The method is suitable for the determination of water vapor volatile aroma compounds in beer.
Volatile aroma compounds are driven out of the sample through steam distillation. The ethanolic distillate is saturated with NaCl. Potassium hydrogen sulfite is added to separate carbonyl groups that might interfere with the analysis. The extraction of the aroma compounds is performed by shaking out with dichloromethane and the phases separated by centrifuging.
The method is suitable for beer brewed to any original gravity or to any alcohol content.
Higher alcohols and esters in beer are determined by gas chromatography using the headspace method, e.g., the volatile compounds are transferred from the gas space in the sample vial to the GC system for analysis. The method is suitable for beer brewed to any original gravity or to any alcohol content.
The method is suitable for beers of all original gravities and of any alcohol content.
The gas chromatography headspace method is used to determine the higher alcohols and esters present in beer, i.e., the volatile compounds are transferred from the headspace in the sample vial into the GC system for analysis. The following substances are measured in this analysis:
Acetaldehyde
Propanol-1
Ethyl acetate
2-Methylpropanol
3-Methylbutanol
2-Methylbutanol
2-Methylpropylacetate
Butyric acid ethyl ester
3-Methylbutyl acetate
2-Methylbutyl acetate
Hexanoic acid ethyl ester
The method is suitable for beers of all original wort ranges and alcohol contents.
Volatile compounds in beer are concentrated through distillation and the distillate is quantitatively determined by direct injection into a gas chromatograph. The linearity of the detector and the determination of the concentrations of analytes in the sample are achieved by using multiple concentration levels within the relevant range and through evaluation of the relative area under the peaks.
This method is suitable for beers exhibiting all ranges of original gravity and alcohol concentrations.
Analysis for determining the content of added vitamin E using HPLC
This analysis is suitable for NAB, juice, beverage bases, energy drinks and vitamin powder.
α-Tocopherol and α-tocopherol acetate are separated using HPLC in reversed phases and determined with a fluorescence detector or a UV detector.
Determination of acetic acid by enzymatic means
This analysis is suitable for malt, wort, beer, beer-based beverages and soft drinks
Acetic acid (acetate) is converted to acetyl-CoA in the presence of the enzyme acetyl-CoA synthetase (ACS) by adenosine-5'-triphosphate (ATP) and coenzyme A (CoA).
Acetate + ATP + CoA \(^{\underrightarrow{ACS}}\) Acetyl-CoA + AMP + pyrophosphate
Acetyl-CoA reacts with oxaloacetate in the presence of citrate synthase (CS) to form citrate.
Acetyl-CoA + oxaloacetate + H2O \(^{\underrightarrow{CS}}\) citrate + CoA
The oxaloacetic acid required for reaction (2) is produced from malic acid and nicotinamide adenine dinucleotide (NAD) in the presence of malate dehydrogenase (MDH). In doing so, NAD is reduced to NADH:
Malate + NAD+ \(^{\underleftrightarrow{L-MDH}}\) oxaloacetate + NADH + H+
The formation of NADH forms the basis of this analysis, which is measured as an increase in the absorbance at 340, 334 or 365 nm. Since this concerns a previous indicator reaction, the quantity of NADH is not linearly proportional to the acetic acid concentration.