Scarlet

Mcrcuryill) iodide, HgL. Scarlet (to 126 C) or yellow substance (HgC L solution plus KI or Hg plus I2)- Forms complex iodides with excess iodide (Nessler s reagent). 

Pelargonin-3-biosides are of widespread occurrence, e.g. in the nasturtium, scarlet runner bean, gloxinia. See anthocyanins. 

Addition of mercury(II) chloride solution to a solution of an iodide gives a scarlet precipitate of mercury(II) iodide, soluble in excess of iodide ... 

Azo-dye formation. Dissolve 2-3 drops of aniline in 1 ml. of cone. HCl and add 3 ml. of water. Shaike to dissolve any hydrochloride which may have separated and cool in ice. Add a few drops of 20% sodium nitrite solution. Add this cold diazonium solution to a cold solution of the phenol in an excess of aqueous NaOH solution. Solutions or precipitates of azo-dyes ranging in colour from orange through scarlet to dark red, according to the phenol used, are obtained. Note in particular that i-naphthol gives a brownish-red, 2-naphthol a scarlet precipitate. Catechol decomposes. 

Textile dyes were, until the nineteenth century invention of aniline dyes, derived from biological sources plants or animals, eg, insects or, as in the case of the highly prized classical dyestuff Tyrian purple, a shellfish. Some of these natural dyes are so-caUed vat dyes, eg, indigo and Tyrian purple, in which a chemical modification after binding to the fiber results in the intended color. Some others are direct dyes, eg, walnut sheU and safflower, that can be apphed directly to the fiber. The majority, however, are mordant dyes a metal salt precipitated onto the fiber facUitates the binding of the dyestuff Aluminum, iron, and tin salts ate the most common historical mordants. The color of the dyed textile depends on the mordant used for example, cochineal is crimson when mordanted with aluminum, purple with iron, and scarlet with tin (see Dyes AND DYE INTERMEDIATES). 

Uses. (9-Nitrotoluene is used in the synthesis of intermediates for azo dyes, sulfur dyes, mbber chemicals, and agriculture chemicals. Typical intermediates are o-toluidine, o-nitrobenzaldehyde, 2-nitro-4-chlorotoluene, 2-nitro-6-chlorotoluene, 2-amino-4-chlorotoluene (Fast Scarlet TR Base), and 2-amino-6-chlorotoluene (Fast Red KB Base). -Nitrotoluene is used principally in the production of intermediates for azo and sulfur dyes. Typical intermediates are -toluidine, -nitrobenzaldehyde, and 4-nitro-2-chlorotoluene. 

B. Scarlet, M. Rippon, and P. J. Lloyd, Proceedings of the Conference on Particle Si Mnalysis, The Society for Analytical Chemistry, London, 1967, p. 242. 

In this way, many green azo dyes have been made by combining separate conjugated systems in the same molecule, eg, one yellow and the other blue. The blocking or the insulating group prevents the electronic interaction of one chromophore system with the second. Chloramine Fast Scarlet 4BS... 

Commercial Disperse Azo Dyes. The first proposal to use insoluble dyes in suspension in an aqueous foam bath, ie, disperse dyes, to dye cellulose acetate was in 1921 (60). Commercialization of disperse dyes began in 1924 with the introduction of the Duranol dyes by British Dyestuffs Corporation (61) and the SRA dyes by British Celanese Company (62). In contrast to the acid monoazo dyes, derivatives of benzene rather than of naphthalene are of the greatest importance as coupling components. Among these components mono- and dialkylariifines (especially A/-P-hydroxyethyl-and A/-(3-acetoxyethylanifine derivatives) are widely used couplers. Nitrodiazobenzenes are widely used as diazo components. A typical example is CeUiton Scarlet B [2872-52-8] (91) (Cl Disperse Red 1 Cl 11110). 

Couplers which form scarlet dyes with 4-nitroani1ine and red dyes with 2-amiQO-6-nitrobenzothiazole yield blue dyes with 3-amiQo-5-nitro-2,l-benzisothiazole [14346-19-1]. 

Kermisic Acid. Many accounts claim that kermisic acid [476-35-7] (Cl Natural Red 3 Cl 75460) is the oldest dyestuff ever recorded (23). The name kermes is derived from an Armenian word meaning Httle worm for which the later Latin equivalent was vermiculus, the basis of the Knglish word Vermillion. The dye was obtained from an oriental shield louse, K. ilicis which infest the holm o5kQuercus ilex and the shmb oak. coccifera. The dye produces a brilliant scarlet color with an alum mordant. Although expensive, it was cheaper than its rival Tyrian Purple. It was in great demand until the sixteenth century when it was displaced by carminic acid. 

Eosin B (Bluish, Eosin Scarlet, 4, 5 -dibromo-2, 7 -dinitrofluorescein disodium salt)... 

Akuanunenine, C20H22O4N2. This base has only been isolated as the scarlet-red picrate, m.p. 225° it contains one methoxyl group. 

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