ZA200208004B - Ambient stable beverage. - Google Patents
Ambient stable beverage. Download PDFInfo
- Publication number
- ZA200208004B ZA200208004B ZA200208004A ZA200208004A ZA200208004B ZA 200208004 B ZA200208004 B ZA 200208004B ZA 200208004 A ZA200208004 A ZA 200208004A ZA 200208004 A ZA200208004 A ZA 200208004A ZA 200208004 B ZA200208004 B ZA 200208004B
- Authority
- ZA
- South Africa
- Prior art keywords
- acid
- ppm
- tea
- tubes
- methyl
- Prior art date
Links
- 235000013361 beverage Nutrition 0.000 title claims description 58
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 114
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims description 84
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 claims description 84
- 235000013985 cinnamic acid Nutrition 0.000 claims description 84
- 229930016911 cinnamic acid Natural products 0.000 claims description 84
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims description 84
- 235000010199 sorbic acid Nutrition 0.000 claims description 79
- 239000004334 sorbic acid Substances 0.000 claims description 78
- 229940075582 sorbic acid Drugs 0.000 claims description 78
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 claims description 77
- 235000010233 benzoic acid Nutrition 0.000 claims description 58
- 239000005711 Benzoic acid Substances 0.000 claims description 57
- 239000000341 volatile oil Substances 0.000 claims description 53
- 239000001695 (2E)-1,1-dimethoxy-3,7-dimethylocta-2,6-diene Substances 0.000 claims description 44
- ZSKAJFSSXURRGL-PKNBQFBNSA-N (2e)-1,1-dimethoxy-3,7-dimethylocta-2,6-diene Chemical compound COC(OC)\C=C(/C)CCC=C(C)C ZSKAJFSSXURRGL-PKNBQFBNSA-N 0.000 claims description 44
- OIGWAXDAPKFNCQ-UHFFFAOYSA-N 4-isopropylbenzyl alcohol Chemical compound CC(C)C1=CC=C(CO)C=C1 OIGWAXDAPKFNCQ-UHFFFAOYSA-N 0.000 claims description 44
- PRNCMAKCNVRZFX-UHFFFAOYSA-N 3,7-dimethyloctan-1-ol Chemical compound CC(C)CCCC(C)CCO PRNCMAKCNVRZFX-UHFFFAOYSA-N 0.000 claims description 27
- RXBQNMWIQKOSCS-UHFFFAOYSA-N (7,7-dimethyl-4-bicyclo[3.1.1]hept-3-enyl)methanol Chemical compound C1C2C(C)(C)C1CC=C2CO RXBQNMWIQKOSCS-UHFFFAOYSA-N 0.000 claims description 24
- JZQKTMZYLHNFPL-BLHCBFLLSA-N (2E,4E)-deca-2,4-dienal Chemical compound CCCCC\C=C\C=C\C=O JZQKTMZYLHNFPL-BLHCBFLLSA-N 0.000 claims description 13
- JZQKTMZYLHNFPL-UHFFFAOYSA-N 2-trans-4-trans-decadienal Natural products CCCCCC=CC=CC=O JZQKTMZYLHNFPL-UHFFFAOYSA-N 0.000 claims description 13
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 claims description 12
- RXBQNMWIQKOSCS-RKDXNWHRSA-N Myrtenol Natural products C1[C@H]2C(C)(C)[C@@H]1CC=C2CO RXBQNMWIQKOSCS-RKDXNWHRSA-N 0.000 claims description 12
- 229940043350 citral Drugs 0.000 claims description 12
- WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 claims description 12
- PFWYHTORQZAGCA-UHFFFAOYSA-N Piperonyl acetate Chemical compound CC(=O)OCC1=CC=C2OCOC2=C1 PFWYHTORQZAGCA-UHFFFAOYSA-N 0.000 claims description 11
- WRYLYDPHFGVWKC-UHFFFAOYSA-N 4-terpineol Chemical compound CC(C)C1(O)CCC(C)=CC1 WRYLYDPHFGVWKC-UHFFFAOYSA-N 0.000 claims description 9
