2009_Book_FoodChemistry

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352 5 Aroma CompoundsFig. 5.9. Apparatus for the gas chromatography–olfactometry of static headspace samples. 1 Sample in thermostatedglass vessel, 2 septum, 3 gastight syringe, 4 injector, 5 hydrophobed glass tube, 6 carrier gas, e. g., helium,7 purge and trap system, 8 cold trap, 9 gas chromatograph with capillary column, 10 sniffing port, 11 flameionization detector (according to Guth and Grosch, 1993)Fig. 5.10. FD chromatogram of static headspace samples of French fries. Ordinate: n, number of 1 + 1 dilutions.Abscissa: retention index (RI) on the capillary SE-54. The following odorants were identified: 1 methanethiol,2 methylpropanal, 3 2,3-butanedione, 4 3-methylbutanal, 5 2-methylbutanal, 6 2,3-pentanedione, 7 hexanal, 8 methional,9 2-acetyl-1-pyrroline, 10 dimethyltrisulfide (according to Wagner and Grosch, 1997)
5.2 Aroma Analysis 353by chromatography on silica gel, as shown in Table5.11 for coffee aroma. To localize the aromasubstances each of the four fractions is analyzedby gas chromatography and olfactometry.Some volatile compounds are aroma active insuch low concentrations that even enrichment bycolumn chromatography does not allow identification,e. g., 3-methyl-2-butenethiol (Fraction Ain Table 5.11) and the two methoxypyrazines(Fraction B) in coffee. In most cases, furtherconcentration is achieved with the help of multidimensionalgas chromatography (MGC). Thefraction which contains the unknown aromaTable 5.11. Column chromatographic preliminaryseparation of an aroma extract of roasted coffeeFraction a Aroma substanceABCD2-Methyl-3-furanthiol, 2-furfurylthiol,bis(2-methyl-3-furyl)disulfide,3-methyl-2-butenethiol2,3-Butanedione, 3-methylbutanal,2,3-pentanedione, trimethylthiazole,3-mercapto-3-methylbutylformiate,3-isopropyl-2-methoxypyrazine,phenylacetaldehyde,3-isobuty1-2-methoxypyrazine,5-methyl-5(H)-cyclopentapyrazine,p-anisaldehyde,(E)-β-damascenoneMethional, 2-ethenyl-3,5-dimethylpyrazine,linalool, 2,3-diethyl-5-methylpyrazine,guaiacol, 2-ethenyl-3-ethyl-5-methylpyrazine,4-ethylguaiacol, 4-vinylguaiacol2-/3-Methylbutyric acid, trimethylpyrazine,3-mercapto-3-methyl-1-butanol,5-ethyl-2,4-dimethylthiazole,2-ethyl-3,5-dimethylpyrazine, 3,4-dimethy1-2-cyclopentenol-1-one, 4-hydroxy-2,5-dimethyl-3(2H)-furanone, 5-ethyl-4-hydroxy-2-methyl-3(2H)-furanone,3-hydroxy-4,5-dimethy1-2(5H)-furanone,5-ethyl-3-hydroxy-4-methyl-2(5H)-furanone, vanillina Chromatography at 10–12 ◦ C on a silica gel column(24 × 1 cm, deactivated with 7% water); elution withmixtures of pentane-diethylether (50 ml, 95 + 5, v/v,fraction A; 30 ml, 75 × 25, v/v, Fraction B; 30 ml,1 + 1, v/v, Fraction C) and with diethylether (100 ml,Fraction D).substance is first subjected to preliminary separationon a polar capillary. The eluate containingthe substance is cut out, rechromatographed ona non-polar capillary and finally analyzed bymass spectrometry. The MGC is also used inquantitative analysis for the preliminary purificationof analyte and internal standard (cf. 5.2.6.1).5.2.4 Chemical StructureIn the structure elucidation of aroma substances,mass spectrometry has become an indispensabletool because the substance amounts eluted by gaschromatography are generally sufficient for anevaluable spectrum. If the corresponding referencesubstance is available, identification of thearoma substance is based on agreement of themass spectrum, retention indices on at least twocapillary columns of different polarity, and ofodor thresholds, which are compared by gas chromatography/olfactometry.If the reference substanceis not available, the following procedureis suitable for the identification of the odorant:The analyte is concentrated until a 1 H-NMRspectrum and, if necessary, a 13 C-spectrum canbe measured. An example is the identification ofthe characteristic odorant of roasted hazelnuts.The mass spectrum of this substance (Fig. 5.11a)indicates an unsaturated carbonyl compound witha molar mass of 126. In conjunction with thestructural elements shown by the 1 H-NMR spectrum(Fig. 5.11b), it was proposed that the odorantis 5-methyl-(E)-2-hepten-4-one (Filbertone).It goes without saying that the synthesis of theproposed aroma substance was part of the identification.It was also guaranteed that its chromatographicand sensory properties correspond withthose of the unknown odorant.5.2.5 Enantioselective AnalysisIn the case of chiral aroma substances, elucidationof the absolute configuration anddetermination of the enantiomeric ratio, which isusually given as the enantiomeric excess (ee), areof especial interest because the enantiomers ofa compound can differ considerably in their odorquality and threshold. The compound 3a,4,5,7a-
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Food Chemistry
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Professor Dr. Hans-Dieter Belitz
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viPrefacewill prove useful to both
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viiiContents1.2.4.4 ReactionsofAmin
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xContents2.2.4 IsolationandPurifica
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xiiContents3 Lipids ...............
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xivContents3.8.3.2 Analysis........
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xviContents4.4.4.8.3 Utilization .
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xviiiContents5.3 Individual Aroma C
