ZA200303305B - Solvent extraction process. - Google Patents
Solvent extraction process. Download PDFInfo
- Publication number
- ZA200303305B ZA200303305B ZA200303305A ZA200303305A ZA200303305B ZA 200303305 B ZA200303305 B ZA 200303305B ZA 200303305 A ZA200303305 A ZA 200303305A ZA 200303305 A ZA200303305 A ZA 200303305A ZA 200303305 B ZA200303305 B ZA 200303305B
- Authority
- ZA
- South Africa
- Prior art keywords
- solvent
- extraction
- composition
- extract
- compound
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 97
- 238000000638 solvent extraction Methods 0.000 title description 11
- 238000000605 extraction Methods 0.000 claims abstract description 92
- 239000002904 solvent Substances 0.000 claims abstract description 89
- 239000000203 mixture Substances 0.000 claims abstract description 47
- 150000001875 compounds Chemical class 0.000 claims abstract description 46
- 239000002994 raw material Substances 0.000 claims description 30
- 239000007788 liquid Substances 0.000 claims description 29
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 21
- 239000006184 cosolvent Substances 0.000 claims description 15
- UKACHOXRXFQJFN-UHFFFAOYSA-N heptafluoropropane Chemical compound FC(F)C(F)(F)C(F)(F)F UKACHOXRXFQJFN-UHFFFAOYSA-N 0.000 claims description 14
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 12
- YFMFNYKEUDLDTL-UHFFFAOYSA-N 1,1,1,2,3,3,3-heptafluoropropane Chemical compound FC(F)(F)C(F)C(F)(F)F YFMFNYKEUDLDTL-UHFFFAOYSA-N 0.000 claims description 9
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 9
- 239000002243 precursor Substances 0.000 claims description 8
- 239000004567 concrete Substances 0.000 claims description 7
- 239000000470 constituent Substances 0.000 claims description 7
- 239000003205 fragrance Substances 0.000 claims description 6
- 229930195733 hydrocarbon Natural products 0.000 claims description 6
- 150000002430 hydrocarbons Chemical class 0.000 claims description 6
- 239000000796 flavoring agent Substances 0.000 claims description 5
- 235000019634 flavors Nutrition 0.000 claims description 5
- 239000004215 Carbon black (E152) Substances 0.000 claims description 4
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 4
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 claims description 4
- 150000001335 aliphatic alkanes Chemical class 0.000 claims description 3
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 3
- 239000008601 oleoresin Substances 0.000 claims description 3
- 239000000575 pesticide Substances 0.000 claims description 3
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 claims description 2
- XOBKSJJDNFUZPF-UHFFFAOYSA-N Methoxyethane Chemical compound CCOC XOBKSJJDNFUZPF-UHFFFAOYSA-N 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- 125000005907 alkyl ester group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 150000001924 cycloalkanes Chemical class 0.000 claims description 2
- 239000001294 propane Substances 0.000 claims description 2
- 239000013543 active substance Substances 0.000 claims 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000007787 solid Substances 0.000 abstract description 15
- 239000000341 volatile oil Substances 0.000 abstract description 9
- 239000003463 adsorbent Substances 0.000 abstract description 4
- 150000003505 terpenes Chemical class 0.000 abstract description 4
- 235000007586 terpenes Nutrition 0.000 abstract description 3
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 abstract 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 abstract 1
- 230000000717 retained effect Effects 0.000 abstract 1
- 239000000463 material Substances 0.000 description 32
- 239000003921 oil Substances 0.000 description 29
- 235000019198 oils Nutrition 0.000 description 29
- 239000000284 extract Substances 0.000 description 23
- 229930014626 natural product Natural products 0.000 description 17
- 241000196324 Embryophyta Species 0.000 description 15
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 15
- NPNUFJAVOOONJE-ZIAGYGMSSA-N β-(E)-Caryophyllene Chemical compound C1CC(C)=CCCC(=C)[C@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-ZIAGYGMSSA-N 0.000 description 12
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 10
- 235000019441 ethanol Nutrition 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 8
- CDOSHBSSFJOMGT-UHFFFAOYSA-N beta-linalool Natural products CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 8
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 8
- NVEQFIOZRFFVFW-UHFFFAOYSA-N 9-epi-beta-caryophyllene oxide Natural products C=C1CCC2OC2(C)CCC2C(C)(C)CC21 NVEQFIOZRFFVFW-UHFFFAOYSA-N 0.000 description 7
- 238000009835 boiling Methods 0.000 description 7
- 229940117948 caryophyllene Drugs 0.000 description 7
- 238000004821 distillation Methods 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- FAMPSKZZVDUYOS-UHFFFAOYSA-N alpha-Caryophyllene Natural products CC1=CCC(C)(C)C=CCC(C)=CCC1 FAMPSKZZVDUYOS-UHFFFAOYSA-N 0.000 description 6
- NPNUFJAVOOONJE-UHFFFAOYSA-N beta-cariophyllene Natural products C1CC(C)=CCCC(=C)C2CC(C)(C)C21 NPNUFJAVOOONJE-UHFFFAOYSA-N 0.000 description 6
- NPNUFJAVOOONJE-UONOGXRCSA-N caryophyllene Natural products C1CC(C)=CCCC(=C)[C@@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-UONOGXRCSA-N 0.000 description 6
