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Aminoethyl piperazine

N1 -acylsulfanilamides, 23 508 A21-heterocyclic derivatives, 23 508 Ar -heterocyclic-Ar -acylsulfanilamides, 23 508 A21-heterocyclic sulfanilamides, 23 507—508 2V-(2-aminoethyl)-l,3-propylenediamine physical properties, 5 486t 2V-(2-aminoethyl)-piperazine (AEP), 5 485 N2 oxidation, Birkeland-Eyde process of, 27 291-292, 316. See also Dinitrogen entries Nitrogen entries N3 -P5 phosphoramidates, 27 630-631 Na+, detection in blood, 24 54. See also Sodium entries Nabarro-Herring creep, 5 626 Nacol 18, chain length and linearity, 2 10t Nacreous pigments, 7 836-837 19 412 Nacrite, 6 659... [Pg.608]

Aminoethyl)piperazine [140-31-8] Desipramine hydrochloride [58-28-6] 172B I(3)437D, N(1)330C TK8050000 USP... [Pg.1053]

DIISOPROPYLAMINE DI-n-PROPYLAMINE n-HEXYLAMINE TRIETHYLAMINE 6-AMINOHEXANOL DIISOPROPANOLAMINE TRIETHANOLAMINE N-AMINOETHYL PIPERAZINE TRIETHYL PHOSPHATE HEXAMETHYLENEDIAMINE HEXAMETHYL PHOSPHORAHIDE TRIETHYLENE TETRAMINE HEXAMETHYLDISILOXANE... [Pg.14]

Leong et al. evaluated a hyperbranched poly(amino ester) synthesized in a novel A3+2BB B approach by Michael addition polymerization of trimethylol-propane triacrylate (TMPTA) (A3-type monomer, triacrylate), with a double molar of l-(2-aminoethyl) piperazine (AEPZ) (BB B -type monomer, trifunctional amine) (Fig. 11) [127]. To check its DNA condensation behavior and cytotoxicity, the poly(TMPTAl-AEPZ2) obtained was protonated. Due to the protonation ability of... [Pg.114]

Fig. 13 (a) Possible structures of hyperbranched polymer (p(X-Y)) from the conjugate addition of X (diacrylate) and Y (trifunctional amines), (b) Structures of diacrylates and trifunctional amine monomers used for the synthesis 4-(aminomethyl)piperidine) (AMP), A-methylethylenediamine (MEDA), l-(2-aminoethyl)piperazine (AEPZ), ethylene glycol diacrylate (EGDA), 1,4-butanediol diacrylate (BDDA), and 1,6-hexanediol diacrylate (HDDA). Adapted with permission from [124], Copyright 2005 Elsevier... [Pg.117]

SYNS AMINOETHYLPIPERAZINE N-(P-AMINOETHYL)PIPERAZINE N-(2-AMINOETHYL)-PIPERAZINE l-(2-AMINOETHYL)PIPERAZINE USAF DO-46... [Pg.57]

Symmetrical anhydride couplings with annino acid or peptide esters are complete within a few minutes and are quantitative when 1.4 equivalents of anhydride is used. The excess anhydride can be removed by treatment of the nnixture with A-(2-aminoethyl)piperazine. [Pg.502]

C6H12 trans-2-hexene 4050-45-7 9.100E-f-09 64.740 9247 C6H15N3 N-aminoethyl piperazine 140-31-8 1.106E+10 84.330... [Pg.653]

See other pages where Aminoethyl piperazine is mentioned: [Pg.10]    [Pg.88]    [Pg.127]    [Pg.1049]    [Pg.1055]    [Pg.40]    [Pg.67]    [Pg.95]    [Pg.160]    [Pg.186]    [Pg.144]    [Pg.493]    [Pg.257]    [Pg.260]    [Pg.10]    [Pg.96]    [Pg.379]    [Pg.385]    [Pg.96]    [Pg.116]    [Pg.238]    [Pg.307]    [Pg.400]    [Pg.403]    [Pg.405]    [Pg.408]    [Pg.104]    [Pg.502]    [Pg.30]    [Pg.133]    [Pg.226]    [Pg.336]    [Pg.611]    [Pg.714]    [Pg.1721]   
See also in sourсe #XX -- [ Pg.114 ]

See also in sourсe #XX -- [ Pg.354 ]



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Aminoethylation

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Piperazin

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