Sulfate, cupric

Chemical dosimeters based on ferrous sulfate, ferrous cupric sulfate, or ceric sulfate are generally used. Color-change process indicators are also used, but these cannot measure the radiation dose, only the extent of sterilization. 

Colorimetric Methods. Numerous colorimetric methods exist for the quantitative determination of carbohydrates as a group (8). Among the most popular of these is the phenol—sulfuric acid method of Dubois (9), which rehes on the color formed when a carbohydrate reacts with phenol in the presence of hot sulfuric acid. The test is sensitive for virtually all classes of carbohydrates. Colorimetric methods are usually employed when a very small concentration of carbohydrate is present, and are often used in clinical situations. The Somogyi method, of which there are many variations, rehes on the reduction of cupric sulfate to cuprous oxide and is appHcable to reducing sugars. 

Technical-grade dimethylformamide is stirred over anhydrous cupric sulfate, filtered, and distilled under reduced pressure. The submitters used reagent-grade dimethylformamide without purifieation. 

CUPRIC CHLORATE CUPRIC CHLORIDE CUPRIC NITRATE CUPRIC OXALATE CUPRIC SULFATE... 

CUPRIC SULFATE, AMMONIATED CUPRIC TARTRATE CUPRIETHYLENEDIAMINE... 

ChemicalDesignations-Synonym Blue Vitriol Copper Sulfate Pentahydrate Cupric Sulfate Sulfate of Copper Chemical Formula CuS04-5Hj0. 

A combination of the preceding type of synthesis and of cyclization of 4-amino-5-arylazopyrimidine can be seen in the novel procedure of Richter and Taylor. Proceeding from phenylazomalonamide-amidine hydrochloride (180), they actually close both rings in this synthesis. The pyrimidine ring (183) is closed by formamide, the triazole (181) one by oxidative cyclization in the presence of cupric sulfate. Both possible sequences of cyclization were used. The synthetic possibilities of this procedure follow from the combination of the two parts. The synthesis was used for 7-substituted 2-phenyl-l,2,3-triazolo[4,5-d]-pyrimidines (184, 185). An analogous procedure was employed to prepare the 7-amino derivatives (188) from phenylazomalondiamidine (186). 

Attempts to obtain 5-nitro-l,7-naphthyridine and 3,6-dinitro-l,8-naph-thyridine (83) from the corresponding 8-chloro-5-nitro-l,7-naphthyridine and 2-chloro-3,6-dinitro-l,8-naphthyridine using the similar reaction failed (85JHC761 98MI2). However, 3,6-dinitro-l,8-naphthyridine (83) could be prepared in 21% yield by hydrazino-dechlorination of 2-chloro-3,6-dinitro-1,8-naphthyridine (82) and subsequent cupric sulfate oxidation of the intermediate 2-hydrazino-3,6-dinitro-l,8-naphthyridine (93LA471). 

Triazolo[4,5-/i]quinoline 143 and triazolo[4,5-/i]quinoline-5-arsonic acid 144 were isolated from mother liquors after reduction and bis-diazotization of 5,7-dinitro-8-(4-toluenesulfone)aminoquinoline in the presence of cupric sulfate with trisodium arsenite (32JCS2196). 

Cupri-. cupric, copper(II). -azetst, n. cupric acetate, copper(II) acetate, -carbonat, n. cupric carbonate, copper(II) carbonate, -chlorid, n. cupric chloride, copper(II) chloride. -hydroxyd, n. cupric hydroxide, cop-per(II) hydroxide. -ion, n. cupric ion, copper(II) ion. -ozalat, n. cupric oxalate, copper(II) oxalate, -oxyd, n. cupric oxide, copper(II) oxide. -salz, n. cupric salt, copper(II) salt, -suifat, n. cupric sulfate. copper(II) sulfate, -sulfid, n. cupric sulfide, copper(II) sulfide, -verbihdung, /. cupric compound, copper(II) compound, -wein-saure, /. cupritartaric acid. 

The increase in production due to the addition of riboflavin was very noticeable in the above example. A similar effect was reported for cupric sulfate pentahydrate addition according to U.S. Patent 3,050,446. 

Kondo maintained his interest in this area, and with his collaborators [62] he recently made detailed investigations on the polymerization and preparation of methyl-4-vinylphenyl-sulfonium bis-(methoxycarbonyl) meth-ylide (Scheme 27) as a new kind of stable vinyl monomer containing the sulfonium ylide structure. It was prepared by heating a solution of 4-methylthiostyrene, dimethyl-diazomalonate, and /-butyl catechol in chlorobenzene at 90°C for 10 h in the presence of anhydride cupric sulfate, and Scheme 27 was polymerized by using a, a -azobisi-sobutyronitrile (AIBN) as the initiator and dimethylsulf-oxide as the solvent at 60°C. The structure of the polymer was confirmed by IR and NMR spectra and elemental analysis. In addition, this monomeric ylide was copolymerized with vinyl monomers such as methyl methacrylate (MMA) and styrene. 