- -1 isopropylbenzyl alcohol Chemical compound 0.000 claims description 9
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 claims description 9
- BATOPAZDIZEVQF-MQQKCMAXSA-N (E,E)-2,4-hexadienal Chemical compound C\C=C\C=C\C=O BATOPAZDIZEVQF-MQQKCMAXSA-N 0.000 claims description 8
- KRCZYMFUWVJCLI-UHFFFAOYSA-N Dihydrocarveol Chemical compound CC1CCC(C(C)=C)CC1O KRCZYMFUWVJCLI-UHFFFAOYSA-N 0.000 claims description 8
- ZYEMGPIYFIJGTP-UHFFFAOYSA-N O-methyleugenol Chemical compound COC1=CC=C(CC=C)C=C1OC ZYEMGPIYFIJGTP-UHFFFAOYSA-N 0.000 claims description 8
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 claims description 8
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 claims description 8
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 claims description 8
- KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 claims description 8
- CBOQJANXLMLOSS-UHFFFAOYSA-N ethyl vanillin Chemical compound CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 claims description 8
- VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 claims description 8
- IJXHLVMUNBOGRR-UHFFFAOYSA-N methyl nonanoate Chemical compound CCCCCCCCC(=O)OC IJXHLVMUNBOGRR-UHFFFAOYSA-N 0.000 claims description 8
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 claims description 8
- BATOPAZDIZEVQF-UHFFFAOYSA-N sorbic aldehyde Natural products CC=CC=CC=O BATOPAZDIZEVQF-UHFFFAOYSA-N 0.000 claims description 8
- KMPQYAYAQWNLME-UHFFFAOYSA-N undecanal Chemical compound CCCCCCCCCCC=O KMPQYAYAQWNLME-UHFFFAOYSA-N 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- XXRCUYVCPSWGCC-UHFFFAOYSA-N Ethyl pyruvate Chemical compound CCOC(=O)C(C)=O XXRCUYVCPSWGCC-UHFFFAOYSA-N 0.000 claims description 6
- 229940117360 ethyl pyruvate Drugs 0.000 claims description 6
- 239000000284 extract Substances 0.000 claims description 6
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 claims description 6
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 claims description 5
- KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 claims description 5
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- NZGWDASTMWDZIW-MRVPVSSYSA-N (+)-pulegone Chemical compound C[C@@H]1CCC(=C(C)C)C(=O)C1 NZGWDASTMWDZIW-MRVPVSSYSA-N 0.000 claims description 4
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 claims description 4
- IDEYZABHVQLHAF-GQCTYLIASA-N (e)-2-methylpent-2-enal Chemical compound CC\C=C(/C)C=O IDEYZABHVQLHAF-GQCTYLIASA-N 0.000 claims description 4
- IDEYZABHVQLHAF-UHFFFAOYSA-N 2-Methyl-2-pentenal Natural products CCC=C(C)C=O IDEYZABHVQLHAF-UHFFFAOYSA-N 0.000 claims description 4
- WRYLYDPHFGVWKC-SNVBAGLBSA-N 4-Terpineol Natural products CC(C)[C@]1(O)CCC(C)=CC1 WRYLYDPHFGVWKC-SNVBAGLBSA-N 0.000 claims description 4
- UVZMNGNFERVGRC-UHFFFAOYSA-N 4-cyclohexylbutanoic acid Chemical compound OC(=O)CCCC1CCCCC1 UVZMNGNFERVGRC-UHFFFAOYSA-N 0.000 claims description 4
- CRTCWNPLKVVXIX-UHFFFAOYSA-N 5-(2-Hydroxyethyl)-4-methylthiazole acetate Chemical compound CC(=O)OCCC=1SC=NC=1C CRTCWNPLKVVXIX-UHFFFAOYSA-N 0.000 claims description 4
