Aluminum acetate chloride

Acetic acid, boric acid, benzalkonium chloride, aluminum acetate, benzethonium chloride—provide antifungal or antibacterial action... 

The aqueous oxidation of D-[l-14C]glucose and D-[6-14C]glucose at 100 °C afforded formic, acetic, and glycolic acids, and carbon dioxide. The last is mainly produced from C-2 to C-5, the formic acid from C-l, and the acetic acid from C-6.96 Addition of aluminum(III) chloride greatly increased the yield of carbon dioxide. Oxidation of D-glucose and D-fructose, studied with lsO-enriched oxygen, showed that they decompose via the C-l and C-2 hydroperoxides to give D-erythronic acid as the main product.76... 

Bauxite aluminum oxide (alumina, corundum, emery, ruby, sapphire) aluminum sulfate alum ammonium alum. Aluminum chloride aluminum acetate. Uses of aluminum compounds. 

AlCl j method) 1.18 g (8.87 mmol) of aluminum(lll) chloride arc added to a mixture of 0.60 g (2.26 mmol) of the acetal and 0.38 g (2.23 mmol) of 1-trimethylsilyloxycyclohexene in dry CH2C1, a1 —78 C under nitrogen. When TLC analysis indicates that the starting materials have been consumed (ca. 4 h), the reaction mixture is poured into 50 mL of water and given a normal CH2CL workup followed by flash chromatography to afford the cyclized product as one diastercomcr (55%). 

Aluminum Diacetate- Bisiaceto-0)hydroxyalumi-num hydroxybis(acetato)aluminum basic aluminum acetate aluminum subacetate aluminum hydroxyacetate Lenicet Casil. C4H7A Os mol wt 162.08. C 29.64%, H 4.36%. Al 16.64%, O 49.36%. AKOHXCHjCO j. Prepd from aluminum hydroxide and acetic acid or from sodium acetate and aluminum chloride hexahydrate Hood, Hide. J. Am. Cheat. Soc. 72, 2094 (1950). Other methods of prepn Gmelin s Aluminum (8th ed.) 35B, p 296 (1934). Also prepd in eq solution, see Aluminum Subacetate Solution. 

Acetyl chloride Acrylic acid Acrylonitrile Adipic acid Allyl alcohol Allyl chloride Alum Aluminum acetate Aluminum chloride, aqueous 90 32... 

Alkyl acetone Alkyl alcohol Alkyl benzene Alkyl chloride Alkyl sulfide Aluminum acetate Aluminum bromide Aluminum chlorate Aluminum chloride Aluminum ethylate Aluminum fluoride Aluminum fluorosilicate Aluminum formate Aluminum hydroxide Aluminum nitrate Aluminum oxalate Aluminum phosphate Aluminum sulfate Alum... 

Aluminum acetate Aluminum caprylate Aluminum distearate Aluminum myristates/palmitates Aluminum stearate Aluminum tristearate N-2-Aminoethyl-3-aminopropyl trimethoxysilane Aminoethylethanolamine Aminomethyl propanol Aminopropyltriethoxysilane Aminopropyltrimethoxysilane Ammonium benzoate Ammonium borate Ammonium citrate dibasic Ammonium laureth sulfate Ammonium laureth-5 sulfate Ammonium laureth-7 sulfate Ammonium laureth-12 sulfate Ammonium laureth-30 sulfate Ammonium lauryl sulfate Ammonium maleic anhydride/diisobutylene copolymer Ammonium oleate Ammonium persulfate Ammonium polyacrylate Ammonium potassium hydrogen phosphate Ammonium stearate Ammonium sulfamate Ammonium thiocyanate Ammonium thiosulfate Amyl acetate Antimony trioxide Asbestos Asphalt Azelaic acid 2,2 -Azobisisobutyronitrile Barium acetate Barium peroxide Barium sulfatej Bentonite Benzalkonium chloride Benzene Benzethonium chloride Benzothiazyl disulfide Benzoyl peroxide Benzyl alcohol Benzyl benzoate 1,3-Bis (2-benzothiazolylmercaptomethyl) urea 1,2-Bis (3,5-di-t-butyl-4-hydroxyhydrocinnamoyl) hydrazine 4,4 -Bis (a,a-dimethylbenzyl) diphenylamine Bisphenol A Bis (trichloromethyl) sulfone Boric acid 2-Bromo-2-nitropropane-1,3-diol 1,4-Butanediol Butoxydiglycol Butoxyethanol Butoxyethanol acetate n-Butyl acetate Butyl acetyl ricinoleate Butyl alcohol Butyl benzoate Butyl benzyl phthalate Butyidecyl phthalate Butylene glycol t-Butyl hydroperoxide... 

Acid blue 93 Aluminum acetate Aluminum chloride anhydrous Amyris (Amyris balsamifera) oil Basic blue 9 Basic green 1 Basic orange 2 Basic yellow 2 Bay (Pimenta acris) oil Benzethonium chloride... 

Myristalkonium chloride Nissan Cation M2-100 205-354-1 Aluminum acetate 205-355-7 Entarex Acid Hampshire NTA Acid Nitrilotriacetic acid SEQ NT-15 Trilon AS 205-358-3... 

Pitaro J, Mood Z, Daniel SJ. Ototoxicity of aluminum acetate/benzethonium chloride otic solution in the chinchilla animal model. Lar)mgo-scope2013 123(10) 2521-5. 

Aluminum Acetate Aluminum Chloride Ammonia (anhydrous) Ammonium Bicarbonate Ammonium Carbonate Ammonium Chloride Ammonium Hydroxide Ammonium Nitrate Ammonium Oxalate Ammonium Persulfate Ammonium Phosphate Ammonium Sulfide Amyl Acetate Arsenic Acid Azo Dyestuffs... 

