228982
苄基三甲基氯化铵
97%
别名:
Amberlite IRC 178(Cl), 三甲基苄基氯化铵, 苄基三甲基氯化铵(6CI)
方案
97%
mp
239 °C (dec.) (lit.)
SMILES字符串
[Cl-].C[N+](C)(C)Cc1ccccc1
InChI
1S/C10H16N.ClH/c1-11(2,3)9-10-7-5-4-6-8-10;/h4-8H,9H2,1-3H3;1H/q+1;/p-1
InChI key
KXHPPCXNWTUNSB-UHFFFAOYSA-M
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应用
苄基三甲基氯化铵可用作以下反应的相催化剂:
- 在 1,3-二氯-5,5-二甲基乙内酰脲 (DCH) 存在的情况下由硫醇和二硫化物合成烷基和芳基磺酰胺。
- 以过氧化氢为氧化剂,将苯甲醇选择性氧化为苯甲醛。
- 乙醇和月桂酸的酯化反应。
警示用语:
Danger
危险分类
Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Muta. 2
储存分类代码
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
WGK
WGK 2
个人防护装备
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Convenient one-pot Synthesis of sulfonamides from thiols and disulfides using 1, 3-dichloro-5, 5-dimethylhydantoin (DCH)
Veisi Hojat
Bull. Korean Chem. Soc., 33(2), 383-386 (2012)
Kinetics of the reaction of ethanol and lauric acid catalyzed by deep eutectic solvent based on benzyltrimethylammonium chloride
Li Kun, et al.
The Canadian Journal of Chemical Engineering, 97(5), 1144-1151 (2019)
Selective oxidation of benzyl alcohol with hydrogen peroxide over reaction-controlled phase-transfer catalyst
Weng Z, et al.
Catalysis Communications, 8(10), 1493-1496 (2007)
R Daniel Peluffo et al.
The Journal of general physiology, 123(3), 249-263 (2004-02-26)
The effects of organic quaternary amines, tetraethylammonium (TEA) chloride and benzyltriethylammonium (BTEA) chloride, on Na,K pump current were examined in rat cardiac myocytes superfused in extracellular Na(+)-free solutions and whole-cell voltage-clamped with patch electrodes containing a high Na(+)-salt solution. Extracellular
Correlation analysis in a set of X-benzyltrimethylammonium derivatives with antimuscarinic activity.
M De Amici et al.
Il Farmaco; edizione scientifica, 42(6), 409-424 (1987-06-01)
The results of a pharmacological investigation on a series of meta-substituted benzyltrimethylammonium salts possessing an antimuscarinic activity are reported. Correlative analysis shows that the pharmacodynamic activity is a function of the hydrophobic-lipophilic parameter associated with the substituent.
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