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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: dermal

Currently viewing:

Administrative data

Endpoint:
acute toxicity: dermal
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
1990
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: The study was conducted according to a protocol equivalent to current OECD guideline, but not in compliance with GLP.

Data source

Reference
Reference Type:
publication
Title:
A simple method for screening assessment of acute toxicity of chemicals
Author:
Yamanaka
Year:
1990
Bibliographic source:
Arch. Toxicol. 64: 262-268

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: Toxicity Guidelines of Japan (Ministry of Health and Welfare in Japan 1984)
GLP compliance:
not specified
Test type:
fixed dose procedure
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Ammonium sulphate
EC Number:
231-984-1
EC Name:
Ammonium sulphate
Cas Number:
7783-20-2
Molecular formula:
N2H8SO4
IUPAC Name:
diammonium sulfate
Constituent 2
Reference substance name:
Ammonium sulfate
IUPAC Name:
Ammonium sulfate
Details on test material:
- Name of test material (as cited in study report): Ammonium sulfate CAS 7783-20-2
- Molecular formula (if other than submission substance):
- Molecular weight (if other than submission substance):
- Smiles notation (if other than submission substance):
- InChl (if other than submission substance):
- Structural formula attached as image file (if other than submission substance): see Fig.
- Substance type:
- Physical state:
- Analytical purity:
- Impurities (identity and concentrations):
- Composition of test material, percentage of components:
- Isomers composition:
- Purity test date:
- Lot/batch No.:
- Expiration date of the lot/batch:
- Radiochemical purity (if radiolabelling):
- Specific activity (if radiolabelling):
- Locations of the label (if radiolabelling):
- Expiration date of radiochemical substance (if radiolabelling):
- Stability under test conditions:
- Storage condition of test material:
- Other:

Test animals

Species:
other: rats and mice
Strain:
other: rats: Wistar, mice: ddy
Sex:
male/female

Administration / exposure

Type of coverage:
open
Vehicle:
not specified
Duration of exposure:
Single application
Doses:
2000, 200, 20 mg/kg
No. of animals per sex per dose:
3 rats and 3 mice of both sexes
Control animals:
no

Results and discussion

Effect levelsopen allclose all
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Remarks on result:
other: rat
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Remarks on result:
other: mouse

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The LD50 values of >2000 mg/kg bw in rat and >2000 mg/kg bw in mice are reported in a published study conducted according to a protocol similar to current guideline, but not in compliance with GLP.