logo

SICHUAN HONGRI PHARMA-TECH CO., LTD

Sales & Support
Request A Quote - Email
Select Language
Home
Products
About Us
Factory Tour
Quality Control
Contact Us
Request A Quote
Home ProductsImpurities(Standards)

95+ White Powder Levosimendan Impurity 35 CAS 1630760-90-5

95+ White Powder Levosimendan Impurity 35 CAS 1630760-90-5

95+ White Powder Levosimendan Impurity 35 CAS 1630760-90-5
95+ White Powder Levosimendan Impurity 35 CAS 1630760-90-5

Large Image :  95+ White Powder Levosimendan Impurity 35 CAS 1630760-90-5 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 35 CAS No: 1630760-90-5
M.W: 222.67 MF: C11H11ClN2O
Appearance: White Powder Purity: 95+
EINECS No: - Storage: 5-25°C

 

Product Description

 

White Powder Levosimendan Impurity 35 CAS 1630760-90-5 95+

 

Name: Levosimendan Impurity 35

CAS NO1630760-90-5

M.W: 222.67

Appearance: White Powder

Purity: 95+   

SynonymsLevosimendan Impurity 35

 

Application

 

The specific applications of Levosimendan Impurity 35 are not well-defined as it typically refers to a specific chemical impurity rather than a standalone compound or product. Levosimendan Impurity 35 could be one of the impurities generated during the synthesis or production of Levosimendan, a positive inotropic agent primarily used in the treatment of heart failure.

 

However, impurities like Levosimendan Impurity 35 are typically not used for pharmacological or biological applications as they may not possess the therapeutic activity or safety profile required for drugs. The presence of impurities needs to be controlled during drug manufacturing to ensure the quality and safety of the medication.

 

In drug development and production, the study and control of impurities are crucial. These impurities can potentially affect the stability, safety, and efficacy of drugs. Therefore, research on impurities may involve understanding their chemical properties, sources, concentrations in the drug product, and their impact on the quality and safety of the medication.

 

Package

 

 95+ White Powder Levosimendan Impurity 35 CAS 1630760-90-5 0     95+ White Powder Levosimendan Impurity 35 CAS 1630760-90-5 1 

95+ White Powder Levosimendan Impurity 35 CAS 1630760-90-5 295+ White Powder Levosimendan Impurity 35 CAS 1630760-90-5 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 35 CAS 1630760-90-5 495+ White Powder Levosimendan Impurity 35 CAS 1630760-90-5 5

95+ White Powder Levosimendan Impurity 35 CAS 1630760-90-5 695+ White Powder Levosimendan Impurity 35 CAS 1630760-90-5 7

95+ White Powder Levosimendan Impurity 35 CAS 1630760-90-5 895+ White Powder Levosimendan Impurity 35 CAS 1630760-90-5 9

Contact Details
SICHUAN HONGRI PAHRM-TECH CO., LTD

Contact Person: admin

Send your inquiry directly to us