• 99% Pure Pharmaceutical Raw Materials Pantoprazole Sodium 138786-67-1
  • 99% Pure Pharmaceutical Raw Materials Pantoprazole Sodium 138786-67-1
  • 99% Pure Pharmaceutical Raw Materials Pantoprazole Sodium 138786-67-1
  • 99% Pure Pharmaceutical Raw Materials Pantoprazole Sodium 138786-67-1
  • 99% Pure Pharmaceutical Raw Materials Pantoprazole Sodium 138786-67-1
  • 99% Pure Pharmaceutical Raw Materials Pantoprazole Sodium 138786-67-1

99% Pure Pharmaceutical Raw Materials Pantoprazole Sodium 138786-67-1

Powder: Yes
Customized: Non-Customized
Certification: GMP, HSE, ISO 9001, USP, BP
Suitable for: Adult
State: Solid
Purity: >99%
Samples:
US$ 10/gram 1 gram(Min.Order)
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Customization:

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Rating: 4.9/5

Basic Info.

Model NO.
TGY022019042407
Product Name
Pantoprazole Sodium
Appearance
White Powder
Test Methods
HPLC
Shelf Life
2 Years
Shipping Methods
DHL, FedEx, TNT and EMS
MOQ
1g
CAS No.
138786-67-1
Storage
2 Years
Spe
99%
Transport Package
Foil Bag, Box, Drum
Specification
99% min
Trademark
TGY
Origin
China
HS Code
3002200000
Production Capacity
1500kg/Month

Product Description


99% Pure Pharmaceutical Raw Materials Pantoprazole Sodium 138786-67-199% Pure Pharmaceutical Raw Materials Pantoprazole Sodium 138786-67-1
PANTOPRAZOLE SODIUM
Synonyms: 5-(Difluoromethoxy)-2-(((3,4-dimethoxy-2-pyridinyl)methyl) sulfinyl)-1H-benzimidazole sodium
CAS: 138786-67-1 
MF: C16H14F2N3NaO4S 
MW: 405.35 
mp  199-202°C 
storage temp.  -20°C Freezer 
Chemical Properties White to Off-White Solid 
Usage An antiulcerative. Gastric pump inhibitor 
Purity: 99%
Usage: API
Package: 1KG foil bag; 25Kg drum
Intravenous drip. Once 40~80mg, 1~2 times a day, inject 10ml of 0.9% sodium chloride injection into the lyophilized powder vial before use, and add the dissolved drug solution into 100~250ml of 0.9% sodium chloride injection. After intravenous drip. Intravenous drip requires 15 to 60 minutes to complete the drip.
This product must be used within 4 hours after dissolving and diluting. Do not use other solvents or other drugs to dissolve and dilute.
Adverse reactions
Occasionally, symptoms such as dizziness, insomnia, drowsiness, nausea, diarrhea, constipation, skin rash, muscle pain, etc. Arrhythmia, elevated transaminases, altered renal function, and decreased granulocytes may occur during high doses.
Contraindication 
1, disabled for allergies to this product;
2, pregnant and lactating women disabled.
Precautions
1, this product inhibits the strong role of gastric acid secretion, long time, so the application of this product should not be taken at the same time other antacids or acid inhibitors. In order to prevent over-suppression of acid, long-term application of large doses (except Zhuo-ai's syndrome) is not recommended in general peptic ulcers and other diseases.
2. People with impaired renal function do not need to adjust the dosage; those with impaired liver function need to reduce dosage as appropriate.
3, the treatment of ulcers should be excluded after the use of this product in order to avoid delay in diagnosis and treatment.
Storage
Protect from light and airtight and store in a cool place (not exceeding 20°C).

 

99% Pure Pharmaceutical Raw Materials Pantoprazole Sodium 138786-67-1

99% Pure Pharmaceutical Raw Materials Pantoprazole Sodium 138786-67-1

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