- 239000001913 cellulose Substances 0.000 description 6
- 229920002678 cellulose Polymers 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- NDVASEGYNIMXJL-UHFFFAOYSA-N sabinene Chemical compound C=C1CCC2(C(C)C)C1C2 NDVASEGYNIMXJL-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 5
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 5
- 235000010254 Jasminum officinale Nutrition 0.000 description 5
- 240000005385 Jasminum sambac Species 0.000 description 5
- 238000011156 evaluation Methods 0.000 description 5
- 235000001510 limonene Nutrition 0.000 description 5
- 229940087305 limonene Drugs 0.000 description 5
- 229930007744 linalool Natural products 0.000 description 5
- 230000001953 sensory effect Effects 0.000 description 5
- SCCDQYPEOIRVGX-UHFFFAOYSA-N Acetyleugenol Chemical compound COC1=CC(CC=C)=CC=C1OC(C)=O SCCDQYPEOIRVGX-UHFFFAOYSA-N 0.000 description 4
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 4
- 239000005770 Eugenol Substances 0.000 description 4
- 241001469893 Oxyzygonectes dovii Species 0.000 description 4
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 4
- 244000223014 Syzygium aromaticum Species 0.000 description 4
- 235000016639 Syzygium aromaticum Nutrition 0.000 description 4
- 244000269722 Thea sinensis Species 0.000 description 4
- BQOFWKZOCNGFEC-UHFFFAOYSA-N carene Chemical compound C1C(C)=CCC2C(C)(C)C12 BQOFWKZOCNGFEC-UHFFFAOYSA-N 0.000 description 4
- 239000012809 cooling fluid Substances 0.000 description 4
- 229960002217 eugenol Drugs 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- -1 hydrocarbon ethers Chemical class 0.000 description 4
- 150000002576 ketones Chemical class 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 description 4
- 239000012925 reference material Substances 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- RUVINXPYWBROJD-ONEGZZNKSA-N trans-anethole Chemical compound COC1=CC=C(\C=C\C)C=C1 RUVINXPYWBROJD-ONEGZZNKSA-N 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- NDVASEGYNIMXJL-NXEZZACHSA-N (+)-sabinene Natural products C=C1CC[C@@]2(C(C)C)[C@@H]1C2 NDVASEGYNIMXJL-NXEZZACHSA-N 0.000 description 3
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-Phenylethanol Natural products OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- 239000002028 Biomass Substances 0.000 description 3
- 239000005792 Geraniol Substances 0.000 description 3
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 3
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 3
- XMLSXPIVAXONDL-PLNGDYQASA-N Jasmone Chemical compound CC\C=C/CC1=C(C)CCC1=O XMLSXPIVAXONDL-PLNGDYQASA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 244000203593 Piper nigrum Species 0.000 description 3
- 235000008184 Piper nigrum Nutrition 0.000 description 3
- 238000000944 Soxhlet extraction Methods 0.000 description 3
- 235000009499 Vanilla fragrans Nutrition 0.000 description 3
- 244000263375 Vanilla tahitensis Species 0.000 description 3
- 235000012036 Vanilla tahitensis Nutrition 0.000 description 3
- 235000006886 Zingiber officinale Nutrition 0.000 description 3
- 244000273928 Zingiber officinale Species 0.000 description 3
- KGEKLUUHTZCSIP-HOSYDEDBSA-N [(1s,4s,6r)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] acetate Chemical compound C1C[C@]2(C)[C@H](OC(=O)C)C[C@H]1C2(C)C KGEKLUUHTZCSIP-HOSYDEDBSA-N 0.000 description 3
- KQAZVFVOEIRWHN-UHFFFAOYSA-N alpha-thujene Natural products CC1=CCC2(C(C)C)C1C2 KQAZVFVOEIRWHN-UHFFFAOYSA-N 0.000 description 3
- 239000010692 aromatic oil Substances 0.000 description 3
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 3
- CRPUJAZIXJMDBK-UHFFFAOYSA-N camphene Chemical compound C1CC2C(=C)C(C)(C)C1C2 CRPUJAZIXJMDBK-UHFFFAOYSA-N 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 229940113087 geraniol Drugs 0.000 description 3
- 235000008397 ginger Nutrition 0.000 description 3
- 238000000622 liquid--liquid extraction Methods 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- 229930006696 sabinene Natural products 0.000 description 3
- XMLSXPIVAXONDL-UHFFFAOYSA-N trans-jasmone Natural products CCC=CCC1=C(C)CCC1=O XMLSXPIVAXONDL-UHFFFAOYSA-N 0.000 description 3
- LFJQCDVYDGGFCH-UHFFFAOYSA-N β-phellandrene Chemical compound CC(C)C1CCC(=C)C=C1 LFJQCDVYDGGFCH-UHFFFAOYSA-N 0.000 description 3
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 2
- WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 description 2
- XHXUANMFYXWVNG-ADEWGFFLSA-N (-)-Menthyl acetate Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1OC(C)=O XHXUANMFYXWVNG-ADEWGFFLSA-N 0.000 description 2
- GRWFGVWFFZKLTI-IUCAKERBSA-N (-)-α-pinene Chemical compound CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 2
- JSNRRGGBADWTMC-UHFFFAOYSA-N (6E)-7,11-dimethyl-3-methylene-1,6,10-dodecatriene Chemical compound CC(C)=CCCC(C)=CCCC(=C)C=C JSNRRGGBADWTMC-UHFFFAOYSA-N 0.000 description 2
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 description 2
- WEEGYLXZBRQIMU-UHFFFAOYSA-N 1,8-cineole Natural products C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 2
- XBGUIVFBMBVUEG-UHFFFAOYSA-N 1-methyl-4-(1,5-dimethyl-4-hexenylidene)-1-cyclohexene Chemical compound CC(C)=CCCC(C)=C1CCC(C)=CC1 XBGUIVFBMBVUEG-UHFFFAOYSA-N 0.000 description 2
- RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 description 2
- 235000002566 Capsicum Nutrition 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 241000207199 Citrus Species 0.000 description 2
- 244000089742 Citrus aurantifolia Species 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- 235000005979 Citrus limon Nutrition 0.000 description 2
- 244000131522 Citrus pyriformis Species 0.000 description 2
- VLXDPFLIRFYIME-GZBLMMOJSA-N Copaene Natural products C1C=C(C)[C@H]2[C@]3(C)CC[C@H](C(C)C)[C@H]2[C@@H]31 VLXDPFLIRFYIME-GZBLMMOJSA-N 0.000 description 2
- 235000003392 Curcuma domestica Nutrition 0.000 description 2
- 244000008991 Curcuma longa Species 0.000 description 2
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 2
- 244000133098 Echinacea angustifolia Species 0.000 description 2
- ZFMSMUAANRJZFM-UHFFFAOYSA-N Estragole Chemical compound COC1=CC=C(CC=C)C=C1 ZFMSMUAANRJZFM-UHFFFAOYSA-N 0.000 description 2
- WEEGYLXZBRQIMU-WAAGHKOSSA-N Eucalyptol Chemical compound C1C[C@H]2CC[C@]1(C)OC2(C)C WEEGYLXZBRQIMU-WAAGHKOSSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- 235000008100 Ginkgo biloba Nutrition 0.000 description 2
- 244000194101 Ginkgo biloba Species 0.000 description 2
- 235000010469 Glycine max Nutrition 0.000 description 2
- 244000068988 Glycine max Species 0.000 description 2
- 235000008227 Illicium verum Nutrition 0.000 description 2
- 240000007232 Illicium verum Species 0.000 description 2
- BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 description 2
- 241001673966 Magnolia officinalis Species 0.000 description 2
- 239000006002 Pepper Substances 0.000 description 2
- 235000016761 Piper aduncum Nutrition 0.000 description 2
- 235000017804 Piper guineense Nutrition 0.000 description 2
- PXRCIOIWVGAZEP-UHFFFAOYSA-N Primaeres Camphenhydrat Natural products C1CC2C(O)(C)C(C)(C)C1C2 PXRCIOIWVGAZEP-UHFFFAOYSA-N 0.000 description 2
- 241000220317 Rosa Species 0.000 description 2
- 244000178231 Rosmarinus officinalis Species 0.000 description 2
- 235000006468 Thea sinensis Nutrition 0.000 description 2
- 244000299461 Theobroma cacao Species 0.000 description 2
- 235000009470 Theobroma cacao Nutrition 0.000 description 2
- 235000013832 Valeriana officinalis Nutrition 0.000 description 2
- 244000126014 Valeriana officinalis Species 0.000 description 2
- OJOBTAOGJIWAGB-UHFFFAOYSA-N acetosyringone Chemical compound COC1=CC(C(C)=O)=CC(OC)=C1O OJOBTAOGJIWAGB-UHFFFAOYSA-N 0.000 description 2
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 2
- YHBUQBJHSRGZNF-HNNXBMFYSA-N alpha-bisabolene Natural products CC(C)=CCC=C(C)[C@@H]1CCC(C)=CC1 YHBUQBJHSRGZNF-HNNXBMFYSA-N 0.000 description 2
- IPZIYGAXCZTOMH-UHFFFAOYSA-N alpha-eudesmol Natural products CC1=CCCC2CCC(CC12)C(C)(C)O IPZIYGAXCZTOMH-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 229940011037 anethole Drugs 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 229940007550 benzyl acetate Drugs 0.000 description 2
- 229930003493 bisabolene Natural products 0.000 description 2
- 235000020279 black tea Nutrition 0.000 description 2
- 229930006739 camphene Natural products 0.000 description 2
- ZYPYEBYNXWUCEA-UHFFFAOYSA-N camphenilone Natural products C1CC2C(=O)C(C)(C)C1C2 ZYPYEBYNXWUCEA-UHFFFAOYSA-N 0.000 description 2
- 229930006737 car-3-ene Natural products 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- NVEQFIOZRFFVFW-RGCMKSIDSA-N caryophyllene oxide Chemical compound C=C1CC[C@H]2O[C@]2(C)CC[C@H]2C(C)(C)C[C@@H]21 NVEQFIOZRFFVFW-RGCMKSIDSA-N 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- 229960005233 cineole Drugs 0.000 description 2
- BJIOGJUNALELMI-ARJAWSKDSA-N cis-isoeugenol Chemical compound COC1=CC(\C=C/C)=CC=C1O BJIOGJUNALELMI-ARJAWSKDSA-N 0.000 description 2
- 235000020971 citrus fruits Nutrition 0.000 description 2
- 238000010549 co-Evaporation Methods 0.000 description 2
- 235000009508 confectionery Nutrition 0.000 description 2
- 239000013256 coordination polymer Substances 0.000 description 2
- VLXDPFLIRFYIME-BTFPBAQTSA-N copaene Chemical compound C1C=C(C)[C@H]2[C@]3(C)CC[C@@H](C(C)C)[C@H]2[C@@H]31 VLXDPFLIRFYIME-BTFPBAQTSA-N 0.000 description 2
- 238000012937 correction Methods 0.000 description 2
- 235000003373 curcuma longa Nutrition 0.000 description 2
- 238000006731 degradation reaction Methods 0.000 description 2
- 235000014134 echinacea Nutrition 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- WWULHQLTPGKDAM-UHFFFAOYSA-N gamma-eudesmol Natural products CC(C)C1CC(O)C2(C)CCCC(=C2C1)C WWULHQLTPGKDAM-UHFFFAOYSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 235000009569 green tea Nutrition 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 2
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 2
- UWKAYLJWKGQEPM-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 150000002828 nitro derivatives Chemical class 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 description 2
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229940067107 phenylethyl alcohol Drugs 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 2
- 235000013976 turmeric Nutrition 0.000 description 2
- 235000016788 valerian Nutrition 0.000 description 2
