1,3-Diaminopropane, 98%, Thermo Scientific Chemicals

General References:

1. The potassium derivative (KAPA) is a very strong base, valuable for its ability to cause the migration of acetylenic unsaturation to the terminal positions of alkynes (known as the zip reaction). In the presence of excess amine, reaction occurs within seconds; the driving force is the formation of a stable acetylide anion: J. Am. Chem. Soc., 97, 891 (1975). For example, with acetylenic carbinols: J. Chem. Soc., Chem. Commun., 959 (1976); Tetrahedron Lett., 2565 (1976); Can. J. Chem., 62, 1333 (1984). For a further example (2- to 9-decynol), using a combination of Potassium tert-butoxide, A13947, and Li 3-aminopropanamide, see: Org. Synth. Coll., 8, 146 (1993). This technique avoids the use of KH. For the use of KAPA for the isomerization of ß-pinene to the thermodynamically-more stable ɑ-pinene, see: Org. Synth. Coll., 8, 553 (1993).
2. For procedures for the generation of Na or K 3-amino-propylamides from the metals by ultrasound irradiation or in the presence of Fe(NO₃)₃, see: J. Org. Chem., 49, 2494 (1984).
3. Bag, P.; Ghosh, A. B.; Dutta, A. K.; Flörke, U.; Nag, K. Sandwich-type lanthanide(III) complexes of a tetraiminodiphenol macrocyclic ligand derived from 4-methyl-2,6-diformylphenol and 1,3-diaminopropane: structure, NMR and luminescence. Polyhedron 2015, 102, 539-548.
4. Liang, K. L.; Lin, Y. F.; Leron, R. B.; Li, M. H. Molar heat capacity of aqueous solutions of 1, 3-diaminopropane and 1, 4-diaminobutane and their piperazine blends. Thermochim. Acta 2015, 616, 42-48.