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Description
Chlorpromazine Hydrochloride inhibits calmodulin-dependent stimulation of cyclic nucleotide phosphodiesterase and nitric oxide synthase, and it is reported to uncouple and inhibit oxidative phosphorylation at 10-3 – 10-4 M.
- Demonstrates cytotoxic and antiproliferative activity against leukemic cells, but does not affect the viability of normal lymphocytes
- Phenothiazine antipsychotic
- D2 dopamine and H1 histamine receptors antagonist
- Possibly a photo-genotoxic agent in humans
- Helps to induce hypothermia in mice in the dose range of 12.5–100mg/kg
- A substitute for benzidine, o-dianisidine, and o-tolidine in the determination of microquantities of hemoglobin and peroxidase
Specifications
Specifications
| Melting Point | 194°C to 199°C |
| Loss on Drying | ≤1.0% |
| Quantity | 1 kg |
| Solubility Information | Soluble in water (50mg/mL - clear, colorless to faint yellow-grey solution), methanol, ethanol, chloroform; practically insoluble in ether, benzene. |
| Formula Weight | 355.3g/mol |
| Physical Form | Powder |
Safety and Handling
| Recommended Storage | Store at Room Temperature (15–30°C) |
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