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Diflucortolone valerate

pharmaceutical raw materials
Diflucortolone valerate structure

Diflucortolone valerate 

structure
  • CAS No:

    59198-70-8

  • Formula:

    C27H36F2O5

  • Chemical Name:

    Diflucortolone valerate

  • Synonyms:

    Pregna-1,4-diene-3,20-dione,6,9-difluoro-11-hydroxy-16-methyl-21-[(1-oxopentyl)oxy]-,(6α,11β,16α)-;(6α,11β,16α)-6,9-Difluoro-11-hydroxy-16-methyl-21-[(1-oxopentyl)oxy]pregna-1,4-diene-3,20-dione;Diflucortolone valerate;Nerisona;Temetex;Nerisone;Diflucortolone 21-valerate;Nerisone Forte;Neriforte;Texmeten;Travazol;60864-98-4;60945-23-5;87980-40-3

  • Categories:

    Active Pharmaceutical Ingredients  >  Other Chemical Drugs

Description

Diflucortolone valerate is a corticosteroid hormone.

Diflucortolone valerate Basic Attributes

478.57

478.57

261-655-8

1A63Z067C8

DTXSID1048598

Characteristics

80.7 Ų

1.1227 (estimate)

220°C

578.5±50.0 °C(Predicted)

Approx LD50 in mice, rats: >4, 3.1 g/kg orally; 180, 13 mg/kg s.c.; 450, 98 mg/kg i.p. (Gunzel).

12.89±0.70

Safety Information

|Danger|H360 (89.66%): May damage fertility or the unborn child [Danger Reproductive toxicity]|P201, P202, P260, P264, P270, P281, P308+P313, P314, P405, and P501|Aggregated GHS information provided by 29 companies from 5 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

Substances that reduce or suppress INFLAMMATION. (See all compounds classified as Anti-Inflammatory Agents.)

Claral

Diflucortolone valerate Use and Manufacturing

Methods of Manufacturing

16α-Methyl-6α,9α-difluoro-δ4-pregnene-11α,21-diol-3,20-dione-21-acetate (MP = 229°/232°-234°C (with decomposition) is dehydrogenated in 1.2- position by means of Bacillus lentus, Mutant MB 284, whereby the 21-acetate group is simultaneously saponified. (It is possible under the same conditions to start with the free 21-hydroxyl compound.) For this purpose a fermenter made of stainless steel having a 50 liter capacity is charged with 30 liters of a nutrient solution of 0.1% yeast extract, 0.5% cornsteep and 0.2% glucose, heated for one-half hour at 120°C for sterilization purposes, and after cooling, inoculated with a bacterial suspension of Bacillus lentus MB 284. After 24 hours of growth at 28°C under stirring (220 revolutions per minute) and aeration (1.65 m3/hr), 1.8 liters of the obtained culture is removed under sterile conditions and transferred with 28 liters of the same sterilized nutrient medium into a fermenter of the same size. Simultaneously, 6 g of 16α-methyl-6α,9α-difluoro-δ4-pregnene-11β,21-diol3,20-dione-21-acetate in 200 cc of dimethylformamide are added and the fermentation is continued for 50 hours under the same conditions. The course of the fermentation is tested by removal of samples which are extracted with methyl isobutyl ketone. The extracts are analyzed by thin layer chromatography using a system of benzene/ethyl acetate (4:1). After further working up there is obtained an oily crystalline residue which is subjected to chromatography on silica gel. The 16α-methyl-6α,9α-difluoroδ1,4-pregnadien-11β,21-diol-3,20-dione is eluated with ethyl acetatechloroform (1:2), it is recrystallized from ethyl acetate/ether and then formed to melt at 240°/242°-244°C. The yield is 60% of the theoretical. The product is reacted with valeric acid chloride to give the valerate ester.

Uses

The 9α-fluoro derivative of Fluocortolone (F500500). Anti-inflammmatory.

Computed Properties

Molecular Weight:478.6
XLogP3:4.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:7
Exact Mass:478.25308057
Monoisotopic Mass:478.25308057
Topological Polar Surface Area:80.7
Heavy Atom Count:34
Complexity:943
Defined Atom Stereocenter Count:9
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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