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33097-U

Supelco

trimethylanilinium hydroxide (TMAH)

0.2 M in methanol

Synonym(s):

Trimethylphenylammonium hydroxide solution, Phenyltrimethylammonium hydroxide, TMAH

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About This Item

Linear Formula:
(CH3)3N(OH)C6H5
CAS Number:
1899-02-1
Molecular Weight:
153.22
Beilstein:
3917033
MDL number:
MFCD00041899
UNSPSC Code:
12000000
PubChem Substance ID:
329754455

grade

for GC derivatization

reaction suitability

reagent type: derivatization reagent
reaction type: Esterifications

packaging

pkg of 1 × 10 mL (33097-U)

concentration

0.2 M in methanol

SMILES string

[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

InChI key

HADKRTWCOYPCPH-UHFFFAOYSA-M

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General description

Trimethylanilinium hydroxide (TMAH) is an alkylating agent, which is effectively used esterification of carboxylic acids, etherfication of alcohols and N-alkylation of amino groups.

Application

It is used to derivatize the serum sample for determination of Topiramate in Epileptic patients using GC-MS analysis.

Other Notes

Reagent for carboxylic acid methyl ester, methyl esters.

Signal Word

Danger

Hazard Classifications

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

Target Organs

Eyes

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

51.8 °F - closed cup

Flash Point(C)

11 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
LC23665V
LC19061V
LC16326V
LC15133
LC12701

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E.W. Robb and J.J. Westbrook III
Analytical Chemistry, 35, 1644-1644 (1963)
A capillary GC method using nitrogen phosphorus detection for determination of topiramate in patients with epilepsy.
Malakova, J., et al.
Chromatographia, 66, 363-367 (2007)
Vladimir Zaikin, John M. Halket
A Handbook of Derivatives for Mass Spectrometry, 218-219 (2009)
Neera Singh
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 41(1), 17-29 (2006-01-06)
The study aims to prepare the organoclay complexes of metolachlor and metribuzin so as to reduce their downward mobility in soil profile. The organoclays were preadsorbed with phenyltrimethylammonium (PTMA) (50% of cation exchange capacity [CEC]) and hexadecyltrimethylammonium (HDTMA) (100% of
Petr Gebauer et al.
Electrophoresis, 29(5), 1067-1076 (2008-01-26)
In electrophoresis, the introduction of a sample into the BGE creates two new zone boundaries, the front and rear boundary of the sample zone which is sandwiched between the BGE. During an electrophoresis run, these boundaries move and split into
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