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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: inhalation
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
secondary literature

Data source

Reference
Reference Type:
other company data
Title:
Unnamed
Year:
1978
Report date:
2009

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
In this study the groups of 5 male and 5 female Charles River CD rats were exposed for 6 hours to 48.9 mg/L.
GLP compliance:
no
Test type:
acute toxic class method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Trimethoxypropylsilane
EC Number:
213-926-7
EC Name:
Trimethoxypropylsilane
Cas Number:
1067-25-0
Molecular formula:
C6H16O3Si
IUPAC Name:
trimethoxy(propyl)silane
Test material form:
liquid
Specific details on test material used for the study:
TX-1499 (176 g/mol) in a cover sheeet identified as propyltrimethoxysilane, although the molecular weight of propyltrimethoxysilane is 164 g/mol.

Test animals

Species:
rat
Strain:
other: Charles River CD rats
Sex:
male/female

Administration / exposure

Route of administration:
inhalation
Type of inhalation exposure:
not specified
Vehicle:
not specified
Analytical verification of test atmosphere concentrations:
no
Duration of exposure:
ca. 6 h
Concentrations:
High dose level: 48.9 mg/L
No. of animals per sex per dose:
5 female and 5 male
Control animals:
not specified
Details on study design:
6 hours inhalation, 14 days observation period

Results and discussion

Effect levels
Key result
Sex:
male/female
Dose descriptor:
LC50
Remarks:
surrogate LC50
Effect level:
ca. 48.9 mg/L air
Based on:
not specified
Exp. duration:
6 h
Remarks on result:
other: mortality of 3 rats, poor documentation
Mortality:
3 rats during the 14 days observation period

Applicant's summary and conclusion

Interpretation of results:
other: valid, but poor documented due to old standards of 1978
Conclusions:
LC50 for acute inhalation (6 hours inhalation, 14 days observation period) in rats = 48,9 mg/L
Executive summary:

LC50 in this study = 48.9 mg/L