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CAS No 51333-22-3 , S-budesonide

  • Name: S-budesonide
  • Synonyms: S-budesonide;Budesonide;
  • CAS Registry Number:
  • Flash Point: 201.8 °C
  • Boiling Point: 599.7 °C at 760mmHg
  • Density: 1.27 g/cm3
  • Refractive index: 1.592
  • Safety Statements: R40,
  • Hazard Symbols: Xn:Harmful;
  • HS Code: 29372900
  • Flash Point: 201.8 °C
  • EINECS: 257-139-7
  • Molecular Weight: 430.54
  • InChI: InChI=1/C25H34O6/c1-4-5-21-30-20-11-17-16-7-6-14-10-15(27)8-9-23(14,2)22(16)18(28)12-24(17,3)25(20,31-21)19(29)13-26/h8-10,16-18,20-22,26,28H,4-7,11-13H2,1-3H3/t16-,17-,18-,20-,21?,22+,23-,24-,25+/m0/s1
  • Risk Statements: S22,S36,
  • Molecular Formula: C25H34O6
  • Molecular Structure:CAS No:51333-22-3 S-budesonide

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51333-22-3 Budesonide

  • China Hangzhou Sage Chemical Co., Ltd. [Manufacturer]
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51333-22-3 S-budesonide

  • China Wuxi Mizat Chemical Technology Co., Ltd. [Manufacturer]
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51333-22-3 Budesonide

  • Budesonide Kind API Species Corticosteroid CAS NO 51333-22-3 Formula C25H34O6 Contact person: Maggie Ma E-mail: topworkfinebs@hotmail.com MSN: topworkfinebs@hotmail.com Skype:topwork08 Mobile: +86 15902206342 Tel: +86-22-6687 7188 Fax: +86-22-6687 71...
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References of S-budesonide
Title: Budesonide
CAS Registry Number: 51333-22-3
CAS Name: (11b,16a)-16,17-[Butylidenebis(oxy)]-11,21-dihydroxypregna-1,4-diene-3,20-dione
Synonyms: (R,S)-11b,16a,17,21-tetrahydroxypregna-1,4-diene-3,20-dione cyclic 16,17-acetal with butyraldehyde
Manufacturers' Codes: S-1320
Trademarks: Bidien (IDI); Budeson (Fujisawa); Cortivent (Leiras); Entocort (AstraZeneca); Novopulmon (Viatris); Preferid (Yamanouchi); Pulmicort (AstraZeneca); Rhinocort (AstraZeneca); Spirocort (AstraZeneca)
Molecular Formula: C25H34O6
Molecular Weight: 430.53
Percent Composition: C 69.74%, H 7.96%, O 22.30%
Literature References: Non-halogenated glucocorticoid related to triamcinolone hexacetonide, q.v. with a high ratio of topical to systemic activity. Prepn: R. L. Brattsand et al., DE 2323215; eidem, US 3929768 (1973, 1975 both to Bofors). Synthesis and anti-inflammatory properties: A. Thalén, R. L. Brattsand, Arzneim.-Forsch. 29, 1787 (1979). Pharmacokinetic study: A. Ryrfeldt et al., J. Steroid Biochem. 10, 317 (1979). HPLC determn of epimers, impurities, content: G. Roth et al., J. Pharm. Sci. 69, 766 (1980). Review of pharmacodynamics and efficacy in asthma and rhinitis: S. P. Clissold, R. C. Heel, Drugs 28, 485-518 (1984).
Properties: Crystals, mp 221-232° (dec). Mixture of two isomers; the content of the S-isomer in the mixture varies between 40-51%. [a]D25 +98.9° (c = 0.28 in methylene chloride).
Melting point: mp 221-232° (dec)
Optical Rotation: [a]D25 +98.9° (c = 0.28 in methylene chloride)
Therap-Cat: Anti-inflammatory.
Keywords: Antiasthmatic (Steroidal, Inhalant); Glucocorticoid.