51-93-4 Usage
Description
ETHYLTRIMETHYLAMMONIUM IODIDE is a quaternary ammonium salt that consists of an ethyltrimethylammonium cation and an iodide anion. It is a compound with unique properties that make it suitable for various applications across different industries.
Uses
Used in Pharmaceutical Industry:
ETHYLTRIMETHYLAMMONIUM IODIDE is used as a pharmaceutical compound for its potential therapeutic applications. It can be utilized in the development of new drugs or as a component in existing medications due to its unique chemical structure and properties.
Used in Chemical Synthesis:
In the chemical industry, ETHYLTRIMETHYLAMMONIUM IODIDE can be used as a reagent or intermediate in the synthesis of other complex organic compounds. Its quaternary ammonium salt structure makes it a versatile building block for creating a wide range of molecules.
Used in Analytical Chemistry:
ETHYLTRIMETHYLAMMONIUM IODIDE can be employed as an analytical reagent in various techniques such as chromatography, electrophoresis, and spectroscopy. Its unique properties allow for the separation, detection, and quantification of different substances in a sample.
Used in Material Science:
In the field of material science, ETHYLTRIMETHYLAMMONIUM IODIDE can be used to modify the properties of various materials, such as polymers, nanoparticles, and surfaces. Its cationic nature enables it to interact with different materials, leading to improved performance or new functionalities.
Used in Environmental Applications:
ETHYLTRIMETHYLAMMONIUM IODIDE can be utilized in environmental applications, such as water treatment and soil remediation. Its ability to interact with various contaminants and pollutants can help in their removal or transformation, leading to a cleaner and safer environment.
Used in Agricultural Industry:
In agriculture, ETHYLTRIMETHYLAMMONIUM IODIDE can be employed as a component in the development of new pesticides, herbicides, or fertilizers. Its unique properties may contribute to improved efficacy, reduced environmental impact, or enhanced crop yield.
Used in Textile Industry:
In the textile industry, ETHYLTRIMETHYLAMMONIUM IODIDE can be used as a finishing agent, providing specific properties to the fabric, such as antimicrobial activity, water repellency, or soil release. Its cationic nature allows it to interact with the fibers, leading to improved performance and durability of the textile products.
Used in Cosmetics Industry:
ETHYLTRIMETHYLAMMONIUM IODIDE can be utilized in the cosmetics industry as an ingredient in various personal care products, such as hair care, skin care, and oral care formulations. Its unique properties may contribute to improved product performance, enhanced efficacy, or additional benefits for the consumer.
Check Digit Verification of cas no
The CAS Registry Mumber 51-93-4 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 5 and 1 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51-93:
(4*5)+(3*1)+(2*9)+(1*3)=44
44 % 10 = 4
So 51-93-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H14N.HI/c1-5-6(2,3)4;/h5H2,1-4H3;1H/q+1;/p-1
51-93-4Relevant articles and documents
Conformational Analysis of Charged Flexible Molecules in Water by Application of a New Karplus Equation Combined with MM2 Computations: Conformations of Carnitine and Acetylcarnitine
Colucci, William J.,Gandour, Richard D.,Mooberry, Edward A.
, p. 7141 - 7147 (1986)
The solution conformations of carnitine and acetylcarnitine in D2O are estimated from high-resolution 1H NMR coupling data.Conformations and populations of conformers are calculated from vicinal coupling constants by employing a new Karplus relationship with empirically derived substituent constants (Colucci, W.J.; Jungk, S.J.; Gandour, R.D.Magn.Reson.Chem. 1985, 23, 335-343).For this study, substituent constants are assigned for the monosubstituted ethanes: XCH2CH3, where X=-COOH, -OAc, -OH, -N+Me3, -CH2N+Me3, -CH2COOH.Solvent effects are accounted for by measuring the coupling constants of the monosubstituted ethanes under the same conditions employed in the measurement of the carnitine and acetylcarnitine spectra.The assignment of diasteriotopic protons of carnitine and acetylcarnitine is made by analogy with previous experimental work and comparison with the lowest energy conformation as determined by molecular mechanics (MM2) calculations parameterized with atomic charges from ab initio (3-21G) calculations.The vicinal coupling constants are then used to calculate populations of conformers, arising from rotation about the C2-C3 and C3-C4 bonds, in solution.Both compounds adopt a highly preferred g- conformation about the N1-C4-C3-O3 torsion angle.In contrast, the C1-C2-C3-C4 torsion angle exhibits substantial rotational freedom between g- and a.In carnitine, the anti conformer dominates, regardless of the solution pD, whereas in acetylcarnitine the g- conformer is most prevalent.In either compound, ionization from cation to zwitterion results in a net population increase of g-, g- (folded) conformer over the a,g- (extended) conformer.The relative energetics of extended and folded conformers suggest that binding of either carnitine or acetylcarnitine to the enzyme carnitine acetyltransferase occurs with the folded form.
CONFORMATION OF DIMETHYLAMINOETHANOL, ITS METHYL ETHER AND OF THE CORRESPONDING TRIMETHYLAMMONIUM IODIDES. NMR AND VIBRATIONAL SPECTRA
Stokr, Jan,Schneider, Bohdan,Doskocilova, Danica,Sevcik, Stanislav,Pradny, Martin
, p. 1256 - 1271 (2007/10/02)
By analysis of fully coupled 13C NMR spectra and of 1H NMR spectra of dimethylaminoethanol, its methyl ether, and of the corresponding trimethylammonium iodides, populations of isomers generated by rotation about the bonds N-CH2, CH2-CH2, and CH2-O in these compounds in solution were determined.By analysis of Raman and infrared spectra of these compounds in the solid and liquid states it was found that in the crystalline state these compounds form structures with parallel N-CH3 and O-CH2 bonds, which are also preffered in the liquid state.
