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Stock Solutions preparation

Stock solution. Prepare a 200- ug mL stock solution in ACN Fortification solutions. Prepare 0.04 and 0.2 lagmL fortification solutions by dilution of the stock solution in acetonitrile (trinexapac-ethyl). Prepare 0.05 and 0.25 j.gmL fortification solutions by dilution of the stock solution in water (trinexapac). [Pg.593]

The major problem with the intravenous route in children is dosing errors. Because of the unavailability of stock solutions prepared for pediatric doses, errors in dilution of an adult stock solution have resulted in 10- to 20-fold errors in administered doses [87,88], A secondary problem is the maintenance of patent intravenous lines in infants and nonsedated children. [Pg.673]

Place about 25 mL of the stock solution, prepared as directed in the Assay, in a 50 mL beaker, and evaporate on a steam bath with the aid of a current of filtered air to dryness. Dry the residue at 105 °C for 10 min the infrared absorption spectrum of a potassium bromide dispersion of it so obtained exhibits maxima only at the same wavelengths as that of similar preparations of USP Miconazole Nitrate RS. [Pg.34]

SMPB contains a hydrophobic cross-bridge and relatively nonpolar ends, which allows the reagent to permeate membrane structures. Due to its water-insolubility, it must be dissolved in an organic solvent prior to adding an aliquot to a reaction mixture. The solvents DMF and DMSO work well for this purpose. A concentrated stock solution prepared in these solvents allows for easy addition of a small amount to a conjugation reaction. Long-term storage in these solvents is not recommended due to slow water pickup and possible hydrolysis of the NHS ester end. [Pg.291]

Prepare five identical dilutions of the stock solution prepared in step 1 by diluting 10 mL of the solution to 100 mL. Use a clean 10-mL volumetric pipet and a clean 100-mL volumetric flask, and make the measurement and transfer as carefully as possible (see Table 4.1). Label each as 2/1, 2/2, etc., to indicate that they are solutions 1 to 5 prepared in step 2. [Pg.93]

Prepare four calibration standards with concentrations of 0.0435,0.0870,0.174, and 0.261 g/L in the alkane solvent by diluting the stock solution prepared in step 1. Use the 25-mL volumetric flasks prepared in step 1. [Pg.234]

Nitrite stock solution. Prepare a 10 mg/L NOj stock solution of potassium nitrite. [Pg.330]

From this stock solution, prepare four standard solutions, using methanol as the solvent, having concentrations of 0.05,0.1,0.15, and 0.2 mg of methyl paraben per milliliter, in 50-mL volumetric flasks. Filter these solutions into vials as you did the sample in Part A. [Pg.387]

From the stock solutions, prepare a mixture of 10 pg PI and 10 U RNaseA in a total volume of 1 mL PBS. Add it to the isolated nuclear suspension. [Pg.277]

Freshly distilled diglyme (5 g, 37.3 mmol) is added to a diethyl ether stock solution prepared as described in Section 11. A. The resulting solution is concentrated on a rotary evaporator at room temperature to a final volume of 25 ruL. A copious mass of yellow crystals forms in the process. The solid is collected by vacuum filtration, washed with two 5-mL portions of diethyl ether, and dried under mild vacuum, lypical yield, with regard to the initial molybdate, is 7.0 g (74%). A second crop of crystals is obtained by concentrating the combined mother liquor and washings, followed by cooling at — 30°C for 2 h. Overall yield 8.5 g (90%). [Pg.51]

Stock solutions Prepare stock solutions A to E using the amounts indicated below. Measure each component to the nearest 0.1 mg and add to a 100-ml volumetric flask. Bring to volume with HPLC-grade water and mix well. Store up to 1 month at 4°C. Stock solution A 200 mg tartaric acid, 150 mg each acetic, isocitric, and lactic acid. Stock solution B 1.000 g L(-)-malic acid. [Pg.1125]

