EP4076344A1 - Low-molecular gelling agent as fragrant substance dispensing system - Google Patents
Low-molecular gelling agent as fragrant substance dispensing systemInfo
- Publication number
- EP4076344A1 EP4076344A1 EP20824935.9A EP20824935A EP4076344A1 EP 4076344 A1 EP4076344 A1 EP 4076344A1 EP 20824935 A EP20824935 A EP 20824935A EP 4076344 A1 EP4076344 A1 EP 4076344A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- group
- alkyl
- alkyl group
- oil
- compounds
- 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.)
- Pending
Links
- 239000003349 gelling agent Substances 0.000 title abstract description 16
- 239000000126 substance Substances 0.000 title description 11
- 239000000203 mixture Substances 0.000 claims abstract description 143
- 239000002304 perfume Substances 0.000 claims abstract description 128
- 238000003860 storage Methods 0.000 claims abstract description 55
- 238000000034 method Methods 0.000 claims abstract description 27
- 239000007864 aqueous solution Substances 0.000 claims abstract description 24
- 239000004753 textile Substances 0.000 claims abstract description 21
- 238000005406 washing Methods 0.000 claims abstract description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000003921 oil Substances 0.000 claims description 184
- -1 benzylidene alditols Chemical class 0.000 claims description 138
- 150000001875 compounds Chemical class 0.000 claims description 88
- 239000003795 chemical substances by application Substances 0.000 claims description 50
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 42
- 239000003205 fragrance Substances 0.000 claims description 37
- 125000000217 alkyl group Chemical group 0.000 claims description 33
- 125000003277 amino group Chemical group 0.000 claims description 28
- 239000002245 particle Substances 0.000 claims description 27
- 239000004094 surface-active agent Substances 0.000 claims description 26
- 239000002562 thickening agent Substances 0.000 claims description 25
- 125000003118 aryl group Chemical group 0.000 claims description 24
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical group CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 claims description 20
- 229910052757 nitrogen Inorganic materials 0.000 claims description 20
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 19
- 150000001768 cations Chemical class 0.000 claims description 18
- 239000006185 dispersion Substances 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 16
- 239000006254 rheological additive Substances 0.000 claims description 16
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 15
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 15
- 229920001223 polyethylene glycol Polymers 0.000 claims description 14
- 239000000975 dye Substances 0.000 claims description 13
- 125000001072 heteroaryl group Chemical group 0.000 claims description 13
- BXRNXXXXHLBUKK-UHFFFAOYSA-N piperazine-2,5-dione Chemical class O=C1CNC(=O)CN1 BXRNXXXXHLBUKK-UHFFFAOYSA-N 0.000 claims description 13
- 238000004519 manufacturing process Methods 0.000 claims description 12
- 239000007764 o/w emulsion Substances 0.000 claims description 12
- 238000004140 cleaning Methods 0.000 claims description 11
- 239000011159 matrix material Substances 0.000 claims description 11
- 229940114072 12-hydroxystearic acid Drugs 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 238000010438 heat treatment Methods 0.000 claims description 10
- 238000011282 treatment Methods 0.000 claims description 9
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- 229930195733 hydrocarbon Natural products 0.000 claims description 8
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 8
- 239000003112 inhibitor Substances 0.000 claims description 8
- 238000003756 stirring Methods 0.000 claims description 8
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 7
- FMZUHGYZWYNSOA-VVBFYGJXSA-N (1r)-1-[(4r,4ar,8as)-2,6-diphenyl-4,4a,8,8a-tetrahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-yl]ethane-1,2-diol Chemical compound C([C@@H]1OC(O[C@@H]([C@@H]1O1)[C@H](O)CO)C=2C=CC=CC=2)OC1C1=CC=CC=C1 FMZUHGYZWYNSOA-VVBFYGJXSA-N 0.000 claims description 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 6
- 125000003435 aroyl group Chemical group 0.000 claims description 6
- 125000004104 aryloxy group Chemical group 0.000 claims description 6
- 239000004359 castor oil Substances 0.000 claims description 6
- 229940087101 dibenzylidene sorbitol Drugs 0.000 claims description 6
- 229910052731 fluorine Inorganic materials 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 6
- 150000005846 sugar alcohols Chemical class 0.000 claims description 6
- 239000004215 Carbon black (E152) Substances 0.000 claims description 5
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 5
- 125000005333 aroyloxy group Chemical group 0.000 claims description 5
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 5
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 5
- 125000001424 substituent group Chemical group 0.000 claims description 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 4
- 229920002472 Starch Polymers 0.000 claims description 4
- 125000004423 acyloxy group Chemical group 0.000 claims description 4
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 235000019438 castor oil Nutrition 0.000 claims description 4
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- 150000002302 glucosamines Chemical class 0.000 claims description 4
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims description 4
- 239000004615 ingredient Substances 0.000 claims description 4
- 229910052740 iodine Inorganic materials 0.000 claims description 4
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 claims description 4
- 229920000053 polysorbate 80 Polymers 0.000 claims description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 4
- 239000008107 starch Substances 0.000 claims description 4
- 235000019698 starch Nutrition 0.000 claims description 4
- 229920001285 xanthan gum Polymers 0.000 claims description 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 3
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 claims description 3
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 claims description 3
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical group C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 claims description 3
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 3
- 125000004442 acylamino group Chemical group 0.000 claims description 3
- 229940072056 alginate Drugs 0.000 claims description 3
- 235000010443 alginic acid Nutrition 0.000 claims description 3
- 229920000615 alginic acid Polymers 0.000 claims description 3
- 239000004599 antimicrobial Substances 0.000 claims description 3
- 239000003963 antioxidant agent Substances 0.000 claims description 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 3
- 230000002070 germicidal effect Effects 0.000 claims description 3
- 239000000787 lecithin Substances 0.000 claims description 3
- 235000010445 lecithin Nutrition 0.000 claims description 3
- 229940067606 lecithin Drugs 0.000 claims description 3
- 229920002545 silicone oil Polymers 0.000 claims description 3
- JSUVMLHNHUCJTE-UHFFFAOYSA-N 2-acetyloxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCOC(C)=O JSUVMLHNHUCJTE-UHFFFAOYSA-N 0.000 claims description 2
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 claims description 2
- 244000007835 Cyamopsis tetragonoloba Species 0.000 claims description 2
- 102000004190 Enzymes Human genes 0.000 claims description 2
- 108090000790 Enzymes Proteins 0.000 claims description 2
- 229920002385 Sodium hyaluronate Polymers 0.000 claims description 2
- LWZFANDGMFTDAV-BURFUSLBSA-N [(2r)-2-[(2r,3r,4s)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O LWZFANDGMFTDAV-BURFUSLBSA-N 0.000 claims description 2
- 239000006096 absorbing agent Substances 0.000 claims description 2
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims description 2
- 239000003125 aqueous solvent Substances 0.000 claims description 2
- 239000000969 carrier Substances 0.000 claims description 2
- 239000008139 complexing agent Substances 0.000 claims description 2
- 239000003792 electrolyte Substances 0.000 claims description 2
- 229940095399 enema Drugs 0.000 claims description 2
- 239000007920 enema Substances 0.000 claims description 2
- 239000007850 fluorescent dye Substances 0.000 claims description 2
- 239000006260 foam Substances 0.000 claims description 2
- 239000000417 fungicide Substances 0.000 claims description 2
- 239000003752 hydrotrope Substances 0.000 claims description 2
- 239000011859 microparticle Substances 0.000 claims description 2
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 claims description 2
- 229940068968 polysorbate 80 Drugs 0.000 claims description 2
- 239000012748 slip agent Substances 0.000 claims description 2
- 229940010747 sodium hyaluronate Drugs 0.000 claims description 2
- JAJWGJBVLPIOOH-IZYKLYLVSA-M sodium taurocholate Chemical compound [Na+].C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCCS([O-])(=O)=O)C)[C@@]2(C)[C@@H](O)C1 JAJWGJBVLPIOOH-IZYKLYLVSA-M 0.000 claims description 2
- YWIVKILSMZOHHF-QJZPQSOGSA-N sodium;(2s,3s,4s,5r,6r)-6-[(2s,3r,4r,5s,6r)-3-acetamido-2-[(2s,3s,4r,5r,6r)-6-[(2r,3r,4r,5s,6r)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2- Chemical compound [Na+].CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 YWIVKILSMZOHHF-QJZPQSOGSA-N 0.000 claims description 2
- 229940035044 sorbitan monolaurate Drugs 0.000 claims description 2
- 235000011067 sorbitan monolaureate Nutrition 0.000 claims description 2
- 230000008961 swelling Effects 0.000 claims description 2
- 238000012546 transfer Methods 0.000 claims description 2
- 239000002216 antistatic agent Substances 0.000 claims 1
- 238000005260 corrosion Methods 0.000 claims 1
- 230000007797 corrosion Effects 0.000 claims 1
- 238000010409 ironing Methods 0.000 claims 1
- 230000000087 stabilizing effect Effects 0.000 abstract description 3
- 235000019198 oils Nutrition 0.000 description 166
- 239000000499 gel Substances 0.000 description 47
- 150000003254 radicals Chemical class 0.000 description 34
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 33
- 239000012071 phase Substances 0.000 description 29
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 16
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 16
- 239000011734 sodium Substances 0.000 description 16
- 125000004432 carbon atom Chemical group C* 0.000 description 15
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 12
- 239000003599 detergent Substances 0.000 description 12
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 10
- 150000002191 fatty alcohols Chemical class 0.000 description 10
- ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 10
- 239000012459 cleaning agent Substances 0.000 description 9
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 9
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 8
- 229940007550 benzyl acetate Drugs 0.000 description 8
- NEHNMFOYXAPHSD-UHFFFAOYSA-N citronellal Chemical compound O=CCC(C)CCC=C(C)C NEHNMFOYXAPHSD-UHFFFAOYSA-N 0.000 description 8
- 239000000839 emulsion Substances 0.000 description 8
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 8
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 8
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000003945 anionic surfactant Substances 0.000 description 7
- 239000002537 cosmetic Substances 0.000 description 7
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 7
- NTPLXRHDUXRPNE-UHFFFAOYSA-N 4-methoxyacetophenone Chemical compound COC1=CC=C(C(C)=O)C=C1 NTPLXRHDUXRPNE-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- LHXDLQBQYFFVNW-UHFFFAOYSA-N Fenchone Chemical compound C1CC2(C)C(=O)C(C)(C)C1C2 LHXDLQBQYFFVNW-UHFFFAOYSA-N 0.000 description 6
