Methylprednisolone

Methylprednisolone structural formula

CAS Number83-43-2
Molecular FormulaC22H30O5
Molecular Weight374.477
InChI KeyVHRSUDSXCMQTMA-PJHHCJLFSA-N
LogP1.86
Synonyms
  • Methylprednisolone
  • (6alpha,11beta)-11,17,21-Trihydroxy-6-methylpregna-1,4-diene-3,20-dione
  • Pregna-1,4-diene-3,20-dione, 11,17,21-trihydroxy-6-methyl-, (6alpha,11beta)-
  • 83-43-2
  • MP
  • MPL
  • 4-08-00-03498
  • Pregna-1,4-diene-3,20-dione, 11,17,21-trihydroxy-6-methyl-, (6?,11?)-
  • 11?,17,21-Trihydroxy-6?-methylpregna-1,4-diene-3,20-dione
  • 11?,17?,21-Trihydroxy-6?-methyl-1,4-pregnadiene-3,20-dione
  • 6?-Methyl-11?,17?,21?-trihydroxy-1,4-pregnadiene-3,20-dione
  • 6-?-Methylprednisolone
  • 6?-Methylprednisolone
  • A-Methapred
  • Besonia
  • Dopomedrol
  • Medesone
  • Medorol
  • Medralone
  • Medrate
  • Medrone
  • Metastab
  • Methylprednisolon
  • Methypred
  • Metilbetasone
  • metilprednisolona
  • Metipred
  • Metrisone
  • Moderin
  • M-Prednisol
  • Noretona
  • NSC 19987
  • Pregna-1,4-diene-3,20-dione, 11?,17,21-trihydroxy-6?-methyl-
  • Promacortine
  • Suprametil
  • Urbason
  • Urbasone
  • Urbazone
  • Wyacort
  • ?1-6?-Methylhydrocortisone
  • Artisone-wyeth
  • BRN 2340300
  • EINECS 201-476-4
  • Medrol adt pak
  • Medrol dosepak
  • Mesopren
  • Methyleneprednisolone
  • delta(1)-6alpha-Methylhydrocortisone
  • 6-alpha-Methylprednisolone
  • 6alpha-Methylprednisolone
  • NSC-19987
  • Prednisolone, methyl-
  • Prednisolone, 6alpha-methyl-
  • Pregna-1,4-diene-3,20-dione, 11beta,17,21-trihydroxy-6alpha-methyl-
  • delta(sup 1)-6-alpha-Methylhydrocortisone
  • 11beta,17alpha,21-Trihydroxy-6alpha-methyl-1,4-pregnadiene-3,20-dione
  • 11-beta,17,21-Trihydroxy-6-alpha-methylpregna-1,4-diene-3,20-dione
  • Esametone
  • Firmacort
  • Medixon
  • Metrocort
  • Metysolon
  • Nirypan
  • Predni N Tablinen
  • Prednol- L
  • Reactenol
  • Sieropresol
  • Solomet
  • Summicort;
  • Methylprednisolonum
  • Metilprednisolone
  • UNII-X4W7ZR7023
  • (6alpha,11beta)-11,17,21-trihydroxy-6-methylpregna-1,4-diene-3,20-dione
  • 1-dehydro-6alpha-methylhydrocortisone
  • 6alpha-methyl-11beta,17alpha,21-triol-1,4-pregnadiene-3,20-dione
  • Delta(1)-6alpha-methylhydrocortisone
  • 121673-01-6
  • 570-35-4

Applications:

HPLC Method for Analysis of  Methylprednisolone on Primesep B Column

January 29, 2024

HPLC Method for Analysis of Methylprednisolone on Primesep B by SIELC Technologies

HPLC Method for Analysis of Methylprednisolone on Primesep B Column by SIELC Technologies


 High Performance Liquid Chromatography (HPLC) Method for Analysis of Methylprednisolone

Methylprednisolone is a synthetic corticosteroid with anti-inflammatory and immunosuppressive properties. It is a derivative of prednisolone and, like prednisone, belongs to the class of glucocorticoids. Methylprednisolone is used for various medical conditions to reduce inflammation and modify the immune response.

