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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
Mar - May 2006
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2006
Report date:
2006

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
Version / remarks:
2001
Deviations:
no
GLP compliance:
yes (incl. QA statement)
Test type:
acute toxic class method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
4-{[(2-methoxyphenyl)formamido]sulfonyl}benzoyl chloride
EC Number:
617-251-2
Cas Number:
816431-72-8
Molecular formula:
C15H12ClNO5S
IUPAC Name:
4-{[(2-methoxyphenyl)formamido]sulfonyl}benzoyl chloride
Test material form:
solid: bulk

Test animals

Species:
rat
Strain:
Wistar
Sex:
female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
other: tap water with 2% Cremophor EL
Doses:
2000 mg/kg body weight (bw)
No. of animals per sex per dose:
3 female rats
Control animals:
no
Details on study design:
dosing of 3 additional animals with the same dose (2000 mg/kg)

Results and discussion

Effect levels
Key result
Sex:
female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
test mat.
Mortality:
none
Gross pathology:
no findings

Any other information on results incl. tables

A dose of 2000 mg/kg body weight was tolerated by female rats without mortalities,

clinical signs, effects on weight gain and gross pathological findings.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
the test item is of low acute oral toxicity.
Executive summary:

The single oral administration of the test substance (Amidchlorid, CAS 816431-72-8) to female rats at a dose of 2000 mg/kg was tolerated without any mortality. No compound-related clinical signs were observed and there were no macroscopic pathological signs.


The LD50 acute oral toxicity of Amidchlorid (CAS 816431-72-8) in rats is therefore above 2000 mg/kg body weight.