Chapter XIX: Front Matter (19)

=Mixture, Effervescing.= (P. Cod.) _Syn._ MISTURA EFFERVESCENS; POTION GAZEUSE DE RIVIÈRE. _Prep._ Dissolve 1/2 dr. of bicarbonate of potash in 2 oz. of water, and add 4 dr. of syrup. Mix also 1/2 dr. of citric acid with 1/3 oz. of syrup of citric acid and 2 oz. of water. Mix an equal quantity of each, and give it while effervescing.

=Mixture of Elaterium.= (Dr Ferriar.) _Syn._ MISTURA ELATERII. _Prep._ Elaterium, 1 gr.; spirit of nitric ether, 2 fl. oz.; tincture of squills, 1/2 oz.; oxymel of colchicum, 1/2 oz.; syrup of buckthorn, 1 fl. oz.——_Dose_, 1 dr. 3 times a day in water.

=Mixture, Emet′ic.= _Syn._ MISTURA EMETICA, L. _Prep._ 1. (Copland.) Sulphate of zinc, 40 gr.; ipecacuanha wine and tincture of serpentary, of each 4 fl. dr.; tincture of capsicum, 40 drops; oil of chamomile, 12 drops; peppermint water, 4-1/2 fl. oz. As an excitant emetic; in cases of poisoning by narcotics, &c.

2. (Magendie.) Coloured emetine, 4 gr. (or white emetine, 1 gr.); acetic acid, 8 drops; mix, and add of infusion of orange leaves or lime flowers, 3-1/2 fl. oz.; syrup of marshmallows, 1 fl. oz.

3. (A. T. Thomson.) Ipecacuanha, 1/2 dr.; tartar emetic, 1 gr.; tincture of squills, 1 fl. dr.; water, 6 fl. oz. _Dose_, 1 to 2 table-spoonfuls, followed by half the quantity every 10 or 15 minutes, until vomiting is produced; at the same time assisting the action of the medicine by drinking copiously of warm water.

=Mixture, Emmen′agogue.= See MIXTURE, STEEL, &c.

=Mixture, Expec′torant.= _Syn._ MISTURA EXPECTORANS, L. _Prep._ 1. (Collier.) Oxymel of squills and mucilage, of each 1 oz.; syrup of marshmallows, 2 oz.; camphor julep, 3 fl. oz.——_Dose_, 1 to 2 table-spoonfuls, 2 or 3 times a day; in coughs, hoarseness, asthma, &c.

2. (A. T. Thomson.) Almond mixture, 5 fl. oz.; ipecacuanha wine and tincture of squills, of each 1 fl. dr.; syrup of tolu, 6 fl. dr.——_Dose_, 1 table-spoonful; in humoral asthma, catarrh, &c., when the cough is urgent.

=Mixture, Feb′rifuge.= _Syn._ MISTURA FEBRIFUGA, L. See ACETATE OF AMMONIA MIXTURE, DIAPHORETIC M., &c.

=Mixture of Gentian.= (Ph. B.) _Syn._ MISTURA GENTIANÆ. _Prep._ Macerate gentian root, sliced, 1/4 oz.; bitter orange peel, cut small, and coriander fruit, bruised, of each 30 gr., in proof spirit, 2 fl. oz., for 2 hours. Add distilled water, 8 fl. oz.; macerate again for 2 hours, and strain through calico.——_Dose_, 1 oz.

=Mixture, Gentian (Compound).= Gentian, bruised, 1-1/2; bitter orange peel, bruised, 3/4; cardamom seeds, bruised, 1/4; proof spirit, 20: macerate for forty-eight hours with 15 of the spirit, agitating occasionally, pack in a percolator, let it drain, and then pour on the remaining spirit; when it ceases to drop, wash the marc with spirit to make up 20.——_Dose_, 1 to 2 drachms.

=Mixture, Gregory’s.= See POWDERS.

=Mixture, Griffith’s.= See MIXTURE, STEEL.

=Mixture, Guai′acum.= _Syn._ EMULSION OF GUAIACUM, MILI OF G.; MISTURA GUAIACI (B. P.), (Ph. L. & E.), LAC G., L. _Prep._ (Ph. L.) Gum guaiacum, 3 dr.; white sugar, 1/2 oz.; gum acacia, 2 dr. (all in powder); triturate together, and to these, whilst rubbing, gradually add of cinnamon water, 1 pint.

2. (Ph. E.) Guaiacum, 3 dr.; sugar, 1/2 oz.; mucilage, 1/2 fl. oz.; cinnamon water, 19-1/2 fl. oz.; as before.——_Dose_, 1 to 3 table-spoonfuls, 2 or 3 times a day; in chronic rheumatism, gout, &c.

3. (B. P.) Guaiac resin, in powder, 2; sugar, 2; gum Arabic, in powder, 1; cinnamon water, 80; triturate, adding the cinnamon water gradually.——_Dose_, 1/2 to 2 oz.

=Mixture, Gum.= _Syn._ MUCILAGE; MISTURA ACACIÆ (Ph. L.), MUCILAGO (Ph. E.), MUCILAGO ACACIÆ (Ph. D.), MUCILAGO ARABICI GUMMI, L. _Prep._ 1. (Ph. L.) Gum acacia (in powder), 13 oz.; boiling distilled water, 1 pint; rub the gum with the water, gradually poured in, until solution is complete.

2. (Ph. E.) Gum, 9 oz.; cold water, 1 pint; macerate, with occasional stirring, until dissolved, then strain through linen or calico.

3. (Ph. D.) Gum (coarsely powdered), 4 oz.; water (cold), 6 fl. oz.; dissolve, and strain through flannel.

_Uses, &c._ Mucilage of gum acacia is chiefly employed to render oily and resinous substances miscible with water. “Oils require about 3/4 their weight; balsams and spermaceti, equal parts; resins, 2 parts; and musk, 5 times its weight,” for this purpose. (Montgomery.) The GUM MIXTURE, Ph. E., will be found under ‘EMULSION,’

=Mixture of Hemidesmus.= (Mid. Hosp.) _Syn._ MISTURA HEMIDESMI. _Prep._ Bruised root of hemidesmus, 10 oz.; extract of liquorice, 10 gr.; distilled water, 10 oz. Digest for 12 hours, heat the strained liquor to 180° F., and strain again.——_Dose_, 1/3 part 3 times a day.

=Mixture of Hemlock, Compound.= (Guy’s Hosp.) _Syn._ MISTURA CONII COMPOSITA. _Prep._ Extract of hemlock, 1 dr.; carbonate of soda, 1-1/2 dr.; decoction of liquorice, 11 oz.; spirit of pimento, 6 dr.——_Dose_, 1 oz. to 2 oz. Myrrh mixture is sometimes substituted for decoction of liquorice.

=Mixture of Horseradish, Compound.= (Dr Paris.) _Syn._ MISTURA ARMORACIÆ COMPOSITA. _Prep._ Horseradish root, 1/2 oz.; mustard seed, 1/2 oz.; boiling water, 1 pint. Macerate for an hour, and to 7 oz. of the strained infusion add aromatic spirit of ammonia, 1 fl. dr.; spirit of pimento, 1/2 oz. In paralysis.

