Oleyl alcohol
Based on 1 Customer Validation
Oleyl alcohol is an anti-tumor compound that inhibits tumor growth. Oleyl alcohol induces cytotoxicity, cell death and apoptosis. The intracellular accumulation of Oleyl alcohol correlates with its cytotoxicity against tumor cells. Oleyl alcohol forms enhancer-enriched fluid domains in stratum corneum lipids, increases the retention of diclofenac diethylamine in ex vivo human epidermis and dermis, and enhances the skin permeability of diclofenac diethylamine. Oleyl alcohol can be used in studies related to neuroblastoma.
For research use only. We do not sell to patients.
- Purity: 98.00%
- CAS No.: 143-28-2
- Formula: C18H36O
- Molecular Weight:268.48
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Storage:Pure form -20°C, 3 years ; In solvent -80°C, 6 months , -20°C, 1 month
To place orders, for customer services and technical support, please contact: MedChemExpress USA
Tel: 609-228-6898 E-mail: [email protected] [email protected]
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Biological Activity
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Chemical Information
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Solvent & Solubility
- Purity & Documentation
- References
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Help & FAQs
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Biological Activity
Oleyl alcohol (5-50 μg/mL; 24 h) induces dose-dependent cytotoxicity in human neuroblastoma HTLA-230 cells, with PSO 2% 10:1 complexes showing the highest potency (IC50 = 10.1 μg/mL) and PSO 3% 3:1 complexes showing the lowest potency (IC50 = 41.6 μg/mL) after 24 h of treatment[1].
Oleyl alcohol (0.75% w/v; 24-48 h) increases DIC-DEA permeation through ex vivo human skin 2.8-fold after a single 24 h dose and 2.7-fold after four repeated doses over 48 h[3].
Oleyl alcohol (0.75% w/v; 24 h) does not adversely affect TEWL or electrical impedance of ex vivo human skin, with all barrier effects fully reversible within 24 h after sample removal[3].
Oleyl alcohol (0.75% w/v; 8-24 h) does not fluidize ex vivo human SC lipid chains after 8 or 24 h of application, forms fluid enhancer-rich domains in SC lipids after 24 h[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:Human neuroblastoma HTLA-230 cell line
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Concentration:5-50 μg/mL
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Incubation Time:24 h
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Result:Induced dose-dependent cell death, with cytotoxicity correlating with release rates.
Reached an IC50 of 10.1 μg/mL for PSO 2% 10:1 complexes.
Reached an IC50 of 12.7 μg/mL for PSO 2% 5:1 complexes.
Reached an IC50 of 15.6 μg/mL for PSO 2% 3:1 complexes.
Reached an IC50 of 24.4 μg/mL for PSO 3% 10:1 complexes.
Reached an IC50 of 30.3 μg/mL for PSO 3% 5:1 complexes.
Reached an IC50 of 41.6 μg/mL for PSO 3% 3:1 complexes.
Showed no cytotoxicity for pure polymers at concentrations up to 500 μg/mL.
Chemical Information
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CAS No. 143-28-2
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Appearance Liquid (Density: 0.8489 g/cm³)
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Molecular Weight 268.48
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Formula C18H36O
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Color Colorless to light yellow
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SMILES
CCCCCCCC/C=C\CCCCCCCCO
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Shipping
Room temperature in continental US; may vary elsewhere.
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Storage
Pure form -20°C 3 years In solvent -80°C 6 months -20°C 1 month
Solvent & Solubility
DMSO : ≥ 30 mg/mL (111.74 mM; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)
* "≥" means soluble, but saturation unknown.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
Purity & Documentation
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Data Sheet (267 KB)
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SDS (393 KB)
- English - EN (393 KB)
- Français - FR (393 KB)
- Deutsch - DE (393 KB)
- Norwegian - NO (393 KB)
- Español - ES (393 KB)
- Swedish - SV (393 KB)
- Italian - IT (393 KB)
- Korean - KR (393 KB)
- Portuguese - PT (393 KB)
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Handling Instructions (2659 KB)
References
[1]. Orienti I, et al. Enhancement of oleyl alcohol anti tumor activity through complexation in polyvinylalcohol amphiphilic derivatives. Drug delivery. 2007 Apr;14(4):209-17. [Content Brief]
[3]. Kováčik A, et al. Time-Dependent Differences in the Effects of Oleic Acid and Oleyl Alcohol on the Human Skin Barrier. Molecular pharmaceutics. 2023 Dec 04;20(12):6237-6245. [Content Brief]
Complete Stock Solution Preparation Table
Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month. When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.
| Optional Solvent | Concentration Solvent Mass | 1 mg | 5 mg | 10 mg | 25 mg |
|---|---|---|---|---|---|
| DMSO | 1 mM | 3.7247 mL | 18.6234 mL | 37.2467 mL | 93.1168 mL |
| 5 mM | 0.7449 mL | 3.7247 mL | 7.4493 mL | 18.6234 mL | |
| 10 mM | 0.3725 mL | 1.8623 mL | 3.7247 mL | 9.3117 mL | |
| 15 mM | 0.2483 mL | 1.2416 mL | 2.4831 mL | 6.2078 mL | |
| 20 mM | 0.1862 mL | 0.9312 mL | 1.8623 mL | 4.6558 mL | |
| 25 mM | 0.1490 mL | 0.7449 mL | 1.4899 mL | 3.7247 mL | |
| 30 mM | 0.1242 mL | 0.6208 mL | 1.2416 mL | 3.1039 mL | |
| 40 mM | 0.0931 mL | 0.4656 mL | 0.9312 mL | 2.3279 mL | |
| 50 mM | 0.0745 mL | 0.3725 mL | 0.7449 mL | 1.8623 mL | |
| 60 mM | 0.0621 mL | 0.3104 mL | 0.6208 mL | 1.5519 mL | |
| 80 mM | 0.0466 mL | 0.2328 mL | 0.4656 mL | 1.1640 mL | |
| 100 mM | 0.0372 mL | 0.1862 mL | 0.3725 mL | 0.9312 mL |
Oleyl alcohol Related Classifications
HY-141573 Related Classifications
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