Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: study conducted by GLP accredited lab according to recognised guideline method. Data provided by ECHA from migrated NONS file. Litle detail available.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1990

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: Annex V
GLP compliance:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Copper(II) methanesulfonate
EC Number:
405-400-2
EC Name:
Copper(II) methanesulfonate
Cas Number:
54253-62-2
Molecular formula:
C2H6CuO6S2
IUPAC Name:
copper(2+) dimethanesulfonate
Test material form:
not specified

Test animals

Species:
rabbit
Strain:
New Zealand White

Test system

Type of coverage:
semiocclusive
Vehicle:
water
Amount / concentration applied:
0.5g
Duration of treatment / exposure:
4h
Observation period:
7 days
Number of animals:
3

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
other: max value
Time point:
other: 72h
Max. score:
2
Reversibility:
fully reversible within: 7 days
Remarks on result:
other: no additional information provided
Irritation parameter:
edema score
Time point:
other: 48h
Max. score:
2
Reversibility:
fully reversible within: 7 days
Remarks on result:
other: no additional information provided

Any other information on results incl. tables

Erythema/eschar persisted for 72h and had a maximum score of 2.

Oedema persisted for 48h and had a maximum score of 2.

All changes were reversible within 7 days.

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
the substance is not a skin irritant