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xxContents7.2.2 Potassium..........
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xxiiContents8.15.3 SyntheticEmulsif
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xxivContents10.2.7 IceCream........
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xxviContents12.3.6 Guanidine Compou
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xxviiiContents13.1.4.3 Other N-Comp
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xxxContents14.5.3.1 Lipolysis .....
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xxxiiContents15.4.3.3.2 WhiteBreadC
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xxxivContents18 Fruits and Fruit Pr
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xxxviContents19.1.3 Nutritional/Phy
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xxxviii Contents20.1.4.4 Wort Boili
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xlContents21.1.3.3.2 Carbohydrates
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xliiContents22.3.1 Production . ...
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xlivIntroductionThis brief outline
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2 0 WaterH-bridges. This structure
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4 0 WaterTable 0.4. Water activity
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6 0 WaterTable 0.7. T ′ g and W
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1 Amino Acids, Peptides, Proteins1.
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10 1 Amino Acids, Peptides, Protein
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94 2 EnzymesTable 2.1. Examples of
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96 2 Enzymes2.2.4 Isolation and Pur
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98 2 Enzymeslation are specified in
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100 2 EnzymesTable 2.4. Systematic
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102 2 Enzymes2.3.1.2 Adenosine Trip
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104 2 Enzymes(2.14)of the amino aci
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106 2 EnzymesTable 2.5. Redox poten
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108 2 Enzymeswith a number of prote
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110 2 EnzymesFig. 2.12. A schematic
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112 2 EnzymesFig. 2.13. Example of
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114 2 Enzymestions simultaneously:(
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116 2 EnzymesFig. 2.18. Postulated
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118 2 Enzymestermediary enzyme-subs
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120 2 EnzymesTable 2.9. Rate consta
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122 2 Enzymesmechanism:(2.51)In an
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124 2 EnzymesFig. 2.26. Plotting sl
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126 2 Enzymesand concentration of i
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128 2 Enzymesbitor; K m is unchange
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130 2 EnzymesIn order to better und
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132 2 EnzymesFor the reaction rate
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134 2 EnzymesFig. 2.35. Fungal α-a
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136 2 EnzymesFig. 2.40. Blanching o
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138 2 Enzymes2.6.1 Substrate Determ
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140 2 EnzymesTable 2.17. Enzyme con
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142 2 EnzymesTable 2.18. Examples f
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144 2 Enzymesnitude due to amplific
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146 2 EnzymesTable 2.20. Examples f
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148 2 EnzymesFig. 2.47. Enzyme immo
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150 2 EnzymesTable 2.21. Michaelis
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152 2 Enzymes2.7.2.2.6 α-D-Galacto
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154 2 Enzymes2.7.2.2.15 TannasesTan
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156 2 EnzymesBlow, D.M., Birktoft,
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3 Lipids3.1 ForewordLipids are form
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160 3 LipidsTable 3.3. Aroma thresh
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162 3 Lipids3.2.1.2 Unsaturated Fat
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164 3 LipidsTable 3.9. Taste of uns
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166 3 Lipidsin Fig. 3.2. The dimer
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168 3 Lipidsproceeds under mild con
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170 3 LipidsFig. 3.5. Biosynthesis
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172 3 LipidsTable 3.13. Crystalliza
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174 3 LipidsFig. 3.7. Composition o
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176 3 LipidsAlternatively, the ster
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178 3 Lipids3.3.2.2 Physical Proper
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180 3 Lipidsble bond in the cis-con
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182 3 Lipids(3.40a)(3.40b)(3.41)(3.
