20565-75-7

Basic information

• Product Name: (Z)-2-(8-heptadecenyl)-4,5-dihydro-1H-imidazole-1-ethylamine
• Synonyms: (Z)-2-(8-heptadecenyl)-4,5-dihydro-1H-imidazole-1-ethylamine;2-[(Z)-8-Heptadecenyl]-2-imidazoline-1-ethanamine;2-[(Z)-8-Heptadecenyl]-4,5-dihydro-1H-imidazole-1-ethanamine;Einecs 243-882-4;1-(2-Aminoethyl)-2-(cis-8-heptadecen-1-yl)imidazoline;Casamine O
• CAS NO: 20565-75-7
• Molecular Formula: C₂₂H₄₃N₃
• Molecular Weight: 349.59692
• EINECS: 243-882-4
• Mol File: 20565-75-7.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 490.6°Cat760mmHg
• Flash Point: 250.5°C
• Appearance: /
• Density: 0.94g/cm³
• Vapor Pressure: 9.02E-10mmHg at 25°C
• Refractive Index: 1.507
• PKA: 10.63±0.60(Predicted)
• CAS DataBase Reference: (Z)-2-(8-heptadecenyl)-4,5-dihydro-1H-imidazole-1-ethylamine(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-2-(8-heptadecenyl)-4,5-dihydro-1H-imidazole-1-ethylamine(20565-75-7)
• EPA Substance Registry System: (Z)-2-(8-heptadecenyl)-4,5-dihydro-1H-imidazole-1-ethylamine(20565-75-7)

Safety Data

• Hazardous Substances Data: 20565-75-7(Hazardous Substances Data)

Usage

Description

(Z)-2-(8-heptadecenyl)-4,5-dihydro-1H-imidazole-1-ethylamine is a chemical compound characterized by a long hydrocarbon chain and an imidazole ring. It is an amine derivative with a unique structure that offers potential applications in the pharmaceutical and agricultural industries. As an amine, it can function as a base and engage in various chemical reactions. The presence of a long hydrocarbon chain suggests surfactant or emulsifying properties, which could be beneficial in personal care product formulations or industrial applications. Additionally, the imidazole ring endows it with the potential to be a bioactive molecule, given the prevalence of imidazoles in biologically active compounds. (Z)-2-(8-heptadecenyl)-4,5-dihydro-1H-imidazole-1-ethylamine holds promise for use in chemical synthesis and for exhibiting biological activity.

Uses

Used in Pharmaceutical Industry:
(Z)-2-(8-heptadecenyl)-4,5-dihydro-1H-imidazole-1-ethylamine is used as a chemical intermediate for the synthesis of pharmaceutical compounds due to its unique structure and reactivity as an amine derivative.
Used in Agricultural Industry:
(Z)-2-(8-heptadecenyl)-4,5-dihydro-1H-imidazole-1-ethylamine is used as a bioactive agent in the agricultural industry, potentially serving as a component in the development of new pesticides or fertilizers, given its imidazole ring which is common in biologically active molecules.
Used in Personal Care Products:
(Z)-2-(8-heptadecenyl)-4,5-dihydro-1H-imidazole-1-ethylamine is used as a surfactant or emulsifier in personal care products, leveraging its long hydrocarbon chain to improve the formulation's stability and performance.
Used in Industrial Applications:
In industrial settings, this compound is used as an additive to enhance the properties of various products, such as improving the emulsification or surfactant capabilities in different formulations.

InChI:InChI=1/C22H43N3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-22-24-19-21-25(22)20-18-23/h9-10H,2-8,11-21,23H2,1H3

Upstream product

• 112-80-1 cis-Octadecenoic acid 
• 111-40-0 3-azapentane-1,5-diamine 
• 15566-80-0 N-[2-[(2-aminoethyl)amino]ethyl]oleylamide 

Downstream Products

• 1238663-26-7 C₂₄H₄₆N₃O₂⁽¹⁺⁾*Cl^(1-) 

Relevant articles and documents

Thermally stable imidazoline-based sulfonate copolymers for enhanced oil recover

Novel imidazoline-based sulfonate copolymers (noted PAMDSCM and PAMPSCM) were successfully prepared by copolymerization of acrylamide (AM), acrylic acid (AA), 1-acrylamido ethyl-2-oleic imidazoline (ACEIM) with the sodium salts of 3-(diallyl-amino)-2-hydroxypropyl (NDS) or 2-acrylamido-2-methylpropane sulfonic acid (AMPS), respectively. The copolymers were characterized by infrared (IR) spectroscopy, 1H nuclear magnetic resonance (1H NMR) spectroscopy, pyrene fluorescence probe spectroscopy, viscosimetry and thermogravimetry (TG). Both PAMDSCM and PAMPSCM copolymers had excellent high-temperature tolerance in comparison with the same concentration of HPAM, and the residual viscosities were 32.0 mPa s and 31.3 mPa s (viscosity retention rates were 38.8% and 37.1%) at 140 °C, respectively. The copolymers possessed superior long-term thermal stability and their residual viscosity rates were up to 81.8% and 63.8% (52.9 mPa s and 47.1 mPa s) lasting 1.5 hours at 100 °C and 170 s-1, respectively.

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

The invention discloses a corrosion inhibition bactericide and a preparation method thereof, and a corrosion inhibition bactericide for CO2 flooding production well, and belongs to the field of oilfield chemistry. The corrosion inhibition bactericide comprises an imidazoline quaternary ammonium salt modified product, dodecyl dimethyl benzyl ammonium chloride, dithiocyano-methane and an anti-freezing agent according to a mass ratio of (3-5):(1-2):(0.1-0.3):(3-6), the chemical structural formula of the imidazoline quaternary ammonium salt modified product is defined in the specification, and inthe formula, R is branched hydrocarbon containing 12-17 carbon atoms, and n is any positive integer from 2 to 5. The corrosion inhibition bactericide has excellent corrosion inhibition, sterilizationand anti-freezing properties, and can be applied to corrosion prevention and sterilization environments of high and cold and winter low-temperature environments.

Carbamido contained bis-imidazoline corrosion inhibitor and preparation method thereof

The invention provides a carbamido contained bis-imidazoline corrosion inhibitor and a preparation method thereof. The corrosion inhibitor is bis-imidazoline which is produced through a reaction of imidazoline and urea and contains carbamido in molecules; the preparation method mainly comprises steps as follows: step one, imidazoline is produced from organic acid and diethylenetriamine; step two, imidazoline and urea are subjected to a reaction at the high temperature, and carbamido contained bis-imidazoline is produced. According to imidazoline prepared with the method, multi-point adsorption can be formed on the metal surface through multiple nitrogen atoms in the molecules, carbamido in carbamido contained bis-imidazoline molecules is prone to forming hydrogen bonds with hydroxide radicals on the metal surface, so that the film forming capacity of imidazoline by adsorption on the metal surface is further enhanced, the desorption speed of the corrosion inhibitor from the metal surface at the high temperature is reduced, and corrosion inhibition efficiency is remarkably improved.