- 239000005973 Carvone Substances 0.000 claims description 4
- KKVZAVRSVHUSPL-GQCTYLIASA-N Cassiastearoptene Chemical compound COC1=CC=CC=C1\C=C\C=O KKVZAVRSVHUSPL-GQCTYLIASA-N 0.000 claims description 4
- NOTFZGFABLVTIG-UHFFFAOYSA-N Cyclohexylethyl acetate Chemical compound CC(=O)OCCC1CCCCC1 NOTFZGFABLVTIG-UHFFFAOYSA-N 0.000 claims description 4
- NRVPMFHPHGBQLP-UHFFFAOYSA-N Ethyl 3-cyclohexylpropionate Chemical compound CCOC(=O)CCC1CCCCC1 NRVPMFHPHGBQLP-UHFFFAOYSA-N 0.000 claims description 4
- XMLSXPIVAXONDL-PLNGDYQASA-N Jasmone Chemical compound CC\C=C/CC1=C(C)CCC1=O XMLSXPIVAXONDL-PLNGDYQASA-N 0.000 claims description 4
- NZGWDASTMWDZIW-UHFFFAOYSA-N Pulegone Natural products CC1CCC(=C(C)C)C(=O)C1 NZGWDASTMWDZIW-UHFFFAOYSA-N 0.000 claims description 4
- ACWQBUSCFPJUPN-UHFFFAOYSA-N Tiglaldehyde Natural products CC=C(C)C=O ACWQBUSCFPJUPN-UHFFFAOYSA-N 0.000 claims description 4
- USMNOWBWPHYOEA-UHFFFAOYSA-N alpha-thujone Natural products CC1C(=O)CC2(C(C)C)C1C2 USMNOWBWPHYOEA-UHFFFAOYSA-N 0.000 claims description 4
- UDEWPOVQBGFNGE-UHFFFAOYSA-N benzoic acid n-propyl ester Natural products CCCOC(=O)C1=CC=CC=C1 UDEWPOVQBGFNGE-UHFFFAOYSA-N 0.000 claims description 4
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 claims description 4
- KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 claims description 4
- 229940117916 cinnamic aldehyde Drugs 0.000 claims description 4
- 235000000484 citronellol Nutrition 0.000 claims description 4
- 229930007024 dihydrocarveol Natural products 0.000 claims description 4
- 229940073505 ethyl vanillin Drugs 0.000 claims description 4
- 150000002596 lactones Chemical class 0.000 claims description 4
- 229940102398 methyl anthranilate Drugs 0.000 claims description 4
- OLXYLDUSSBULGU-UHFFFAOYSA-N methyl pyridine-4-carboxylate Chemical compound COC(=O)C1=CC=NC=C1 OLXYLDUSSBULGU-UHFFFAOYSA-N 0.000 claims description 4
- 229960001047 methyl salicylate Drugs 0.000 claims description 4
- 229940116837 methyleugenol Drugs 0.000 claims description 4
- PRHTXAOWJQTLBO-UHFFFAOYSA-N methyleugenol Natural products COC1=CC=C(C(C)=C)C=C1OC PRHTXAOWJQTLBO-UHFFFAOYSA-N 0.000 claims description 4
- KKVZAVRSVHUSPL-UHFFFAOYSA-N o-methoxycinnamic aldehyde Natural products COC1=CC=CC=C1C=CC=O KKVZAVRSVHUSPL-UHFFFAOYSA-N 0.000 claims description 4
- 229930007459 p-menth-8-en-3-one Natural products 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- XMLSXPIVAXONDL-UHFFFAOYSA-N trans-jasmone Natural products CCC=CCC1=C(C)CCC1=O XMLSXPIVAXONDL-UHFFFAOYSA-N 0.000 claims description 4
- KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 claims description 4
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 claims description 4
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 claims description 4
- 235000012141 vanillin Nutrition 0.000 claims description 4
- MOZDKDIOPSPTBH-UHFFFAOYSA-N Benzyl parahydroxybenzoate Chemical compound C1=CC(O)=CC=C1C(=O)OCC1=CC=CC=C1 MOZDKDIOPSPTBH-UHFFFAOYSA-N 0.000 claims description 3
- YKFKEYKJGVSEIX-UHFFFAOYSA-N cyclohexanone, 4-(1,1-dimethylethyl)- Chemical compound CC(C)(C)C1CCC(=O)CC1 YKFKEYKJGVSEIX-UHFFFAOYSA-N 0.000 claims description 3
