CAS 1010-19-1: Benzenaminium, N,N,N-triethyl-, iodide (1:1)
Formula:C12H20N·I
InChI:InChI=1S/C12H20N.HI/c1-4-13(5-2,6-3)12-10-8-7-9-11-12;/h7-11H,4-6H2,1-3H3;1H/q+1;/p-1
InChI key:InChIKey=WMSWXWGJYOIACA-UHFFFAOYSA-M
SMILES:[N+](CC)(CC)(CC)C1=CC=CC=C1.[I-]
Synonyms:- Ammonium, triethylphenyl-, iodide
- Benzenaminium, N,N,N-triethyl-, iodide
- Benzenaminium, N,N,N-triethyl-, iodide (1:1)
- N,N,N-triethylanilinium
- Nsc 97254
- Phenyl triethyl ammonium iodide
- Triethylphenylammonium iodide
- N,N,N-Triethylanilinium iodide
- N,N,N-Triethylanilinium iodide
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Found 5 products.
N,N,N-Triethylbenzenaminium iodide
CAS:Purity:95.0%Color and Shape:Liquid, No data available.Molecular weight:305.2030029296875Benzenaminium, N,N,N-triethyl-, iodide (1:1)
CAS:Formula:C12H20INPurity:98%Color and Shape:SolidMolecular weight:305.1984Triethylphenylammonium Iodide
CAS:Formula:C12H20INPurity:>98.0%(T)(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:305.20Triethylphenylammonium Iodide
CAS:Triethylphenylammonium Iodide is a hydrogenated sodium salt of the fatty acid, phenyl-3-ethoxypropanoic acid. It is used as a solid catalyst for the polymerization of vinyl chloride monomer and has been shown to be an effective treatment for tissue infection. The mechanism of action of triethylphenylammonium iodide is not well understood but it is thought to involve adsorption onto the surface of bacteria. This may be due to its hydroxyl group, which can form hydrogen bonds with water molecules on the bacterial cell wall. Triethylphenylammonium iodide also has a carbonic group that can react with CO2 in the air, leading to dissolution in water.Formula:C12H20INPurity:Min. 95%Molecular weight:305.2 g/molRef: 3D-FT62875
Discontinued product
