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10 Gram |
Negotiable |
Offer 95635-56-6 95635-56-6 own lab /supplier /factory Own lab offer 95635-56-6 for An orally active and potent cholesterol ester transfer protein (CETP) inhibitor for the treatment of atherosclerosis, in particular dyslipidemia.
1. Certificate Of Analysis (COA)
2. Material Safety Data Sheet (MSDS)
3. Route of synthesis (ROS)
4. Method of Aanlysis (MOA)
5. Nuclear Magnetic Resonance (NMR)
6. Packing pictures and loading video before loading
7. Free Sample
9. Factory audit
10. Strong after-sale service
Ranolazine dihydrochloride Basic information |
Product Name: | Ranolazine dihydrochloride |
Synonyms: | (+/-)-4-[2-HYDROXY-3-(O-METHOXYPHENOXY)PROPYL]-1-PIPERAZINEACETO-2',6'-XYLIDIDE DIHYDROCHLORIDE;n-(2,6-dimethylphenyl)-2-[4-[2-hydroxy-3-(2-methoxyphenoxy)propyl]piperazin-1-yl]acetamide dihydrochloride;(+/-)-N-(2,6-DIMETHYLPHENYL)-4-[2-HYDROXY-3-(2-METHOXYPHENOXY)PROPYL]-1-PIPERAZINEACETAMIDE DIHYDROCHLORIDE;RANOLAZINE DIHYDROCHLORIDE;RANOLAZINE HCL;Ranolazine DiHCI;Ranolazine and salt;(±)-N-(2,6-dimethylphenyl)-4-[2-hydroxy-3-(2-methoxyphenoxy)propyl]-1-piperazineacetamide |
CAS: | 95635-56-6 |
MF: | C24H35Cl2N3O4 |
MW: | 500.46 |
EINECS: | |
Product Categories: | Active Pharmaceutical Ingredients;Aromatics Compounds;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Ranolazine;Cardiovascular APIs |
Mol File: | 95635-56-6.mol |
Ranolazine dihydrochloride Chemical Properties |
mp | 222-229.5 °C(lit.) |
storage temp. | Desiccate at RT |
solubility | H2O: 10 mg/mL, soluble |
form | solid |
color | off-white |
CAS DataBase Reference | 95635-56-6(CAS DataBase Reference) |
Safety Information |
Safety Statements | 22-24/25 |
WGK Germany | 3 |
MSDS Information |
Provider | Language |
---|---|
SigmaAldrich | English |
Ranolazine dihydrochloride Usage And Synthesis |
Chemical Properties | White Crystalline Powder |
Usage | Anti-ischemic agent which modulates myocardial metabolism. Antianginal |
Usage | treatment of angina and congestive heart failure |
Biological Activity | Antianginal agent with antiarrhythmic properties that acts as a partial fatty acid oxidation inhibitor. Activates pyruvate dehydrogenase in ischemic myocytes to promote glucose oxidation, switching substrate utilization from fatty acids to glucose. Also shown to inhibit late I Na and I Kr currents. |
PRODUCT INFORMATION :
COMPANY INFORMATION :
1. Mixed container, we can mix different items in one container.
2. Quality control, before shipment, free sample for test. after shipment, keep sample for 3 years
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