- YURDCJXYOLERLO-LCYFTJDESA-N (2E)-5-methyl-2-phenylhex-2-enal Chemical compound CC(C)C\C=C(\C=O)C1=CC=CC=C1 YURDCJXYOLERLO-LCYFTJDESA-N 0.000 claims description 2
- YURDCJXYOLERLO-UHFFFAOYSA-N 5-Methyl-2-phenyl-2-hexenal Natural products CC(C)CC=C(C=O)C1=CC=CC=C1 YURDCJXYOLERLO-UHFFFAOYSA-N 0.000 claims description 2
- 241001122767 Theaceae Species 0.000 claims 4
- SPEUIVXLLWOEMJ-UHFFFAOYSA-N 1,1-dimethoxyethane Chemical compound COC(C)OC SPEUIVXLLWOEMJ-UHFFFAOYSA-N 0.000 claims 2
- ZAUAFFKABKNGKX-QPJJXVBHSA-N (e)-3-(2-methylphenyl)prop-2-enal Chemical compound CC1=CC=CC=C1\C=C\C=O ZAUAFFKABKNGKX-QPJJXVBHSA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 229960005235 piperonyl butoxide Drugs 0.000 claims 1
- 125000004591 piperonyl group Chemical group C(C1=CC=2OCOC2C=C1)* 0.000 claims 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 144
- 235000013616 tea Nutrition 0.000 description 112
- 244000269722 Thea sinensis Species 0.000 description 105
- 230000012010 growth Effects 0.000 description 98
- 235000014680 Saccharomyces cerevisiae Nutrition 0.000 description 91
- 239000011159 matrix material Substances 0.000 description 71
- 235000012098 RTD tea Nutrition 0.000 description 53
- 239000003755 preservative agent Substances 0.000 description 41
- 230000002301 combined effect Effects 0.000 description 35
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- 239000012470 diluted sample Substances 0.000 description 26
- 230000003287 optical effect Effects 0.000 description 26
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 21
- 230000000694 effects Effects 0.000 description 18
- 238000002474 experimental method Methods 0.000 description 18
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 14
- 239000000796 flavoring agent Substances 0.000 description 8
- 235000019634 flavors Nutrition 0.000 description 8
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- 229940041514 candida albicans extract Drugs 0.000 description 7
- 239000008103 glucose Substances 0.000 description 7
- 229910001629 magnesium chloride Inorganic materials 0.000 description 7
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 7
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- 230000002335 preservative effect Effects 0.000 description 6
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- 235000019640 taste Nutrition 0.000 description 4
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- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910001425 magnesium ion Inorganic materials 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- 229930007503 menthone Natural products 0.000 description 1
- IJFXRHURBJZNAO-UHFFFAOYSA-N meta--hydroxybenzoic acid Natural products OC(=O)C1=CC=CC(O)=C1 IJFXRHURBJZNAO-UHFFFAOYSA-N 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 229940017219 methyl propionate Drugs 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- YKYONYBAUNKHLG-UHFFFAOYSA-N n-Propyl acetate Natural products CCCOC(C)=O YKYONYBAUNKHLG-UHFFFAOYSA-N 0.000 description 1
