Chemistry Testing
2, 4 D (HERBICIDE): 2, 4 D is extracted in methanol and detected with reversed phase HPLC with a binary mobile phase.
ACID INSOLUBLE ASH: Muffle Furnace
ADDED SUBSTANCE CALCULATION : Requires moisture, salt and protein determinations
ADDED WATER: Requires moisture and protein determinations
AFLATOXINS: Samples are prepared by mixing with a methanol/water extraction solution, blending and filtering. The extract is applied to a column containing monoclonal antibody specific for aflatoxins. Aflatoxins bind to the antibody on the column. The column is then washed and aflatoxins are eluted with methanol. Total aflatoxins are quantitated by a fluorometer.
ALKALINITY: Titration
ARSENIC: Inductively Coupled Plasma Emission
ASH: Muffle Furnace
BENZOIC SORBIC ACIDS: Benzoic and sorbic acids are separated on a C18 HPLC column and quantitated with an ultraviolet detector.
BRIX: Refractometer
CADMIUM: Inductively Coupled Plasma Emission
CAFFEINE: Caffeine is separated on a reverse phase HPLC column and detected and quantitated with an ultraviolet detector.
CALCIUM IN FOOD: Inductively Coupled Plasma Emission
CALORIES CALCULATION: Requires moisture, protein, fat and ash determinations
CALORIES FROM FAT: Requires fat determination
CAPTAN: Gas Chromatography
CARBAMATE PESTICIDES: N-Methyl carbamates are extracted from fruits and vegetables by blending with methanol and partitioning into methylene chloride. The extract is then dried down and redissolved in acidified water. The carbamates are detected by a gradient HPLC fluorescence method with post-column derivitization.
CARBAMATES PESTICIDES IN NONFATTY FOOD PRODUCTS: Gas Chromatography
CARBOHYDRATES CALCULATION: Requires moisture, protein, fat and ash determinations
CARBONATE: Distillation
CHLORAMPHENICOL: Chloramphenicol is extracted with ethyl acetate, evaporated to dryness, and reconstituted in a mixture of organic solvents and water. Detection is based on a competitive-type ELISA, with detection limits down to 3 ppb.
CHLORIDE: Titration
CHLORINATED PESTICIDE RESIDUES: Chlorinated hydrocarbon pesticides are extracted from various food matrices with various organic solvents. Extracts are concentrated, solvent-exchanged, cleaned up, then concentrated again for detection on a gas chromatograph with an electron capture detector.
CHOLESTEROL: Samples are saponified and the unsaponified fraction, containing cholesterol and other sterols, is extracted with hexane. The cholesterol content is determined quantitatively by gas chromatography with a flame ionization detector.
COLLAGEN: Precipitation
CONDUCTIVITY: Conductivity meter
COPPER: Inductively Coupled Plasma Emission
CRUDE FIBER: Muffle Furnace
CYANIDE: Spectrophotometer
DIQUAT: Gas Chromatography
DITHIOCARBAMATE FUNGICIDES: Dithiocarbamate residues are decomposed by refluxing with dilute acid. Dithiocarbamate concentration is calculated from evolved carbon disulfide detected colorimetrically.
EDTA: EDTA is isolated by extraction with water and the formation of a copper chelate. Reversed phase HPLC is used with an ultraviolet detector for quantitation.
EGG ALLERGEN: ELISA
ETHANOL: Gas Chromatography
ETHYLENE OXIDE: Ethylene oxide is distilled and converted to ethylene iodohydrin, which is determined by gas chromatography using electron capture detector.
FAT BY ACID HYDROLYSIS: Acid Hydrolysis/Mojonnier
FATTY ACID PROFILE – SATURATED: Fat is extracted with a mixture of methanol and chloroform. The fat is saponified, and the fatty acids are derivatized to the methyl ester form in the presence of boron trifluoride in methanol. The sample is refluxed and the fatty acids are extracted into hexane. The fatty acids are identified and quantitated by a gas chromatograph with a flame ionization detector.
FATTY ACID PROFILE – TRANS: Fat is extracted with a mixture of methanol and chloroform. The fat is saponified, and the fatty acids are derivatized to the methyl ester form in the presence of boron trifluoride in methanol. The sample is refluxed and the fatty acids are extracted into hexane. The fatty acids are identified and quantitated by a gas chromatograph with a flame ionization detector.
FD & C ARTIFICIAL COLORS (BLUE): HPLC
FD & C ARTIFICIAL COLORS (RED): HPLC
FD & C ARTIFICIAL COLORS (YELLOW): HPLC
FLUORIDE: Spectrophotometer
FORMALDEHYDE: Formaldehyde is extracted with acetonitrile and its concentration is determined with isocratic reverse phase HPLC with ultraviolet absorption detection.
FREE FATTY ACIDS: Oil or fat is reacted with alkaline ethanol and titrated to a neutral endpoint. The volume of sodium hydroxide used to neutralize the sample is indicative of the concentration of free fatty acids in the sample.
GLUTEN: ELISA
GLYPHOSATE: Glyphosate is extracted with acetonitrile and water and isolated and detected on an HPLC with an amine column.
HEAVY FILTH: Isolation: sieve, flotation, filtration, etc.
HEAVY METALS: Inductively Coupled Plasma Emission
HISTAMINE: ELISA or fluorometric
ICAP SCAN (FOODS): Inductively Coupled Plasma Emission
IODINE: Spectrophotometer
IRON: Inductively Coupled Plasma Emission
LEAD: Inductively Coupled Plasma Emission
LIGHT FILTH: Isolation: sieve, flotation, filtration, etc.