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184 3 LipidsFig. 3.12. Separation o
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186 3 LipidsFig. 3.14. Arrangement
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188 3 Lipidssince the free C 4 -C 1
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190 3 LipidsTable 3.24. Free fatty
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192 3 LipidsTable 3.26. Induction p
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194 3 LipidsFig. 3.20. Autoxidation
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196 3 LipidsPeroxy radicals with is
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198 3 Lipidsagreement with the abov
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200 3 LipidsTable 3.29. Linoleic ac
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202 3 LipidsTable 3.30. Rate consta
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204 3 LipidsTable 3.32. Sensory pro
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206 3 LipidsFig. 3.27. Proton-catal
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208 3 LipidsFig. 3.29. Lipoxygenase
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210 3 Lipidshydrolysis, the allene
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212 3 LipidsTable 3.35. Products ob
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214 3 Lipidstexture, decreases in p
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216 3 Lipidspherols secure the stab
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218 3 Lipidsincludes the 2,3-double
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220 3 Lipidscomplex heavy metal ion
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222 3 LipidsTable 3.45. Volatile co
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224 3 LipidsTable 3.46. Relative st
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226 3 LipidsFig. 3.41. Fungal degra
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228 3 LipidsTable 3.49. Cholesterol
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230 3 LipidsFig. 3.42. Photochemica
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232 3 LipidsGas chromatographic-mas
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234 3 LipidsFig. 3.45. Tocopherols
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236 3 Lipidsname “carotene”, de
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238 3 LipidsThis xanthophyll occurs
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240 3 LipidsBixin (XVIII) (3.138)Bi
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242 3 LipidsTable 3.59. Aroma compo
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244 3 Lipids(3.143)3.8.4.5 Use of C
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246 3 LipidsFoti, M., Piattelli, M.
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4 Carbohydrates4.1 ForewordCarbohyd
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250 4 CarbohydratesCorrespondingly,
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252 4 Carbohydrates(4.8)(4.9)Fig. 4
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254 4 CarbohydratesThe reaction rat
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256 4 Carbohydratestion a mixture e
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258 4 CarbohydratesTable 4.8. Speci
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260 4 CarbohydratesFig. 4.5. Temper
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262 4 Carbohydratescopyranosyl mann
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264 4 CarbohydratesDehydrating Reac
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266 4 CarbohydratesWith the 2,3-ene
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268 4 Carbohydrates(4.44)reactive a
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270 4 CarbohydratesAmmonia catalyze
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272 4 Carbohydrates(4.52)The reason
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274 4 Carbohydrates(4.57)(4.58)4.2.
