- Product Details
Keywords
- Stereoisomer of 9,10,12,13,14,21,22,23,24,25,26,27,32,33,34, 34a-hexadecahydro-9,27-dihydroxy-3-[2-(4-hydroxy-3- methoxycyclohexyl)-1-methylethyl]-10,21-dimethoxy-6,8,12,14, 20, 26-hexamethyl-23,27-ep
- RAP
- Sirolimus [USAN:BAN:INN]
Quick Details
- ProName: Rapamycin
- CasNo: 53123-88-9
- Molecular Formula: C51H79NO13
- Appearance: Colorless to yellow
- DeliveryTime: With in 3 days
- PackAge: 1kg/bag
- Port: Shanghai
- ProductionCapacity: 100 Kilogram/Week
- Purity: 99%
- Storage: 2-8℃
- LimitNum: 1 Kilogram
Superiority
Hubei Centro Pharmaceutical is a company mainly engaged in Contract Manufacturing, Research and export of products including, without limitation, pharmaceutical raw materials both for vet and human, Intermediates, Fine chemicals, Vitamins, Amino Acids, Plant extract, Feed and food additives.
With our years effort, we have been providing a wide range of pharmaceutical products to a variety of markets in Southeast Asia, Central America, LATAM, CIS, and Africa. We are committed to being flexible, responsive and innovative in addressing the evolving needs of our customers.
Custom Development – Centro Pharma can offer a unique research environment for custom synthesis and process development. Centro Pharmaceutical’s expert staff and laboratory in collaboration with highly respected outside resources offers the skills and experience to expedite the development process.
Custom Manufacturing – Working on an Exclusive Basis with a number of domestic and international cGMP manufacturers, Centro Pharma can supply those difficult to produce generics and new pharmaceuticals in a time frame that enables quick market entry.
Custom Production Facilities – Whether your requirements demand large-scale fermentation capacity or clean room scale synthesis, Centro Pharma has the range of capabilities to satisfy your needs. Should your requirements demand it, experienced engineers can design and build a facility quickly and efficiently. Through our own laboratory, we can provide analytical services from methods development to methods validation. All projects are conducted under cGMP conditions and are supported with DMF filings or product registration.