2498-27-3

Basic information

• Product Name: TRIMETHYL(3-HYDROXYPHENYL)AMMONIUMIODIDE
• Synonyms: TRIMETHYL(3-HYDROXYPHENYL)AMMONIUMIODIDE;(M-Hydroxyphenyl)triMethylaMMoniuM Iodide;3-(TriMethylaMMonio)phenol Iodide;3-Hydroxy-N,N,N-triMethylbenzenaMiniuM Iodide;3-HydroxyphenyltriMethylaMMoniuM Iodide;M-(DiMethylaMino)phenol Methiodide;M-Hydroxy-N-triMethylaniliniuM Iodide;M-HydroxytriMethylaniliniuM Iodide
• CAS NO: 2498-27-3
• Molecular Formula: C₉H₁₄NO*I
• Molecular Weight: 279.11803
• Product Categories: Amines, Aromatics, Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 2498-27-3.mol
• Article Data: 3

Chemical Properties

• Melting Point: 195-197 °C(Solv: ethanol (64-17-5))
• Appearance: /
• Storage Temp.: Refrigerator
• Solubility: DMSO, Water
• CAS DataBase Reference: TRIMETHYL(3-HYDROXYPHENYL)AMMONIUMIODIDE(CAS DataBase Reference)
• NIST Chemistry Reference: TRIMETHYL(3-HYDROXYPHENYL)AMMONIUMIODIDE(2498-27-3)
• EPA Substance Registry System: TRIMETHYL(3-HYDROXYPHENYL)AMMONIUMIODIDE(2498-27-3)

Safety Data

• Hazardous Substances Data: 2498-27-3(Hazardous Substances Data)

Usage

Uses

3-Hydroxyphenyltrimethylammonium iodide is an acetylcholinesterase inhibitor.

InChI:InChI=1/C10H15NO.HI/c1-11(2,3)8-9-5-4-6-10(12)7-9;/h4-7H,8H2,1-3H3;1H

Upstream product

• 591-27-5 m-Hydroxyaniline 
• 74-88-4 methyl iodide 
• 84649-54-7 3-decanoyloxy-N-trimethylanilinium iodide 
• 84649-53-6 3-octanoyloxy-N-trimethylanilinium iodide 
• 17427-00-8 3-acetoxy-N-trimethylanilinium iodide 
• 77-78-1 dimethyl sulfate 
• 99-07-0 3-Dimethylaminophenol 

Downstream Products

• 99-07-0 3-Dimethylaminophenol 
• 31061-59-3 meta-(trimethylammonio)phenolate betaine 
• 100-02-7 4-nitro-phenol 

Relevant articles and documents

C-H Nickelation of Aryl Phosphinites: Mechanistic Aspects

The present report describes the results of a combined experimental and computational study on the mechanism of aryl phosphinite cyclonickelation. The reaction of ArOP(i-Pr)2 with [(i-PrCN)NiBr2]n proceeds more readily in

Role of Solvation and Desolvation in Polymer "Catalysis". 7. The Influence of High Pressures on the Alkaline Hydrolyses of Neutral and Cationic Esters Catalyzed by Macroions

The alkaline hydrolyses of electrically neutral esters and positively charged esters are influenced by macroions under high pressures up to 2000 bar.The polyelectrolytes used are sodium poly(styrenesulfonate) (NaPSS) and poly(trimethylvinylbenzylammonium chloride) (PMVA).All of the volumes, enthalpies, and entropies of activation of the reactions examined increase on the addition of hydrophobic macroanions (NaPSS), whereas they decrease on the addition of the hydrophobic and cationic macroions (PMVA).The significant role of the hydrophobic hydration effects of macroions, i.e., the formation of the "iceberg" water structure around the hydrophobic reactants and macroions, is demonstrated for the observed rate acceleration and deceleration with PMVA and NaPSS, respectively.