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Fludarabine for system suitability
Fludarabine for system suitability

Fludarabine for system suitability

MOQ : 1 Kilograms

Fludarabine for system suitability Specification

  • Usage
  • Fludarabine is FDA approved to treat people who have chronic lymphocytic leukemia (CLL) who have not responded to at least one standard alkylting-agent-containing regimen or whose disease has progressed during treatment with such a regimen.
  • Melting Point
  • (°C), 260
  • Molecular Formula
  • C10H13FN5O7P
  • Purity
  • 98%
  • Molecular Weight
  • 365.212 Grams (g)
 

Fludarabine for system suitability Trade Information

  • Minimum Order Quantity
  • 1 Kilograms
  • Payment Terms
  • Cash Advance (CA), Cash in Advance (CID)
  • Supply Ability
  • 500 Kilograms KG Per Month
  • Delivery Time
  • 2-8 Week
  • Sample Available
  • Yes
  • Sample Policy
  • Sample costs shipping and taxes has to be paid by the buyer
  • Packaging Details
  • Carton and Poly Bag.
  • Main Export Market(s)
  • Australia, Middle East, Central America, Africa, South America, Western Europe, Asia, Eastern Europe, North America
  • Main Domestic Market
  • All India
 

About Fludarabine for system suitability

Fludarabine for system suitabilitySynonym: 2-Fluoro-9-(5-O-phosphono--D-arabinofuranosyl)-9H-purin-6-amine, Fludarabine phosphate Empirical Formula (Hill Notation): C10H13FN5O7PMolecular Weight: 365.21CAS Number: 75607-67-9

FAQs of Fludarabine for system suitability:


Q: What is the molecular weight of Fludarabine?

A: The molecular weight of Fludarabine is 365.212 grams (g).

Q: What is the molecular formula of Fludarabine?

A: The molecular formula of Fludarabine is C10H13FN5O7P.

Q: What is the melting point of Fludarabine?

A: The melting point of Fludarabine is 260C.

Q: What is the purity specification of Fludarabine?

A: Fludarabine has a purity of 98%.

Q: What is the approved use of Fludarabine by the FDA?

A: Fludarabine is FDA approved to treat chronic lymphocytic leukemia (CLL) in individuals who have not responded to at least one standard alkylating-agent-containing regimen or whose disease has progressed during treatment with such a regimen.

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