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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
short-term repeated dose toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study
Justification for type of information:
A study according to OECD TG 422 is commissioned and will be finished in Q4 2022. Results will be reported as soon as available

Data source

Reference
Title:
Unnamed
Year:
2022

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 422 (Combined Repeated Dose Toxicity Study with the Reproduction / Developmental Toxicity Screening Test)
Deviations:
no
GLP compliance:
yes (incl. QA statement)

Test material

Constituent 1
Chemical structure
Reference substance name:
2-ethylhexyl 3-mercaptopropionate
EC Number:
256-589-1
EC Name:
2-ethylhexyl 3-mercaptopropionate
Cas Number:
50448-95-8
Molecular formula:
C11H22O2S
IUPAC Name:
2-ethylhexyl 3-sulfanylpropanoate

Test animals

Species:
rat
Strain:
Wistar

Administration / exposure

Route of administration:
oral: gavage
Control animals:
yes, concurrent vehicle

Results and discussion

Effect levels

Dose descriptor:
NOAEL
Effect level:
0 mg/kg bw/day (actual dose received)
Sex:
male/female
Basis for effect level:
other:
Remarks on result:
other: results will be reported as soon as the study is finalized

Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion