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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
basic toxicokinetics in vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
study well documented, meets generally accepted scientific principles, acceptable for assessment

Data source

Reference
Reference Type:
publication
Title:
The Fate of [14C]Thiodipropionates in Rats
Author:
Reynolds, R.C., Astill, B. D., and Fassett, D.W.
Year:
1974
Bibliographic source:
TOXICOLOGY AND APPLIED PHARMACOLOGY 28, 133-141 (1974)

Materials and methods

Objective of study:
toxicokinetics
Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 417 (Toxicokinetics)
Version / remarks:
limited documentation
GLP compliance:
no
Remarks:
predates GLP

Test material

Constituent 1
Reference substance name:
3,3'-Thiobispropanoic acid
IUPAC Name:
3,3'-Thiobispropanoic acid
Specific details on test material used for the study:
14]Thiodipropionate, specific activity 1.71 mCi/mmol
Radiolabelling:
yes

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: 215 - 325g
- Fasting period before study: yes
- Housing: in glass metabolism cages, for collection of urine, feces and exhaled carbon dioxide
- Individual metabolism cages: yes

Administration / exposure

Route of administration:
other: oral: gavage / feed
Vehicle:
other: ethanol: water 1:1
Duration and frequency of treatment / exposure:
single treatment
Doses / concentrationsopen allclose all
Dose / conc.:
3.1 mg/kg bw/day
Remarks:
(gavage)
Dose / conc.:
551 mg/kg bw/day
Remarks:
(gavage)
Dose / conc.:
572 mg/kg bw/day
Remarks:
(gavage)
Dose / conc.:
650 mg/kg bw/day
Remarks:
(gavage)
Dose / conc.:
241 mg/kg bw/day
Remarks:
(feed)
No. of animals per sex per dose / concentration:
1
Control animals:
no
Positive control reference chemical:
no

Results and discussion

Main ADME resultsopen allclose all
Type:
absorption
Results:
Complete absorption of thiodipropionic acid
Type:
excretion
Results:
as acid labile conjugate of thiodipropionic acid or free thiodipropionic acid, >90% in urine, less than 5% as carbon dioxide

Metabolite characterisation studies

Metabolites identified:
yes
Details on metabolites:
Dithiopropionic acid is recovered as a acid-labile conjugate if given at a dose of 3.1 mg/kg bw. At 650 mg/kg bw, the major fraction is recovered in the non-conjugated form. The acid-labile conjugate is not or only to a small fraction a glucuronidate. Further identification was not performed.

Any other information on results incl. tables

Cumulative elimination in the rat after gavage and feed application

Rat no.

dose [mg/kg bw]

dose [μCi]

gavage/feed

time [days]

Elimination

urine

carbon dioxide

feces

total

1

3.1

9.3

gavage 

4

90.10%

3.10%

0.50%

93.60%

2

650

9

gavage 

4

78.10%

8.20%

0.50%

86.80%

3

572

9.3

gavage 

4

84.50%

2.80%

0.90%

88.40%

4

551

8.9

gavage 

8

88.50%

7.20%

0.20%

95.90%

5

241

8.2

feed

34

87.40%

3.30%

0.10%

90.70%

 

Applicant's summary and conclusion

Conclusions:
No bioaccumulation potential based on study results.