AC-11590 - 3-dimethylaminopropylamine-99 | 109-55-7
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N,N-Dimethyl-1,3-propanediamine, 99%
CAS:<p>Useful for cleavage of N-alkylphthalimide derivatives to give primary amines, as an alternative to methyl hydrazine. DMAPA is also used directly as a hardener in epoxy resins in the plastics industry, as a cross linking agent for cellulose fibers in the paper industry and as an anti-shriking agent f</p>Formula:C5H14N2Purity:99%Color and Shape:Liquid, Clear colorless to pale yellowMolecular weight:102.183-(Dimethylamino)-1-propylamine
CAS:Controlled ProductFormula:C5H14N2Color and Shape:NeatMolecular weight:102.18N,N-Dimethyl-1,3-propylenediamine
CAS:Controlled Product<p>Applications N,N-Dimethyl-1,3-propylenediamine is a useful catalyst for Knoevenagel condensation. It is also a useful hardening agent for expoxy resin.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Li, G. et al.: Green Chem., 13, 1828 (2011); Kroupa, J. et al.: Cgem. Prum., 26, 477 (1976); Caldwell, J. et al.: Polym. Preprints, 8, 687 (1967);<br></p>Formula:C5H14N2Color and Shape:ColourlessMolecular weight:102.18N,N-Dimethyl-1,3-propanediamine
CAS:Formula:C5H14N2Purity:>99.0%(GC)(T)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:102.18N,N-Dimethyl-1,3-propanediamine
CAS:N,N-Dimethyl-1,3-propanediaminePurity:98%Color and Shape:Colourless LiquidMolecular weight:102.18g/mol3-(Dimethylamino)-1-propylamine
CAS:Formula:C5H14N2Purity:98.0%Color and Shape:Colourless liquidMolecular weight:102.181(3-Dimethylamino)-1-propylamine
CAS:<p>3-Dimethylamino)-1-propylamine is a nitrogenous organic chemical compound. This molecule has been studied by surface methodology, which includes titration calorimetry and experimental solubility data. It is soluble in water and can be made stable with sodium salts or potassium dichromate. The optimum concentration of this compound is at 1 Molar, while the stability range is from 0.5 to 3 Molar concentrations. 3-Dimethylamino)-1-propylamine reacts as a nucleophile with an electrophile in the presence of an enzyme form to form a cyclic peptide. The mechanism for this reaction involves formation of a covalent bond between the amine group's lone electron pair and the electrophile's carbonyl carbon atom to form an imine intermediate that releases ammonia (NH3) on hydrolysis.</p>Formula:C5H14N2Purity:Min. 99 Area-%Color and Shape:Colorless Clear LiquidMolecular weight:102.18 g/mol









