scholarly journals Methods of Quantitative Determination of Catechol in Cigarette Smoke Condensate/Methoden der quantitativen Bestimmung des Brenzcatechins im Cigarettenrauch

Author(s):  
P. Waltz ◽  
M. Häusermann ◽  
A. Krull

AbstractThree methods of quantitative determination of catechol in cigarette smoke condensate are presented. The procedures are based on:a.Column chromatography of a smoke condensate solution in chloroform over polyamide powder, followed by elution with ethyl acetate and a spectrophotometric measure in methanol solution;b.Liquid-liquid partitions of the smoke condensate, followed by a spectrophotometric measure based on a bathochromic shift of the absorption spectrum of catechol; andc.Vapour-phase chromatography of the phenolic smoke components in the form of their methyl ethers. The procedure a. is best suited as a routine method, as it is easy to execute and gives fairly accurate and precise results. The procedures b. and c. both give less reproducible results, and c. shows insufficient analytical yields. Their advantages are the rapid execution of method b. and the high specificity of method c.Contents between 200 and 500 µg of catechol per cigarette were found in the smoke of cigarettes.

1972 ◽  
Vol 55 (6) ◽  
pp. 1226-1227
Author(s):  
Mark A Litchman ◽  
Lewis A Turano ◽  
Ronald P Upton

Abstract A method is described for the quantitative determination of hexane in modified hop extract by head-space gas-liquid chromatography. A sample of extract is weighed into a serum vial and water-methanol solution is added. The vial is sealed tightly and heated 1 hr in a 70°C bath. A sample of the head-space gas over the solution is injected onto a Porapak Q gas chromatographic column for determination. Recovery of 2–29 ppm hexane added to potassium isohumulone was 95.5–114.8%. The method may be applicable to other hop extracts.


1964 ◽  
Vol 46 (4) ◽  
pp. 552-562 ◽  
Author(s):  
Ingrid Ernest ◽  
Britt Håkansson ◽  
Jörgen Lehmann ◽  
Björn Sjögren

ABSTRACT The accuracy of two routine methods for the determination of urinary steroids – 17-ketosteroids (17-KS) and Porter-Silber chromogens – has been investigated by chromatographic separation and quantitative determination of individual 17-KS and Porter-Silber reacting steroids in 141 urine samples. For this purpose urine was submitted to enzyme hydrolysis and subsequent solvolysis. The pertinent steroids were separated by column chromatography into three groups, 11-deoxy-17-KS, 11-oxy-17-KS and Porter-Silber reacting steroids. The final separation was accomplished by paper chromatography. As a mean, the urinary excretion of true 17-KS corresponded to about 40–50 per cent of the routine figures. Due to non specific chromogens, individual routine figures were completely unreliable and probably had no more significance than showing a difference between a high and a low urinary content of 17-KS A true figure, however, was never higher than that indicated by the routine method. The routine method for determination of Porter-Silber chromogens also overestimated the urinary content of steroids, the true excretion of Porter-Silber steroids being, on an average, about 25 % lower. Again, the significance of individual determinations was low. The determination of 17-KS and Porter-Silber steroids by column chromatography was found to be rather simple and reliable as only minor amounts of unspecific chromogens were included in the results. Moreover with this method, the 17-KS were separated into 11-deoxy-17-KS and 11-oxy-17-KS.


1974 ◽  
Vol 97 (1) ◽  
pp. 79-82 ◽  
Author(s):  
Madelyn S. Baggett ◽  
Gerald P. Morie ◽  
Mary W. Simmons ◽  
Jack S. Lewis

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