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Factory supply good quality Benzyltriethylammonium chloride (BTEAC) 56-37-1 with stock We supply high quality Benzyltriethylammonium chloride (CAS 56-37-1), in stock, factory directly supply to clients, lower prices, more competitiveness.
Benzyltriethylammonium chloride is white to light yellow crystallize powder, while it's Molecular Formula is C13H22ClN. Benzyltriethylammonium chloride is used as a catalyst in the preparation of 2-phenylbutyronitrile from phenyl acetonitrile. It is involved in the Knoevenagel condensation of carbonyl compounds with active methylene compounds to give olefinic products. It acts as a phase transfer catalyst used in the alkylation reaction. It reacts with 1H-Pyridine-2-thione to get 2-Benzylsulfanyl-pyridine.
The CAS number of Benzyltriethylammonium chloride is 56-37-1.
More information of Benzyltriethylammonium chloride 56-37-1 are:
Synonyms |
Ammonium,benzyltriethyl-, chloride (8CI);Benzenemethanaminium, N,N,N-triethyl-,chloride (9CI);Benzyltriethylammonium chloride (6CI);BAC-TE;N,N,N-Triethyl-N-benzylammonium chloride;TEBA;TEBAC;Triethylbenzylammoniumchloride;Benzenemethanaminium, N,N,N-triethyl-, chloride; |
CAS Number |
56-37-1 |
Molecular Formula |
C13H22ClN |
Molecular Weight |
227.777 |
Density |
1.08 g/mL at 25 °C |
Melting Point |
239 °C (dec.)(lit.) |
Boiling Point |
366.11°C (rough estimate) |
Flash Point |
> 100 °C |
HS CODE |
2923.90 |
PSA |
0.00000 |
LogP |
0.06710 |
Benzyltriethylammonium chloride (TEBAC) is a phase transfer catalyst (PTC) used in organic synthesis to facilitate reactions between immiscible phases, such as aqueous and organic layers. It has been employed in the synthesis of 6-methoxytryptamine, where it enhances the alkylation step by improving the reactivity of the reactants in a biphasic system. Additionally, it serves as a chloride source in radical-mediated chlorodecarboxylation reactions, influencing product distributions based on its concentration. Its role as a PTC also extends to the synthesis of heterocyclic compounds like N-thioamido-β-lactams, where it increases reaction efficiency and yield under mild conditions.
InChI:InChI=1/C13H22N.ClH/c1-4-14(5-2,6-3)12-13-10-8-7-9-11-13;/h7-11H,4-6,12H2,1-3H3;1H/q+1;/p-1
Articles related to Benzyltriethylammonium chloride:
Article |
Source |
Activation of C-Cl Bonds in Chloroalkanes by Nickel Oxide Nanoparticles: Formation of Tetrasubstituted Ammonium Salts from Tertiary Amines |
Park, Kang Hyun,Jung, Il Gu,Chung, Young Keun,Han, Jin Wook , p. 411 - 416 (2007) |
Thermal stability of quaternary ammonium hexafluorophosphates and halides |
Zhuravlev,Nikol'skii,Voronchikhina , p. 824 - 830 (2014/02/14) |
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