API Product Detail

Cyclophosphamide Monohydrate

Explore technical data, documentation access, molecular information and enquiry options for this Clearsynth research product.

Product Code: CS-O-06288 API Research Use Only
Cyclophosphamide Monohydrate
Category
API
API Family
Cyclophosphamide
Product Code
CS-O-06288
Research Status
For Laboratory Use

Cyclophosphamide Monohydrate

Cyclophosphamide API
Stock Status: In Stock
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CAT No.
CS-O-06288
CAS No.
6055-19-2
Molecular Formula
C7H17Cl2N2O3P
Molecular Weight
279.10
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There is no hazardous surcharge associated with this product.
There is no packaging charge associated with this product.
For Research Purposes only. Not for Personal or Veterinary use.
All compounds supplied are strictly intended for laboratory, research, analytical, and scientific use only. They are not meant for human consumption, therapeutic use, or any form of clinical application.
CAS No.
6055-19-2
Product Code
CS-O-06288
M.F.
C7H17Cl2N2O3P
M.W.
279.10
Smiles
ClCCN(P1(OCCCN1)=O)CCCl.[H]O[H]
Category
API
API Family
Cyclophosphamide
Storage Condition
Store at refrigerator (2-8°C) for long term storage
IUPAC Name
2-[Bis(2-chloroethyl)amino]tetrahydro-2H-1,3,2-oxazaphosphorine 2-oxide monohydrate
References
"Wheeler; A,G,; et al,: Toxcol, Appl, Pharmcol,; 4; 324 (1962); Fraiser; L,H,; et al,: Drugs; 42; 781 (1991);colvin; O,M,; et al,:curr, Pharmceut, Design; 5; 555 (1999);"
Synonyms
2H-1,3,2-Oxazaphosphorine, 2-[bis(2-chloroethyl)amino]tetrahydro-, 2-oxide, monohydrate (8CI); 2-[Bis(2-chloroethyl)amino]tetrahydro-2H-1,3,2-oxazaphosphorine-2-oxide monohydrate; Cyclophosphamide hydrate
Application Notes
"It is a cytotoxic nitrogen mustard derivative widely used in cancer chemotherapy. It cross-links DNA, causes strand breakage, and induces mutations. Its clinical activity is associated with a decrease in aldehyde dehydrogenase 1 (ALDH1) activity. This sub"
Purity by HPLC
Not less than 90%
Hazard Compound
Refer MSDS for accurate information.
Overview
"It is a cytotoxic nitrogen mustard derivative widely used in cancer chemotherapy. It cross-links DNA, causes strand breakage, and induces mutations. Its clinical activity is associated with a decrease in aldehyde dehydrogenase 1 (ALDH1) activity. This sub"

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