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Carbonyl compounds from lipid oxidation

Describes a simple and sensitive spectrophotometric method to estimate the content of total carbonyl compounds in rancid fats and foods by trapping them with 2,4-DNPH the technique determines total carbonyls, including those that are nonvolatile, decreasing the ability of the assay to correlate well with sensory data. Although gas chromatographic techniques are better suited for determining volatile carbonyl compounds from lipid oxidation, this is still the classical colorimetric assay. [Pg.564]

According to the Cd 18-90 AOCS ° official method, the ANV is 100 times the optical density measured in a 1 cm cell, at 350 nm, of a solution containing 1.00 g of oil in 100 ml of the test solution. The measured absorbance is due to Schiff bases (167) formed when p-anisidine (166) undergoes condensation reaction with carbonyl compounds, according to equation 55. The carbonyl compounds are secondary oxidation products of lipids, such as a, S-unsaturated aldehydes and ketones derived from the hydroperoxides (see Scheme 1 in Section n.A.2.c), and their presence points to advanced oxidation of the oil. [Pg.666]

Phospholipids contribute specific aroma to heated milk, meat and other cooked foods through lipid oxidation derived volatile compounds and interaction with Maillard reaction products. Most of the aroma significant volatiles from soybean lecithin are derived from lipid decomposition and Maillard reaction products including short-chain fatty acids, 2-heptanone, hexanal, and short-chain branched aldehydes formed by Strecker degradation (reactions of a-dicarbonyl compounds with amino acids). The most odor-active volatiles identified from aqueous dispersions of phosphatidylcholine and phos-phatidylethanolamine include fra 5 -4,5-epoxy-c/5-2-decenal, fran5,fran5-2,4-decadienal, hexanal, fra 5, d5, d5 -2,4,7-tridecatrienal (Table 11.9). Upon heating, these phospholipids produced cis- and franj-2-decenal and fra 5-2-undecenal. Besides fatty acid composition, other unknown factors apparently affect the formation of carbonyl compounds from heated phospholipids. [Pg.318]

Not all of the potent volatile compounds are derived from lipid oxidation, including a number of lactones that come from naturally occurring hydroxy fatty acids, diacetyl and vanillin in butter oil (from melted butter). The concentrations of the mixtures of carbonyl compounds exceed the flavor threshold values for individual aldehydes, and the oxidized flavor results from a combination of volatile compounds. [Pg.327]

Flavor is one of the major characteristics that restricts the use of legume flours and proteins in foods. Processing of soybeans, peas and other legumes often results in a wide variety of volatile compounds that contribute flavor notes, such as grassy, beany and rancid flavors. Many of the objectionable flavors come from oxidative deterioration of the unsaturated lipids. The lipoxygenase-catalyzed conversion of unsaturated fatty acids to hydroperoxides, followed by their degradation to volatile and non-volatile compounds, has been identified as one of the important sources of flavor and aroma components of fruits and vegetables. An enzyme-active system, such as raw pea flour, may have most of the necessary enzymes to produce short chain carbonyl compounds. [Pg.32]

The major cause of deterioration of food products is lipid oxidation, from which low-molecular-weight, off-flavor compounds are formed. This deterioration is often caused by the oxidation of the unsaturated lipids present in foods. Off-flavor compounds are created when the hydroperoxides, formed during the initial oxidation, are degraded into secondary reaction compounds. Free radicals are also formed which can participate in reactions with secondary products and with proteins. Interactions with the latter can result in carbonyl amino... [Pg.535]

NOTE Solutions and extracts of oil or lipid samples should be protected from undue exposure to light and air before use in order to prevent deterioration of the existing carbonyl compounds as well as further oxidation of the lipid. [Pg.553]

Solutions and extracts of lipid for the test should be protected from undue exposure to light and air before use in order to prevent deterioration of the existing carbonyl compounds as well as further oxidation of the lipid. The solvents must be of high purity to eliminate any interference from existing carbonyls. Fading of color for the test sample occurs after the addition of the alkanolic base solution. For this reason, absorbance readings should be read exactly 10 min after the alkali addition. If the analysis is performed <1 hr after preparation of the sample, data obtained are reliable. [Pg.561]

Heterocyclic aroma compounds found in meat primarily arise from interactions between mono- and dicarbonyl compounds, H2S and ammonia. The carbonyl compounds are derived from the Maillard reaction, including Strecker degradation of amino acids, oxidation of lipids and aldolization reactions. H2S is produced by thermal degradation of sulfur amino acids and ammonia by amino acid pyrolysis. [Pg.430]

Flavors and aromas commonly associated with seafoods have been intensively investigated in the past forty years ( l-7), but the chemical basis of these flavors has proven elusive and difficult to establish. Oxidized fish oils can be described as painty, rancid or cod-liver-oil like (j ), and certain volatile carbonyls arising from the autoxidation of polyunsaturated fatty acids have emerged as the principal contributors to this type of fish-like aroma ( 3, 5, 9-10). Since oxidized butterfat (9, 11-12) and oxidized soybean and linseed oils (13) also can develop similar painty, fish-like aromas, confusion has arisen over the compounds and processes that lead to fish-like aromas. Some have believed that the aromas of fish simply result from the random autoxidation of the polyunsaturated fatty acids of fish lipids (14-17). This view has often been retained because no single compound appears to exhibit an unmistakable fish aroma. Still, evidence has been developed which indicates that a relatively complex mixture of autoxidatively-derived volatiles, including the 2,4-heptadienals, the 2,4-decadienals, and the 2,4,7-decatrienals together elicit unmistakable, oxidized fish-oil aromas (3, 9, 18). Additionally, reports also suggest that contributions from (Z -4-heptenal may add characteristic notes to the cold-store flavor of certain fish, especially cod (4-5). [Pg.201]

