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Postion:Product Catalog >Analytical Chemistry>Standard>Pharmaceutical Impurity Reference Standards>Rizatriptan EP Impurity A
Rizatriptan EP Impurity A
  • Rizatriptan EP Impurity A
  • Rizatriptan EP Impurity A
  • Rizatriptan EP Impurity A
  • Rizatriptan EP Impurity A

Rizatriptan EP Impurity A NEW

Price Get Latest Price
Package 10mg
Min. Order: 10mg
Supply Ability: 5g
Update Time: 2026-03-12

Product Details

Product Name: Rizatriptan EP Impurity A CAS No.: 887001-08-3
Min. Order: 10mg Purity: 0.98
Supply Ability: 5g Release date: 2026/03/12

Article illustration

Product information:

English name :    Rizatriptan EP Impurity A

Chemical name: 2-(5-((1H-1,2,4-triazol-1-yl)methyl)-2-((3-(2-(dimethylamino)ethyl)-1H-indol-5-yl)methyl)-1H-indol-3-yl)-N,N-dimethylethanamine

CAS number:887001-08-3

Molecular form:  C28H35N7

Molecular weight :  469.62


Shenzhen Hengfeng Wanda Pharmaceutical Technology is a professional supplier of drug impurity control products. Products with short delivery time, covering more than 90% of cutting-edge generic drug projects; All products must check LCMS and HPLC within a year.The company has 300 flat warehouse, 42 sets of -20℃ refrigerator; Under the brands "H&D" and "Molcoo", we provide customized 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, analysis and testing and customized compound synthesis services. The company can provide professional technical services.


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, standard products, pharmaceutical intermediates, and drug impurity preparation, separation and purification business. Our company is located in Wuhan, a city with abundant talents and a thoroughfare of nine provinces.The company enjoys more rich academic foundation and convenient and fast logistics speed.


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. All standard products will be provided by Molcoo quality assurance and related certificates (COA), H-NMR, MS, HPLC and other structure confirmation to meet the basic needs.Customers can also test C-NMR, QNMR, IR, etc., according to their own needs, we can also provide atlas analysis services for new and old customers Provides a simple synthetic route.


We can provide ull set of stock.Our products are subject to strict quality control to ensure excellent quality. So we will carry out strict quality testing on each product before delivery. We also have a professional sales customer service team , so that you can rest assured before and after sales.


Impurity Sales Manager: Manager Sun


Impurity consultation phone: +8618672472998

Email:sale@hdimpurity.com

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.

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