4-Hydroperoxy Cyclophosphamide-d4

Product Name 4-Hydroperoxy Cyclophosphamide-d4
Alternate Names Cyclophosphamide Stable Isotopes, Stable Isotopes of Cyclophosphamide
CAT No. CS-T-78084
CAS No. 1246816-71-6
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Cyclophosphamide
Smileys OOC1NP(OCC1)(N(CC([2H])([2H])Cl)CC([2H])([2H])Cl)=O
Canonical Smiles C1COP(=O)(NC1OO)N(CCCl)CCCl
InchIKey VPAWVRUHMJVRHU-BYUTVXSXSA-N
Inchl InChI=1S/C7H15Cl2N2O4P/c8-2-4-11(5-3-9)16(13)10-7(15-12)1-6-14-16/h7,12H,1-6H2,(H,10,13)/i2D2,4D2
IUPAC N-(2-chloroethyl)-N-(2-chloro-1,1,2,2-tetradeuterioethyl)-4-hydroperoxy-2-oxo-1,3,2lambda5-oxazaphosphinan-2-amine
Controlled No
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4-Hydroperoxy Cyclophosphamide-d4 is a deuterated form of the cyclophosphamide drug, which is used in chemotherapy to treat various types of cancer. This drug is an alkylating agent that works by damaging the DNA of cancer cells, preventing them from dividing and growing. The deuterated form of this drug is used in research and development to better understand the mechanism of action and pharmacokinetics of the drug. Chemically, 4-Hydroperoxy Cyclophosphamide-d4 has the molecular formula C7H12CIN2O4P and a molar mass of 296.6 g/mol. It is a yellowish solid that is soluble in water and organic solvents like ethanol and methanol. The deuterated form is labeled with four deuterium atoms, which are stable isotopes of hydrogen. In terms of usage, 4-Hydroperoxy Cyclophosphamide-d4 is primarily used in preclinical studies to investigate the pharmacokinetics and metabolism of the cyclophosphamide drug. It is also used in the development of new drugs that can be used in cancer treatment. The deuterated form of the drug allows researchers to track its movement in the body and determine the effects of different doses and formulations. Overall, 4-Hydroperoxy Cyclophosphamide-d4 is an important tool in cancer research and drug development. Its unique properties allow researchers to better understand the mechanism of action of the cyclophosphamide drug and develop new treatments for cancer.

Related Compounds

Cyclophosphamide D4 | N-Dechloroethyl Cyclophosphamide-d4 | Cyclophosphamide D8 | Cyclophosphamide D6 |

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