Purity: | 99%-102% |
---|---|
Brand Name: | Hande |
Grade Standard: | Medicine Grade |
Type: | Antineoplastic Agents |
CAS No.: | 33069-62-4 |
Place of Origin: | China (Mainland) |
Quick Details
Specifications
Paclitaxel is a monomeric diterpenoid alkaloid compound derived from Taxus genus.It is a white crystalline powder,slightly soluble in water,and easily soluble in organic solvents such as chloroform and acetone.It has good anticancer activity,especially for advanced metastases.Sexual ovarian cancer,breast cancer,lung cancer has a very significant effect.At present,paclitaxel is divided into natural paclitaxel and 10-DAB semi-synthetic paclitaxel.
1.Product Information
Name:10-DAT Semi-synthetic Paclitaxel
CAS number:33069-62-4
Chemical formula:C47H51NO14
Specifications:99%-102%
Color:white or nearly white powder
Source:Taxus yunnanensis,Taxus chinensis
Type:APIs
2.the History of Hande GMP
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.
3.Hande production capacity
Hande capacity:600-800kg/year
4.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.
1.Product Information
Name:10-DAT Semi-synthetic Paclitaxel
CAS number:33069-62-4
Chemical formula:C47H51NO14
Specifications:99%-102%
Color:white or nearly white powder
Source:Taxus yunnanensis,Taxus chinensis
Type:APIs
2.the History of Hande GMP
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.
3.Hande production capacity
Hande capacity:600-800kg/year
4.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.