Yunnan Hande Biotechnology Co., Ltd.| Manufacturer

Yunnan Hande Biotechnology Co., Ltd.

[ Yunnan, China ]
Business Type: Manufacturer
Brand(s): Hande
Main Markets: North America, South America, Eastern Europe
Main Product: Pharmaceutical APIs, Pharmaceutical Intermediates, Plant Extracts, Natural Paclitaxel, Ecdysterone, Melatonin
Year Established: 1993
Years OEM Experience: 20
Employ Number: 101 - 500 People
Annual Sales Volume: US$5 Million - US$10 Million
Factory Size: 5,000-10,000 square meters
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Yunnan Hande Biotechnology Co., Ltd.

China Manufacturer with main products: Pharmaceutical APIs, Pharmaceutical Intermediates, Plant Extracts, Natural Paclitaxel, Ecdysterone, Melatonin

Home  >Products Catalog > Pharmaceutical Intermediates > Docetaxel Trihydrate CAS 148408-66-6 Raw Material of Docetaxel Trihydrate

Docetaxel Trihydrate CAS 148408-66-6 Raw Material of Docetaxel Trihydrate

FOB Price: 200.00 - 300.00 USD/Gram
In Stock

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Export Markets: North America, South America, Eastern Europe, Southeast Asia, Africa, Oceania, Mid East, Eastern Asia, Western Europe
Place of Origin: Yunnan in China

Quick Details

  • Purity: 99%
  • Brand Name: 148408-66-6
  • Grade Standard: Medicine Grade
  • Type: Antineoplastic Agents
  • CAS No.: 148408-66-6

Specifications

Docetaxel Trihydrate CAS 148408666 Raw Material of Docetaxel Trihydrate
Docetaxel Trihydrate is a semisynthetic analog of paclitaxel that attenuates the effects of bcl-2 and bcl-xL gene expression.Docetaxel Trihydrate arrests the G2/M cell cycle,leading to apoptosis.Hande Bio provides Docetaxel Trihydrate CAS 148408-66-6 Raw Material of Docetaxel Trihydrate.for more details,please contact us online.

1.Product Information

Name:Docetaxel Trihydrate

CAS number:148408-66-6

Chemical formula:C43H59NO17

Specifications:99-101%

Color:white to off-white powder

Source:Branches and leaves of plants of the genus Taxaceae

Type:Intermediate

2.Shelf life

Storage conditions:sealed,protected from light,dry,controlled at room temperature(15-30°C)

3.Hande production capacity

Production cycle:2-3 weeks,batch 20kg.

4.Hande GMP process

1996,the quality system was established and obtained DMF.

2004,FDA on-site inspection obtained CGMP certificate.

2009,semi-synthetic paclitaxel DMF and natural paclitaxel CEP were obtained.

2011,semi-synthetic paclitaxel CEP was obtained.

2012,passed the TGA on-site inspection,obtained GMP certification,and passed the FDA on-site inspection.

2013,passed the CGMP site.

2015,India was registered and Japan was registered.

5.Our services

1.Products:Provide high-quality,high-purity plant extracts,pharmaceutical raw materials,and pharmaceutical intermediates.

2.Technical services:Customized extracts with special specifications according to customer requirements.




Service Process

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