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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
in vivo mammalian germ cell study: cytogenicity / chromosome aberration
Type of information:
experimental study planned
Justification for type of information:
OECD 473 shows cytotoxicity and chromosome aberation. Therefore, according to Regulation (EC) No. 1907/2006 an OECD 475 study is required.

- Available GLP studies
no studies avaible for the substance

- Available non-GLP studies
no studies avaible for the substance

- Grouping and read-across
no studies avaible for possible read across substances

- Historical human data
no historical human data avaible

- (Q)SAR
out of prediction range, Regulation requires in vivo study

- In vitro methods
Regulation requires in vivo study

- Weight of evidence
not possible based on data lacking

- Substance-tailored exposure driven testing [if applicable]
n.a.

Data source

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 475 (Mammalian Bone Marrow Chromosome Aberration Test)
Deviations:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Silicic acid (H4SiO4), tetraethyl ester, reaction products with bis(acetyloxy)dibutylstannane
EC Number:
300-344-4
EC Name:
Silicic acid (H4SiO4), tetraethyl ester, reaction products with bis(acetyloxy)dibutylstannane
Cas Number:
93925-42-9
Molecular formula:
C12H24O4Sn.C8H20O4Si
IUPAC Name:
Acetic acid, 1,1'-(dibutylstannylene) ester, reaction products with silicic acid (H4SiO4) tetra-Et ester
Details on test material:
UL03475

Results and discussion

Applicant's summary and conclusion