=Mixture, Hydrocyan′ic.= _Syn._ MIXTURE OF PRUSSIC ACID; MISTURA ACIDI HYDROCYANICI, L. _Prep._ From medicinal prussic acid, 15 drops; simple syrup (pure), 1 fl. oz.; distilled water, 5 fl. oz.;——_Dose_, 1 table-spoonful, 2 or 3 times daily. Each dose contains 1-1/4 drop of medicinal prussic acid. The bottle should be shaken before pouring out the dose. Magendie’s formulæ for this mixture are omitted, because the acid which he orders is not kept in the shops in England.

=Mixture of Iodine with Sarsaparilla.= (Magendie.) _Syn._ MISTURA IODINII CUM SARZA. _Prep._ Decoction of sarsaparilla, 1-1/2 pint; iodide of potassium, 1 dr.; syrup of orange, 2 oz.

=Mixture, I′ron.= See MIXTURE, STEEL.

=Mixture, I′ron (Compound).= See MIXTURE, STEEL.

=Mixture, Marshmallow.= _Syn._ MISTURA ALTHÆÆ (Ph. E.), L. _Prep._ (Ph. E.) Marshmallow root (dried), 4 oz.; stoned raisins, 2 oz.; water, 5 pints; boil to 3 pints, strain through linen, and after the sediment has subsided, decant the clear portion.

2. (Ph. D.) See DECOCTION. Demulcent.——_Dose._ A few spoonfuls _ad libitum_, so as to take 1 to 3 pints in the 24 hours; in strangury, calculus, coughs, fevers, &c.

=Mixture of Monesia.= (Neligan.) _Syn._ MISTURA MONESIÆ. _Prep._ Extract of monesia, 2 scruples; water, 7-1/2 oz.; compound tincture of cardamoms, 1/2{?} oz.

=Mixture of Musk.= (Ph. L.) _Syn._ MISTURA MOSCHI. _Prep._ Musk, 3 dr.; triturate it with white sugar, 3 dr.; gum acacia, 3 dr.; and gradually add rose water, 1 pint.——_Dose_, 1 to 2 oz.

=Mixture of Musk-seed.= (Dr Reece.) _Syn._ MISTURA ABELMOSCHI. _Prep._ Tincture of musk-seeds, 1 oz.; aromatic spirit of ammonia, 3 fl. dr.; compound spirit of lavender, 4 fl. dr.; camphor mixture, 6 oz.——_Dose_, 1/2 oz. to 1 oz.

=Mixture, Myrrh.= _Syn._ EMULSION OF MYRRH; MISTURA MYRRHÆ, L. _Prep._ (Copland.) Myrrh, 1-1/2 dr.; add to it gradually, triturating all the time, decoction of liquorice, 6 fl. oz., and strain.——_Dose_, 1 to 2 table-spoonfuls, twice or thrice a day, combined with carbonate of soda, dilute hydrochloric acid, or paregoric; in debility, and diseases of the digestive organs.

=Mixture, Narcot′ic.= _Syn._ MISTURA NARCOTICA, M. FEBRIFUGA, L. _Prep._ 1. Tincture of henbane, 2 fl. dr.; solution of acetate of ammonia, 3 fl. oz.; water, 2-3/4 fl. oz.; mix.——_Dose_, 1 to 2 table-spoonfuls, to relieve pain, procure sleep in fevers, &c.

2. (W. Cooley.) Laudanum, 1-1/2 fl. dr.; syrup of poppies, sulphuric ether, and spirit of cinnamon, of each 1 oz.; tincture of henbane, 2-1/2 fl. dr.; tincture of capsicum, 4 fl. dr.; water 2 fl. oz.——_Dose_, 1 to 2 table-spoonfuls, at the commencement of the hot fit of ague.

=Mixture, Oleo-balsam′ic.= _Syn._ MISTURA OLEO-BALSAMICA, L. _Prep._ (Hamb. Cod.) Oils of cedrat, cinnamon, cloves, lavender, mace, and marjoram, of each 20 drops; oil of rue, 10 drops; balsam of Peru, 1/2 dr.; rectified spirit, 10 oz.; digest and filter.

=Mixture of Oxalic Acid.= (Nardo.) _Syn._ MISTURA ACIDI OXALICI. _Prep._ Oxalic acid, 8 gr.; mucilage, 3 oz.; syrup, 1 oz. In inflammation, of the fauces and digestive tube.

=Mixture of Phosphorus.= (Soubeiran.) _Syn._ MISTURA PHOSPHORICI. _Prep._ Phosphorated oil, 2 dr.; powdered gum acacia, 2 dr.; peppermint water, 3 oz.; syrup, 2 oz. Mix the gum with 10 dr. of water, and thin with the oil, and gradually add the others. Contains 1 gr. of phosphorus.——_Dose_, 1/2 fl. oz.

=Mixture of Platinum Chloride.= (Hoeffer.) _Syn._ MISTURA PLATINI CHLORIDI. _Prep._ Perchloride of platinum, 1-1/2 gr.; gum juleps, 6 oz.

=Mixture of Potassium Iodide.= (Cazenave.) _Syn._ MISTURA POTASSII IODIDI. _Prep._ Iodide of potassium, 2 dr.; distilled water, 16 oz.; syrup, 2 fl. oz. 2 or 3 table-spoonfuls per diem.

=Mixture, Pur′gative.= _Syn._ MISTURA CATHARTICA, M. LAXATIVA, M. PURGANS. L. _Prep._ 1. From any of the purging salts (Epsom, Glauber, tasteless, &c.), 2 oz.; infusion of senna, 5 fl. oz.; syrup of orange peel, 1 fl. oz.; tincture of ginger, 1/2 fl. oz.; spirit of pimento, 2 fl. dr.; mix.——_Dose_, 1 to 3 table-spoonfuls, early in the morning; as an aperient in stomach complaints, &c.

2. (Dr Copland.) Manna, 1-1/2 oz.; cream of tartar, 1/2 oz.; whey, 1 quart. By wine-glassfuls, as an aperient drink, in fevers, &c.

3. (Corvisart.) Borotartrate of potassa (soluble tartar), 1 oz.; tartar emetic, 1/2 gr.; sugar, 2 oz.; water, 1-1/2 pint; dissolve. By wine-glassfuls, until it begins to operate. This has been called ‘NAPOLEON’S MEDICINE,’ from its having been frequently taken by Napoleon I. See MIXTURES OF SCAMMONY, SENNA, &c.

=Mixture of Quinine and Coffee.= _Syn._ MISTURA QUINIÆ ET CAFFEÆ; CAFÉ QUININE. Prepare 5 oz. of infusion from 4 dr. of ground coffee by percolation, and add 24 gr. of neutral sulphate of quinine and 4 dr. of sugar.——_Dose._ A tablespoonful. The coffee conceals the bitterness of the quinine.

=Mixture of Quinine with Iron.= _Syn._ MISTURA QUINIÆ CUM FERRO. Sulphate of quinine, 1 gr.; sulphate of iron, 2 gr.; dilute sulphuric acid, 5 minims; water, 1 oz. For 1 dose.