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276 4 Carbohydrates(4.63)by reducti
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278 4 Carbohydrates(4.70)re-formati
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280 4 Carbohydrates(4.79)(4.80)inst
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282 4 CarbohydratesVarious oxidatio
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284 4 Carbohydrates4.2.4.4.8 Format
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286 4 Carbohydrates(4.96)Pyridosine
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288 4 Carbohydrates(4.100)(4.101)Ta
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290 4 CarbohydratesThis then reacts
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292 4 Carbohydratestrimethylchloros
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294 4 Carbohydratestose and the C-2
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296 4 Carbohydratescontain shorter
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298 4 CarbohydratesFig. 4.13. Stabi
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300 4 Carbohydrates4.4.3 Properties
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Page 384 and 385: 5 Aroma Compounds5.1 Foreword5.1.1
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402 5 Aroma CompoundsSaxby, M.J. (E
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404 6 Vitaminsciency can result in
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406 6 Vitaminsby cleavage of the ce
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408 6 Vitamins(6.3)6.2.3.3 Stabilit
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410 6 VitaminsTable 6.7. ContinuedF
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412 6 Vitaminsdrate metabolism, the
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414 6 Vitaminspyridoxal phosphate,
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416 6 Vitamins(6.16)fer single carb
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418 6 Vitaminsvegetables from winte
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420 6 VitaminsFig. 6.4. Ascorbic ac
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422 7 MineralsTable 7.2. Mineral co
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424 7 Minerals7.2.3 MagnesiumThe co
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426 7 Mineralssuch as arginase, ami
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428 7 Minerals7.3.3.4 SiliconSilico
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430 8 Food Additivesis made to legi
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432 8 Food Additivesintensive α-ke
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434 8 Food AdditivesFig. 8.4. Model
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436 8 Food AdditivesTable 8.3. Tast
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438 8 Food AdditivesTable 8.5. Amin
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440 8 Food Additivesand the thiocar
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442 8 Food Additivesinto amino acid
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444 8 Food AdditivesTable 8.12. Exa
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446 8 Food AdditivesTable 8.13. Str
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448 8 Food Additives8.10.6 Lactic A
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450 8 Food Additives(pK a = 4.19) i
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452 8 Food AdditivesThe microbial a
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454 8 Food Additives“gaseous rins
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456 8 Food AdditivesIn the producti
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458 8 Food Additives(mechanical des
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460 8 Food Additivessaponification
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462 8 Food AdditivesUnlike acetem a
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464 8 Food Additives• introductio
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466 8 Food Additivesing” compound
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468 9 Food ContaminationADI: the AD
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470 9 Food Contaminationin trace an
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472 9 Food Contaminationtion is cha
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474 9 Food ContaminationTable 9.3.
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476 9 Food Contaminationthe recomme
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478 9 Food ContaminationFig. 9.2. (
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482 9 Food Contaminationcan destroy
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488 9 Food ContaminationFig. 9.3. S
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490 9 Food Contamination(9.3)As a r
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492 9 Food Contaminationamide can a
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494 9 Food ContaminationNitrosamine
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496 9 Food Contaminationlife (aqueo
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10 Milk and Dairy Products10.1 Milk
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500 10 Milk and Dairy ProductsTable
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506 10 Milk and Dairy ProductsFig.
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510 10 Milk and Dairy ProductsFig.
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512 10 Milk and Dairy ProductsHence
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518 10 Milk and Dairy Products10.1.
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520 10 Milk and Dairy Products• C
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524 10 Milk and Dairy Productsferme
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526 10 Milk and Dairy Productsfat g
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528 10 Milk and Dairy Productsis co
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532 10 Milk and Dairy ProductsRipen
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534 10 Milk and Dairy Productsty ac
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542 10 Milk and Dairy ProductsAmong
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544 10 Milk and Dairy Products10.4
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11 Eggs11.1 ForewordEggs have been
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548 11 EggsTable 11.3. Amino acid c
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550 11 Eggssequence:-Glu-Lys-Thr-As
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552 11 EggsTable 11.7. Amino acid s
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554 11 Eggsrange of 5 to 221 kdal.
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556 11 EggsTable 11.12. Fatty acid
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558 11 EggsFig. 11.5. Schematic pre
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560 11 EggsTable 11.14. Composition
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562 11 EggsPalmer, H.H., Ijichi, K.
