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Ammonia assay

El30 Sundberg, M.W., Becker, R.W., Esders, T.W., Figueras, J. and Goodhue, C.T. (1983). An enzymic creatinine assay and a direct ammonia assay in coated thin films. Clin. Chem. 29,645-649. [Pg.278]

E527 Kirk, J.M. (1989). Probable cefotaxime interference in enzymatic ammonia assay - A cautionary note. Ann. Qin. Biochem. 26,195-196. [Pg.300]

E610 Fricker, R., Doptis, P., Hornak, M. and Li, C. (1990). Development of an optimized ammonia assay for the Kodak Ektachem analyzer. Clin. Chem. 56, 1072, Abstr. 561. [Pg.305]

EN81 Bach, P.R. (1992). Interfering reactions in an ammonia assay using glutamate dehydrogenase. Clin. Chem. 38, 1024, Abstr. 383. [Pg.315]

Yamaguchi F, Etoh T, Takahashi M, Misaki H, Sakuraba H, Ohshiraa T. A new enzymatic cycling method for ammonia assay using NAD synthetase. Clin Chim Acta 2005 352 165-73. [Pg.1847]

Analytical Procedures. Standard methods for analysis of food-grade adipic acid are described ia the Food Chemicals Codex (see Refs, ia Table 8). Classical methods are used for assay (titration), trace metals (As, heavy metals as Pb), and total ash. Water is determined by Kad-Fisher titration of a methanol solution of the acid. Determination of color ia methanol solution (APHA, Hazen equivalent, max. 10), as well as iron and other metals, are also described elsewhere (175). Other analyses frequendy are required for resia-grade acid. For example, hydrolyzable nitrogen (NH, amides, nitriles, etc) is determined by distillation of ammonia from an alkaline solution. Reducible nitrogen (nitrates and nitroorganics) may then be determined by adding DeVarda s alloy and continuing the distillation. Hydrocarbon oil contaminants may be determined by ir analysis of halocarbon extracts of alkaline solutions of the acid. [Pg.246]

CoF is used for the replacement of hydrogen with fluorine in halocarbons (5) for fluorination of xylylalkanes, used in vapor-phase soldering fluxes (6) formation of dibutyl decalins (7) fluorination of alkynes (8) synthesis of unsaturated or partially fluorinated compounds (9—11) and conversion of aromatic compounds to perfluorocycHc compounds (see Fluorine compounds, organic). CoF rarely causes polymerization of hydrocarbons. CoF is also used for the conversion of metal oxides to higher valency metal fluorides, eg, in the assay of uranium ore (12). It is also used in the manufacture of nitrogen fluoride, NF, from ammonia (13). [Pg.178]

Manufacture, Shipment, and Analysis. In the United States, sodium and potassium thiocyanates are made by adding caustic soda or potash to ammonium thiocyanate, followed by evaporation of the ammonia and water. The products are sold either as 50—55 wt % aqueous solutions, in the case of sodium thiocyanate, or as the crystalline soHds with one grade containing 5 wt % water and a higher assay grade containing a maximum of 2 wt % water. In Europe, the thiocyanates may be made by direct sulfurization of the corresponding cyanide. The acute LD q (rat, oral) of sodium thiocyanate is 764 mg/kg, accompanied by convulsions and respiratory failure LD q (mouse, oral) is 362 mg/kg. The lowest pubhshed toxic dose for potassium thiocyanate is 80—428 mg/kg, with hallucinations, convulsions, or muscular weakness. The acute LD q (rat, oral) for potassium thiocyanate is 854 mg/kg, with convulsions and respiratory failure. [Pg.152]

ThioglycoHc acid can be identified by its in spectmm or by gas chromatography. Most of the by-products and self-esterification products are also detected by liquid chromatography, eg, thiodiglycolic acid, dithiodiglycolic acid, linear dimers, and polymers. Iron content can be assayed by the red sensitive complex of 1,10-phenanthroline [66-71-7] and ferrous ion of a mineralised sample. Ferric ion turns an aqueous ammonia solution deep red-violet. [Pg.4]

Reduction. Triaryknethane dyes are reduced readily to leuco bases with a variety of reagents, including sodium hydrosulfite, 2inc and acid (hydrochloric, acetic), 2inc dust and ammonia, and titanous chloride in concentrated hydrochloric acid. Reduction with titanium trichloride (Knecht method) is used for rapidly assaying triaryknethane dyes. The TiCl titration is carried out to a colorless end point which is usually very sharp (see Titanium COMPOUNDS, inorganic). [Pg.269]

Cyanuric acid can also be prepared by pyrolysis of urea derivatives. Biuret and triuret give less aminotria ines due to reduced ammonia evolution. Urea cyanurate also provides a higher assay product. [Pg.420]

A solution of 2.25 g (25 mmol) of D-glyccraldehyde in 300 mL of water is combined with a solution of 20 mmol of dihydroxyacetonc phosphate (DIIAP) in 200 mL of water freshly adjusted to pH 6.8. The mixture is incubated with 100 U of L-rhamnulose 1-phosphate aldolase at r.t. for 24 h with monitoring of conversion by TLC (2-propanol/sat. ammonia/water 6 4 2) and by enzymatic assay for DHAP55. [Pg.589]