- 235000019354 vermiculite Nutrition 0.000 description 2
- 229910052902 vermiculite Inorganic materials 0.000 description 2
- 239000010455 vermiculite Substances 0.000 description 2
- NZGWDASTMWDZIW-MRVPVSSYSA-N (+)-pulegone Chemical compound C[C@@H]1CCC(=C(C)C)C(=O)C1 NZGWDASTMWDZIW-MRVPVSSYSA-N 0.000 description 1
- NFLGAXVYCFJBMK-IUCAKERBSA-N (-)-isomenthone Chemical compound CC(C)[C@@H]1CC[C@H](C)CC1=O NFLGAXVYCFJBMK-IUCAKERBSA-N 0.000 description 1
- NFLGAXVYCFJBMK-BDAKNGLRSA-N (-)-menthone Chemical compound CC(C)[C@@H]1CC[C@@H](C)CC1=O NFLGAXVYCFJBMK-BDAKNGLRSA-N 0.000 description 1
- KXSDPILWMGFJMM-DJBFQZMMSA-N (1R,5R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hexan-2-ol Chemical compound CC1(O)CC[C@@]2(C(C)C)[C@H]1C2 KXSDPILWMGFJMM-DJBFQZMMSA-N 0.000 description 1
- CXENHBSYCFFKJS-UHFFFAOYSA-N (3E,6E)-3,7,11-Trimethyl-1,3,6,10-dodecatetraene Natural products CC(C)=CCCC(C)=CCC=C(C)C=C CXENHBSYCFFKJS-UHFFFAOYSA-N 0.000 description 1
- 239000001605 (5-methyl-2-propan-2-ylcyclohexyl) acetate Substances 0.000 description 1
- 239000001169 1-methyl-4-propan-2-ylcyclohexa-1,4-diene Substances 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 1
- 240000000560 Citrus x paradisi Species 0.000 description 1
- 235000007129 Cuminum cyminum Nutrition 0.000 description 1
- 244000304337 Cuminum cyminum Species 0.000 description 1
- XHXUANMFYXWVNG-UHFFFAOYSA-N D-menthyl acetate Natural products CC(C)C1CCC(C)CC1OC(C)=O XHXUANMFYXWVNG-UHFFFAOYSA-N 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- 235000019501 Lemon oil Nutrition 0.000 description 1
- 235000006679 Mentha X verticillata Nutrition 0.000 description 1
- 244000246386 Mentha pulegium Species 0.000 description 1
- 235000016257 Mentha pulegium Nutrition 0.000 description 1
- 235000002899 Mentha suaveolens Nutrition 0.000 description 1
- 235000004357 Mentha x piperita Nutrition 0.000 description 1
- 235000001636 Mentha x rotundifolia Nutrition 0.000 description 1
- 229930191564 Monensin Natural products 0.000 description 1
- GAOZTHIDHYLHMS-UHFFFAOYSA-N Monensin A Natural products O1C(CC)(C2C(CC(O2)C2C(CC(C)C(O)(CO)O2)C)C)CCC1C(O1)(C)CCC21CC(O)C(C)C(C(C)C(OC)C(C)C(O)=O)O2 GAOZTHIDHYLHMS-UHFFFAOYSA-N 0.000 description 1
- GLZPCOQZEFWAFX-JXMROGBWSA-N Nerol Natural products CC(C)=CCC\C(C)=C\CO GLZPCOQZEFWAFX-JXMROGBWSA-N 0.000 description 1
- 229930012538 Paclitaxel Natural products 0.000 description 1
- 240000004371 Panax ginseng Species 0.000 description 1
- 235000002789 Panax ginseng Nutrition 0.000 description 1
- 229930182555 Penicillin Natural products 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- ATTZFSUZZUNHBP-UHFFFAOYSA-N Piperonyl sulfoxide Chemical compound CCCCCCCCS(=O)C(C)CC1=CC=C2OCOC2=C1 ATTZFSUZZUNHBP-UHFFFAOYSA-N 0.000 description 1
- 235000011751 Pogostemon cablin Nutrition 0.000 description 1
- 240000002505 Pogostemon cablin Species 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- NZGWDASTMWDZIW-UHFFFAOYSA-N Pulegone Natural products CC1CCC(=C(C)C)C(=O)C1 NZGWDASTMWDZIW-UHFFFAOYSA-N 0.000 description 1
- 244000007853 Sarothamnus scoparius Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229930013930 alkaloid Natural products 0.000 description 1
- USMNOWBWPHYOEA-UHFFFAOYSA-N alpha-thujone Natural products CC1C(=O)CC2(C(C)C)C1C2 USMNOWBWPHYOEA-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 239000003443 antiviral agent Substances 0.000 description 1
- 229940121357 antivirals Drugs 0.000 description 1
- 239000001387 apium graveolens Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 235000001053 badasse Nutrition 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- UAHWPYUMFXYFJY-UHFFFAOYSA-N beta-myrcene Chemical compound CC(C)=CCCC(=C)C=C UAHWPYUMFXYFJY-UHFFFAOYSA-N 0.000 description 1
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 1
- 235000013614 black pepper Nutrition 0.000 description 1
- 229940115397 bornyl acetate Drugs 0.000 description 1
- 239000013590 bulk material Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- RSYBQKUNBFFNDO-UHFFFAOYSA-N caryophyllene oxide Natural products CC1(C)CC2C(=C)CCC3OC3(C)CCC12C RSYBQKUNBFFNDO-UHFFFAOYSA-N 0.000 description 1
- 238000004113 cell culture Methods 0.000 description 1
- 229940043350 citral Drugs 0.000 description 1
- 239000001279 citrus aurantifolia swingle expressed oil Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 235000008504 concentrate Nutrition 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- JVHIPYJQMFNCEK-UHFFFAOYSA-N cytochalasin Natural products N1C(=O)C2(C(C=CC(C)CC(C)CC=C3)OC(C)=O)C3C(O)C(=C)C(C)C2C1CC1=CC=CC=C1 JVHIPYJQMFNCEK-UHFFFAOYSA-N 0.000 description 1
- ZMAODHOXRBLOQO-UHFFFAOYSA-N cytochalasin-A Natural products N1C(=O)C23OC(=O)C=CC(=O)CCCC(C)CC=CC3C(O)C(=C)C(C)C2C1CC1=CC=CC=C1 ZMAODHOXRBLOQO-UHFFFAOYSA-N 0.000 description 1
- IRAQOCYXUMOFCW-UHFFFAOYSA-N di-epi-alpha-cedrene Natural products C1C23C(C)CCC3C(C)(C)C1C(C)=CC2 IRAQOCYXUMOFCW-UHFFFAOYSA-N 0.000 description 1
- 150000001983 dialkylethers Chemical class 0.000 description 1
