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Lead sugar

Preparation of Lead(Il) Acetate (Lead Sugar). Dissolve 3 g of lead(II) oxide in a calculated amount of a hot 50% acetic acid solution. Filter the solution, and add 1 ml of acetic acid with the same concentration to the filtrate. Evaporate the latter up to half of its initial volume and let it stand for crystallization. Separate the crystals from the mother liquor on a Buchner funnel and wash them with small portions of ethanol, and then with ether (for what purpose ), What is the composition of the product ... [Pg.271]

Heat a small part of the crystals in a dry test tube, first carefully, and then more strongly (280 °C). What happens to the lead acetate in the air and when heated Can lead sugar be dried in a desiccator over sulphuric acid ... [Pg.271]

Lead(fl) ethanoate, Pb(02CCH3)2,3H20, sugar of lead. Soluble in water (ethanoic acid and ethanoic anhydride plus Pb304). [Pg.237]

Lead formate is only slightly soluble in cold water, and insoluble in hot absolute ethanol it can therefore be readily distinguished from lead acetate or sugar of lead because, quite apart from chemical tests, the acetate is readily soluble in cold water and moderately soluble in ethanol. [Pg.114]

Acetone was originally observed about 1595 as a product of the distillation of sugar of lead (lead acetate). In the nineteenth century it was obtained by the destmctive distillation of metal acetates, wood, and carbohydrates with lime, and pyrolysis of citric acid. Its composition was determined by Liebig and Dumas in 1832. [Pg.94]

Phenylalanine- and Tyrosine-Derived Alkaloids. Carbohydrate metaboHsm leads via a seven-carbon sugar, ie, a heptulose, derivative to shikimic acid [138-59-0] (57), C H qO, which leads in turn to prephenic acid [126-49-8] (58), (43). [Pg.539]

NIDDM is a much more common disease than IDDM, accounting for about 85—90% of all cases of diabetes meUitus. Whereas NIDDM may be present at any age, the incidence increases dramatically with advanced age over 10% of the population reaching 70 years of age has NIDDM. Patients with NIDDM do not require insulin treatment to maintain life or prevent the spontaneous occurrence of diabetic ketoacidosis. Therefore, NIDDM is frequendy asymptomatic and unrecognized, and diagnosis requires screening for elevations in blood or urinary sugar. Most forms of NIDDM are associated with a family history of the disease, and NIDDM is commonly associated with and exacerbated by obesity. The causes of NIDDM are not well understood and there may be many molecular defects which lead to NIDDM. [Pg.338]

Basic Lead Acetate. Basic lead acetate [1335-32-6] (lead subacetate), 2Pb(0H)2-Pb(C2H3 02 )2, is a heavy white powder which is used for sugar analyses. Some physical properties are given in Table 4. Reagent grade is available in 11.3-kg cartons and in 45- and 147-kg fiber dmms. [Pg.71]

At least six specifications of standards for granulated sugar quaUty are appHcable ia the United States. These include Codex JUimentarius Food Chemicals Codex (ECC) (4), US. Pharmacopeia (USP) and National Formula (NE) (5), National Soft Drink Association (6), National Canners Association, and Mihtary Standard-900 for white sugar. These standards are intended to set limits on various components, including, but not necessarily limited to, polarization, invert or reducing sugar, ash, moisture, color, sulfur dioxide, arsenic, lead, and copper. [Pg.9]

Sugar analysis by hplc has advanced greatly as a result of the development of columns specifically designed for carbohydrate separation. These columns fall into several categories. (/) Aminopropyl-bonded siHca used in reverse-phase mode with acetonitrile—water as the eluent. (2) Ion-moderated cation-exchange resins using water as the eluent. Efficiency of these columns is enhanced at elevated temperature, ca 80—90°C. Calcium is the usual counterion for carbohydrate analysis, but lead, silver, hydrogen, sodium, and potassium are used to confer specific selectivities for mono-, di-, and... [Pg.10]

Moisture. Moisture is usually determined by a vacuum oven-dry method at 80°C. Moisture levels of more than 0.05% are likely to lead to caking or lumping problems which can make storage and transfer of bulk sugar difficult. The usual standard is 0.03%, which manufacturers can easily meet. Care must be taken to avoid temperature differentials ia storage which cause moisture to migra te and estabUsh pockets of unacceptably high moisture levels. [Pg.30]

Etherification. The reaction of alkyl haUdes with sugar polyols in the presence of aqueous alkaline reagents generally results in partial etherification. Thus, a tetraaHyl ether is formed on reaction of D-mannitol with aHyl bromide in the presence of 20% sodium hydroxide at 75°C (124). Treatment of this partial ether with metallic sodium to form an alcoholate, followed by reaction with additional aHyl bromide, leads to hexaaHyl D-mannitol (125). Complete methylation of D-mannitol occurs, however, by the action of dimethyl sulfate and sodium hydroxide (126). A mixture of tetra- and pentabutyloxymethyl ethers of D-mannitol results from the action of butyl chloromethyl ether (127). Completely substituted trimethylsilyl derivatives of polyols, distillable in vacuo, are prepared by interaction with trim ethyl chi oro s il an e in the presence of pyridine (128). Hexavinylmannitol is obtained from D-mannitol and acetylene at 25.31 MPa (250 atm) and 160°C (129). [Pg.51]


See other pages where Lead sugar is mentioned: [Pg.3]    [Pg.3]    [Pg.400]    [Pg.2]    [Pg.15]    [Pg.749]    [Pg.1189]    [Pg.149]    [Pg.58]    [Pg.315]    [Pg.63]    [Pg.165]    [Pg.3]    [Pg.3]    [Pg.400]    [Pg.2]    [Pg.15]    [Pg.749]    [Pg.1189]    [Pg.149]    [Pg.58]    [Pg.315]    [Pg.63]    [Pg.165]    [Pg.376]    [Pg.275]    [Pg.69]    [Pg.424]    [Pg.449]    [Pg.42]    [Pg.208]    [Pg.71]    [Pg.71]    [Pg.296]    [Pg.482]    [Pg.537]    [Pg.251]    [Pg.9]    [Pg.9]    [Pg.14]    [Pg.24]    [Pg.27]    [Pg.27]    [Pg.29]    [Pg.49]    [Pg.50]   
See also in sourсe #XX -- [ Pg.149 ]




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Lead acetate sugar

Lead hydroxide, reaction with sugars

Lead tetraacetate action of, on the sugars

Oxidation lead tetraacetate, of sugars

Perlin, A. S., Action of Lead Tetraacetate on the Sugars

Sugar of lead

Sugars action of lead tetraacetate

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