Distilled water

Water (distilled) 100° Non-inflammable To be used whenever suitable. ... 

Reflux 1 ml. of the ether with 5 ml. of freshly distilled, constant boiling point hydriodic acid (Section 11,49,2), b.p. 126-128°, for 2-3 hours. Add 10 ml. of water, distil and collect about 7 ml. of liquid. Decolourise the distillate by the addition of a httle sodium bisulphite, and separate the two layers by means of a dropper pipette (Fig. 11,27,1). Determine the b.p. of the resulting iodide by the Siwoloboff method (Section 11,12) and prepare a crystalline derivative (Section 111,42). 

Into a 750 ml. round-bottomed flask furnished with a reflux condenser place a solution of 34 g. (18-5 ml.) of concentrated sulphuric acid in 100 ml, of water add 33 g. of di-n-butyl cyanamide and a few fragments of porous porcelain. Reflux gently for 6 hours. Cool the resulting homogeneous solution and pour in a cold solution of 52 g. of sodium hydroxide in 95 ml. of water down the side of the flask so that most of it settles at the bottom without mixing with the solution in the flask. Connect the flask with a condenser for downward distillation and shake it to mix the two layers the free amine separates. Heat the flask when the amine with some water distils continue the distillation until no amine separates from a test portion of the distillate. Estimate the weight of water in the distillate anp add about half this amount of potassium hydroxide in the form of sticks, so that it dissolves slowly. 

Place 5 g. of lard (or any fat or fatty oil), 3 g. of potassium hydroxide and 40 ml. of alcohol in a 250 ml. round-bottomed flask, attach a reflux condenser, and boil for about 30 minutes. The reaction is complete when no globules of oil are present when a few drops of the mixture are mixed with a little water. Distil the reaction mixture (Fig. II, 13, 3) and recover the alcohol dissolve the residue in 75 ml. of hot water. C arry out the following experiments with the resulting solution —... 

The following is a modification of the process described and gives quite satisfactory results. Wash the crude mixture of benzonitrile and dibromopentane with sodium carbonate solution until the latter remains alkaline, and then with water. Distil it under reduced pressure and collect the fraction boiling up to 120°/18 mm. Dissolve this in twice its volume of light petroleum, b.p. 40-60°, which has previously been shaken with small volumes of concentrated sulphuric acid until the acid remains colourless. Shake the solution with 6 per cent, of its volume of concentrated sulphuric acid, allow to settle, and run ofi the sulphuric acid layer repeat the extraction until the acid is colourless or almost colourless. Wash successively with water, sodium carbonate solution and water, dry over anhydrous calcium chloride or calcium sulphate, and distil off the solvent. Distil the residue under diminished pressure and collect the 1 6-dibromopentane at 98- 100°/13 mm. 

Water. Distilled water must be (a) redistilled in an all-Pyrex glass apparatus or (b) purified by passage through a column of cation exchange resin in the sodium form. For storage, polyethylene bottles are most satisfactory, particularly for very dilute (0.00 lAf) EDTA solutions. 

Pommade. These are botanical extracts prepared by the enfleurage method wherein flower petals are placed on a layer of fat which extracts the essential oil. This method is appHed to low odored flowers, which do not yield appreciable oil on steam or water distillation, or flowers of valuable but dehcate odor (such as jasmin), which are destroyed on such treatment. Pommades, as such, are seldom used by the industry at present (ca 1995), but are further processed to provide more concentrated extracts such as absolutes. Absolutes, being alcohol-soluble, are much more convenient forms for the perfumer. 

Wintergreen Oil. Water distillation of the leaves of Gaultheriaprocumbens L. yields an oil which consists of essentially one chemical constituent, methyl saUcylate. Because of this, the oil has been almost totally replaced by the synthetic chemical. Natural oil of wintergreen [68917-75-9] is a pale yellow to pinkish colored mobile Hquid of intensely sweet-aromatic odor and flavor. The oil or its synthetic replacement find extensive use in pharmaceutical preparations, candy, toothpaste, industrial products, and in rootbeer flavor. In perfumery, it is used in fougnre or forest-type fragrances. 

RGA Example In order to illustrate use of the RGA method, consider the following steady-state version of a transfer function model for a pilot-scale, methanol-water distillation column (Wood and Berry, Terminal Composition Control of a Binaiy Distillation Column, Chem. Eng. Sci, 28, 1707, 1973) Ku = 12.8, K = -18.9, K. i = 6.6, and Koo = —19.4. It follows that A = 2 and... 

In this study in order to eompare the green and yellow leaves of plant they were separately eolleeted and their essential oils were extraeted by water-distillation method and analyzed by GC and GC/MS. The main eonstituents were separated and analyzed by TLC, IR, NMR and UV methods. 

Water-filled motors These arc initially filled with clean water. Distilled water was originally used as an initial filler, but with the passage of time, clean w atcr was found to be a better substitute and now only clean water is used as an initial filler. 

Cyclohexanol [108-93-0] M 100.2, m 25.2", b 161.1", d 0.946, n 1.466, n s 1.437, n 1.462. Refluxed with freshly ignited CaO, or dried with Na2C03, then fractionally distd. Redistd from Na. Further purified by fractional crystn from the melt in dry air. Peroxides and aldehydes can be removed by prior washing with ferrous sulfate and water, followed by distillation under nitrogen from 2,4-dinitrophenylhydrazine, using a short fractionating column water distils as the azeotrope. Dry cyclohexanol is very hygroscopic. 

Fractionally crystd from its melt or from water. Distils in vacuo. 

Isoquinuclidone A 5-g portion of cis- and rra/ij-4-aminocyclohexanecarboxylic acid is mixed with 30 ml of Dowtherm At and heated rapidly to reflux in a flask fitted with a short distilling column. Water distils during the heating, which is continued for about 20 minutes. At this time, the mixture is homogeneous. The cooled solution is... 

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