 Methylprednisolone can be retained, and analyzed using a Primesep B mixed-mode stationary phase column. The analysis utilizes an isocratic method with a simple mobile phase consisting of water, acetonitrile (MeCN), and sulfuric acid as a buffer. Detection is achieved using UV 245 nm

ColumnPrimesep B, 4.6 x 150 mm, 5 µm, 100 A
Mobile PhaseMeCN/H2O – 35%
BufferH2SO4 – 0.1%
Flow Rate1.0 ml/min
DetectionUV 245 nm

Class of Compounds
Corticosteroids
Analyzing CompoundsMethylprednisolone

Application Column

Primesep B

Column Diameter: 4.6 mm
Column Length: 150 mm
Particle Size: 5 µm
Pore Size: 100 A

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Application Analytes:
Methylprednisolone

Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

HPLC Method for Separating Corticosteroids such as Prednisone, Prednisolone and Methylprednisolone on Primesep B Column

January 29, 2024

HPLC Method for Prednisone, Prednisolone, Methylprednisolone on Primesep B by SIELC Technologies

HPLC method for separating corticosteroids such as Prednisone, Prednisolone, and Methylprednisolone on Primesep B Column
HPLC Method for Analysis of Prednisone, Prednisolone, Methylprednisolone on Primesep B Column by SIELC Technologies


 High Performance Liquid Chromatography (HPLC) Method for Analysis of Prednisone, Prednisolone, Methylprednisolone

All three compounds have potent anti-inflammatory effects, making them valuable in treating conditions where inflammation plays a role.

Prednisone:

  • Mechanism of Action: Prednisone is a synthetic corticosteroid that mimics the action of cortisol, a natural steroid produced by the adrenal glands. It primarily exerts its effects by binding to glucocorticoid receptors and regulating gene expression.
  • Medical Uses: It is commonly used to treat inflammatory conditions, autoimmune disorders, allergic reactions, and certain cancers.

Prednisolone:

  • Derived Form: Prednisolone is the active form of prednisone. When prednisone is ingested, the liver converts it into prednisolone.
  • Mechanism of Action: Similar to prednisone, it has anti-inflammatory and immunosuppressive properties.

Methylprednisolone:

  • Potency: Methylprednisolone is considered to be more potent than prednisone.
  • Medical Uses: It is used in various conditions, including severe allergic reactions, inflammatory conditions, and as a part of immunosuppressive regimens.

Corticosteroids can be retained, separated, and analyzed using a Primesep B mixed-mode stationary phase column. The analysis utilizes an isocratic method with a simple mobile phase consisting of water, acetonitrile (MeCN), and sulfuric acid as a buffer. Detection is achieved using UV at 245 nm

ColumnPrimesep B, 4.6 x 150 mm, 5 µm, 100 A
Mobile PhaseMeCN/H2O – 35/35%
BufferH3PO4 -0.1%
Flow Rate1.0 ml/min
DetectionUV 245 nm

Class of Compounds
Corticosteroids
Analyzing CompoundsPrednisone, Prednisolone, Methylprednisolone

Application Column

Primesep B

Column Diameter: 4.6 mm
Column Length: 150 mm
Particle Size: 5 µm
Pore Size: 100 A

Add to cart
Application Analytes:
Methylprednisolone
Prednisolone
Prednisone

Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

Separation of Methylprednisolone on Newcrom R1 HPLC column

February 19, 2018
Separation of Methylprednisolone on Newcrom C18 HPLC column

Methylprednisolone can be analyzed by this reverse phase (RP) HPLC method with simple conditions. The mobile phase contains an acetonitrile (MeCN), water, and phosphoric acid. For Mass-Spec (MS) compatible applications the phosphoric acid needs to be replaced with formic acid. Smaller 3 µm particles columns available for fast UPLC applications. This liquid chromatography method is scalable and can be used for isolation impurities in preparative separation. It also suitable for pharmacokinetics.

Application Column

Newcrom R1

The Newcrom columns are a family of reverse-phase-based columns. Newcrom A, AH, B, and BH are all mixed-mode columns with either positive or negative ion-pairing groups attached to either short (25 Å) or long (100 Å) ligand chains. Newcrom R1 is a special reverse-phase column with low silanol activity.

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Application Analytes:
Methylprednisolone
The result was obtained by a proprietary SIELC algorithm. It may deviate from the actual experimental data. The experimental data are available upon request. Contact us by e-mail: support@sielc.com or by phone: 847-229-2629.