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By H. Stephen and T. Stephen

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Additional resources for Binary Systems. Solubilities of Inorganic and Organic Compounds, Volume 1, Part 1

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4780 M 0 - 8 1588 K/l. % g/1 Continuation . 508 661, 662 661, 662 4 8? 0925 1/1. 87 562 Ba(JO,). ),, 20 a Anthracenesulfonate a Dimethyl amino a * >• CdtCMHuNaOaS), 20bensene-25 sulfonate H „ N . O ) ( C 1 0 ) , 20 Hexa»antipyrinecad~ C d ( C M 6 4 mium Perchlorate 20 a -antipyrinecadiun , C d ( C H N 0 ) . Cl) a 9 Unite Compound BaGe0 80 9 33 s e e Teble 773 i i1 Continuation Compound Formula KM. % Peroxydiaulfate BaS 0 0 • a Cnromate 0 9 3 a8 BaCr0 4 1842 20 t/1. 0 2118 BaI,-Hg(CN) 20 • 6,03 1772 Ba(Re0 ) 9 9 9 4 4 4a BaP0 F 3 BaaFefCNVeHjO 9 Iodide.

A 1-Naphthylamine -2,4,7-trisulfonate | a PCOWPW * Carboxypropanesulfonate a isobutyl Phosphate a Acetoneglycerophosphate v0 Methyladipate 8? a a a • a M I a £-Glycerophosphate Succinnate . a a . a . ^Glycerophosphate ^ P a P o a P a P p a „ Isopropyl Phosphate Glycerophosphate - a S? 27 I Reference No 270 00 m a 8? , a m 00 P o P a Methyl Hydrogenphoaphate a-Chlorocarbo* xyethenesulfonate a-Bromocarboxyethanesulfonate a-Carboxyethane#sulfonate # Phosphate AUyl B3 o a a P OO? 0406 1497 Ba(C H 0 ) 6 n 7a Ba(C H 0 Cl) 25 25 20 «/l.

G/1. 7. phenylhydroxy1 amine 20 25 t/1. 06 20 25 3 9/1. % 2088 s e e Table 915 2088 2088 0 . 0042 1302 1302 1546 t/1. 025 1548 • Chloride. Oxide Chloride. 5 459 Pb(I0 ) 25 g/i. 47 17721 Nitrate Pb(N0 ) 20 m Sulfide PbS Sulfate. Oxide Sulfate. Lead Nitrrte 1 X P b ( N 0 ) - 1 2 H 0 32 2 44 18 2 g/1. 7753 338 s e e T a b l e 4 932 8 . 6 - 1 0 - 4 12033 4 2 . 2 - 1 0 - 1450 6 . 8 . 63 see Table Name „ead Methanedisulfonate m Oxalate tt Maleate Unit! 77 376 Pb(C H. ClS0 ) 18 t/1. 0420 1497 Nitrosoy0-phenylhydoxyl amine Gluconate Cinnamate Pb(C H,N 0 ) 25 18 t/1.

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