10182-92-0

Basic information

• Product Name: trimethyltetradecylammonium
• Synonyms: trimethyltetradecylammonium;tetradecyltrimethylammonium;Myristyltrimethylammonium;N,N,N-Trimethyl-1-tetradecanaminium;Tetradecyltrimethylaminium;Trimethyl(tetradecyl)aminium;Trimethyltetradecylaminium;1119-97-7 (Bromide)
• CAS NO: 10182-92-0
• Molecular Formula: C₁₇H₃₈N
• Molecular Weight: 256.49032
• EINECS: 233-454-5
• Mol File: 10182-92-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: trimethyltetradecylammonium(CAS DataBase Reference)
• NIST Chemistry Reference: trimethyltetradecylammonium(10182-92-0)
• EPA Substance Registry System: trimethyltetradecylammonium(10182-92-0)

Safety Data

• Hazardous Substances Data: 10182-92-0(Hazardous Substances Data)

Usage

General Description

Trimethyltetradecylammonium is a quaternary ammonium compound with the chemical formula C17H38N+. It is commonly used as a surfactant and fabric softener in various household and industrial products. This chemical compound is known for its antimicrobial properties and is often found in various disinfectants and cleaning agents. Additionally, trimethyltetradecylammonium is used in the synthesis of other organic compounds and can also be found in some pesticides. However, it is important to note that this compound can have toxic effects on aquatic life and should be handled with caution to avoid environmental harm.

InChI:InChI=1/C17H38N.CH4O4S/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18(2,3)4;1-5-6(2,3)4/h5-17H2,1-4H3;1H3,(H,2,3,4)/q+1;/p-1

Upstream product

• 158400-60-3 Br^(1-)*C₁₇H₃₈N⁽¹⁺⁾*C₄₈H₈₀O₄₀ 

Related news

Peculiar solubilization thermodynamics of pentan-1-ol in mixed surfactant solutions of benzyldimethyltetradecylammonium chloride and trimethyltetradecylammonium (cas 10182-92-0) chloride: a calorimetric investigation07/19/2019

The thermodynamics of micellar solubilization were obtained from precise calorimetric measurements for pentan-1-ol in surfactant mixtures of benzyldimethyltetradecylammonium chloride (BzCl) and trimethyltetradecylammonium chloride (TACl) (system I). The partition coefficient P of pentan-1-ol bet...detailed

Relevant articles and documents

Effects of ionic surfactants and cyclodextrins on hydride-transfer reaction of l-Benzyl-l,4-dihydronicotinamide with methylene blue

The kinetics of the hydride-transfer reaction between methylene blue (MB+) and 1 -benzyl-1,4-dihydronictinamide (BNAH) were studied in media containing cyclodextrins (β- and γ-CD) and surfactants (sodium dodecyl sulfate (SDS), dodecyltrimethylammonium bromide, tetradecyltrimethylammonium bromide, and hexadecyltrimethylammonium bromide). Cationic surfactants decreased the apparent first-order rate constant (k obsd) above the cmc, while SDS increased kobsd just above the cmc and then decreased kobsd with increasing surfactant concentration. This behavior for cationic surfactants was typical of micellar effects due to a separation of the reactants by the micelles. BNAH associated with micelles, whereas MB+ ions were repelled from the cationic interface of the micelles. Binding of BNAH and MB to the same SDS micelle enhanced the reaction, but dilution of reagents within the micellar interface with the increase in [SDS] caused a decrease in Kobsd. In β-CD-cationic surfactant mixtures, the results were interpreted in terms of the model which takes into account the formation of CD-BNAH, CD-MB+, and CD-surfactant complexes and the association of BNAH with micelles. The decrease in Kobsd with increasing surfactant concentration observed in γ-CD-cationic surfactant mixtures can be explained by the decrease in the concentration of free γ-CD by the formation of 1:1 and 2:1 complexes of surfactant monomer with β-CD.