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Methylprednisolone Acetate EP Impurity F



Chemical Properties

CAT No. :

CS-EO-00458
Parent API : Methylprednisolone
CAS Registry No. : NA
Category : Impurity Standards
Molecular Weight: 398.5
Molecular Formula : C24H30O5
Controlled Substance : NO
Synonyms : 2-oxo-2-((6S,8S,9S,10R,13S,14S,17S)-6,10,13-trimethyl-3,11-dioxo-6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-17-yl)ethyl acetate ; 6α-methyl-3,11,20-trioxopregna-1,4-dien-21-yl acetate,
Custom Duty : Applicable
Documents:  View Sample COA   View Sample MSDS
Port of Loading : Canada
Expected Dispatch : 2-3 Weeks
Taxes : Not Applicable
Refund Policy : 30-days money back


More information about Methylprednisolone Acetate EP Impurity F


Methylprednisolone (Depo-Medrol, Medrol, Solu-Medrol) is a synthetic glucocorticoid, primarily prescribed for its anti-inflammatory and immunosuppressive effects. It is either used at low doses for chronic illnesses or used concomitantly at high doses during acute flares. Methylprednisolone and its derivatives can be administered orally or parenterally.

Regardless of route of administration, methylprednisolone integrates systemically as exhibited by its effectiveness to quickly reduce inflammation during acute flares. It is associated with many adverse reactions that require tapering off the drug as soon as the disease is under control. Serious side effects include iatrogenic Cushing's Syndrome, hypertension, osteoporosis, diabetes, infection, and skin atrophy.

Chemically, methylprednisolone is a synthetic pregnane steroid hormone derived from hydrocortisone and prednisolone. It belongs to a class of synthetic glucocorticoids and more generally, corticosteroids. It acts as a mineralocorticoid and glucocorticoid receptor agonist. In comparison to other exogenous glucocorticoids, methylprednisolone has a higher affinity to glucocorticoid receptors than to mineralocorticoid receptors.

Glucocorticoid's name was derived after the discovery of their involvement in regulating carbohydrate metabolism. The cellular functions of glucocorticoids, such as methylprednisolone, are now understood to regulate homeostasis, metabolism, development, cognition, and inflammation. They play a critical role in adapting and responding to environmental, physical and emotional stress.

Methylprednisolone was first synthesized and manufactured by The Upjohn Company (now Pfizer) and FDA approved in the United States in October 1957. In 2019, it was the 161st most commonly prescribed medication in the United States, with more than 3\u00a0million prescriptions. Methylprednisolone is also on the World Health Organization's List of Essential Medicines for its effects against lymphoid leukemia.


This page contains information about Methylprednisolone Acetate EP Impurity F , Methylprednisolone Acetate EP Impurity F cas, Methylprednisolone Acetate EP Impurity F synthesis, Methylprednisolone Acetate EP Impurity F suppliers

What is Methylprednisolone Acetate EP Impurity F ?
Methylprednisolone Acetate EP Impurity F falls under Impurity Standards of Methylprednisolone.
What is the CAS Number of Methylprednisolone Acetate EP Impurity F?
The CAS Number of Methylprednisolone Acetate EP Impurity F is NA
Who are the suppliers of Methylprednisolone Acetate EP Impurity F?
CLEARSYNTH is a worldwide supplier of Methylprednisolone Acetate EP Impurity F

Related compounds of Methylprednisolone Acetate EP Impurity F

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