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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Immunotoxicity

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Administrative data

Endpoint:
immunotoxicity: sub-chronic oral
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Data originally provided for the HPV programme, but study report it no longer available. Study summary provided for information purposes only.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1981
Report date:
1981

Materials and methods

Principles of method if other than guideline:
Male and female rats were dosed in feed for 3 months with monooctyltin trichloride at 3, 10, 30, and 100 ppm.
GLP compliance:
not specified
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Trichlorooctylstannane
EC Number:
221-435-4
EC Name:
Trichlorooctylstannane
Cas Number:
3091-25-6
Molecular formula:
C8H17Cl3Sn
IUPAC Name:
trichlorooctylstannane
Details on test material:
Monooctyltin Trichloride [CAS No. 3091-25-6]:Dioctyltin Dichloride [CAS No. 3542-36-7] (65:35% mixture)

Test animals

Species:
rat
Sex:
male/female

Administration / exposure

Route of administration:
oral: feed
Vehicle:
not specified
Doses / concentrations
Remarks:
Doses / Concentrations:
3, 10, 30, and 100 ppm
Basis:
no data

Results and discussion

Results of examinations

Gross pathological findings:
effects observed, treatment-related
Description (incidence and severity):
ignificant reduction in thymus weight observed in males and  females in the 100 ppm dose group.  Marginal decrease observed at 30 ppm.   No histopathological changes were observed in the thymic tissue.
Details on results:
GROSS PATHOLOGY
Significant reduction in thymus weight observed in males and  females in the 100 ppm dose group.  Marginal decrease observed at 30 ppm.   No histopathological changes were observed in the thymic tissue.

Effect levels

open allclose all
Dose descriptor:
NOEL
Effect level:
0.87 mg/kg bw/day
Based on:
not specified
Sex:
male
Dose descriptor:
NOEL
Effect level:
0.88 mg/kg bw/day
Based on:
not specified
Sex:
female

Applicant's summary and conclusion

Conclusions:
A significant reduction in thymus weight was observed in males and  females in the 100 ppm dose group with less apparent decrease in the 30 ppm group. No histopathological changes were observed in the thymic tissue.