=Mixture of Rhubarb with Magnesia.= (St Thom. Hosp.) _Syn._ MISTURA RHEI CUM MAGNESIA. _Prep._ Rhubarb, 7-1/2 gr.; carbonate of magnesia, 15 gr.; peppermint water, 1-1/2 oz. For 1 dose.

=Mixture, Saline.= _Syn._ MISTURA SALINA, L. See DRAUGHT and LEMONADE.

=Mixture, Scam′mony.= _Syn._ SCAMMONY MILK; MISTURA SCAMMONII (B. P.), L. _Prep._ 1. (Ph. E.) Resin of scammony, 7 gr.; unskimmed milk, 3 fl. oz.: gradually mix, triturating all the time, so as to form an emulsion. Purgative.——_Dose._ One half.

2. (Planche’s PURGATIVE POTION.) To the last add of white sugar, 1/4 oz.; cherry-laurel (or bitter-almond) water, 4 or 5 drops. The above are the most tasteless and pleasant purgatives of an active character known.

3. (B. P.) Resin of scammony, 4 gr.; fresh milk, 2 oz.; triturate and form an emulsion.——_Dose._ The quantity of the formula for an adult, half for a child.

=Mixture, Senega, with Ammonia.= (St Th. H.) _Syn._ MISTURA SENEGÆ CUM AMMONIA. _Prep._ Infusion of senega, 1 oz.; carbonate of ammonia, 4 gr. For 1 dose.

=Mixture, Sen′na (Compound).= _Syn._ BLACK DRAUGHT, ABERNETHY’S D., CATHARTIC MIXTURE; MISTURA SENNÆ COMPOSITA (B. P.), L. _Prep._ 1. Infusion of senna, 3/4 pint; tincture of senna, 1-1/2 fl. oz.; Epsom salts, 4 oz.; carbonate of ammonia, 1/2 dr.; sugar, 3 oz.; agitate until the solids are dissolved.

2. Senna, 13 oz.; boiling water, 2 quarts; digest for 4 hours in a hot place, then press out the liquor in a tincture press, and add, of compound tincture of senna, 3/4 pint; Epsom salts, 1 lb.

3. East India senna, 2 lbs.; boiling water, 9 quarts; tincture of senna and Epsom salts, of each 3-1/4 lbs.; as the last.

4. Senna, 8 lbs.; boiling water, 9 galls.; Epsom salts, 16 lbs.; tincture of senna, 1-1/2 galls.; treacle and colouring, of each 1 quart.

5. (Guy’s Hosp.) Senna and mint, of each 1-1/4 oz. (say 1-1/2 oz.); boiling water, 1 quart; Epsom salts, 7-1/2 oz. (say 1/2 lb.).

6. (Redwood.) Infusion of senna, 18 oz.; tincture of senna, 3 oz.; sulphate of magnesia, 6 oz.; extract of liquorice and spirit of sal volatile, of each 3/4 oz.; oil of cloves, 6 drops.

7. (B. P.) Infusion of senna, 14; sulphate of magnesia, 4; extract of liquorice, 1/2; tincture of senna, 2-1/2; compound tincture of cardamoms, 1-1/4: dissolve and mix.——_Dose_, 1 to 1-1/2 oz.

_Obs._ As the above mixture contains very little spirit, and from its great consumption being made in large quantities at a time, it frequently spoils before the whole is sold especially in hot weather. To avoid this, 1-1/2 dr. of cloves, and 3 dr. of mustard seed, both bruised, may be added to every gall. of the strained liquor at the same time with the salts, spirit, and colouring, after which it must be shaken up repeatedly for a few days, and then allowed to repose for a few days more when it will become quite clear. It may be filtered through a flannel bag, but there is much loss and delay, owing to the consistence of the liquid. It is purgative in doses of 1 to 1-1/2 fl. oz.

It is a singular circumstance, that although an enormous quantity of this preparation is consumed in these countries, there is no standard formula for it in the British Pharmacopœias. See MIXTURE, APERIENT, &c.

=Mixture, Steel.= _Syn._ MISTURA FERRI COMPOSITA (B. P.), MISTURA CHALYBEATA, L. Two compounds of this class are officinal:——

1. (GRIFFITH’S MIXTURE, COMPOUND IRON M.; MISTURA FERRI, M. F. PROTOXYDI, M. F. COMPOSITA——Ph. L. E. & D.) _Prep._——_a._ (Ph. L. & E.) Carbonate of potassa, 1 dr.; powdered myrrh, 2 dr.; spirit of nutmeg, 1 fl. oz.; triturate together, and whilst rubbing, add gradually, of sugar, 2 dr.; rose water, 18 fl. oz.; mix well; then add of sulphate of iron (powdered), 50 gr.; and place it at once in a bottle, which must be kept closely corked.

_b._ (Ph. D.) Powdered myrrh and sugar, of each 1 dr.; carbonate of potassa, 1/2 dr.; essence of nutmeg, 1 fl. dr.; rose water, 7 fl. oz.; sulphate of iron, 1/2 dr.; (dissolved in) rose water, 1 fl. oz.;——_Dose_, 1 to 2 oz., 3 or 4 times a day, as a mild and genial chalybeate tonic and stimulant; in amenorrhœa, chlorosis, debility, &c., when there is no determination of blood to the head.

2. (HEBERDEN’S MIXTURE, H.’S INK; ATRAMENTUM HEBERDII; MISTURA FERRI AROMATICA——Ph. D.) Pale cinchona bark, 1 oz.; calumba root, 3 dr. (both in coarse powder;) cloves (bruised), 2 dr.; iron filings, 1/2 oz.; peppermint water, 16 fl. oz.; digest in a close vessel for 3 days, agitating frequently, then strain, and add of tincture of cardamoms (comp.), 3 fl. oz.; tincture of orange peel, 3 fl. dr. Bitter, stomachic, and aromatic.——_Dose_, 1 or 2 table-spoonfuls, or more, 3 or 4 times a day. It is very slightly chalybeated. See also MIXTURE, AROMATIC IRON.

3. Sulphate of iron, 25 gr.; carbonate of potash, 30 gr.; myrrh, 60 gr.; sugar, 60 gr.; spirit of nutmegs, 4 dr.; rose water, 9-1/2 oz. Reduce the myrrh to powder, add the carbonate of potash of sugar, and triturate them with a small quantity of rose water so as to form a thin paste, then gradually add more rose water, and the spirit of nutmegs, continuing the trituration and further addition of rose water until about eight fluid ounces of milky liquid is formed, then add the sulphate of iron previously dissolved in the remainder of the rose water and cork the bottle immediately.——_Dose_, 1 to 2 oz. as a stimulating tonic.

=Mixture of Sulphuric Acid.= (Ph. G.) _Syn._ MISTURA ACIDI SULPHURICI; HALLER’S ELIXIR. _Prep._ To 3 oz. (by weight) of rectified spirit add gradually 1 oz. (by weight) of pure sulphuric acid.——_Dose_, 5 to 20 drops diluted.

