69485
甲基三辛基氯化铵
≥97.0% (AT)
别名:
三辛基甲基氯化铵
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关于此项目
线性分子式:
[CH3(CH2)6CH2]3N(Cl)CH3
化学文摘社编号:
分子量:
404.16
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
EC Number:
264-120-7
Beilstein/REAXYS Number:
4039255
MDL number:
InChI
1S/C25H54N.ClH/c1-5-8-11-14-17-20-23-26(4,24-21-18-15-12-9-6-2)25-22-19-16-13-10-7-3;/h5-25H2,1-4H3;1H/q+1;/p-1
InChI key
XKBGEWXEAPTVCK-UHFFFAOYSA-M
SMILES string
[Cl-].CCCCCCCC[N+](C)(CCCCCCCC)CCCCCCCC
assay
≥97.0% (AT)
Quality Level
form
liquid
impurities
~1% water
Application
甲基三辛基氯化铵可用于：
- 作为催化剂，在超声波辐射下由芳香醛、双甲酮和胺合成吖啶二酮衍生物。
- 作为催化剂，合成芳香醛和甲基吡嗪的延伸π体系。
- 作为催化体系的组成部分，用于多种芳基和杂芳基氯化物在水中的Suzuki-Miyaura交叉偶联反应。
signalword
Danger
Hazard Classifications
Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Repr. 1B - Skin Corr. 1A - STOT RE 2
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
235.4 °F
flash_point_c
113 °C
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Quaternary ammonium salt-assisted synthesis of extended pi-systems from methyldiazines and aromatic aldehydes
Vanden E, et al.
Synthetic Communications, 31(20), 3167-3173 (2001)
A highly active catalytic system for Suzuki--Miyaura cross-coupling reactions of aryl and heteroaryl chlorides in water
Mao S, et al.
Organic & Biomolecular Chemistry, 10(47), 9410-9417 (2012)
Xin Di et al.
Journal of separation science, 43(15), 3129-3135 (2020-06-09)
A green extractant, hydrophobic deep eutectic solvent was first introduced for extraction of tetracycline, oxytetracycline, and chlortetracycline from environmental water samples prior to high-performance liquid chromatography determination. Deep eutectic solvents consist of methyltrioctylammonium chloride and various medium-chain alcohols/acids, and are
Methyltrioctylammonium chloride catalysed sonochemical synthesis of acridine diones
Kaur B and Kumar H
Journal of Chemical Sciences (Bangalore), 125(5), 989-992 (2013)
Anja Stojanovic et al.
Journal of chromatography. A, 1209(1-2), 179-187 (2008-09-23)
Several hydrophobic ionic liquids (ILs) based on long-chain aliphatic ammonium- and phosphonium cations and selected aromatic anions were analyzed by reversed-phase high-performance liquid chromatography (RP-HPLC) employing trifluoroacetic acid as ion-pairing additive to the acetonitrile-containing mobile phase and adopting a step-gradient
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