- 235000015872 dietary supplement Nutrition 0.000 description 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- OJYLAHXKWMRDGS-UHFFFAOYSA-N ethyl gingerone Natural products COC1=CC(CCC(C)=O)=CC=C1O OJYLAHXKWMRDGS-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000001781 evernia prunasti lichen concrete Substances 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 229930009668 farnesene Natural products 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229930001612 germacrene Natural products 0.000 description 1
- YDLBHMSVYMFOMI-SDFJSLCBSA-N germacrene Chemical compound CC(C)[C@H]1CC\C(C)=C\CC\C(C)=C\C1 YDLBHMSVYMFOMI-SDFJSLCBSA-N 0.000 description 1
- 229940002508 ginger extract Drugs 0.000 description 1
- 235000020708 ginger extract Nutrition 0.000 description 1
- 239000010649 ginger oil Substances 0.000 description 1
- 235000008434 ginseng Nutrition 0.000 description 1
- 229940107131 ginseng root Drugs 0.000 description 1
- 239000010651 grapefruit oil Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 235000001050 hortel pimenta Nutrition 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- NFLGAXVYCFJBMK-UHFFFAOYSA-N isomenthone Natural products CC(C)C1CCC(C)CC1=O NFLGAXVYCFJBMK-UHFFFAOYSA-N 0.000 description 1
- 244000056931 lavandin Species 0.000 description 1
- 235000009606 lavandin Nutrition 0.000 description 1
- 239000010501 lemon oil Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229960005358 monensin Drugs 0.000 description 1
- GAOZTHIDHYLHMS-KEOBGNEYSA-N monensin A Chemical compound C([C@@](O1)(C)[C@H]2CC[C@@](O2)(CC)[C@H]2[C@H](C[C@@H](O2)[C@@H]2[C@H](C[C@@H](C)[C@](O)(CO)O2)C)C)C[C@@]21C[C@H](O)[C@@H](C)[C@@H]([C@@H](C)[C@@H](OC)[C@H](C)C(O)=O)O2 GAOZTHIDHYLHMS-KEOBGNEYSA-N 0.000 description 1
- 125000004971 nitroalkyl group Chemical group 0.000 description 1
- 125000004999 nitroaryl group Chemical group 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 1
- 239000000346 nonvolatile oil Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229930007459 p-menth-8-en-3-one Natural products 0.000 description 1
- 229960001592 paclitaxel Drugs 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 150000002960 penicillins Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 239000010668 rosemary oil Substances 0.000 description 1
- 229940058206 rosemary oil Drugs 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 235000013599 spices Nutrition 0.000 description 1
- 229940045955 star anise extract Drugs 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
-
- 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
- A23F3/40—Tea flavour; Tea oil; Flavouring of tea or tea extract
- A23F3/42—Isolation or recuperation of tea flavour or tea oil
- A23F3/423—Isolation or recuperation of tea flavour or tea oil by solvent extraction; Tea flavour from tea 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
- A23L27/10—Natural spices, flavouring agents or condiments; Extracts thereof
-
- 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
- A23L27/10—Natural spices, flavouring agents or condiments; Extracts thereof
- A23L27/11—Natural spices, flavouring agents or condiments; Extracts thereof obtained by solvent extraction
-
- 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
- A23L27/10—Natural spices, flavouring agents or condiments; Extracts thereof
- A23L27/12—Natural spices, flavouring agents or condiments; Extracts thereof from fruit, e.g. essential oils
-
- 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
- A23L33/00—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof
- A23L33/10—Modifying nutritive qualities of foods; Dietetic products; Preparation or treatment thereof using additives
- A23L33/105—Plant extracts, their artificial duplicates or their derivatives
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/02—Recovery or refining of essential oils from raw materials
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Nutrition Science (AREA)
- Health & Medical Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Botany (AREA)
- Mycology (AREA)
- Analytical Chemistry (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Fats And Perfumes (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Extraction Or Liquid Replacement (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- Treatment Of Liquids With Adsorbents In General (AREA)
- Compounds Of Unknown Constitution (AREA)
- Crystals, And After-Treatments Of Crystals (AREA)
- Silicon Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0027047.0A GB0027047D0 (en) | 2000-11-06 | 2000-11-06 | Process for reducing the concentration of undesired compounds in a composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200303305B true ZA200303305B (en) | 2005-07-29 |
Family
ID=9902612
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200303305A ZA200303305B (en) | 2000-11-06 | 2003-04-29 | Solvent extraction process. |
| ZA200303097A ZA200303097B (en) | 2000-11-06 | 2005-04-22 | Process for reducing the concentration of undesired compounds in a composition |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200303097A ZA200303097B (en) | 2000-11-06 | 2005-04-22 | Process for reducing the concentration of undesired compounds in a composition |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US7250185B2 (fr) |
| EP (1) | EP1332201B1 (fr) |
| JP (1) | JP2004513215A (fr) |
| KR (1) | KR20030059227A (fr) |
