| Identification | More | [Name]
D(+)-2-Octanol | [CAS]
6169-06-8 | [Synonyms]
D(+)-2-OCTANOL
D-2-OCTANOL
(S)-(+)-2-HYDROXYOCTANE
(S)-2-HYDROXYOCTANE
(S)-(+)-2-OCTANOL
(S)-2-OCTANOL
(S)-(+)-N-HEXYLMETHYLCARBINOL
(S)-(+)-OCTANOL
(s)-2-octano
(S)-octan-2-ol
PLUS-2-OCTANOL
2-Octanol, (2S)-
(S)-(+)-Hexylmethylcarbinol
(2S)-Octan-2-ol
2-Octanol, (S)-
(1S)-1-Methyl-1-heptanol | [EINECS(EC#)]
228-213-6 | [Molecular Formula]
C8H18O | [MDL Number]
MFCD00064283 | [Molecular Weight]
130.23 | [MOL File]
6169-06-8.mol |
| Chemical Properties | Back Directory | [Appearance]
Colorless to light yellow liqui | [Melting point ]
-61.15°C (estimate) | [alpha ]
9.5 º (neat) | [Boiling point ]
175 °C (lit.) | [density ]
0.822 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.426(lit.)
| [Fp ]
160 °F
| [storage temp. ]
Sealed in dry,Room Temperature | [solubility ]
1.28g/l | [form ]
clear liquid | [pka]
15.44±0.20(Predicted) | [color ]
Colorless to Almost colorless | [Odor]
at 1.00 % in dipropylene glycol. mushroom oily fatty creamy grape | [Stability:]
Stable. Combustible. Incompatible with strong oxidizing agents | [explosive limit]
0.8%(V) | [Odor Type]
mushroom | [optical activity]
[α]20/D +9.5°, neat | [Water Solubility ]
1 g/L (20 ºC) | [Merck ]
14,6752 | [BRN ]
1719323 | [InChIKey]
SJWFXCIHNDVPSH-QMMMGPOBSA-N | [LogP]
2.721 (est) | [CAS DataBase Reference]
6169-06-8(CAS DataBase Reference) | [NIST Chemistry Reference]
2-Octanol, (S)-(6169-06-8) | [EPA Substance Registry System]
2-Octanol, (2S)- (6169-06-8) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [TSCA ]
Yes | [HS Code ]
29051620 |
| Questions And Answer | Back Directory | [Description]
2-Octanol is a fatty alcohol. It is directly produced from vegetal chemistry. In industry, it is produced by a cracking process from castor oil.
2-octanol is mainly used as a raw material to produce caproic acid, an intermediate in flavor. It is used as a green solvent for various resins intended for paints and coatings or adhesives sectors. It can be employed as a defoamer in different processes, as an additive for lubricants, and as a solvent in rare minerals extraction. In coal industry, it is used as floatation agent and as a frother in mineral flotation. As an intermediate, 2-octanol can be used in synthesis of a wide range of plasticizers, esters, and surfactants, which include alcohol alkoxylates and sulfates for detergency and personal care markets; adipates, aebacates, palmitates, stearates for applications in cosmetic, paints and coatings, plastic, paper, textile, etc…; phthalates; acrylates and maleates for coatings and adhesives markets; salicylate, myristate, méthoxycinnamate for application in fragrances.
| [References]
[1] https://en.wikipedia.org/wiki/2-Octanol
[2] Robert A. Levis (2016) Hawley's Condensed Chemical Dictionary
[3] http://www.castoroil.in/castor/castor_seed/castor_oil/2_octanol/2_octanol.html
|
| Hazard Information | Back Directory | [Chemical Properties]
Colorless to light yellow liqui | [Uses]
(S)-(+)-2-Octanol is used as chiral compounds. | [Definition]
ChEBI: (2S)-octan-2-ol is an octan-2-ol. It is an enantiomer of a (2R)-octan-2-ol. |
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