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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1992

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
GLP compliance:
yes
Test type:
acute toxic class method

Test material

Constituent 1
Chemical structure
Reference substance name:
3-[(2E)-2-benzylidenehydrazino]-4-sulfonatobenzoate, disodium salt
EC Number:
601-577-7
Cas Number:
118969-29-2
Molecular formula:
C14H10N2Na2O5S
IUPAC Name:
3-[(2E)-2-benzylidenehydrazino]-4-sulfonatobenzoate, disodium salt
Test material form:
other: solid

Test animals

Species:
rat
Strain:
other: Tif:RAI f (SPF)
Sex:
male/female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
water
Remarks:
distilled
Doses:
2000 mg/kg
No. of animals per sex per dose:
5 males
5 females

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
2 000 mg/kg bw

Any other information on results incl. tables

Observations

Piloerection, hunched posture, and dyspnea were seen, being common symptoms in acute tests. Additionally, reduced locomotor activity and diarrhea was observed in all animals. The animals recovered within 6 days. At necropsy, no deviations from normal morphology were found in all animals.

Applicant's summary and conclusion

Conclusions:
No adverse effect observed with 2000mg/kg bw
Executive summary:

No adverse effect observed with 2000mg/kg bw