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 6
- 229920000426 Microplastic Polymers 0.000 description 6
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 6
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 description 6
- 230000003750 conditioning effect Effects 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 6
- 238000005538 encapsulation Methods 0.000 description 6
- 235000019441 ethanol Nutrition 0.000 description 6
- CBOQJANXLMLOSS-UHFFFAOYSA-N ethyl vanillin Chemical compound CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 description 6
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 235000019645 odor Nutrition 0.000 description 6
- DTUQWGWMVIHBKE-UHFFFAOYSA-N phenylacetaldehyde Chemical compound O=CCC1=CC=CC=C1 DTUQWGWMVIHBKE-UHFFFAOYSA-N 0.000 description 6
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 6
- YGFGZTXGYTUXBA-UHFFFAOYSA-N (±)-2,6-dimethyl-5-heptenal Chemical compound O=CC(C)CCC=C(C)C YGFGZTXGYTUXBA-UHFFFAOYSA-N 0.000 description 5
- 239000004480 active ingredient Substances 0.000 description 5
- 229910001413 alkali metal ion Inorganic materials 0.000 description 5
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 description 5
- JNGZXGGOCLZBFB-IVCQMTBJSA-N compound E Chemical compound N([C@@H](C)C(=O)N[C@@H]1C(N(C)C2=CC=CC=C2C(C=2C=CC=CC=2)=N1)=O)C(=O)CC1=CC(F)=CC(F)=C1 JNGZXGGOCLZBFB-IVCQMTBJSA-N 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 5
- 150000002430 hydrocarbons Chemical group 0.000 description 5
- WPFVBOQKRVRMJB-UHFFFAOYSA-N hydroxycitronellal Chemical compound O=CCC(C)CCCC(C)(C)O WPFVBOQKRVRMJB-UHFFFAOYSA-N 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 description 5
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 5
- 239000002736 nonionic surfactant Substances 0.000 description 5
- BOPPSUHPZARXTH-UHFFFAOYSA-N ocean propanal Chemical compound O=CC(C)CC1=CC=C2OCOC2=C1 BOPPSUHPZARXTH-UHFFFAOYSA-N 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- KYWIYKKSMDLRDC-UHFFFAOYSA-N undecan-2-one Chemical compound CCCCCCCCCC(C)=O KYWIYKKSMDLRDC-UHFFFAOYSA-N 0.000 description 5
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 5
- YYMCVDNIIFNDJK-XFQWXJFMSA-N (z)-1-(3-fluorophenyl)-n-[(z)-(3-fluorophenyl)methylideneamino]methanimine Chemical compound FC1=CC=CC(\C=N/N=C\C=2C=C(F)C=CC=2)=C1 YYMCVDNIIFNDJK-XFQWXJFMSA-N 0.000 description 4
- CHLICZRVGGXEOD-UHFFFAOYSA-N 1-Methoxy-4-methylbenzene Chemical compound COC1=CC=C(C)C=C1 CHLICZRVGGXEOD-UHFFFAOYSA-N 0.000 description 4
- MZZRKEIUNOYYDF-UHFFFAOYSA-N 2,4-dimethylcyclohex-3-ene-1-carbaldehyde Chemical compound CC1C=C(C)CCC1C=O MZZRKEIUNOYYDF-UHFFFAOYSA-N 0.000 description 4
- XSAYZAUNJMRRIR-UHFFFAOYSA-N 2-acetylnaphthalene Chemical compound C1=CC=CC2=CC(C(=O)C)=CC=C21 XSAYZAUNJMRRIR-UHFFFAOYSA-N 0.000 description 4
- NFAVNWJJYQAGNB-UHFFFAOYSA-N 2-methylundecanal Chemical compound CCCCCCCCCC(C)C=O NFAVNWJJYQAGNB-UHFFFAOYSA-N 0.000 description 4
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 4
- 241000379225 Abies procera Species 0.000 description 4
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 4
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 4
- FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 description 4
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 4
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 4
- ZYEMGPIYFIJGTP-UHFFFAOYSA-N O-methyleugenol Chemical compound COC1=CC=C(CC=C)C=C1OC ZYEMGPIYFIJGTP-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 150000001299 aldehydes Chemical class 0.000 description 4
- IGODOXYLBBXFDW-UHFFFAOYSA-N alpha-Terpinyl acetate Chemical compound CC(=O)OC(C)(C)C1CCC(C)=CC1 IGODOXYLBBXFDW-UHFFFAOYSA-N 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 4
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 4
- 239000008346 aqueous phase Substances 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 4
- AKGGYBADQZYZPD-UHFFFAOYSA-N benzylacetone Chemical compound CC(=O)CCC1=CC=CC=C1 AKGGYBADQZYZPD-UHFFFAOYSA-N 0.000 description 4
- 229960000541 cetyl alcohol Drugs 0.000 description 4
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 4
- 229930003633 citronellal Natural products 0.000 description 4
- 235000000983 citronellal Nutrition 0.000 description 4
- KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 description 4
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
- 238000002296 dynamic light scattering Methods 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 4
- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 4
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 4
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 4
- UWKAYLJWKGQEPM-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 description 4
- 125000002960 margaryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
- VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 description 4
- OSWPMRLSEDHDFF-UHFFFAOYSA-N methyl salicylate Chemical compound COC(=O)C1=CC=CC=C1O OSWPMRLSEDHDFF-UHFFFAOYSA-N 0.000 description 4
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 4
- 125000001196 nonadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 4
- GYHFUZHODSMOHU-UHFFFAOYSA-N nonanal Chemical compound CCCCCCCCC=O GYHFUZHODSMOHU-UHFFFAOYSA-N 0.000 description 4
- 125000002958 pentadecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 239000010668 rosemary oil Substances 0.000 description 4
- 229940058206 rosemary oil Drugs 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 229940012831 stearyl alcohol Drugs 0.000 description 4
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 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
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- LHXDLQBQYFFVNW-XCBNKYQSSA-N (+)-Fenchone Natural products C1C[C@]2(C)C(=O)C(C)(C)[C@H]1C2 LHXDLQBQYFFVNW-XCBNKYQSSA-N 0.000 description 3
- KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 description 3
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 3
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N 1-Tetradecanol Natural products CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 3
- UEGBWDUVDAKUGA-UHFFFAOYSA-N 2,6,10-trimethylundec-9-enal Chemical compound CC(C)=CCCC(C)CCCC(C)C=O UEGBWDUVDAKUGA-UHFFFAOYSA-N 0.000 description 3
- HMKKIXGYKWDQSV-SDNWHVSQSA-N 2-Pentyl-3-phenyl-2-propenal Chemical compound CCCCC\C(C=O)=C/C1=CC=CC=C1 HMKKIXGYKWDQSV-SDNWHVSQSA-N 0.000 description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- PRNCMAKCNVRZFX-UHFFFAOYSA-N 3,7-dimethyloctan-1-ol Chemical compound CC(C)CCCC(C)CCO PRNCMAKCNVRZFX-UHFFFAOYSA-N 0.000 description 3
- OHRBQTOZYGEWCJ-UHFFFAOYSA-N 3-(3-propan-2-ylphenyl)butanal Chemical compound CC(C)C1=CC=CC(C(C)CC=O)=C1 OHRBQTOZYGEWCJ-UHFFFAOYSA-N 0.000 description 3
- ORMHZBNNECIKOH-UHFFFAOYSA-N 4-(4-hydroxy-4-methylpentyl)cyclohex-3-ene-1-carbaldehyde Chemical compound CC(C)(O)CCCC1=CCC(C=O)CC1 ORMHZBNNECIKOH-UHFFFAOYSA-N 0.000 description 3
- 235000007173 Abies balsamea Nutrition 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- 235000019489 Almond oil Nutrition 0.000 description 3
- 239000004857 Balsam Substances 0.000 description 3
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 description 3
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 3
- 241000723346 Cinnamomum camphora Species 0.000 description 3
- 244000223760 Cinnamomum zeylanicum Species 0.000 description 3
- 235000013162 Cocos nucifera Nutrition 0.000 description 3
- 244000060011 Cocos nucifera Species 0.000 description 3
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 3
- 239000005770 Eugenol Substances 0.000 description 3
- 244000018716 Impatiens biflora Species 0.000 description 3
- BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-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
- 239000004435 Oxo alcohol Substances 0.000 description 3
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 3
- 239000005844 Thymol Substances 0.000 description 3
- 229940022663 acetate Drugs 0.000 description 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 3
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 3
- 239000008168 almond oil Substances 0.000 description 3
- 230000000845 anti-microbial effect Effects 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 3
- FZJUFJKVIYFBSY-UHFFFAOYSA-N bourgeonal Chemical compound CC(C)(C)C1=CC=C(CCC=O)C=C1 FZJUFJKVIYFBSY-UHFFFAOYSA-N 0.000 description 3
- 229960000846 camphor Drugs 0.000 description 3
- 229930008380 camphor Natural products 0.000 description 3
- 239000003093 cationic surfactant Substances 0.000 description 3
- 239000003518 caustics Substances 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 description 3
- 235000017803 cinnamon Nutrition 0.000 description 3
- BJIOGJUNALELMI-ARJAWSKDSA-N cis-isoeugenol Chemical compound COC1=CC(\C=C/C)=CC=C1O BJIOGJUNALELMI-ARJAWSKDSA-N 0.000 description 3
- 229940043350 citral Drugs 0.000 description 3
- 125000006165 cyclic alkyl group Chemical group 0.000 description 3
- NGPCLOGFGKJCBP-UHFFFAOYSA-N cyclo(tyrosyl-tyrosyl) Chemical compound C1=CC(O)=CC=C1CC1C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)N1 NGPCLOGFGKJCBP-UHFFFAOYSA-N 0.000 description 3
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N dodecahydrosqualene Natural products CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- 229960002217 eugenol Drugs 0.000 description 3
- 229930006735 fenchone Natural products 0.000 description 3
- 239000007863 gel particle Substances 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- 150000004702 methyl esters Chemical class 0.000 description 3
- JPTOCTSNXXKSSN-UHFFFAOYSA-N methylheptenone Chemical compound CCCC=CC(=O)CC JPTOCTSNXXKSSN-UHFFFAOYSA-N 0.000 description 3
- 229940043348 myristyl alcohol Drugs 0.000 description 3
- 125000001624 naphthyl group Chemical group 0.000 description 3
- NUJGJRNETVAIRJ-UHFFFAOYSA-N octanal Chemical compound CCCCCCCC=O NUJGJRNETVAIRJ-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 3
- 229940100595 phenylacetaldehyde Drugs 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- ZMQAAUBTXCXRIC-UHFFFAOYSA-N safrole Chemical compound C=CCC1=CC=C2OCOC2=C1 ZMQAAUBTXCXRIC-UHFFFAOYSA-N 0.000 description 3
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 229960002920 sorbitol Drugs 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 239000003760 tallow Substances 0.000 description 3
- 229960000790 thymol Drugs 0.000 description 3
- 125000005424 tosyloxy group Chemical group S(=O)(=O)(C1=CC=C(C)C=C1)O* 0.000 description 3
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 3
- XMLSXPIVAXONDL-UHFFFAOYSA-N trans-jasmone Natural products CCC=CCC1=C(C)CCC1=O XMLSXPIVAXONDL-UHFFFAOYSA-N 0.000 description 3
- 238000002604 ultrasonography Methods 0.000 description 3
- KMPQYAYAQWNLME-UHFFFAOYSA-N undecanal Chemical compound CCCCCCCCCCC=O KMPQYAYAQWNLME-UHFFFAOYSA-N 0.000 description 3
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 3
- 235000012141 vanillin Nutrition 0.000 description 3
- ZFNVDHOSLNRHNN-UHFFFAOYSA-N xi-3-(4-Isopropylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)C)C=C1 ZFNVDHOSLNRHNN-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
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 2
- NFLGAXVYCFJBMK-RKDXNWHRSA-N (+)-isomenthone Natural products CC(C)[C@H]1CC[C@@H](C)CC1=O NFLGAXVYCFJBMK-RKDXNWHRSA-N 0.000 description 2
- CRDAMVZIKSXKFV-FBXUGWQNSA-N (2-cis,6-cis)-farnesol Chemical compound CC(C)=CCC\C(C)=C/CC\C(C)=C/CO CRDAMVZIKSXKFV-FBXUGWQNSA-N 0.000 description 2
- MBDOYVRWFFCFHM-SNAWJCMRSA-N (2E)-hexenal Chemical compound CCC\C=C\C=O MBDOYVRWFFCFHM-SNAWJCMRSA-N 0.000 description 2
