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Home ProductsImpurities(Standards)

95+ White Powder Levosimendan Impurity 8 CAS 274263-65-9

95+ White Powder Levosimendan Impurity 8 CAS 274263-65-9

95+ White Powder Levosimendan Impurity 8 CAS 274263-65-9
95+ White Powder Levosimendan Impurity 8 CAS 274263-65-9

Large Image :  95+ White Powder Levosimendan Impurity 8 CAS 274263-65-9 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 8 CAS No: 274263-65-9
M.W: 298.3 MF: C14H14N6O2
Appearance: White Powder Purity: 95+
EINECS No: - Storage: 5-25°C

 

Product Description

 

White Powder Levosimendan Impurity 8 CAS 274263-65-9 Purity 95+

 

Name: Levosimendan Impurity 8

CAS NO274263-65-9

M.W: 298.3

Appearance: White Powder

Purity: 95+   

SynonymsLevosimendan Impurity 8

 

Application

 

Quality Control: Monitoring and controlling the level of Levosimendan Impurity 8 is crucial in ensuring the quality and safety of the final Levosimendan product. Manufacturers need to ensure that the impurity levels meet established quality standards.

 

Stability Studies: By studying the formation and stability of Levosimendan Impurity 8 under various conditions, scientists can gain insights into the degradation pathways and rates of Levosimendan, thereby predicting its stability during storage and use.

 

Drug Development: Researching Levosimendan Impurity 8 can aid in optimizing synthetic routes, reducing impurity formation, and improving the purity of the drug during the drug development phase. This not only enhances production efficiency but also helps to reduce production costs.

 

Safety Assessment: While Levosimendan Impurity 8 itself may not have therapeutic activity, its presence may pose potential risks to human health. Therefore, a thorough safety assessment of the impurity is an essential part of the drug development process.

 

Regulatory Compliance: Manufacturers are required to demonstrate the safety and efficacy of their products to meet the requirements of drug regulatory agencies. Extensive research on Levosimendan Impurity 8 is an important component of fulfilling these regulatory requirements.

 

Package

 

 95+ White Powder Levosimendan Impurity 8 CAS 274263-65-9 0     95+ White Powder Levosimendan Impurity 8 CAS 274263-65-9 1 

95+ White Powder Levosimendan Impurity 8 CAS 274263-65-9 295+ White Powder Levosimendan Impurity 8 CAS 274263-65-9 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 8 CAS 274263-65-9 495+ White Powder Levosimendan Impurity 8 CAS 274263-65-9 5

95+ White Powder Levosimendan Impurity 8 CAS 274263-65-9 695+ White Powder Levosimendan Impurity 8 CAS 274263-65-9 7

95+ White Powder Levosimendan Impurity 8 CAS 274263-65-9 895+ White Powder Levosimendan Impurity 8 CAS 274263-65-9 9

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