=Mixture, Ton′ic.= _Syn._ STRENGTHENING MIXTURE; MISTURA TONICA, L. _Prep._ 1. Infusion of cascarilla, 5 fl. oz.; tincture of orange peel, 7 fl. dr.; aromatic sulphuric acid, 2 fl. dr.

2. (Collier.) Decoction of bark, 5-1/2 fl. oz.; tincture of do., 3 fl. dr.; aromatic confection, 20 gr.; aromatic spirit of ammonia, 1 fl. dr.

3. (Thomson.) Infusion of calumba, 5-1/2 fl. oz.; compound tincture of cinnamon and syrup of orange peel, of each 2 fl. dr.——_Dose_, 1 to 3 table-spoonfuls, 2 or 3 times a day; in debility of the digestive organs, loss of appetite, to check nausea and vomiting, &c.

=Mixture of Wine.= (Guy’s Hosp.) _Syn._ MISTURA VINI. White wine, 6 fl. oz.; yolks of 2 eggs; sugar, 1/2 oz.; oil of cinnamon, 3 drops.——_Dose_, 1 oz.

=Mixture, Worm.= _Syn._ MISTURA ANTHELMINTICA, M. VERMIFUGA, L. _Prep._ 1. (Collier.) Sulphate of iron, 20 gr.; infusion of quassia, 8 fl. oz.——_Dose._ Two table-spoonfuls every morning fasting.

2. (Copland.) Valerian, 2 dr.; worm-seed, 4 dr.; boiling water, 8 fl. oz.; macerate 1 hour, strain, and add of assafœtida, 1 dr., previously triturated with the yolk of one egg. As the last.

3. (Richard.) Root of male fern, 1 oz.; water, 9 fl. oz.; boil to 6 fl. oz., strain, and add, of sulphuric ether, 1 dr.; syrup of tansy, 1 fl. oz. In tapeworm; as above.

=Mixture, Zinc.= _Syn._ MISTURA ZINCI, M. Z. SULPHATIS, L. _Prep._ (Collier.) Sulphate of zinc, 5 gr.; sulphate of quinine, 10 gr.; compound infusion of roses, 2 fl. oz. Tonic.——_Dose._ A teaspoonful 2 or 3 times a day, in a glass of water. Said to be very efficacious in the cure of coughs of a spasmodic character.

=MIXTURES (Arithmetic of).= The constantly recurring necessity in business and chemical manipulations of determining the value of mixtures, and of producing articles and preparations of different strengths or prices to those already in stock, has rendered a ready means of making such calculations an indispensable qualification in almost every department of trade and industrial art. As we address ourselves to the intelligent operative and busy tradesman, as well as to those more blessed by education and leisure, we feel we are bestowing a boon on many of our readers in giving a short, but sufficient, outline of this useful branch of commercial arithmetic, which is most intimately connected with the objects of the present work.

1. To determine the price of a mixture from the value and quantity of each ingredient of which it is composed.——RULE. Divide the ‘gross value’ by the ‘gross saleable’ or ‘useful quantity,’ the quotient is the value or cost per gallon, pound, &c., as the case may be.——_Example._ Required, the value per gallon of a hogshead of wine containing——

_s._ _d._ £ _s._ _d._

30 gallons @ 10 6 = 15 15 0
20 ” ” 12 6 = 12 10 0
13 ” ” 14 6 = 9 8 6
—— ---------------
63 divide into 37 13 6
---------------
Cost per gallon 0 11 11-1/2

2. To determine the proportions of substances or articles of different values or strengths which must be taken to prepare a mixture of any other value or strength.——RULE. Arrange the ‘prices’ or ‘strengths of the ingredients’ in a column, and link them together in pairs; each of those above the required price being always connected with another below it. Then set the difference between the required price and these numbers, alternately against those they are linked to; when they will indicate the quantities to be taken, as in the following examples:——_a._ Required the proportions of tea at 3_s._, 4_s._, 6_s._, and 7_s._, that must be taken to produce a mixture 5_s._ the pound. Here——

{ 3——+ 1, or 1 lb. @ 3_s._
{ 4——|——+ 2, ” 2 ” ” 4_s._
5 { 6——+ | 2, ” 2 ” ” 6_s._
{ 7-----+ 1, ” 1 ” ” 7_s._

_b._ (When the number of the ingredients or prices is odd.) Required the proportions of teas at 3_s._, 5_s._, and 6_s._, the pound, to sell at 4_s._ Here the odd number must be taken a second time:——

{ 3——+——+ 1 + 2 or 3 lbs @ 3_s._
4 { 5——+ | 1, ” 1 ” ” 6_s._
{ 6-----+ 1, ” 1 ” ” 6_s._

_c._ (When the number of the ingredients is not merely odd, but the prices are unequally distributed either above or below the required price.) A dealer having wines of the same name at 7_s._, 9_s._, 11_s._, 12_s._, and 14_s._, per gallon, wishes to produce a mixture of them worth 10_s._ per gallon:——

{ 7——+---+ 1 + 4, or 5 galls. @ 7_s._
{ 9——+-+ | 2, ” 2 ” ” 9_s._
10 { 11——+ | | 3, ” 3 ” ” 11_s._
{ 12----+ | 1, ” 1 ” ” 12_s._
{ 14------+ 3, ” 3 ” ” 14_s._

It will be seen that by varying the manner of linking the numbers, different answers may often be obtained to the same question. It also often happens that the dealer or operator desires to use a given quantity of one particular article, or to produce a certain quantity only of the mixture instead of those indicated by the above calculations. In these instances he has simply to apply the common rule of ‘practice’ or the ‘rule of three,’ as the particular case may demand.

In the above manner the proportions of the constituents of a compound may be determined from their specific gravity, when no change of volume has arisen from their admixture; but when this is the case, as in alloys, alcoholic mixtures, &c., it is either quite inapplicable or the results obtained are mere approximations to the truth. It may, however, be conveniently employed for calculations connected with the ‘mixing’ and ‘reduction’ of spirits and other liquids, by substituting their per-centage value in ‘proof gallons’ or other corresponding denomination, for the prices in the above examples; water, when introduced be reckoned, =0. Thus:——A spirit merchant having two puncheons of rum of the strengths of 17 and 21 o. p., wishes to know what proportions of each and of water he must take to form a spirit 10 u. up. The proof value of 100 gallons of these spirits are respectively equal to 121, 117, 90, and 0 (water). Therefore——

| 0----+ 27 + 31, or 58 g. water.
90 | 117——| | 90, ” 90 ” rum @ 117 o.p.
| 121----+ 90, ” 90 ” rum ” 121 ”

Suppose the dealer required to use different proportions of the spirits referred to, instead of equal measures, he has only to take such aliquot parts of the quantities thus found referring to the smaller proportion; or such multiples of those referring to the larger one, as he wishes them to bear to each in the new mixture. Numerous other applications of this rule will occur to the ingenious reader.

Questions in ‘alligation,’ as the department of arithmetic above referred to is called, are very easily resolved by the ‘method of indeterminate analysis,’ even by persons but slightly conversant with rudimentary algebra; of which, indeed, they form a simple class of problems, often admitting of an almost indefinite number of solutions.

