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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: oral

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Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Test procedure in accordance with national standard methods with acceptable restrictions

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1977
Report date:
1977

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Undiluted propane-2-thiol was administered by stomach tube to 2 groups of 6 rats. Surviving animals were observed for 7 days
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Propane-2-thiol
EC Number:
200-861-4
EC Name:
Propane-2-thiol
Cas Number:
75-33-2
Molecular formula:
C3H8S
IUPAC Name:
propane-2-thiol
Test material form:
liquid
Details on test material:
No details available

Test animals

Species:
rat
Strain:
other: WBS/W
Sex:
male
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: 200 g

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
unchanged (no vehicle)
Doses:
2000 and 5000 mg/kg
No. of animals per sex per dose:
6
Control animals:
no
Details on study design:
- Duration of observation period following administration: 7 days
- Frequency of observations and weighing: no data
- Necropsy of survivors performed: yes
Statistics:
Not appropriate

Results and discussion

Effect levelsopen allclose all
Sex:
male
Dose descriptor:
LD50
Effect level:
> 2 000 - < 5 000 mg/kg bw
Based on:
test mat.
Sex:
male
Dose descriptor:
approximate LD50
Effect level:
3 730 mg/kg bw
Based on:
test mat.
Remarks on result:
other: Calculated with the standard probit method
Mortality:
0/6 at 2000 mg/kg.
6/6 at 5000 mg/kg (time for death (h): 3, >4, >4, >4, 20, 96)
Clinical signs:
other: Muscular hypothonia, motor ataxia, loss of righting reflex, recovery of righting reflex.
Gross pathology:
Findings were not significant

Applicant's summary and conclusion

Interpretation of results:
Category 5 based on GHS criteria
Conclusions:
The LD50 was between 2000 and 5000 mg/kg bw.
Executive summary:

In a pre-guideline study, male WBS/W rats were dosed with iso-propyl mercaptan at doses of 2000 and 5000 mg/kg bw and followed for 7 days. Mortality was 0 and 5 of the 6 animals per group, respectively.  Signs included hypotonia, ataxia, loss of righting reflex and body weight loss. Recovery was complete in 4 days. The LD50 was between 2000 and 5000 mg/kg bw and approximately 3730 mg/kg bw when calculated with the standard probit method .