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Carminative orange

Capsandiin, capsorubin, paprika, paprika E 160c Paprika (Capsicum annum L) reddish (carmine) orange 0... [Pg.586]

METHYL ORANGE METHYL RED BROMTHYMOLBLUE PHENOLPHTHALEIN AUZAR1N YELLOW R INDIGO CARMINE... [Pg.492]

Procedure. Weigh out accurately from a weighing bottle about 0.2 g of the pure sodium carbonate into a 250 mL conical flask (Note 1), dissolve it in 50-75 mL of water, and add 2 drops of methyl orange indicator (Note 2) or preferably of methyl orange-indigo carmine indicator (Section 10.9), which gives a very much more satisfactory end point (Note 3). Rinse a clean burette three times with 5 mL portions of the acid fill the burette to a point 2-3 cm above the zero mark and open the stopcock momentarily, in order to fill the jet with liquid. Examine the jet to see that no air bubbles are enclosed. If there are, more liquid must be run out until the jet is completely filled. Re-fill, if necessary, to bring the level above the zero mark then slowly run out the liquid until the level is between the 0.0 and 0.5 mL marks. Read the position of the meniscus to 0.01 mL (Section 3.12). [Pg.286]

If the solution contains carbonate (Procedure A), methyl orange, methyl orange-ihdigo carmine, or bromophenol blue must be used in standardisation against hydrochloric acid of known molar concentration. Phenolphthalein or indicators with a similar pH range, which are affected by carbon dioxide, cannot... [Pg.292]

Procedure A with standard hydrochloric acid. Place the standardised (approx. 0.1 M) hydrochloric acid in the burette. Transfer 25 mL of the sodium hydroxide solution into a 250 mL conical flask with the aid of a pipette, dilute with a little water, add 1-2 drops of methyl orange or 3-4 drops of methyl orange-indigo carmine indicator, and titrate with the previously standardised hydrochloric acid. Repeat the titrations until duplicate determinations agree within 0.05 mL of each other. [Pg.293]

Titration of 25.00 mL of the carbonate solution with 0.1060M HC1, using methyl orange-indigo carmine as indicator. [Pg.295]

Another titration is performed with methyl orange, methyl orange-indigo carmine or bromophenol blue as indicator. Let the volume of acid be V mL. [Pg.298]

Procedure B. The experimental details for the preparation of the initial solution are similar to those given under Procedure A. Titrate 25 or 50 mL of the cold solution with standard 0.1M hydrochloric acid and methyl orange, methyl orange-indigo carmine, or bromophenol blue as indicator. Titrate another 25 or 50 mL of the cold solution, diluted with an equal volume of water, slowly with the standard acid using phenolphthalein or, better, the thymol-blue cresol red mixed indicator in the latter case, the colour at the end point is rose. Calculate the result as described in the Discussion above. [Pg.299]

The two methods available for this determination are modifications of those described in Section 10.32 for hydroxide/carbonate mixtures. In the first procedure, which is particularly valuable when the sample contains relatively large amounts of carbonate and small amounts of hydrogencarbonate, the total alkali is first determined in one portion of the solution by titration with standard 0.1M hydrochloric acid using methyl orange, methyl orange-indigo carmine, or bromophenol blue as indicator ... [Pg.299]

Another sample of equal volume is then titrated with the same standard acid using methyl orange, methyl orange-indigo carmine or bromophenol blue as indicator. The volume of acid used (say, ymL) corresponds to carbonate+ hydrogencarbonate. Hence 2y = carbonate, and y — 2Y = hydrogencarbonate. [Pg.299]

In the direct method, a solution of the ammonium salt is treated with a solution of a strong base (e.g. sodium hydroxide) and the mixture distilled. Ammonia is quantitatively expelled, and is absorbed in an excess of standard acid. The excess of acid is back-titrated in the presence of methyl red (or methyl orange, methyl orange-indigo carmine, bromophenol blue, or bromocresol green). Each millilitre of 1M monoprotic acid consumed in the reaction is equivalent to 0.017032 g NH3 ... [Pg.301]

In the indirect method, the ammonium salt (other than the carbonate or bicarbonate) is boiled with a known excess of standard sodium hydroxide solution. The boiling is continued until no more ammonia escapes with the steam. The excess of sodium hydroxide is titrated with standard acid, using methyl red (or methyl orange-indigo carmine) as indicator. [Pg.301]

Carminic acid is orange in acidic media (pH 3), red in nearly neutral media (pH 5.5), and purple at pH 7. It forms complexes with metals such as tin and aluminum to make brilliant red pigments. Carmine is easily bleached by sulfur dioxide. [Pg.112]

Cochineal, carminic acid, and carmines are approved as food colorants in the EU under code E 120, and their purity criteria are regulated.The amount of E 120 permitted in food ranges from 50 to 500 mg/kg. Carminic acid and carmine are considered very good food colorants due to their high stability and tinctorial properties. Solutions of carminic acid are yellow to orange, while carmines show various stable brilliant red hues. - ... [Pg.335]

Carminic acid and carmine, cochineal E 120 Yes Female cochineal insect orange to red, pink to red ... [Pg.586]

E 110 Sunset Yellow FCF, Orange Yellow S E 120 Cochineal, carminic acid, carmines... [Pg.32]

Its solutions in dilute hydrobromic acid are a carmine-red (0.025 M PoBr4) and in more dilute solution (10 3 M), orange red. The tetrabromide is soluble in ethanol, acetone and some other ketones, and is sparingly soluble in liquid bromine. It is hygroscopic and is easily hydrolyzed to a white, basic bromide of variable composition. It forms a yellow ammine in ammonia gas and this yields polonium dibromide and polonium metal on standing, presumably because of radiation decomposition of the ammonia and subsequent hydrogen reduction of the tetrabromide (7). [Pg.217]

We are of opinion, that many of the nitrates might be advantageously employed in the manufacture of fire works. Some, as nitrate of strontian, communicate a red color to flame, as the flame of alcohol. Nitrate of lime also might be used.. . . Muriate of strontian, mixed with alcohol, or spirit of wine, will give a carmine-red flame. For this experiment, one part of the muriate is added to three or four parts of alcohol. Muriate of lime produces, with alcohol, an orange-coloured flame. Nitrate of copper produces an emerald-green flame. Common salt and nitre, with alcohol, give a yellow flame.14... [Pg.60]

Biebrich s scarlet is recognised by boiling the substance with ammonia in presence of this colouring matter the liquid assumes an orange-red tint, whilst with pure carmine a purple-red liquid is obtained. [Pg.422]


See other pages where Carminative orange is mentioned: [Pg.113]    [Pg.113]    [Pg.113]    [Pg.113]    [Pg.945]    [Pg.284]    [Pg.287]    [Pg.287]    [Pg.295]    [Pg.297]    [Pg.297]    [Pg.297]    [Pg.298]    [Pg.868]    [Pg.112]    [Pg.335]    [Pg.590]    [Pg.595]    [Pg.187]    [Pg.1214]    [Pg.266]    [Pg.7]    [Pg.184]    [Pg.348]    [Pg.194]    [Pg.342]    [Pg.421]    [Pg.110]    [Pg.473]    [Pg.486]    [Pg.678]    [Pg.174]    [Pg.431]    [Pg.54]   
See also in sourсe #XX -- [ Pg.479 ]




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Carminative

Carmine

Carminic

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