logo
Send Message
Hefei Home Sunshine Pharmaceutical Technology Co.,Ltd
products
products
Home > products > Chemical Intermediates > Pantoprazole CAS 1026-25-70-7

Pantoprazole CAS 1026-25-70-7

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

Get Best Price
Highlight:
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
Pantoprazole CAS 1026-25-70-7

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.

 

 

If you are interested in our products or have any questions, please feel free to contact us!

 

 

Products under patent are offered for R & D purpose only. However, the final responsibility lies exclusively with the buyer.