Of the four possible 5-deoxy-pent-4-enofuranoses, the D-erythro-isomer was of interest as a potential source of derivatives of L-lyxofuranose. For this purpose, a vinyl ether having the D-en/ hro-configuration has been prepared from derivatives of D-ribose. Condensation of D-ribose with acetone in the presence of methanol, cupric sulfate and sulfuric acid at 30°C., as described by Levene and Stiller(30) afforded a sirupy product consisting mainly of methyl 2,3-O-isopropylidene-D-ribofuranose (40). Treatment of a pyridine solution of the sirup with tosyl chloride... 

The completion of the synthesis of key intermediate 2 requires only a straightforward sequence of functional group manipulations. In the presence of acetone, cupric sulfate, and camphorsulfonic acid (CSA), the lactol and secondary hydroxyl groups in 10 are simultaneously protected as an acetonide (see intermediate 9). The overall yield of 9 is 55 % from 13. Cleavage of the benzyl ether in 9 with lithium metal in liquid ammonia furnishes a diol (98% yield) which is subsequently converted to selenide 20 according to Grie-co s procedure22 (see Scheme 6a). Oxidation of the selenium atom... 

Irradiation Conditions. The gamma (cobalt-60) radiation facility and the source calibration are described by Holm and Jarrett (4). Irradiation doses were 3-4 Mrad and 6-7.5 Mrad at 9 X 102 rads per second for the screening study. Irradiation temperatures were 5, —30, and — 90°C. The gamma source was calibrated with the ferrous sulfate-cupric sulfate dosimeter. 

The CuCl precipitate was obtained by mixing an aqueous solution of cupric sulfate and sodium sulfite to produce the reactions ... 

Densification is also influenced by the presence of supporting electrolyte. As shown in the last line of Table II, the relative densification in acidified cupric sulfate is less than that in binary cupric sulfate solution. In the case of the supported redox reaction, that is, in the presence of KOH or NaOH, the migration effect makes the density difference larger than that expected from overall reaction stoichiometry. 

A SELECTIVE, HETEROGENEOUS OXIDATION USING A MIXTURE OF POTASSIUM PERMANGANATE AND CUPRIC SULFATE (3aS,7aR)-HEXAHYDRO-(3S,6R)-DIMETHYL-2(3H)-BENZOFURANONE (2(3H)-Benzofuranone, hexahydro-3,6-dimethyl-,... 

Chemical and other names Copper Cupric sulfate, blue vitriol, cupric sulfate, Roman vitriol, Salzburg vitriol, blue copperas, copper (II) sulfate)... 

Patio [Spanish, a courtyard] A medieval process for extracting silver from argentite, Ag2S. The ore was mixed with salt, mercury, and roasted pyrites, which contains cupric sulfate. This mixture was crashed by stones dragged by mules walking on the paved floor of a courtyard. The overall reactions are ... 

Russell A process for extracting silver from aigentite, Ag2S, using a solution of sodium thiosulfate and cupric sulfate. Invented by E. H. Russell in 1884, following his use of this solution to remove sodium sulfide from soda ash. 

Pseudoephedrine hydrochloride in syrup formulations has been analyzed by colorimetry. Pseudoephedrine forms a stable blue-colored chelate with cupric sulfate at pH 12.5. The complex has a maximum absorbance at 500 nm. The complex is extracted from an aqueous layer with 1-pentanol. Interfering substances such as glycerine and sugars normally found in syrup formulations, which form complexes with cupric sulfate, are not extracted into 1-pentanol.21... 

A number of 2H-1,2,3-triazole 1-oxides 72 were prepared by chemists at the Cassella Company as potential NO-donors in view of their formal structural similarity with furoxan derivatives [18]. Derivative 72a was studied in depth. It was obtained by cupric sulfate oxidation of intermediate 79, derived from the action of the substituted phenylhydrazine 78 on the oximino acetoacetic acid amide 77 (Scheme 6.13). 

To prepare the 3-nonene-2-one condense excess acetone with n-hexaldehyde (or 2,3-dimethyloctanal for 5,6-dimethyl-undec-3-ene-2-one) in the presence of NaOH in an inert medium if desired (benzene, toluene, xylene, etc.), at 10-70° C to get (T). Dehydrate (I) with sodium sulfate or cupric sulfate in an inert medium at reflux temperature or simply reflux in benzene, xylene or toluene. 

Polymerizations were carried out in a jacketed, 1-gal, stirred, pressure tank reactor. Typical reactions were run by adding water, alcohol, or chain transfer agent, phosphate buffer, and persulfate to the reactor. The reactor was pressurized with CTFE monomer. Sulfite solution was fed at a rate to maintain reaction. Copper and iron ions were used at times as catalysts by adding cupric sulfate or ferrous sulfate.3 The product was filtered, washed with 90 10 water methanol followed with deionized water. The product was dried at 110°C. 

Sodium Nitrotetrazolate Dihydrate (NaNT) Anhydrous aminotetra-zole (8.48 g, 0.10 mol) and copper sulfate pentahydrate (0.2 g, 0.8 mmol) were added to a solution of nitric acid (9 mL, 65 %) in distilled water (60 mL). This was added to a pre-cooled solution of sodium nitrite (20.8 g, 0.30 mol) and cupric sulfate pentahydrate (11 g, 0.044 mol) in distilled water (100 mL). The solution was maintained at 15 to 18 °C during the addition by means of a cool water bath. After addition, the solution was stirred for 30 min at the same temperature... 

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