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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
key study
Study period:
2012
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2012

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
EPA OPPTS 870.1100 (Acute Oral Toxicity)
GLP compliance:
yes
Test type:
up-and-down procedure
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Allyl isothiocyanate
EC Number:
200-309-2
EC Name:
Allyl isothiocyanate
Cas Number:
57-06-7
Molecular formula:
C4H5NS
IUPAC Name:
3-isothiocyanatoprop-1-ene
Test material form:
liquid

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
female

Administration / exposure

Route of administration:
oral: gavage
Doses:
175, 55, 175, 550, 2000, 550, 2000, 550 mg/kg bw
No. of animals per sex per dose:
8

Results and discussion

Effect levels
Key result
Sex:
female
Dose descriptor:
LD50
Effect level:
425.4 mg/kg bw

Applicant's summary and conclusion

Interpretation of results:
Category 4 based on GHS criteria
Conclusions:
Under the conditions of this study, the acute LD50 of IR9804 is estimated to be 425.4 mg/kg bw (based on maximum likelihood and an assumed sigma of 0.5) in female rats with a 95% PL (Profile-Likelihood based confidence interval) Confidence interval of 0 mg/kg (lower) to greater than 20,000 mg/kg (upper).