Carbonyl compounds in oxidized lipids are the secondary oxidation products resulting from the decomposition of the hydroperoxides. They can be quantified by the reaction with 2,4-dinitrophenylhydrazine and the resulting colored hydrazones are measured spectrophotometrically at 430-460 nm. The carbonyl value is directly related to sensory evaluation, because many of the carbonyl molecules are those responsible for off-flavor in oxidized oil. The anisidine value is a measure of carbonyl compounds that have medium molecular weight and are less volatile (Frankel 1998). It can be used to discover something about the prior oxidation or processing history of an oil. [Pg.46]

Oxidation of unsaturated acyl chains of lipids is a major route to volatile compounds during cooking of fat-containing food of either animal or vegetable origin. The unsaturated fatty acids, readily susceptible to the attack by oxygen, form hydroperoxides which in themselves are odorless and tasteless. The compounds that influence the flavor of the product result from a further breakdown of these hydroperoxides, and, normally, include saturated and unsaturated aldehydes, alcohols, and ketones. The carbonyl compounds resulting from autoxidation impart specific flavors that are normally detrimental to food products (Table 9.3). It should be pointed out, however, that they may also contribute to the desirable characteristic flavor of foods [48]. [Pg.299]

The formation of off-flavours in beer has been reviewed [40], Autoxidation of the lipids present in beer produces carbonyl compounds with very low taste thresholds. In particular, linoleic acid is oxidized to trihydroxyoctadecenoic acids (Table 22.7) which break down into 2-/mAz.y-nonenal. This aldehyde and related compounds impart a cardboard flavour to beer at very low concentrations. Other carbonyl are formed from the lipids in beer by irradiation with light including the C9, Cjo, and Cu-alka-2,4-dienals (thresholds 0 5, 0 3 and 0 01 ppb respectively) [40]. The level of diacetyl and pentane-2,3-dione in a range of commercial beers is given in Table 22.11. Quantities in excess of 0 15 ppm impart a buttery flavour more noticeable in lagers than in ales. Bacterial contamination and petite mutants of yeast result in high levels of diacetyl. The sulphur compounds characterized in beer are listed in Table 22.19 with some threshold data. Dimethyl sulphide is the major volatile... [Pg.474]

The origin of meat flavor has been shown to arise from the combination of two primary sources. The first is the tissue fat, both extracellular and intracellular, which produces carbonyl and other lipid and lipid-oxidation products. The fat component of meat flavor is viewed as being responsible for the species specific flavor in meat (9). The second major component of meat flavor is the lean portion. The proteins, peptides, and amino acids of the lean, add not only to the muscle food s general meaty flavor, but also undergo Maillard reactions with sugars to produce Amadori and Heyns compounds having meat flavor characteristics. [Pg.50]

Sugars and carbonyl compounds interact with amino acids or proteins in a sequence of complex reactions known as the Maillard reaction or as non-enzymatic browning. The browning products from this reaction have a marked influence on lipid oxidation. They generally retard lipid oxidation in foods, and contribute to meat flavors. Lipid oxidation products can also react with proteins and amino acids, leading to the loss of essential amino acids with impact on the oxidative stability and the nutritional quality of foods. [Pg.311]

The structure of the food matrix is also known to affect the release of volatile compounds having an impact on flavors and aroma. Changes in flavor result from the interactions of lipid-derived carbonyl compounds by aldolization with the amino groups of proteins. Undesirable flavors are produced when beef or chicken are fried in oxidized fats by the interaction of secondary lipid oxidation... [Pg.317]

Aldehydes foimd in various dairy products include those derived from the hydroperoxides of polyunsaturated fatty acid components, and further oxidation products of polyunsaturated aldehydes (Table 11.12). Havors imparted by these carbonyl compounds are described as oxidized, fishy, metaUic, cardboard, painty and tallowy. Higher alkanals and alkenals with more than six carbons and ketones are typical volatiles produced by lipid oxidation. A powerful technique, known as aroma extract dilution analysis, was used to... [Pg.324]


See other pages where Carbonyl compounds from lipid oxidation is mentioned: [Pg.330]    [Pg.47]    [Pg.61]    [Pg.214]    [Pg.412]    [Pg.2685]    [Pg.299]    [Pg.98]    [Pg.566]    [Pg.661]    [Pg.955]    [Pg.980]    [Pg.661]    [Pg.955]    [Pg.980]    [Pg.396]    [Pg.663]    [Pg.118]    [Pg.561]    [Pg.411]    [Pg.412]    [Pg.412]    [Pg.140]    [Pg.400]    [Pg.168]    [Pg.449]    [Pg.165]    [Pg.111]    [Pg.70]    [Pg.204]    [Pg.325]    [Pg.479]    [Pg.122]    [Pg.543]   
See also in sourсe #XX -- [ Pg.369 ]




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Carbonyl oxidation

Carbonyl oxide

Carbonylation oxide

From carbonyl compounds

Lipid compounds

Lipidic Compound

Oxidation carbonylative

Oxidation oxidative carbonylation

Oxidative carbonylation

Oxidative carbonylations

Oxidized lipids

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