Urease assay. When Proteus mirabilis grows in a urea-containing medium it hydrolyses the urea to ammonia and consequently raises the pH of the medium. This production of urease is inhibited by aminoglycoside antibiotics (inhibitors of protein synthesis Chapter 8). In practice, it is difficult to obtain reliable results by this method. [Pg.481]

The metabolic and pharmacokinetic profile of sucralose (this is a novel intense sweetener with a potency about 600 times that of sucrose) in human volunteers was studied by Roberts and coworkers [82]. Part of this study was realized using PLC in the following chromatographic system in which the stationary phase was silica gel and the mobile phase was ethyl acetate-methanol-water-concentrated ammonia (60 20 10 2, v/v). Separated substances were scraped off separately, suspended in methanol, and analyzed by filtration, scintillation counting, or enzymatic assay. It was shown that the characteristics of sucralose include poor absorption, rapid elimination, limited conjugative metabolism of the fraction absorbed, and lack of bio-accumulative potential. [Pg.223]

Normal phase silica column Chloroform-methanol-ammonia solution (86.8 12.5 0.7) 254 nm Assay of primaquine and hepatic targeting neoglycoalbumin-primaquine in whole blood and liver of mouse by reversed-phase HPLC. [105]... [Pg.193]

In a different approach a super-high-throughput ee-assay was developed on the basis of chirally modified capillary array electrophoresis (CAE).90 CAE was used in the Human Genome Project, and commercially available instruments have been developed which comprise a high number of capillaries in parallel, for example the 96-capillary unit MegaBACE consisting of 6 bundles of 16 capillaries.91 The system can address a 96-well microtiter plate. It was adapted to perform ee-determinations of chiral amines, which are potentially accessible by catalytic reductive amination of ketones, transition metal catalyzed Markovnikov addition of ammonia, or enzymatic hydrolysis of acetamides (Scheme 14).90... [Pg.529]

A specific assay of bromocriptine mesilate in the dosage form may be carried out by tic followed by uv-spectrophotometry (26)(The system can also serve for identification purposes). The drug substance is extracted with methanol in the absence of light, the chromatographic conditions are Merck plates F 254, mobile phase dichloromethane/dioxane/ ethanol abs./conc. ammonia 180 15 5 0.1 per volume. [Pg.77]

Note also that ammonium sulfate is absent from the recommended binding buffer formulations despite its general popularity in the field. Ammonium ions become fully titrated at alkaline pH and convert to ammonia gas. Buffer pH may become unstable as a result and causticity of the free ammonia may partially hydrolyze the proteins in a sample, creating a source of assay variability.617 18 At small buffer volumes used for analytical applications, liberated ammonia gas may not be a significant health hazard, but precautions may still be necessary to meet regulations. For all these reasons, ammonium salts are best avoided at alkaline pH. [Pg.88]

No evidence of mutagenicity was seen in Ames bacterial assays. Diethylamine has an ammonia-like odor that is detectable at... [Pg.248]

Reflectance measurements provided an excellent means for building an ammonium ion sensor involving immobilization of a colorimetric acid-base indicator in the flow-cell depicted schematically in Fig. 3.38.C. The cell was furnished with a microporous PTFE membrane supported on the inner surface of the light window. The detection limit achieved was found to depend on the constant of the immobilized acid-base indicator used it was lO M for /7-Xylenol Blue (pAT, = 2.0). The response time was related to the ammonium ion concentration and ranged from 1 to 60 min. The sensor remained stable for over 6 months and was used to determine the analyte in real samples consisting of purified waste water, which was taken from a tank where the water was collected for release into the mimicipal waste water treatment plant. Since no significant interference fi-om acid compounds such as carbon dioxide or acetic acid was encountered, the sensor proved to be applicable to real samples after pH adjustment. The ammonium concentrations provided by the sensor were consistent with those obtained by ion chromatography, a spectrophotometric assay and an ammonia-selective electrode [269]. [Pg.184]

Urease. An enzyme of the hydrolase class that catalyzes the hydrolysis of urea to COj and ammonia. It is nickel protein found in micro-organisms and plant that is frequently used in clinical assays of plasma urea concentrations. [Pg.578]

Combination of the A and B chains 8,11 involved deprotection of Cys(Bzl), Lys(Tos), and Arg(Tos) or Arg(N02) by sodium in liquid ammonia and slow air oxidation to form the intrachain A6-An disulfide and the two interchain A7-B7 and A20-B19 disulfides. In some experiments, the 5-sulfonates were utilized for combination of the chains. All three syntheses produced material with insulin activity in the mouse convulsion assay or the glucose oxidation assay. [Pg.6]

Fig. 2.1.2a-c A Urine amino acids in a patient with cystinuria assayed by an amino acid analyzer (AAA). The indicated peaks are 1 glycine, 2 cystine, 3 ammonia, 4 ornithine, 5 lysine, 6 arginine, i.s. internal standard (S-amino thyl-cysteine). Cystinuria treatment is best followed-up by analyzing an early morning urine specimen, which usually shows the highest amino acid concentrations. b-c see next page... [Pg.66]


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