142-81-4 | N-Hexylamine HCl

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$26.00	$18.00
25g	98%	in stock	$92.00	$65.00
100g	98%	in stock	$299.00	$209.00

Description

• Catalog Number: AA69186
• Chemical Name: N-Hexylamine HCl
• CAS Number: 142-81-4
• Molecular Formula: C6H16ClN
• Molecular Weight: 137.6509
• MDL Number: MFCD00043792
• SMILES: CCCCCCN.Cl
• NSC Number: 210910

Computed Properties

• Complexity: 27.4
• Covalently-Bonded Unit Count: 2
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 1
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 4

Literature

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  Physical chemistry chemical physics : PCCP 20121021

• Active site residue involvement in monoamine or diamine oxidation catalysed by pea seedling amine oxidase.

  The FEBS journal 20110401

• Determination of picropodophyllin and its isomer podophyllotoxin in human serum samples with electrospray ionization of hexylamine adducts by liquid chromatography-tandem mass spectrometry.

  Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20110215

• A photosensing system composed of photosystem I, molecular wire, gold nanoparticle, and double surfactants in water.

  Chemical communications (Cambridge, England) 20100421

• Ultraperformance liquid chromatography with electrospray ionization ion trap mass spectrometry for chondroitin disaccharide analysis.

  Analytical biochemistry 20100201

• Functional expression of amine oxidase from Aspergillus niger (AO-I) in Saccharomyces cerevisiae.

  Molecular biology reports 20090101

• Discovery of synergistic permeation enhancers for oral drug delivery.

  Journal of controlled release : official journal of the Controlled Release Society 20080604

• CEC separation of aromatic compounds and proteins on hexylamine-functionalized N-acryloxysuccinimide monoliths.

  Journal of separation science 20071101

• Functional reactivity of oxanine: its biological meanings and biotechnological applications.

  Nucleic acids symposium series (2004) 20070101

• Functionalization of indium tin oxide.

  Langmuir : the ACS journal of surfaces and colloids 20061219

• Monodentate phosphines provide highly active catalysts for Pd-catalyzed C-N bond-forming reactions of heteroaromatic halides/amines and (H)N-heterocycles.

  Angewandte Chemie (International ed. in English) 20061006

• Simultaneous quantitative analysis of metabolites using ion-pair liquid chromatography-electrospray ionization mass spectrometry.

  Analytical chemistry 20060915

• Hydrogen storage in chemically reducible mesoporous and microporous Ti oxides.

  Journal of the American Chemical Society 20060913

• Enhanced skin permeation of salicylate by ion-pair formation in non-aqueous vehicle and further enhancement by ethanol and l-menthol.

  Chemical & pharmaceutical bulletin 20060401

• Mechanistic insights into the Pd(BINAP)-catalyzed amination of aryl bromides: kinetic studies under synthetically relevant conditions.

  Journal of the American Chemical Society 20021127

• Modification of the upper rim of homooxacalix[3]arenes and complexation between a nitrohomooxacalix[3]arene derivative and n-hexylamine.

  The Journal of organic chemistry 20021115

• Principles for measurement of chemical exposure based on recognition-driven anchoring transitions in liquid crystals.

  Science (New York, N.Y.) 20010817