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Home ProductsImpurities(Standards)

95+ White Powder Granisetron EP Impurity A CAS 127472-42-8

95+ White Powder Granisetron EP Impurity A CAS 127472-42-8

95+ White Powder Granisetron EP Impurity A CAS 127472-42-8
95+ White Powder Granisetron EP Impurity A CAS 127472-42-8

Large Image :  95+ White Powder Granisetron EP Impurity A CAS 127472-42-8 Get Best Price

Product Details:
Place of Origin: CHINA
Brand Name: Enlai Biotech
Certification: ISO 9001 COA HPLC NMR
Payment & Shipping Terms:
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Inside: double PE bag Outside: paper drum
Delivery Time: In Stock
Payment Terms: T/T
Supply Ability: 100 kilograms per month
Detailed Product Description
Product Name: Granisetron EP Impurity A CAS No: 127472-42-8
M.W: 312.41 MF: C18H24N4O
Appearance: White Powder Purity: 95+
EINECS No: - Storage: 5-25°C
Highlight:

95 Granisetron EP Impurity A

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Granisetron EP Impurity A 127472-42-8

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95 Granisetron EP Impurity A

 

Product Description

 

White Powder Granisetron EP Impurity A CAS 127472-42-8 95+

 

Name: Granisetron EP Impurity A

CAS NO127472-42-8

M.W312.41

Appearance: White Powder

Purity: 95+   

SynonymsGranisetron EP Impurity A

 

Application

 

Quality Control and Assurance: Monitoring the presence and quantity of Granisetron EP Impurity A is crucial for ensuring the purity and quality of Granisetron. It serves as a key indicator in the quality control process, allowing manufacturers to assess whether the drug meets regulatory standards and ensures its safety for patients. By accurately detecting and quantifying this impurity, quality control teams can maintain the consistency and reliability of the final product.

 

Drug Research and Development: Studying Granisetron EP Impurity A can provide valuable insights to researchers and developers working on improving the synthesis and formulation of Granisetron. Understanding the formation mechanisms, reactivity, and potential pharmacological properties of this impurity can assist in optimizing the production process, enhancing drug stability, and potentially discovering new therapeutic benefits.

 

Production Process Monitoring: Monitoring Granisetron EP Impurity A during the production of Granisetron helps manufacturers identify potential issues in the production process, such as contamination of raw materials or incomplete reactions. By detecting this impurity, engineers can promptly adjust production parameters or introduce corrective measures to ensure product quality and maintain high production efficiency.

 

Package

 

 95+ White Powder Granisetron EP Impurity A CAS 127472-42-8 0     95+ White Powder Granisetron EP Impurity A CAS 127472-42-8 1 

95+ White Powder Granisetron EP Impurity A CAS 127472-42-8 295+ White Powder Granisetron EP Impurity A CAS 127472-42-8 3

Transportation

 

Small package(1g, 25g, 1Kg, 25Kg) can be shipped by Express. (DHL, FedEx, EMS, etc.)
Large package(100kg and more than100Kg) can be transported by Air or Sea.

All transportation is in accordance with the customer's needs.

 

Company Profile

 

95+ White Powder Granisetron EP Impurity A CAS 127472-42-8 495+ White Powder Granisetron EP Impurity A CAS 127472-42-8 5

95+ White Powder Granisetron EP Impurity A CAS 127472-42-8 695+ White Powder Granisetron EP Impurity A CAS 127472-42-8 7

95+ White Powder Granisetron EP Impurity A CAS 127472-42-8 895+ White Powder Granisetron EP Impurity A CAS 127472-42-8 9

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