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Introduction
Product name | Cyclophosphamide |
CAS | 50-18-0 |
Appearance | white powder |
Assay | 99% |
Storage | Cool and Protect from light |
Function
Product Name:Cyclophosphamide
CAS:50-18-0
MF:C7H15Cl2N2O2P
MW:261.085961
EINECS:200-015-4
Mol File:50-18-0.mol
Melting point:41-45°C
Boiling point:336.1±52.0 °C(Predicted)
Density 1.33±0.1 g/cm3(Predicted)
form solid
pka2.84±0.20(Predicted)
Water Solubility Soluble. 1-5 g/100 mL at 23 ºC
Stability:Stable, but light sensitive. Incompatible with oxidizing agents.
Application
Cyclophosphamide is one of the most successful anticancer agents ever synthesized. Even today, 50 years after its synthesis, cyclophosphamide is still widely used as a chemotherapeutic agent and in the mobilization and conditioning regimens for blood and marrow trans plantation (BMT). Among 1,000 selected compounds and antibiotics tested against 33 tumors, cyclophosphamide was the most effective molecule. The initial clinical trials[1, 2] of cyclophosphamide for the treatment of cancer were performed in 1958, and in 1959 it became the eighth cytotoxic anticancer agent approved by the FDA. It is also approved for minimal change disease of the kidney in children (a disease that causes nephrotic syndrome), but despite its widespread use in other autoimmune disorders and BMT, it has never been approved for these indications.
Specification
Item | Specification |
Description | White crystalline powder |
Identification A | IR , UV conform |
Identification B | Should conform |
PH Value | Between 3.9 to 7.1 |
Wate | Between 5.7%~6.8% |
Heavy Metals | Not more than 0.002% |
Chlorides | Not more than 0.018% |
Melting range | Between 48.5°C and 52°C |
Related | A: Not more than 0.06 B: Not more than 0.06 C: Not more than 0.06 D: Not more than 0.06 |
LIMIT OF PROPANOLAMINE | ≤ 0.025 % |
LIMIT OF PHOSPHATE | ≤ 0.01 % |
Residual solvents | Alcohol : not more than 5000ppm Aceton : not more than 5000ppm |
Assay | Between 97.0 and 103.0% |