CAS 199191-66-7
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7 produits trouvés.
Duloxetine Related Compound H ((S)-4-{Methyl[3-(naphthalen-1-yloxy)-3-(thiophen-2-yl)propyl]amino}-4-oxobutanoic acid)
CAS :Nucleic acids and their salts, whether or not chemically defined; other heterocyclic compounds, nesoiFormule :C22H23NO4SCouleur et forme :White Crystalline PowderMasse moléculaire :397.13478Duloxetine USP Related Compound H
CAS :Formule :C22H23NO4SCouleur et forme :White To Off-White SolidMasse moléculaire :397.49(S)-Duloxetine Succinamide
CAS :Produit contrôléImpurity Duloxetine USP Related Compound H
Stability Hygroscopic
Applications An impurity of Duloxetine hydrochloride (D721000). It is formed by interaction of Duloxetine-HCl with enteric polymers. Duloxetine USP Related Compound H.
References Jansen, P.J., et al.: J. Pharmaceut. Sci., 87, 81 (1998),Formule :C22H23NO4SCouleur et forme :NeatMasse moléculaire :397.49(S)-Duloxetine succinamide
CAS :Duloxetine succinamide is a chromatographic, solid, acidic compound. It has been synthesized by reacting (S)-duloxetine hydrochloride with succinic anhydride in the presence of triethylamine and acetonitrile. The reaction mixture was purified by high-performance liquid chromatography to produce the desired product. The purity of the compound was confirmed by postulating that it should have a reversed-phase HPLC profile similar to that of duloxetine succinate. Duloxetine succinamide is not soluble in water and is insoluble in organic solvents such as acetone, chloroform, ether, or benzene. The compound is stable at room temperature but decomposes when heated at higher temperatures. !--Formule :C22H23NO4SDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :397.49 g/mol(S)-Duloxetine-d7 Succinamide
CAS :Produit contrôléApplications A labelled impurity of Duloxetine hydrochloride (D721000). It is formed by interaction of Duloxetine-HCl with enteric polymers.
References Jansen, P.J., et al.: J. Pharmaceut. Sci., 87, 81 (1998),Formule :C22D7H16NO4SCouleur et forme :NeatMasse moléculaire :404.531
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