- QQZOPKMRPOGIEB-UHFFFAOYSA-N n-butyl methyl ketone Natural products CCCCC(C)=O QQZOPKMRPOGIEB-UHFFFAOYSA-N 0.000 description 1
- UUIQMZJEGPQKFD-UHFFFAOYSA-N n-butyric acid methyl ester Natural products CCCC(=O)OC UUIQMZJEGPQKFD-UHFFFAOYSA-N 0.000 description 1
- HNBDRPTVWVGKBR-UHFFFAOYSA-N n-pentanoic acid methyl ester Natural products CCCCC(=O)OC HNBDRPTVWVGKBR-UHFFFAOYSA-N 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- WASNIKZYIWZQIP-AWEZNQCLSA-N nerolidol Natural products CC(=CCCC(=CCC[C@@H](O)C=C)C)C WASNIKZYIWZQIP-AWEZNQCLSA-N 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 238000009928 pasteurization Methods 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- QCCDLTOVEPVEJK-UHFFFAOYSA-N phenylacetone Chemical compound CC(=O)CC1=CC=CC=C1 QCCDLTOVEPVEJK-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 230000029553 photosynthesis Effects 0.000 description 1
- 238000010672 photosynthesis Methods 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000004302 potassium sorbate Substances 0.000 description 1
- 235000010241 potassium sorbate Nutrition 0.000 description 1
- 229940069338 potassium sorbate Drugs 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 229940090181 propyl acetate Drugs 0.000 description 1
- YQUVCSBJEUQKSH-UHFFFAOYSA-N protochatechuic acid Natural products OC(=O)C1=CC=C(O)C(O)=C1 YQUVCSBJEUQKSH-UHFFFAOYSA-N 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 229960001811 quinine hydrochloride Drugs 0.000 description 1
- WSWCOQWTEOXDQX-MQQKCMAXSA-N sorbic acid group Chemical group C(\C=C\C=C\C)(=O)O WSWCOQWTEOXDQX-MQQKCMAXSA-N 0.000 description 1
- 150000003398 sorbic acids Chemical class 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- JKUYRAMKJLMYLO-UHFFFAOYSA-N tert-butyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OC(C)(C)C JKUYRAMKJLMYLO-UHFFFAOYSA-N 0.000 description 1
- 230000035922 thirst Effects 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- RUVINXPYWBROJD-ONEGZZNKSA-N trans-anethole Chemical compound COC1=CC=C(\C=C\C)C=C1 RUVINXPYWBROJD-ONEGZZNKSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- ZHYZQXUYZJNEHD-UHFFFAOYSA-N trans-geranic acid Natural products CC(C)=CCCC(C)=CC(O)=O ZHYZQXUYZJNEHD-UHFFFAOYSA-N 0.000 description 1
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 1
- QURCVMIEKCOAJU-UHFFFAOYSA-N trans-isoferulic acid Natural products COC1=CC=C(C=CC(O)=O)C=C1O QURCVMIEKCOAJU-UHFFFAOYSA-N 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- WKOLLVMJNQIZCI-UHFFFAOYSA-N vanillic acid Chemical compound COC1=CC(C(O)=O)=CC=C1O WKOLLVMJNQIZCI-UHFFFAOYSA-N 0.000 description 1
- TUUBOHWZSQXCSW-UHFFFAOYSA-N vanillic acid Natural products COC1=CC(O)=CC(C(O)=O)=C1 TUUBOHWZSQXCSW-UHFFFAOYSA-N 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 235000014101 wine Nutrition 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/42—Preservation of non-alcoholic beverages
- A23L2/44—Preservation of non-alcoholic beverages by adding preservatives
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23F—COFFEE; TEA; THEIR SUBSTITUTES; MANUFACTURE, PREPARATION, OR INFUSION THEREOF
