| Identification | Back Directory | [Name]
PINANOL 85 | [CAS]
473-54-1 | [Synonyms]
Pinanol
2-pinanol
PINANOL 85
Pinan-2-ol
DL-pinan-3-ol
TRANS-2-PINANOL
(2R)-Pinane-3α-ol
cis+trans-2-pinanol
2,6,6-trimethylnorpinan-2-ol
2,7,7-trimethylbicyclo[3.1.1]heptan-2-ol
2,6,6-trimethylbicyclo[3.1.1]heptan-3-ol
2,6,6-trimethyl-bicyclo(3.1.1)heptan-2-o
2,6,6-trimethyl-bicyclo[3.1.1]heptan-2-o
2,6,6-trimethyl-Bicyclo[3.1.1]heptan-2-ol
2,6,6-trimethylbicyclo[3.1.1]heptane-3-ol
Bicyclo3.1.1heptan-2-ol, 2,6,6-trimethyl- | [EINECS(EC#)]
207-466-6 | [Molecular Formula]
C10H18O | [MDL Number]
MFCD00013739 | [MOL File]
473-54-1.mol | [Molecular Weight]
154.25 |
| Chemical Properties | Back Directory | [Melting point ]
55 - 60°C | [storage temp. ]
Refrigerator, under inert atmosphere | [solubility ]
Chloroform (Slightly), Diethyl Ether (Slightly), Methanol (Slightly) | [form ]
Solid | [color ]
White to Off-White | [LogP]
2.650 (est) | [EPA Substance Registry System]
2-Pinanol (473-54-1) |
| Hazard Information | Back Directory | [Uses]
trans-2-Pinanol is an essential oil component found in a variety of plants. | [Production Methods]
cis-2-Pinanol is produced industrially by the catalytic hydrogenation of 2-pinane hydroperoxide. Alternatively 2-pinane hydroperoxide can be treated with sodium sulfide in aqueous sodium hydroxide or with sodium methoxide. cis-2-Pinanol can also be obtained directly from pinane by air oxidation in the presence of alkalis, such as sodium hydroxide, at 80–100 ℃. |
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