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Note: this service is for Research Use Only and Not intended for clinical use.
The United States is the fourth largest wine producer in the world, after France, Italy and Spain. Wine is produced in 50 states across the country, while California produces 89% of the country's total. As a new world wine producer, the United States has a history of 300 years of wine production. Wine is a special kind of thing that has multiple properties: in its essence, wine is a substance, a mixed beverage containing various chemical components such as acid, ester, aldehyde, alcohol, etc., and the main component of which is ethanol (alcohol). It can be directly absorbed by the intestines without going through the digestive system. A few minutes after drinking, alcohol is first taken to the liver by the blood, filtered by the liver, reaching the heart, then to the lungs, back from the lungs to the heart, then through the aorta to the veins, to the brain and the advanced nerve center, and then has a wonderful effect on human physiology and psychology. However, drinking safety is based on quality assurance. Alfa Chemistry offers a strong array of capabilities and testing services to the liquor industry. From authenticity testing to microbiology, Alfa Chemistry provides incredible service and credible results. Alfa Chemistry is your one-stop-shop laboratory performing all of your liquor analysis.
Samples tested by Alfa Chemistry include but not limited to:
Wine
Beer
Brandy
Whisky
Vodka
Champagne
Alfa Chemistry's testing services for alcohol include but not limited to:
The gas chromatograph (GC) is used to analyze volatile components in beverages, such as aroma compounds and additives.
High-Performance Liquid Chromatograph (HPLC)
The high-performance liquid chromatograph (HPLC) is used to detect non-volatile compounds, such as pigments, acids, and sugars.
Mass Spectrometer (MS)
The mass spectrometer (MS) is used in conjunction with chromatographs for quantitative and qualitative analysis to identify complex components and impurities.
Fourier Transform Infrared Spectrometer (FTIR)
The Fourier transform infrared spectrometer (FTIR) is used to analyze the molecular structure and functional groups in beverages, assessing their components.
Nuclear Magnetic Resonance Spectrometer (NMR)
The nuclear magnetic resonance spectrometer (NMR) is used to determine the structure and concentration of compounds in beverages.
Alcohol Meter
The alcohol meter is used to measure the alcohol content in beverages.
pH Meter
The pH meter is used to measure the acidity of beverages, ensuring their flavor and quality.
Heavy Metal Detector
The heavy metal detector is used to detect heavy metal content in beverages, ensuring safety.
Microbial Testing Equipment
Microbial testing equipment includes incubators and ATP fluorescence detectors, used to detect microbial contamination in beverages.
Moisture Meter
The moisture meter is used to measure the moisture content in beverages, ensuring their quality and stability.
Industry articles
Determination of Non-Glycosidic Cyanogens in Fermentation Materials of Chinese Liquor
Zhu, Xiaochun, Shuang Chen, and Yan Xu. Food Control 140 (2022): 109101.
Non-glycosidic cyanogens present in sorghum, wheat, and fermented grains during the fermentation process of Chinese liquor can easily decompose and release toxic cyanide ions, affecting the quality and safety of liquor and potentially posing a threat to public health.
In this study, a simple and practical method for determining non-glycosidic cyanogens was developed using QuEChERS sample preparation combined with spectrophotometry. The recovery rates of analytes in spiked samples were optimized by adjusting the QuEChERS extraction solvent, buffer solution, and SPE adsorbent. Under optimal conditions, the linear range for cyanide determination was 0.02–0.44 μg/mL, with a correlation coefficient of 0.99 and a limit of detection (LOD) of 0.0023 μg/mL. The recoveries of spiked samples (82.11–115.12%) and relative standard deviations (RSD; 4.87–9.62%) were considered satisfactory.
Determination of Ethanol in Alcoholic Beverages
Somboon, Titikan, et al. LWT 154 (2022): 112593.
To ensure the quality and authenticity of beverage products, it is necessary to assess the ethanol content in alcoholic drinks.
A simple and environmentally friendly method for the quantitative determination of ethanol concentration is introduced, based on conductivity measurements and a non-catalytic esterification reaction. The reaction progress between ethanol and acetic acid is monitored by measuring conductivity, which corresponds to the amount of hydrogen ions and acetate anions produced by the dissociation of acetic acid. By fixing the concentration of acetic acid, a decrease in conductivity was observed as ethanol concentration increased. A successful inverse linear relationship between conductivity and ethanol concentration in the range of 0.0-99.9% v/v was established. This method allows for the effective quantification of ethanol content with good intra- and inter-day precision (RSD < 3.45%). The method has been successfully applied to determine ethanol concentration in alcoholic beverage samples and validated using gas chromatography.
Simultaneous Determination of 124 Pesticide Residues in Chinese Liquor
Liquor is one of the oldest distilled spirits in the world, typically made from grains, with sorghum as a primary ingredient. However, in modern agriculture, due to the occurrence of pests, diseases, and weeds, large amounts of pesticides are inevitably used during the sorghum growing process to ensure high yield and quality. This can lead to pesticide residues in sorghum, which may transfer into liquor, posing potential risks to human health. Therefore, monitoring pesticide residues in liquor and its brewing raw materials (sorghum and rice husks) is crucial for human health.
A multi-residue analytical method was developed for the determination of 124 pesticide residues in Chinese liquor and brewing raw materials (sorghum and rice husks) using rapid multi-plug filtration cleanup (m-PFC) and GC-MS/MS detection. The dispersive solid-phase extraction (d-SPE) procedure was optimized for each matrix by adjusting different combinations and ratios of adsorbents. The 124 pesticides exhibited good linearity with regression coefficients (R2) greater than 0.9901. Except for cycloprothrin, pyraclonil, and prothioconazole, the average recoveries for the other 121 pesticides ranged from 71% to 121%, with relative standard deviations (RSD) below 16.8%. The limits of quantification (LOQ) for the 124 pesticides in the matrices ranged from 1.0 × 10-4 to 5.0 × 10-3 mg/kg, and the limits of detection (LOD) ranged from 3.0 × 10-5 to 1.5 × 10-3 mg/kg. The results demonstrated that the m-PFC procedure is superior to the d-SPE method and can be used for routine monitoring of pesticide residues in market samples.
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