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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: study conducted according to accepted scientific criteria

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1971
Report date:
1971

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Deviations:
not specified
Principles of method if other than guideline:
15 male rats per dose were dosed by gavage. Symptoms and deaths were recorded.
GLP compliance:
no
Test type:
standard acute method

Test material

Constituent 1
Chemical structure
Reference substance name:
N-phenyl-N-[(trichloromethyl)thio]benzenesulphonamide
EC Number:
218-915-0
EC Name:
N-phenyl-N-[(trichloromethyl)thio]benzenesulphonamide
Cas Number:
2280-49-1
Molecular formula:
C13H10Cl3NO2S2
IUPAC Name:
N-phenyl-N-[(trichloromethyl)sulfanyl]benzenesulfonamide
Test material form:
other: solid
Details on test material:
no data on purity; the compound tested was 98% N-Phenyi-N-[(trichloromethyl)thio]benzenesulphonamide and 2% magnesium carbonate.

Test animals

Species:
rat
Strain:
Wistar
Sex:
male

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
other: aceton:oil 1:10
Doses:
100, 250, 500, 1000, 2500 g/kg bw
No. of animals per sex per dose:
15 males per group
Control animals:
no

Results and discussion

Effect levels
Sex:
male
Dose descriptor:
LD0
Effect level:
> 2 500 mg/kg bw
Based on:
test mat.

Any other information on results incl. tables

Dose level; No of deaths/ no of animals with symptoms/no of deaths.

100; 0/0/15

250; 0/15/15; Animals were free of symptoms on day 2

500;0/15/15; Animals were free of symptoms on day 2

1000; 0/15/15; Animals were free of symptoms on day 4

2500; 0/15/15; Animals were free of symptoms on day 4

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Executive summary:

No animal died even at the highest dose 2500 mg/kg.