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95+ White Powder Etrapopa Ethanolamine impurity CAS 1437383-35-1

95+ White Powder Etrapopa Ethanolamine impurity CAS 1437383-35-1

95+ White Powder Etrapopa Ethanolamine impurity CAS 1437383-35-1
95+ White Powder Etrapopa Ethanolamine impurity CAS 1437383-35-1

Large Image :  95+ White Powder Etrapopa Ethanolamine impurity CAS 1437383-35-1 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: Etrapopa Ethanolamine Impurity CAS No: 1437383-35-1
M.W: 456.49 MF: C26H24N4O4
Appearance: White Powder Purity: 95+
EINECS No: - Storage: 5-25°C

 

Product Description

 

White Powder Etrapopa Ethanolamine impurity CAS 1437383-35-1 Purity 95+

 

Name: Etrapopa Ethanolamine impurity

CAS NO1437383-35-1

M.W: 456.49

Appearance: White Powder

Purity: 95+   

SynonymsEtrapopa Ethanolamine impurity

 

Application

 

EtrapopaEthanolamine impurity, also referred to as eltrombopag ethanolamine impurity, is a potential impurity that may arise during the synthesis or manufacturing of eltrombopag, a drug used to treat thrombocytopenia and other blood disorders. This impurity does not have direct therapeutic applications but rather serves as an indicator for quality control and safety evaluation of the drug.

 

In the pharmaceutical industry, the presence of impurities like EtrapopaEthanolamine impurity is carefully monitored and controlled to ensure the safety and efficacy of the final drug product. The study and analysis of this impurity are crucial for understanding its origin, quantity, and potential effects on the stability, purity, and safety of eltrombopag.

 

The primary application of EtrapopaEthanolamine impurity lies in quality control and assurance during drug development and production. Manufacturers employ rigorous analytical methods to detect and quantify this impurity, allowing them to adjust production processes, optimize manufacturing techniques, and ensure that the final drug product meets the required standards for safety and efficacy.

 

Additionally, the characterization of EtrapopaEthanolamine impurity may contribute to pharmacokinetic and metabolism studies. By understanding how this impurity behaves in the body, researchers can gain insights into the metabolic pathways of eltrombopag and the formation of its metabolites. This information can guide further optimization of the drug and its safety profile.

 

Package

 

 95+ White Powder Etrapopa Ethanolamine impurity CAS 1437383-35-1 0     95+ White Powder Etrapopa Ethanolamine impurity CAS 1437383-35-1 1 

95+ White Powder Etrapopa Ethanolamine impurity CAS 1437383-35-1 295+ White Powder Etrapopa Ethanolamine impurity CAS 1437383-35-1 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 Etrapopa Ethanolamine impurity CAS 1437383-35-1 495+ White Powder Etrapopa Ethanolamine impurity CAS 1437383-35-1 5

95+ White Powder Etrapopa Ethanolamine impurity CAS 1437383-35-1 695+ White Powder Etrapopa Ethanolamine impurity CAS 1437383-35-1 7

95+ White Powder Etrapopa Ethanolamine impurity CAS 1437383-35-1 895+ White Powder Etrapopa Ethanolamine impurity CAS 1437383-35-1 9

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