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Merck
CN

74202

Supelco

四甲基氯化铵

suitable for ion pair chromatography, LiChropur, ≥99.0% (AT)

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别名:
TMA
线性分子式:
(CH3)4N(Cl)
CAS号:
分子量:
109.60
Beilstein:
3911201
EC 号:
MDL编号:
UNSPSC代码:
12000000
PubChem化学物质编号:
NACRES:
NB.21

描述

cationic

质量水平

检测方案

≥99.0% (AT)

形式

crystals

质量

LiChropur

技术

ion pair chromatography: suitable

mp

>300 °C (lit.)

λ

10 % in H2O

紫外吸收

λ: 220 nm Amax: 0.05
λ: 230 nm Amax: 0.04
λ: 250 nm Amax: 0.03
λ: 260 nm Amax: 0.02
λ: 500 nm Amax: 0.02

适用性

corresponds to standard for RP gradient test
corresponds to standard for filter test

SMILES字符串

[Cl-].C[N+](C)(C)C

InChI

1S/C4H12N.ClH/c1-5(2,3)4;/h1-4H3;1H/q+1;/p-1

InChI key

OKIZCWYLBDKLSU-UHFFFAOYSA-M

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一般描述

四甲基氯化铵(TMAC)在结构上类似于烷基三甲基铵盐。TMAC的氧化产生甲醛和三甲胺。由于它不溶于有机介质,因此被认为是大多数反应的不良相转移催化剂。但是,它非常适合作为相转移催化剂,与碱金属氟化物一起氟化氯苯甲醛,从而产生1,2,2,2-四氟乙基二氟甲基醚。

应用

TMAC可用于离子交换程序中,以显示pH的增加,以使用Knoevenagel缩合模型了解催化剂[CTA]Si-MCM-41的化学行为。

法律信息

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

警示用语:

Danger

危险分类

Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Aquatic Chronic 2 - Skin Irrit. 2 - STOT SE 1 Oral

靶器官

Central nervous system

WGK

WGK 3

个人防护装备

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Surfactant containing Si-MCM-41: An efficient basic catalyst for the Knoevenagel condensation.
Martins, Leandro, et al.
Applied Catalysis A: General, 312, 77-85 (2006)
Fundamentals, Applications, and Industrial Perspectives
C.M. Starks, M. Halper
Phase Transfer Catalysis (Academic Press), 182 -182 (2012)
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The Fbw7 tumor suppressor targets a broad network of proteins for ubiquitylation. Here we show critical functions for Fbw7 dimerization in regulating the specificity and robustness of degradation. Dimerization enables Fbw7 to target substrates through concerted binding to two suboptimal
Wei Shen et al.
Chemical communications (Cambridge, England), 49(73), 8114-8116 (2013-08-08)
A simple and low-cost colorimetric assay utilizing ferrofluidic nanoparticulate probes (FNPs) and a ligase for single-nucleotide polymorphism genotyping is described. Excellent sensitivity and selectivity were accomplished through the engagement of the FNPs and a ligase chain reaction.
Marco I Ries et al.
The Journal of biological chemistry, 288(52), 37289-37295 (2013-11-15)
Metabolic profiling and structural elucidation of novel secondary metabolites obtained from derived deletion strains of the filamentous fungus Penicillium chrysogenum were used to reassign various previously ascribed synthetase genes of the roquefortine/meleagrin pathway to their corresponding products. Next to the

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