| CN (1) | CN1484689A (fr) |
| AT (1) | ATE321114T1 (fr) |
| AU (1) | AU2002212511A1 (fr) |
| BR (1) | BR0115152A (fr) |
| CA (1) | CA2426904A1 (fr) |
| DE (1) | DE60118234T2 (fr) |
| GB (1) | GB0027047D0 (fr) |
| IL (1) | IL155631A0 (fr) |
| MX (1) | MXPA03003979A (fr) |
| NZ (1) | NZ525476A (fr) |
| RU (1) | RU2003116902A (fr) |
| WO (1) | WO2002036720A1 (fr) |
| ZA (2) | ZA200303305B (fr) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0027047D0 (en) | 2000-11-06 | 2000-12-20 | Ici Plc | Process for reducing the concentration of undesired compounds in a composition |
| EP1524019B1 (fr) * | 2002-06-03 | 2013-10-23 | Central Research Institute of Electric Power Industry | Procede servant a retirer l'eau contenue dans un solide au moyen d'un materiau liquide |
| GB0306399D0 (en) * | 2003-03-20 | 2003-04-23 | Ineos Fluor Holdings Ltd | Process for reducing the concentration of undesired compounds in a composition |
| DE10322564A1 (de) * | 2003-05-20 | 2004-12-09 | Degussa Ag | Verfahren zur selektiven Abtrennung von Wertstoffen |
| US7727401B2 (en) | 2004-11-09 | 2010-06-01 | Air Products And Chemicals, Inc. | Selective purification of mono-terpenes for removal of oxygen containing species |
| US8158180B2 (en) | 2007-12-17 | 2012-04-17 | Symrise Gmbh & Co. Kg | Process for the preparation of a flavoring concentrate |
| EP2075320A1 (fr) * | 2007-12-17 | 2009-07-01 | Symrise GmbH & Co. KG | Procédé destiné à la fabrication d'un concentré d'arômes et concentré d'arômes |
| US9968564B2 (en) | 2009-06-05 | 2018-05-15 | Intercontinental Great Brands Llc | Delivery of functional compounds |
| US20100307542A1 (en) * | 2009-06-05 | 2010-12-09 | Kraft Foods Global Brands Llc | Method of Reducing Surface Oil on Encapsulated Material |
| US20100310726A1 (en) | 2009-06-05 | 2010-12-09 | Kraft Foods Global Brands Llc | Novel Preparation of an Enteric Release System |
| US8859003B2 (en) * | 2009-06-05 | 2014-10-14 | Intercontinental Great Brands Llc | Preparation of an enteric release system |
| ES2362850B1 (es) * | 2011-04-28 | 2012-01-13 | Dallant, S.A. | Procedimiento de enriquecimiento de aceites esenciales. |
| BR102012021282A2 (pt) * | 2012-08-24 | 2015-09-22 | Cdg Participaç Es E Investimentos Ltda | composição para bebida energética a base de semente de chia |
| US8859005B2 (en) | 2012-12-03 | 2014-10-14 | Intercontinental Great Brands Llc | Enteric delivery of functional ingredients suitable for hot comestible applications |
| WO2015192137A2 (fr) * | 2014-06-13 | 2015-12-17 | Buese Mark A | Extracteur, concentrateur et isolateur chimiques en continu |
| EP3002327A1 (fr) * | 2014-10-02 | 2016-04-06 | Sensient Flavors Limited | Procédé de modification de la composition d'huiles essentielles |
| US11399652B2 (en) * | 2016-12-29 | 2022-08-02 | Koninklijke Philips N.V. | Method and device for providing a coffee beverage with reduced terpene content |
| ES2908561T3 (es) * | 2017-04-24 | 2022-05-03 | Biotage Ab | Eliminación de iones metálicos de aceites esenciales |
| US10503631B1 (en) * | 2017-07-31 | 2019-12-10 | Cisco Technology, Inc. | Runtime intelligence within an integrated development environment |
| US10596487B2 (en) * | 2017-09-27 | 2020-03-24 | Rj Lee Group, Inc. | Methods and apparatus for clarification of pyrolysis oils |
| CN112539638A (zh) * | 2020-12-22 | 2021-03-23 | 广西南宁墨子新能源有限公司 | 一种八角烘干及细胞液提取设备及工艺 |
| JP2025083892A (ja) * | 2023-11-21 | 2025-06-02 | 栗田工業株式会社 | 油分含有廃液からの油分回収方法 |
Family Cites Families (57)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2712008A (en) | 1951-06-29 | 1955-06-28 | Justus G Kirchner | Production of terpeneless essential oils |
| US3155523A (en) | 1958-08-15 | 1964-11-03 | Standard Brands Inc | Extraction of coffee aroma and flavor |
| GB928594A (en) | 1958-09-29 | 1963-06-12 | Albert Verley & Company | Manufacture of perfumes |
| FR1211820A (fr) * | 1958-10-10 | 1960-03-18 | Essences pour la parfumerie et leur procédé de fabrication | |
| US3150050A (en) | 1959-10-28 | 1964-09-22 | Albert Verley & Company | Extraction of essential perfume fragrance components with fluorinated hydrocarbons |
| US3649296A (en) | 1970-01-19 | 1972-03-14 | Gen Foods Corp | Stabilized roasted coffee aroma |
| US3612066A (en) | 1970-02-05 | 1971-10-12 | Reynolds Tobacco Co R | Denicotinizing process |
| US3769033A (en) | 1970-04-24 | 1973-10-30 | Gen Foods Corp | Green bean decaffination employing fluorinated hydrocarbons |
| DE2127618C2 (de) | 1971-06-03 | 1973-06-14 | Hag Ag | Verfahren zur Gewinnung von Hopfenextrakten |
| CH574603A5 (fr) | 1972-05-08 | 1976-04-15 | Ciba Geigy Ag | |
| GB1419958A (en) | 1972-07-19 | 1975-12-31 | Brooke Bond Liebig Ltd | Extraction of flavour and fragrance components from plant material |
| US3867262A (en) * | 1973-05-21 | 1975-02-18 | Us Agriculture | Production of terpeneless essential oils |
| US3954678A (en) | 1974-07-11 | 1976-05-04 | E. I. Du Pont De Nemours And Company | Semipermeable microcapsules containing a silica gel |
| US3928579A (en) | 1974-11-25 | 1975-12-23 | Warner Lambert Co | Process for the purification of coal tar |
| DE2621974A1 (de) | 1976-05-18 | 1977-11-24 | Max Planck Gesellschaft | Verfahren zur herstellung eines zur kovalenten bindung mit biologisch aktivem material befaehigten traegermaterials |
