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Merck

79266

Supelco

Trimethylphenylammonium hydroxide solution

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

Synonim(y):

Phenyltrimethylammonium hydroxide, TMAH

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About This Item

Wzór liniowy:
(CH3)3N(OH)C6H5
Numer CAS:
Masa cząsteczkowa:
153.22
Beilstein:
3917033
Numer MDL:
Kod UNSPSC:
12000000
Identyfikator substancji w PubChem:
NACRES:
NA.22

klasa czystości

for GC derivatization

Poziom jakości

Postać

liquid

jakość

LiChropur

przydatność reakcji

reagent type: derivatization reagent
reaction type: Esterifications

stężenie

~0.5 M (CH3)3N(OH)C6H5 in methanol

metody

gas chromatography (GC): suitable

zanieczyszczenia

≤0.2% halides (as chloride)

temp. przechowywania

2-8°C

ciąg 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

Klucz InChI

HADKRTWCOYPCPH-UHFFFAOYSA-M

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Opis ogólny

Trimethylphenylammonium hydroxide (TMAH) is a methylating reagent.

Zastosowanie

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.

Inne uwagi

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

Informacje prawne

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
This page may contain text that has been machine translated.

Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

Klasyfikacja zagrożeń

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

Organy docelowe

Eyes

Kod klasy składowania

3 - Flammable liquids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

51.8 °F - closed cup

Temperatura zapłonu (°C)

11 °C - closed cup

Środki ochrony indywidualnej

Faceshields, Gloves, Goggles


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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

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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