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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
February to March 1978
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Comparable to guideline study with acceptable restrictions

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1978
Report date:
1978

Materials and methods

Principles of method if other than guideline:
Internal Guideline Hoechst AG
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2-[(p-aminophenyl)sulphonyl]ethyl hydrogensulphate
EC Number:
219-669-7
EC Name:
2-[(p-aminophenyl)sulphonyl]ethyl hydrogensulphate
Cas Number:
2494-89-5
Molecular formula:
C8H11NO6S2
IUPAC Name:
[2-(4-aminobenzenesulfonyl)ethoxy]sulfonic acid
Details on test material:
- Name of test material (as cited in study report): p-Base-Ester

Test animals

Species:
rat
Strain:
Wistar
Sex:
female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
water
Details on oral exposure:
VEHICLE
- Concentration in vehicle: 25g / 100 ml
- Amount of vehicle (if gavage): 5000 mg/kg bw
- Justification for choice of vehicle: provide homogeneous suspension
Doses:
5 g/kg body weight
No. of animals per sex per dose:
10 females
Control animals:
no
Details on study design:
Weight range at start: 164 to 170 g
Test substance concentration: 25%
Withhold of food 16 hours prior to test substance administration
Observation period: 7 days after test substance administration
Statistics:
Exact determination of LD50 not possible - only one of ten rats died --> LD50 >5000 mg/kg

Results and discussion

Effect levels
Sex:
female
Dose descriptor:
LD50
Effect level:
> 5 000 mg/kg bw
Mortality:
one of 10 rats at 5000 mg/kg died
Gross pathology:
no data
Other findings:
no data

Applicant's summary and conclusion

Interpretation of results:
practically nontoxic
Remarks:
Migrated information Criteria used for interpretation of results: expert judgment
Conclusions:
LD50 above 5000 mg/kg bw.
No classification required.