- 239000000260 (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol Substances 0.000 description 2
- ZHYZQXUYZJNEHD-CLFYSBASSA-N (2z)-3,7-dimethylocta-2,6-dienoic acid Chemical compound CC(C)=CCC\C(C)=C/C(O)=O ZHYZQXUYZJNEHD-CLFYSBASSA-N 0.000 description 2
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 2
- 239000001147 (3aR,5aS,9aS,9bR)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1H-benzo[e][1]benzofuran Substances 0.000 description 2
- NGPCLOGFGKJCBP-IYBDPMFKSA-N (3r,6s)-3,6-bis[(4-hydroxyphenyl)methyl]piperazine-2,5-dione Chemical compound C1=CC(O)=CC=C1C[C@@H]1C(=O)N[C@@H](CC=2C=CC(O)=CC=2)C(=O)N1 NGPCLOGFGKJCBP-IYBDPMFKSA-N 0.000 description 2
- KHWTYGFHPHRQMP-UHFFFAOYSA-N (4-propan-2-ylcyclohexyl)methanol Chemical compound CC(C)C1CCC(CO)CC1 KHWTYGFHPHRQMP-UHFFFAOYSA-N 0.000 description 2
- 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 description 2
- NVIPUOMWGQAOIT-UHFFFAOYSA-N (E)-7-Hexadecen-16-olide Natural products O=C1CCCCCC=CCCCCCCCCO1 NVIPUOMWGQAOIT-UHFFFAOYSA-N 0.000 description 2
- OOCCDEMITAIZTP-QPJJXVBHSA-N (E)-cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 2
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 2
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 2
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 2
- OHBQPCCCRFSCAX-UHFFFAOYSA-N 1,4-Dimethoxybenzene Chemical compound COC1=CC=C(OC)C=C1 OHBQPCCCRFSCAX-UHFFFAOYSA-N 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 2
- OFHHDSQXFXLTKC-UHFFFAOYSA-N 10-undecenal Chemical compound C=CCCCCCCCCC=O OFHHDSQXFXLTKC-UHFFFAOYSA-N 0.000 description 2
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- XFOQWQKDSMIPHT-UHFFFAOYSA-N 2,3-dichloro-6-(trifluoromethyl)pyridine Chemical compound FC(F)(F)C1=CC=C(Cl)C(Cl)=N1 XFOQWQKDSMIPHT-UHFFFAOYSA-N 0.000 description 2
- 229940029225 2,6-dimethyl-5-heptenal Drugs 0.000 description 2
- HGDVHRITTGWMJK-UHFFFAOYSA-N 2,6-dimethylheptan-2-ol Chemical compound CC(C)CCCC(C)(C)O HGDVHRITTGWMJK-UHFFFAOYSA-N 0.000 description 2
- DNRJTBAOUJJKDY-UHFFFAOYSA-N 2-Acetyl-3,5,5,6,8,8-hexamethyl-5,6,7,8- tetrahydronaphthalene Chemical compound CC(=O)C1=C(C)C=C2C(C)(C)C(C)CC(C)(C)C2=C1 DNRJTBAOUJJKDY-UHFFFAOYSA-N 0.000 description 2
- GUMOJENFFHZAFP-UHFFFAOYSA-N 2-Ethoxynaphthalene Chemical compound C1=CC=CC2=CC(OCC)=CC=C21 GUMOJENFFHZAFP-UHFFFAOYSA-N 0.000 description 2
- FLUWAIIVLCVEKF-UHFFFAOYSA-N 2-Methyl-1-phenyl-2-propanyl acetate Chemical compound CC(=O)OC(C)(C)CC1=CC=CC=C1 FLUWAIIVLCVEKF-UHFFFAOYSA-N 0.000 description 2
- RQXTZKGDMNIWJF-UHFFFAOYSA-N 2-butan-2-ylcyclohexan-1-one Chemical compound CCC(C)C1CCCCC1=O RQXTZKGDMNIWJF-UHFFFAOYSA-N 0.000 description 2
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 2
- QPRQEDXDYOZYLA-UHFFFAOYSA-N 2-methylbutan-1-ol Chemical compound CCC(C)CO QPRQEDXDYOZYLA-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
- VNWOJVJCRAHBJJ-UHFFFAOYSA-N 2-pentylcyclopentan-1-one Chemical compound CCCCCC1CCCC1=O VNWOJVJCRAHBJJ-UHFFFAOYSA-N 0.000 description 2
- WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 description 2
- ZQWZOXZKTPYDHR-UHFFFAOYSA-N 3,6-bis[(4-phenylmethoxyphenyl)methyl]piperazine-2,5-dione Chemical compound O=C1NC(CC=2C=CC(OCC=3C=CC=CC=3)=CC=2)C(=O)NC1CC(C=C1)=CC=C1OCC1=CC=CC=C1 ZQWZOXZKTPYDHR-UHFFFAOYSA-N 0.000 description 2
- GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 description 2
- BBWGOIQLDWZWMM-UHFFFAOYSA-N 3-(5-benzyl-3,6-dioxopiperazin-2-yl)propanoic acid Chemical compound N1C(=O)C(CCC(=O)O)NC(=O)C1CC1=CC=CC=C1 BBWGOIQLDWZWMM-UHFFFAOYSA-N 0.000 description 2
- URQMEZRQHLCJKR-UHFFFAOYSA-N 3-Methyl-5-propyl-2-cyclohexen-1-one Chemical compound CCCC1CC(C)=CC(=O)C1 URQMEZRQHLCJKR-UHFFFAOYSA-N 0.000 description 2
- VAJVDSVGBWFCLW-UHFFFAOYSA-N 3-Phenyl-1-propanol Chemical compound OCCCC1=CC=CC=C1 VAJVDSVGBWFCLW-UHFFFAOYSA-N 0.000 description 2
- OQQPOHUVAQPSHJ-UHFFFAOYSA-N 3-benzyl-6-propan-2-ylpiperazine-2,5-dione Chemical compound N1C(=O)C(C(C)C)NC(=O)C1CC1=CC=CC=C1 OQQPOHUVAQPSHJ-UHFFFAOYSA-N 0.000 description 2
- YGCZTXZTJXYWCO-UHFFFAOYSA-N 3-phenylpropanal Chemical compound O=CCCC1=CC=CC=C1 YGCZTXZTJXYWCO-UHFFFAOYSA-N 0.000 description 2
- GNKZMNRKLCTJAY-UHFFFAOYSA-N 4'-Methylacetophenone Chemical compound CC(=O)C1=CC=C(C)C=C1 GNKZMNRKLCTJAY-UHFFFAOYSA-N 0.000 description 2
- TXFPEBPIARQUIG-UHFFFAOYSA-N 4'-hydroxyacetophenone Chemical compound CC(=O)C1=CC=C(O)C=C1 TXFPEBPIARQUIG-UHFFFAOYSA-N 0.000 description 2
- TZJLGGWGVLADDN-UHFFFAOYSA-N 4-(3,4-Methylenedioxyphenyl)-2-butanone Chemical group CC(=O)CCC1=CC=C2OCOC2=C1 TZJLGGWGVLADDN-UHFFFAOYSA-N 0.000 description 2
- MSHFRERJPWKJFX-UHFFFAOYSA-N 4-Methoxybenzyl alcohol Chemical compound COC1=CC=C(CO)C=C1 MSHFRERJPWKJFX-UHFFFAOYSA-N 0.000 description 2
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 2
- MUDSDYNRBDKLGK-UHFFFAOYSA-N 4-methylquinoline Chemical compound C1=CC=C2C(C)=CC=NC2=C1 MUDSDYNRBDKLGK-UHFFFAOYSA-N 0.000 description 2
- NVIPUOMWGQAOIT-DUXPYHPUSA-N 7-hexadecen-1,16-olide Chemical compound O=C1CCCCC\C=C\CCCCCCCCO1 NVIPUOMWGQAOIT-DUXPYHPUSA-N 0.000 description 2
- QGFSQVPRCWJZQK-UHFFFAOYSA-N 9-Decen-1-ol Chemical compound OCCCCCCCCC=C QGFSQVPRCWJZQK-UHFFFAOYSA-N 0.000 description 2
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 2
- 240000007087 Apium graveolens Species 0.000 description 2
- 235000015849 Apium graveolens Dulce Group Nutrition 0.000 description 2
- 235000010591 Appio Nutrition 0.000 description 2
- 241000208983 Arnica Species 0.000 description 2
- ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 description 2
- UYWQUFXKFGHYNT-UHFFFAOYSA-N Benzylformate Chemical compound O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 2
- 241000717739 Boswellia sacra Species 0.000 description 2
- 235000002566 Capsicum Nutrition 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 2
- 244000037364 Cinnamomum aromaticum Species 0.000 description 2
- 235000014489 Cinnamomum aromaticum Nutrition 0.000 description 2
- 240000001251 Cucumis anguria Species 0.000 description 2
- 235000009075 Cucumis anguria Nutrition 0.000 description 2
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 2
- 235000007129 Cuminum cyminum Nutrition 0.000 description 2
- 244000304337 Cuminum cyminum Species 0.000 description 2
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 2
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 2
- QSJXEFYPDANLFS-UHFFFAOYSA-N Diacetyl Chemical compound CC(=O)C(C)=O QSJXEFYPDANLFS-UHFFFAOYSA-N 0.000 description 2
- 240000002943 Elettaria cardamomum Species 0.000 description 2
- KBEBGUQPQBELIU-CMDGGOBGSA-N Ethyl cinnamate Chemical compound CCOC(=O)\C=C\C1=CC=CC=C1 KBEBGUQPQBELIU-CMDGGOBGSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- JUWUWIGZUVEFQB-UHFFFAOYSA-N Fenchyl acetate Chemical compound C1CC2C(C)(C)C(OC(=O)C)C1(C)C2 JUWUWIGZUVEFQB-UHFFFAOYSA-N 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- 239000004863 Frankincense Substances 0.000 description 2
- DUKPKQFHJQGTGU-UHFFFAOYSA-N Hexyl salicylic acid Chemical compound CCCCCCOC(=O)C1=CC=CC=C1O DUKPKQFHJQGTGU-UHFFFAOYSA-N 0.000 description 2
- 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 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 2
- VHVOLFRBFDOUSH-NSCUHMNNSA-N Isosafrole Chemical compound C\C=C\C1=CC=C2OCOC2=C1 VHVOLFRBFDOUSH-NSCUHMNNSA-N 0.000 description 2
- VHVOLFRBFDOUSH-UHFFFAOYSA-N Isosafrole Natural products CC=CC1=CC=C2OCOC2=C1 VHVOLFRBFDOUSH-UHFFFAOYSA-N 0.000 description 2
- VNHJXYUDIBQDDX-UHFFFAOYSA-N L-cis-Cyclo(aspartylphenylalanyl) Chemical compound N1C(=O)C(CC(=O)O)NC(=O)C1CC1=CC=CC=C1 VNHJXYUDIBQDDX-UHFFFAOYSA-N 0.000 description 2
- 235000019501 Lemon oil Nutrition 0.000 description 2
- 240000007794 Melaleuca viridiflora Species 0.000 description 2
- NFLGAXVYCFJBMK-UHFFFAOYSA-N Menthone Chemical compound CC(C)C1CCC(C)CC1=O NFLGAXVYCFJBMK-UHFFFAOYSA-N 0.000 description 2
- 244000174681 Michelia champaca Species 0.000 description 2
- GLZPCOQZEFWAFX-JXMROGBWSA-N Nerol Natural products CC(C)=CCC\C(C)=C\CO GLZPCOQZEFWAFX-JXMROGBWSA-N 0.000 description 2
- 235000011203 Origanum Nutrition 0.000 description 2
- 241001529744 Origanum Species 0.000 description 2
- 239000006002 Pepper Substances 0.000 description 2
- OHUXOEXBXPZKPT-STQMWFEESA-N Phe-His Chemical compound C([C@H](N)C(=O)N[C@@H](CC=1N=CNC=1)C(O)=O)C1=CC=CC=C1 OHUXOEXBXPZKPT-STQMWFEESA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 241000218657 Picea Species 0.000 description 2
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 2
- 235000011613 Pinus brutia Nutrition 0.000 description 2
- 241000018646 Pinus brutia Species 0.000 description 2
- 235000016761 Piper aduncum Nutrition 0.000 description 2
- 240000003889 Piper guineense Species 0.000 description 2
- 235000017804 Piper guineense Nutrition 0.000 description 2
- 235000008184 Piper nigrum Nutrition 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- 241000218636 Thuja Species 0.000 description 2
- 235000007212 Verbena X moechina Moldenke Nutrition 0.000 description 2
- 240000001519 Verbena officinalis Species 0.000 description 2
- 235000001594 Verbena polystachya Kunth Nutrition 0.000 description 2
- 235000007200 Verbena x perriana Moldenke Nutrition 0.000 description 2
- 235000002270 Verbena x stuprosa Moldenke Nutrition 0.000 description 2
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 2
- 125000002252 acyl group Chemical group 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- OOCCDEMITAIZTP-UHFFFAOYSA-N allylic benzylic alcohol Natural products OCC=CC1=CC=CC=C1 OOCCDEMITAIZTP-UHFFFAOYSA-N 0.000 description 2
- UZFLPKAIBPNNCA-BQYQJAHWSA-N alpha-ionone Chemical compound CC(=O)\C=C\C1C(C)=CCCC1(C)C UZFLPKAIBPNNCA-BQYQJAHWSA-N 0.000 description 2
- YPZUZOLGGMJZJO-LQKXBSAESA-N ambroxan Chemical compound CC([C@@H]1CC2)(C)CCC[C@]1(C)[C@@H]1[C@]2(C)OCC1 YPZUZOLGGMJZJO-LQKXBSAESA-N 0.000 description 2
- 239000002280 amphoteric surfactant Substances 0.000 description 2
- 229940011037 anethole Drugs 0.000 description 2
- 239000001408 angelica archangelica l. root oil Substances 0.000 description 2
- 239000010617 anise oil Substances 0.000 description 2
- 235000006708 antioxidants Nutrition 0.000 description 2
- 239000010619 basil oil Substances 0.000 description 2
- 229940018006 basil oil Drugs 0.000 description 2
- 239000010620 bay oil Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 2
- 239000012965 benzophenone Substances 0.000 description 2
- LRTSNNDRHYCIQY-UHFFFAOYSA-N benzyl 3-(5-benzyl-3,6-dioxopiperazin-2-yl)propanoate Chemical compound C(C1=CC=CC=C1)C1C(NC(C(N1)=O)CCC(=O)OCC1=CC=CC=C1)=O LRTSNNDRHYCIQY-UHFFFAOYSA-N 0.000 description 2
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 2
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 description 2
- 229940115397 bornyl acetate Drugs 0.000 description 2
- 239000010629 calamus oil Substances 0.000 description 2
- 239000010624 camphor oil Substances 0.000 description 2
- 229960000411 camphor oil Drugs 0.000 description 2
- 239000001444 canarium indicum l. oil Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 235000005300 cardamomo Nutrition 0.000 description 2
- RECUKUPTGUEGMW-UHFFFAOYSA-N carvacrol Chemical compound CC(C)C1=CC=C(C)C(O)=C1 RECUKUPTGUEGMW-UHFFFAOYSA-N 0.000 description 2
- MIZGSAALSYARKU-UHFFFAOYSA-N cashmeran Chemical compound CC1(C)C(C)C(C)(C)C2=C1C(=O)CCC2 MIZGSAALSYARKU-UHFFFAOYSA-N 0.000 description 2
- 239000001913 cellulose Substances 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 239000000919 ceramic Substances 0.000 description 2
- 239000010628 chamomile oil Substances 0.000 description 2
- 235000019480 chamomile oil Nutrition 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 235000012000 cholesterol Nutrition 0.000 description 2
- 229940107161 cholesterol Drugs 0.000 description 2
- 235000013985 cinnamic acid Nutrition 0.000 description 2
