amino alcohol


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amino alcohol

[ə′mē‚nō ′al·kə‚hȯl]
(organic chemistry)
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Three new mononuclear copper(II) complexes possessing ONNO type Schiff bases of chiral amino alcohol were synthesized.
has patented an aqueous cleaning composition comprising an ionic liquid that is a polypropoxylated 2-(trialkylammonio)ethanol salt; an amino alcohol; a component selected from the group consisting of a quaternary benzyl ammonium surfactant, a nonionic surfactant, an aminopolycarboxylate chelating agent, or mixtures thereof; and water.
Three different means were tried to stabilize the Sweet Sap to prevent fermentation: (a) doping with amino alcohol and maintaining at higher pH; (b) addition of 5% methylated spirit (Trial 1); addition of 2% fungicides (Trial 2).
The reduction of amino acids [25, 26] is considered important transformation in organic synthesis, the amino alcohol obtained in this transformation plays vital role in asymmetric synthesis [1] and peptide synthesis.
The complex chemical compound hydrogen fluoride pyridine is widely used in the preparation of beta-fluoroamines through reaction with amino alcohols. Moreover, hydrogen fluoride pyridine is also used in the preparation of gem-difluorides by reacting with ketoximes in associated with nitrosonium tetrafluorborate.
A number of custom-designed hydrophobic amino alcohols and hydrophobic amino diols have been developed that are used to manufacture a variety of amine technology HEUR products.
Occurrence and characteristics of amino alcohols and cyclohexenone, components of fungal mycosporines.
Also, weak amines and amino alcohols have also been used as activators in combinations with the metal oxides.
Such reagents provide versatile methods to prepare chiral cyclobutanones, amino acids and amino alcohols with enantiomeric excesses in some cases of |is greater than~ 98%.
ANGUS' ULTRA PC portfolio of amino alcohols, with their high purity and excellent water- and alcohol-solubility properties, helps formulators achieve unmatched performance in many home and personal care products.
Since the pioneering work of Julia and Colonna [9-11], a variety of efficient organocatalysts have been explored for this reaction, for instance, polyamino acids [12], amino alcohols [13-19], phase-transfer catalysts (PTCs) [20-22], amines [23], chiral ketones [24] and chiral peroxides [25, 26].