79266
三甲基苯基氢氧化铵 溶液
~0.5 M (CH3)3N(OH)C6H5 in methanol, derivatization grade (GC derivatization), LiChropur™
别名:
苯基三甲基氢氧化铵
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关于此项目
线性分子式:
(CH3)3N(OH)C6H5
化学文摘社编号:
分子量:
153.22
UNSPSC Code:
41115710
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3917033
Concentration:
~0.5 M (CH3)3N(OH)C6H5 in methanol
Form:
liquid
Grade:
derivatization grade (GC derivatization)
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
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General description
Trimethylphenylammonium hydroxide (TMAH) is a methylating reagent.
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.
Other Notes
Reagent for n-methyl and methyl esters.
Legal Information
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany
Disclaimer
Sales restrictions may apply
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
存储类别
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
法规信息
危险化学品
此项目有
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)
Timothy J Jensen et al.
Journal of photochemistry and photobiology. B, Biology, 100(2), 100-111 (2010-06-19)
Five cationic porphyrins bearing one to four -N(CH(3))(3)(+) groups linked to the p-phenyl positions of 5,10,15,20-tetraphenylporphyrin (TPP) were synthesized in order to study the effect of overall charge and its distribution on the cellular uptake, phototoxicity and intracellular localization using
A Ranz et al.
Journal of biochemical and biophysical methods, 69(1-2), 3-14 (2006-03-28)
In the present study, a derivatization method for the determination of acidic herbicides has been investigated. This procedure involves the methylation with the quaternary ammonium salt trimethylanilinium hydroxide (TMAH) directly in the gas chromatographic auto-sampler vial for analysis by gas
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
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
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