91219-68-0

Basic information

• Product Name: 1,6-bis(aminooxy)hexane
• CAS NO: 91219-68-0
• Molecular Formula: C₆H₁₆N₂O₂
• Molecular Weight: 148.2034
• Mol File: 91219-68-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 297°C at 760 mmHg
• Flash Point: 150.4°C
• Density: 1.003g/cm³
• Vapor Pressure: 0.00138mmHg at 25°C
• Refractive Index: 1.459
• CAS DataBase Reference: 1,6-bis(aminooxy)hexane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,6-bis(aminooxy)hexane(91219-68-0)
• EPA Substance Registry System: 1,6-bis(aminooxy)hexane(91219-68-0)

Safety Data

• Hazardous Substances Data: 91219-68-0(Hazardous Substances Data)

Usage

Solubility

Water-soluble

Functional groups

Contains two aminooxy functional groups

Application

Selective labeling of aldehydes and ketones in biological samples

Usage

Wide range of applications in biochemical research

Studies

Protein-carbohydrate interactions, protein structure, and enzyme catalysis

Target

Specifically targets and labels carbonyl groups

Fields

Valuable tool in biochemistry, molecular biology, and biomedical research

Upstream product

• 95006-51-2 N,N'-hexane-1,6-diyldioxy-bis-phthalimide 
• 629-03-8 1 ,6-dibromohexane 

Relevant articles and documents

Synthesis and characterization of Salamo-type bisoxime compounds based on 2-hydroxy-4-methoxybenzaldehyde and bis(aminooxy)alkane

There new Salamo-type bisoxime compounds H2L1-H2L3 have been synthesized from 2-hydroxy-4-methoxybenzaldehye and 1,5-bis(aminooxy)pentane, 1,6-bis(aminooxy)hexane or 1,9-bis(aminooxy)nonane in hot ethanol medium, respectivel and characterized by elemental analysis, IR and 1HNMR spectroscopy.

Synthesis and characterization of multihalogen substituted salamo-type bisoximes

Four tetrahalogen substituted Salamo-type bisoximes H2L1-H2L4 have been synthesized from 3-bromo-5-chloro-2-hydroxybenzaldehyde and 1,3-bis(aminooxy) propane, 1,4-bis(aminooxy)butane, 1,5-bis(aminooxy)pentane or 1,6-bis(aminooxy)hexane in ethanol solution

Uracil-directed ligand tethering: An efficient strategy for uracil DNA glycosylase (UNG) inhibitor development

Uracil DNA glycosylase (UNG) is an important DNA repair enzyme that recognizes and excises uracil bases in DNA using an extrahelical recognition mechanism. It is emerging as a desirable target for small-molecule inhibitors given its key role in a wide ran