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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: oral

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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: Reliable with restrictions; comparable to guideline study with acceptable restrictions.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1973

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: no information on method
Principles of method if other than guideline:
no information on method
GLP compliance:
no
Test type:
other: LD50
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Nicotinonitrile
EC Number:
202-863-0
EC Name:
Nicotinonitrile
Cas Number:
100-54-9
Molecular formula:
C6H4N2
IUPAC Name:
pyridine-3-carbonitrile
Constituent 2
Reference substance name:
Pyridine-3-carbonitrile
IUPAC Name:
Pyridine-3-carbonitrile
Details on test material:
Purity of Nicotinonitrile: not stated

Test animals

Species:
rat
Strain:
other: Sherman-Wistar
Sex:
male
Details on test animals or test system and environmental conditions:
Rats weighed 200-300g

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
water
Details on oral exposure:
Rats were deprived of food, but not water, for 24 hours prior to dosing. Food and water were available ad libitum post dose.
Doses:
Concentrations of 250, 500, 1000, 2000 and 4000 mg/kg.
No. of animals per sex per dose:
Five male rats per group were dosed at 50% w/v suspension in water

Results and discussion

Effect levels
Sex:
male
Dose descriptor:
LD50
Effect level:
1 100 mg/kg bw
Based on:
test mat.
95% CL:
960 - 1 500
Mortality:
250 mg/kg = 0/5
500 mg/kg = 0/5
1000 mg/kg = 2/5 — within 24 hours, animals were semi-comatose, which prevaled for five days during which time two animals died, one at three days post dose and the other four days post dose.
2000 mg/kg = 5/5
4000 mg/kg = 5/5
Clinical signs:
other: No signs of toxicity were observed at the 250 mg/kg dose level. At 500 mg/kg, the rats were depressed one hour post dose and lethargic. They appeared normal 24 hours post dose.
Gross pathology:
Findings revealed nothing remarkable.
Other findings:
Rats in the 1000 mg/kg dose group were extremely depressed 30 minutes post dose and exhibited shallow breathing. Within 24 hours they were semi-comatose. The surviving rats appeared normal eight to nine days post dose. At 2000 mg/kg and 4000 mg/kg the animals died within 1-3 hours.

Applicant's summary and conclusion

Interpretation of results:
Toxicity Category IV
Remarks:
Migrated information LD50 > 300 mg/kg and < 2000 mg/kg Criteria used for interpretation of results: EU
Conclusions:
The acute oral LD50 of 3-cyanopyridine has been adequately characterized at 1100 mg/kg (95% Confidence limits = 960-1500 mg/kg)