During September and October 1976, 6 samples of peanuts (Arachis hY1Jogaea L. var. Florunner) from a plot at the Coastal Plain Experiment Station, Tifton, Georgia were hand picked and brought immediately to the laboratory, washed, towel-dried and separated into physiological maturity stages according to Pattee et 01. (5). The various stages were quickly separated into hull, seed coat and seed. Peanuts from the same plot were later harvested and cured; and the fruits visually judged mature were likewise separated into hull, seed coat and seed. Fruit parts (20-30) were immediately ground in 150 ml methanol for I min in a Waring Blendor and statically extracted for 48 hours. The supernatant was decanted and 2-3 similar static extractions were performed.Tannin content ofeach extract was measured with Folin-Denis reagent by the Association of Official Analytical Chemists' method (1). Aromatic hydroxyl groups react with the Folin-Denis reagents to form a blue color. Assays were performed on 0.5 ml of methanol extract, and when clouding occurred, the test solution was filtered through Reeve Angel 934H glass fiber filter. Absorbance of the test solution at 760 nm was determined on a Bausch and Lomb Spectronic 70.