=MO′HAIR.= The hair of a goat indigenous in Asia Minor. It is dyed and manufactured by similar materials and in a similar manner to wool.

=MOIL.= See CIDER.

=MOIRÉE METALLIQUE.= [Fr.] A beautiful crystalline appearance produced on the surface of tin plate by acids. The tin plate is submitted for a few seconds, whilst gently heated, to the action of dilute aqua regia, by which it acquires a variegated primrose appearance. It is afterwards washed in hot water, dried, and lacquered. The degree of heat and dilution of the acid modifies the beauty and character of the surface. The effect is also varied by employing dilute sulphuric acid, either alone or mixed with a portion of nitric or hydrochloric acid; or by using a solution of citric acid or caustic potassa. According to Herberger, the best metal for the purpose is plate iron, which has been coated by dipping it into a tin bath composed of pure tin, 200 parts; copper, 3 parts; arsenic, 1 part. The varnish should consist of copal in highly rectified spirit. Moirée metallique is in much less demand now than formerly.

=MO′LASSES.= See TREACLE.

=MOLES.= The small, soft excrescences and discolorations of the skin which are popularly known under this name may, when slight, be removed by touching them every day with a little concentrated acetic acid, by means of a hair pencil, observing due care to prevent the application from spreading to the surrounding parts. This does not discolour the skin. The application of lunar caustic is also very effective, but it turns the spot temporarily black. In the pure mole there is always a considerable production of hair. When other means fail, they may be easily and safely removed by surgical means. The operation is trifling; and when judiciously performed no trace of such a proceeding is left behind.

=MOLUC′CA BALM.= See LIQUEUR.

=MOLYBDATE OF AMMONIUM.= (NH_{4})_{2} MoO_{4}. _Syn._ MOLYBDENIC ACID, PEROXIDE OF MOLYBDENUM; ACIDUM MOLYBDICUM, L. _Prep._ Native sulphide of molybdenum, after being well roasted, is reduced to fine powder, digested with ammonia, and the mixture filtered, and the filtrate evaporated to dryness; the residue, molybdate of ammonium, is then dissolved in water, purified by crystallisation; and, lastly, decomposed by heat.

_Prop., &c._ Small white scales, soluble in 570 parts of water; the solution reddens litmus paper; dissolves in the alkalies, forming alkaline molybdates, from which it is again precipitated by strong acids. It is used in the preparation of molybdenum blue, and in calico-printing, but its scarcity precludes its extensive employment in the arts. Molybdate of ammonium is the salt principally used in dyeing. Silks and cottons passed through a solution of this salt, then through a bath soured with hydrochloric acid, and, lastly (without washing), through another of protochloride of tin, are dyed of a rich and permanent blue colour. A solution of molybdate of ammonia in excess of nitric acid forms a valuable agent as a test for phosphates, with which it gives a beautiful yellow precipitate (phospho-molybdate of ammonia). See PHOSPHORIC ACID.

=MOLYB′DENUM.= Mo. A very rare metal, having a white colour, discovered by Hielm in 1782.

_Prep._ By exposing molybdic acid, mixed with charcoal and placed in a covered crucible, to the strongest heat of a smith’s forge.

_Prop., &c._ It is brittle and very infusible; when heated in contact with the air, it is converted into molybdic anhydride, MoO_{3}.

=MOMOR′DICINE.= See ELATERIN.

=MOMRAUGHAN FOR HARNESS, &c.= A correspondent of the ‘Field’ newspaper gives the following formulæ for momraughan, a substance used in India for preserving saddles and every description of leather. It is made as follows:——1 lb. white wax, 3 lb. mutton fat, 1 pint spirits of turpentine; melt, and mix well together while liquid. The saddle or leather should be rubbed well with a lime in the sun, then scrubbed with a brush with soap and water; when thoroughly dry, rub it well with the momraughan (letting it soak in) in the sun. One tablespoonful will be enough for a saddle. Another recipe is:——1 pint neats-foot oil, 2 oz. beeswax, 2 oz. spirits of turpentine, other directions as above. This latter mixture, with the addition of 1 oz. Burgundy pitch, makes a very good waterproof composition for boots.

=MONE′SIA.= _Syn._ MONESIA BARK, BURANHEIM B.; CORTEX MONESIÆ, L. The bark of _Chrysophyllum Buranheim_, a tree growing in the Brazils. The rough, imported extract of this drug also commonly passes under the name of MONESIA. It is astringent, and possesses no advantage over rhatany or catechu.——_Dose_ (of the latter), 18 to 20 gr.

=MONE′SIN.= A peculiar acrid principle, analogous to saponin, found in monesia bark, to the extent of 4·7%.

=MONOBROMATED CAMPHOR.= See CAMPHOR, MONOBROMATED.

=MONOMA′NIA.= See INSANITY.

=MOR′DANT.= In _dyeing_ and _calico printing_, any substance employed to fix the colouring matter of dye-stuffs in the fibres of organic bodies, and to give it brilliancy and permanency. This it effects either by serving as a bond of union between the two, owing to its attraction for each of them; or it acts by uniting with the colouring particles in the minute pores of the fibres, and rendered them insoluble in the alkaline, soapy, and other liquids, to the action of which they will subsequently be exposed. When an infusion of some dye-stuff, as cochineal or madder, for example, is mixed with alum or acetate of alumina, and a little alkali, a precipitate immediately forms, consisting of alumina in combination with colouring matter, constituting a LAKE. It is by a similar reaction occurring within the fibres that the permanent dyeing of the cloth is effected. Here the colouring matter of the dyeing materials not only passes from the soluble to the insoluble form, but it enters into chemical combination with other substances, and in the new compounds it assumes greater brilliancy and permanency than it previously possessed. Annotta and safflower afford instances of the second mode of action above referred to, by which substances operate as mordants. The colouring matter of these dye-stuffs is soluble in alkaline lyes, and into a solution of this kind the cloth is dipped. It has now received an extremely fugitive colour only; but by passing it through acidulated water the alkaline solvent is abstracted, and the tinctorial matter is precipitated in an insoluble and minutely divided state within its pores, and it becomes permanently dyed. A similar reaction takes place in dyeing with the ‘indigo vat,’ in which atmospheric oxygen performs the part of a mordant. It is believed that even in these cases the colouring principle, during its transition from the liquid to the solid form, enters into combination with the fibres of the organic substance, and that, in proportion to the affinity existing between the two, is the integrity and excellence of the dye. In wool and silk the affinity between their filaments and the tinctorial particles of the dye-bath is, in general, so considerable, that a permanent stain is very easily communicated to them; but with cotton and flax, the materials of which calico and linen goods are made, the reverse is the case, and the intervention of a third material, in the shape of a mordant, is absolutely necessary to dye them of a permanent colour.

