DE2044781C3 - Nahrungs- und Genußmittel mit Kaffeegeschmack - Google Patents
Nahrungs- und Genußmittel mit KaffeegeschmackInfo
- Publication number
 - DE2044781C3 DE2044781C3 DE2044781A DE2044781A DE2044781C3 DE 2044781 C3 DE2044781 C3 DE 2044781C3 DE 2044781 A DE2044781 A DE 2044781A DE 2044781 A DE2044781 A DE 2044781A DE 2044781 C3 DE2044781 C3 DE 2044781C3
 - Authority
 - DE
 - Germany
 - Prior art keywords
 - coffee
 - taste
 - trans
 - aroma
 - nonenal
 - Prior art date
 - Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
 - Expired
 
Links
- 235000013305 food Nutrition 0.000 title claims description 41
 - 239000008373 coffee flavor Substances 0.000 title claims description 16
 - BSAIUMLZVGUGKX-BQYQJAHWSA-N (E)-non-2-enal Chemical compound CCCCCC\C=C\C=O BSAIUMLZVGUGKX-BQYQJAHWSA-N 0.000 claims description 156
 - 235000013353 coffee beverage Nutrition 0.000 claims description 102
 - 235000016213 coffee Nutrition 0.000 claims description 96
 - NSSALFVIQPAIQK-BQYQJAHWSA-N (E)-non-2-en-1-ol Chemical compound CCCCCC\C=C\CO NSSALFVIQPAIQK-BQYQJAHWSA-N 0.000 claims description 50
 - NSSALFVIQPAIQK-UHFFFAOYSA-N trans-non-2-en-1-ol Natural products CCCCCCC=CCO NSSALFVIQPAIQK-UHFFFAOYSA-N 0.000 claims description 49
 - 239000007787 solid Substances 0.000 claims description 21
 - 125000004432 carbon atom Chemical group C* 0.000 claims description 4
 - 239000000654 additive Substances 0.000 claims 1
 - 230000000996 additive effect Effects 0.000 claims 1
 - 235000019640 taste Nutrition 0.000 description 138
 - 240000007154 Coffea arabica Species 0.000 description 94
 - 239000000203 mixture Substances 0.000 description 58
 - 239000000796 flavoring agent Substances 0.000 description 52
 - 235000019634 flavors Nutrition 0.000 description 50
 - 235000021539 instant coffee Nutrition 0.000 description 29
 - XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 26
 - 150000001875 compounds Chemical class 0.000 description 22
 - 239000000523 sample Substances 0.000 description 17
 - 239000000243 solution Substances 0.000 description 17
 - 239000000284 extract Substances 0.000 description 16
 - OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
 - 239000012141 concentrate Substances 0.000 description 15
 - RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 14
 - 239000003921 oil Substances 0.000 description 14
 - 235000019198 oils Nutrition 0.000 description 14
 - 239000007921 spray Substances 0.000 description 12
 - 235000013361 beverage Nutrition 0.000 description 11
 - LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
 - 235000019568 aromas Nutrition 0.000 description 10
 - BSAIUMLZVGUGKX-UHFFFAOYSA-N non-2-enal Chemical compound CCCCCCC=CC=O BSAIUMLZVGUGKX-UHFFFAOYSA-N 0.000 description 10
 - MIDXCONKKJTLDX-UHFFFAOYSA-N 3,5-dimethylcyclopentane-1,2-dione Chemical compound CC1CC(C)C(=O)C1=O MIDXCONKKJTLDX-UHFFFAOYSA-N 0.000 description 9
 - KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
 - 235000013736 caramel Nutrition 0.000 description 9
 - 230000000052 comparative effect Effects 0.000 description 8
 - 239000000126 substance Substances 0.000 description 7
 - XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
 - LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
 - CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
 - 150000001299 aldehydes Chemical class 0.000 description 6
 - 238000002474 experimental method Methods 0.000 description 6
 - 239000000047 product Substances 0.000 description 6
 - VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 6
 - -1 Aldehydes Dimethyl Acetals Chemical class 0.000 description 5
 - 235000019658 bitter taste Nutrition 0.000 description 5
 - 238000001035 drying Methods 0.000 description 5
 - 230000000694 effects Effects 0.000 description 5
 - 238000004519 manufacturing process Methods 0.000 description 5
 - 238000010992 reflux Methods 0.000 description 5
 - UXFSPRAGHGMRSQ-UHFFFAOYSA-N 3-isobutyl-2-methoxypyrazine Chemical compound COC1=NC=CN=C1CC(C)C UXFSPRAGHGMRSQ-UHFFFAOYSA-N 0.000 description 4
 - IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
 - 239000000969 carrier Substances 0.000 description 4
 - 239000010635 coffee oil Substances 0.000 description 4
 - 238000011156 evaluation Methods 0.000 description 4
