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201812-64-8

201812-64-8 Structure

201812-64-8 Structure
IdentificationBack Directory
[Name]

DesfluoroMethyl Fluticasone Propionate Disulfide
[CAS]

201812-64-8
[Synonyms]

Fluticasone EP Imp H
Propionate Impurity H
Fluticasone Impurity 9
Fluticasone Disulphane Impurity
Fluticasone Propionate EP Impurity H
Fluticasone Propionate Disulfide Dimer Impurity
DesfluoroMethyl Fluticasone Propionate Disulfide
Fluticasone Impurity 8(Fluticasone EP Impurity H)
Androsta-1,4-dien-3-one, 17,17'- (dithiodicarbonyl)bis[6,9- difluoro-11-hydroxy-16-Methyl-17-(1-oxopropoxy)-, (6α,11β, 16α,17α)-(6'α,11'β,16'α,17'α)-
Fluticasone Propionate EP Impurity H/Fluticasone Disulphane Impurity/Desfluoromethyl Fluticasone Propionate Disulfide/17,17′-(Disulphanediyldicarbonyl)bis(6α,9-difluoro-11β-hydroxy-16α-methyl-3-oxoandrosta-1,4-dien-17α-yl) dipropanoate
[Molecular Formula]

C48H58F4O10S2
[MDL Number]

MFCD21363598
[MOL File]

201812-64-8.mol
[Molecular Weight]

935.092
Chemical PropertiesBack Directory
[Melting point ]

>200°C
[Boiling point ]

905.0±75.0 °C(Predicted)
[density ]

1.38±0.1 g/cm3(Predicted)
[storage temp. ]

Refrigerator
[solubility ]

Chloroform (Slightly), DMSO (Slightly)
[form ]

Solid
[pka]

12.20±0.70(Predicted)
[color ]

Off-White to Light Yellow
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Health Hazard (GHS08)
GHS07,GHS08
[Signal word ]

Danger
[Hazard statements ]

H312-H317-H302-H332-H360-H334
[Precautionary statements ]

P261-P272-P280-P302+P352-P333+P313-P321-P363-P501-P264-P270-P301+P312-P330-P501-P261-P271-P304+P340-P312-P280-P302+P352-P312-P322-P363-P501-P261-P285-P304+P341-P342+P311-P501
Hazard InformationBack Directory
[Uses]

Desfluoromethyl Fluticasone Propionate Disulfide is the disulfide conjugated dimer of Fluticasone Propionate (F599500), a derivative of flumethasone and an anti-inflammatory agent.
[Synthesis]

This is an impurity formed during the synthesis of Fluticasone Propionate. Its formation involves key steps: oxidative cleavage of the C-17 hydroxymethyl group in flumetasone, activation of the resulting acid and reaction with H₂S to give a thiocarboxylic
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