
Olivetol CAS: 500-66-3
3,5-hydroxypentylbenzene/Olivetol Usage: Intermediates used in poliomyelitis and other pharmaceutical intermediates. 3,5-hydroxypentylbenzene/Olivetol Packaging and Shipping: 1kg per bag or 25kg/...
Category:Pharmaceutical Materials
Introduction
3,5-hydroxypentylbenzene/Olivetol Usage: Intermediates used in poliomyelitis and other pharmaceutical intermediates. 3,5-hydroxypentylbenzene/Olivetol Packaging and Shipping: 1kg per bag or 25kg/carton or as required by buyer 3,5-hydroxypentylbenzene/Olivetol Storage: Stored in a dry and ventilated warehouse;Stay out of the sun;Avoid fire;Avoid dampness.
Name | 3,5-hydroxypentylbenzene |
Synonyms | Olivetol Oilvetol OLIVETOL AURORA KA-7378 n-Amylresolcinol 5-AMYL RESORCINOL 5-Pentylresorcinol 5-PENTYLRESORCINOL 5-N-PENTYLRESORCINOL 5-pentyl-3-benzenediol 3,5-dihydro-amylbenzene 5-pentylbenzene-1,3-diol 5-PENTYL 1,3-BENZENEDIOL 3,5-hydroxypentylbenzene 3,5-dihydroxyamylbenzene 5-Pentyl-1,3-benzenediol Pentyl-3,5-dihydroxybenzene 5-Pentyl3,5-Dihydroxyamylbenzene |
CAS | 500-66-3 |
EINECS | 207-908-8 |
InChI | InChI=1/C11H16O2/c1-2-3-4-5-9-6-10(12)8-11(13)7-9/h6-8,12-13H,2-5H2,1H3 |
InChIKey | IRMPFYJSHJGOPE-UHFFFAOYSA-N |
Molecular Formula | C11H16O2 |
Molar Mass | 180.24 |
Density | 1.068±0.06 g/cm3(Predicted) |
Melting Point | 46-48°C(lit.) |
Boling Point | 164 °C |
Flash Point | >230°F |
Solubility | Soluble in water (partly miscible), chloroform, and methanol. |
Vapor Presure | 0.000273mmHg at 25°C |
Appearance | Solid |
Color | Colourless to Beige Oil to Low-Melting |
pKa | 9.59±0.10(Predicted) |
Storage Condition | Keep in dark place,Inert atmosphere,Room temperature |
Stability | Light Sensitive |
Refractive Index | 1.546 |
MDL | MFCD00002293 |
In vitro study | Olivetol inhibits the (S)-mephenytoin 4′-hydroxylase activity of CYP2C19 activity with an IC 50 of 15.3 μM and a K i of 2.71 μM. Olivetol also inhibits AMMC O-demethylase activity of recombinant CYP2D6 with an IC 50 of 7.21 μM and a K i of 2.87 μM. Olivetol is a competitive inhibitor of the cannabinoid receptors CB1 and CB2. |
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