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378-44-9

  • Product Name:Betamethasone
  • Molecular Formula:C22H29FO5
  • Appearance:white to off-white solid
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Product Details

Appearance:white to off-white solid

Purity:99%

Best Price Betamethasone 378-44-9 In Medicine

378-44-9 Name

Name

Betamethasone

Synonym

17,21-trihydr;betamethasone standard;(8S,9R,10S,11S,13S,14S,16S,17R)-9-fluoro- 11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl- 6,7,8,9,10,11,12,13,14,15,16,17-dodecahydro-3H-cyclopenta[a]phenanthren-3-one;Betamethasone Base & Salts;Betamethasone,9α-Fluoro-11β,17α,21-trihydroxy-16β-methylpregna-1,4-diene-3,20-dione, 9α-Fluoro-16β-methyl-11β,17α,21-trihydroxy-1,4-pregnadiene-3,20-dione, 9α-Fluoro-16β-methylprednisolone;Betamethasone (200 mg);BetaMethasone (Celestone);BetaMethasone SolutioM

 

378-44-9 Biological Activity

Related Catalog

Signaling Pathways >> GPCR/G Protein >> Glucocorticoid Receptor

Research Areas >> Inflammation/Immunology

 

378-44-9 Chemical & Physical Properties

Melting point 

235-237°C

Boiling point

568.2±50.0 °C at 760 mmHg

Density

1.3±0.1 g/cm3

Molecular Formula

C22H29FO5

Molecular Weight

392.461

Flash Point

297.5±30.1 °C

PSA

94.83000

LogP

1.87

Exact Mass

392.199890

Vapour Pressure

0.0±3.5 mmHg at 25°C

Index of Refraction

1.592

Betamethasone 378-44-9 In Medicine

Betamethasone, a corticosteroid drug used in the clinic for its anti-inflammatory and immunosuppressive effects, were effective in reducing the intensity of epileptic seizures. Betamethasone (BM) is the drug of choice for antenatal corticosteroid therapy for women at risk of preterm delivery because it induces fetal lung maturation and enhances survival after birth.

InChI:InChI=1/C22H29FO5/c1-12-8-16-15-5-4-13-9-14(25)6-7-19(13,2)21(15,23)17(26)10-20(16,3)22(12,28)18(27)11-24/h6-7,9,12,15-17,24,26,28H,4-5,8,10-11H2,1-3H3/t12-,15+,16+,17+,19+,20+,21+,22+/m1/s1

378-44-9 Relevant articles

A variation of Mattox rearrangement mechanism under alkaline condition

Li, Min,Chen, Bin,Lin, Mingxiang,Chan, Tze-Ming,Fu, Xiaoyong,Rustum, Abu

, p. 3901 - 3905 (2007)

A variation of the Mattox rearrangement, a key degradation pathway under acidic conditions for corticosteroids possessing the 1,3-dihydroxyacetone side chain, has been found to occur for the 17,21-diesters of these corticosteroids but under the alkaline condition. The mechanism of this variation of the original Mattox rearrangement is proposed.

Review of Calcipotriene and Betamethasone Dipropionate Cream in the Treatment of Psoriasis

Alexandra Taylor, BS , Rohan Singh, BS , and Steven R. Feldman, MD, PhD

Paragraph 0038; 0039; 0041, (2017/07/22)

To review the pharmacokinetics, efficacy, and safety of recently approved calcipotriene and betamethasone dipropionate (C-BD) cream. Newly FDA-approved C-BD cream with novel polyaphron dispersion (PAD) technology provides a safe efficacious combination therapy for mild-to-moderate psoriasis which may be preferred by some patients.

378-44-9 Process route

betamethasone dipropionate
5593-20-4

betamethasone dipropionate

betamethasone
378-44-9

betamethasone

Betamethasone propionate
5534-13-4

Betamethasone propionate

betamethasone 21-monopropionate

betamethasone 21-monopropionate

Conditions
Conditions Yield
With sulfuric acid; In acetonitrile; at 20 ℃; for 20h; Further Variations:; Temperatures; Product distribution;
 
betamethasone dipropionate
5593-20-4

betamethasone dipropionate

betamethasone
378-44-9

betamethasone

Betamethasone propionate
5534-13-4

Betamethasone propionate

6β-hydroxybetamethasone
24703-00-2,24703-12-6,55879-47-5

6β-hydroxybetamethasone

6β-hydroxybetamethasone 17-propionate
78144-00-0,91677-33-7

6β-hydroxybetamethasone 17-propionate

Conditions
Conditions Yield
With phosphate buffer; air; plasma of 20 d pregnant Sprague-Dawley rat; at 37 ℃; for 1h; Product distribution; metabolism with tissues (plasma, liver, brain, placenta) from mothers and fetuses of Sprague-Dawley rats sacrificed on day 20 of pregnancy and mice on day 17 of pregnancy, further in vivo;
67.8 % Chromat.
2.3 % Chromat.
14.8 % Chromat.
1.4 % Chromat.

378-44-9 Upstream products

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