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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: other routes
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
other: only orientating information about acute toxicity
Rationale for reliability incl. deficiencies:
other: only orientating information

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1961
Report date:
1961

Materials and methods

Principles of method if other than guideline:
according to BASF-internal standard
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Sodium 3-nitrobenzenesulphonate
EC Number:
204-857-3
EC Name:
Sodium 3-nitrobenzenesulphonate
Cas Number:
127-68-4
Molecular formula:
C6H5NO5S.Na
IUPAC Name:
sodium 3-nitrobenzenesulphonate
Test material form:
solid: particulate/powder
Remarks:
migrated information: powder
Details on test material:
Name of the test substance used in the study report: Ludigol
Purity: 95%

Test animals

Species:
mouse
Strain:
other: Tuebinger
Sex:
male/female

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
water
Doses:
4-30% solution (= 400, 800, 1600 or 3200 mg/kg)
No. of animals per sex per dose:
10
Control animals:
not specified

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
ca. 2 300 mg/kg bw
Mortality:
400, 800 and 1600 mg/kg: no animal died
3200 mg/kg: 9/10 males and 10/10 females after 24 hours
Clinical signs:
As a reaction to the high dose (3200 mg/kg b.w.), the animals showed strong tonic convulsion and dyspnea. Some mice died within 24 h.
Gross pathology:
Gross pathological examination of the deceased animals revealed redness of the small intestine at the site of injection. The animals that were sacrificed at the end of the observation period were without pathological findings.

Applicant's summary and conclusion