Is an aliphatic secondary amine widely used as an organic base in organic synthesis. Its standard molar enthalpy of formation and combustion has been measured by static-bomb calorimetry. May be used in the following syntheses: diisopropylamine methyl urea (DMU), N,N-diisopropyl quinoline-2-carboxamide, 3-N-sulfonylamidine coumarins, N-chloroamine, an intermediate to generate amides. Used as a precursor to prepare lithium diisopropylamide and sulfenamides, which are used in rubber vulcanization. It is also involved in the synthesis of N,N-Diisopropylethylamine (Hünig's base) obtained by alkylation with diethyl sulfate. Diisopropylammonium bromide is a bromide salt of DIPA used as an inert alternative to barium titanate. It is widely used as solvent as well as an intermediate in the the synthesis of pharmaceuticals, dyes, mineral flotation agents and emulsifiers.
(iso-C3H7)2NH; Bis(isopropyl)amine; Bis(methylethyl)amine; Diisopropylamin; Diisopropylamine; DIPA; N-(1-Methyethyl)-2-propanamine; N-(1-Methylethyl)-2-propamine; N-(1-Methylethyl)-2-propanamine; N,N-Diisoproplyamine; N-Isopropyl-1-amino-2-methylethane; N-Isopropylpropan-2-amine; N-Propan-2-ylpropan-2-amine; Beilstein/REAXYS Number: 605284; CAS Number: 108-18-9; EC Number: 203-558-5; MDL number: MFCD00008862; Molecular Formula: (CH3)2CHNHCH(CH3)2; Molecular Formula: C6H15N; Molecular Weight: 101.19;