 - 239000007788 liquid Substances 0.000 description 4
 - 238000000034 method Methods 0.000 description 4
 - 239000000843 powder Substances 0.000 description 4
 - ADLXTJMPCFOTOO-BQYQJAHWSA-N (E)-non-2-enoic acid Chemical compound CCCCCC\C=C\C(O)=O ADLXTJMPCFOTOO-BQYQJAHWSA-N 0.000 description 3
 - WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
 - UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
 - WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
 - CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 3
 - VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
 - 229910010082 LiAlH Inorganic materials 0.000 description 3
 - DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
 - GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
 - 229910052794 bromium Inorganic materials 0.000 description 3
 - 239000003085 diluting agent Substances 0.000 description 3
 - 239000006185 dispersion Substances 0.000 description 3
 - 238000004821 distillation Methods 0.000 description 3
 - 238000004108 freeze drying Methods 0.000 description 3
 - FXHGMKSSBGDXIY-UHFFFAOYSA-N heptanal Chemical compound CCCCCCC=O FXHGMKSSBGDXIY-UHFFFAOYSA-N 0.000 description 3
 - 239000010410 layer Substances 0.000 description 3
 - 238000002156 mixing Methods 0.000 description 3
 - 229910000029 sodium carbonate Inorganic materials 0.000 description 3
 - 235000019614 sour taste Nutrition 0.000 description 3
 - 239000012086 standard solution Substances 0.000 description 3
 - XWYRENPAWWXFNI-BQYQJAHWSA-N (e)-non-2-enoyl chloride Chemical compound CCCCCC\C=C\C(Cl)=O XWYRENPAWWXFNI-BQYQJAHWSA-N 0.000 description 2
 - SPEUIVXLLWOEMJ-UHFFFAOYSA-N 1,1-dimethoxyethane Chemical compound COC(C)OC SPEUIVXLLWOEMJ-UHFFFAOYSA-N 0.000 description 2
 - 244000215068 Acacia senegal Species 0.000 description 2
 - CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
 - 240000008067 Cucumis sativus Species 0.000 description 2
 - 229920000084 Gum arabic Polymers 0.000 description 2
 - OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
 - JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
 - PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
 - ACIAHEMYLLBZOI-ZZXKWVIFSA-N Unsaturated alcohol Chemical compound CC\C(CO)=C/C ACIAHEMYLLBZOI-ZZXKWVIFSA-N 0.000 description 2
 - 235000010489 acacia gum Nutrition 0.000 description 2
 - 239000000205 acacia gum Substances 0.000 description 2
 - DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 2
 - 150000001241 acetals Chemical class 0.000 description 2
 - 230000009286 beneficial effect Effects 0.000 description 2
 - 230000015572 biosynthetic process Effects 0.000 description 2
 - 238000009835 boiling Methods 0.000 description 2
 - 238000006243 chemical reaction Methods 0.000 description 2
 - 238000001816 cooling Methods 0.000 description 2
 - SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 2
 - 239000012153 distilled water Substances 0.000 description 2
 - 239000000839 emulsion Substances 0.000 description 2
 - 238000000605 extraction Methods 0.000 description 2
 - 235000013355 food flavoring agent Nutrition 0.000 description 2
 - 230000007062 hydrolysis Effects 0.000 description 2
 - 238000006460 hydrolysis reaction Methods 0.000 description 2
 - 229910052757 nitrogen Inorganic materials 0.000 description 2
 - 239000012044 organic layer Substances 0.000 description 2
 - 230000003647 oxidation Effects 0.000 description 2
 - 238000007254 oxidation reaction Methods 0.000 description 2
 - SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 2
 - 229910052938 sodium sulfate Inorganic materials 0.000 description 2
 - 235000011152 sodium sulphate Nutrition 0.000 description 2
 - 238000003756 stirring Methods 0.000 description 2
 - 238000003786 synthesis reaction Methods 0.000 description 2
 - 235000012976 tarts Nutrition 0.000 description 2
 - FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
 - 238000005406 washing Methods 0.000 description 2
 - VKWXFMOLPWWLDR-MDZDMXLPSA-N (e)-1,1-dimethoxynon-2-ene Chemical compound CCCCCC\C=C\C(OC)OC VKWXFMOLPWWLDR-MDZDMXLPSA-N 0.000 description 1
 - HIKLFLVBBNMALF-UHFFFAOYSA-N 2-bromo-1,1-dimethoxynonane Chemical compound CCCCCCCC(Br)C(OC)OC HIKLFLVBBNMALF-UHFFFAOYSA-N 0.000 description 1