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564 12 MeatTable 12.1. Continuation
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566 12 MeatFig. 12.1. The structura
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568 12 Meat12.3 Muscle Tissue: Comp
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570 12 MeatFig. 12.9. Schematic rep
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572 12 MeatFig. 12.10. A schematic
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574 12 Meatoxygen to myoglobin. The
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576 12 MeatNO, N − 3), low-spin c
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578 12 MeatTable 12.6. Amino acid c
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580 12 MeatZ ∗ M S Y G Y D E K S
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582 12 Meatnoline content was highe
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584 12 MeatThe transition of collag
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586 12 Meat12.3.8 Purines and Pyrim
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588 12 MeatFig. 12.22. Post-mortem
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590 12 MeatTable 12.15. Endopeptida
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592 12 MeatFig. 12.28. Swelling of
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594 12 MeatTable 12.16. Average com
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596 12 MeatTable 12.18. Oxidative f
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598 12 MeatTable 12.19. Effect of c
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600 12 Meat12.7.2.2.1 Raw SausagesT
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602 12 MeatTable 12.21. Chemical co
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604 12 Meataromas are used as the t
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606 12 MeatTable 12.23. Concentrati
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608 12 Meatdrolysate is used as the
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610 12 MeatFig. 12.39. Animal speci
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612 12 Meathousehold as meat tender
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614 12 Meatcontain milk, egg or soy
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616 12 MeatTraub, W., Piez, K. A.:
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618 13 Fish, Whales, Crustaceans, M
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14 Edible Fats * and Oils14.1 Forew
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642 14 Edible Fats and OilsTable 14
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644 14 Edible Fats and Oilscontains
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650 14 Edible Fats and Oilsor ident
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654 14 Edible Fats and Oilsthe aque
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656 14 Edible Fats and Oilsfining s
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658 14 Edible Fats and Oils14.4.2.3
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660 14 Edible Fats and OilsThe appl
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662 14 Edible Fats and OilsFig. 14.
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666 14 Edible Fats and OilsThe dete
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15 Cereals and Cereal Products15.1
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672 15 Cereals and Cereal ProductsT
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676 15 Cereals and Cereal ProductsF
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680 15 Cereals and Cereal Productsc
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698 15 Cereals and Cereal Products1
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702 15 Cereals and Cereal Productsa
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704 15 Cereals and Cereal Productse
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708 15 Cereals and Cereal Productss
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714 15 Cereals and Cereal Productsi
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718 15 Cereals and Cereal Productsi
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744 15 Cereals and Cereal ProductsK
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16 Legumes16.1 ForewordRipe seeds o
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748 16 LegumesTable 16.1. (Continue
Page 794 and 795:
750 16 LegumesTable 16.6. Amino aci
Page 796 and 797:
752 16 LegumesTable 16.8. Amino aci
Page 798 and 799:
754 16 LegumesTable 16.11. Examples
Page 800 and 801:
756 16 LegumesTable 16.13. Active c
Page 802 and 803:
758 16 LegumesTable 16.16. Destruct
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760 16 LegumesTable 16.21. Carbohyd
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762 16 LegumesTable 16.24. Fatty ac
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764 16 LegumesSaponins contribute t
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766 16 LegumesFig. 16.6. Soybean pr
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768 16 Legumesacid), heated (100
Page 814 and 815:
17 Vegetables and Vegetable Product
Page 816 and 817:
772 17 Vegetables and Vegetable Pro
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Page 820 and 821:
Page 822 and 823:
Page 824 and 825:
Page 826 and 827:
Page 828 and 829:
Page 830 and 831:
Page 832 and 833:
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Page 840 and 841:
Page 842 and 843:
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Page 850 and 851:
Page 852 and 853:
808 18 Fruits and Fruit ProductsTab
Page 854 and 855:
Page 856 and 857:
Page 858 and 859:
Page 860 and 861:
Page 862 and 863:
Page 864 and 865:
820 18 Fruits and Fruit Productsint
Page 866 and 867:
Page 868 and 869:
Page 870 and 871:
826 18 Fruits and Fruit Products(18
Page 872 and 873:
Page 874 and 875:
830 18 Fruits and Fruit Productscya
Page 876 and 877:
832 18 Fruits and Fruit Productsis
Page 878 and 879:
Page 880 and 881:
Page 882 and 883:
Page 884 and 885:
Page 886 and 887:
842 18 Fruits and Fruit Products(cf
Page 888 and 889:
844 18 Fruits and Fruit ProductsFig
Page 890 and 891:
846 18 Fruits and Fruit Products18.