- 229930016911 cinnamic acid Natural products 0.000 description 2
- KBEBGUQPQBELIU-UHFFFAOYSA-N cinnamic acid ethyl ester Natural products CCOC(=O)C=CC1=CC=CC=C1 KBEBGUQPQBELIU-UHFFFAOYSA-N 0.000 description 2
- CCRCUPLGCSFEDV-UHFFFAOYSA-N cinnamic acid methyl ester Natural products COC(=O)C=CC1=CC=CC=C1 CCRCUPLGCSFEDV-UHFFFAOYSA-N 0.000 description 2
- 229940117916 cinnamic aldehyde Drugs 0.000 description 2
- 239000010630 cinnamon oil Substances 0.000 description 2
- NNWHUJCUHAELCL-UHFFFAOYSA-N cis-Methyl isoeugenol Natural products COC1=CC=C(C=CC)C=C1OC NNWHUJCUHAELCL-UHFFFAOYSA-N 0.000 description 2
- NNWHUJCUHAELCL-PLNGDYQASA-N cis-isomethyleugenol Chemical compound COC1=CC=C(\C=C/C)C=C1OC NNWHUJCUHAELCL-PLNGDYQASA-N 0.000 description 2
- 239000010632 citronella oil Substances 0.000 description 2
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000001111 citrus aurantium l. leaf oil Substances 0.000 description 2
- 239000001524 citrus aurantium oil Substances 0.000 description 2
- 239000010634 clove oil Substances 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 239000001555 commiphora myrrha gum extract Substances 0.000 description 2
- 239000010636 coriander oil Substances 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 239000001939 cymbopogon martini roxb. stapf. oil Substances 0.000 description 2
- 239000010639 cypress oil Substances 0.000 description 2
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 2
- 235000018417 cysteine Nutrition 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- QGGZBXOADPVUPN-UHFFFAOYSA-N dihydrochalcone Chemical compound C=1C=CC=CC=1C(=O)CCC1=CC=CC=C1 QGGZBXOADPVUPN-UHFFFAOYSA-N 0.000 description 2
- 229940095104 dimethyl benzyl carbinyl acetate Drugs 0.000 description 2
- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 2
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 2
- 229940073505 ethyl vanillin Drugs 0.000 description 2
- 239000010642 eucalyptus oil Substances 0.000 description 2
- 229940044949 eucalyptus oil Drugs 0.000 description 2
- 239000002979 fabric softener Substances 0.000 description 2
- 229940043259 farnesol Drugs 0.000 description 2
- 229930002886 farnesol Natural products 0.000 description 2
- 239000010643 fennel seed oil Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000010645 fir oil Substances 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- 239000010649 ginger oil Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 150000002301 glucosamine derivatives Chemical class 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- 229930182470 glycoside Natural products 0.000 description 2
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 2
- FXHGMKSSBGDXIY-UHFFFAOYSA-N heptanal Chemical compound CCCCCCC=O FXHGMKSSBGDXIY-UHFFFAOYSA-N 0.000 description 2
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- FVDRFBGMOWJEOR-UHFFFAOYSA-N hexadecan-2-ol Chemical compound CCCCCCCCCCCCCCC(C)O FVDRFBGMOWJEOR-UHFFFAOYSA-N 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- ZOCHHNOQQHDWHG-UHFFFAOYSA-N hexan-3-ol Chemical compound CCCC(O)CC ZOCHHNOQQHDWHG-UHFFFAOYSA-N 0.000 description 2
- JARKCYVAAOWBJS-UHFFFAOYSA-N hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 description 2
- AOGQPLXWSUTHQB-UHFFFAOYSA-N hexyl acetate Chemical compound CCCCCCOC(C)=O AOGQPLXWSUTHQB-UHFFFAOYSA-N 0.000 description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000001735 hyssopus officinalis l. herb oil Substances 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- ZYTMANIQRDEHIO-KXUCPTDWSA-N isopulegol Chemical compound C[C@@H]1CC[C@@H](C(C)=C)[C@H](O)C1 ZYTMANIQRDEHIO-KXUCPTDWSA-N 0.000 description 2
- 239000001851 juniperus communis l. berry oil Substances 0.000 description 2
- 239000000171 lavandula angustifolia l. flower oil Substances 0.000 description 2
- 239000010501 lemon oil Substances 0.000 description 2
- SDQFDHOLCGWZPU-UHFFFAOYSA-N lilial Chemical compound O=CC(C)CC1=CC=C(C(C)(C)C)C=C1 SDQFDHOLCGWZPU-UHFFFAOYSA-N 0.000 description 2
- 235000001510 limonene Nutrition 0.000 description 2
- 229940087305 limonene Drugs 0.000 description 2
- 229930007744 linalool Natural products 0.000 description 2
- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 2
- 239000001525 mentha piperita l. herb oil Substances 0.000 description 2
- 229940041616 menthol Drugs 0.000 description 2
- 229930007503 menthone Natural products 0.000 description 2
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 2
- KVWWIYGFBYDJQC-UHFFFAOYSA-N methyl dihydrojasmonate Chemical compound CCCCCC1C(CC(=O)OC)CCC1=O KVWWIYGFBYDJQC-UHFFFAOYSA-N 0.000 description 2
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 2
- CCRCUPLGCSFEDV-BQYQJAHWSA-N methyl trans-cinnamate Chemical compound COC(=O)\C=C\C1=CC=CC=C1 CCRCUPLGCSFEDV-BQYQJAHWSA-N 0.000 description 2
- SBENKNZHVXGNTP-UHFFFAOYSA-N methylconiferyl ether Natural products COCC=CC1=CC=C(O)C(OC)=C1 SBENKNZHVXGNTP-UHFFFAOYSA-N 0.000 description 2
- 239000001186 myroxylon pereirae klotzsch oil Substances 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 235000019720 niaouli oil Nutrition 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- NMRPBPVERJPACX-UHFFFAOYSA-N octan-3-ol Chemical compound CCCCCC(O)CC NMRPBPVERJPACX-UHFFFAOYSA-N 0.000 description 2
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-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
- LVECZGHBXXYWBO-UHFFFAOYSA-N pentadecanolide Natural products CC1CCCCCCCCCCCCC(=O)O1 LVECZGHBXXYWBO-UHFFFAOYSA-N 0.000 description 2
- PGMYKACGEOXYJE-UHFFFAOYSA-N pentyl acetate Chemical compound CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- 235000019477 peppermint oil Nutrition 0.000 description 2
- MDHYEMXUFSJLGV-UHFFFAOYSA-N phenethyl acetate Chemical compound CC(=O)OCCC1=CC=CC=C1 MDHYEMXUFSJLGV-UHFFFAOYSA-N 0.000 description 2
- ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 2
- 150000003904 phospholipids Chemical class 0.000 description 2
- 239000001622 pimenta officinalis fruit oil Substances 0.000 description 2
- SATCULPHIDQDRE-UHFFFAOYSA-N piperonal Chemical compound O=CC1=CC=C2OCOC2=C1 SATCULPHIDQDRE-UHFFFAOYSA-N 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 239000001738 pogostemon cablin oil Substances 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- KRIOVPPHQSLHCZ-UHFFFAOYSA-N propiophenone Chemical compound CCC(=O)C1=CC=CC=C1 KRIOVPPHQSLHCZ-UHFFFAOYSA-N 0.000 description 2
- 235000018102 proteins Nutrition 0.000 description 2
- 108090000623 proteins and genes Proteins 0.000 description 2
- 102000004169 proteins and genes Human genes 0.000 description 2
- HEBKCHPVOIAQTA-ZXFHETKHSA-N ribitol Chemical compound OC[C@H](O)[C@H](O)[C@H](O)CO HEBKCHPVOIAQTA-ZXFHETKHSA-N 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 239000010671 sandalwood oil Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 229920001059 synthetic polymer Polymers 0.000 description 2
- 239000010678 thyme oil Substances 0.000 description 2
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 2
- CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 description 2
- 235000013311 vegetables Nutrition 0.000 description 2
- WJUFSDZVCOTFON-UHFFFAOYSA-N veratraldehyde Chemical compound COC1=CC=C(C=O)C=C1OC WJUFSDZVCOTFON-UHFFFAOYSA-N 0.000 description 2
- 239000010679 vetiver oil Substances 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 239000011782 vitamin Substances 0.000 description 2
- 235000013343 vitamin Nutrition 0.000 description 2
- 229930003231 vitamin Natural products 0.000 description 2
- 229940088594 vitamin Drugs 0.000 description 2
- 235000019154 vitamin C Nutrition 0.000 description 2
- 239000011718 vitamin C Substances 0.000 description 2
- 235000019165 vitamin E Nutrition 0.000 description 2
- 239000011709 vitamin E Substances 0.000 description 2
- 239000000341 volatile oil Substances 0.000 description 2
- 239000009637 wintergreen oil Substances 0.000 description 2
- 239000002023 wood 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
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 description 1
- 239000001563 (1,5,5-trimethyl-6-bicyclo[2.2.1]heptanyl) acetate Substances 0.000 description 1
- BGCIAWBDYRWKEK-UHFFFAOYSA-N (1-butylcyclohexyl) acetate Chemical compound CCCCC1(OC(C)=O)CCCCC1 BGCIAWBDYRWKEK-UHFFFAOYSA-N 0.000 description 1
- 239000001871 (1R,2R,5S)-5-methyl-2-prop-1-en-2-ylcyclohexan-1-ol Substances 0.000 description 1
- HZYHMHHBBBSGHB-UHFFFAOYSA-N (2E,6E)-2,6-Nonadienal Natural products CCC=CCCC=CC=O HZYHMHHBBBSGHB-UHFFFAOYSA-N 0.000 description 1
- KIUKXJAPPMFGSW-DNGZLQJQSA-N (2S,3S,4S,5R,6R)-6-[(2S,3R,4R,5S,6R)-3-Acetamido-2-[(2S,3S,4R,5R,6R)-6-[(2R,3R,4R,5S,6R)-3-acetamido-2,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-2-carboxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O[C@H]2[C@@H]([C@@H](O[C@H]3[C@@H]([C@@H](O)[C@H](O)[C@H](O3)C(O)=O)O)[C@H](O)[C@@H](CO)O2)NC(C)=O)[C@@H](C(O)=O)O1 KIUKXJAPPMFGSW-DNGZLQJQSA-N 0.000 description 1
- HZYHMHHBBBSGHB-DYWGDJMRSA-N (2e,6e)-nona-2,6-dienal Chemical compound CC\C=C\CC\C=C\C=O HZYHMHHBBBSGHB-DYWGDJMRSA-N 0.000 description 1
- GUTXMPQWQSOAIY-HOTGVXAUSA-N (2r)-2-benzamido-3-[[(2r)-2-benzamido-2-carboxyethyl]disulfanyl]propanoic acid Chemical compound N([C@@H](CSSC[C@@H](C(=O)O)NC(=O)C=1C=CC=CC=1)C(O)=O)C(=O)C1=CC=CC=C1 GUTXMPQWQSOAIY-HOTGVXAUSA-N 0.000 description 1
- MESCLBRMEHFBJF-CHWSQXEVSA-N (3R,6R)-3-(4-aminobutyl)-6-benzylpiperazine-2,5-dione Chemical compound C(C1=CC=CC=C1)[C@@H]1C(N[C@@H](C(N1)=O)CCCCN)=O MESCLBRMEHFBJF-CHWSQXEVSA-N 0.000 description 1
- NGPCLOGFGKJCBP-HZPDHXFCSA-N (3r,6r)-3,6-bis[(4-hydroxyphenyl)methyl]piperazine-2,5-dione Chemical compound C1=CC(O)=CC=C1C[C@@H]1C(=O)N[C@H](CC=2C=CC(O)=CC=2)C(=O)N1 NGPCLOGFGKJCBP-HZPDHXFCSA-N 0.000 description 1
- OQQPOHUVAQPSHJ-RYUDHWBXSA-N (3s,6s)-3-benzyl-6-propan-2-ylpiperazine-2,5-dione Chemical compound N1C(=O)[C@H](C(C)C)NC(=O)[C@@H]1CC1=CC=CC=C1 OQQPOHUVAQPSHJ-RYUDHWBXSA-N 0.000 description 1
- CIXAYNMKFFQEFU-UHFFFAOYSA-N (4-Methylphenyl)acetaldehyde Chemical compound CC1=CC=C(CC=O)C=C1 CIXAYNMKFFQEFU-UHFFFAOYSA-N 0.000 description 1
- MMLYERLRGHVBEK-XYOKQWHBSA-N (4e)-5,9-dimethyldeca-4,8-dienal Chemical compound CC(C)=CCC\C(C)=C\CCC=O MMLYERLRGHVBEK-XYOKQWHBSA-N 0.000 description 1
- ZXGMEZJVBHJYEQ-UKTHLTGXSA-N (5e)-2,6,10-trimethylundeca-5,9-dienal Chemical compound O=CC(C)CC\C=C(/C)CCC=C(C)C ZXGMEZJVBHJYEQ-UKTHLTGXSA-N 0.000 description 1
- YYGNTYWPHWGJRM-UHFFFAOYSA-N (6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene Chemical compound CC(C)=CCCC(C)=CCCC(C)=CCCC=C(C)CCC=C(C)CCC=C(C)C YYGNTYWPHWGJRM-UHFFFAOYSA-N 0.000 description 1
- 239000001306 (7E,9E,11E,13E)-pentadeca-7,9,11,13-tetraen-1-ol Substances 0.000 description 1
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
- 239000001674 (E)-1-(2,6,6-trimethyl-1-cyclohexenyl)but-2-en-1-one Substances 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- NSSALFVIQPAIQK-BQYQJAHWSA-N (E)-non-2-en-1-ol Chemical compound CCCCCC\C=C\CO NSSALFVIQPAIQK-BQYQJAHWSA-N 0.000 description 1
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 1
- WUOACPNHFRMFPN-SECBINFHSA-N (S)-(-)-alpha-terpineol Chemical compound CC1=CC[C@@H](C(C)(C)O)CC1 WUOACPNHFRMFPN-SECBINFHSA-N 0.000 description 1
- CMWOCHXOAOFYCY-HOTGVXAUSA-N (S,S)-2,5-di-(p-hydroxybenzyl)piperazine Chemical compound Oc1ccc(C[C@H]2CN[C@@H](Cc3ccc(O)cc3)CN2)cc1 CMWOCHXOAOFYCY-HOTGVXAUSA-N 0.000 description 1
- RUJPNZNXGCHGID-UHFFFAOYSA-N (Z)-beta-Terpineol Natural products CC(=C)C1CCC(C)(O)CC1 RUJPNZNXGCHGID-UHFFFAOYSA-N 0.000 description 1
- XEJGJTYRUWUFFD-FNORWQNLSA-N (e)-1-(2,6,6-trimethyl-1-cyclohex-3-enyl)but-2-en-1-one Chemical compound C\C=C\C(=O)C1C(C)C=CCC1(C)C XEJGJTYRUWUFFD-FNORWQNLSA-N 0.000 description 1
