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Diethylaminoethyl Alcohol

The physical properties of /3-diethylaminoethyl alcohol are described in detail by Headlee, Collett, and Lazzell.  [Pg.29]

Synonyms AI3-16309 BRN 0741863 CCRIS 4793 DEAE Diethylaminoethanol p Diethyl-aminoethanol TV-Diethylaminoethanol 2-A-Diethylaminoethanol 2-Diethylaminoethyl alcohol P-Diethylaminoethyl alcohol Diethylethanolamine A7A-Diethylethanolamine Diethyl(2-hy-droxyethyl)amine A,7V-Diethyl-A-(P-hydroxyethyl)amine EINECS 202-845-2 2-Hydroxytrieth-ylamine NSC 8759 Perdilaton UN 2686. [Pg.449]

A solution of 205 g. (1.75 moles) of 2-diethylaminoethyl alcohol in 500 ml. of dry thiophene-free benzene is cooled in an ice-salt bath... [Pg.116]

Synonyms/Trade Names Diethylaminoethanol 2-Diethylaminoethyl alcohol N,N-Diethylethaholamihe Diethyl-(2-hydroxyethyl)amine 2-Hydroxytriethylamine ... [Pg.107]

Diethylaminoethyl alcohol has been prepared by reduction of diethylaminoacetic ester with sodium and alcohol, by the action of ethylene chlorohydrin on diethylamine, and by the action of ethylene oxide on diethylamine. ... [Pg.29]

SYNS DEAE DIAETHYLAMINOAETHANOL (GERMAN) DIETHYLAMINOETHANOL (3-DIETHYLAMINOETHANOL n-diethylamino-ETHANOL 2-(DIETHYLAMIN0)ETIL N0L 2-N-DIETHYLAMINOETHANOL DIETHYLAMINOETHANOL (DOT) P-DIETHYLAMINOETHYL ALCOHOL DIETHYLETHANOLAMINE N,N-DIETHYLETHANOLAMINE N,N-DIETHYL-N-(P-HYDR0XYETHYL)AMINE 2-HYDROXYTRIETH-YLAMINE... [Pg.481]

Amino alcohols are commonly made by the amination of halo alcohols or by alkylation of amino alcohols. Thus (S-diethylaminoethyl alcohol is synthesized from diethylamine and ethylene chlorohydrin (70%)/ Higher amino alcohols are made in a similar manner. No isomerization... [Pg.786]

Di-w-butyl carbinol, 15,11 Diethylamine, 10, 58 14, 28 /3-Diethylaminoethyl alcohol, 14, 28 Diethyl carbonate, 11, 98 Diethyl zinc, 12, 86... [Pg.50]

DIETHYLAMINO)ETHANOL or 2-iV-DIETHYLAMINOETHANOL or iV-DI-ETHYL-AMINOETHANOL or P-DIETHYLAMINOETHANOL or 2-(DIETHYL-AMINO) ETHYL ALCOHOL or P-DIETHYLAMINOETHYL ALCOHOL (100-37-8)... [Pg.415]

An understanding of the metabolism of local anesthetics is important in clinical practice, because the overall toxicity of a drug depends not only on its uptake and tissue distribution but also on how it is deactivated in vivo. The amino ester-type local anesthetics are rapidly hydrolyzed by plasma cholinesterase (also known as pseudocholinesterase), which is widely distributed in body tissues. These compounds can therefore be metabolized in the blood, kidneys, and liver and, to a lesser extent, at the site of administration. For example, both procaine and benzocaine are easily hydrolyzed by cholinesterase into PABA and the corresponding N,N -diethylaminoethyl alcohol. [Pg.679]

P-Diethylaminoethyl alcohol. See Diethylaminoethanol 2-Diethyl ami noethyl p-ami nobenzoate 4-(Diethylamino) ethyl 4-ami nobenzoate p-Diethylaminoethyl-4-aminobenzoate Diethylaminoethyl-p-aminobenzoate. See Procaine... [Pg.1299]

Synonyms DEAE 2-Diethylaminoethanol P-Diethylaminoethanol N-Diethylami-noethanol N,N-Diethyl-2-aminoethanol P-Diethylaminoethyl alcohol Diethyletha-nolamine N,N-Diethylethanolamine N,N-Diethyl-N-(P-hydroxyethyl) amine Ethanol, 2-(diethylamino)- 2-Hydroxytriethylamine Ciassification Aliphatic amino alcohol Empiricai CeH sNO Formuia (C2H5)2NCH2CH20H... [Pg.2074]

Diethylamino) ethyl acrylate P-Diethylaminoethyl acrylate N,N-Diethylami-noethyl acrylate. See Diethylaminoethyl acrylate P-Diethylaminoethyl alcohol. See Diethylaminoethanol Diethylaminoethyl cocoate... [Pg.2074]

See other pages where Diethylaminoethyl Alcohol is mentioned: [Pg.1476]    [Pg.21]    [Pg.565]    [Pg.20]    [Pg.28]    [Pg.83]    [Pg.1476]    [Pg.48]    [Pg.96]    [Pg.18]    [Pg.21]    [Pg.39]    [Pg.344]    [Pg.491]    [Pg.565]    [Pg.319]    [Pg.319]    [Pg.17]    [Pg.20]    [Pg.38]    [Pg.15]    [Pg.69]    [Pg.1298]    [Pg.319]    [Pg.319]    [Pg.430]    [Pg.194]   
See also in sourсe #XX -- [ Pg.29 , Pg.319 ]

See also in sourсe #XX -- [ Pg.107 ]

See also in sourсe #XX -- [ Pg.29 , Pg.319 ]



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2- diethylaminoethyl

Diethylamine 3-Diethylaminoethyl alcohol

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