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Ammonium lactate is a compound with formula NH 4 (C 2 H 4 (OH)COO). It is the ammonium salt of lactic acid. It has mild anti-bacterial properties. It has E number "E328" and is the active ingredient of the skin lotions Amlactin and Lac-Hydrin. [1] Ammonium lactate is the chemical combination of lactic acid and ammonium hydroxide.
The combination of urea and ammonium nitrate has an extremely low critical relative humidity (18% at 30 °C) and can therefore only be used in liquid fertilizers. The most commonly used grade of these fertilizer solutions is UAN 32.0.0 (32%N) known as UN32 or UN-32, which consists of 45% ammonium nitrate , 35% urea and only 20% water.
The structure of the molecule of urea is O=C(−NH 2) 2.The urea molecule is planar when in a solid crystal because of sp 2 hybridization of the N orbitals. [8] [9] It is non-planar with C 2 symmetry when in the gas phase [10] or in aqueous solution, [9] with C–N–H and H–N–H bond angles that are intermediate between the trigonal planar angle of 120° and the tetrahedral angle of 109.5°.
Ammonia solution, also known as ammonia water, ammonium hydroxide, ammoniacal liquor, ammonia liquor, aqua ammonia, aqueous ammonia, or (inaccurately) ammonia, is a solution of ammonia in water. It can be denoted by the symbols NH 3 (aq). Although the name ammonium hydroxide suggests a salt with the composition [NH + 4][OH −
DEF is a 32.5% solution of urea, (NH 2) 2 CO. When it is injected into the hot exhaust gas stream, the water evaporates and the urea thermally decomposes [13] to form ammonia (NH 3) and isocyanic acid (HNCO): (NH 2) 2 CO → NH 3 + HNCO. The isocyanic acid reacts with the water vapor and hydrolyses to carbon dioxide and ammonia: HNCO + H 2 O ...
ATC code B05 Blood substitutes and perfusion solutions is a therapeutic subgroup of the Anatomical Therapeutic Chemical Classification System, a system of alphanumeric codes developed by the World Health Organization (WHO) for the classification of drugs and other medical products.
An additional proof of the chemical transformation is obtained by adding a solution of oxalic acid which forms urea oxalate as a white precipitate. [3] Alternatively the reaction can be carried out with lead cyanate and ammonia. [4] The actual reaction taking place is a double displacement reaction to form ammonium cyanate:
The first pentavalent antimonial, urea stibamine, was synthesised by the Indian scientist Upendranath Brahmachari in 1922. Though it caused a dramatic decline in deaths due to leishmaniasis, it fell out of favour in the 1950s due to higher toxicity compared to sodium stibogluconate.
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