- VLUMOWNVWOXZAU-VQHVLOKHSA-N (e)-2-methyl-3-phenylprop-2-enal Chemical compound O=CC(/C)=C/C1=CC=CC=C1 VLUMOWNVWOXZAU-VQHVLOKHSA-N 0.000 description 1
- MTVBNJVZZAQKRV-BJMVGYQFSA-N (e)-2-methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-en-1-ol Chemical compound OCC(/C)=C/CC1CC=C(C)C1(C)C MTVBNJVZZAQKRV-BJMVGYQFSA-N 0.000 description 1
- CWRKZMLUDFBPAO-VOTSOKGWSA-N (e)-dec-4-enal Chemical compound CCCCC\C=C\CCC=O CWRKZMLUDFBPAO-VOTSOKGWSA-N 0.000 description 1
- HBBONAOKVLYWBI-MDZDMXLPSA-N (e)-dodec-3-enal Chemical compound CCCCCCCC\C=C\CC=O HBBONAOKVLYWBI-MDZDMXLPSA-N 0.000 description 1
- JHEPBQHNVNUAFL-AATRIKPKSA-N (e)-hex-1-en-1-ol Chemical compound CCCC\C=C\O JHEPBQHNVNUAFL-AATRIKPKSA-N 0.000 description 1
- JRJBVWJSTHECJK-LUAWRHEFSA-N (z)-3-methyl-4-(2,6,6-trimethylcyclohex-2-en-1-yl)but-3-en-2-one Chemical compound CC(=O)C(\C)=C/C1C(C)=CCCC1(C)C JRJBVWJSTHECJK-LUAWRHEFSA-N 0.000 description 1
- QMMJWQMCMRUYTG-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=C(Cl)C(Cl)=CC(Cl)=C1Cl QMMJWQMCMRUYTG-UHFFFAOYSA-N 0.000 description 1
- QZMQKPGVXNSITP-UHFFFAOYSA-N 1,3-benzodioxole-4-carbaldehyde Chemical compound O=CC1=CC=CC2=C1OCO2 QZMQKPGVXNSITP-UHFFFAOYSA-N 0.000 description 1
- WEEGYLXZBRQIMU-UHFFFAOYSA-N 1,8-cineole Natural products C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 1
- CRIGTVCBMUKRSL-FNORWQNLSA-N 1-(2,6,6-trimethylcyclohex-2-en-1-yl)but-2-enone Chemical compound C\C=C\C(=O)C1C(C)=CCCC1(C)C CRIGTVCBMUKRSL-FNORWQNLSA-N 0.000 description 1
- FXCYGAGBPZQRJE-UHFFFAOYSA-N 1-(2,6,6-trimethylcyclohex-2-en-1-yl)hepta-1,6-dien-3-one Chemical compound CC1=CCCC(C)(C)C1C=CC(=O)CCC=C FXCYGAGBPZQRJE-UHFFFAOYSA-N 0.000 description 1
- BGTBFNDXYDYBEY-UHFFFAOYSA-N 1-(2,6,6-trimethylcyclohexen-1-yl)but-2-en-1-one Chemical compound CC=CC(=O)C1=C(C)CCCC1(C)C BGTBFNDXYDYBEY-UHFFFAOYSA-N 0.000 description 1
- NPMRPDRLIHYOBW-UHFFFAOYSA-N 1-(2-butoxyethoxy)propan-2-ol Chemical compound CCCCOCCOCC(C)O NPMRPDRLIHYOBW-UHFFFAOYSA-N 0.000 description 1
- QWOZZTWBWQMEPD-UHFFFAOYSA-N 1-(2-ethoxypropoxy)propan-2-ol Chemical compound CCOC(C)COCC(C)O QWOZZTWBWQMEPD-UHFFFAOYSA-N 0.000 description 1
- NGTMQRCBACIUES-UHFFFAOYSA-N 1-(3,3-dimethyl-2-bicyclo[2.2.1]heptanyl)ethanone Chemical compound C1CC2C(C)(C)C(C(=O)C)C1C2 NGTMQRCBACIUES-UHFFFAOYSA-N 0.000 description 1
- GSUYZVWMHZWMGJ-UHFFFAOYSA-N 1-(4-methylpent-3-enyl)cyclohex-3-ene-1-carbaldehyde Chemical compound CC(C)=CCCC1(C=O)CCC=CC1 GSUYZVWMHZWMGJ-UHFFFAOYSA-N 0.000 description 1
- OEVIJAZJVZDBQL-UHFFFAOYSA-N 1-(5,5-dimethylcyclohexen-1-yl)pent-4-en-1-one Chemical compound CC1(C)CCC=C(C(=O)CCC=C)C1 OEVIJAZJVZDBQL-UHFFFAOYSA-N 0.000 description 1
- DZSVIVLGBJKQAP-RYUDHWBXSA-N 1-[(1s,5s)-2-methyl-5-propan-2-ylcyclohex-2-en-1-yl]propan-1-one Chemical compound CCC(=O)[C@H]1C[C@@H](C(C)C)CC=C1C DZSVIVLGBJKQAP-RYUDHWBXSA-N 0.000 description 1
- SRXJYTZCORKVNA-UHFFFAOYSA-N 1-bromoethenylbenzene Chemical compound BrC(=C)C1=CC=CC=C1 SRXJYTZCORKVNA-UHFFFAOYSA-N 0.000 description 1
- JOLQKTGDSGKSKJ-UHFFFAOYSA-N 1-ethoxypropan-2-ol Chemical compound CCOCC(C)O JOLQKTGDSGKSKJ-UHFFFAOYSA-N 0.000 description 1
- 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 description 1
- LKGPPAYTKODBGI-UHFFFAOYSA-N 1-methyl-3-(4-methylpentyl)cyclohex-3-ene-1-carbaldehyde Chemical compound CC(C)CCCC1=CCCC(C)(C=O)C1 LKGPPAYTKODBGI-UHFFFAOYSA-N 0.000 description 1
- VUIWFNRBSGUSIN-UHFFFAOYSA-N 1-methyl-4-(4-methylpent-3-enyl)cyclohex-3-ene-1-carbaldehyde Chemical compound CC(C)=CCCC1=CCC(C)(C=O)CC1 VUIWFNRBSGUSIN-UHFFFAOYSA-N 0.000 description 1
- 239000001169 1-methyl-4-propan-2-ylcyclohexa-1,4-diene Substances 0.000 description 1
- UUFQTNFCRMXOAE-UHFFFAOYSA-N 1-methylmethylene Chemical compound C[CH] UUFQTNFCRMXOAE-UHFFFAOYSA-N 0.000 description 1
- WAPNOHKVXSQRPX-UHFFFAOYSA-N 1-phenylethanol Chemical compound CC(O)C1=CC=CC=C1 WAPNOHKVXSQRPX-UHFFFAOYSA-N 0.000 description 1
- FENFUOGYJVOCRY-UHFFFAOYSA-N 1-propoxypropan-2-ol Chemical compound CCCOCC(C)O FENFUOGYJVOCRY-UHFFFAOYSA-N 0.000 description 1
- GQCZPFJGIXHZMB-UHFFFAOYSA-N 1-tert-Butoxy-2-propanol Chemical compound CC(O)COC(C)(C)C GQCZPFJGIXHZMB-UHFFFAOYSA-N 0.000 description 1
- GIEMHYCMBGELGY-UHFFFAOYSA-N 10-undecen-1-ol Chemical compound OCCCCCCCCCC=C GIEMHYCMBGELGY-UHFFFAOYSA-N 0.000 description 1
- PUKWIVZFEZFVAT-UHFFFAOYSA-N 2,2,5-trimethyl-5-pentylcyclopentan-1-one Chemical compound CCCCCC1(C)CCC(C)(C)C1=O PUKWIVZFEZFVAT-UHFFFAOYSA-N 0.000 description 1
- WCOXQTXVACYMLM-UHFFFAOYSA-N 2,3-bis(12-hydroxyoctadecanoyloxy)propyl 12-hydroxyoctadecanoate Chemical compound CCCCCCC(O)CCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC(O)CCCCCC)COC(=O)CCCCCCCCCCC(O)CCCCCC WCOXQTXVACYMLM-UHFFFAOYSA-N 0.000 description 1
- CTLDWNVYXLHMAS-UHFFFAOYSA-N 2,4,4,7-tetramethyloct-6-en-3-one Chemical compound CC(C)C(=O)C(C)(C)CC=C(C)C CTLDWNVYXLHMAS-UHFFFAOYSA-N 0.000 description 1
- ZTNFZIHZMITMGE-UHFFFAOYSA-N 2,6-dimethylcyclohex-2-ene-1-carbaldehyde Chemical compound CC1CCC=C(C)C1C=O ZTNFZIHZMITMGE-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- LAUVMIDRJMQUQL-UHFFFAOYSA-N 2-(3,7-dimethylocta-2,6-dienoxy)acetaldehyde Chemical compound CC(C)=CCCC(C)=CCOCC=O LAUVMIDRJMQUQL-UHFFFAOYSA-N 0.000 description 1
- VVUMWAHNKOLVSN-UHFFFAOYSA-N 2-(4-ethoxyanilino)-n-propylpropanamide Chemical compound CCCNC(=O)C(C)NC1=CC=C(OCC)C=C1 VVUMWAHNKOLVSN-UHFFFAOYSA-N 0.000 description 1
- FSKGFRBHGXIDSA-UHFFFAOYSA-N 2-(4-propan-2-ylphenyl)acetaldehyde Chemical compound CC(C)C1=CC=C(CC=O)C=C1 FSKGFRBHGXIDSA-UHFFFAOYSA-N 0.000 description 1
- 125000000134 2-(methylsulfanyl)ethyl group Chemical group [H]C([H])([H])SC([H])([H])C([H])([H])[*] 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- LUZDYPLAQQGJEA-UHFFFAOYSA-N 2-Methoxynaphthalene Chemical compound C1=CC=CC2=CC(OC)=CC=C21 LUZDYPLAQQGJEA-UHFFFAOYSA-N 0.000 description 1
- ZKPFRIDJMMOODR-UHFFFAOYSA-N 2-Methyloctanal Chemical compound CCCCCCC(C)C=O ZKPFRIDJMMOODR-UHFFFAOYSA-N 0.000 description 1
- MJTPMXWJHPOWGH-UHFFFAOYSA-N 2-Phenoxyethyl isobutyrate Chemical compound CC(C)C(=O)OCCOC1=CC=CC=C1 MJTPMXWJHPOWGH-UHFFFAOYSA-N 0.000 description 1
- RNDNSYIPLPAXAZ-UHFFFAOYSA-N 2-Phenyl-1-propanol Chemical compound OCC(C)C1=CC=CC=C1 RNDNSYIPLPAXAZ-UHFFFAOYSA-N 0.000 description 1
- COBPKKZHLDDMTB-UHFFFAOYSA-N 2-[2-(2-butoxyethoxy)ethoxy]ethanol Chemical compound CCCCOCCOCCOCCO COBPKKZHLDDMTB-UHFFFAOYSA-N 0.000 description 1
- WFSMVVDJSNMRAR-UHFFFAOYSA-N 2-[2-(2-ethoxyethoxy)ethoxy]ethanol Chemical compound CCOCCOCCOCCO WFSMVVDJSNMRAR-UHFFFAOYSA-N 0.000 description 1
- KNHGOYVXAHUDHP-UHFFFAOYSA-N 2-[2-(4-methylcyclohex-3-en-1-yl)propyl]cyclopentan-1-one Chemical compound C1CC(C)=CCC1C(C)CC1CCCC1=O KNHGOYVXAHUDHP-UHFFFAOYSA-N 0.000 description 1
- ZJVJPPNOQCMEPI-UHFFFAOYSA-N 2-[ethyl(methyl)amino]-2-phenylacetic acid Chemical compound CCN(C)C(C(O)=O)C1=CC=CC=C1 ZJVJPPNOQCMEPI-UHFFFAOYSA-N 0.000 description 1
- GUTXMPQWQSOAIY-UHFFFAOYSA-N 2-benzamido-3-[(2-benzamido-2-carboxyethyl)disulfanyl]propanoic acid Chemical compound C=1C=CC=CC=1C(=O)NC(C(=O)O)CSSCC(C(O)=O)NC(=O)C1=CC=CC=C1 GUTXMPQWQSOAIY-UHFFFAOYSA-N 0.000 description 1
- RITMXTLCKYLIKW-UHFFFAOYSA-N 2-benzylpiperazine Chemical compound C=1C=CC=CC=1CC1CNCCN1 RITMXTLCKYLIKW-UHFFFAOYSA-N 0.000 description 1
- 125000005999 2-bromoethyl group Chemical group 0.000 description 1
- 125000000069 2-butynyl group Chemical group [H]C([H])([H])C#CC([H])([H])* 0.000 description 1
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 description 1
- PJXHBTZLHITWFX-UHFFFAOYSA-N 2-heptylcyclopentan-1-one Chemical compound CCCCCCCC1CCCC1=O PJXHBTZLHITWFX-UHFFFAOYSA-N 0.000 description 1
- QSZQTGNYQLNKAQ-UHFFFAOYSA-N 2-hydroxy-3-phenylprop-2-enal Chemical compound O=CC(O)=CC1=CC=CC=C1 QSZQTGNYQLNKAQ-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- PFNHSEQQEPMLNI-UHFFFAOYSA-N 2-methyl-1-pentanol Chemical compound CCCC(C)CO PFNHSEQQEPMLNI-UHFFFAOYSA-N 0.000 description 1
- RIWRBSMFKVOJMN-UHFFFAOYSA-N 2-methyl-1-phenylpropan-2-ol Chemical compound CC(C)(O)CC1=CC=CC=C1 RIWRBSMFKVOJMN-UHFFFAOYSA-N 0.000 description 1
- YLQPSXZFPBXHPC-UHFFFAOYSA-N 2-methyl-3-(2-propan-2-ylphenyl)propanal Chemical compound O=CC(C)CC1=CC=CC=C1C(C)C YLQPSXZFPBXHPC-UHFFFAOYSA-N 0.000 description 1
- FJCQUJKUMKZEMH-UHFFFAOYSA-N 2-methyl-4-(2,6,6-trimethylcyclohexen-1-yl)but-2-enal Chemical compound O=CC(C)=CCC1=C(C)CCCC1(C)C FJCQUJKUMKZEMH-UHFFFAOYSA-N 0.000 description 1
- LBICMZLDYMBIGA-UHFFFAOYSA-N 2-methyldecanal Chemical compound CCCCCCCCC(C)C=O LBICMZLDYMBIGA-UHFFFAOYSA-N 0.000 description 1
- QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 description 1
- 125000004924 2-naphthylethyl group Chemical group C1=C(C=CC2=CC=CC=C12)CC* 0.000 description 1
- XFFILAFLGDUMBF-UHFFFAOYSA-N 2-phenoxyacetaldehyde Chemical compound O=CCOC1=CC=CC=C1 XFFILAFLGDUMBF-UHFFFAOYSA-N 0.000 description 1
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- IQVAERDLDAZARL-UHFFFAOYSA-N 2-phenylpropanal Chemical compound O=CC(C)C1=CC=CC=C1 IQVAERDLDAZARL-UHFFFAOYSA-N 0.000 description 1
- RPJGEHBYOXRURE-UHFFFAOYSA-N 2-propylbicyclo[2.2.1]hept-5-ene-3-carbaldehyde Chemical compound C1C2C=CC1C(CCC)C2C=O RPJGEHBYOXRURE-UHFFFAOYSA-N 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- PANBRUWVURLWGY-UHFFFAOYSA-N 2-undecenal Chemical compound CCCCCCCCC=CC=O PANBRUWVURLWGY-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- BRRVXFOKWJKTGG-UHFFFAOYSA-N 3,3,5-trimethylcyclohexanol Chemical compound CC1CC(O)CC(C)(C)C1 BRRVXFOKWJKTGG-UHFFFAOYSA-N 0.000 description 1
- IXIYWQIFBRZMNR-UHFFFAOYSA-N 3,4,5,6,6-pentamethylhept-3-en-2-one Chemical compound CC(C)(C)C(C)C(C)=C(C)C(C)=O IXIYWQIFBRZMNR-UHFFFAOYSA-N 0.000 description 1
- YXRXDZOBKUTUQZ-UHFFFAOYSA-N 3,4-dimethyloct-3-en-2-one Chemical compound CCCCC(C)=C(C)C(C)=O YXRXDZOBKUTUQZ-UHFFFAOYSA-N 0.000 description 1
- WTPYRCJDOZVZON-UHFFFAOYSA-N 3,5,5-Trimethylhexanal Chemical compound O=CCC(C)CC(C)(C)C WTPYRCJDOZVZON-UHFFFAOYSA-N 0.000 description 1
- DEMWVPUIZCCHPT-UHFFFAOYSA-N 3,5,6-trimethylcyclohex-3-ene-1-carbaldehyde Chemical compound CC1C=C(C)CC(C=O)C1C DEMWVPUIZCCHPT-UHFFFAOYSA-N 0.000 description 1
- JUAPMRSLDANLAS-UHFFFAOYSA-N 3,6-dibenzylpiperazine-2,5-dione Chemical compound O=C1NC(CC=2C=CC=CC=2)C(=O)NC1CC1=CC=CC=C1 JUAPMRSLDANLAS-UHFFFAOYSA-N 0.000 description 1
- DLHQZZUEERVIGQ-UHFFFAOYSA-N 3,7-dimethyl-3-octanol Chemical compound CCC(C)(O)CCCC(C)C DLHQZZUEERVIGQ-UHFFFAOYSA-N 0.000 description 1
- UCSIFMPORANABL-UHFFFAOYSA-N 3,7-dimethyloctanal Chemical compound CC(C)CCCC(C)CC=O UCSIFMPORANABL-UHFFFAOYSA-N 0.000 description 1
- ITJHALDCYCTNNJ-UHFFFAOYSA-N 3-(2-ethylphenyl)-2,2-dimethylpropanal Chemical compound CCC1=CC=CC=C1CC(C)(C)C=O ITJHALDCYCTNNJ-UHFFFAOYSA-N 0.000 description 1
- 229940019847 3-(3,4-methylenedioxyphenyl)-2-methylpropanal Drugs 0.000 description 1
- QCAHUFWKIQLBNB-UHFFFAOYSA-N 3-(3-methoxypropoxy)propan-1-ol Chemical compound COCCCOCCCO QCAHUFWKIQLBNB-UHFFFAOYSA-N 0.000 description 1
- MESCLBRMEHFBJF-UHFFFAOYSA-N 3-(4-aminobutyl)-6-benzylpiperazine-2,5-dione Chemical compound N1C(=O)C(CCCCN)NC(=O)C1CC1=CC=CC=C1 MESCLBRMEHFBJF-UHFFFAOYSA-N 0.000 description 1
- VLFBSPUPYFTTNF-UHFFFAOYSA-N 3-(4-methoxyphenyl)-2-methylpropanal Chemical compound COC1=CC=C(CC(C)C=O)C=C1 VLFBSPUPYFTTNF-UHFFFAOYSA-N 0.000 description 1
- NMRPBPVERJPACX-QMMMGPOBSA-N 3-Octanol Natural products CCCCC[C@@H](O)CC NMRPBPVERJPACX-QMMMGPOBSA-N 0.000 description 1
- DDFGFKGJBOILQZ-GHMZBOCLSA-N 3-[(1S,5R)-6,6-dimethyl-2-bicyclo[3.1.1]hept-2-enyl]propanal Chemical compound C1[C@H]2C(C)(C)[C@@H]1CC=C2CCC=O DDFGFKGJBOILQZ-GHMZBOCLSA-N 0.000 description 1
- GRWVBLRIPRGGPD-UHFFFAOYSA-N 3-benzyl-6-[(4-hydroxyphenyl)methyl]piperazine-2,5-dione Chemical compound C1=CC(O)=CC=C1CC1C(=O)NC(CC=2C=CC=CC=2)C(=O)N1 GRWVBLRIPRGGPD-UHFFFAOYSA-N 0.000 description 1
