ChemicalBook--->CAS DataBase List--->92340-57-3

92340-57-3

92340-57-3 Structure

92340-57-3 Structure
IdentificationBack Directory
[Name]

5-HYDROXY OMEPRAZOLE
[CAS]

92340-57-3
[Synonyms]

Hydroxyomeprazole
5-HYDROXY OMEPRAZOLE
5-hydroxymethylomeprazole
HydroxyoMeprazole SodiuM Salt
5-HYDROXY OMEPRAZOLE USP/EP/BP
Esomeprazole Sodium Impurity 31
5-Hydroxy Omeprazole Sodium Salt
5-Hydroxy OMeprazole (~5% TriethylaMine as stabilizer)
2-[(5-HYDROXYMETYL-4-METHOXY-3-METHYL-PYRIDIN-2-YL)-METHYLSULFO]-BENZIMIDAZOLE
4-Methoxy-6-[[(5-methoxy-1H-benzimidazol-2-yl)sulfinyl]methyl]-5-methyl-3-pyridinemethanol
[4-Methoxy-6-[(6-methoxy-1H-benzimidazol-2-yl)sulfinylmethyl]-5-methylpyridin-3-yl]methanol
3-Pyridinemethanol, 4-methoxy-6-[[(6-methoxy-1H-benzimidazol-2-yl)sulfinyl]methyl]-5-methyl-
5-Methoxy-2-{[(5-hydroxymethyl-4-methoxy-3-methyl-2-pyridinyl)methyl]sulfinyl}-1H-benzimidazole
4-Methoxy-6-[[(5-Methoxy-1H-benziMidazol-2-yl)sulfinyl]Methyl]-5-Methyl-3-pyridineMethanol SodiuM Salt
[Molecular Formula]

C17H19N3O4S
[MDL Number]

MFCD00869771
[MOL File]

92340-57-3.mol
[Molecular Weight]

361.42
Chemical PropertiesBack Directory
[Melting point ]

144-146?C
[Boiling point ]

656.3±65.0 °C(Predicted)
[density ]

1.45±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C Freezer, Under Inert Atmosphere
[solubility ]

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

neat
[pka]

8.50±0.10(Predicted)
[color ]

White to Pale Brown
[BRN ]

8439890
[Stability:]

Hygroscopic, Temperature Sensitive
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

2
Hazard InformationBack Directory
[Chemical Properties]

Off-White to Pale Yellow Solid
[Uses]

5-Hydroxy Omeprazole is the main metabolite of Omeprazole (O635000), which binds covalently to proton pump. It inhibits gastric secretion. Used as an anttiulcerative.
[Uses]

A metabolite of Omeprazole
[Uses]

The main metabolite of Omeprazole.
[Definition]

ChEBI: A sulfoxide that is omeprazole in which one of the methyl hydrogens at position 5 on the pyridine ring is substituted by a hydroxy group.
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