Name: Prednisolone Acetate
Brand: Mikromol
SKU: MM0194.00-0250

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Product Overview

Product Code

MM0194.00-0250

CAS Number

52-21-1

EP Description

Hydrocortisone Acetate Impurity C, Methylprednisolone Acetate Impurity E, Prednisolone Impurity C, Prednisone Impurity L

Product Format

Neat

Molecular Formula

C23 H30 O6

Molecular Weight

402.48

API Family

Prednisolone, Methylprednisolone Acetate, Prednisone, Hydrocortisone Acetate, Prednisolone Acetate

Product Categories

API Reference Standards & Research Materials, Impurity Reference Materials , Cardiac drugs and beta blockers, Respiratory drugs, Steroids and derivatives, Mikromol

Product Type

Impurity, API

Drug Type

Glucocorticoids

Documentation

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Product Information

Analyte Data

Analyte Name

Prednisolone Acetate

CAS Number

52-21-1

Molecular Formula

C23 H30 O6

Molecular Weight

402.48

Accurate Mass

402.2042

SMILES

CC(=O)OCC(=O)[C@@]1(O)CC[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@H]3[C@@H](O)C[C@]12C

InChI

InChI=1S/C23H30O6/c1-13(24)29-12-19(27)23(28)9-7-17-16-5-4-14-10-15(25)6-8-21(14,2)20(16)18(26)11-22(17,23)3/h6,8,10,16-18,20,26,28H,4-5,7,9,11-12H2,1-3H3/t16-,17-,18-,20+,21-,22-,23-/m0/s1

IUPAC

[2-[(8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-10,13-dimethyl-3-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-yl]-2-oxoethyl] acetate

Product Data

Storage Temperature

+5°C

Shipping Temperature

Room Temperature

Country of Origin

GERMANY

Product Type

API; Impurity

Product Format

Neat

Impurity Type

Degradation product; Intermediate

API Family

Prednisolone; Methylprednisolone Acetate; Prednisone; Hydrocortisone Acetate; Prednisolone Acetate

Product citations

Why work with us?

At Mikromol, we go beyond the standard to produce high-quality, globally relevant pharmaceutical reference standards that you can trust. For more than 25 years we have delivered quality reference standards for analytical development, method validation, and stability and release testing to customers around the world.

Alongside a market-leading product range accredited to ISO 17034, the majority of our 5,000+ impurity, API and excipient reference standards are manufactured under ISO/IEC 17025 and accompanied by an extensive Certificate of Analysis.

With unparalleled depth of knowledge, decades of manufacturing experience and unrivalled scientific excellence, we work tirelessly to help you create ever better, safer medicines.

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