| US4059604A (en) | 1976-11-29 | 1977-11-22 | Kresse Herman J | Separation of mature okra seed into component fractions |
| SU1002350A1 (ru) | 1978-12-29 | 1983-03-07 | Харьковский Научно-Исследовательский Химико-Фармацевтический Институт | Способ получени масла шиповника |
| JPS5653458A (en) | 1979-10-06 | 1981-05-13 | Hitachi Chem Co Ltd | Specific solvent column for gel permeation |
| DE3011185A1 (de) | 1980-03-22 | 1981-10-01 | Kali-Chemie Pharma Gmbh, 3000 Hannover | Verfahren zur gewinnung von fuer physiologische zwecke direkt verwendbarem rin(paragraph)lecithin |
| FR2543155B1 (fr) * | 1983-03-25 | 1985-11-15 | Artozoul Jacques | Procede de fabrication d'aromes purs a partir d'huiles essentielles et aromes obtenus |
| US4522995A (en) | 1983-05-02 | 1985-06-11 | E. I. Du Pont De Nemours And Company | Fluorinated alkyl ether-containing ethylenes, precursors thereto, and copolymers thereof with tetrafluoroethylene |
| US4597943A (en) | 1984-11-29 | 1986-07-01 | Morinaga & Co., Ltd. | Apparatus for analyzing solid sample with supercritical fluid |
| US4673733A (en) | 1985-04-11 | 1987-06-16 | Sudhish Chandra | Treatment of biological and pharmaceutical products adsorbed on a solid phase with virus and pyrogen inactivating agents |
| JPS6267036A (ja) | 1985-09-20 | 1987-03-26 | Jgc Corp | アルコ−ルの分離方法 |
| CA1279864C (fr) | 1985-12-27 | 1991-02-05 | Rocco Difoggio | Methode pour determiner la quantite de petrole absorbe par une eponge de carottage |
| FR2601883B1 (fr) | 1986-07-25 | 1988-11-25 | Elf Aquitaine | Procedes et dispositifs de separation a l'aide d'un fluide supercritique |
| US4802986A (en) | 1986-09-09 | 1989-02-07 | The United States Of America As Represented By The Secretary Of The Air Force | Hydrocarbon group-type analyzer system |
| US4826603A (en) | 1986-09-09 | 1989-05-02 | United States Of America As Represented By The Secretary Of The Air Force | Hydrocarbon group-type analyzer system |
| US5092983A (en) | 1986-09-12 | 1992-03-03 | The Standard Oil Company | Process for separating extractable organic material from compositions comprising said extractable organic material intermixed with solids and water using a solvent mixture |
| DE3769089D1 (de) | 1986-11-15 | 1991-05-08 | British Petroleum Co | Transportdetektorsystem. |
| US5018540A (en) | 1986-12-29 | 1991-05-28 | Philip Morris Incorporated | Process for removal of basic materials |
| US4767670A (en) | 1987-01-21 | 1988-08-30 | E. I. Du Pont De Nemours And Company | Chromatographic supports for separation of oligonucleotides |
| US4816159A (en) | 1987-08-31 | 1989-03-28 | Aluminum Company Of America | Supercritical fluid chromatography packing material |
| SU1557154A1 (ru) | 1987-11-03 | 1990-04-15 | Горский Сельскохозяйственный Институт | Способ получени масла лоха узколистного |
| FR2632826B1 (fr) | 1988-06-17 | 1991-10-18 | Air Liquide | Procede d'extraction d'epices |
| GB2225205A (en) | 1988-09-22 | 1990-05-30 | Trevor William Smith | Oil-reduced snack foods |
| DE3834988A1 (de) * | 1988-10-14 | 1990-04-19 | Sueddeutsche Kalkstickstoff | Verfahren zur entfernung von terpenen aus etherischen oelen |
| US4865741A (en) | 1988-12-23 | 1989-09-12 | Texaco Inc. | Separation of oil into fractions of asphaltenes, resins, aromatics, and saturated hydrocarbons |
| EP0527019B1 (fr) | 1991-08-03 | 1999-04-21 | Asahi Kasei Kogyo Kabushiki Kaisha | Solvent contenant de l'halogène, solution avec ce solvent et procédé pour la fabrication de fibres tri-dimensionelles |
| IT1251964B (it) | 1991-10-21 | 1995-05-27 | Ausimont Spa | Procedimento per separare tra loro specie non funzionali, monofunzionali e bifunzionali presenti nei perfluoropoliossialchileni. |
| IT1251965B (it) | 1991-10-21 | 1995-05-27 | Ausimont Spa | Procedimento per separare tra loro le specie non funzionali, monofunzionali e bifunzionali presenti nei perfluoropoliossialchileni. |
| US5281732A (en) | 1991-12-31 | 1994-01-25 | University Research & Marketing | Solvent extraction of oil from oil-bearing materials |
| US5516923A (en) | 1992-04-27 | 1996-05-14 | Agritech International | Extracting oil from oil bearing plant parts |
| US5405633A (en) | 1992-10-08 | 1995-04-11 | Skw Trostberg Aktiengesellschaft | Process for the extraction of fats and oils |
| GB2276392B (en) | 1993-02-22 | 1997-03-26 | D G P | Improved production of natural flavours and fragrances |
| US5440055A (en) | 1993-03-12 | 1995-08-08 | Aphios Corporation | Method and apparatus for extracting taxol from source materials |
| US5481058A (en) * | 1994-01-07 | 1996-01-02 | Minnesota Mining And Manufacturing Company | Supercritical fluid extraction involving hydrofluoroalkanes |
| GB9406423D0 (en) | 1994-03-31 | 1994-05-25 | Ici Plc | Solvent extraction process |
| GB9407886D0 (en) | 1994-04-21 | 1994-06-15 | Ici Plc | Purification process |
| US5562857A (en) | 1995-12-22 | 1996-10-08 | Bayer Corporation | Azeotrope-like compositions of 1,1,1,3,3-pentafluoropropane and 2-methyl butane |
| GB2355006B (en) | 1996-12-06 | 2001-07-04 | Advanced Phytonics Ltd | Materials treatment |
| GB9707130D0 (en) | 1997-04-08 | 1997-05-28 | Advanced Phytonics Ltd | Solvent extraction |
