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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1975
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
comparable to guideline study with acceptable restrictions

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1975
Report date:
1975

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
GLP compliance:
no
Remarks:
study was conducted prior to the GLP legislation
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
3-mercaptopropane-1,2-diol
EC Number:
202-495-0
EC Name:
3-mercaptopropane-1,2-diol
Cas Number:
96-27-5
Molecular formula:
C3H8O2S
IUPAC Name:
3-sulfanylpropane-1,2-diol
Test material form:
liquid: viscous
Specific details on test material used for the study:
Batch 297-1382

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female
Details on test animals or test system and environmental conditions:
BW: 200-300 g

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
unchanged (no vehicle)
Remarks:
except for 0.05 and 0.25 mg/kg dose, which were administered as 1% solution in water
Details on oral exposure:
animals were fasted for 24 h before dosing
Doses:
0.05, 0.25, 0.50, 1.00, 5.00 mL/kg bw
62, 312, 623, 1247, 6234 mg/kg bw (using density of 1.25 g/mL)
No. of animals per sex per dose:
5 (3m / 2f)
Control animals:
no
Details on study design:
- Duration of observation period following administration: 14 days
Statistics:
Probit analysis (Miller & Tainter, Proc Soc Biol Med 57, 261 (1944))

Results and discussion

Effect levelsopen allclose all
Sex:
male/female
Dose descriptor:
LD50
Effect level:
0.52 mL/kg bw
Based on:
test mat.
Key result
Sex:
male/female
Dose descriptor:
LD50
Effect level:
648 mg/kg bw
Based on:
test mat.
Mortality:
mg/kg bw dead total mortality
62 0 5 0%
312 0 5 0%
623 2 5 40%
1247 5 5 100%
6234 5 5 100%
Clinical signs:
other: not reported
Gross pathology:
not reported

Applicant's summary and conclusion

Interpretation of results:
Category 4 based on GHS criteria
Conclusions:
Based on an LD50 of 648 mg/kg bw, monothioglycerol should be classified as Acute Tox 4 - H302: Harmful if swallowed