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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Report date:
2017

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
GLP compliance:
yes
Test type:
acute toxic class method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2-propylvaleronitrile
EC Number:
236-338-2
EC Name:
2-propylvaleronitrile
Cas Number:
13310-75-3
Molecular formula:
C8H15N
IUPAC Name:
2-propylpentanenitrile

Test animals

Species:
rat
Strain:
other: Crl:WI(Han)
Sex:
female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
unchanged (no vehicle)
Doses:
300 and 2000 mg/kg
No. of animals per sex per dose:
3 females/dose
Control animals:
no

Results and discussion

Effect levels
Key result
Sex:
female
Dose descriptor:
LD50
Effect level:
>= 300 - <= 2 000 mg/kg bw
Based on:
test mat.
Mortality:
There were no deaths at a dose level of 300 mg/kg. Two animals dosed at 2000 mg/kg were found dead two days after dosing on Day 3. One other animal was humanely killed due to the severity of the clinical signs at this time point.
Clinical signs:
No clinical signs were seen at a dose level of 300 mg/kg.
Piloerection and ataxia or decreased activity were noted in all animals treated at 2000 mg/kg one day after dosing. Piloerection, ataxia, decreased activity and hunched posture were noted in these animals on Day 3. One animal treated at 2000 mg/kg was prone and gasping on Day 3 and was humanely killed. All surviving animals appeared normal from Day 4.
Body weight:
All surviving rats achieved body weight gains during the first and second weeks of the study except for one animal treated at 2000 mg/kg which showed a slight loss in body weight during the first week.
Gross pathology:
No abnormalities were noted at necropsy.

Applicant's summary and conclusion

Interpretation of results:
Category 4 based on GHS criteria
Conclusions:
The acute median lethal oral dose level of the test article, 2-propylvaleronitrile (CAS 13310-75-3), was found to be between 300 and 2000 mg/kg.
The test material was classified as Category 4 in respect of its acute oral toxicity according to the Globally Harmonized System of Classification and Labelling of Chemicals (GHS).