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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Study period:
1944
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Study well documented, meets generally accepted scientific principles, acceptable for assessment (taking into account the publication year)

Data source

Reference
Reference Type:
publication
Title:
Unnamed
Year:
1944

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
3 different doses: 200 mg/kg , 350 mg/kg , 400 mg/kg
8-16 rats/dose
Intravenous injection
GLP compliance:
no
Remarks:
no GLP at this time

Test material

Constituent 1
Reference substance name:
Succinchlorimide
IUPAC Name:
Succinchlorimide

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
intravenous
Vehicle:
not specified
Doses:
200 mg/kg
350 mg/kg
400 mg/kg
No. of animals per sex per dose:
200 mg/kg: 16 animals
350 mg/kg: 8 animals
400 mg/kg: 10 animals
Control animals:
not specified
Details on study design:
Succinchlorimide is acid in reaction and must be neutralized.

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
> 200 - < 400 mg/kg bw
Based on:
test mat.
Mortality:
200 mg/kg: 19 % mortality
350 mg/kg: 12 % mortality
400 mg/kg: 90 % mortality

Applicant's summary and conclusion

Conclusions:
Acute toxicity when injected intravenously:
200 mg/kg: 19 % mortality
350 mg/kg: 12 % mortality
400 mg/kg: 90 % mortality
Executive summary:

The acute toxicity of Succinchlorimide was tested when injected intravenously to group of 8 -16 rats. 3 different doses were applied: 200, 350, 400 mg/kg.

Mortalities:

200 mg/kg: 19 % mortality

350 mg/kg: 12 % mortality

400 mg/kg: 90 % mortality