First outlines of a dictionary of solubilities of chemical substances / by Frank H. Storer.
- Francis Humphreys Storer
- Date:
- 1864
Licence: Public Domain Mark
Credit: First outlines of a dictionary of solubilities of chemical substances / by Frank H. Storer. Source: Wellcome Collection.
Provider: This material has been provided by the National Library of Medicine (U.S.), through the Medical Heritage Library. The original may be consulted at the National Library of Medicine (U.S.)
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![Acetyl (of Gerhardt, &c). Not isolated. (Acetoxyl.) C4 1I3 0, AcetylAldehyde. Vid. Hydride of Acetyl. Acetylamin. Vid. Acetosamin. Acetylammonium (of Natanson). Vid. Ace- tosamin. Acetylammonium. Vid. Acetylide of Am- C4II7N02 monium. AcetylAnilin. Vid. PhenylAcetosamin. AcetylBenzoin. Insoluble in water. Read- er H14 08 = ^» u°21 o2 J1y soluble in alcohol, and 32 « • c4H362 j * ether> Warm alcohol dis- solves nearly twice its weight of this compound. (Zinin.) Acetylide of Ammonium. Miscible in all (AldehydeAmmonia.) proportions with water ; less C4H7N02=c*^3g2| soluble in alcohol. Very * sparingly soluble in ether. (Gerhardt.) Not at all soluble in ether. (Liebig) Decomposed by dilute acids, like acetic acid. AcETTLIDE OF AMMONIUM with NlTRATE OF 2C4H3(NH,)0,; AgO,N05 Silver. Very soluble in water. Sparingly sol- uble in alcohol. Acetylide of Potassium. Soluble in water. (Aldehydate of Potash.) 04 H3 K 02 Acetylide of Silver. Easily soluble in wa- (Aldehydate of Silver.) ter. Sparingly soluble in b4H3 Ag02 alcohol. Acetylium. Vid. Acetosamin. TkraAcETYLiUM. Vid. tetraVinylium. AcetylMercaptan. Vid. Hydride of Sulph- Acetyl. AcetylMethyl. Vid. Acetone. AcetylNitroPhloretic Acid. Sparingly C22 Hu N 0n = C18 H7 (N 04) (C4 H3 02) 06> H O soluble in wa- ter. Soluble in alcohol, (v. Gilm.) AcetylPhloretic Acid. Sparingly soluble C22H1208 = C18H8(C4H302)05,HO in cold, easily soluble in boil- ing water. Easily soluble in ether, (v. Gilm.) AcetylSalicylic Acid. Insoluble in cold, C18H808 somewhat soluble in boiling water. Ea- sily soluble in alcohol, and ether, (v. Gilm.) AcettlSulphide of X. Vid. ThiAcetate of X. AcetylUrea. [See also MethylUrea.] More c C2 02 readily soluble in hot than Ce He N2 °i = N2 \ C. H3 02 jn com water, and al- 3 cohol. (Moldenhauer.) Very sparingly soluble in cold water. Soluble in 100 pts. of cold alcohol. Soluble in 10 pts. of boiling alcohol. Much more soluble in boiling water than in boiling alcohol. Insoluble in ether. (Zinin.) Achilleic Acid. Soluble in 2 pts. of water (Perhaps identical with Malic Acid. (Gmelin.) at 12.5°. (Zanon.) Achilleate of Ammonia. Very soluble in water. Insoluble in alcohol. Achilleate of Lead. Ppt. Achilleate of Lime* Insoluble in alcohol. Achilleate of Magnesia. Soluble in water. Achilleate of Potash. Permanent. Very soluble in water. Sparingly soluble in alcohol. Achilleate of Quinine. Easily soluble in water, and alcohol. Achilleate of Soda. Very soluble in water. Sparingly soluble in alcohol. AchIllein. (From Achillea millefolium.) Hy- groscopic. Easily soluble in water, and in boiling alcohol. Insoluble in ether, but soluble in acidu- lated ether. Also soluble in ammonia-water. (Za- non.) Acichloride. ) Names proposed by Berzelius Acisulphide. ) for compounds of an acid and chloride, or sulphide. (See Berzelius's Juhresbe- richt, 20. (2. Abth.) p. 478.) AconitAnilic Acid. Vid. PhenylAconitamic Acid. AconitAnilid. Soluble in cold alcohol. C48 H21N3 06 (?) Partially soluble in ammonia-wa- ter. (Pebal.) Aconitic Acid. Permanent. Soluble in 3 (Citridic Acid. Er/uisctic pts. of water at 15°, and Acid. Achilleic Add.) in a smaner quantity of c12n6o12 = c12u3o9,<mu hotwater (Baup.) Very readily soluble in water, either hot or cold, being much more soluble than its isomer fumaric acid. (Buchner.) Soluble in 2 pts. of alcohol, of 88% at 12°. (Baup.) Readily soluble in alcohol, and ether. (Crasso.) Most of the normal aconitates are easily soluble in water. ACONITATE OF AMMONIA. a ■= tri, or normal. Readily soluble in water ; but the solution loses ammonia when exposed to the air. 6 = mono. Soluble in 6.5 pts. water at 15°; CuHgCNH^Ou more soluble in hot water. (Baup, Ann. Ch.et Phys., (3.) 30. 322.) c = acid. More soluble than the monobasic C12 H3 (N H4) 3 012; C12 H0 0^ salt, but is decomposed, with separation of the latter, as soon as it dissolves. (Baup, loc. cit., p. 321.) Aconitate of Baryta. Scarcely at all solu- C^H3Ba30^ + 6Aq ble in water. Soluble in an aqueous solution of aconitic acid. (Buchner.) By precipitating equisetic acid Regnault obtained a gelatinous baryta salt solu- ble in 9 pts. of water at 20°. Aconitate of Copper. Somewhat soluble in water. Aconitate of Ethyl. Soluble in an alco- C2iH18012 = C12H3(C4H5)3012 holic solution of chlor- hydric acid, from which it separates on the addition of water. (Crasso.) Aconitate of peroxide of Iron. Ppt. Aconitate of Lead. Very sparingly soluble C12H3Pb30]2-|-3Aq in boiling water. (Buchner.) Aconitate of Lime. At first it is soluble in CuHjjCajO^ + eAq water, but after having crystal- lized it is but slowly soluble. Soluble in 98 f© 99 pts. water at 15°. Soluble in dilute nitric acid. (Baup, Ann. Ch. et Phys., (3.) 30. 323.) Aconitate of Magnesia. Very soluble in water. Aconitate of Manganese. ' Permanent. Cnn3Mn30a +12Aq Sparingly soluble in cold, more readily soluble in hot water. Partially decomposed by boiling water. (Baup, Ann. Ch. et Phys., (3.) 30. 323.)](https://iiif.wellcomecollection.org/image/b21157091_0029.jp2/full/800%2C/0/default.jpg)