary and conclusion