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Merck
CN

79266

Trimethylphenylammonium hydroxide solution

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

Synonym(s):

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
UNSPSC Code:
41115710
NACRES:
NA.22
PubChem Substance ID:
329768356
MDL number:
MFCD00041899
Beilstein/REAXYS Number:
3917033

Key Documents

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Product Name

Trimethylphenylammonium hydroxide solution, ~0.5 M (CH3)3N(OH)C6H5 in methanol, derivatization grade (GC derivatization), LiChropur™

InChI

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

SMILES string

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

InChI key

HADKRTWCOYPCPH-UHFFFAOYSA-M

grade

derivatization grade (GC derivatization)

form

liquid

quality

LiChropur™

reaction suitability

reagent type: derivatization reagent
reaction type: Esterifications

concentration

~0.5 M (CH3)3N(OH)C6H5 in methanol

technique(s)

gas chromatography (GC): suitable

impurities

≤0.2% halides (as chloride)

storage temp.

2-8°C

Quality Level

100

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Application

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.

Disclaimer

Sales restrictions may apply

General description

Trimethylphenylammonium hydroxide (TMAH) is a methylating reagent.

Other Notes

Reagent for n-methyl and methyl esters.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

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

target_organs

Eyes

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

51.8 °F - closed cup

flash_point_c

11 °C - closed cup

ppe

Faceshields, Gloves, Goggles

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCN6600
BCCF7109
STBJ1243
STBH7120
STBG9018

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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)
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
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
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.
Hearing research, 232(1-2), 78-86 (2007-07-31)
Local delivery of drugs to the inner ear is increasingly being used in both clinical and experimental studies. Although direct injection of drugs into perilymph appears to be the most promising way of administering drugs quantitatively, no studies have yet
View All Related Papers

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