Safaei-Ghomi et al. (2004) reported microwave enhanced Diels-Alder reactions of furan, 2,5-dimetylfiiran, 1,3-cyclohexadiene and anthracene with dimethyl acet-ylenedicarboxylate (DMAD) and diethyl acetylenedicarboxylate (DEAD) to give [4+2]-cycloadducts in high yields in domestic microwave oven. Aluminum (III) chloride and dichloromethane were used in combination with microwave irradiation for increasing the reaction rate. 

Hydrogen chloride Acetic anhydride, aluminum, 2-aminoethanol, ammonia, chlorosulfonic acid, ethylenediamine, fluorine, metal acetylides and carbides, oleum, perchloric acid, potassium permanganate, sodium, sulfuric acid... 

Acetic acid, fp 16.635°C ((1), bp 117.87°C at 101.3 kPa (2), is a clear, colorless Hquid. Water is the chief impurity in acetic acid although other materials such as acetaldehyde, acetic anhydride, formic acid, biacetyl, methyl acetate, ethyl acetoacetate, iron, and mercury are also sometimes found. Water significantly lowers the freezing point of glacial acetic acid as do acetic anhydride and methyl acetate (3). The presence of acetaldehyde [75-07-0] or formic acid [64-18-6] is commonly revealed by permanganate tests biacetyl [431-03-8] and iron are indicated by color. Ethyl acetoacetate [141-97-9] may cause slight color in acetic acid and is often mistaken for formic acid because it reduces mercuric chloride to calomel. Traces of mercury provoke catastrophic corrosion of aluminum metal, often employed in shipping the acid. 

Nearly all commercial acetylations are realized using acid catalysts. Catalytic acetylation of alcohols can be carried out using mineral acids, eg, perchloric acid [7601-90-3], phosphoric acid [7664-38-2], sulfuric acid [7664-93-9], benzenesulfonic acid [98-11-3], or methanesulfonic acid [75-75-2], as the catalyst. Certain acid-reacting ion-exchange resins may also be used, but these tend to decompose in hot acetic acid. Mordenite [12445-20-4], a decationized Y-zeohte, is a useful acetylation catalyst (28) and aluminum chloride [7446-70-0], catalyzes / -butanol [71-36-3] acetylation (29). 

The synthesis of 2,4-dihydroxyacetophenone [89-84-9] (21) by acylation reactions of resorcinol has been extensively studied. The reaction is performed using acetic anhydride (104), acetyl chloride (105), or acetic acid (106). The esterification of resorcinol by acetic anhydride followed by the isomerization of the diacetate intermediate has also been described in the presence of zinc chloride (107). Alkylation of resorcinol can be carried out using ethers (108), olefins (109), or alcohols (110). The catalysts which are generally used include sulfuric acid, phosphoric and polyphosphoric acids, acidic resins, or aluminum and iron derivatives. 2-Chlororesorcinol [6201-65-1] (22) is obtained by a sulfonation—chloration—desulfonation technique (111). 1,2,4-Trihydroxybenzene [533-73-3] (23) is obtained by hydroxylation of resorcinol using hydrogen peroxide (112) or peracids (113). 

Derivatives. Oxidation of pyrogaHol trimethyl ether with nitric acid, followed by reduction ia acetic anhydride and treatment of the product with aluminum chloride, affords 3,6-dihydroxy-2,4-dimethoxyacetophenone (228). 3,4,5-Trimethoxyphenol (antiarol) has been prepared by treatment of... 

Friedel-Crafts Acylation. The Friedel-Crafts acylation procedure is the most important method for preparing aromatic ketones and thein derivatives. Acetyl chloride (acetic anhydride) reacts with benzene ia the presence of aluminum chloride or acid catalysts to produce acetophenone [98-86-2], CgHgO (1-phenylethanone). Benzene can also be condensed with dicarboxyHc acid anhydrides to yield benzoyl derivatives of carboxyHc acids. These benzoyl derivatives are often used for constmcting polycycHc molecules (Haworth reaction). For example, benzene reacts with succinic anhydride ia the presence of aluminum chloride to produce P-benzoylpropionic acid [2051-95-8] which is converted iato a-tetralone [529-34-0] (30). 

Zinc chloride is a Lewis acid catalyst that promotes cellulose esterification. However, because of the large quantities required, this type of catalyst would be uneconomical for commercial use. Other compounds such as titanium alkoxides, eg, tetrabutoxytitanium (80), sulfate salts containing cadmium, aluminum, and ammonium ions (81), sulfamic acid, and ammonium sulfate (82) have been reported as catalysts for cellulose acetate production. In general, they require reaction temperatures above 50°C for complete esterification. Relatively small amounts (<0.5%) of sulfuric acid combined with phosphoric acid (83), sulfonic acids, eg, methanesulfonic, or alkyl phosphites (84) have been reported as good acetylation catalysts, especially at reaction temperatures above 90°C. 

With Acyl Halides, Hydrogen Halides, and Metallic Halides. Ethylene oxide reacts with acetyl chloride at slightly elevated temperatures in the presence of hydrogen chloride to give the acetate of ethylene chlorohydrin (70). Hydrogen haUdes react to form the corresponding halohydrins (71). Aqueous solutions of ethylene oxide and a metallic haUde can result in the precipitation of the metal hydroxide (72,73). The haUdes of aluminum, chromium, iron, thorium, and zinc in dilute solution react with ethylene oxide to form sols or gels of the metal oxide hydrates and ethylene halohydrin (74). 

Aminoisoxazoles are obtained by reduction of 4-nitroisoxazoles with amalgamated aluminum, tin(II) chloride and hydrochloric acid, or zinc dust and acetic acid (62HC(17)1, p. 73). 

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