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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: oral
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Data from secondary source

Data source

Reference
Reference Type:
other: MSDS
Title:
Unnamed
Year:
2010

Materials and methods

Principles of method if other than guideline:
Method unknown
GLP compliance:
not specified

Test material

Constituent 1
Chemical structure
Reference substance name:
11β,17,21-trihydroxypregna-1,4-diene-3,20-dione 21-methanesulphonate
EC Number:
252-549-2
EC Name:
11β,17,21-trihydroxypregna-1,4-diene-3,20-dione 21-methanesulphonate
Cas Number:
35410-28-7
Molecular formula:
C22H30O7S
IUPAC Name:
2-[(1R,3aS,3bS,9aR,9bS,10S,11aS)-1,10-dihydroxy-9a,11a-dimethyl-7-oxo-1H,2H,3H,3aH,3bH,4H,5H,7H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-1-yl]-2-oxoethyl methanesulfonate
Constituent 2
Reference substance name:
Prednisolone mesylate
IUPAC Name:
Prednisolone mesylate

Test animals

Species:
rat

Administration / exposure

Route of administration:
oral: unspecified

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
With a LD50 above 2000 mg/kg, the substance is not toxic via oral route.