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| 4-Hydroxyphenyl-beta-D-glucopyranoside |
| Hydroquinone-beta-D-glucopyranoside |
| Arbutin |
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Predict NMR spectrum
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| InChI: |
1S/C12H16O7/c13-5-8-9(15)10(16)11(17)12(19-8)18-7-3-1-6(14)2-4-7/h1-4,8-17H,5H2/t8-,9-,10+,11-,12-/m1/s1 |
| InChIKey: |
BJRNKVDFDLYUGJ-RMPHRYRLSA-N |
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| H donor: |
5 |
| H acceptor: |
7 |
| Rotatable bond: |
3 |
| Stereocenter: |
5 |
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| cLogP: |
-0.727 |
| cLogS: |
-0.91 |
| Polar surface: |
119.61 |
| NEW: 3D model: |
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Click on a product name to get more information on that compound, on a supplier name to get more information on that supplier.
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Supplier
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Description
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Reference
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| amadischem
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Arbutin, 98%
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| advtechind
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arbutin, 99.5% by hplc natural
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5MG |
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on request |
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10MG |
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on request |
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25MG |
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on request |
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| alfa-chemistry
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Arbutin, 98%
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| leapchem
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arbutin
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| alfa-chemistry
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Arbutin is a natural active substance derived from green plants. It combines the "green plant, safe and reliable" and "high-efficiency discoloration" into a skin decolorizing component, which can quickly penetrate into the skin without affecting cell proliferation. At the same time, it can effectively inhibit the activity of tyrosinase in the skin, block the formation of melanin, and directly combine with tyrosinase to accelerate the decompositio;n and excretion of melanin, thereby reducing skin pigmentation, eliminating pigmentation and Freckles, and do not produce toxic, irritating, sensitizing and other side effects on melanocytes, as well as bactericidal and anti-inflammatory effects., 98%
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| leapchem
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arbutin
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| leapchem
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deoxyarbutin, 98%
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| cm-finechemicals
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Arbutin
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| bocsci
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Arbutin, ≥ 98%
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| chemieliva
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Arbutin, 98%
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| carbonesci
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Deoxyarbutin, 98%
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| oakwood
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| biosynth
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| manchesterorganics
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| (2R,3S,4S,5R,6S)-2-(Hydroxymethyl)-6-(4-hydroxyphenoxy)tetrahydropyran-3,4,5-triol |
| , 97%
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| rosewachem
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Arbutin
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| fmect
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β-Arbutin
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| cslabs
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b-Arbutin
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| kinbester
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Beta-Arbutin
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| bocsci
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Arbutin, ≥ 98%
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| aceschem
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hydroquinone O-β-D-glucopyranoside, 98%NLT
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