In such cases, Thiamine pyrophosphate acts as a co-factor.
The normal ortho-phosphate, Pb3(P04)2, is a white precipitate obtained by adding sodium phosphate to lead acetate; the acid phosphate, PbHPO 4, is produced by precipitating a boiling solution of lead nitrate with phosphoric acid; the pyrophosphate and meta-phosphate are similar white precipitates.
Other precipitants of phosphoric acid or its salts in solution are: ammonium molybdate in nitric acid, which gives on heating a canary-yellow precipitate of ammonium phosphomolybdate, 12[M00 3] (NH 4) 3 PO 4, insoluble in acids but readily soluble in ammonia; magnesium chloride, ammonium chloride and ammonia, which give on standing in a warm place a white crystalline precipitate of magnesium ammonium phosphate, Mg(NH 4)PO 4.6H 2 0, which is soluble in acids but highly insoluble in ammonia solutions, and on heating to redness gives magnesium pyrophosphate, Mg 2 P 2 0 7; uranic nitrate and ferric chloride, which give a yellowish-white precipitate, soluble in hydrochloric acid and ammonia, but insoluble in acetic acid; mercurous nitrate which gives a white precipitate, soluble in nitric acid, and bismuth nitrate which gives a white precipitate, insoluble in nitric acid.
Crystals may be obtained by heating di-calcium pyrophosphate, Ca2P207, with water under pressure.
When heated to 100° C., it loses five molecules of water of crystallization, and at a higher temperature loses the remainder of the water and also ammonia, leaving a residue of magnesium pyrophosphate, Mg 2 P 2 0 7.