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| | D(+)-2-Octanol Chemical Properties |
| 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 | | Odor Type | mushroom | | optical activity | [α]20/D +9.5°, neat | | explosive limit | 0.8%(V) | | Water Solubility | 1 g/L (20 ºC) | | Merck | 14,6752 | | BRN | 1719323 | | Stability: | Stable. Combustible. Incompatible with strong oxidizing agents | | 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) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36-37/39 | | WGK Germany | 3 | | TSCA | Yes | | HS Code | 29051620 |
| | D(+)-2-Octanol Usage And Synthesis |
| 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
| | Chemical Properties | Colorless to light yellow liqui | | Uses | (S)-(+)-2-Octanol is used as chiral compounds. | | Uses | (S)-(+)-2-Octanol can be used:
- To prepare the solution of 5-(benzyloxy)-isophthalic acid derivative, which is used as a 2D chiral self-assembly system comprising pyrolytic graphite.
- As a chiral template in the study of enantioselective glycidol esterification.
- As a starting material for the preparation of (+)-(S)-2-octyI tosylate, an intermediate used to prepare (?)-(R)-2-halo and azido octanes.
| | Definition | ChEBI: (2S)-octan-2-ol is an octan-2-ol. It is an enantiomer of a (2R)-octan-2-ol. |
| | D(+)-2-Octanol Preparation Products And Raw materials |
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