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Merck

69485

Sigma-Aldrich

Methyltrioctylammonium chloride

≥97.0% (AT)

Sinónimos:

Trioctylmethylammonium chloride

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About This Item

Fórmula lineal:
[CH3(CH2)6CH2]3N(Cl)CH3
Número de CAS:
Peso molecular:
404.16
Beilstein/REAXYS Number:
4039255
EC Number:
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥97.0% (AT)

impurities

~1% water

SMILES string

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

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

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Application

Methyltrioctylammonium chloride can be used:
  • As a catalyst in the synthesis of acridine dione derivatives from aromatic aldehyde, dimedone and amines under ultrasonic irradiations.
  • As a catalyst in the synthesis of extended π-systems using aromatic aldehydes and methyldiazines.
  • As a component of a catalytic system used in the Suzuki-Miyaura cross-coupling reaction of a variety of aryl and heteroaryl chlorides in H2O.

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

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

235.4 °F

flash_point_c

113 °C

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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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)
Methyltrioctylammonium chloride catalysed sonochemical synthesis of acridine diones
Kaur B and Kumar H
Journal of Chemical Sciences (Bangalore), 125(5), 989-992 (2013)
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
Noorbasha N Meeravali et al.
Talanta, 80(1), 173-178 (2009-09-29)
A novel cloud point phase separation of cationic surfactant, Aliquat-336 and capabilities of its reactive solubilizing sites for selective extraction of chromium species at ultra trace levels was examined in natural water. The phase separation behavior of Aliquat-336 is studied

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