Acetate ammonium

Ammonia causes intense irritation of eyes, nose and respiratory tract which can lead to tears, respiratory distress, chest pain, and pulmonary edema. A few minutes exposure to 3,000 ppm can cause severe blistering of skin, lung edema, and asphyxia which can lead to death (Patnaik, P. 1992. A Comprehensive Guide to the Hazardous Properties of Chemical Substances, p. 304. New York, Van Nostrand Reinhold). Contact with liquid ammonia can cause serious blistering and destruction of skin tissues. LC50 inhalation (mouse) 4,200 ppm/hr. 

Fire or explosion hazard may arise from the foUowing ammonia reactions Reaction with halogens produces nitrogen trihahdes which explode on heating its mixture with fluorine bursts into flame reacts with gold, silver, or mercury to form unstable fulminate-type shock-sensitive compounds similarly, shock-sensitive nitrides are formed when ammonia reacts with sulfur or certain metal chlorides, such as mercuric, or silver chloride liquid ammonia reacts violently with alkah metal chlorates and ferricyanides. 

Ammonium acetate is used for preserving meats as a mordant in the dyeing of wool in analytical chemistry for standardization of electrodes, and in titra- 

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Fig. XI-14. Effect of hydrocarbon chain length on the f potential of quartz in solutions of alkylammonium acetates and in solutions of ammonium acetate. (From Ref. 183.)...

Pashley R M, McGuiggan P M, Ninham B W, Brady J and Evans D F 1986 Direct measurements of surface forces between bilayers of double-chained quaternary ammonium acetate and bromide surfactants J. Phys. Chem. 90 1637-42... 

Dehydration of the corresponding ammonium salt. Thus ammonium acetate on heating loses water giving acetamide. An excess of acetic acid is... 

Ammonium acetate CH3COONH4 Acetamide CH CONHj Acetonitrile CH CN Phthalimide C,H,(CO),NU Acetanilide C H,NHCOCH,... 

An excess of acetic acid is usually added before heating in order to repress the hydrolysis (and also the thermal dissociation) of the ammonium acetate, thus preventing the escape of ammonia. The excess of acetic acid, together with the water, is removed by slow fractional distillation. The method is rarely used except for the preparation of acetamide. 

ACETAMIDE (from Ammonium Acetate or from Acetic Acid)... 

Ammonium acetate method. Place 77 g. of ammonium acetate and 84 g. (80 ml.) of glacial acetic acid in a 250 ml. round bottomed flask (1)... 

The formation of ethyl isopropylidene cyanoacetate is an example of the Knoevenagel reaction (see Discussion before Section IV,123). With higher ketones a mixture of ammonium acetate and acetic acid is an effective catalyst the water formed is removed by azeotropic distillation with benzene. The essential step in the reaction with aqueous potassium cyanide is the addition of the cyanide ion to the p-end of the ap-double bond ... 

The versatility of this reaction is quite apparent. One can use ammonium acetate to make MDA or amphetamine, or methylamine in methanol for MDMA. But methylamine is optimal because it gives higher yield and less byproducts. Also, if ammonium acetate is used, one must use either ammonia (NH3) or a primary amine (any of one s choosing. Strike supposes) in place of the triethyla-mine in the reaction. 

In articles like this one, the scientists don t have the time nor the space to write out the details and amounts of reactants used for every single substrate they tried things on. So they pick just a few of the precursors they tried and use their numbers as an example of how the reaction typically goes. All one does is just substitute an equal amount of their favorite phenylacetone for the one in the example while keeping everything else the same. This will not be too big of a stretch of the old imagination with the first example below. The example ketone is just phenylbutanone. One little carbon more than phenylacetone, but a methyl ketone nonetheless (don t ask). They react exactly the same. As it so happens this first example is also the one using ammonium acetate to make MDA. Sweet ... 

Anyway, with catalyst in hand it is time to proceed with the reductive amination [56]. As far as Strike can see, this method will not work well in making MDA. It will not use ammonium acetate in the same way as NaBHaCN. So one is stuck with making MDMA or meth using this method. And without further ado, here s your recipe ... 

This procedure has been performed in a variety of ways [28 p714, 38-42] with variations in solvent, base and time of reaction. For piperonal conversion, the consensus is toward the use of acetic acid as the solvent, ammonium acetate as the base and 4 hours of reflux time. Dr. Alexander Shulgin, a giant in this field, prefers the use of cyclohexylamine as the base. Strike would not tend to doubt this man s choice, especially since Strike is also getting the... 

In a flask the chemist mixes 50g piperonal into 200mL glacial acetic acid, then adds 45mL nitroethane and 17g ammonium acetate. The solution is then refluxed 4 hours and takes on the color of yellow to yellow-orange. After 4 hours and cooling, yellowish crystals of p-nitropropene will spontaneously form. If not, the solution can be diluted with 50ml of dHjO and chilled in an ice bath for an hour to form the crystals with some slushy glacial acetic acid and water intermixed. The mass of crystals is broken up and plopped into a Buchner funnel to be vacuum filtered. The filter cake is washed with a little extra acetic acid or water. All of the filtrate is saved. 

It has been shown that by doubling the amount of nitroethane respective to that of the aldehyde in a ratio of 2 to 1, then the amount of ammonium acetate used can be reduced considerably [28 p703J. 

An interesting new synthesis of 2,4,5-trisubstituted and 2,4-disubstituted alkylthiazoles has been reported by Dubs (807). Heating the easily obtainable derivatives (276) with ammonium acetate in acetic acid gives thiazoles (10), Rj, Rj = alkyl and R3 = H or alkyl in good yields (Scheme 143). 

Likewise the experimentally measured pattern of carbon-oxygen bond lengths m acetic acid is different from that of acetate ion Acetic acid has a short C=0 and a long C—O distance In ammonium acetate though both carbon-oxygen distances are equal... 

Even high-quality ammonium acetate contains a significant amount of iron. Why is this source of iron not a problem ... 

Since all samples and standards are prepared using the same volume of ammonium acetate buffer, the contribution of this source of iron is accounted for by the calibration curve s reagent blank. 

After being formed as a spray, many of the droplets contain some excess positive (or negative) electric charge. Solvent (S) evaporates from the droplets to form smaller ones until, eventually, ions (MH+, SH+) from the sample M and solvent begins to evaporate to leave even smaller drops and clusters (S H+ n = I, 2, 3, etc,). Later, collisions between ions and molecules (Cl) leave [M + H]" ions, which proceed on into the mass analyzer. Ion yield can be enhanced by including a volatile ionic compound (e.g., ammonium acetate) in the initial solution before it reaches the spraying zone. 

Most commercial routes for the production of acetamide involve dehydration of ammonium acetate [631 -31 -8] ... 

The covalent character of mercury compounds and the corresponding abiUty to complex with various organic compounds explains the unusually wide solubihty characteristics. Mercury compounds are soluble in alcohols, ethyl ether, benzene, and other organic solvents. Moreover, small amounts of chemicals such as amines, ammonia (qv), and ammonium acetate can have a profound solubilizing effect (see COORDINATION COMPOUNDS). The solubihty of mercury and a wide variety of mercury salts and complexes in water and aqueous electrolyte solutions has been well outlined (5). 

Both normal or neutral ammonium acetate [631-61-8], NH4C2H2O2, and the acid salt are known. The normal salt results from exact neutralization of acetic acid using ammonia the acid salt is composed of the neutral salt and acetic acid. 

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