Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: dermal
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
supporting study
Reliability:
3 (not reliable)

Data source

Reference
Reference Type:
other: read across with Pravastatin sodium
Title:
Unnamed
Year:
2012
Report date:
2012

Materials and methods

GLP compliance:
not specified

Test material

Constituent 1
Reference substance name:
Pravastatin sodium
IUPAC Name:
Pravastatin sodium

Results and discussion

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
not classified
Executive summary:

Pravastatin sodium LD50, dermal 3172 mg/kg (rat) which is more than the classification limit 2000 mg/kg. ( read-across)