Oleyl alcohol
Structural formula
| Business number | 03W2 |
|---|---|
| Molecular formula | C18H36O |
| Molecular weight | 268.48 |
| label |
Olive oil alcohol, cis-9-octadecene-1, cis-9-octadecen-1-ol, 9-n-Octadecenol, Oleic alcohol, (Z)-9-Octadecen-1-ol, detergents, emulsifiers, alcohol solvent |
Numbering system
CAS number:143-28-2
MDL number:MFCD00002993
EINECS number:205-597-3
RTECS number:RG4120000
BRN number:1723962
PubChem number:24898063
Physical property data
1. Properties: colorless or light yellow oily liquid
2. Relative density (25/4℃): 0.8489
3. Refraction Rate (n20D): 1.461
4. Flash point (ºC): 120.7
5. Melting point (℃): 6~7
6. Boiling point (ºC, 2kpa): 333, 207ºC (2kpa)
7. Solubility: soluble in ethanol, Ether, insoluble in water.
Toxicological data
None
Ecological data
Other harmful effects: This substance may be harmful to the environment, and special attention should be paid to water bodies.
Molecular structure data
1. Molar refractive index: 87.03
2. Molar volume (cm3/mol): 316.7
3. Isotonic specific volume (90.2K ): 752.2
4. Surface tension (dyne/cm): 31.7
5. Polarizability (10-24cm3): 34.50
Compute chemical data
1. Reference value for hydrophobic parameter calculation (XlogP): 7.4
2. Number of hydrogen bond donors: 1
3. Number of hydrogen bond acceptors: 1
4. Number of rotatable chemical bonds: 15
5. Topological molecular polar surface area (TPSA): 20.2
6. Number of heavy atoms: 19
7. Surface charge: 0
8. Complexity: 175
9. Number of isotope atoms: 0
10. Determine the number of atomic stereocenters : 0
11. The number of uncertain atomic stereocenters: 0
12. The number of determined chemical bond stereocenters: 1
13. Uncertain chemical bond stereocenters Number of structural centers: 0
14. Number of covalent bond units: 1
Properties and stability
1. Stable under normal temperature and pressure.
2. Incompatible materials: strong oxidizing agents.
3. Exist in mainstream smoke.
Storage method
Store at -20℃.
Synthesis method
1. Mix ethyl oleate and anhydrous acetic acid, quickly add metal sodium flakes, and the reaction proceeds vigorously. After the reaction eases, add absolute ethanol and heat until the sodium metal completes the reaction. Then add water and reflux for 1 hour to saponify unreacted ethyl oleate. cool downAfter that, it is extracted with ether, neutralized and washed; after drying, the ether is evaporated, and fractionation is carried out under reduced pressure to collect the 150-152°C (0.133kPa) fraction, which is oleyl alcohol. The yield is about 50%.
Purpose
1. Used in the manufacture of detergents; wetting agents; defoaming agents; lubricants for metal cutting; plasticizers and fabric softeners.
2. Used in organic synthesis , raw materials for special surfactants, which can be used to produce oil additives, cold-resistant auxiliary plasticizers, lubricants and solvents, etc.
3. Fat-enriching agent is a raw material for the production of wetting agents, emulsifiers, detergents, and dispersants. It is also suitable for use in cosmetics and medicines. The oily component of the preparation.
