ChemicalBook--->CAS DataBase List--->164579-32-2

164579-32-2

164579-32-2 Structure

164579-32-2 Structure
IdentificationBack Directory
[Name]

PantoprazoleSodiumSesquihydrate
[CAS]

164579-32-2
[Synonyms]

Unii-6871619Q5x
BY1023 (sodium hydrate)
SKF-96022 SODIUM HYDRATE
Pantoprazole sodium hydrate
Pantoprazole sodium sesquihydrate CRS
Pantoprazole for system suitability CRS
Pantoprazole Sodium sesqui hydrate- IP/BP/USP
6-(Difluoromethoxy)-2-[[(3,4-dimethoxy-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole sodium salt hydrate (2:2:3)
1H-Benzimidazole, 5-(difluoromethoxy)-2-(((3,4-dimethoxy-2-pyridinyl)methyl)sulfinyl)-, sodium salt, hydrate (2:3)
Pantoprazole Sodium SesquihydrateQ: What is Pantoprazole Sodium Sesquihydrate Q: What is the CAS Number of Pantoprazole Sodium Sesquihydrate Q: What is the storage condition of Pantoprazole Sodium Sesquihydrate
[EINECS(EC#)]

1312995-182-4
[Molecular Formula]

C16H15F2N3O4S.3/2H2O.Na
[MDL Number]

MFCD16879010
[MOL File]

164579-32-2.mol
[Molecular Weight]

864.75
Chemical PropertiesBack Directory
[Appearance]

White or almost white powder.
[storage temp. ]

4°C, protect from light
[solubility ]

Freely soluble in water and in ethanol (96 per cent), practically insoluble in hexane.
[form ]

neat
[color ]

White to off-white
[Major Application]

pharmaceutical (small molecule)
[InChI]

1S/C16H16F2N3O4S.Na.H2O/c1-23-13-5-6-19-12(14(13)24-2)8-26(22)16-20-10-4-3-9(25-15(17)18)7-11(10)21-16;;/h3-7,15-16,21H,8H2,1-2H3;;1H2/q-1;+1;
[InChIKey]

QHNXIKDJFYGZTL-UHFFFAOYSA-N
[SMILES]

[Na+].FC(F)Oc1cc2c(cc1)[N-]C(N2)[S](=O)Cc3nccc(c3OC)OC.O
Hazard InformationBack Directory
[Chemical Properties]

White or almost white powder.
[Uses]

Treatment of various acid-related gastrointestinal diseases, including acute erosive esophagitishealing and maintenance, treatment of hypersecretory conditions, Zollinger-Ellison Syndrome (ZES), and eradication of Helicobacter pylori infection.
[Brand name]

Protonix (Wyeth).
[in vivo]

Pantoprazole sodium hydrate (BY1023 sodium hydrate; 200 mg/kg; IP; once a week for 3 weeks) significantly increases tumor growth delay of MCF-7 xenografts combined with Doxorubicin[1].
Pantoprazole sodium hydrate (0.3-3 mg/kg, p.o.) dose-dependently decreases both basal acid secretion in pylorus-ligated rats and the stimulated acid secretion induced by mepirizole in acute fistula rats[4].

Animal Model:Mice bearing MCF-7 or A431 xenografts[1]
Dosage:200 mg/kg
Administration:IP; once a week for 3 weeks; alone or 2 hours before Doxorubicin (6 mg/kg i.v.)
Result:Showed even greater growth delay of MCF-7 xenografts with Doxorubicin compared with the single-dose combination.
Significantly increased tumor growth delay with a single dose with Doxorubicin.
There is no effect on growth delay alone.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P301+P312+P330
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

nwg
[HS Code ]

2933399090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Spectrum DetailBack Directory
[Spectrum Detail]

PantoprazoleSodiumSesquihydrate(164579-32-2)1HNMR
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