- CNXWPOWVDIUTPS-UHFFFAOYSA-N 3-benzyl-6-methylpiperazine-2,5-dione Chemical compound N1C(=O)C(C)NC(=O)C1CC1=CC=CC=C1 CNXWPOWVDIUTPS-UHFFFAOYSA-N 0.000 description 1
- MFKRHJVUCZRDTF-UHFFFAOYSA-N 3-methoxy-3-methylbutan-1-ol Chemical compound COC(C)(C)CCO MFKRHJVUCZRDTF-UHFFFAOYSA-N 0.000 description 1
- YCIXWYOBMVNGTB-UHFFFAOYSA-N 3-methyl-2-pentylcyclopent-2-en-1-one Chemical compound CCCCCC1=C(C)CCC1=O YCIXWYOBMVNGTB-UHFFFAOYSA-N 0.000 description 1
- OXYRENDGHPGWKV-UHFFFAOYSA-N 3-methyl-5-phenylpentan-1-ol Chemical compound OCCC(C)CCC1=CC=CC=C1 OXYRENDGHPGWKV-UHFFFAOYSA-N 0.000 description 1
- DFJMIMVMOIFPQG-UHFFFAOYSA-N 3-methyl-5-phenylpentanal Chemical compound O=CCC(C)CCC1=CC=CC=C1 DFJMIMVMOIFPQG-UHFFFAOYSA-N 0.000 description 1
- YLNYLLVKHRZLGO-UHFFFAOYSA-N 4-(1-ethoxyethenyl)-3,3,5,5-tetramethylcyclohexan-1-one Chemical compound CCOC(=C)C1C(C)(C)CC(=O)CC1(C)C YLNYLLVKHRZLGO-UHFFFAOYSA-N 0.000 description 1
- DCSKAMGZSIRJAQ-UHFFFAOYSA-N 4-(2-methylbutan-2-yl)cyclohexan-1-one Chemical compound CCC(C)(C)C1CCC(=O)CC1 DCSKAMGZSIRJAQ-UHFFFAOYSA-N 0.000 description 1
- UNDXPKDBFOOQFC-UHFFFAOYSA-N 4-[2-nitro-4-(trifluoromethyl)phenyl]morpholine Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=CC=C1N1CCOCC1 UNDXPKDBFOOQFC-UHFFFAOYSA-N 0.000 description 1
- AZRRZGIBBLWSSQ-UHFFFAOYSA-N 4-ethyl-7-phenyl-3,5-diazabicyclo[2.2.2]octane-2,6-dione Chemical compound N1C(=O)C2C(=O)NC1(CC)CC2C1=CC=CC=C1 AZRRZGIBBLWSSQ-UHFFFAOYSA-N 0.000 description 1
- DKKRDMLKVSKFMJ-UHFFFAOYSA-N 4-propan-2-ylcyclohexan-1-ol Chemical compound CC(C)C1CCC(O)CC1 DKKRDMLKVSKFMJ-UHFFFAOYSA-N 0.000 description 1
- MBZRJSQZCBXRGK-UHFFFAOYSA-N 4-tert-Butylcyclohexyl acetate Chemical compound CC(=O)OC1CCC(C(C)(C)C)CC1 MBZRJSQZCBXRGK-UHFFFAOYSA-N 0.000 description 1
- JGVWYJDASSSGEK-UHFFFAOYSA-N 5-methyl-2-propan-2-ylidenecyclohexan-1-ol Chemical compound CC1CCC(=C(C)C)C(O)C1 JGVWYJDASSSGEK-UHFFFAOYSA-N 0.000 description 1
- LGVYUZVANMHKHV-UHFFFAOYSA-N 6,10-Dimethylundec-9-en-2-one Chemical compound CC(=O)CCCC(C)CCC=C(C)C LGVYUZVANMHKHV-UHFFFAOYSA-N 0.000 description 1
- HDQVGGOVPFQTRB-UHFFFAOYSA-N 6,8-dimethylnonan-2-ol Chemical compound CC(C)CC(C)CCCC(C)O HDQVGGOVPFQTRB-UHFFFAOYSA-N 0.000 description 1
- XJHRZBIBSSVCEL-ONEGZZNKSA-N 6E-Nonen-1-ol Chemical compound CC\C=C\CCCCCO XJHRZBIBSSVCEL-ONEGZZNKSA-N 0.000 description 1
- IDWULKZGRNHZNR-UHFFFAOYSA-N 7-methoxy-3,7-dimethyloctanal Chemical compound COC(C)(C)CCCC(C)CC=O IDWULKZGRNHZNR-UHFFFAOYSA-N 0.000 description 1
- NBESWRYPFPFRAP-UHFFFAOYSA-N 8,8-dimethyl-2,3,4,4a,5,8a-hexahydro-1h-naphthalene-2-carbaldehyde Chemical compound C1CC(C=O)CC2C(C)(C)C=CCC21 NBESWRYPFPFRAP-UHFFFAOYSA-N 0.000 description 1
- AQJANVUPNABWRU-UHFFFAOYSA-N 8,8-dimethyl-2,3,4,5,6,7-hexahydro-1h-naphthalene-2-carbaldehyde Chemical compound C1C(C=O)CCC2=C1C(C)(C)CCC2 AQJANVUPNABWRU-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 235000009051 Ambrosia paniculata var. peruviana Nutrition 0.000 description 1
- 235000003097 Artemisia absinthium Nutrition 0.000 description 1
- 240000001851 Artemisia dracunculus Species 0.000 description 1
- 235000017731 Artemisia dracunculus ssp. dracunculus Nutrition 0.000 description 1
- 235000003261 Artemisia vulgaris Nutrition 0.000 description 1
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Natural products OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 1
- GTPBQABGXGLMBM-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)C1=CC=CC=C1.C(C1=CC=CC=C1)CC(=O)C1=CC=CC=C1 Chemical compound C(C1=CC=CC=C1)(=O)C1=CC=CC=C1.C(C1=CC=CC=C1)CC(=O)C1=CC=CC=C1 GTPBQABGXGLMBM-UHFFFAOYSA-N 0.000 description 1
- GBULKWSESKKEQH-UHFFFAOYSA-N C(C1=CC=CC=C1)C(C(=O)O)(C)C1CCCCC1 Chemical compound C(C1=CC=CC=C1)C(C(=O)O)(C)C1CCCCC1 GBULKWSESKKEQH-UHFFFAOYSA-N 0.000 description 1
- YUBBNBZAMAPEGF-UHFFFAOYSA-N C(C1=CC=CC=C1)C1C(N(C(C(N1)=O)C=1N=CNC1)C)=O Chemical compound C(C1=CC=CC=C1)C1C(N(C(C(N1)=O)C=1N=CNC1)C)=O YUBBNBZAMAPEGF-UHFFFAOYSA-N 0.000 description 1
- 240000007436 Cananga odorata Species 0.000 description 1
- 235000005747 Carum carvi Nutrition 0.000 description 1
- 240000000467 Carum carvi Species 0.000 description 1
- 239000005973 Carvone Substances 0.000 description 1
- KKVZAVRSVHUSPL-GQCTYLIASA-N Cassiastearoptene Chemical compound COC1=CC=CC=C1\C=C\C=O KKVZAVRSVHUSPL-GQCTYLIASA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 235000019499 Citrus oil Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- 235000010919 Copernicia prunifera Nutrition 0.000 description 1
- 244000180278 Copernicia prunifera Species 0.000 description 1
- 241001327300 Cymbopogon schoenanthus Species 0.000 description 1
- HEBKCHPVOIAQTA-QWWZWVQMSA-N D-arabinitol Chemical compound OC[C@@H](O)C(O)[C@H](O)CO HEBKCHPVOIAQTA-QWWZWVQMSA-N 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- RUPBZQFQVRMKDG-UHFFFAOYSA-M Didecyldimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCC[N+](C)(C)CCCCCCCCCC RUPBZQFQVRMKDG-UHFFFAOYSA-M 0.000 description 1
- ZXGMEZJVBHJYEQ-UHFFFAOYSA-N Dihydroapofarnesal Natural products O=CC(C)CCC=C(C)CCC=C(C)C ZXGMEZJVBHJYEQ-UHFFFAOYSA-N 0.000 description 1
- ZDQWESQEGGJUCH-UHFFFAOYSA-N Diisopropyl adipate Chemical compound CC(C)OC(=O)CCCCC(=O)OC(C)C ZDQWESQEGGJUCH-UHFFFAOYSA-N 0.000 description 1
- 108010016626 Dipeptides Proteins 0.000 description 1
- 241000668724 Dipterocarpus turbinatus Species 0.000 description 1
- 241000402754 Erythranthe moschata Species 0.000 description 1
- GYCKQBWUSACYIF-UHFFFAOYSA-N Ethyl salicylate Chemical compound CCOC(=O)C1=CC=CC=C1O GYCKQBWUSACYIF-UHFFFAOYSA-N 0.000 description 1
- WEEGYLXZBRQIMU-WAAGHKOSSA-N Eucalyptol Chemical compound C1C[C@H]2CC[C@]1(C)OC2(C)C WEEGYLXZBRQIMU-WAAGHKOSSA-N 0.000 description 1
- 239000001293 FEMA 3089 Substances 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 239000005792 Geraniol Substances 0.000 description 1
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 1
- 241000208152 Geranium Species 0.000 description 1
- 229920002581 Glucomannan Polymers 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 229920002683 Glycosaminoglycan Polymers 0.000 description 1
- 241000147041 Guaiacum officinale Species 0.000 description 1
- PMGCQNGBLMMXEW-UHFFFAOYSA-N Isoamyl salicylate Chemical compound CC(C)CCOC(=O)C1=CC=CC=C1O PMGCQNGBLMMXEW-UHFFFAOYSA-N 0.000 description 1
- DTGKSKDOIYIVQL-MRTMQBJTSA-N Isoborneol Natural products C1C[C@@]2(C)[C@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-MRTMQBJTSA-N 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- HEBKCHPVOIAQTA-IMJSIDKUSA-N L-arabinitol Chemical compound OC[C@H](O)C(O)[C@@H](O)CO HEBKCHPVOIAQTA-IMJSIDKUSA-N 0.000 description 1
- FBPFZTCFMRRESA-BXKVDMCESA-N L-mannitol Chemical compound OC[C@H](O)[C@H](O)[C@@H](O)[C@@H](O)CO FBPFZTCFMRRESA-BXKVDMCESA-N 0.000 description 1
- 229930182842 L-mannitol Natural products 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 241000234269 Liliales Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 239000006001 Methyl nonyl ketone Substances 0.000 description 1
- RXBQNMWIQKOSCS-RKDXNWHRSA-N Myrtenol Natural products C1[C@H]2C(C)(C)[C@@H]1CC=C2CO RXBQNMWIQKOSCS-RKDXNWHRSA-N 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- WQDRZTIUAGZBQW-UHFFFAOYSA-N O-Acetyl-limonol Natural products CC(=O)OC1CC2C(C)(C)OC3CC(=O)OCC23C4CCC5(C)C(OC(=O)C6OC56C14C)c7cocc7 WQDRZTIUAGZBQW-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 235000019502 Orange oil Nutrition 0.000 description 1
- 235000006484 Paeonia officinalis Nutrition 0.000 description 1
- 244000170916 Paeonia officinalis Species 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 240000006711 Pistacia vera Species 0.000 description 1
- 235000017304 Ruaghas Nutrition 0.000 description 1
- BHEOSNUKNHRBNM-UHFFFAOYSA-N Tetramethylsqualene Natural products CC(=C)C(C)CCC(=C)C(C)CCC(C)=CCCC=C(C)CCC(C)C(=C)CCC(C)C(C)=C BHEOSNUKNHRBNM-UHFFFAOYSA-N 0.000 description 1
- 240000002657 Thymus vulgaris Species 0.000 description 1
- 235000007303 Thymus vulgaris Nutrition 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 238000005411 Van der Waals force Methods 0.000 description 1
- 229930003268 Vitamin C Natural products 0.000 description 1
- 229930003427 Vitamin E Natural products 0.000 description 1
- LMETVDMCIJNNKH-UHFFFAOYSA-N [(3,7-Dimethyl-6-octenyl)oxy]acetaldehyde Chemical compound CC(C)=CCCC(C)CCOCC=O LMETVDMCIJNNKH-UHFFFAOYSA-N 0.000 description 1
- JBBRZDLNVILTDL-XNTGVSEISA-N [(3s,8s,9s,10r,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl] 16-methylheptadecanoate Chemical compound C([C@@H]12)C[C@]3(C)[C@@H]([C@H](C)CCCC(C)C)CC[C@H]3[C@@H]1CC=C1[C@]2(C)CC[C@H](OC(=O)CCCCCCCCCCCCCCC(C)C)C1 JBBRZDLNVILTDL-XNTGVSEISA-N 0.000 description 1
- BQOWUDKEXDCGQS-UHFFFAOYSA-N [CH]1CCCC1 Chemical compound [CH]1CCCC1 BQOWUDKEXDCGQS-UHFFFAOYSA-N 0.000 description 1
- YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical compound [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 description 1
- IKHGUXGNUITLKF-XPULMUKRSA-N acetaldehyde Chemical compound [14CH]([14CH3])=O IKHGUXGNUITLKF-XPULMUKRSA-N 0.000 description 1
- HHCJRIXDMXVJQC-UHFFFAOYSA-N acetaldehyde;tert-butylbenzene Chemical compound CC=O.CC(C)(C)C1=CC=CC=C1 HHCJRIXDMXVJQC-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000004996 alkyl benzenes Chemical group 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940061720 alpha hydroxy acid Drugs 0.000 description 1
- 150000001280 alpha hydroxy acids Chemical class 0.000 description 1
- CRIGTVCBMUKRSL-UHFFFAOYSA-N alpha-Damascone Natural products CC=CC(=O)C1C(C)=CCCC1(C)C CRIGTVCBMUKRSL-UHFFFAOYSA-N 0.000 description 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 1
- GUUHFMWKWLOQMM-NTCAYCPXSA-N alpha-hexylcinnamaldehyde Chemical compound CCCCCC\C(C=O)=C/C1=CC=CC=C1 GUUHFMWKWLOQMM-NTCAYCPXSA-N 0.000 description 1
- UZFLPKAIBPNNCA-UHFFFAOYSA-N alpha-ionone Natural products CC(=O)C=CC1C(C)=CCCC1(C)C UZFLPKAIBPNNCA-UHFFFAOYSA-N 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- QUMXDOLUJCHOAY-UHFFFAOYSA-N alpha-methylbenzyl acetate Natural products CC(=O)OC(C)C1=CC=CC=C1 QUMXDOLUJCHOAY-UHFFFAOYSA-N 0.000 description 1
- DCAYPVUWAIABOU-UHFFFAOYSA-N alpha-n-hexadecene Natural products CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 1
- GUUHFMWKWLOQMM-UHFFFAOYSA-N alpha-n-hexylcinnamic aldehyde Natural products CCCCCCC(C=O)=CC1=CC=CC=C1 GUUHFMWKWLOQMM-UHFFFAOYSA-N 0.000 description 1
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 229940062909 amyl salicylate Drugs 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 description 1
- 230000001166 anti-perspirative effect Effects 0.000 description 1
- 239000003213 antiperspirant Substances 0.000 description 1
- 229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 1
- 125000001204 arachidyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- VUEDNLCYHKSELL-UHFFFAOYSA-N arsonium Chemical group [AsH4+] VUEDNLCYHKSELL-UHFFFAOYSA-N 0.000 description 1
- 239000001138 artemisia absinthium Substances 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 229940092738 beeswax Drugs 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- UKXSKSHDVLQNKG-UHFFFAOYSA-N benzilic acid Chemical compound C=1C=CC=CC=1C(O)(C(=O)O)C1=CC=CC=C1 UKXSKSHDVLQNKG-UHFFFAOYSA-N 0.000 description 1
- 239000001518 benzyl (E)-3-phenylprop-2-enoate Substances 0.000 description 1
- 229960002903 benzyl benzoate Drugs 0.000 description 1
- NGHOLYJTSCBCGC-QXMHVHEDSA-N benzyl cinnamate Chemical compound C=1C=CC=CC=1\C=C/C(=O)OCC1=CC=CC=C1 NGHOLYJTSCBCGC-QXMHVHEDSA-N 0.000 description 1
- YZJCDVRXBOPXSQ-UHFFFAOYSA-N benzyl pentanoate Chemical compound CCCCC(=O)OCC1=CC=CC=C1 YZJCDVRXBOPXSQ-UHFFFAOYSA-N 0.000 description 1
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 description 1
