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Home ProductsImpurities(Standards)

95+ White Powder Levosimendan Impurity 16 CAS 2290570-69-1

95+ White Powder Levosimendan Impurity 16 CAS 2290570-69-1

95+ White Powder Levosimendan Impurity 16 CAS 2290570-69-1
95+ White Powder Levosimendan Impurity 16 CAS 2290570-69-1

Large Image :  95+ White Powder Levosimendan Impurity 16 CAS 2290570-69-1 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: Levosimendan Impurity 16 CAS No: 2290570-69-1
M.W: 188.23 MF: C11H12N2O
Appearance: White Powder Purity: 95+
EINECS No: - Storage: 5-25°C

 

Product Description

 

White Powder Levosimendan Impurity 16 CAS 2290570-69-1 Purity 95+

 

Name: Levosimendan Impurity  16

CAS NO2290570-69-1

M.W: 298.3

Appearance: White Powder

Purity: 95+   

SynonymsLevosimendan Impurity 16

 

Application

 

Drug Research and Development: Studying Levosimendan Impurity 16 aids in understanding the by-products and reaction mechanisms involved in the synthesis of the drug. This knowledge can optimize the synthesis route, minimize impurity formation, and enhance the purity and quality of the final drug product. Additionally, analyzing the structure and properties of the impurity can provide valuable insights for drug structure design and optimization.

 

Quality Control: Monitoring and controlling Levosimendan Impurity 16 during production is crucial for ensuring the quality and safety of the drug. Rigorous control of impurity levels can promptly identify potential production issues, ensuring product consistency and stability.

 

Stability Studies: Examining the stability and degradation pathways of Levosimendan Impurity 16 under various conditions can predict the stability of the drug during storage and use. This information is essential for determining appropriate storage conditions and setting expiration dates.

 

Safety Assessment: Although Levosimendan Impurity 16 may not possess therapeutic activity, its presence could pose potential risks to human health. Therefore, a thorough safety assessment of the impurity is essential in the drug development process. Detailed studies of the impurity can provide robust support for drug safety evaluations.

 

Package

 

 95+ White Powder Levosimendan Impurity 16 CAS 2290570-69-1 0     95+ White Powder Levosimendan Impurity 16 CAS 2290570-69-1 1 

95+ White Powder Levosimendan Impurity 16 CAS 2290570-69-1 295+ White Powder Levosimendan Impurity 16 CAS 2290570-69-1 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 Levosimendan Impurity 16 CAS 2290570-69-1 495+ White Powder Levosimendan Impurity 16 CAS 2290570-69-1 5

95+ White Powder Levosimendan Impurity 16 CAS 2290570-69-1 695+ White Powder Levosimendan Impurity 16 CAS 2290570-69-1 7

95+ White Powder Levosimendan Impurity 16 CAS 2290570-69-1 895+ White Powder Levosimendan Impurity 16 CAS 2290570-69-1 9

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