- A23F3/00—Tea; Tea substitutes; Preparations thereof
- A23F3/16—Tea extraction; Tea extracts; Treating tea extract; Making instant tea
- A23F3/163—Liquid or semi-liquid tea extract preparations, e.g. gels, liquid extracts in solid capsules
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
- A23L2/00—Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
- A23L2/52—Adding ingredients
- A23L2/68—Acidifying substances
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Dispersion Chemistry (AREA)
- Tea And Coffee (AREA)
- Non-Alcoholic Beverages (AREA)
- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0011676.4A GB0011676D0 (en) | 2000-05-15 | 2000-05-15 | Ambient stable beverage |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200208004B true ZA200208004B (en) | 2003-10-06 |
Family
ID=9891617
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200208004A ZA200208004B (en) | 2000-05-15 | 2002-10-04 | Ambient stable beverage. |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US6761919B2 (da) |
| EP (1) | EP1282370B1 (da) |
| JP (1) | JP4519391B2 (da) |
| CN (1) | CN1263404C (da) |
| AR (1) | AR028098A1 (da) |
| AT (1) | ATE311769T1 (da) |
| AU (1) | AU2001267391B2 (da) |
| BR (1) | BR0110688A (da) |
| CA (1) | CA2408933C (da) |
| DE (1) | DE60115632T2 (da) |
| DK (1) | DK1282370T3 (da) |
| ES (1) | ES2252248T3 (da) |
| GB (1) | GB0011676D0 (da) |
| HU (1) | HUP0302137A3 (da) |
| MX (1) | MXPA02011243A (da) |
| MY (1) | MY128418A (da) |
| PL (1) | PL199165B1 (da) |
| WO (1) | WO2001087095A1 (da) |
| ZA (1) | ZA200208004B (da) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005514924A (ja) * | 2002-01-02 | 2005-05-26 | キンタロー・サケ・カンパニー・リミテッド・ライアビリティ・カンパニー | 浸出日本酒およびその製造方法 |
| JP4657715B2 (ja) * | 2002-08-12 | 2011-03-23 | ロンザ インコーポレイテッド | 抗菌性組成物 |
| GB2408933A (en) * | 2003-12-12 | 2005-06-15 | Reckitt Benckiser Healthcare | Antimicrobial composition |
| GB0416200D0 (en) * | 2004-07-20 | 2004-08-18 | Unilever Plc | Tea-based beverage |
| EP1629732A1 (en) * | 2004-08-27 | 2006-03-01 | Purac Biochem BV | Composition for inactivating yeasts or molds in soft drinks |
| JP4500874B2 (ja) | 2005-05-23 | 2010-07-14 | キャドバリー アダムス ユーエスエー エルエルシー | 味覚増強剤組成物及び味覚増強剤組成物を含有する飲料 |
| JP4694619B2 (ja) * | 2005-05-23 | 2011-06-08 | キャドバリー・アダムズ・ユーエスエイ・エルエルシー | エラストマー成分、調理済み糖成分および改善した放出成分を含む菓子組成物 |
| WO2007120544A2 (en) * | 2006-04-12 | 2007-10-25 | Alexander Rayna L | Compositions comprising pyruvate alkyl esters and uses thereof |
| US20070275140A1 (en) * | 2006-05-26 | 2007-11-29 | Paula Safko | Beverage compositions comprising a preservative system |
| US20080193616A1 (en) * | 2007-02-13 | 2008-08-14 | The Coca-Cola Company | Beverage compositions comprising polylysine and at least one weak acid |
| GB0710884D0 (en) * | 2007-06-07 | 2007-07-18 | Univ Nottingham | Preservative |
| US8945655B2 (en) * | 2007-07-10 | 2015-02-03 | Conopco, Inc. | Stable and consumable compositions |
