Privately Coenzyme Q10 Powder Fat Soluble 98% Water Soluble 40% 20% 10%

• Powder: Yes
• Customized: Customized
• Certification: GMP, ISO 9001
• Suitable for: Elderly, Children, Adult
• Purity: >98%
• Product Name: Coenzyme Q10 Powder
• Model NO.: WH3
• Appearance: Yellow to Orange Crystalline Powder
• Storage: 2-8°c(Protect From Light)
• Usage: Pharmaceutical Industry
• Package Details: 25kg/Drum
• Mf: C20h18o10
• Packaging: 1kg/Bag, 25kg/Drum
• Shelf Life: 2 Years
• CAS No: 03-98-0
• Product Specification: 10%, 98%
• Transport Package: Carton
• Specification: 1kg/bag 25kg/drum
• Origin: China
• Production Capacity: 100000000 Kg/Year

Product Description

Manufacturer Supply High Quality Bifendate / BifendatatuM API / CAS 73536-69-3

Product Name	Manufacturer Supply High Quality Bifendate / BifendatatuM API / CAS 73536-69-3
CAS NO.	73536-69-3
Appearance	White Powder
Purity	99%
Melting Point	179-181 °C
Boiling Point	606.9±55.0 °C
Density	1.390±0.06 g/cm3
Storage	2-8°C(protect from light)
Application	Pharmaceutical raw materials; The raw material; Intermediates
Usage	Bifendate is commonly used in the pharmaceutical industry.

Bifendate is a synthetic intermediate of Schisandrin C and also an anti-HBV drug used in Chinese medicine for the treatment of chronic hepatitis B. Following the intake of Bifendate in rats, the drug was observed to improve liver function by increasing the detoxification process, reducing pathological lesions, and accelerating hepatocyte regeneration. Bifendate can also function as a membrane-stabilizing agent to protect the cell from damage. After treatment with Bifendate, the protein metabolic processes of hepatitis patients were improved, with increased serum albumin levels and decreased globulin levels. Bifendate is a potent inducer of cytochrome proteins (CYPs) and can result in clinically significant interactions. It has been proposed that the increased detoxification capability of Bifendate originates from an increase in the level of P450. Bifendate may function as a protecting agent to prevent drug-induced liver dysfunction by increasing the activity of CYP450.
 

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