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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
data from handbook or collection of data

Data source

Referenceopen allclose all

Reference Type:
publication
Title:
NIOSH Exchange Chemicals. Vol. NX#03763
Author:
U.S. Army Armament Research & Development Command, Chemical Systems Laboratory
Reference Type:
secondary source
Title:
Succinimide
Author:
EPA
Year:
2011
Bibliographic source:
ACToR:Aggregated Computational Toxicology Resource; http://actor.epa.gov/actor/faces/GenericChemical.jsp

Materials and methods

Test guideline
Guideline:
other: no data
Principles of method if other than guideline:
Acute intravenous toxicity study in mice
GLP compliance:
not specified

Test material

Constituent 1
Reference substance name:
Succinimid
IUPAC Name:
Succinimid
Details on test material:
- Name: Succinimid (German)
- Amount: 50 g
- Storage of the test substance: 4°C
Specific details on test material used for the study:
not specified

Test animals

Species:
mouse
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
not specified

Administration / exposure

Route of administration:
unspecified
Vehicle:
not specified
Details on exposure:
not specified
Doses:
not specified
No. of animals per sex per dose:
not specified
Control animals:
not specified
Details on study design:
not specified
Statistics:
not specified

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
320 mg/kg bw
Based on:
not specified
Mortality:
not specified
Clinical signs:
not specified
Body weight:
not specified
Gross pathology:
not specified
Other findings:
not specified

Applicant's summary and conclusion

Conclusions:
In an acute oral toxicity in mice, an LD50 value of 320 mg/kg bw was determined.
Executive summary:

In an acute oral toxicity in mice, an LD50 value of 320 mg/kg bw was determined.