112-90-3
Chemical Structure
Oleylamine, 80-90%
Synonym(s): cis-1-Amino-9-octadecene, 80-90%
- CAS No.: 112-90-3
- Formula:C18H37N
- Molecular Weight:267.49
IUPAC Name: (Z)-octadec-9-en-1-amine
InChIKey: QGLWBTPVKHMVHM-KTKRTIGZSA-N
SMILES: CCCCCCCC/C=C\CCCCCCCCN
Biological Activity: Oleylamine, 80-90% (cis-1-Amino-9-octadecene, 80-90%) is a multifunctional reagent used for metal ion coordination and nanoparticle surface modification, and acts as a solvent, surfactant and reducing agent in the synthesis of metal oxide nanoparticles. Oleylamine, 80-90% regulates nanoparticle morphology, magnetization intensity and water proton relaxation rate via thiol-ene "click" reaction, and enhances the colloidal stability of nanoparticles in organic reagents. Oleylamine, 80-90% is mainly used in research and applications in fields such as nanomaterial synthesis, biomedical imaging (MRI contrast agents, fluorescent probes), cancer cell targeting and drug delivery[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Oleylamine, 80-90% | 89.08% | Oleylamine, 80-90% (cis-1-Amino-9-octadecene, 80-90%) is a multifunctional reagent used for metal ion coordination and nanoparticle surface modification, and acts as a solvent, surfactant and reducing agent in the synthesis of metal oxide nanoparticles. Oleylamine, 80-90% regulates nanoparticle morphology, magnetization intensity and water proton relaxation rate via thiol-ene "click" reaction, and enhances the colloidal stability of nanoparticles in organic reagents. Oleylamine, 80-90% is mainly used in research and applications in fields such as nanomaterial synthesis, biomedical imaging (MRI contrast agents, fluorescent probes), cancer cell targeting and drug delivery. | ||||||||||||||||||||
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Oleyl alcohol | 98.00% | 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. | ||||||||||||||||||||
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7(E)-Nonadecenol | 7(E)-Nonadecenol ((E)-Nonadec-7-en-1-ol) is an ester product. | |||||||||||||||||||||
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(Z)-Nonadec-7-en-1-ol | (Z)-Nonadec-7-en-1-ol ((7Z)-7-Nonadecen-1-ol) is an ester product. | |||||||||||||||||||||
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11(E)-Octadecenol | 11(E)-Octadecenol (11-Octadecen-1-ol; (E)-,11-trans-Octadecenol) is an ester product. | |||||||||||||||||||||
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6(E)-Octadecenol | 6(E)-Octadecenol is an ester product. | |||||||||||||||||||||
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6(Z)-Octadecenol | 6(Z)-Octadecenol (6-cis-Octadecenol; Petroselinyl alcohol) is an ester product. | |||||||||||||||||||||
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(Z)-9-Nonadecene | 98.0% | (Z)-9-Nonadecene is the anal secretion of a species of thrips. | ||||||||||||||||||||
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Oleyl bromide | 98.67% | Oleyl bromide ((Z)-1-Bromooctadec-9-ene) is a hydrophobic compound that can carry out ring-opening reaction through a process called "encapsulation". Oleyl bromine can also be used as the starting material in the synthesis of oleylphosphonates. | ||||||||||||||||||||
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trans-9-Octadecenol | Trans-9-Octadecenol is an organic compound belonging to the group of alcohols. It has a mild fatty smell and is commonly found in a variety of foods, such as meat and dairy products. Trans-9-Octadecenol has several applications in the flavor and fragrance industry, especially as a fragrance agent in products such as perfumes, colognes and air fresheners. In addition, it has potential utility in inhibiting inflammation-related diseases and cancer. | |||||||||||||||||||||
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(Z)-11-Octadecen-1-ol | (Z)-11-Octadecen-1-ol is a marking secretion deposited by wasps on repeated flight paths, isolated from the paired labial glands of North American male bumblebees. | |||||||||||||||||||||
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References
- [1]. Georgiadou V, et al. Oleylamine as a beneficial agent for the synthesis of CoFe₂O₄ nanoparticles with potential biomedical uses. Dalton Trans. 2014;43(17):6377-6388. [Content Brief]
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[2]. Yoo S, et al. Oleylamine‐induced pustular irritant contact dermatitis. Contact Dermatitis (01051873). 2019 Dec 1;81(6).
[Content Brief] - [3]. Mourdikoudis S, et al. Oleic acid/oleylamine ligand pair: a versatile combination in the synthesis of colloidal nanoparticles. Nanoscale Horiz. 2022;7(9):941-1015. Published 2022 Aug 22. [Content Brief]
