Customization: | Available |
---|---|
CAS No.: | 63393-96-4 |
Formula: | [CH3(CH2)7]3nch3c |
Suppliers with verified business licenses
Audited by an independent third-party inspection agency
Aliquat 336 is used as a phase transfer catalyst,[2] including in the catalytic oxidation of cyclohexene to 1,6-hexanedioic acid.[3] This reaction is more environmentally friendly. It is an example of green chemistry, compared with the traditional method of oxidizing cyclohexanol or cyclohexanone with nitric acid or potassium permanganate, which produce hazardous wastes.[4]
Aliquat 336 was used in the total synthesis of manzamine A by Darren Dixon in an early step to the electrophile.[5]
Aliquat 336 has been used for the extraction of metals, it does so by acting as a liquid anion exchanger. It is often used while diluted in hydrocarbon solvents such as aromatic kerosene. It is possible to use it in aliphatic kerosene but in such solvents often a phase modifier (typically a long chain alcohol) must be added to prevent the formation of third phase.
Identifiers | |
---|---|
CAS Number
|
|
3D model (JSmol)
|
|
ChemSpider |
|
ECHA InfoCard | 100.023.542 |
PubChem CID
|
|
RTECS number |
|
UNII |
|
CompTox Dashboard (EPA)
|
|
show
InChI
|
|
show
SMILES
|
|
Properties | |
Chemical formula
|
C25H54ClN |
Molar mass | 404.16 g·mol−1 |
Appearance | Colorless viscous liquid |
Density | 0.884 g/cm3 |
Melting point | −20 °C (−4 °F; 253 K) |
Boiling point | 225 °C (437 °F; 498 K) |
Viscosity | 1500 mPa·s at 30 °C |