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Cyclophosphamide Monohydrate
Cyclophosphamide Monohydrate
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| 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 substance is listed as a known human carcinogen. | | | Catalog # | 007349 | | Melting Point | 44-45°C | | Solubility | Chloroform | | Method for Determining Identity | Proton NMR Spectroscopic and Mass Spectrometric Analysis | | Water Content | 7.0% | | TLC Conditions | SiO2; Dichloromethane: Methanol = 9:1; Visualized with UV, Ninhydrin and KMnO4; Single spot; Rf=0.45 | | Storage and Stability | May be stored at RT for short-term only. Long-term storage is recommended at 4°C. For maximum recovery of product, centrifuge the original vial prior to removing the cap. | | Important Note | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological. | | Toxicity and Hazards | All products should be handled by qualified personnel only, trained in laboratory procedures. | | CAS Number | 6055-19-2 | | Molecular Formula | C7H17Cl2N2O3P | | Molecular Weight | 279.1 | | Purity | ~90% | | Form | Supplied as a white solid. | | | Important Note | This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological. | | Alternate names | N,N-Bis(2-chloroethyl)tetrahydro-2H-1,3,2-oxazaphosphorin-2-amine 2-Oxide Monohydrate; Cycloblastin; Cyclostin; Cytoxan; Endoxan; Genoxal; Hexadrin; Mitoxan; NSC 26271; |
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