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Exposure to light

C10H10N4O2S. White powder, which darkens on exposure to light m.p. 255-256 C. Prepared by condensing p-acet-amidobenzenesulphonyl chloride with 2-aminopyrimidine and subsequent hydrolysis. Soluble sulphadiazine is the sodium salt. Sulphadiazine is the least toxic of the more potent sulphonamides. ... [Pg.376]

Chloroform was formerly used in medicine as an anaesthetic. One disadvantage for this purpose is the ready oxidation which chloroform undergoes on exposure to light and air, generating the poisonous phosgene, or carbonyl chloride, COCU- This is counteracted by storing the liquid in dark amber-... [Pg.91]

Ethyl iodide is a heavy liquid, of b.p. 72° and of d, 1 94 insoluble in water, When freshly distilled it is colourless, but on prolonged exposure to light it darkens in colour owing to the liberation of free iodine. Its chemical properties are almost identical with those of ethyl bromide given on pp. 102 and 103. [Pg.107]

Phenylhydrazine is, however, frequently supplied in the form of its hydro chloride or sulphate, since these salts on exposure to light darken less rapidly than the free base. If these salts are used, however, osazone formation is unsatisfactory, partly because the mineral acid formed by hydrolysis of... [Pg.138]

Iodobenzene, as usually prepared, is a very pale yellow liquid of b.p. 188°, and d, 1 83. The freshly distilled pure liquid i colourless, but soon redevelops the yellow colour on exposure to light. Iodobenzene is insoluble in water. [Pg.185]

Pure phenol is a colourless crystalline substance, having m.p. 43°, and b.p. 182° on exposure to air, it slowly sublimes, and on exposure to light, develops a pink colour. It has a characteristic odour, and a limited solubility in water. Phenol in dilute aqueous solution has strongly antiseptic properties, but the crystalline substance should not be allowed to come in contact with the skin, as it may cause severe blistering. [Pg.197]

Phenylhydrazine on exposure to light slowly darkens and eventually becomes deep red in colour salts of the base share this property but to a lesser degree, the sulphate and acetate (of the common salts) being most stable to light. Phenylhydrazine is largely used in organic chemistry to characterise aldehydes and ketones as their phenyl-hydrazones (pp. 342, 345), and carbohydrates as their osazones (pp. 136-140). It is readily reduced thus in the process of osazone formation some of the phenylhydrazine is reduced to aniline and ammonia. On the... [Pg.199]

Chloroform undergoes oxidation to the very poisonous phosgene upon exposure to light and air. Commercial specimens are therefore stored in brown bottles and contain 1-2 per cent, of alcohol the latter converts the toxic phosgene into the harmless substance diethyl carbonate ... [Pg.298]

Its conductivity increases slightly with exposure to light. It can be doped with silver, copper, gold, tin, or other elements. In air, tellurium burns with a greenish-blue flames, forming the dioxide. Molten tellurium corrodes iron, copper, and stainless steel. [Pg.120]

From the perspective of laboratory practice, the sensitivity of many indoles to acids, oxygen and light prescribes the use of an inert atmosphere for most reactions involving indoles and the avoidance of storage with exposure to light. This sensitivity is greatly attenuated by electron-withdrawing (EW) substituents. [Pg.3]

A second degradation process is oxidation, often photo-induced especially by exposure to light not filtered for uv. The radicals resulting from this reaction promote depolymerization of the cellulose, as well as yellowing and fa ding of paper and media. Aging causes paper to become more crystalline and fragile, and this can be exacerbated particularly if the paper is subjected to poor conditions. [Pg.428]

TetrabromophthalicAnhydride. Tetrabromophthalic anhydride [632-79-1] (TBPA) is widely used as a reactive flame retardant in unsaturated polyesters as weU as the precursor to a number of other fine retardants. Polyesters prepared from this compound have relatively poor photochemical stabiUty and tend to discolor upon exposure to light. This tendency to discolor can be reduced, but not eliminated, by the use of uv stabilizers. [Pg.470]

Color Centers. Characteristics of a color center (1,3,7) include production by irradiation and destmction by heating. Exposure to light or even merely time in the dark may be sufficient to destroy these centers. Color arises from light absorption either from an electron missing from a normally occupied position, ie, a hole color center, or from an extra electron, ie, an electron color center. If the electron is a valence electron of a transition element, the term color center is not usually used. [Pg.222]

Grades and Specifications. Two grades of phloroglucinol, ie, grades 2 and pure, are offered in the United States by Haake, Inc., who resell material made by Fisons (Table 1). The product discolors slowly on exposure to light. [Pg.384]


See other pages where Exposure to light is mentioned: [Pg.130]    [Pg.184]    [Pg.236]    [Pg.311]    [Pg.360]    [Pg.1379]    [Pg.208]    [Pg.212]    [Pg.599]    [Pg.637]    [Pg.641]    [Pg.838]    [Pg.1041]    [Pg.195]    [Pg.269]    [Pg.223]    [Pg.160]    [Pg.160]    [Pg.160]    [Pg.271]    [Pg.365]    [Pg.366]    [Pg.366]    [Pg.68]    [Pg.255]    [Pg.38]    [Pg.462]    [Pg.440]    [Pg.440]    [Pg.443]    [Pg.446]    [Pg.447]    [Pg.447]    [Pg.456]    [Pg.515]    [Pg.23]    [Pg.378]   
See also in sourсe #XX -- [ Pg.354 ]




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Color Changes Upon Exposure to Light

Effect of exposure to light

Exposure to light sources

Light exposure

TL and OSL after Exposure to UV Light

To light

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