| US20090074927A1 (en) | 2007-09-18 | 2009-03-19 | Pepsico, Inc. | Cinnamic Acid To Inhibit Heat- And Light-Induced Benzene Formation In Benzoate-Preserved Carbonated And Non-Carbonated Beverages And Foods While Maintaining Or Improving Product Microbial Stability |
| EP2312958A1 (en) * | 2008-08-07 | 2011-04-27 | PepsiCo, Inc. | Extension of beverage shelf-stability by solute-ligand complexes |
| US20100151104A1 (en) * | 2008-10-27 | 2010-06-17 | Pepsico, Inc. | Preservative System For Beverages Based On Combinations Of Trans-Cinnamic Acid, Lauric Arginate, And Dimethyl Dicarbonate |
| US8628812B2 (en) | 2008-12-30 | 2014-01-14 | Pepsico, Inc. | Preservative system for acidic beverages based on sequestrants |
| FR2967055B1 (fr) * | 2010-11-08 | 2012-12-21 | Biochimie Appliquee Solabia | Compositions cosmetiques a base d'esters de piperonyle et leur utilisation en sosmetique en tant qu'anti-vieillissement cutane et agent depigmentant |
| CN103347407A (zh) * | 2011-02-07 | 2013-10-09 | 弗门尼舍有限公司 | 抗真菌调味成分和组合物 |
| MX2013012646A (es) | 2011-04-29 | 2014-02-11 | Intercontinental Great Brands Llc | Acido encapsulado, metodo para la preparacion del mismo y goma de mascar que comprende el mismo. |
| EP2583568A1 (en) * | 2011-10-18 | 2013-04-24 | Purac Biochem N.V. | Preservative combinations comprising vanillin and cinnamic acid |
| EP2583567A1 (en) * | 2011-10-18 | 2013-04-24 | Purac Biochem N.V. | Preservative combinations comprising propionic acid and vanillin and/or cinnamic acid |
| CN102406209B (zh) * | 2011-11-28 | 2013-04-10 | 新疆和田阳光沙漠玫瑰有限公司 | 一种含玫瑰精油有效成份的液态饮及其制备方法 |
| EP2995201A1 (en) | 2014-09-04 | 2016-03-16 | Purac Biochem B.V. | Preservation of meat products with a composition comprising a vanilin and a cinnamate component |
| GB201503581D0 (en) * | 2015-03-03 | 2015-04-15 | Woodall Guy | A beverage |
| BR112021013871A2 (pt) * | 2019-02-14 | 2021-09-14 | Unilever Ip Holdings B.V. | Alimento conservado, bebida conservada e método para preparar um alimento conservado |
| MX2021009710A (es) * | 2019-02-14 | 2021-09-14 | Unilever Ip Holdings B V | Producto de bebida de te negro en conserva. |
| AU2020220265B2 (en) | 2019-02-14 | 2022-08-25 | Unilever Ip Holdings B.V. | Preserved tea product |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2148431B1 (da) | 1971-08-12 | 1978-03-03 | Nestle Sa | |
| JPS57194775A (en) * | 1981-05-21 | 1982-11-30 | Asama Kasei Kk | Storing and quality improving agent of food |
| JPS61148110A (ja) * | 1984-12-20 | 1986-07-05 | Pola Chem Ind Inc | 化粧料の防腐方法 |
| JPH0578219A (ja) * | 1991-05-15 | 1993-03-30 | Nippon Sanso Kk | 鳥獣類忌避剤 |
| JPH05255126A (ja) * | 1992-03-04 | 1993-10-05 | Zeria Pharmaceut Co Ltd | 苦味低減組成物 |
| US5441979A (en) | 1994-01-27 | 1995-08-15 | Buckman Laboratories International, Inc. | Synergistic antimicrobial compositions containing methylene-bis(thiocyanate) and an organic acid |
| FR2728462B1 (fr) | 1994-12-21 | 1998-04-24 | Chicouri Marcel | Nouvelles compositions laxatives et leur procede d'obtention |
| RU2113133C1 (ru) * | 1995-12-01 | 1998-06-20 | Всероссийский научно-исследовательский институт пищевых ароматизаторов, кислот и красителей | Пищевой ароматизатор со вкусом и ароматом тропических плодов |
