Azilsartan impurity Z NEW

$0.00 10mg

$0.00 20mg

$0.00 50mg

Min. Order10mg
Purity98%
Cas No
Supply Ability500mg
Update time2024-09-20

ShenZhen H&D Pharmaceutical Technology Co., LTD

1YR

China

Since

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Chemical Properties

Product Name	Azilsartan impurity Z
CAS No
EC-No
Min. Order	10mg
Purity	98%
Supply Ability	500mg
Release date	2024/09/20

CAS Number:

136285-65-9

Molecular formula:

C14H18N2O6

Molecular weight:

310.3

Email:sale@hdimpurity.com

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ShenZhen H&D Pharmaceutical Technology Co., LTD is a professional supplier of drug impurity control products. Products cove more than 90% of cutting-edge generic drug projects. All products must check LCMS and HPLC within a year.We provide customized synthesis and preparation of small molecule compounds.

ShenZhen H&D Pharmaceutical Technology Co., LTD has its own laboratory. The company focuses on providing pharmaceutical research and development units with new drug and generic drug registration and application of chemical products.

The company focuses on providing pharmaceutical research and development units with new drugs and generic drug registration and application of chemical products, including drug impurity reference products and standard products. Our delivery standard is not less than 98% purity (HPLC).If the purity is less than 98%, we will give special instructions to the customer.

Impurity Sales Manager: Mr. Sun

Email:sale@hdimpurity.com

Price wire negotiation

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Company Profile Introduction

ShenZhen H&D Pharmaceutical Technology Co., LTD is a professional supplier of pharmaceutical impurity control products. Short product delivery time, covering more than 90% of cutting-edge generic drug projects; All products must be checked for LCMS and HPLC within one year. We offer custom synthesis and preparation of small molecule compounds. The company has its own research and development center, focusing on providing pharmaceutical research and development units with new drug and generic drug registration and application of chemical products, including drug standards, drug impurity reference products, characteristic intermediates, analytical testing and custom compound synthesis services. Our delivery standard is not less than 98% purity (HPLC). The company focuses on providing pharmaceutical research and development units with new drug and generic drug registration applications and chemical products, including drug impurity reference products, standards, pharmaceutical intermediates, as well as drug impurity preparation, separation and purification business.