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

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

Uses

Used in Household and Industrial Products:
Trimethyltetradecylammonium is used as a surfactant and fabric softener for its ability to reduce surface tension and improve the texture and feel of fabrics.
Used in Disinfectants and Cleaning Agents:
Trimethyltetradecylammonium is used as an antimicrobial agent for its effectiveness in killing or inhibiting the growth of microorganisms, thereby enhancing the sanitizing properties of disinfectants and cleaning agents.
Used in Synthesis of Organic Compounds:
Trimethyltetradecylammonium is utilized as a reagent or intermediate in the synthesis of other organic compounds, contributing to the production of various chemical products.
Used in Pesticides:
Trimethyltetradecylammonium is used in some pesticides for its ability to control pests by leveraging its antimicrobial properties to target and eliminate harmful organisms.

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.