scholarly journals DETERMINAÇÃO DE ACETOÍNA E METANOL EM VINAGRES DE VINHO BRASILEIROS

Author(s):  
LUIZ ANTENOR RIZZON ◽  
ALBERTO MIELE

Visou-se a caracterização do vinagre de vinho brasileiro, mediante determinação do teor de acetoína e de metanol. Analisaram-se 29 amostras de diferentes marcas comerciais de vinagre de vinho tinto e 18 de vinagre de vinho branco. As análises de acetoína e de metanol foram efetuadas mediante cromatografia a gás. Constatou-se variabilidade acentuada no teor de acetoína e de metanol do vinagre de vinho brasileiro. Detectou-se que 61,0% dos vinagres de vinho branco e 39,4% dos vinagres de vinho tinto apresentaram menos de 40 mg/L de acetoína. Observou-se, também, que 66,6% dos vinagres de vinho branco apresentaram menos de 25 mg/L de metanol e 53,6% dos vinagres de vinho tinto menos de 50 mg/L. O estabelecimento de limite mínimo pela legislação brasileira para a acetoína e o metanol do vinagre de vinho contribuiria para a determinação da genuinidade desse produto. A cromatografia a gás mostrou-se adequada para a determinação da acetoína e do metanol nos vinagres de vinho. DETERMINATION OF ACETOIN AND METHANOL IN BRAZILIAN WINE VINEGARS Abstract The aim of this work was to characterize Brazilian wine vinegars, by determination of acetoin and methanol content. Twenty-nine samples of different commercial red wine vinegars and 18 samples of white wine vinegars were analysed. The analyses of acetoin and methanol were made by gas chromatography. High variability in the acetoin and methanol contents were observed. It was remarked that 61.0% of the white wine vinegars and 39.4% of the red wine vinegars showed less than 40 mg/L of acetoin. It was showed that 66.6% of the white wine vinegars showed less than 25 mg/L of methanol and 53.6% of the red wine vinegars had less than 50 mg/L of this alcohol. The setting up of limitation by Brazilian legislation for the acetoin and methanol in the vinegar components contribute to its genuinity. The gas chromatography showed to be suitable, for acetoin and methanol determination in wine vinegars.

2014 ◽  
Vol 97 (2) ◽  
pp. 498-505 ◽  
Author(s):  
Steve Kupina ◽  
Mark Roman ◽  
D Anderson ◽  
S Bhandari ◽  
M S Cardozo ◽  
...  

Abstract An international collaborative study was conducted of an HPLC-refractive index (RI) detector method for the determination of the combined amounts of sugars, glycerol, organic acids, and phenolic compounds in wines and wine-like beverages. Nine collaboratinglaboratories representing major winery, contract laboratories, and government laboratories tested eight different materials as blind duplicates using the proposed method. Sample materials included red and white wines, port, wine cooler, and nonalcoholic wine. One material was a negative control, and one material was a reference material. Samples were either treated with an ion-exchange resin to remove interferingorganic acids prior to analysis or left untreated toinclude organic acids and phenolics. Red wine samples were treated with polyvinylpolypyrrolidone to remove potential interferences from phenolics prior to analysis. The HPLC analyses were performed on a Bio-Rad Fast Acid Analysis Column using RI detection. Reproducibility (RSDR) for untreated samples(sugars + phenolics + organic acids) ranged from 6.6% for Titrivin AA4 reference material to 11.0% for dry red wine. RSDR for treated samples (sugars only) ranged from 6.8% for white zinfandel to 18.9% for dry white wine. RSDR for treatedsamples (sugars only) + glycerol ranged from 6.4% for white zinfandel to 19.8% for dry red wine. Based on these results, the method was adopted as Official First Action status for determination of total carbohydrates in wine and wine-like beverages.


2001 ◽  
Vol 84 (6) ◽  
pp. 1818-1827 ◽  
Author(s):  
Angelo Visconti ◽  
Michelangelo Pascale ◽  
Gianluca Centonze ◽  
E Anklam ◽  
A M Betbeder ◽  
...  

Abstract The accuracy, repeatability, and reproducibility characteristics of a liquid chromatographic method for the determination of ochratoxin A (OTA) in white wine, red wine, and beer were established in a collaborative study involving 18 laboratories in 10 countries. Blind duplicates of blank, spiked, and naturally contaminated materials at levels ranging from ≤0.01 to 3.00 ng/mL were analyzed. Wine and beer samples were diluted with a solution containing polyethylene glycol and sodium hydrogen carbonate, and the diluted samples were filtered and cleaned up on an immunoaffinity column. OTA was eluted with methanol and quantified by reversed-phase liquid chromatography with fluorometric detection. Average recoveries from white wine, red wine, and beer ranged from 88.2 to 105.4% (at spiking levels ranging from 0.1 to 2.0 ng/mL), from 84.3 to 93.1% (at spiking levels ranging from 0.2 to 3.0 ng/mL), and from 87.0 to 95.0% (at spiking levels ranging from 0.2 to 1.5 ng/mL), respectively. Relative standard deviations for within-laboratory repeatability (RSDr) ranged from 6.6 to 10.8% for white wine, from 6.5 to 10.8% for red wine, and from 4.7 to 16.5% for beer. Relative standard deviations for between-laboratories reproducibility (RSDR) ranged from 13.1 to 15.9% for white wine, from 11.9 to 13.6% for red wine, and from 15.2 to 26.1% for beer. HORRAT values were ≤0.4 for the 3 matrixes.


2016 ◽  
Vol 196 ◽  
pp. 1131-1136 ◽  
Author(s):  
Fernando J. Lona-Ramirez ◽  
Guillermo Gonzalez-Alatorre ◽  
Vicente Rico-Ramírez ◽  
Ma.Cristina I. Perez-Perez ◽  
Edgar O. Castrejón-González

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