The lipid component of orange juice has received considerable attention because of its possible influence on flavor changes which develop in the canned juice during storage. Several investigators (2,4,5, 7,8,9,10,11) have presented analytical data, both qualitative and quantitative, on this fraction. Huskins, Swift, and Veldhuis ( 4 ) analyzed the lipids from canned pasteurized orange juice stored for 2 years under normal climatic conditions at Winter Haven, Florida (annual mean temperature about 22°C.). They found that the phosphorus had decreased to one-tenth of its original value and the nitrogen to one-fifth, choline having entirely disappeared. Also, the amount of lipid which could be extracted from the stored juice had decreased. They concluded that the phosphatides had hydrolyzed and that the choline and ethanolamine, as well as part of the phosphorus, had been lost to the aqueous phase of the juice. These investigators also noted changes in the fatty acid constituents, which could have been the result of oxidation. I n this previous work, no attempt was made to establish whether these changes occurred rapidly o r slowly. The present analyses of the lipid from pasteurized, stored Valencia orange juice were carried out to study this question. Attention was given only to the changes in the phosphorus, nitrogen, and fatty acid constituents. EXPERIMENTAL Extraction of lipids. Fresh Valencia orange juice was obtained from a local cannery in 1950. I n the laboratory i t was mixed, pasteurized at 88"C., canned, and quickly cooled.About one-third of the cans were held at 0-5°C. for 2 days until the lipid could be extracted. The extraction was carried out by passing the juice through an Oliver Precoat filter and then extracting the lipid from the filter-aid with acetone as described by Huskins, Swift, and Veldhuis (4,5). The solvent was evaporated and the lipid taken up in petroleum ether. This step eliminated the water which the acetone also extracts from the damp filter-aid. The petroleum ether solution of the lipids was then stored under refrigeration (0-5°C.) until the analysis could be made.After storage periods of 6 and 13 months, portions of the stored juice were processed f o r lipids as outlined above.Prior to analysis, the petroleum ether solutions of the lipids were treated as follows: each solution, in a 3-necked flask equipped with a mechanical stirrer, condenser, and vacuum gauge, was warmed over a steam bath to evaporate most of the solvent at atmospheric pressure. Then the flask was immersed in cold water, the stirrer was started,The remaining two-thirds of the cans were stored in the laboratory loft.