LOSS ON DRYING: Mechanical Convection Oven
MAGNESIUM: Inductively Coupled Plasma Emission
MANGANESE: Inductively Coupled Plasma Emission
MAXIMUM INTERNAL TEMPERATURE: Water Bath
MERCURY IN FOOD: Cold Vapor Atomic Absorption
METHYL MERCURY (FISH & SHELLFISH): Gas Chromatography
MILK ALLERGEN: ELISA
MOISTURE IN FOODS: Mechanical Convection or Vacuum Oven
MOISTURE/PROTEIN RATIO: Requires moisture and protein determinations
MOLYBDENUM: Inductively Coupled Plasma Emission
MONO- AND POLY-UNSATURATED FATTY ACIDS PROFILE: Fat is extracted with a mixture of methanol and chloroform. The fat is saponified, and the fatty acids are derivatized to the methyl ester form in the presence of boron trifluoride in methanol. The sample is refluxed and the fatty acids are extracted into hexane. The fatty acids are identified and quantitated by a gas chromatograph with a flame ionization detector.
NET WEIGHT – DRAINED: Analytical balance
NICKEL: Inductively Coupled Plasma Emission
NITRATE in water: Spectrophotometer
NITRATE, AS NANO3: Spectrophotometer
NITRITE: Spectrophotometer
NUTRITIONAL LABELING: ESHA Software
ORGANIC ACIDS: HPLC
ORGANOPHOPHORUS PESTICIDE RESIDUES: Organophosphate pesticides are extracted from various food matrices with various organic solvents. Extracts are concentrated, solvent-exchanged, cleaned up, then concentrated again for detection on a gas chromatograph with a pulsed flame photometric detector.
PAPAIN: Tyrosine is liberated from the specified casein substrate by proteolytic papain enzyme. The tyrosine is then analyzed by an ultraviolet spectrophotometer and correlated to the concentration of papain in the sample.
PARABENS: Methyl, ethyl, propyl, and butyl parabens can be separated and detected by extraction of sample in acetonitrile and quantitation using reverse phase HPLC with ultraviolet detection.
PATULIN: Patulin is extracted with ethyl acetate and cleaned up with sodium carbonate. Patulin is quantitatively determined by HPLC with ultraviolet detection.
PEANUT ALLERGEN: ELISA
PECTIN: Colorimetric
PERCENT BONE: Requires calcium determination
PERCENT SOLIDS: Drying Oven
PEROXIDE VALUE: Titration
PH: pH meter
PHOSPHATE: Requires phosphorus determination
PHOSPHORUS: Inductively Coupled Plasma Emission
POTASSIUM: Inductively Coupled Plasma Emission
PROPYLENE GLYCOL: Propylene glycol is extracted in water and detected by either HPLC with ultraviolet detection or GC with a flame ionization detector.
PROTEIN: Foss Kjeldahl Instrument
PROTEIN FAT FREE CALCULATION: Requires protein and fat determinations
PUNGENCY/SCOVILLE UNITS: The pungency of capsicums is determined by the Scoville heat test. Capsaicin content is determined from alcoholic extracts of samples run through an HPLC with a fluorescence detector.
RESIDUAL CHLORINE: Colorimetric
SALT: Titration
SCOTT RECOVERABLE OIL- CITRUS: Recoverable oil is codistilled with isopropanol, then determined by titration with standard potassium bromide-potassium bromate solution.
SODIUM: Inductively Coupled Plasma Emission
SODIUM BENZOATE: HPLC
SODIUM NITRITE: Spectrophotometer
SOLUBLE SOLIDS: Drying Ocen
SOXHLET FATS: Petroleum ether extraction
SOY ALLERGEN: ELISA
SOY PROTEIN CONCENTRATE: Centrifuge
SPECIFIC GRAVITY: Analytical balance
STARCH: Spectrophotometer
SUGAR ALCOHOLS: HPLC
SUGARS: Sugars are extracted with water and analyzed by HPLC with a refractive index detector. Individual sugars in the sugar screen (fructose, glucose, sucrose, maltose, and lactose) are quantitated based on response factors of known standards.
SULFATE: Spectrophotometer
TANNIN: Tannins are polyphenolic compounds found naturally in fruit and vegetable products. Total soluble tannins are measured spectrophotometrically based on the ability of the tannins to reduce Folin-Ciocalteu`s reagent in the presence of sodium carbonate.
TBZ IN JUICE: Thiabendazole is extracted with methanol and water and quantitated by reverse phase HPLC with fluorescence detection.
TETRACYCLINE AND RELATED ANTIBIOTICS: HPLC
THIOBARBITURIC ACID: Spectrophotometer
TITRATABLE ACIDITY: Titration
TOTAL DIETARY FIBER: Extraction, ashing and protein determination
TOTAL HARDNESS: Titration
TOTAL ORGANIC CARBON: Spectrophotometer
TURBIDITY (PWS026): Turbidimeter
VITAMIN A: Retinol and beta-carotene are extracted with organic solvents and quantitated independently by reversed phase high performance liquid chromatography with ultraviolet detection. These values are combined to provide the amount of Vitamin A Activity in a sample.
VITAMIN C: Total vitamin C is extracted from food with aqueous solvent and assayed as ascorbic acid by reversed phase high performance liquid chromatography with ultraviolet detection and an acidic mobile phase.
VITAMIN D: Vitamin D samples are saponified, extracted, and cleaned up. Vitamin D is quantitated using reverse phase HPLC with ultraviolet detection.
WATER ACTIVITY: Humidity Measurement
WATER PHASE SALT: Requires moisture and salt determinations
WEIGHT: Analytical balance
ZINC: Inductively Coupled Plasma Emission