Use of Glacial Acetic Acid in the Determination of Metol in Developer Solutions

1951 ◽  
Vol 57 (5) ◽  
pp. 411-415 ◽  
Author(s):  
William R. Crowell ◽  
Harvey E. Gausman ◽  
Harlan L. Baumbach
Keyword(s):  
Acetic Acid ◽  
Glacial Acetic Acid

Reverse Phase Liquid Chromatographic Determination of Chlorophacinone and Diphacinone in Bait Formulations

1982 ◽  
Vol 65 (4) ◽  
pp. 927-929
Author(s):  
Brian R Bennett ◽  
Gregory S Grimes
Keyword(s):  
Acetic Acid ◽  
Glacial Acetic Acid ◽  
Chromatographic Determination ◽  
Reverse Phase ◽  
Target Concentration ◽  
External Standard ◽  
Liquid Chromatographic Determination ◽  
Phase Liquid ◽  
Liquid Chromatographic

Abstract Chlorophacinone and diphacinone are extracted at the 0.005% level from grain or paraffinized baits with glacial acetic acid. The target concentration is 0.01 mg/mL. The filtered supernate is chromatographed on a Partisil PXS ODS10/25 liquid chromatography column with premixed and degassed glacial acetic acid-tetrahydrofuran-water (14 + 2 + 9) and detected at 288 nm. The concentration is calculated by using an external standard. The recovery from spiked samples averaged 96.6% for both analytes. The response is linear from 0.001 to 0.040 mg/mL. The coefficient of variation of within-day replicates ranged from 1.1 to 2.5%.

Method for the accurate determination of specific rotation. Specific rotation of valine and leucine

1969 ◽  
Vol 47 (15) ◽  
pp. 2739-2746 ◽  
Author(s):  
J. C. MacDonald
Keyword(s):  
Acetic Acid ◽  
Glacial Acetic Acid ◽  
Optical Rotation ◽  
Accurate Determination ◽  
Computer Calculation ◽  
Specific Rotation ◽  
Best Fit

The optical rotation of various concentrations of L-valine and L-leucine, dissolved in glacial acetic acid, or 5 or 6 M HCl, was measured with a photoelectric polarimeter at the nominal wavelengths 589, 578, 546, 436, and 365 nm and temperatures of 20, 25, and 30 °C. The specific rotation for any one wavelength, solute, and solvent could be defined by the equation [α]λT = A(1 + D(T − 25)) + BC, where T is temperature in °C, C is concentration in grams of solute per 100 ml of solution, and A, B, and D are constants. The best fit values of the constants were determined by computer calculation and are listed. Constants are also given for calculating a specific rotation based on grams of solute per 100 g of solution.

Determination of acetaldehyde in glacial acetic acid by gas chromatography

1974 ◽  
Vol 46 (11) ◽  
pp. 1584-1584 ◽  
Author(s):  
Harold J. Rhodes ◽  
David W. Bode ◽  
Martin I. Blake
Keyword(s):  
Gas Chromatography ◽  
Acetic Acid ◽  
Glacial Acetic Acid

Bromination of Acridine

2018 ◽  
Vol 71 (4) ◽  
pp. 285
Author(s):  
Graham S. Chandler ◽  
Wolfgang H. F. Sasse
Keyword(s):  
Acetic Acid ◽  
Sulfuric Acid ◽  
Quantitative Determination ◽  
Glacial Acetic Acid ◽  
Tiny Amount ◽  
Concentrated Sulfuric Acid

The quantitative determination of the products of bromination of acridine in concentrated sulfuric acid and glacial acetic acid is described. In both cases, the only monobromo products were the 2- and 4-substituted compounds. With sulfuric acid, the 4-isomer predominates whereas in acetic acid, the 2-isomer is predominant. This work expands substantially on the tiny amount of previous work on halogenation of dibenzo-annelated pyridines.

Rapid and Simple Determination of Oxyphenbutazone in Dosage Forms by Biamperometric Titration

1986 ◽  
Vol 69 (2) ◽  
pp. 191-192
Author(s):  
Daniela Šebková ◽  
Luděk Šafařík
Keyword(s):  
Acetic Acid ◽  
Hydrochloric Acid ◽  
Glacial Acetic Acid ◽  
Platinum Electrode ◽  
Potassium Bromide ◽  
Dosage Forms ◽  
End Point

Abstract Oxyphenbutazone was determined in the presence of glacial acetic acid, hydrochloric acid, and potassium bromide by bromometric titration with biamperometric end point indication. The course of the titration was followed with double platinum electrode with 100 mV of polarizing voltage

Iodimetric determinations in organic solvents: Determination of manganese oxidation states in methylene chloride solutions

1990 ◽  
Vol 68 (1) ◽  
pp. 79-81 ◽  
Author(s):  
Joaquin F. Perez-Benito ◽  
Enrique Brillas ◽  
Conchita Arias
Keyword(s):  
Acetic Acid ◽  
Quaternary Ammonium ◽  
Glacial Acetic Acid ◽  
Methylene Chloride ◽  
Oxidation States ◽  
Manganese Oxidation ◽  
Chloride Solutions ◽  
Tetrabutylammonium Iodide ◽  
Organic Solutions

An iodimetric technique has been developed to quantitatively analyze the oxidants present in organic solutions. Addition of excess tetrabutylammonium iodide and excess glacial acetic acid results in the formation of tetrabutylammonium triiodide, whose concentration can be measured spectrophotometrically at 295 or 365 nm. Application of this technique to the determination of the final oxidation state of manganese in permanganate reactions in methylene chloride solutions is described. The equilibrium constant for formation of tetrabutylammonium triiodide in methylene chloride has been measured: K = (3.48 ± 0.12) × 104 at 25.0 °C. Keywords: iodimetric determinations, manganese oxidation states, methylene chloride, quaternary ammonium permanganate, quaternary ammonium triiodide.

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