- WHGYBXFWUBPSRW-FOUAGVGXSA-N beta-cyclodextrin Chemical compound OC[C@H]([C@H]([C@@H]([C@H]1O)O)O[C@H]2O[C@@H]([C@@H](O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O[C@H]3O[C@H](CO)[C@H]([C@@H]([C@H]3O)O)O3)[C@H](O)[C@H]2O)CO)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H]3O[C@@H]1CO WHGYBXFWUBPSRW-FOUAGVGXSA-N 0.000 description 1
- POIARNZEYGURDG-FNORWQNLSA-N beta-damascenone Chemical compound C\C=C\C(=O)C1=C(C)C=CCC1(C)C POIARNZEYGURDG-FNORWQNLSA-N 0.000 description 1
- POIARNZEYGURDG-UHFFFAOYSA-N beta-damascenone Natural products CC=CC(=O)C1=C(C)C=CCC1(C)C POIARNZEYGURDG-UHFFFAOYSA-N 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 229940116229 borneol Drugs 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- OCKPCBLVNKHBMX-UHFFFAOYSA-N butylbenzene Chemical group CCCCC1=CC=CC=C1 OCKPCBLVNKHBMX-UHFFFAOYSA-N 0.000 description 1
- 125000004063 butyryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 125000004181 carboxyalkyl group Chemical group 0.000 description 1
- 229920001525 carrageenan Chemical class 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000001862 carum carvi l. seed oil Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 229940106189 ceramide Drugs 0.000 description 1
- 150000001783 ceramides Chemical class 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- WQDRZTIUAGZBQW-AATXCISZSA-N chembl2271673 Chemical compound C=1([C@@H]2[C@]3(C)CC[C@@H]4[C@]56COC(=O)C[C@@H]6OC(C)(C)[C@@H]5C[C@H]([C@]4([C@]33O[C@@H]3C(=O)O2)C)OC(=O)C)C=COC=1 WQDRZTIUAGZBQW-AATXCISZSA-N 0.000 description 1
- 229960005233 cineole Drugs 0.000 description 1
- IVLCENBZDYVJPA-ARJAWSKDSA-N cis-Jasmone Natural products C\C=C/CC1=C(C)CCC1=O IVLCENBZDYVJPA-ARJAWSKDSA-N 0.000 description 1
- NGHOLYJTSCBCGC-UHFFFAOYSA-N cis-cinnamic acid benzyl ester Natural products C=1C=CC=CC=1C=CC(=O)OCC1=CC=CC=C1 NGHOLYJTSCBCGC-UHFFFAOYSA-N 0.000 description 1
- 239000001507 cistus ladaniferus l. oil Substances 0.000 description 1
- 235000000484 citronellol Nutrition 0.000 description 1
- 239000001279 citrus aurantifolia swingle expressed oil Substances 0.000 description 1
- 239000001926 citrus aurantium l. subsp. bergamia wright et arn. oil Substances 0.000 description 1
- 239000010500 citrus oil Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000011258 core-shell material Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- JUAPMRSLDANLAS-HOTGVXAUSA-N cyclo(L-phenylalanyl-L-phenylalanyl) Chemical compound C([C@@H]1NC([C@@H](NC1=O)CC=1C=CC=CC=1)=O)C1=CC=CC=C1 JUAPMRSLDANLAS-HOTGVXAUSA-N 0.000 description 1
- NGPCLOGFGKJCBP-HOTGVXAUSA-N cyclo(L-tyrosyl-L-tyrosyl) Chemical compound C1=CC(O)=CC=C1C[C@H]1C(=O)N[C@@H](CC=2C=CC(O)=CC=2)C(=O)N1 NGPCLOGFGKJCBP-HOTGVXAUSA-N 0.000 description 1
- YKFKEYKJGVSEIX-UHFFFAOYSA-N cyclohexanone, 4-(1,1-dimethylethyl)- Chemical compound CC(C)(C)C1CCC(=O)CC1 YKFKEYKJGVSEIX-UHFFFAOYSA-N 0.000 description 1
- NUQDJSMHGCTKNL-UHFFFAOYSA-N cyclohexyl 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1CCCCC1 NUQDJSMHGCTKNL-UHFFFAOYSA-N 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 239000001941 cymbopogon citratus dc and cymbopogon flexuosus oil Substances 0.000 description 1
- HEBKCHPVOIAQTA-NGQZWQHPSA-N d-xylitol Chemical compound OC[C@H](O)C(O)[C@H](O)CO HEBKCHPVOIAQTA-NGQZWQHPSA-N 0.000 description 1
- AKMSQWLDTSOVME-UHFFFAOYSA-N dec-9-enal Chemical compound C=CCCCCCCCC=O AKMSQWLDTSOVME-UHFFFAOYSA-N 0.000 description 1
- SASYSVUEVMOWPL-NXVVXOECSA-N decyl oleate Chemical compound CCCCCCCCCCOC(=O)CCCCCCC\C=C/CCCCCCCC SASYSVUEVMOWPL-NXVVXOECSA-N 0.000 description 1
- UZILCZKGXMQEQR-UHFFFAOYSA-N decyl-Benzene Chemical group CCCCCCCCCCC1=CC=CC=C1 UZILCZKGXMQEQR-UHFFFAOYSA-N 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002781 deodorant agent Substances 0.000 description 1
- 229960004670 didecyldimethylammonium chloride Drugs 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 238000004851 dishwashing Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 229960000735 docosanol Drugs 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- QQQMUBLXDAFBRH-UHFFFAOYSA-N dodecyl 2-hydroxypropanoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)O QQQMUBLXDAFBRH-UHFFFAOYSA-N 0.000 description 1
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical group CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 1
- SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical compound CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 description 1
- JAYVEHKNGGQSSZ-UHFFFAOYSA-N ethane-1,2-diol;pentane Chemical compound OCCO.CCCCC JAYVEHKNGGQSSZ-UHFFFAOYSA-N 0.000 description 1
- VQNUNMBDOKEZHS-UHFFFAOYSA-N ethoxymethoxycyclododecane Chemical compound CCOCOC1CCCCCCCCCCC1 VQNUNMBDOKEZHS-UHFFFAOYSA-N 0.000 description 1
- NYNCZOLNVTXTTP-UHFFFAOYSA-N ethyl 2-(1,3-dioxoisoindol-2-yl)acetate Chemical compound C1=CC=C2C(=O)N(CC(=O)OCC)C(=O)C2=C1 NYNCZOLNVTXTTP-UHFFFAOYSA-N 0.000 description 1
- BMOAQMNPJSPXIU-UHFFFAOYSA-N ethyl 2-(3-fluoro-4-nitrophenyl)propanoate Chemical compound CCOC(=O)C(C)C1=CC=C([N+]([O-])=O)C(F)=C1 BMOAQMNPJSPXIU-UHFFFAOYSA-N 0.000 description 1
- 229940005667 ethyl salicylate Drugs 0.000 description 1
- 125000006260 ethylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 239000001148 ferula galbaniflua oil terpeneless Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 description 1
- 229940113087 geraniol Drugs 0.000 description 1
- FQMZVFJYMPNUCT-UHFFFAOYSA-N geraniol formate Natural products CC(C)=CCCC(C)=CCOC=O FQMZVFJYMPNUCT-UHFFFAOYSA-N 0.000 description 1
- HIGQPQRQIQDZMP-DHZHZOJOSA-N geranyl acetate Chemical compound CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 150000002338 glycosides Chemical class 0.000 description 1
- 239000010503 gourd oil Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 229940091561 guaiac Drugs 0.000 description 1
- 239000000118 hair dye Substances 0.000 description 1
- 239000010653 helichrysum oil Substances 0.000 description 1
- CUKAXHVLXKIPKF-UHFFFAOYSA-N hept-4-en-1-ol Chemical compound CCC=CCCCO CUKAXHVLXKIPKF-UHFFFAOYSA-N 0.000 description 1
- DWMMZQMXUWUJME-UHFFFAOYSA-N hexadecyl octanoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)CCCCCCC DWMMZQMXUWUJME-UHFFFAOYSA-N 0.000 description 1
- 125000003104 hexanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 229920002674 hyaluronan Polymers 0.000 description 1
- 229960003160 hyaluronic acid Drugs 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 125000005020 hydroxyalkenyl group Chemical group 0.000 description 1
- 229920003063 hydroxymethyl cellulose Polymers 0.000 description 1
- 229940031574 hydroxymethyl cellulose Drugs 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 125000002883 imidazolyl group Chemical group 0.000 description 1
- 125000006302 indol-3-yl methyl group Chemical group [H]N1C([H])=C(C2=C([H])C([H])=C([H])C([H])=C12)C([H])([H])* 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- MGFYSGNNHQQTJW-UHFFFAOYSA-N iodonium Chemical compound [IH2+] MGFYSGNNHQQTJW-UHFFFAOYSA-N 0.000 description 1
- YJSUCBQWLKRPDL-UHFFFAOYSA-N isocyclocitral Chemical compound CC1CC(C)=CC(C)C1C=O YJSUCBQWLKRPDL-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- XUGNVMKQXJXZCD-UHFFFAOYSA-N isopropyl palmitate Chemical compound CCCCCCCCCCCCCCCC(=O)OC(C)C XUGNVMKQXJXZCD-UHFFFAOYSA-N 0.000 description 1
- 229940095045 isopulegol Drugs 0.000 description 1
- 239000010656 jasmine oil Substances 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- UEYGVZMYXRRXJN-UHFFFAOYSA-N limonyl acetate Natural products CC(=O)CC1CC2C(C)(C)OC3CC(=O)OCC23C4CCC5(C)C(OC(=O)C6OC56C14C)c7cocc7 UEYGVZMYXRRXJN-UHFFFAOYSA-N 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 239000007937 lozenge Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000001098 melissa officinalis l. leaf oil Substances 0.000 description 1
- 239000001683 mentha spicata herb oil Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
- GVOWHGSUZUUUDR-UHFFFAOYSA-N methyl N-methylanthranilate Chemical compound CNC1=CC=CC=C1C(=O)OC GVOWHGSUZUUUDR-UHFFFAOYSA-N 0.000 description 1
- XCLFXSUTXZKNFU-UHFFFAOYSA-N methyl uguenenoate Natural products OCC12C(CC(=O)OC)OC(C)(C)C2CC(=O)C(C23OC2C(=O)O2)(C)C1CCC3(C)C2C=1C=COC=1 XCLFXSUTXZKNFU-UHFFFAOYSA-N 0.000 description 1
- 229940100573 methylpropanediol Drugs 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 238000000386 microscopy Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000008164 mustard oil Substances 0.000 description 1
- 229940078812 myristyl myristate Drugs 0.000 description 1
- IBOBFGGLRNWLIL-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)[O-] IBOBFGGLRNWLIL-UHFFFAOYSA-N 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- JXTPJDDICSTXJX-UHFFFAOYSA-N n-Triacontane Natural products CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC JXTPJDDICSTXJX-UHFFFAOYSA-N 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001038 naphthoyl group Chemical group C1(=CC=CC2=CC=CC=C12)C(=O)* 0.000 description 1
- 125000004923 naphthylmethyl group Chemical group C1(=CC=CC2=CC=CC=C12)C* 0.000 description 1
- 239000002018 neem oil Substances 0.000 description 1
- ZYTMANIQRDEHIO-UHFFFAOYSA-N neo-Isopulegol Natural products CC1CCC(C(C)=C)C(O)C1 ZYTMANIQRDEHIO-UHFFFAOYSA-N 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- LIXVMPBOGDCSRM-UHFFFAOYSA-N nonylbenzene Chemical group CCCCCCCCCC1=CC=CC=C1 LIXVMPBOGDCSRM-UHFFFAOYSA-N 0.000 description 1
- KKVZAVRSVHUSPL-UHFFFAOYSA-N o-methoxycinnamic aldehyde Natural products COC1=CC=CC=C1C=CC=O KKVZAVRSVHUSPL-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940060184 oil ingredients Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000010502 orange oil Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 238000012858 packaging process Methods 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 239000011049 pearl Substances 0.000 description 1
- 150000007875 phellandrene derivatives Chemical class 0.000 description 1
- 229960003742 phenol Drugs 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 229960005323 phenoxyethanol Drugs 0.000 description 1
- 229960000969 phenyl salicylate Drugs 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 235000020777 polyunsaturated fatty acids Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- 125000001325 propanoyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000005344 pyridylmethyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 125000006413 ring segment Chemical group 0.000 description 1
- 239000010666 rose oil Substances 0.000 description 1
- 235000019719 rose oil Nutrition 0.000 description 1
- 239000010670 sage oil Substances 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 238000004626 scanning electron microscopy Methods 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 230000001953 sensory effect Effects 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- ZFRKQXVRDFCRJG-UHFFFAOYSA-N skatole Chemical compound C1=CC=C2C(C)=CNC2=C1 ZFRKQXVRDFCRJG-UHFFFAOYSA-N 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000010356 sorbitol Nutrition 0.000 description 1
- 235000019721 spearmint oil Nutrition 0.000 description 1
- 239000012177 spermaceti Substances 0.000 description 1
- 229940084106 spermaceti Drugs 0.000 description 1
- 229940032094 squalane Drugs 0.000 description 1
- 229940031439 squalene Drugs 0.000 description 1
- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 150000003445 sucroses Chemical class 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- QJVXKWHHAMZTBY-GCPOEHJPSA-N syringin Chemical compound COC1=CC(\C=C\CO)=CC(OC)=C1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 QJVXKWHHAMZTBY-GCPOEHJPSA-N 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- BORJONZPSTVSFP-UHFFFAOYSA-N tetradecyl 2-hydroxypropanoate Chemical compound CCCCCCCCCCCCCCOC(=O)C(C)O BORJONZPSTVSFP-UHFFFAOYSA-N 0.000 description 1
- DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 description 1