Page 892 and 893:
848 18 Fruits and Fruit Productsbut
Page 894 and 895:
Page 896 and 897:
852 18 Fruits and Fruit Productsmar
Page 898 and 899:
854 18 Fruits and Fruit Productslat
Page 900 and 901:
856 18 Fruits and Fruit Productsinv
Page 902 and 903:
Page 904 and 905:
860 18 Fruits and Fruit Productsbev
Page 906 and 907:
19 Sugars, Sugar Alcohols and Honey
Page 908 and 909:
864 19 Sugars, Sugar Alcohols and H
Page 910 and 911:
Page 912 and 913:
Page 914 and 915:
Page 916 and 917:
Page 918 and 919:
Page 920 and 921:
Page 922 and 923:
Page 924 and 925:
Page 926 and 927:
Page 928 and 929:
Page 930 and 931:
Page 932 and 933:
Page 934 and 935:
Page 936 and 937:
20 Alcoholic BeveragesAlcoholic bev
Page 938 and 939:
894 20 Alcoholic BeveragesTable 20.
Page 940 and 941:
Page 942 and 943:
898 20 Alcoholic Beveragesharvested
Page 944 and 945:
900 20 Alcoholic Beveragesenzyme in
Page 946 and 947:
902 20 Alcoholic BeveragesThus, for
Page 948 and 949:
904 20 Alcoholic Beverages7-8%; mal
Page 950 and 951:
Page 952 and 953:
908 20 Alcoholic BeveragesFig. 20.4
Page 954 and 955:
Page 956 and 957:
Page 958 and 959:
914 20 Alcoholic Beveragesto 50 ◦
Page 960 and 961:
916 20 Alcoholic Beveragesthe insta
Page 962 and 963:
918 20 Alcoholic Beveragesstability
Page 964 and 965:
920 20 Alcoholic Beverageslimit is
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Page 968 and 969:
Page 970 and 971:
926 20 Alcoholic Beveragescentratio
Page 972 and 973:
928 20 Alcoholic Beveragesthe spark
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Page 976 and 977:
932 20 Alcoholic BeveragesDuring di
Page 978 and 979:
934 20 Alcoholic BeveragesIn the pr
Page 980 and 981:
936 20 Alcoholic BeveragesAllasch,
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21 Coffee, Tea, Cocoa21.1 Coffee an
Page 984 and 985:
940 21 Coffee, Tea, Cocoaclean flav
Page 986 and 987:
942 21 Coffee, Tea, Cocoachanges in
Page 988 and 989:
944 21 Coffee, Tea, Cocoaand theoph
Page 990 and 991:
946 21 Coffee, Tea, CocoaTable 21.1
Page 992 and 993:
948 21 Coffee, Tea, Cocoa(21.4)Tabl
Page 994 and 995:
950 21 Coffee, Tea, Cocoatemperatur
Page 996 and 997:
952 21 Coffee, Tea, CocoaIndia and
Page 998 and 999:
954 21 Coffee, Tea, Cocoaof great i
Page 1000 and 1001:
956 21 Coffee, Tea, Cocoathe peroxi
Page 1002 and 1003:
958 21 Coffee, Tea, Cocoa21.2.7 Pac
Page 1004 and 1005:
960 21 Coffee, Tea, Cocoapulp surro
Page 1006 and 1007:
962 21 Coffee, Tea, Cocoatinesteras
Page 1008 and 1009:
964 21 Coffee, Tea, Cocoa21.3.2.3.7
Page 1010 and 1011:
966 21 Coffee, Tea, Cocoaand porous
Page 1012 and 1013:
968 21 Coffee, Tea, CocoaTable 21.2
Page 1014 and 1015:
970 21 Coffee, Tea, CocoaSchieberle
Page 1016 and 1017:
972 22 Spices, Salt and VinegarTabl
Page 1018 and 1019:
Page 1020 and 1021:
