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Home ProductsImpurities(Standards)

95+ White Powder Enzalutamide EP Impurity C CAS NO. 179232-29-2

95+ White Powder Enzalutamide EP Impurity C CAS NO. 179232-29-2

95+ White Powder Enzalutamide EP Impurity C CAS NO. 179232-29-2
95+ White Powder Enzalutamide EP Impurity C CAS NO. 179232-29-2 95+ White Powder Enzalutamide EP Impurity C CAS NO. 179232-29-2

Large Image :  95+ White Powder Enzalutamide EP Impurity C CAS NO. 179232-29-2 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: Enzalutamide EP Impurity C CAS No: 179232-29-2
M.W: 233.03 MF: C8H6BrFO2
Appearance: White Powder Purity: 95+
EINECS No: - Storage: 5-25°C

 

Product Description

 

White Powder Enzalutamide EP Impurity C CAS NO. 179232-29-2 Purity 95+

 

Name: Enzalutamide EP Impurity C

CAS NO:179232-29-2

M.W: 233.03

Appearance: White Powder

Purity: 95+   

SynonymsEnzalutamide EP Impurity C

 

Application

 

Impurities are any other substances in a drug other than the main active ingredient. They can be unreacted starting materials, byproducts, degradation products, or substances introduced during the manufacturing process. During the production of drugs, impurities need to be strictly controlled to ensure the safety and efficacy of the final product.

 

In general, the study and control of impurities is a crucial aspect of drug research and development as well as production. Impurities can affect the stability, safety, and efficacy of drugs, so they require in-depth research and analysis to ensure the quality and safety of the final product.

 

As a potential impurity of Enzalutamide, Enzalutamide EP Impurity C may have an impact on the quality and safety of the drug. Therefore, it requires strict detection and control in the production and quality control of Enzalutamide.

 

Safety assessment: Before a drug enters the market, extensive safety assessments are conducted, including evaluating the potential impact of impurities such as Enzalutamide Impurity 14 on patient health.

 

Package

 

 95+ White Powder Enzalutamide EP Impurity C CAS NO. 179232-29-2 0     95+ White Powder Enzalutamide EP Impurity C CAS NO. 179232-29-2 1 

95+ White Powder Enzalutamide EP Impurity C CAS NO. 179232-29-2 295+ White Powder Enzalutamide EP Impurity C CAS NO. 179232-29-2 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 Enzalutamide EP Impurity C CAS NO. 179232-29-2 495+ White Powder Enzalutamide EP Impurity C CAS NO. 179232-29-2 5

95+ White Powder Enzalutamide EP Impurity C CAS NO. 179232-29-2 695+ White Powder Enzalutamide EP Impurity C CAS NO. 179232-29-2 7

95+ White Powder Enzalutamide EP Impurity C CAS NO. 179232-29-2 895+ White Powder Enzalutamide EP Impurity C CAS NO. 179232-29-2 9

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