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Abstract
Se propone la síntesis del ácido β-mercaptoetilaminotriacético, HO2CCH2SC2H4N(CH2CO2H)2 (MET, H3A), en base a la reacción a fondo de cistamina, S2(C2H4NH2)2, con cloroacetato en medio alcalino, con rendimiento (70%) superior al descrito para la condensación de cisteamina (HSC2H4NH2) con cloroacetato (42%). Se discute la estructura más probable de las especies de MET en disolución a partir de los valores de pKa (1.93, 2.27, 3.52 y 9.05, para. I=0.1 M (KN03) y 25cº) y datos de (1H)-RMN. Los espectros IR y datos de análisis térmico (TG,ATD) informan del ordenamiento estructural de MET.H20 y MET.HC1.H20 en estado sólido.
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