Beclomethasone Dipropionate

CAS: 5534-09-8

Ref. TR-B131030

Produktinformation

• Name: Beclomethasone Dipropionate
• Synonyme: 9-Chloro-11beta-hydroxy-16beta-methyl-3,20-dioxopregna-1,4-diene-17,21-diyl Dipropanoate, Beclometasone Dipropionate, Betamethasone Dipropionate Imp. E (Pharmeuropa), (11β,16β)-9-Chloro-11-hydroxy-16-methyl-17,21-bis(1-oxopropoxy)pregna-1,4-diene-3,20-dione, 9-Chloro-11β,17,21-trihydroxy-16β-methylpregna-1,4-diene-3,20-dione 17,21-dipropionate, 9α-Chloro-16β-methylprednisolone 17,21-dipropionate, Aerobec, Aldecin, Aldecin AQ nasal, Anceron, Andion, Beclacin, Beclate, Beclazone, Beclazone 250, Beclazone 50, Beclomet, Beclometasone 17,21-dipropionate, Beclometasone dipropionate, Beclomethasone 17,21-dipropionate, Beclomethasone 17α,21-dipropionate, Beclotide, Beclotide 100, Becloval, Beclovent, Beclovent Inhaler, Becodisks, Beconase, Beconase AQ, Becotide, Belchlorhinol, Belcoforte, Belcomet, Clenil A, Entyderma, Inalone O, Inalone R, Korbutone, Propaderm, Propaderm Forte, QVAR, Qvar 50, Rino-Clenil, Sanasthmax, Sanasthmyl, Sanasthymyl, Sch 8020W, Vancenase, Vancenase AQ, Vanceril, Vanceril DS, Ventolair, Viarex, Viarox
• Marke: TRC
• Beschreibung: Impurity Betamethasone Dipropionate EP Impurity EApplications Beclomethasone Dipropionate (Betamethasone Dipropionate EP Impurity E) is an antiallergic, antiasthmatic (inhalate). Anti-inflammatory (topical).References Laube, B., et al.: J. Allergy Clin. Immunol., 101, 475 (1998), Harrison, L., et al.: Eur. J. Clin. Pharmacol., 58, 191 (2002), Maneechotesuwan, K., et al.: J. Allergy Clin. Immunol., 121, 43 (2008).

Chemische Eigenschaften

• Molekulargewicht: 521.04
• Formel: C₂₈H₃₇ClO₇
• Farbe/Form: White
• InChl: InChI=1S/C28H37ClO7/c1-6-23(33)35-15-22(32)28(36-24(34)7-2)16(3)12-20-19-9-8-17-13-18(30)10-11-25(17,4)27(19,29)21(31)14-26(20,28)5/h10-11,13,16,19-21,31H,6-9,12,14-15H2,1-5H3/t16-,19-,20-,21-,25-,26-,27-,28-/m0/s1
• InChI Key: InChIKey=JEEXYCNTHWXJMQ-XGLYSLNUSA-N
• SMILES: CCC(=O)O.CCC(=O)O.CCC(=O)OCC(=O)[C@@]1(OC(=O)CC)[C@@H](C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)C3(Cl)[C@@H](O)C[C@@]21C