Quercetin dihydrate NEW
| Price | Get Latest Price |
| Package | 25KG |
| Min. Order: | 1KG |
| Supply Ability: | 50000KG/month |
| Update Time: | 2023-08-29 |
Product Details
| Product Name: Quercetin dihydrate | CAS No.: 6151-25-3 |
| EC-No.: 612-158-3 | Min. Order: 1KG |
| Purity: 99% | Supply Ability: 50000KG/month |
| Release date: 2023/08/29 |
| CAS: | 6151-25-3 |
| MF: | C15H14O9 |
| MW: | 338.27 |
| EINECS: | 612-158-3 |
| Product Categories: | Flavanols;Biochemistry;Flavonoids;C15 to C38;Carbonyl Compounds;Ketones;Signalling;Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Tyrosine Kinase Inhibitors;Inhibitors;TROXEPURE |
| Mol File: | 6151-25-3.mol |
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| Quercetin dihydrate Chemical Properties |
| Melting point | >300 °C(lit.) |
| density | 1.680 g/cm3 |
| storage temp. | -20°C |
| solubility | Soluble in DMSO > 10 mM |
| form | Yellow solid |
| Colour Index | 75670 |
| color | Yellow |
| Water Solubility | practically insoluble |
| Merck | 14,8034 |
| BRN | 317313 |
| InChIKey | GMGIWEZSKCNYSW-UHFFFAOYSA-N |
| LogP | 2.075 (est) |
| CAS DataBase Reference | 6151-25-3(CAS DataBase Reference) |
| Quercetin dihydrate Usage And Synthesis |
| Chemical Properties | yellow crystalline powder |
| Uses | capillary protectant, antioxidant. antineoplastic, anti-HIV |
| Uses | bioflavenoid, antioxidant, antiviral, antimicrobial, enzyme inhibitor |
| Uses | Quercetin dihydrate used as a Inhibitor of protein tyrosine kinase, mitochondrial ATPase and phosphodiesterase inhibitor. It Inhibits PI3-kinase activity and slightly inhibits PIP kinase activity. |
| General Description | Produced and qualified by HWI pharma services GmbH. Exact content by quantitative NMR can be found on the certificate. |
| Biochem/physiol Actions | Quercetin dihydrate is a flavonoid with anticancer activity. Quercetin is a mitochondrial ATPase and phosphodiesterase inhibitor. It Inhibits PI3-kinase activity and slightly inhibits PIP kinase activity. Quercetin has antiproliferative effects on cancer cell lines, reduces cancer cell growth via type II estrogen receptors, and arrests human leukemic T cells in late G1 phase of the cell cycle. |
| target | HMG-CoA Reductase | SOD | Antifection |
| storage | Room temperature |
| Purification Methods | Crystallise the flavone from aqueous EtOH and dry at 100o. It also sublimes in a vacuum. IR: 2.5 and 16.7 (KBr). max It complexes with Cu2+, Al3+, Ca2+, Ge4+, Zn2+, Ti4+, Zr4+, Th4+, UO4+ . [Beilstein 18 H 242, 18 I 242, 18 II 236, 18 III/IV 3470, 18/5 V 494.] |
Product picture
Packing &shipping&Payment
Shipping:by sea or by air
Payment:T/T,western union,moneygram
Packaging Details drum
Port:Tianjin
Lead Time :
| Quantity(Kilograms) | 1 - 10000 | >10000 |
| Est. Time(days) | 5 | To be negotiated |
Company information
Hebei Mojin Biotechnology Co., Ltd, Our company is a professional in 4'-Methylacetophenone,Levamisole hydrochloride ,N-Methylformamide and other chemical reagents research and development production enterprises. Our business covers more than 30 countries, most of the big customers come from Europe, America and other countries in the world, we can guarantee the quality and price. In recent decades, with the efforts of all employees, we have established many cooperative companies in shandong, henan, guangdong and other places. Our corporate purpose is based on the market, enhance the strength, take the road of scientific and environmental sustainable development, relying on the country. Technology r & d center, increase the investment in r & d, based on the domestic market, expand the international market, manufacturing quality products, sincere service to the society, into a modern, ecological, scientific and technological enterprise world.
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