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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Study period:
1969
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Followed appropriate guidelines.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1969
Report date:
1969

Materials and methods

Principles of method if other than guideline:
Oral LD50 according to a modification of the method of E.J. de Beer
GLP compliance:
not specified
Remarks:
Oral LD50 according to a modification of the method of E.J. de Beer
Test type:
other: Oral LD50 according to a modification of the method of E.J. de Beer

Test material

Constituent 1
Chemical structure
Reference substance name:
Adiponitrile
EC Number:
203-896-3
EC Name:
Adiponitrile
Cas Number:
111-69-3
Molecular formula:
C6H8N2
IUPAC Name:
hexanedinitrile
Details on test material:
- Name of test material (as cited in study report): Refined Adiponitrile
- Lot/batch No.: 957

Test animals

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

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
corn oil
Doses:
The doses given to the rats were 158 mg/kg, 200 mg/kg, 251 mg/kg and 316 mg/kg.
No. of animals per sex per dose:
Three female and two male were dosed at 158 mg/kg.
Three male and two female were dosed at 200 mg/kg.
Three female and two male were dosed at 251 mg/kg.
Three male and two female were dosed at 316 mg/kg.

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
215 other: mg/kg
Remarks on result:
other: 198-235 mg/kg (lower and upper limits)

Applicant's summary and conclusion

Interpretation of results:
moderately toxic
Remarks:
Migrated information Criteria used for interpretation of results: not specified
Conclusions:
The oral LD 50 for male and female rats was placed at 215 milligrams per kilogram with lower and upper limits of 198 to 235 milligrams per kilogram.
Executive summary:

The oral LD 50 for male and female rats was placed at 215 milligrams per kilogram with lower and upper limits of 198 to 235 milligrams per kilogram. The compound was classed as moderately toxic by oral ingestion in male and female rats. Survival time was several hours to five days with most deaths occuring within two days. Toxic symptons included reduced appetite and activitiy, increasing weakness, and collapse. At autopsy there was liver discoloration, lung hyperemia, gaseous and inflammed intestinal tract, and distended coronaries. Surviving animals were sacrified nine days after dosing. Viscera of the animals on lower test level hyperemia was noted on the upper test levels.