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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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
产品名称
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™
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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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
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)
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
Alec N Salt et al.
Hearing research, 182(1-2), 24-33 (2003-09-02)
Our understanding of the perilymph kinetics of drugs depends largely on data obtained by the analysis of perilymph samples. Although a number of studies have demonstrated qualitatively that perilymph samples may be contaminated by cerebrospinal fluid (CSF), and some investigations
Jie Zhang et al.
Journal of chromatography. A, 1216(44), 7527-7532 (2009-04-07)
A method has been established for the determination of four pharmaceutically active compounds (ibuprofen, ketoprofen, naproxen and clofibric acid) in water samples using dynamic hollow fiber liquid-phase microextraction (HF/LPME) followed by gas chromatography (GC) injection port derivatization and GC-mass spectrometric
Alec N Salt et al.
Hearing research, 283(1-2), 14-23 (2011-12-20)
It has been widely believed that drug entry from the middle ear into perilymph occurs primarily via the round window (RW) membrane. Entry into scala vestibuli (SV) was thought to be dominated by local, inter-scala communication between scala tympani (ST)
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