| US6824789B2 (en) | 1998-05-20 | 2004-11-30 | Kemin Industries, Inc. | Method of extracting antioxidants from lamiaceae species and the extract products thereof |
| US6746695B1 (en) | 1998-10-02 | 2004-06-08 | Armadillo Pharmaceuticals, Inc. | Pharmaceutical preparations of bioactive substances extracted from natural sources |
| GB9909136D0 (en) | 1999-04-22 | 1999-06-16 | Ici Plc | Solvent extraction process |
| JP2003500452A (ja) | 1999-05-27 | 2003-01-07 | アーマディーロ・ファーマシューティカルス・インコーポレーテッド | 天然資源から抽出した生物活性物質の医薬製剤 |
| GB0027047D0 (en) | 2000-11-06 | 2000-12-20 | Ici Plc | Process for reducing the concentration of undesired compounds in a composition |
-
2000
- 2000-11-06 GB GBGB0027047.0A patent/GB0027047D0/en not_active Ceased
-
2001
- 2001-11-06 DE DE60118234T patent/DE60118234T2/de not_active Revoked
- 2001-11-06 AU AU2002212511A patent/AU2002212511A1/en not_active Abandoned
- 2001-11-06 BR BR0115152-5A patent/BR0115152A/pt not_active IP Right Cessation
- 2001-11-06 US US10/415,862 patent/US7250185B2/en not_active Expired - Fee Related
- 2001-11-06 KR KR10-2003-7006210A patent/KR20030059227A/ko not_active Withdrawn
- 2001-11-06 WO PCT/GB2001/004920 patent/WO2002036720A1/fr not_active Ceased
- 2001-11-06 RU RU2003116902/13A patent/RU2003116902A/ru not_active Application Discontinuation
- 2001-11-06 MX MXPA03003979A patent/MXPA03003979A/es not_active Application Discontinuation
- 2001-11-06 CN CNA018217214A patent/CN1484689A/zh active Pending
- 2001-11-06 EP EP01980723A patent/EP1332201B1/fr not_active Revoked
- 2001-11-06 JP JP2002539466A patent/JP2004513215A/ja not_active Withdrawn
- 2001-11-06 NZ NZ525476A patent/NZ525476A/en not_active Application Discontinuation
- 2001-11-06 CA CA002426904A patent/CA2426904A1/fr not_active Abandoned
- 2001-11-06 AT AT01980723T patent/ATE321114T1/de not_active IP Right Cessation
- 2001-11-06 IL IL15563101A patent/IL155631A0/xx unknown
-
2003
- 2003-04-29 ZA ZA200303305A patent/ZA200303305B/en unknown
-
2005
- 2005-04-22 ZA ZA200303097A patent/ZA200303097B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU2002212511A1 (en) | 2002-05-15 |
| IL155631A0 (en) | 2003-11-23 |
| NZ525476A (en) | 2004-10-29 |
| BR0115152A (pt) | 2003-12-30 |
| CN1484689A (zh) | 2004-03-24 |
| DE60118234D1 (de) | 2006-05-11 |
| CA2426904A1 (fr) | 2002-05-10 |
| ATE321114T1 (de) | 2006-04-15 |
| KR20030059227A (ko) | 2003-07-07 |
| ZA200303097B (en) | 2006-12-27 |
| US7250185B2 (en) | 2007-07-31 |
| GB0027047D0 (en) | 2000-12-20 |
| JP2004513215A (ja) | 2004-04-30 |
| RU2003116902A (ru) | 2004-12-10 |
| WO2002036720A1 (fr) | 2002-05-10 |
| MXPA03003979A (es) | 2003-08-19 |
| US20040069713A1 (en) | 2004-04-15 |
| EP1332201B1 (fr) | 2006-03-22 |
| EP1332201A1 (fr) | 2003-08-06 |
| DE60118234T2 (de) | 2007-03-08 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US20040105899A1 (en) | Solvent extraction process | |
| ZA200303305B (en) | Solvent extraction process. | |
| Moyler | Extraction of essential oils with carbon dioxide | |
| KR100362918B1 (ko) | 용매추출방법 | |
| Coelho et al. | Supercritical carbon dioxide extraction of Foeniculum vulgare volatile oil | |
| CA2115599C (fr) | Extraction de fragrance | |
| Teng et al. | New developments on ultrasound-assisted processing and flavor detection of spices: A review | |
| Bocevska et al. | Supercritical CO2 extraction of essential oil from yarrow | |
| Tuan et al. | Liquid CO2 extraction of essential oil from star anise fruits (Illicium verum H.) | |
| Baldino et al. | Supercritical CO2 processing strategies for pyrethrins selective extraction | |
| Della Porta et al. | Isolation of eucalyptus oil by supercritical fluid extraction | |
| Balakrishnan | Postharvest and industrial processing of ginger | |
| Sovilj et al. | Critical review of supercritical fluid extraction of selected spice plant materials | |
| JPH04227680A (ja) | シソ科ハーブの酸化防止剤抽出プロセス及び酸化防止組成物 | |
| Rout et al. | Extraction and composition of volatiles from Zanthoxylum rhesta: Comparison of subcritical CO2 and traditional processes | |
| Monteiro et al. | Extraction of the soluble material from the shells of the bacuri fruit (Platonia insignis Mart) with pressurized CO2 and other solvents | |
| Immaroh et al. | Eucalyptus globulus essential oil extraction method | |
| Sanders | Food legislation and the scope for increased use of near-critical fluid extraction operations in the food, flavouring and pharmaceutical industries | |
| Coelho et al. | Supercritical fluid extraction of compounds from spices and herbs | |
| Norkaew et al. | Supercritical fluid extraction and gas chromatographic-mass spectrometric analysis of terpenoids in fresh kaffir lime leaf oil | |
| AU765058B2 (en) | Solvent extraction process | |
| Gopalakrishnan et al. | Composition of clove (Syzygium aromaticum) bud oil extracted using carbon dioxide | |
| Chiou et al. | Recovery of mint essential oil through pressure-releasing distillation during subcritical water treatment | |
| Nguyen et al. | Influence of spray drying parameters on the physicochemical characteristics of microencapsulated orange (Citrus sinensis L.) essential oil | |
| T Santos et al. | Extraction of volatile oils by supercritical fluid extraction: patent survey |