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Merck

79266

Supelco

Trimethylphenylammonium hydroxide solution

~0.5 M (CH3)3N(OH)C6H5 in methanol, for GC derivatization, LiChropur

Sinónimos:

Phenyltrimethylammonium hydroxide, TMAH

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About This Item

Fórmula lineal:
(CH3)3N(OH)C6H5
Número de CAS:
Peso molecular:
153.22
Beilstein:
3917033
Número MDL:
Código UNSPSC:
12000000
ID de la sustancia en PubChem:
NACRES:
NA.22

grado

for GC derivatization

Nivel de calidad

formulario

liquid

calidad

LiChropur

idoneidad de la reacción

reagent type: derivatization reagent
reaction type: Esterifications

concentración

~0.5 M (CH3)3N(OH)C6H5 in methanol

técnicas

gas chromatography (GC): suitable

impurezas

≤0.2% halides (as chloride)

temp. de almacenamiento

2-8°C

cadena SMILES

[OH-].C[N+](C)(C)c1ccccc1

InChI

1S/C9H14N.H2O/c1-10(2,3)9-7-5-4-6-8-9;/h4-8H,1-3H3;1H2/q+1;/p-1

Clave InChI

HADKRTWCOYPCPH-UHFFFAOYSA-M

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Descripción general

Trimethylphenylammonium hydroxide (TMAH) is a methylating reagent.

Aplicación

Learn more in the Product Information
Suitable for the derivatization of amino acids, n-methyl and n-aryl carbamates and fatty acids, clonidine, and substituted phenylureas.
TMAH may be used as a 0.1 mole/litre solution in methanol to determine plasma concentrations of carbamazepine and other anticonvulsant drugs, including phenobarbital, diphenylhydantoin, primidone, and mephenytoin using Gas-Liquid Chromatography.

Otras notas

Reagent for n-methyl and methyl esters.
Sales restrictions may apply

Información legal

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Palabra de señalización

Danger

Clasificaciones de peligro

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 1

Órganos de actuación

Eyes

Código de clase de almacenamiento

3 - Flammable liquids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

51.8 °F - closed cup

Punto de inflamabilidad (°C)

11 °C - closed cup

Equipo de protección personal

Faceshields, Gloves, Goggles


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Simultaneous determination of carbamazapine ("Tegretol") and other anticonvulsants in human plasma by gas-liquid chromatography.
J C Roger et al.
Clinical chemistry, 19(6), 590-592 (1973-06-01)
Y El-Nahhal et al.
Journal of agricultural and food chemistry, 48(10), 4791-4801 (2000-10-29)
This study aimed to design formulations of hydrophobic herbicides, alachlor and metolachlor, by adsorbing them on the clay mineral montmorillonite preadsorbed by the small organic cation phenyltrimethylammonium (PTMA). An adsorption model that considers electrostatics and specific binding and the possibility
Alec N Salt et al.
Hearing research, 283(1-2), 14-23 (2011-12-20)
It has been widely believed that drug entry from the middle ear into perilymph occurs primarily via the round window (RW) membrane. Entry into scala vestibuli (SV) was thought to be dominated by local, inter-scala communication between scala tympani (ST)
Alec N Salt et al.
Hearing research, 182(1-2), 24-33 (2003-09-02)
Our understanding of the perilymph kinetics of drugs depends largely on data obtained by the analysis of perilymph samples. Although a number of studies have demonstrated qualitatively that perilymph samples may be contaminated by cerebrospinal fluid (CSF), and some investigations
Jie Zhang et al.
Journal of chromatography. A, 1216(44), 7527-7532 (2009-04-07)
A method has been established for the determination of four pharmaceutically active compounds (ibuprofen, ketoprofen, naproxen and clofibric acid) in water samples using dynamic hollow fiber liquid-phase microextraction (HF/LPME) followed by gas chromatography (GC) injection port derivatization and GC-mass spectrometric

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