 - FUSSDBPSTWJYKS-UHFFFAOYSA-N 3,4-dibromoundec-3-enoic acid Chemical compound CCCCCCCC(Br)=C(CC(O)=O)Br FUSSDBPSTWJYKS-UHFFFAOYSA-N 0.000 description 1
 - YZIVXOSGZIXDGD-UHFFFAOYSA-N 3-bromo-1,1-dichlorononane Chemical compound CCCCCCC(Br)CC(Cl)Cl YZIVXOSGZIXDGD-UHFFFAOYSA-N 0.000 description 1
 - HGINADPHJQTSKN-UHFFFAOYSA-M 3-ethoxy-3-oxopropanoate Chemical compound CCOC(=O)CC([O-])=O HGINADPHJQTSKN-UHFFFAOYSA-M 0.000 description 1
 - SJIWUNNSRFWATG-UHFFFAOYSA-N 4-[2-(2-hydroxyethoxy)ethoxy]-4-oxobutanoic acid Chemical compound OCCOCCOC(=O)CCC(O)=O SJIWUNNSRFWATG-UHFFFAOYSA-N 0.000 description 1
 - DJKUVMZEGIWUTP-UHFFFAOYSA-N 9,10,12-trihydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CC(O)C(O)CCCCCCCC(O)=O DJKUVMZEGIWUTP-UHFFFAOYSA-N 0.000 description 1
 - 235000005979 Citrus limon Nutrition 0.000 description 1
 - 244000131522 Citrus pyriformis Species 0.000 description 1
 - 235000009849 Cucumis sativus Nutrition 0.000 description 1
 - 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
 - 244000000626 Daucus carota Species 0.000 description 1
 - 235000002767 Daucus carota Nutrition 0.000 description 1
 - 239000004375 Dextrin Substances 0.000 description 1
 - 229920001353 Dextrin Polymers 0.000 description 1
 - 206010013911 Dysgeusia Diseases 0.000 description 1
 - 239000001828 Gelatine Substances 0.000 description 1
 - 240000005979 Hordeum vulgare Species 0.000 description 1
 - 235000007340 Hordeum vulgare Nutrition 0.000 description 1
 - UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
 - MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
 - DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
 - 235000019483 Peanut oil Nutrition 0.000 description 1
 - 229920002472 Starch Polymers 0.000 description 1
 - NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
 - 235000021307 Triticum Nutrition 0.000 description 1
 - 244000098338 Triticum aestivum Species 0.000 description 1
 - 240000001717 Vaccinium macrocarpon Species 0.000 description 1
 - 239000002253 acid Substances 0.000 description 1
 - 238000005903 acid hydrolysis reaction Methods 0.000 description 1
 - 235000019647 acidic taste Nutrition 0.000 description 1
 - 235000010443 alginic acid Nutrition 0.000 description 1
 - 229920000615 alginic acid Polymers 0.000 description 1
 - 238000004458 analytical method Methods 0.000 description 1
 - 239000007864 aqueous solution Substances 0.000 description 1
 - 125000003118 aryl group Chemical group 0.000 description 1
 - QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
 - 239000011324 bead Substances 0.000 description 1
 - 244000309464 bull Species 0.000 description 1
 - 235000020289 caffè mocha Nutrition 0.000 description 1
 - 235000012970 cakes Nutrition 0.000 description 1
 - 239000001569 carbon dioxide Substances 0.000 description 1
 - 229910002092 carbon dioxide Inorganic materials 0.000 description 1
 - 235000011089 carbon dioxide Nutrition 0.000 description 1
 - 235000012174 carbonated soft drink Nutrition 0.000 description 1
 - 239000003153 chemical reaction reagent Substances 0.000 description 1
 - 239000003795 chemical substances by application Substances 0.000 description 1
 - 239000011248 coating agent Substances 0.000 description 1
 - 238000000576 coating method Methods 0.000 description 1
 - 235000021566 cold tea drink Nutrition 0.000 description 1
 - 238000009833 condensation Methods 0.000 description 1
 - 230000005494 condensation Effects 0.000 description 1
 - 239000013068 control sample Substances 0.000 description 1
 - 238000007796 conventional method Methods 0.000 description 1
 - 235000012343 cottonseed oil Nutrition 0.000 description 1
 - 239000002385 cottonseed oil Substances 0.000 description 1
 - 235000021019 cranberries Nutrition 0.000 description 1
 - 239000006071 cream Substances 0.000 description 1
 - 125000004122 cyclic group Chemical group 0.000 description 1
 - 230000003247 decreasing effect Effects 0.000 description 1
 - 239000007857 degradation product Substances 0.000 description 1
 - 235000011850 desserts Nutrition 0.000 description 1
 - 238000001514 detection method Methods 0.000 description 1
 - 238000011161 development Methods 0.000 description 1
 - 235000019425 dextrin Nutrition 0.000 description 1
 - SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 description 1
 - 239000012895 dilution Substances 0.000 description 1
 - 238000010790 dilution Methods 0.000 description 1
 - 238000009826 distribution Methods 0.000 description 1
 - QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 1
 - 230000001804 emulsifying effect Effects 0.000 description 1
 - 150000002148 esters Chemical class 0.000 description 1
 - ZCSDUGXKKBIICL-MDZDMXLPSA-N ethyl (e)-non-2-enoate Chemical compound CCCCCC\C=C\C(=O)OCC ZCSDUGXKKBIICL-MDZDMXLPSA-N 0.000 description 1
 - 235000019581 fat taste sensations Nutrition 0.000 description 1
 - 238000001914 filtration Methods 0.000 description 1
 - 235000011194 food seasoning agent Nutrition 0.000 description 1
 - 235000003599 food sweetener Nutrition 0.000 description 1
 - 239000007789 gas Substances 0.000 description 1
 - 238000004817 gas chromatography Methods 0.000 description 1
 - 229920000159 gelatin Polymers 0.000 description 1
 - 235000019322 gelatine Nutrition 0.000 description 1
 - 238000009499 grossing Methods 0.000 description 1
 - 238000000265 homogenisation Methods 0.000 description 1
 - 239000001257 hydrogen Substances 0.000 description 1
 - 229910052739 hydrogen Inorganic materials 0.000 description 1
 - 235000015243 ice cream Nutrition 0.000 description 1
 - 239000005457 ice water Substances 0.000 description 1
 - 238000002955 isolation Methods 0.000 description 1
 - 239000012280 lithium aluminium hydride Substances 0.000 description 1
 - 230000000873 masking effect Effects 0.000 description 1
 - 239000000463 material Substances 0.000 description 1
 - 238000002844 melting Methods 0.000 description 1
 - 230000008018 melting Effects 0.000 description 1
 - QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
 - 229940073769 methyl oleate Drugs 0.000 description 1
 - 235000016709 nutrition Nutrition 0.000 description 1
 - 238000007248 oxidative elimination reaction Methods 0.000 description 1
 - 229910052760 oxygen Inorganic materials 0.000 description 1
 - 239000001301 oxygen Substances 0.000 description 1
 - 235000014594 pastries Nutrition 0.000 description 1
 - 239000000312 peanut oil Substances 0.000 description 1
 - 235000010987 pectin Nutrition 0.000 description 1
 - 239000001814 pectin Substances 0.000 description 1
 - 229920001277 pectin Polymers 0.000 description 1
 - 239000000825 pharmaceutical preparation Substances 0.000 description 1
 - 229920000728 polyester Polymers 0.000 description 1
 - 235000011056 potassium acetate Nutrition 0.000 description 1
 - 238000002360 preparation method Methods 0.000 description 1
 - 108090000623 proteins and genes Proteins 0.000 description 1
 - 235000011962 puddings Nutrition 0.000 description 1
 - 238000000746 purification Methods 0.000 description 1
 - UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
 - 239000002994 raw material Substances 0.000 description 1
 - 239000011541 reaction mixture Substances 0.000 description 1
 - 229920006395 saturated elastomer Polymers 0.000 description 1
 - 229910052708 sodium Inorganic materials 0.000 description 1
 - 239000011734 sodium Substances 0.000 description 1
 - 238000001694 spray drying Methods 0.000 description 1
 - 239000003381 stabilizer Substances 0.000 description 1
 - 235000019698 starch Nutrition 0.000 description 1
 - 239000008107 starch Substances 0.000 description 1
 - 239000000021 stimulant Substances 0.000 description 1
 - 238000005728 strengthening Methods 0.000 description 1
 - 235000012094 sugar confectionery Nutrition 0.000 description 1
 - 229910052717 sulfur Inorganic materials 0.000 description 1
 - 239000011593 sulfur Substances 0.000 description 1
 - 239000003765 sweetening agent Substances 0.000 description 1
 - 230000008961 swelling Effects 0.000 description 1
 - 235000019630 tart taste sensations Nutrition 0.000 description 1
 - 230000009967 tasteless effect Effects 0.000 description 1
 - 238000012360 testing method Methods 0.000 description 1
 - 238000012546 transfer Methods 0.000 description 1
 - 235000015112 vegetable and seed oil Nutrition 0.000 description 1
 - 239000008158 vegetable oil Substances 0.000 description 1
 - 239000000341 volatile oil Substances 0.000 description 1
 - 238000005303 weighing Methods 0.000 description 1
 
