Product: Cyclophosphamide Monohydrate
Catalog Number: 17429
CAS Number: 6055-19-2
Synonyms: Cyclophosphamide monohydrate; Cytotoxan;
2-[Bis(2-chloroethyl)amino]tetrahydro-2H-1,3,2-oxazaphosphorine 2-oxide
1 g =  $790   (In Stock) Add to Cart
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Formula: C7H15Cl2N2O2P • H2O
Chemical Purity: >97%
Molecular Weight: 279.10
Structure: Cyclophosphamide Monohydrate
Appearance: White crystalline
Category: Anti-cancer compounds
Stability: Stable under recommended storage conditions.

Keep container tightly closed in a dry and well-ventilated place. Recommended storage temperature: 2-8°C.


IATA: Hazard Class: 6.1; UN Number: UN3464; Packing Group: III; Shipping Name: Organophosphorus compound, toxic, solid, n.o.s. (Cyclophosphamide monohydrate)

Literature References:

Cullion, K., et al., Targeting The Notch1 And MTOR Pathways In A Mouse T-ALL Model. Blood 113, 6172-81, (2009); Tammam, J., et al., Down-regulation Of The Notch Pathway Mediated By A Gamma-secretase Inhibitor Induces Anti-tumour Effects In Mouse Models Of T-cell Leukaemia. Br. J. Pharmacol. 158, 1183-95, (2009); Guerriero, J.L., et al., DNA Alkylating Therapy Induces Tumor Regression Through An HMGB1-Mediated Activation Of Innate Immunity. J. Immunol. 186, 3517-26, (2011); Gibson, L.F., et al., Regulation of BAX and BCL-2 expression in breast cancer cells by chemotherapy. Breast Cancer Res. Treat. 55, 107-117, (1999); Ren, S., et al., Inhibition of human aldehyde dehydrogenase 1 by the 4-hydroxycyclophosphamide degradation product acrolein. Drug Metab. Dispos. 27, 133-137, (1999); Inagawa, H., et al., Mechanisms by which chemotherapeutic agents augment the antitumor effects of tumor necrosis factor: involvement of the pattern shift of cytokines from Th2 to Th1 in tumor lesions. Anticancer Res. 18, 3957-3964, (1998); Merck 14,2747; Aldrich MSDS 1, 537:C / Corp MSDS 1 (1), 992:C / FT-IR 1 (1), 920:C / FT-IR 2 (1), 1582:D / FT-NMR 1 (1), 1500:B / IR-Spectra (3), 552:G / NMR-Reference 2 (2), 872:B / RegBook 1 (1), 1119:E / Sax 6, 1277 / Sigma FT-IR 1 (2), 418:D / Structure Index 1, 173:D:4


Cyclophosphamide 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.