Pantoprazole sodium cas 138786-67-1 CAS NO.138786-67-1

Min.Order: 1 Gram
Payment Terms: L/C,D/A,D/P,T/T,Other

Product Details

Keywords

Pantoprazole sodium
cas 138786-67-1
API

Quick Details

ProName: Pantoprazole sodium cas 138786-67-1
CasNo: 138786-67-1
Molecular Formula: C16H35F2N3NaO4S
Appearance: powder
Application: Animal Pharmaceuticals
DeliveryTime: ASAP
PackAge: as your requests
Port: Ningbo/Shanghai port/other ports
ProductionCapacity: 1000 Kilogram/Month
Purity: 99%
Storage: -20°C Freezer
Transportation: The product will be sent out as soon a...
LimitNum: 1 Gram

Superiority

Jinlan Pharm-Drugs Technology Co.,Limited (with its export company Hangzhou Royall Import & Export Co.,Ltd.)is located in Hangzhou, Zhejiang Province. Neighboring Ningbo port, Shanghai port, Hangzhou Xiaoshan Int’l Airport and Shanghai Pudong Int’l Airport, the transportation and production environment are excellent. JINLAN PHARMA is mainly engaged in R&D, manufacturing and marketing pharmaceuticals, chemical intermediates, Biochemicals, Veterinary medicines and Nutrition products.

With its strong ability in R&D, and world-leading process technology, JINLAN PHARMA develops the new and high-tech chemicals and pharmaceuticals. Synthesis capacity from gram scale, kg scale to mt scale is available.

Details

Nebivolol hydrochloride

cas 152520-56-4

1.Specification:

Product name	Pantoprazole sodium
Other name	5-(Difluoromethoxy)-2-(((3,4-dimethoxy-2-pyridinyl)methyl) sulfinyl)-1H-benzimidazole sodium
Specification	Enterprise Standard.
CAS	138786-67-1
Package	25kg net per drum.
Stock	Fresh stock; good price; samples available
Molecular Structure
Molecular Formula	C16H35F2N3NaO4S
Molecular Weight	425.52

2.Detailed Product Description:

Test Item	Standards Required	Test Result
Characters	White to almost white powder.	Almost white powder.
Identification
A:Infrared Absorption	IR Conforms to standard	Complies
B:HPLC	The retention time of the major peak in the chromatogram of the Assay preparation corresponds to that in the chromatogram of the Standard preparation, as obtained in the Assay.	Complies
C:	It meets the requirements of the pyroantimonate precipitate test for Sodium.	Complies
Water	5.0%-8.0% Method I	6.1%
Heavy Metals	≤0.002% Method II	Complies
Chromatographic purity (HPLC)
Related compound A	≤0.20%	0.04%
Related compound B	≤0.15%	Not detected
Related compound C	≤0.10%	0.04%
Related compound D+E	≤0.20%	Not detected
Related compound F	≤0.10%	Not detected
Any other individual impurity	≤0.10%	0.03%
Total impurities	≤0.5%	0.1%
Assay% on dry basis	98.0% - 102.0%	99.7%
Residual solvent
Methanol	≤3000ppm	157ppm
Ethanol	≤5000ppm	142ppm
Methylene chloride	≤100ppm	Not detected
acetoacetate	≤5000ppm	54ppm
Results: The commodity meets the standard of USP35.