Classifications
- 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
 - C07C57/02—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
 - C07C57/03—Monocarboxylic acids
 
 - 
        
- A—HUMAN NECESSITIES
 - A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
 - A23F—COFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
 - A23F5/00—Coffee; Coffee substitutes; Preparations thereof
 - A23F5/46—Coffee flavour; Coffee oil; Flavouring of coffee or coffee extract
 - A23F5/465—Flavouring with flavours other than natural coffee flavour or coffee oil
 
 - 
        
- A—HUMAN NECESSITIES
 - A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
 - A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
 - A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
 - A23L27/20—Synthetic spices, flavouring agents or condiments
 - A23L27/202—Aliphatic compounds
 - A23L27/2024—Aliphatic compounds having oxygen as the only hetero atom
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
 - C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
 - C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
 - C07C29/14—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
 - C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
 - C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
 - C07C29/147—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
 - C07C45/41—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by hydrogenolysis or reduction of carboxylic groups or functional derivatives thereof
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
 - C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
 - C07C51/353—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by isomerisation; by change of size of the carbon skeleton
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
 - C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
 - C07C51/58—Preparation of carboxylic acid halides
 - C07C51/60—Preparation of carboxylic acid halides by conversion of carboxylic acids or their anhydrides or esters, lactones, salts into halides with the same carboxylic acid part
 
 - 
        
- C—CHEMISTRY; METALLURGY
 - C07—ORGANIC CHEMISTRY
 - C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
 - C07B2200/00—Indexing scheme relating to specific properties of organic compounds
 - C07B2200/09—Geometrical isomers
 
 
Landscapes
- Chemical & Material Sciences (AREA)
 - Organic Chemistry (AREA)
 - Engineering & Computer Science (AREA)
 - Polymers & Plastics (AREA)
 - Life Sciences & Earth Sciences (AREA)
 - Food Science & Technology (AREA)
 - Oil, Petroleum & Natural Gas (AREA)
 - Health & Medical Sciences (AREA)
 - Nutrition Science (AREA)
 - Chemical Kinetics & Catalysis (AREA)
 - Tea And Coffee (AREA)
 - Seasonings (AREA)
 - Pivots And Pivotal Connections (AREA)
 
