Barium acetate citrate

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... 

An aqueous precursorfor 0.75Pb(Zni/3- Nb2/3)O3-0.25BaTiOs solid solution was synthesized by Van Werde et al. (2001). They used acetates of lead and zinc, and Nb(V) peroxocitrato complex. The solution of lead zincate niobate was prepared by adding the compounds into aqueous solution of ammonium citrate. The aqueous solution was stable when pH was higher than 8 and the citrate acid/cation mole ratio was higher than 1.5. The aqueous precursor for barium titanate was prepared by using titanium(IV) peroxocitrato complex and barium acetate. They found that the solid solution of PZN and BT is crystallized as a perovskite phase at temperatures as low as 800°C. 

Lynen, and Virtanen and Sundman have reported that in yeast, acetate is metabolized by way of the tricarboxylic cycle. Wieland and Rosenthal have also shown that kidney contains an enzyme system which can convert acetate or acetoacetate to citrate. Upon addition of oxalacetate along with either of these acids, the yield of citrate is significantly increased. In these experiments barium ions were added to inhibit further breakdown of the resulting citrate. These authors have proposed that oxalacetate and acetoacetate condense to form either acetyl citrate or citroyl acetate which are subsequently hydrolyzed to citrate and acetate. 

Cellulose acetate phthalate is incompatible with ferrous sulfate, ferric chloride, silver nitrate, sodium citrate, aluminum sulfate, calcium chloride, mercuric chloride, barium nitrate, basic lead acetate, and strong oxidizing agents such as strong alkalis and acids. 

Coprecipitation of yttrium, copper and barium is most often done with carboxy-lates (citrates, oxalates, acetates) from solutions of nitrates. Control of the pH, temperature and concentration make the precipitation as quantitative as possible in order to preserve the stoichiometry of the mixture [126-129]. Long-chain carboxy-lates (2-ethylhexanoate, neodecanoate) ensure the solubility of metals in volatile solvents such as xylene or xylene-pyridine mixtures, in order to make drying at... 

---