Product Details
Place of Origin: China
Brand Name: Sunshine
Certification: ISO,COA
Model Number: 1026-25-70-7
Payment & Shipping Terms
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Bag,Drum
Delivery Time: 7-15 days
Payment Terms: L/C, D/A, T/T, Western Union
Supply Ability: TON
CAS NO:: |
1026-25-70-7 |
Appearance:: |
Liquid |
Molecular Formula:: |
C16H15F2N3O4S |
Molecular Weight:: |
383.37 |
EINECS NO:: |
600-331-6 |
MDL NO:: |
NA |
CAS NO:: |
1026-25-70-7 |
Appearance:: |
Liquid |
Molecular Formula:: |
C16H15F2N3O4S |
Molecular Weight:: |
383.37 |
EINECS NO:: |
600-331-6 |
MDL NO:: |
NA |
Product Description:
Product Name: Pantoprazole CAS NO: 1026-25-70-7
Synonyms:
5-(difluoromethoxy)-2-[[(3,4-dimetho-xy-2-yridinyl)methyl]sulfinyl]-1h-benzimidazole;
Pantoprazole (base and/or unspecified salts);
6-(difluoromethoxy)-2-[(3,4-dimetho-xypyridin-2-yl)methylsulfinyl]-1h-benzimidazole;
Chemical & Physical Properties:
Appearance: Liquid
Assay :≥99.00%
Density: 1.51±0.1 g/cm3(Predicted)
Melting Point: 139-140℃(dec)
Boiling Point: 586.9±60.0℃(Predicted)
Safety Information:
Hazard Code: Xn
Risk Statements: R20/21/22-37/38-41-48
Safety Statements: S22-26-36/37/39-45
Hazardous Substances Data: 102625-70-7(Hazardous Substances Data)
Pantoprazole, an irreversible proton pump inhibitor, reached its first market worldwide in Germany for acute treatment of gastric and duodenal ulcers and gastroesophageal reflux disease. Proton pump inhibitors are more effective than other strategies in inhibiting acid secretion since they function at the final step of acid production, therefore, provide superior symptom relief and healing in all acid related diseases. As the third substituted benzimidazole proton pump inhibitor marketed, pantoprazole not only has superior ulcer-preventing effect but also is more potent than omeprazole in healing acetic acid-induced gastric and duodenal ulcers with extremely low acute toxicity. The mechanism of action for this class of compounds has been suggested to be mediated via the protonated form of the molecule which selectively reacts with cysteines present on the extracytoplasmic face of the enzyme to form covalent disulfide bonds.
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