| US6036986A (en) * | 1997-10-28 | 2000-03-14 | Lipton, Division Of Conopco, Inc. | Cinnamic acid for use in tea containing beverages |
| US6022576A (en) * | 1997-10-28 | 2000-02-08 | Lipton, Division Of Conopco, Inc. | Flavoring materials for use in tea containing beverages |
| TR200001149T2 (tr) * | 1997-10-28 | 2000-08-21 | Unilever N.V. | Oda sıcaklığında niteliği bozulmayan niteliği bozulmayan ve esası çay olan bir içecek |
| JP3404703B2 (ja) * | 1998-03-02 | 2003-05-12 | 株式会社 伊藤園 | 青果物の変色防止剤 |
| EP1077034B1 (en) * | 1999-08-18 | 2003-10-22 | Symrise GmbH & Co. KG | Flavor delivery system |
-
2000
- 2000-05-15 GB GBGB0011676.4A patent/GB0011676D0/en not_active Ceased
-
2001
- 2001-05-01 JP JP2001583572A patent/JP4519391B2/ja not_active Expired - Lifetime
- 2001-05-01 WO PCT/EP2001/004856 patent/WO2001087095A1/en active IP Right Grant
- 2001-05-01 AU AU2001267391A patent/AU2001267391B2/en not_active Ceased
- 2001-05-01 HU HU0302137A patent/HUP0302137A3/hu unknown
- 2001-05-01 CA CA002408933A patent/CA2408933C/en not_active Expired - Fee Related
- 2001-05-01 BR BR0110688-0A patent/BR0110688A/pt not_active IP Right Cessation
- 2001-05-01 EP EP01945065A patent/EP1282370B1/en not_active Expired - Lifetime
- 2001-05-01 DK DK01945065T patent/DK1282370T3/da active
- 2001-05-01 PL PL363530A patent/PL199165B1/pl not_active IP Right Cessation
- 2001-05-01 CN CNB01809533XA patent/CN1263404C/zh not_active Expired - Fee Related
- 2001-05-01 AT AT01945065T patent/ATE311769T1/de not_active IP Right Cessation
- 2001-05-01 MX MXPA02011243A patent/MXPA02011243A/es active IP Right Grant
- 2001-05-01 ES ES01945065T patent/ES2252248T3/es not_active Expired - Lifetime
- 2001-05-01 DE DE60115632T patent/DE60115632T2/de not_active Expired - Fee Related
- 2001-05-11 MY MYPI20012215A patent/MY128418A/en unknown
- 2001-05-14 AR ARP010102271A patent/AR028098A1/es active IP Right Grant
- 2001-05-14 US US09/854,877 patent/US6761919B2/en not_active Expired - Lifetime
-
2002
- 2002-10-04 ZA ZA200208004A patent/ZA200208004B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES2252248T3 (es) | 2006-05-16 |
| EP1282370A1 (en) | 2003-02-12 |
| US6761919B2 (en) | 2004-07-13 |
| CA2408933C (en) | 2009-11-10 |
| DK1282370T3 (da) | 2006-01-09 |
| BR0110688A (pt) | 2003-03-18 |
| HUP0302137A2 (hu) | 2003-09-29 |
| PL199165B1 (pl) | 2008-08-29 |
| US20010055646A1 (en) | 2001-12-27 |
| CA2408933A1 (en) | 2001-11-22 |
| MXPA02011243A (es) | 2003-03-10 |
| CN1263404C (zh) | 2006-07-12 |
| ATE311769T1 (de) | 2005-12-15 |
| DE60115632T2 (de) | 2006-06-29 |
| WO2001087095A1 (en) | 2001-11-22 |
| AR028098A1 (es) | 2003-04-23 |
| AU6739101A (en) | 2001-11-26 |
| DE60115632D1 (de) | 2006-01-12 |
| EP1282370B1 (en) | 2005-12-07 |
| MY128418A (en) | 2007-01-31 |
| CN1429079A (zh) | 2003-07-09 |
| PL363530A1 (en) | 2004-11-29 |
| GB0011676D0 (en) | 2000-07-05 |
| HUP0302137A3 (en) | 2005-11-28 |
| JP2003533201A (ja) | 2003-11-11 |
| JP4519391B2 (ja) | 2010-08-04 |
| AU2001267391B2 (en) | 2004-01-08 |
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