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| US85722769A | 1969-09-11 | 1969-09-11 | |
| US86787769A | 1969-10-20 | 1969-10-20 | 
Publications (3)
| Publication Number | Publication Date | 
|---|---|
| DE2044781A1 DE2044781A1 (de) | 1971-03-25 | 
| DE2044781B2 DE2044781B2 (de) | 1977-10-27 | 
| DE2044781C3 true DE2044781C3 (de) | 1978-06-22 | 
Family
ID=27127400
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| DE2044781A Expired DE2044781C3 (de) | 1969-09-11 | 1970-09-10 | Nahrungs- und Genußmittel mit Kaffeegeschmack | 
Country Status (12)
| Country | Link | 
|---|---|
| JP (1) | JPS5527792B1 (en:Method) | 
| BE (1) | BE756028A (en:Method) | 
| CA (1) | CA928139A (en:Method) | 
| CH (1) | CH528871A (en:Method) | 
| DE (1) | DE2044781C3 (en:Method) | 
| DK (1) | DK132926C (en:Method) | 
| FR (1) | FR2061672B1 (en:Method) | 
| GB (1) | GB1287048A (en:Method) | 
| IT (1) | IT988007B (en:Method) | 
| NL (1) | NL163417C (en:Method) | 
| NO (1) | NO132297C (en:Method) | 
| SE (1) | SE367536B (en:Method) | 
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| US3655397A (en) * | 1971-03-30 | 1972-04-11 | Gen Foods Corp | Flavor compositions and processes | 
| US4001454A (en) * | 1975-05-28 | 1977-01-04 | General Foods Corporation | Flavoring foods with 8-methyl-non-2ynol and its derivatives | 
- 
        0
        
- BE BE756028D patent/BE756028A/xx not_active IP Right Cessation
 
 - 
        1970
        
- 1970-09-08 NO NO3410/70A patent/NO132297C/no unknown
 - 1970-09-09 GB GB43233/70A patent/GB1287048A/en not_active Expired
 - 1970-09-10 IT IT53336/70A patent/IT988007B/it active
 - 1970-09-10 DK DK466870A patent/DK132926C/da not_active IP Right Cessation
 - 1970-09-10 DE DE2044781A patent/DE2044781C3/de not_active Expired
 - 1970-09-10 CA CA092770A patent/CA928139A/en not_active Expired
 - 1970-09-11 JP JP7937970A patent/JPS5527792B1/ja active Pending
 - 1970-09-11 CH CH1355770A patent/CH528871A/fr not_active IP Right Cessation
 - 1970-09-11 NL NL7013472.A patent/NL163417C/xx not_active IP Right Cessation
 - 1970-09-11 SE SE12419/70A patent/SE367536B/xx unknown
 - 1970-09-11 FR FR707033105A patent/FR2061672B1/fr not_active Expired
 
 
Also Published As
| Publication number | Publication date | 
|---|---|
| NL7013472A (en:Method) | 1971-03-15 | 
| NO132297C (en:Method) | 1975-10-22 | 
| DK132926C (da) | 1976-09-13 | 
| IT988007B (it) | 1975-04-10 | 
| DE2044781A1 (de) | 1971-03-25 | 
| FR2061672B1 (en:Method) | 1973-04-27 | 
| CH528871A (fr) | 1972-10-15 | 
| NL163417C (nl) | 1980-09-15 | 
| GB1287048A (en) | 1972-08-31 | 
| BE756028A (fr) | 1971-03-11 | 
| NL163417B (nl) | 1980-04-15 | 
| JPS5527792B1 (en:Method) | 1980-07-23 | 
| DK132926B (da) | 1976-03-01 | 
| SE367536B (en:Method) | 1974-06-04 | 
| DE2044781B2 (de) | 1977-10-27 | 
| NO132297B (en:Method) | 1975-07-14 | 
| FR2061672A1 (en:Method) | 1971-06-25 | 
| CA928139A (en) | 1973-06-12 | 
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Legal Events
| Date | Code | Title | Description | 
|---|---|---|---|
| C3 | Grant after two publication steps (3rd publication) | ||
| 8339 | Ceased/non-payment of the annual fee |