976 22 Spices, Salt and Vinegar22.1
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Page 1024 and 1025:
Page 1026 and 1027:
982 22 Spices, Salt and VinegarCont
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984 22 Spices, Salt and Vinegarprov
Page 1030 and 1031:
23 Drinking Water, Mineral and Tabl
Page 1032 and 1033:
988 23 Drinking Water, Mineral and
Page 1034 and 1035:
990 IndexADI-value 467, 468Adipic a
Page 1036 and 1037:
992 Index-, egg 548(T)-, egg white
Page 1038 and 1039:
994 Index-, fruit, content 829(T)-,
Page 1040 and 1041:
996 Index-, saffron 974(T), 977, 97
Page 1042 and 1043:
998 IndexBeer 892-, acid 902-, alco
Page 1044 and 1045:
1000 IndexBrisling 618Broad bean, c
Page 1046 and 1047:
1002 IndexCarboxypeptidase B 077(T)
Page 1048 and 1049:
1004 Index-, -, application of lyso
Page 1050 and 1051:
1006 Index-, sterol 229(T)-, unsapo
Page 1052 and 1053:
1008 IndexCrabs, color retention 14
Page 1054 and 1055:
1010 Index-, production 799, 800(F)
Page 1056 and 1057:
1012 IndexDragée 881Dried fruit, A
Page 1058 and 1059:
1014 Index-, immobilization 147, 14
Page 1060 and 1061:
1016 Index-, -, lipolysis 667-, det
Page 1062 and 1063:
1018 IndexFish sperm 636Fishy off-f
Page 1064 and 1065:
1020 Index-, haze, PVPP 837-, membr
Page 1066 and 1067:
1022 Index-, egg white 549(T)-, leg
Page 1068 and 1069:
1024 Index-, ovomucin 551-, ovomuco
Page 1070 and 1071:
1026 IndexHexenal, (Z)-3--, aroma,
Page 1072 and 1073:
1028 Index-, alginate 301(T), 304-,
Page 1074 and 1075:
1030 IndexKey odorant, example 340(
Page 1076 and 1077:
1032 IndexLinoleic acid, autoxidati
Page 1078 and 1079:
1034 Index-, discovery 011-, guanid
Page 1080 and 1081:
1036 Index-, defect 588-, DFD 588,
Page 1082 and 1083:
1038 Index-, odor threshold value 3
Page 1084 and 1085:
1040 Index-, conformation 254-, con
Page 1086 and 1087:
1042 IndexNon-competitive inhibitio
Page 1088 and 1089:
1044 Index-, structure, melting poi
Page 1090 and 1091:
1046 Index-, saponin content 763(T)
Page 1092 and 1093:
1048 IndexPhenylalanine-free diet 0
Page 1094 and 1095:
1050 Index-, temperature of phase t
Page 1096 and 1097:
1052 Index-, isoionic point 059, 05
Page 1098 and 1099:
1054 IndexRadiation detection, food
Page 1100 and 1101:
1056 IndexSafflower seed, productio
Page 1102 and 1103:
1058 IndexSorbitan fatty acid ester
Page 1104 and 1105:
1060 IndexStarch ester 326Starch et
Page 1106 and 1107:
1062 IndexTable wine 919Tablet 881T
Page 1108 and 1109:
1064 Index-, occurrence 234(T)-, st
Page 1110 and 1111:
1066 IndexVanilla, aroma substance
Page 1112 and 1113:
1068 Index-, -, electropherogram 68
Page 1114:
1070 Index-, solubility 862(F)-, wa
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2009_Book_FoodChemistry

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