“Experience has proved that, of all the bases, those which succeed best as mordants are alumina, tin, and oxide of iron; the first two of which, being naturally white, are the only ones which can be employed for preserving to the colour its original tint, at least without much variation. But whenever the mordant itself is coloured, it will cause the dye to take a compound colour quite different from its own. If, as is usually said, the mordant enters into a real chemical union with the stuff to be dyed, the application of the mordant should obviously be made in such circumstances as are known to be most favorable to the combination taking place; and this is the principle of every day’s practice in the dye-house.

“In order that a combination may result between two bodies, they must not only be in contact, but they must be reduced to their ultimate molecules. The mordants to be united with stuffs are, as we have seen, insoluble in themselves, for which reason their particles must be divided by solution in an appropriate vehicle. Now, this solvent or menstruum will exert in its own favour an affinity for the mordant, which will prove to that extent an obstacle to its attraction for the stuff. Hence we must select such solvents as have a weaker affinity for the mordants than the mordants have for the stuffs. Of all acids which can be employed to dissolve alumina, for example, vinegar (acetic acid) is the one which will retain it with the least energy, for which reason the acetate of alumina is now generally substituted for alum, because the acetic acid gives up the alumina with such readiness that mere elevation of temperature is sufficient to effect the separation of these two substances. Before the substitution of the acetate, alum alone was employed; but without knowing the true reason, all the French dyers preferred the alum of Rome, simply regarding it to be the purest; it is only within these few years that they have understood the real grounds of this preference.

“The two principal conditions, namely, extreme tenuity of particles and liberty of action, being found in a mordant, its operation is certain. But as the combination to be effected is merely the result of the play of affinity between the solvent and the stuff to be dyed, a sort of partition must take place, proportioned to the mass of the solvent, as well as to its attractive force. Hence the stuff will retain more of the mordant when its solution is more concentrated, that is, when the base diffused through it is not so much protected by a large mass of menstruum; a fact applied to very valuable uses by the practical man. On impregnating, in calico printing, for example, different spots of the same web with the same mordant in different degrees of concentration, there is obtained in the dye-bath a depth of colour upon these spots intense in proportion to the strength of their various mordants. Thus, with solution of acetate of alumina in different grades of density, and with madder, every shade can be produced from the fullest red to the lightest pink, and with acetate of iron and madder, every shade from black to pale violet.” (Ure.)

In the employment of mordants in the ordinary processes of dyeing the goods are passed through the solution for a period varying, under different circumstances, according to the object in view. The cloth is subsequently aired, dried, and well rinsed, before immersing it in the colouring bath. In _calico printing_ the mordant is applied partially or topically to the cloth by means of wooden blocks, or some similar contrivance; or certain parts of the cloth are stopped out by a suitable preparation, or ‘resist,’ by which means a pattern is produced, as the colouring matter of the dye-bath is removed from the other portions by the washing or scouring to which it is subsequently subjected. The substances used to thicken the mordant by the calico printers, to prevent them spreading, are starch and British gum. The first is prepared for neutral solutions; the last for acidulous ones. The removal of the undecomposed particles of the mordant, so as to preserve the other portion of the cloth from their action, is effected by the process of DUNGING (which _see_).

The process of GALLING or ROOTING, commonly employed as a preparation of cotton and linen for fast dyes, consists in working the stuff for some time, at a good hand heat, in a decoction of galls or an infusion of sumach. In this case the astringent matter plays the part of a mordant. About 2-1/2 oz. of galls, or 5 oz. of sumach, and 3 or 4 pints of water, are commonly taken for every lb. of cotton. See CALICO PRINTING, DYEING, and the respective dye-stuffs and mordants.

=Mordant.= In _gilding_, any sticky matter by which gold-leaf is made to adhere. _Prep._ 1. Water or beer, rendered adhesive by the addition of a little gum, sugar, or honey, and tinged with a little gamboge or carmine, to mark the parts to which it is applied. Used to attach gold leaf to paper, taffety, vellum, &c.

2. (Mixtion.) From asphaltum, 1 part; mastic, 4 parts; amber, 12 parts; fused together, and then mixed with hot boiled oil, 1 pint. Used for gilding wood, &c. See GOLD SIZE.

=MORPHIA.= C_{17}H_{19}NO_{3}. _Syn._ MORPHINE (Ph. D.), MORPHINA, MORPHIUM, L. The chief active principle of opium. Morphia was discovered by Ludwig in 1688, but it was first obtained pure, and its precise nature pointed out by Sertuerner in 1804. It is peculiar to the _Papaveraceæ_, or poppy family.

_Prep._ 1. (Ph. D.) Turkey opium (cut into thin slices), 1 lb., is macerated for 24 hours in water, 1 quart, and the liquid portion decanted; the residuum is macerated for 12 hours with a second quart of water, and the process is repeated with a third quart of water, after which the insoluble portion is subjected to strong pressure; the mixed liquids are evaporated by water or steam heat to a pint, and filtered through calico; to the filtrate is added a solution formed of chloride of calcium, 6 dr., dissolved in distilled water, 4 fl. oz., and the liquid is further evaporated until it is so far concentrated that nearly the whole of it becomes solid on cooling; this is enveloped in a couple of folds of strong calico, and subjected to powerful pressure, the dark liquid which exudes being preserved for subsequent use; the squeezed cake is next treated with about 1/2 pint of boiling water, and the undissolved portion is washed on a paper filter; the filtered solution is again evaporated, and the solid portion thus obtained submitted to pressure, as before; if the product is not quite white, this process is repeated a third time; the squeezed cake is now dissolved in boiling water, 6 fl. oz., and the solution filtered through animal charcoal (if necessary); to the clear solution is added ammonia, in slight excess; the crystalline precipitate which forms as the liquid cools is collected on a paper filter, washed with cold distilled water, and, lastly, the filter is transferred to a porous brick, in order that the morphia which it contains may become dry. (From the liquids reserved from the expressions more morphia may be obtained by dilution with water, precipitation with ammonia, re-solution in boiling water, and treatment with a little animal charcoal, &c., as before.)

2. (Ph. L. 1836.) Hydrochlorate of morphia, 1 oz., is dissolved in distilled water, 1 pint; and ammonia, 5 fl. dr. (or q. s.), previously diluted with water, 1 fl. oz., is added, with agitation; the precipitate is well washed in distilled water, and dried by a gentle heat. By a similar process morphia may be obtained from its other salts.

3. (Merck.) A cold aqueous infusion of opium is precipitated with carbonate of sodium, in excess; the precipitate washed, first with cold water, and then with cold alcohol of sp. gr. 85; the residuum is dissolved in weak acetic acid, the solution filtered through animal charcoal, and precipitated with ammonia; the precipitate is again washed with cold water, dissolved in alcohol, and crystallised. A good process where spirit is cheap.

4. (Mohr.) Opium, 4 parts, is made into a strong infusion with water, q. s.; lime, 1 part, reduced to a state of milk with water, is then added; the mixture is next heated to boiling, at once filtered through linen, and treated, whilst still hot, with chloride of ammonium, in fine powder, in slight excess (about 1 oz. to each lb. of opium); the morphia is deposited as the liquid cools, and may be purified by a second solution in lime and precipitation by chloride of ammonium. This process is remarkably simple, and in many points is preferable to any other, either on the small or large scale.

