Di n butylamine

Into a 750 ml. round-bottomed flask furnished with a reflux condenser place a solution of 34 g. (18-5 ml.) of concentrated sulphuric acid in 100 ml. of water add 33 g. of di-n-butyl cyanamide and a few fragments of porous porcelain. Reflux gently for 6 hours. Cool the resulting homogeneous solution and pour in a cold solution of 52 g. of sodium hydroxide in 95 ml. of water down the side of the flask so that most of it settles at the bottom without mixing with the solution in the flask. Connect the flask with a condenser for downward distillation and shake it to mix the two layers the free amine separates. Heat the flask when the amine with some water distils continue the distillation until no amine separates from a test portion of the distillate. Estimate the weight of water in the distillate anp add about half this amount of potassium hydroxide in the form of sticks, so that it dissolves slowly. 

Cool the solution in ice while the alkali hydroxide is dissolving some ammonia gas is evolved. When the potassium hydroxide has dissolved, separate the amine, and dry it for 24 hours over sodium hydroxide pellets. Filter into a Claisen flask and distil. Collect the di-n-butylamine at 157-160°. The yield is 31 g. 

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Chemical Reactivity - Reactivity with Water No reaction Reactivity with Common Materials No reactions Stability During Transport Stable Neutralizing Agents for Acids and Caustics Not pertinent Polymerization Polymerization is accelerated by heat and exposure to oxygen, as well as the presence of contamination such as iron rust. Iron surfaces should be treated with an appropriate reducing agent such as sodium nitrate, before being placed into isoprene service Inhibitor of Polymerization Tertiary butyl catechol (0.06 %). Di-n-butylamine, phenyl-beta-naphthylamine andphenyl-alpha-naphthylamine are also recommended. 

The reaction was carried out at 100°C for about two hours until the theoretical isocyanate content, as determined by the di-n-butylamine titration method (27), was reached. The PU prepolymer with or without tertiary amine nitrogen groups was dissolved in dry MEK to obtain a prepolymer solution of 30-40% solids. It was then mixed with a mixture of 1,4-BD/TMP (4 1 by equiv. ratio) at an NCO/OH = 1.05/1.0 ratio in the presence of T-12 catalyst (0.05% based on total weight). The reaction mixture was cast in a metal mold treated with a release agent at ambient temperature. After standing 3-5 hours at room temperature, the mold was placed in an oven and post-cured at 100°C for 16 hours. The samples were then conditioned in a desiccator for one week before testing. 

The deoxygenative ring expansion of nitrobenzene with tri-n-butylphosphine in butanol (77BCJ2013), or with phosphorus trichloride and di-n-butylamine in hexane, followed by catalytic reduction and hydrolysis of the resulting 2-butoxy- or 2-butylamino-3//-azepines have been patented as methods for the production of caprolactam (78JAP(K)78132586, 77GEP2647936 respectively). 

Dibenzoyl Peroxide Diisobutyl Ketone Ethylene Dibromide Ethylene Dibromide Di-N-Butylamine Di-N-Butylamine... 

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