NEW COLOR REACTIONS OF SEDOHEPTULOSAN AND ITS DETERMINATION IN MIXTURES OF RIBOSE AND FRUCTOSE

1954 ◽  
Vol 32 (1) ◽  
pp. 14-18 ◽  
Author(s):  
L. Ujejski ◽  
E. R. Waygood

The reagents carbazole – sulphuric acid, cysteine hydrochloride – sulphuric acid, have been applied successfully to the quantitative colorimetric determination of sedoheptulosan in pure solution or in the presence of ribose and/or fructose. Fructose can be determined quantitatively in the presence of sedoheptulosan and/or ribose by using a combination of the two reagents. Results indicate that while sedoheptulose reacts differently to sedoheptulosan with the orcinol reagent, the reactions with carbazole and cysteine are not altered by hydration and these may form a basis for the determination of the naturally occurring seven carbon sugar sedoheptulose.


1949 ◽  
Vol 27b (7) ◽  
pp. 646-652 ◽  
Author(s):  
R. A. Dunford

The synthetic oestrogens, stilboestrol, hexoestrol, and dienoestrol give color reactions with nitric and nitrous acids, bromine, and certain phenol reagents, some of which can be adapted to their colorimetric determination. The use of Folin and Ciocalteu's phenol reagent is described for determination of the hormones in pharmaceutical products, using a Lumetron photoelectric colorimeter. The interference of other oestrogens and of phenolic preservatives and bactericides is considered and reference is made to a means of identifying the hormones by color reactions with antimony pentachloride in ethylene dichloride, and with an acetic – phosphoric acid reagent.



Author(s):  
L. H. N. Cooper

Phosphorus in plankton has been determined by digestion with sulphuric acid and perhydrol followed by colorimetric determination.Nitrogen has been readily determined by the micro-Kjeldahl method of Parnas and Wagner.



1970 ◽  
Vol 49 (2) ◽  
pp. 301-307 ◽  
Author(s):  
M.R.F. Ashworth ◽  
G. Cappel ◽  
E. Hammer


1928 ◽  
Vol 3 (7) ◽  
pp. 173-179 ◽  
Author(s):  
Junzô Yamazaki


1959 ◽  
Vol 36 (2) ◽  
pp. 193-201 ◽  
Author(s):  
Julius A. Goldbarg ◽  
Esteban P. Pineda ◽  
Benjamin M. Banks ◽  
Alexander M. Rutenburg


2013 ◽  
Vol 12 (7) ◽  
pp. 460-465
Author(s):  
Sameer Amereih ◽  
Zaher Barghouthi ◽  
Lamees Majjiad

A sensitive colorimetric determination of fluoride in drinking water has been developed using a polymeric zirconium complex of 5-(2-Carboxyphenylazo)-8-Hydroxyquinoline as fluoride reagents. The method allowed a reliable determination of fluoride in range of (0.0-1.5) mg L-1. The molar absorptivity of the complex formation is 7695 ± 27 L mol-1 cm-1 at 460 nm. The sensitivity, detection limit, quantitation limit, and percentage recovery for 1.0 mg L-1 fluoride for the proposed method were found to be 0.353 ± 0.013 μg mL-1, 0.1 mg L-1, 0.3 mg L-1, and 101.7 ± 4.1, respectively.



Author(s):  
Abbas Shebeeb Al-kadumi ◽  
Sahar Rihan Fadhel ◽  
Mohammed Abdullah Ahmed ◽  
Luma Amer Musa

We proposed two simple, rapid, and convenient spectrophotometric methods are described for the determination of Amoxicillin in bulk and its pharmaceutical preparations. They are based on the measurement of the flame atomic emission of potassium ion (in first method) and colorimetric determination of the green colored solution for manganite ion at 610 nm formed after reaction of Amoxicillin with potassium permanganate as oxidant agent (in the second method) in basic medium. The working conditions of the methods were investigated and optimized. Beer's law plot showed a good correlation in the concentration range of 5-45 μg/ml. The detection limits and relative standared deviations were (2.573, 2.814 μg/ml) (2.137, 2.498) for the flame emission photometric method and (1.844, 2.016 μg/ml) (1.645,1.932) for colorimetric methods for capsules and suspensions respectively. The methods were successfully applied to the determination of Amoxicillin in capsules and suspensions, and the obtained results were in good agreement with the label claim. No interference was observed from the commonly encountered additives and expectancies.



Kerntechnik ◽  
2008 ◽  
Vol 73 (3) ◽  
pp. 118-121
Author(s):  
T. Heinrich ◽  
L. Funke ◽  
M. Köhler ◽  
U.-K. Schkade ◽  
F. Ullrich ◽  
...  


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