B. From the stock solution prepare solutions containing 10, 20, 30, 50, and 75 mg of naringin per 100 ml of distilled water. [Pg.305]

Dilute 10 mL of stock solution prepared above to 1L. The strength of this secondary standard is 10 mg NH3-N/L or 1 mL = 10 pg NH3-N = 12.2 pg NH3. Prepare a series of Nessler tube standards as follows ... [Pg.175]

A solution of 125ug/LAs(V) in deionized water was prepared by serial dilution of a 1,000 mg/L As(V) stock solution prepared from As205. This solution and the synthetic Grande Ronde groundwater were air-saturated. [Pg.181]

System Suitability Preparation - Pipet 5 ml of the stock solution, prepared as directed under Standard preparation, into a 25-ml volumetric flask, dilute with isooctane to volume, and mix. Heat this solution at reflux for 2 hours, cool, and irradiate for 1 hour under long-wavelength and short-wavelength ultraviolet light. This solution contains cholecalciferol, pre-cholecalciferol, and tachysterol. [Pg.692]

Preparation of DHPC stock solution. Prepare a stock solution of the detergent in water (or D20 if desired for NMR purposes). A 1M solution of DHPC is convenient for preparing bicelles with a total lipid (phospholipids + detergent) concentration of 300 mM (see Note 6). [Pg.135]

To minimize errors occurring when weighing the compounds, HEPES-buffered HBSS may be prepared from three stock solutions. Prepare 1L lOx stock no. 1... [Pg.161]

Dissolve 5.7194 g of H3B03 in water and dilute to 11 to yield a 1.000 g Bl-1 stock solution. Prepare a 100/xgBml-1 stock solution by diluting 100 ml of the 1.000 g Bml-1 stock solution to 11 in a volumetric flask. [Pg.312]

A) Preparation of Diazoaminobenzene. Place in a 150-ml beaker 5 ml of water, 1 ml of aniline, and 1 ml of concentrated hydrochloric acid. Stir, and add 15 ml (0.015 moles) of the benzenediazonium chloride stock solution prepared in Experiment 53 (C). Add 1.5 ml of Q N sodium hydroxide solution drop by drop while stirring. Allow to stand, and proceed with section (B). Later filter the compound, wash several times with water, press, and remove to paper to dry. The yield is 1.8-2.2 g. [Pg.286]

Trypan Blue. Stock solution 1 % trypan blue in distilled water filter and store at 4°C. After 2 to 3 weeks precipitates will form which may greatly falsify the interpretation of dye-uptake into the cells. Working solution 9 volumes LC -i-1 volume trypan blue stock solution prepare just before the experiment and keep at 37°C. [Pg.225]

M CaCl2 stock solution prepare by dissolving 1.47 g CaCb x 2H2O in 10 ml of distilled water. [Pg.264]

GSSG (Sigma) 100 M stock solution Prepare a 0.1 M solution (0.328g GSSG/ 5 mL phosphate buffer) and dilute 1 1000 to 1001aM with phosphate buffer. [Pg.85]

Using your Cr aqueous stock solution prepare a solution of approximately 5 x 10-5 m [Cr(phen)3]3+ (aq) in 50 mM Tris-HCl buffer, determining the actual concentration as precisely as possible. Obtain a UV-vis spectrum and a luminescence spectrum of this solution. [Pg.207]


See other pages where Stock Solutions preparation is mentioned: [Pg.260]    [Pg.181]    [Pg.316]    [Pg.319]    [Pg.245]    [Pg.278]    [Pg.150]    [Pg.16]    [Pg.263]    [Pg.286]    [Pg.290]    [Pg.188]    [Pg.44]    [Pg.331]    [Pg.509]    [Pg.291]    [Pg.229]    [Pg.158]    [Pg.16]    [Pg.245]    [Pg.246]    [Pg.246]    [Pg.264]    [Pg.126]   
See also in sourсe #XX -- [ Pg.30 , Pg.31 ]




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