Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Basic toxicokinetics

Currently viewing:

Administrative data

basic toxicokinetics in vitro / ex vivo
Type of information:
experimental study
Adequacy of study:
key study
Study period:
Study Plan: 19.01.2015 Experimental phase: 22.-23. 01.2015 Draft Report 26.01.2015 Final Report 27.01.2015
2 (reliable with restrictions)

Data source

Reference Type:
study report
Report date:

Materials and methods

Objective of study:
Test guideline
no guideline followed
Principles of method if other than guideline:
The test Item was exposed to a simulated gastric environment (0.1 M HCl solution / 37 °C) for 4 hours. The organic metabolites were extracted with hexane and analyzed by 119Sn-NMR spectroscopy.
GLP compliance:

Test material

Constituent 1
Chemical structure
Reference substance name:
2-ethylhexyl 4,4-dibutyl-10-ethyl-7-oxo-8-oxa-3,5-dithia-4-stannatetradecanoate
EC Number:
EC Name:
2-ethylhexyl 4,4-dibutyl-10-ethyl-7-oxo-8-oxa-3,5-dithia-4-stannatetradecanoate
Cas Number:
Molecular formula:
2-ethylhexyl 4,4-dibutyl-10-ethyl-7-oxo-8-oxa-3,5-dithia-4-stannatetradecan-1-oate
Test material form:
other: liquid
Details on test material:
Name: Dibutyltin bis(2-ethylhexylthioglycolate)

CAS-Nr.: 10584-98-2
IUPAC: 2-ethylhexyl 4,4-dibutyl-10-ethyl-7-oxo-8-oxa-3,5-dithia-4-stannatetradecan-1-oate

Trivial Name: DBTE

Commercial Name: Mark 292

Water solubility: 3.58 x 10ˆ-3 g/l (20°C)

Partition Coefficient: Log Kow = 3.4 (22.1 °C)

Batch No.: AK115/001/00

Results and discussion

Applicant's summary and conclusion

Interpretation of results (migrated information): other: DBTEC (Dibutyltin chloro 2-thyhlhexylester)is the only metabolite of DBTE that was formed in the simulated mammalian gastric environment
DBTE in-vitro metabolism can be monitored using 119Sn-NMR Spectroscopy by the decrease in a relative intensity of the 119Sn-NMR signal at ~72-74 ppm attributable to DBTE and an increase in the relative intensity of the signal at ~31-33 ppm characteristic to DBTEC.
Under the simulated gastric conditions (0.1 M HCl/pH 1.2/37°C) DBTE in-vitro metabolism equilibrated within 4 hours and resulted in the formation of DBTEC (a mono-chloro-ester of DBTE) at about 68%.
DBTC was not detected in the metabolyzed DBTE sample (no peak was found at DBTC = 129 ppm).
Executive summary:

The study showed that under the simulated gastric conditions (0.1 M HCl / pH 1.2 / 37 °C) DBTE hydrolyzes to its mono-chloro-ester DBTEC

It can be concluded that DBTEC is the only metabolite of DBTE that was formed in the simulated mammalian gastric environment. No DBTC was formed under the conditions of this study.

The119Sn-NMR Spectroscopy was used as a valuable analytical tool to directly identify and quantify all organotin components, which are formed as a result of the in-vitro metabolism of the test item.