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Supelco

Trimethylphenylammonium hydroxide solution

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

Sinônimo(s):

Phenyltrimethylammonium hydroxide, TMAH

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About This Item

Fórmula linear:
(CH3)3N(OH)C6H5
Número CAS:
1899-02-1
Peso molecular:
153.22
Beilstein:
3917033
Número MDL:
MFCD00041899
Código UNSPSC:
12000000
ID de substância PubChem:
329768356
NACRES:
NA.22

grau

for GC derivatization

Nível de qualidade

100

forma

liquid

qualidade

LiChropur™

adequação da reação

reagent type: derivatization reagent
reaction type: Esterifications

concentração

~0.5 M (CH3)3N(OH)C6H5 in methanol

técnica(s)

gas chromatography (GC): suitable

Impurezas

≤0.2% halides (as chloride)

temperatura de armazenamento

2-8°C

cadeia de caracteres 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

chave InChI

HADKRTWCOYPCPH-UHFFFAOYSA-M

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Descrição geral

Trimethylphenylammonium hydroxide (TMAH) is a methylating reagent.

Aplicação

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.

Outras notas

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

Informações legais

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Palavra indicadora

Danger

Classificações de perigo

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

Órgãos-alvo

Eyes

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

51.8 °F - closed cup

Ponto de fulgor (°C)

11 °C - closed cup

Equipamento de proteção individual

Faceshields, Gloves, Goggles

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Certificados de análise (COA)

Lot/Batch Number
BCCF7109
STBJ1243
STBH7120
STBG9018
STBF8692V

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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)
R W Gullick et al.
Environmental science & technology, 35(7), 1523-1530 (2001-05-12)
A natural shale and four synthetic organoclays were compared as potential sorbent additives to containment barriers at hazardous waste sites. Trimethylphenyl ammonium bentonite (TMPA-bent) was shown in batch experiments to have the greatest sorption capacities for 1,2,4-trichlorobenzene, trichloroethylene, and methyl
Jeffrey T Auletta et al.
Chemico-biological interactions, 187(1-3), 135-141 (2010-05-25)
Acetylcholinesterase (AChE) contains a narrow and deep active site gorge with two sites of ligand binding, an acylation site (or A-site) at the base of the gorge and a peripheral site (or P-site) near the gorge entrance. The P-site contributes
Anthony A Mikulec et al.
Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology, 30(2), 131-138 (2009-01-31)
Drugs applied to the middle ear enter perilymph through the bony otic capsule. Drugs applied intratympanically in humans are thought to enter the cochlea primarily through the round window membrane (RWM). Local drug treatments of the ear are commonly evaluated
Alec N Salt et al.
Journal of the Association for Research in Otolaryngology : JARO, 13(6), 771-783 (2012-09-13)
Perilymph pharmacokinetics was investigated by a novel approach, in which solutions containing drug or marker were injected from a pipette sealed into the perilymphatic space of the lateral semi-circular canal (LSCC). The cochlear aqueduct provides the outlet for fluid flow
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