5. (PURE.) A filtered solution of opium in tepid water is mixed with acetate of lead in excess; the precipitate (meconate of lead) is separated by a filter, and a stream of sulphuretted hydrogen is passed through the nearly colourless filtrate; the latter is warmed, to expel excess of the gas, once more filtered, and then mixed with a slight excess of ammonia, which throws down narcotine and morphia; these are separated by boiling ether, in which the former is soluble.

_Prop._ The morphia of commerce is a white crystalline powder; but when crystallised from alcohol, it forms brilliant prismatic crystals of adamantine lustre, and the formula C_{17}H_{19}NO_{3}.H_{2}O. It exerts an alkaline reaction on test paper; imparts a perceptible bitter taste to water; requires 1160 parts of cold water, and 94 parts of boiling water, for its solution; insoluble in ether; dissolves in 90 parts of cold and about 30 parts of boiling alcohol; it also dissolves in the fixed and volatile oils, and in solutions of the alkalies; heated in close vessels, it forms a yellow liquid, like melted sulphur, which becomes white and crystalline on cooling; heated in the air, it melts, inflames like a resin, and leaves a small quantity of charcoal behind. With the acids it forms salts, which are mostly soluble and crystallisable. These may all be made by the direct solution of the alkaloid in the dilute acid. The only ones of importance are the acetate, hydrochlorate, and sulphate.

_Pur._ Commercial morphia and its preparations are often contaminated with codeine, narcotine, and colouring matter. The proportion of the first two may be estimated by the loss of weight which the sample suffers when digested in ether; or by dissolving out the morphine by digestion in weak liquor of potassa. Pure morphia “is scarcely soluble in cold water, sparingly so in boiling water, and readily so in alcohol. This solution is alkaline to test paper, and by evaporation leaves crystals, which are wholly dissipated by heat. It is soluble in pure potassa.” (Ph. L. 1836.)

_Tests._ 1. Potassium hydrate and ammonia precipitate morphia from solution of its salts, under the form of a white crystalline powder, which is very soluble in excess of hydrate of potassium, and, with somewhat more difficulty, in excess of ammonia. The solution formed by excess of the first is precipitated on the addition of bicarbonate of potassium. The precipitate in either case is soluble in a solution of chloride of ammonium, and in dilute acetic acid, and is insoluble in ether. A careful inspection of the precipitate through a lens of small power shows it to consist of minute acicular crystals; and seen through a glass which magnifies 100 times, these crystals present the form of right rhombic prisms.——2. The carbonates of potassium and sodium produce the same precipitate as hydrate of potassium, and which is insoluble in excess of the precipitant.——3. The bicarbonates of potassium and sodium also give similar precipitates from neutral solutions, insoluble in excess. In each of the above cases stirring with a glass rod and friction on the sides of the vessel promote the separation of the precipitate.——4. If to a mixture of morphia and oil of vitriol a minute fragment of bichromate of potassium be added, oxide of chromium is set free, and a fine green colour developed.——5. A drop or two of solution of terchloride of gold added to a weak solution of morphia gives a yellow precipitate, which is mostly redissolved on agitating the liquid, which then assumes various hues (green, blue, violet, purple) on the addition of a drop of liquor of potassa.——6. A minute fragment of terchloride of gold and of hydrate of potassium very gently dropped into the liquid, occasion purple clouds or streaks in dilute solutions, followed by a precipitate, which is violet, purple, or blue-black, according to the strength of the liquid.

Another test, given by Siebold,[41] is the following:——“Heat the substance which is believed to be, or to contain, morphia, gently with a few drops of sulphuric acid, add a very small quantity of pure perchlorate of potassium. The liquid immediately surrounding the perchlorate will at once assume a deep brown colour, which will soon spread and extend over the greater part of the acid. Warming increases the delicacy of the test. 0·0001 gramme of morphia can be distinctly recognised in this way, and no other alkaloid is acted upon in a similar way by the substances named. It is indispensable, however, for the success of the experiment that the perchlorate of potassium be absolutely free from chlorate.” See ALKALOIDS.

[Footnote 41: ‘Year Book of Pharmacy,’ 1873.]

The above are the most reliable precipitates for morphia; the first two may, indeed, be regarded as characteristic, and the remainder as almost so. The following are often referred to by medical writers, but are less exclusive and trustworthy:——Morphia and its salts are——7. Reddened by nitric acid, and form orange-red solutions, darkened by ammonia in excess, and ultimately turning yellow, with the production of oxalic acid.——8. They are turned blue by ferric chloride, either at once or on the addition of an alkali, and this colour is destroyed by water and by alkalies, or acids in excess.——9. Iodic acid added to their solutions turns them yellowish brown, by setting iodine free, and the liquid forms a blue compound with starch.

_Uses._ Morphia and its salts are exhibited either in substance, made into pills, or in solution, generally the latter; or externally, in fine powder, applied to the dermis denuded of the cuticle. They are principally employed as anodynes and hypnotics in cases in which opium is inadmissible, and are justly regarded as the most valuable medicines of their class. “In cases wherein both opium and the morphine salts are equally admissible, I prefer the former, its effects being better known and regulated; moreover, opium is to be preferred as a stimulant and sudorific, and for suppressing excessive mucous discharges.” (Pereira.)——_Dose._ Of pure morphia, 1/12 to 1/6 gr.; of its salts, 1/8 to 1/4 gr.; externally, 1/2 to 1-1/2 gr. Morphine is chiefly used for the preparation of the acetate, and some of its other salts.

Good opium yields from 10% to 13% of morphia. See OPIUM.

=Morphia, Ac′etate of.= C_{17}H_{20}NO_{3}C_{2}H_{3}O_{2}. _Syn._ MORPHIÆ ACETAS (Ph. L., E., & D.), L. _Prep._ 1. (Ph. L. 1836.) Morphia, 6 dr.; acetic acid (Ph. L.), 3 fl. dr.; distilled water, 4 fl. oz.; dissolve, gently evaporate, and crystallise.

2. (Ph. E.) Hydrochlorate of morphia, 1 part, is dissolved in warm water, 14 parts; and the solution, when cold, is precipitated with ammonia, in slight excess, the precipitate is washed in cold water, and dissolved by means of acetic acid, in excess, in warm water, 12 parts; from the solution crystals are obtained as before.

3. (Ph. D.) Morphia (in fine powder), 1 oz.; rectified spirit, 8 fl. oz.; mix, apply a gentle heat, and add of acetic acid (sp. gr. 1·044), 4-1/2 fl. dr. or q. s., until a neutral or slightly acid solution is obtained; evaporate this to the consistence of a syrup by steam or water heat, and set aside the residuum for a few days until it solidifies.

4. (Ph. L.) Similar to the Edinburgh process.

_Pur._ “Soluble in water and in rectified spirit” (less so in the former than the latter); “and when the spirit is distilled from the solution, it yields crystals which are totally destroyed by heat.” (Ph. L.) “100 measures of a solution of 10 gr. in 1/2 fl. oz. of water, and 5 minims of acetic acid, heated to 212° and decomposed by a very slight excess of ammonia, yield by agitation a precipitate which, in 24 hours, occupies 15-1/2 measures of the liquid.” (Ph. E.)

