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N,N-Dimethylbutylamine

Base Information
  • Chemical Name:N,N-Dimethylbutylamine
  • CAS No.:927-62-8
  • Molecular Formula:C6H15N
  • Molecular Weight:101.192
  • Hs Code.:29211990
  • European Community (EC) Number:213-156-1
  • UN Number:2734
  • UNII:O0BL4Z8J3H
  • DSSTox Substance ID:DTXSID8047472
  • Nikkaji Number:J43.087K
  • Wikidata:Q23993507
  • Metabolomics Workbench ID:60353
  • ChEMBL ID:CHEMBL2448977
  • Mol file:927-62-8.mol
N,N-Dimethylbutylamine

Synonyms:N,N-Dimethylbutylamine;927-62-8;N-n-Butyldimethylamine;Butyldimethylamine;Dimethylbutylamine;1-Butanamine, N,N-dimethyl-;N,N-dimethylbutan-1-amine;N-Butyldimethylamine;N,N-Dimethyl-1-butanamine;Butylamine, N,N-dimethyl-;(Dimethylamino)butane;butyl-dimethyl-amine;n-C4H9N(CH3)2;AR 84996;N,N-DIMETHYL-N-BUTYLAMINE;EINECS 213-156-1;UNII-O0BL4Z8J3H;O0BL4Z8J3H;1-(N,N-Dimethylamino)butane;DTXSID8047472;CHEBI:59023;EC 213-156-1;N,N-Dimethylaminobutane;dimethylaminobutane;n,n-butyldimethylamine;dimethyl(n-butyl)amine;n,n-dimethyl butylamine;SCHEMBL12592;Dimethyl-1-butanamine, N,N-;N,N-Dimethylbutylamine, 99%;CHEMBL2448977;DTXCID6027472;AMY25818;Tox21_303901;MFCD00043838;AKOS015850715;NCGC00357270-01;CAS-927-62-8;LS-45570;Butylamine, N,N-dimethyl- (6CI,7CI,8CI);D1506;FT-0629524;Q23993507;[1R-(1alpha,2beta,5alpha)]-2-isopropyl-5-methylcyclohexyl5-oxo-L-prolinate

Suppliers and Price of N,N-Dimethylbutylamine
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • N,N-Dimethylbutylamine
  • 10ml
  • $ 60.00
  • TCI Chemical
  • N-Butyldimethylamine
  • 500ML
  • $ 88.00
  • TCI Chemical
  • N-Butyldimethylamine
  • 25ML
  • $ 23.00
  • AK Scientific
  • N,N-Dimethylbutylamine
  • 25ml
  • $ 31.00
  • AK Scientific
  • N,N-Dimethylbutylamine
  • 500ml
  • $ 110.00
  • AHH
  • N-N-Butyldimethylamine 99%
  • 1000ml
  • $ 328.00
Total 92 raw suppliers
Chemical Property of N,N-Dimethylbutylamine
Chemical Property:
  • Appearance/Colour:colourless liquid 
  • Vapor Pressure:44.6mmHg at 25°C 
  • Melting Point:-60 °C 
  • Refractive Index:n20/D 1.398(lit.)  
  • Boiling Point:95.9 °C at 760 mmHg 
  • PKA:9.83±0.28(Predicted) 
  • Flash Point:25°F 
  • PSA:3.24000 
  • Density:0.75 g/cm3 
  • LogP:1.34810 
  • Water Solubility.:3.4 g/100 mL (20 ºC) 
  • XLogP3:1.7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:3
  • Exact Mass:101.120449483
  • Heavy Atom Count:7
  • Complexity:33.2
  • Transport DOT Label:Corrosive Flammable Liquid
Purity/Quality:

99.3% *data from raw suppliers

N,N-Dimethylbutylamine *data from reagent suppliers

Safty Information:
  • Pictogram(s): FlammableF,Corrosive
  • Hazard Codes:F,C 
  • Statements: 11-20/22-34 
  • Safety Statements: 26-36/37/39-45-16 
MSDS Files:

SDS file from LookChem

Useful:
  • Chemical Classes:Nitrogen Compounds -> Amines, Aliphatic
  • Canonical SMILES:CCCCN(C)C
  • Uses Dimethylbutylamine is used as a chemical intermediate. N,N-Dimethylbutylamine (cas# 927-62-8) is in preparation of high-density rigid flame-retardant polyimide foam material. N,N-Dimethylbutylamine is suitable for use in the fabrication of polystyrene-based nano-LC monolithic columns for the separation of protein molecules. It may be used as ion-pairing reagent in a study involving comparison of performance of six ion-pairing reagents as mobile phase modifiers for oligonucleotide LC/MS.
Technology Process of N,N-Dimethylbutylamine

There total 42 articles about N,N-Dimethylbutylamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With acetic acid; at 30 ℃; for 2h;
DOI:10.1016/j.tetlet.2007.08.092
Guidance literature:
N,N-dimethylbutyramide; With bis(cyclopentadienyl)dihydrozirconium; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane; at 20 ℃; Glovebox; Inert atmosphere;
With hydrogenchloride; In diethyl ether; water; for 2h; Glovebox; Inert atmosphere;
DOI:10.1016/S1872-2067(21)63853-6
Guidance literature:
palladium; at 160 ℃; for 5h;
DOI:10.1021/ja00353a025
Refernces

Xantphos as an efficient ligand for palladium-catalyzed cross-coupling reactions of aryl bromides and triflates with allyl acetates and indium

10.1021/jo702279t

The research focuses on the efficiency of Xantphos as a ligand in palladium-catalyzed allyl cross-coupling reactions of aryl bromides and triflates with allylindium reagents, which are generated in situ from allyl acetates and indium. The purpose of this study was to address the need for an efficient catalytic system for these reactions, as previous methods were only successful with aryl iodides and vinyl bromides and triflates. The researchers found that Xantphos, a ligand developed by van Leeuwen, significantly improved the reactivity and selectivity of the catalyst, leading to high yields and good functional group tolerance. The optimal conditions involved the use of 5 mol % of Pd2dba3CHCl3, 20 mol % of Xantphos, indium (2 equivalents), InCl3 (0.5 equivalents), LiCl (3 equivalents), and N,N-dimethyl-n-butylamine (2 equivalents) in DMF at 100 °C under a nitrogen atmosphere. The chemicals used in the process include various aryl bromides and triflates, allyl acetates, indium, indium trichloride, lithium chloride, Pd2dba3CHCl3, Xantphos, and N,N-dimethyl-n-butylamine. The study concluded that Xantphos is an efficient ligand for these cross-coupling reactions, offering a complementary method to existing synthetic methods.

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