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Pharmacopeial Impurities (EP / USP / BP)

Hydrocortisone Acetate EP Impurity F

Reference StandardAvailable on request

Hydrocortisone Acetate EP Impurity F (CAS 1250-97-1) supplier Zemixal: C23H32O6, COA and SDS with every lot, worldwide shipping.

Pack sizes
Hydrocortisone Acetate EP Impurity F chemical structure
CAS number1250-97-1
FormulaC23H32O6
Molar mass404.5 g/mol
Physical formSolid
HS code38229090
InChIKeyALEXXDVDDISNDU-VVCDUNCFSA-N
IUPAC name[2-[(8S,9S,10R,11R,13S,14S,17R)-11,17-dihydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-oxoethyl] acetate

About Hydrocortisone Acetate EP Impurity F

Hydrocortisone Acetate EP Impurity F belongs to the Hydrocortisone reference-standard family in the Zemixal catalogue. For your records (Reference Standard), the material is defined by CAS 1250-97-1, formula C23H32O6 and molar mass 404.5 g/mol. It is handled as a solid.

Use cases we see most often

  • Pharmacopeial method verification
  • Impurity profiling
  • QC release testing
  • ANDA / DMF filings

Order it in 10 mg, 25 mg, 50 mg and 100 mg packs or ask for a bulk quotation. Each lot travels with a certificate of analysis with characterisation data. Add it to your quote list and our team replies with price, lead time and shipping options within one business day.

Reference standards for Hydrocortisone

See every impurity, metabolite and related compound we list for this API.

Hydrocortisone standards

Typical uses

  • Pharmacopeial method verification
  • Impurity profiling
  • QC release testing
  • ANDA / DMF filings

Applications

Pharmaceutical Manufacturing and QCResearch Labs and Universities

Grade guides

Ph. Eur. Grade (European Pharmacopoeia)

Specifications and identifiers

Specifications of Hydrocortisone Acetate EP Impurity F
Product nameHydrocortisone Acetate EP Impurity F
Catalogue numberZX-025018
CAS number1250-97-1
IUPAC name[2-[(8S,9S,10R,11R,13S,14S,17R)-11,17-dihydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-oxoethyl] acetate
Molecular formulaC23H32O6
Molar mass404.5 g/mol
Exact mass404.2199
GradeReference Standard
Physical formSolid
XLogP32.2
H-bond donors / acceptors2 / 6
Topological polar surface area101 Ų
HS code38229090
InChIKeyALEXXDVDDISNDU-VVCDUNCFSA-N
SMILESCC(=O)OCC(=O)[C@]1(CC[C@@H]2[C@@]1(C[C@H]([C@H]3[C@H]2CCC4=CC(=O)CC[C@]34C)O)C)O
PubChem CID102056
SynonymsEpi Hydrocortisone 21-Acetate, Hydrocortisone Acetate - Impurity F, epi-Hydrocortisone acetate, (11alpha)-21-(Acetyloxy)-11,17-dihydroxypregn-4-ene-3,20-dione, 11alpha,17,21-Trihydroxypregn-4-ene-3,20-dione 21-acetate, Epihydrocortisone 21-acetate, 11a,17,21-Trihydroxyprogesterone 21-acetate, 11alpha,17-Dihydroxy-3,20-dioxopregn-4-en-21-yl acetate, (11a)-21-(Acetyloxy)-11,17-dihydroxypregn-4-ene-3,20-dione

Lot values are stated on the batch certificate of analysis. Ask for a typical COA with your quotation.

Safety and GHS hazards

No GHS classification is on file for this item. Handle it as an unknown laboratory chemical and request the SDS with your quotation.

Pack sizes

Pack sizes of Hydrocortisone Acetate EP Impurity F
10 mgQuoted on request
25 mgQuoted on request
50 mgQuoted on request
100 mgQuoted on request

Need a different size? Bulk drums and custom packing are quoted on request through the quote form on this page.

Questions about Hydrocortisone Acetate EP Impurity F

Which CAS number identifies Hydrocortisone Acetate EP Impurity F?
Hydrocortisone Acetate EP Impurity F is registered under CAS 1250-97-1. You may also see it listed as Epi Hydrocortisone 21-Acetate, Hydrocortisone Acetate - Impurity F, epi-Hydrocortisone acetate. Our catalogue number for this item is ZX-025018.
What are the formula and molar mass of Hydrocortisone Acetate EP Impurity F?
For Hydrocortisone Acetate EP Impurity F, its formula is C23H32O6 and its molar mass is 404.5 g/mol. The systematic (IUPAC) name is [2-[(8S,9S,10R,11R,13S,14S,17R)-11,17-dihydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-oxoethyl] acetate. InChIKey ALEXXDVDDISNDU-VVCDUNCFSA-N lets you match it in any structure database.
How is Hydrocortisone Acetate EP Impurity F used in pharmaceutical QC?
Hydrocortisone Acetate EP Impurity F is a characterised reference material linked to Hydrocortisone. Laboratories use it to identify and quantify this impurity during method development and validation, stability work, batch release testing and regulatory submissions.
What grade and pack sizes are available for Hydrocortisone Acetate EP Impurity F?
This listing is Reference Standard grade. Standard packs are 10 mg, 25 mg, 50 mg, 100 mg. Larger quantities and custom packing can be quoted on request.
Which documents come with Hydrocortisone Acetate EP Impurity F?
Each lot ships with a batch certificate of analysis and a 16-section GHS safety data sheet. A typical COA or specification sheet can be shared with the quotation before you order.
Can Zemixal ship Hydrocortisone Acetate EP Impurity F to my country?
Yes. Hydrocortisone Acetate EP Impurity F ships worldwide by express courier, air cargo or sea freight, quoted on the Incoterm you prefer, with full export documents.

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