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| Chemical manufacturer since 1982 | ||||
| Classification | Analytical chemistry >> Standard >> Forensic and veterinary standards |
|---|---|
| Name | 20alpha-Hydroxycholesterol |
| Synonyms | (3S,8S,9S,10R,13S,14S,17S)-17-[(1S)-1-Hydroxy-1,5-Dimethyl-Hexyl]-10,13-Dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-Dodecahydro-1H-Cyclopenta[A]Phenanthren-3-Ol; (3S,8S,9S,10R,13S,14S,17S)-17-[(1S)-1-Hydroxy-1,5-Dimethylhexyl]-10,13-Dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-Dodecahydro-1H-Cyclopenta[A]Phenanthren-3-Ol; (3S,8S,9S,10R,13S,14S,17S)-17-[(2S)-2-Hydroxy-6-Methyl-Heptan-2-Yl]-10,13-Dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-Dodecahydro-1H-Cyclopenta[A]Phenanthren-3-Ol |
| Molecular Structure | ![]() |
| Molecular Formula | C27H46O2 |
| Molecular Weight | 402.66 |
| CAS Registry Number | 516-72-3 |
| SMILES | [C@H]34[C@H]1[C@@H]([C@@]2(C(=CC1)C[C@@H](O)CC2)C)CC[C@@]3([C@@H]([C@@](O)(CCCC(C)C)C)CC4)C |
| InChI | 1S/C27H46O2/c1-18(2)7-6-14-27(5,29)24-11-10-22-21-9-8-19-17-20(28)12-15-25(19,3)23(21)13-16-26(22,24)4/h8,18,20-24,28-29H,6-7,9-17H2,1-5H3/t20-,21-,22-,23-,24-,25-,26-,27-/m0/s1 |
| InChIKey | MCKLJFJEQRYRQT-APGJSSKUSA-N |
| Density | 1.036g/cm3 (Cal.) |
|---|---|
| Boiling point | 512.256°C at 760 mmHg (Cal.) |
| Flash point | 213.089°C (Cal.) |
| SDS | Available |
|---|---|
| (1) | Nachtergaele et al.. Oxysterols are allosteric activators of the oncoprotein Smoothened, Nature Chemical Biology, 2012 |
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| Market Analysis Reports |
| List of Reports Available for 20alpha-Hydroxycholesterol |