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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: The study was conducted according to standard OECD method and under GLP

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2016
Report date:
2016

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
GLP compliance:
yes
Test type:
fixed dose procedure
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
-
EC Number:
419-560-6
EC Name:
-
Cas Number:
4369-14-6
Molecular formula:
C9H18O5Si
IUPAC Name:
3-(trimethoxysilyl)propyl prop-2-enoate
Test material form:
not specified
Details on test material:
no data

Test animals

Species:
rat
Strain:
Crj: CD(SD)
Sex:
male/female
Details on test animals or test system and environmental conditions:
no data

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
olive oil
Doses:
Preliminary sighting study: 200; 500; 100; 20 mg/kg bw
Main study: 2000; 100 mg/kgbw
No. of animals per sex per dose:
Preliminary sighting study: 3 (male)
Preliminary sighting study: 3 (female)
Main study: 5 (male)
Main study: 5 (female)
Control animals:
no
Details on study design:
no data

Results and discussion

Preliminary study:
2000 mg/kg bw: no mortality, no evident toxicity
500 mg/kg bw: no mortality, no evident toxicity
100 mg/kg bw: no mortality, no evident toxicity
20 mg/kg bw: no mortality, no evident toxicity
No animal were found dead
Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
test mat.
Mortality:
One female rat of the 2000 mg/kg bw died
Clinical signs:
Decreased spontaneous locomotion, decreased respiration rate, ptosis, salivation and mucous stool were observed in 1000 and 2000 mg/kg bw of both sexes
Gross pathology:
reddish spots of mucosa in glandular stomach was observed in the dead female rat. Adhesion to diphragm and liver in the forestomach was observed in a rat of 2000 mg/kg bw group

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
According to the results of the acute oral toxicty test acryloxypropyltrimethoxysilane, LD50 > 2000 mg/kg bw no classification is required
Executive summary:

The acute oral toxicty of acryloxypropyltrimethoxysilane is above 2000 mg/kg bw