- Min.Order :500 Gram
- Purity: 99%
- Payment Terms : L/C,T/T,
Keywords
C21H20O6 CAS:118525-40-9 C21H20O6 ICARITIN CAS:118525-40-9 C21H20O6
Quick Details
- Appearance:white poweder
- Application:CAS:118525-40-9 C21H20O6 ICARITIN
- PackAge:Plastic vacuum packaging bag or bucket
- ProductionCapacity:1|Metric Ton|Day
- Storage:under the cool and dry area
- Transportation:by express or by sea
Superiority:
| ICARITIN Basic information |
| Product Name: | ICARITIN |
| Synonyms: | ICARITIN;3,5,7-Trihydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one;3,7-bis(2-hydroxyethyl)icaritin |
| CAS: | 118525-40-9 |
| MF: | C21H20O6 |
| MW: | 368.3799 |
| EINECS: | |
| Product Categories: | Aromatics;Heterocycles;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;plant extract |
| Mol File: | 118525-40-9.mol |
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| ICARITIN Chemical Properties |
| mp | 239℃ |
| density | 1.359 |
| storage temp. | 2-8°C |
| Safety Information |
| ICARITIN Usage And Synthesis |
| Chemical Properties | N/A |
| Usage | A metabolite of Icariin. Icaritin and Desmethylicaritin, two metabolites of Icariin, dramatically inhibit the growth of most malignant cells. They also have significant antiangiogenesis properties, inhibiting or eliminating entirely the development of new malignant cells. |
Details:
| ICARITIN Basic information |
| Product Name: | ICARITIN |
| Synonyms: | ICARITIN;3,5,7-Trihydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one;3,7-bis(2-hydroxyethyl)icaritin |
| CAS: | 118525-40-9 |
| MF: | C21H20O6 |
| MW: | 368.3799 |
| EINECS: | |
| Product Categories: | Aromatics;Heterocycles;Intermediates & Fine Chemicals;Metabolites & Impurities;Pharmaceuticals;plant extract |
| Mol File: | 118525-40-9.mol |
|
|
|
| ICARITIN Chemical Properties |
| mp | 239℃ |
| density | 1.359 |
| storage temp. | 2-8°C |
| Safety Information |
| ICARITIN Usage And Synthesis |
| Chemical Properties | N/A |
| Usage | A metabolite of Icariin. Icaritin and Desmethylicaritin, two metabolites of Icariin, dramatically inhibit the growth of most malignant cells. They also have significant antiangiogenesis properties, inhibiting or eliminating entirely the development of new malignant cells. |
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