15566-80-0

Basic information

• Product Name: (Z)-N-[2-[(2-aminoethyl)amino]ethyl]-9-octadecenamide
• Synonyms: (Z)-N-[2-[(2-aminoethyl)amino]ethyl]-9-octadecenamide;(Z)-N-[2-[(2-Aminoethyl)amino]ethyl]-9-octadeceneamide;N-[2-[(2-Aminoethyl)amino]ethyl]oleic amide;9-Octadecenamide, N-(2-((2-aminoethyl)amino)ethyl)-, (9Z)-;Einecs 239-614-0;Oleic acid, diethylenetriamine amide
• CAS NO: 15566-80-0
• Molecular Formula: C22H45N3O
• Molecular Weight: 367.6122
• EINECS: 239-614-0
• Mol File: 15566-80-0.mol

Chemical Properties

• Boiling Point: 535.5°Cat760mmHg
• Flash Point: 277.6°C
• Appearance: /
• Density: 0.91g/cm³
• Vapor Pressure: 1.54E-11mmHg at 25°C
• Refractive Index: 1.48
• CAS DataBase Reference: (Z)-N-[2-[(2-aminoethyl)amino]ethyl]-9-octadecenamide(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-N-[2-[(2-aminoethyl)amino]ethyl]-9-octadecenamide(15566-80-0)
• EPA Substance Registry System: (Z)-N-[2-[(2-aminoethyl)amino]ethyl]-9-octadecenamide(15566-80-0)

Safety Data

• Hazardous Substances Data: 15566-80-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
(Z)-N-[2-[(2-aminoethyl)amino]ethyl]-9-octadecenamide is used as a surfactant and emulsifier for enhancing the stability and solubility of various pharmaceutical formulations. Its ability to reduce surface tension and improve the dispersion of active ingredients makes it a valuable component in the development of drugs.
Used in Personal Care Products:
In the personal care industry, (Z)-N-[2-[(2-aminoethyl)amino]ethyl]-9-octadecenamide is used as a stabilizing agent and emulsifier in the production of creams, lotions, and other skincare products. Its emulsifying properties help create a uniform mixture of oil and water, ensuring a smooth and consistent texture.
Used in Industrial Coatings:
(Z)-N-[2-[(2-aminoethyl)amino]ethyl]-9-octadecenamide is used as a corrosion inhibitor in the industrial coatings sector. Its ability to form a protective layer on metal surfaces helps prevent corrosion and extends the lifespan of coated materials.
Used in Nanoparticle Synthesis:
(Z)-N-[2-[(2-aminoethyl)amino]ethyl]-9-octadecenamide is used as a stabilizing agent in the synthesis of nanoparticles. Its amphiphilic nature allows it to interact with both the hydrophobic and hydrophilic components of nanoparticles, enhancing their stability and preventing aggregation.
Used in Colloidal Metal Particle Production:
In the production of colloidal metal particles, (Z)-N-[2-[(2-aminoethyl)amino]ethyl]-9-octadecenamide serves as a stabilizing agent. It helps maintain the uniform size and distribution of metal particles, which is crucial for their performance in various applications.
Used in Antimicrobial and Antifungals:
(Z)-N-[2-[(2-aminoethyl)amino]ethyl]-9-octadecenamide has been studied for its potential antimicrobial and antifungal properties. It is being explored for use in applications where controlling the growth of microorganisms is essential, such as in the food industry or medical settings.

InChI:InChI=1/C22H45N3O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-22(26)25-21-20-24-19-18-23/h9-10,24H,2-8,11-21,23H2,1H3,(H,25,26)/b10-9-

Upstream product

• 112-80-1 cis-Octadecenoic acid 
• 111-40-0 3-azapentane-1,5-diamine 
• 112-77-6 (Z)-9-octadecenoyl chloride 

Relevant articles and documents

Combination of antimicrobial and endotoxin-neutralizing activities of novel oleoylamines

A combination of antimicrobial and endotoxin-neutralizing activities is desired in order to prevent progression from infection to sepsis due to the release of lipopolysaccharide from dying gram-negative bacteria. Lipopolyamines have emerged as a new type of endotoxin-neutralizing compound, but their antimicrobial activity has not been investigated. We synthesized a series of 10 oleoylamines differing in the polyamino head group, particularly in the number and separation between nitrogen atoms and the position of the oleoyl moiety. Compounds showed activity against both gram-negative and gram-positive bacteria in the micromolar range. Compounds were able to provide penetration of ethidium bromide into bacteria, indicating effects on the bacterial membrane. Oleoylamines neutralized endotoxin in Limulus amoebocyte lysate assays and by neutralization of tumor necrosis factor alpha release in human blood. Comparison of biological activities of compounds identified structural properties responsible for antimicrobial activity, and quantitative structure-property relationship analysis provided a quantitative model for prediction of activity of oleoylamines. Copyright

Corrosion inhibition bactericide and preparation method thereof, and corrosion inhibition bactericide for CO2 flooding production well

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Imidazoline Mannich base corrosion inhibitor and preparation method thereof

The invention relates to the technical field of corrosion inhibitors, and in particular relates to an imidazoline mannich base corrosion inhibitor and a preparation method thereof. The imidazoline mannich base corrosion inhibitor is of the structure shown in the formula I. The imidazoline mannich base corrosion inhibitor is prepared from, by mass, 10-20% of benzaldehyde, 5-15% of butanone, 40-60%of oleic acid imidazoline, 10-30% of ethanol, 1-5% of concentrated hydrochloric acid and 0.1-0.5% of a catalyst. According to the imidazoline mannich base corrosion inhibitor, a benzene ring, an imidazole ring and an ultra-long hydrophobic alkyl chain on imidazoline are introduced, the benzene ring in benzaldehyde and N atoms in the imidazoline ring have relatively high electron cloud density andcan form a firm coordination bond with an empty d track of metal, and the super-long hydrophobic alkyl chain forms a hydrophobic membrane layer away from the surface of the metal and has a peripheralshielding effect on the surface of the metal, so that the corrosion inhibitor has excellent corrosion inhibition performance in a high-temperature acidification environment.

Some imidazoline derivatives as corrosion inhibitors

In this study, cationic surfactants having different alkyl chain lengths were prepared by amidation of lauric, myristic, palmitic, stearic, oleic acids with diethylene triamine. The products were quaternized using chlo-roacetic acid. The chemical structure of the prepared compounds was elucidated using different spectroscopic techniques. The critical micelle concentration (CMC) and the free energy of the micellization and adsorption of these compounds were determined by surface tension and conductivity measurements. The products were evaluated as surface-active agents as well as corrosion inhibitors for steel alloy in 1 M hydrochloric and sulfuric acid, the results indicate that these materials have a high efficiency as corrosion inhibitors and as surface active agents. These results were correlated with the chemical structure of the prepared compounds. AOCS 2009.