Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
supporting study
Study period:
Not reported
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: The data was only available as a short abstract as part of a MSDS, it is not possible to assess the accuracy of the data from the information presented.

Data source

Reference
Reference Type:
other company data
Title:
Unnamed
Year:
2000
Report date:
2000

Materials and methods

Principles of method if other than guideline:
Information on methods not reported, data presented as a short abstract only.
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
Dioctyltin oxide
EC Number:
212-791-1
EC Name:
Dioctyltin oxide
Cas Number:
870-08-6
Molecular formula:
C16H34OSn
IUPAC Name:
dioctylstannanone
Test material form:
not specified
Details on test material:
- Name of test material (as cited in study report): Dioctyltin oxide

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
not specified
Control animals:
not specified

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
> 4 000 mg/kg bw
Based on:
not specified

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The acute oral LD50 of the test substance was reported to be greater than 4000 mg/kg bw.
Executive summary:

Information pertaining to the methods used to generate the data was not reported, the data was presented as a short abstract only. The acute oral LD50 of the test substance was reported to be greater than 4000 mg/kg bw.