_Obs._ The acetate of morphia of commerce is usually in the form of a whitish powder, and is prepared by the mere evaporation of the solution to dryness by a gentle heat. During the process a portion of the acetic acid is dissipated, and hence this preparation is seldom perfectly soluble in water, unless it has been slightly acidulated with acetic acid. In the Ph. L. 1851 this salt (in crystals) is included in the materia medica. See MORPHIA (_above_).

=Morphia, Hydri′odate of.= C_{17}H_{19}NO_{3},HI. _Syn._ MORPHIÆ HYDRIODAS, L. _Prep._ (A. T. Thomson.) Hydrochlorate of morphia, 2 parts; iodide of potassium, 1 part; dissolve each separately in a little water, mix the solutions, wash the precipitate in a little very cold water, press it in bibulous paper, redissolve it in hot water, and crystallise.

=Morphia, Hydriodate of, with Iodine.= _Syn._ MORPHIÆ HYDRIODAS CUM IODINIO; BOUCHARDAT’S IODURE D’IODHYDRATE, &c.; MORPHINE. _Prep._ Mix an acid solution of sulphate of morphia with an ioduretted solution of iodide of potassium, keeping the liquid at the temperature of 140° for an hour.

Pour off the liquid, wash the scales, and dry them.——_Dose_, 3/4 gr. at bedtime.

=Morphia and Hydriodate of Zinc with Iodine.= (Bouchardat.) _Syn._ MORPHIÆ ET ZINCI HYDRIODAS CUM IODINIO. _Prep._ Boil 1 scruple of ioduretted hydriodate of morphia with 2 fl. oz. of water and 10 scruples of zinc. After some days’ action filter the boiling liquid, which deposits the salt. Make 1-1/2 gr. into 8 pills, with powdered marshmallow root and syrup.

=Morphia, Hydrochlo′′rate of.= C_{17}H_{19}NO_{3},HI. _Syn._ MURIATE OF MORPHIA; MORPHIÆ HYDROCHLORAS (Ph. L. & Ph. B.), MORPHIÆ MURIAS (Ph. E., D. & U. S.), L. _Prep._ 1. (Ph. L. 1836.) Macerate sliced opium, 1 lb., in water, 4 pints, for 30 hours; then bruise it, digest it for 20 hours more, and press it; macerate what remains a second and a third time in water until exhausted, and as often bruise and press it; mix the liquors, and evaporate at 140° Fahr. to the consistence of a syrup; add of water, 3 pints, and after defecation decant the clear portion; gradually add to this liquid crystallised chloride of lead, 2 oz. (or q. s.), dissolved in boiling water, 4 pints, until it ceases to produce a precipitate; decant the clear liquid, wash the residuum with water, and evaporate the mixed liquids, as before, that crystals may form; press these in a cloth, then dissolve them in distilled water, 1 pint, add freshly burnt animal charcoal, 1-1/2 oz., digest at 120°, and filter; finally, the charcoal being washed, cautiously evaporate the mixed liquors, that pure crystals of hydrochlorate of morphia may form. To the decanted liquor from which the crystals were first separated, add of water, 1 pint, and drop in liquor of ammonia, frequently shaking, until all the morphine is precipitated; wash this precipitate with cold distilled water, saturate it with hydrochloric acid, digest with animal charcoal, 2 oz.; filter, wash the filtrate as before, and evaporate the mixed liquors, cautiously, as above, that pure crystals may be obtained.

2. (Ph. E.) Opium, 20 oz., is exhausted with water, 1 gall., in the quantity of a quart at a time, and the mixed liquors are evaporated to a pint; chloride of calcium, 1 oz., dissolved in water, 4 fl. oz., is added, and, after agitation, the liquid is placed aside to settle; the clear decanted liquid, and the washings of the sediment, are next evaporated, so that they may solidify on cooling; the cooled mass, after very strong pressure in a cloth, is redissolved in warm water, a little powdered white marble added, and the whole filtered; the filtrate is acidulated with hydrochloric acid, the solution again concentrated for crystallisation, and the crystals submitted to powerful pressure, as before; the process of solution, clarification, with powdered marble and hydrochloric acid, and crystallisation, is repeated until a snow-white mass is obtained. This is the process of Gregory and Robertson, and is one of the easiest and most productive on the large scale. To procure the salt quite white, 2 to 4 crystallisations are required, according to the power of the press employed. The Edinburgh College recommends, on the small scale, the solution, after two crystallisations, to be decoloured by means of animal charcoal; but, on the large scale, to purify the salt by repeated crystallisations alone.

3. (Ph. B.) Macerate opium, sliced, 1 lb., for 24 hours with distilled water, 2 pints, and decant. Macerate the residue for 12 hours with distilled water, 2 pints, decant, and repeat the process with the same quantity of water, subjecting the insoluble residue to strong pressure.

Unite the liquors, evaporate on a water bath to the bulk of 1 pint, and strain through calico. Pour in now chloride of calcium, 3/4 oz., previously dissolved in 4 fl. oz. of distilled water, and evaporate until the solution is so far concentrated that upon cooling it becomes solid. Envelope the mass in a double fold of strong calico, and subject it to powerful pressure, preserving the dark fluid which exudes. Triturate the squeezed cake with about 1/2 pint of boiling distilled water, and, the whole being thrown upon a paper filter, wash the residue well with boiling distilled water. The filtered fluids having been evaporated as before, cooled, and solidified, again subject the mass to pressure, and if it be still much coloured, repeat this process a third time, the expressed liquids being always preserved. Dissolve the pressed cake in 6 fl. oz. of boiling distilled water, add purified animal charcoal, 1/4 oz., and digest for 20 minutes; filter; wash the filter and charcoal with boiling distilled water, and to the solution thus obtained add solution of ammonia in slight excess. Let the pure crystalline morphia which separates as the liquid cools be collected on a paper filter, and washed with cold distilled water until the washings cease to give a precipitate with solution of nitrate of silver acidulated with nitric acid.

From the dark liquids expressed in the above process an additional product may be obtained by diluting them with distilled water, precipitating with solution of potash added in considerable excess, filtering, and supersaturating the filtrate with hydrochloric acid. This acid liquid, digested with a little animal charcoal, and again filtered, gives upon the addition of ammonia a small quantity of pure morphia. Diffuse the pure morphia obtained as above through 2 oz. of boiling distilled water placed in a porcelain capsule, kept hot, and add, constantly stirring, dilute hydrochloric acid, 2 fl. oz., or q. s., proceeding with caution, so that the morphia may be entirely dissolved and a neutral solution obtained. Set aside to cool and crystallise. Drain the crystals and dry them on filtering paper. By further evaporating the mother liquor, and again cooling, additional crystals are obtained.——_Dose._ From 1/8th to 1/2 gr.

4. (Mohr.) By dissolving the precipitate of morphia (see MORPHIA, _Prep._ 4) in dilute hydrochloric acid, and by crystallisation, as before.