Molecular structure of Oleyl alcohol, CAS Number: 143-28-2
Oleyl alcohol (CAS 143-28-2)
Alternate Names:
Z-9-Dodecen-1-ol; cis-9-Octadecen-1-ol
Application:
Oleyl alcohol is a long-chain, unsaturated fatty alcohol that can be used as an emulsifier, nonionic surfactant and thickener
CAS Number:
143-28-2
Molecular Weight:
268.48
Molecular Formula:
C18H36O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Oleyl alcohol has been recognized for its anti-inflammatory and antioxidant properties, and its ability to inhibit certain bacterial growth. In industrial research, it is investigated for its properties as an emollient and its ability to stabilize emulsions, making it a subject of interest in the development of non-ionic surfactants. As a surfactant, oleyl alcohol can reduce the surface tension of liquids, which aids in its ability to penetrate skin and other tissues, and to interact with proteins and other molecules within. Its interactions with cell membranes may induce changes in cellular structure and functions.
Oleyl alcohol (CAS 143-28-2) References
- Enhancement of oleyl alcohol anti tumor activity through complexation in polyvinylalcohol amphiphilic derivatives. | Orienti, I., et al. 2007. Drug Deliv. 14: 209-17. PMID: 17497353
- Kinetics of enzymatic synthesis of liquid wax ester from oleic acid and oleyl alcohol. | Radzi, SM., et al. 2010. J Oleo Sci. 59: 127-34. PMID: 20124754
- Phase behavior and hydrated solid structure in lysophospholipid/long-chain alcohol/water system and effect of cholesterol addition. | Konno, Y., et al. 2010. J Oleo Sci. 59: 581-7. PMID: 20972358
- Membrane extraction for detoxification of biomass hydrolysates. | Grzenia, DL., et al. 2012. Bioresour Technol. 111: 248-54. PMID: 22361069
- Renewable synthesis of n-butyraldehyde from glucose by engineered Escherichia coli. | Ku, JT., et al. 2017. Biotechnol Biofuels. 10: 291. PMID: 29213330
- Adenosine Triphosphate and Carbon Efficient Route to Second Generation Biofuel Isopentanol. | Eiben, CB., et al. 2020. ACS Synth Biol. 9: 468-474. PMID: 32149502
- Direct production of fatty alcohols from glucose using engineered strains of Yarrowia lipolytica. | Cordova, LT., et al. 2020. Metab Eng Commun. 10: e00105. PMID: 32547923
- Lysine-Based Biodegradable Surfactants: Increasing the Lipophilicity of Insulin by Hydrophobic Ion Paring. | Kurpiers, M., et al. 2021. J Pharm Sci. 110: 124-134. PMID: 32758547
- Group 13 Lewis acid catalyzed synthesis of metal oxide nanocrystals via hydroxide transmetallation. | Gibson, NJ., et al. 2021. Nanoscale. 13: 11505-11517. PMID: 34180490
- Intensification of p-coumaric acid heterologous production using extractive biphasic fermentation. | Combes, J., et al. 2021. Bioresour Technol. 337: 125436. PMID: 34182346
- Seasonal Changes in Essential Oil Constituents of Cystoseira compressa: First Report. | Generalić Mekinić, I., et al. 2021. Molecules. 26: PMID: 34771056
- Photodynamic therapy fortified with topical oleyl alcohol-based transethosomal 8-methoxypsoralen for ameliorating vitiligo: Optimization and clinical study. | Mahmoud, DB., et al. 2022. Int J Pharm. 614: 121459. PMID: 35026313
- Lipase Catalyzed Transesterification of Model Long-Chain Molecules in Double-Shell Cellulose-Coated Oil-in-Water Emulsion Particles as Microbioreactors. | Meir, I., et al. 2022. Int J Mol Sci. 23: PMID: 36292979
- Effective hexanol production from carbon monoxide using extractive fermentation with Clostridium carboxidivorans P7. | Oh, HJ., et al. 2023. Bioresour Technol. 367: 128201. PMID: 36374655
- N-Alkylation of Amines by C1-C10 Aliphatic Alcohols Using A Well-Defined Ru(II)-Catalyst. A Metal-Ligand Cooperative Approach. | Guin, AK., et al. 2023. J Org Chem.. PMID: 37052217
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Oleyl alcohol, 1 g | sc-215628 | 1 g | $219.00 | |||
Oleyl alcohol, 5 g | sc-215628A | 5 g | $801.00 |