- 238000002411 thermogravimetry Methods 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 239000001585 thymus vulgaris Substances 0.000 description 1
- 239000000606 toothpaste Substances 0.000 description 1
- MBDOYVRWFFCFHM-UHFFFAOYSA-N trans-2-hexenal Natural products CCCC=CC=O MBDOYVRWFFCFHM-UHFFFAOYSA-N 0.000 description 1
- DKZBBWMURDFHNE-UHFFFAOYSA-N trans-coniferylaldehyde Natural products COC1=CC(C=CC=O)=CC=C1O DKZBBWMURDFHNE-UHFFFAOYSA-N 0.000 description 1
- NSSALFVIQPAIQK-UHFFFAOYSA-N trans-non-2-en-1-ol Natural products CCCCCCC=CCO NSSALFVIQPAIQK-UHFFFAOYSA-N 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- MCVUKOYZUCWLQQ-UHFFFAOYSA-N tridecylbenzene Chemical group CCCCCCCCCCCCCC1=CC=CC=C1 MCVUKOYZUCWLQQ-UHFFFAOYSA-N 0.000 description 1
- JLGLQAWTXXGVEM-UHFFFAOYSA-N triethylene glycol monomethyl ether Chemical compound COCCOCCOCCO JLGLQAWTXXGVEM-UHFFFAOYSA-N 0.000 description 1
- 229940057400 trihydroxystearin Drugs 0.000 description 1
- KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 1
- XBEADGFTLHRJRB-QPXULEPBSA-N undecylbenzene Chemical group CCCCCCCCCCC[13C]1=[13CH][13CH]=[13CH][13CH]=[13CH]1 XBEADGFTLHRJRB-QPXULEPBSA-N 0.000 description 1
- 125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- OJYLAHXKWMRDGS-UHFFFAOYSA-N zingerone Chemical compound COC1=CC(CCC(C)=O)=CC=C1O OJYLAHXKWMRDGS-UHFFFAOYSA-N 0.000 description 1
- 229930007850 β-damascenone Natural products 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/042—Gels
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/06—Emulsions
- A61K8/062—Oil-in-water emulsions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/11—Encapsulated compositions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
- A61K8/922—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes
- C11D3/502—Protected perfumes
- C11D3/505—Protected perfumes encapsulated or adsorbed on a carrier, e.g. zeolite or clay
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/005—Compositions containing perfumes; Compositions containing deodorants
Definitions
- the present invention relates to a perfume oil storage composition comprising at least one low molecular weight gel former as described herein, at least one perfume oil and water. Furthermore, the present invention is directed to a method for producing such a perfume oil storage composition, to agents comprising such a perfume oil storage composition, the use of such agents for treating surfaces and / or in textile washing and / or in textile care, methods for their use Use and the use of a low molecular weight gel former to stabilize a perfume oil in water or an aqueous solution.
- the detergents, cleaning agents and treatment agents available on the market, including cosmetic products, are usually perfumed.
- encapsulated perfuming is also increasingly being used. Consumers want the product to be adequately scented as well as covering up “bad” side odors. Long-lasting and fresh perfumes are also desired. Such properties can be achieved in an advantageous manner through the use of encapsulated fragrances.
- the fragrances enclosed in microcapsules can be released in a controlled manner, for example through mechanical stress, such as friction.
- Synthetic polymers are largely used for the encapsulation and in most cases the encapsulation takes place through interfacial polymerisation on the surface of finely divided fragrance droplets in an aqueous phase.
- microplastics solid and insoluble plastics that are smaller than 5 mm fall under the term “microplastics” (U.S. National Oceanic and Atmospheric Administration).
- the object on which the present invention is based was therefore to provide a microplastic-free storage and carrier system for beneficial agents, in particular perfume oils, which enables the beneficial agent, in particular the perfume oil, to be released in a controlled manner over a longer period of time.
- the present invention is therefore directed to a perfume oil storage composition
- a perfume oil storage composition comprising a) at least one low molecular weight gel former; b) at least one perfume oil; and c) water, the composition being a dispersion, for example in the form of an oil-in-water emulsion, the dispersed phase of which comprises the at least one low molecular weight gel former and the at least one perfume oil.
- the dispersed phase has the form of (stably dispersed) particles, the at least one low molecular weight gel former forming a matrix or shell which encloses the at least one perfume oil.
- the present invention is directed to a method for producing a perfume oil storage composition as described herein, characterized in that it comprises the following steps: a) providing a mixture comprising at least one low molecular weight gel former and at least one perfume oil; b) dispersing the mixture from step a) in water in order to obtain a dispersion, for example in the form of an oil-in-water emulsion, the dispersed phase of which comprises the at least one low molecular weight gel former and the at least one perfume oil.
- the present invention is directed to the use of a low molecular weight gel former for stabilizing at least one perfume oil in water or in an aqueous solution.
- the present invention is directed to an agent comprising at least one perfume oil storage composition, as described herein, wherein the agent is a detergent, cleaning agent or treatment agent.
- the present invention is directed to the use of an agent described herein for treating surfaces and / or in textile washing and / or in textile care.
- the present invention is finally also directed to a method for treating a surface or for washing and / or caring for textiles, characterized in that an agent as described herein is used in at least one method step.
- At least one refers to 1 or more, for example 1, 2, 3, 4, 5, 6, 7, 8, 9 or more.
- Figure 1 shows the integrals of the aliphatic CHx band peaks of an FTIR gas phase spectrum of emulsion E1 (examples) and of the FTIR gas phase spectrum of the reference emulsion (examples) against time (see example 3).
- the odor stability of a particular conventional perfume used in the end product ie for example in a liquid detergent
- a perfume oil storage composition according to the invention comprising a low molecular weight gelling agent, a perfume oil and water compared to conventionally dosed perfuming in the same end product can be clearly seen can be increased while at the same time the use of microplastics can be dispensed with.
- a first object of the present invention is a perfume oil storage composition
- a perfume oil storage composition comprising a) at least one low molecular weight gel former, b) at least one perfume oil and c) water, the composition being a dispersion, for example an oil-in-water emulsion , the dispersed phase of which comprises the at least one low molecular weight gel former and the at least one perfume oil.
- the perfume oil storage composition may further include at least one water-miscible solvent, for example, but not limited to, selected from monohydric and polyhydric alcohols, in particular polyhydric alcohols that are liquid under standard conditions (20 ° C., 1013 mbar).
- at least one water-miscible solvent for example, but not limited to, selected from monohydric and polyhydric alcohols, in particular polyhydric alcohols that are liquid under standard conditions (20 ° C., 1013 mbar).
- suitable water-miscible solvents can be selected, for example, from ethanol, n-propanol, i-propanol, butanols, glycol, propanediol, butanediol, methylpropanediol, glycerol, diglycol, propyldiglycol, butyldiglycol, hexylene glycol, ethylene glycol methyl ether, ethylene glycol ethyl propane, -butyl ether, diethylene glycol methyl ether, diethylene glycol ethyl ether, propylene glycol methyl ether, propylene glycol ethyl ether,
- Propylene glycol propyl ether dipropylene glycol monomethyl ether, dipropylene glycol monoethyl ether, methoxy triglycol, ethoxy triglycol, butoxy triglycol, 1-butoxyethoxy-2-propanol, 3-methyl-3-methoxybutanol, propylene glycol t-butyl ether and mixtures of these solvents.
- low molecular weight gel former denotes compounds whose molecules have a molar mass of less than 1000 g / mol and are produced by non-covalent interactions such as, without limitation, hydrogen bonds, tt-tt stacking and van- der Waals forces, can form a network of fibers in a liquid matrix. Gels formed in this way are thermo reversible and, moreover, can be completely biodegraded. In particular, the gels formed by low molecular weight gelling agents do not fall under the definition of microplastics.
- some embodiments of the present invention are characterized in that the at least one low molecular weight gel former, as defined herein, has a molar mass of less than 1000 g / mol.
- compounds which come under the above definition of low molecular weight gel formers are in particular selected from the group consisting of
- F compounds from the group of glucosamines.
- n is 0 or 1, preferably 1, m is 0 or 1, preferably 1,
- both said benzylidene alditols in the L configuration or in the D configuration or a mixture of both are suitable. Because of their natural availability, the benzylidene alditol compounds in the D configuration are preferably used according to the invention.
- alditol basic structure of the benzylidene alditol compound according to formula (I) is D-glucitol, D-mannitol, D-arabinitol, D-ribitol, D-xylitol, L-glucitol, L-mannitol , L-arabinitol, L-ribitol or L-xylitol.
- Particularly preferred benzylidene alditol compounds are those which are characterized in that R 1 , R 2 , R 3 , R 4 , R 5 and R 6 according to formula (I) independently of one another represent a hydrogen atom, methyl, ethyl, chlorine, fluorine or Methoxy, preferably a hydrogen atom.
- n according to the benzylidene alditol compound of the formula (I) preferably stands for 1.
- m according to the benzylidene alditol compound of the formula (I) preferably stands for 1.
- those benzylidene alditol compounds of the formula (I) which come under the definition of the following formula (1-1) are very particularly preferred: where, in the compounds of formula (1-1), R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are as defined in formula (I). Most preferably, according to formula (1-1), R 1 , R 2 , R 3 , R 4 , R 5 and R 6 independently of one another represent a hydrogen atom, methyl, ethyl, chlorine, fluorine or methoxy, preferably a hydrogen atom.
- those compounds A) are used which are selected from the group consisting of 1, 3: 2,4-di-0-benzylidene-D-sorbitol; 1, 3: 2,4-di-0- (p-methylbenzylidene) -D-sorbitol; 1, 3: 2,4-di-0- (p-chlorobenzylidene) -D-sorbitol; 1, 3: 2,4-di-0- (2,4-dimethylbenzylidene) -D-sorbitol; 1, 3: 2,4-di-0- (p-ethylbenzylidene) -D-sorbitol; 1, 3: 2,4-di-0- (3,4-dimethylbenzylidene) -D-sorbitol or mixtures of the aforementioned.
- a compound (A) is in particular 1, 3: 2,4-di-0-benzylidene-D-sorbitol (DBS).
- HCO hydrogenated castor oil
- Commercially available compounds include THIXCIN® R from Rheox Inc. (now Elementis). Further examples of suitable HCOs can be found in US Patent No. 5,340,390.
- HCO includes any hydrogenated castor oil or derivative thereof.
- Castor oils include glycerides, especially triglycerides, which carry C10-C22 hydroxyalkyl or hydroxyalkenyl groups. The hydrogenation converts double bonds in the starting oil to give saturated hydroxyalkyl groups such as hydroxystearyl groups.
- HCO can therefore, for example, from trihydroxystearin, Dihydroxystearin and mixtures thereof.
- Low molecular weight gel formers of this type preferred in the context of the present invention are also described, for example, in US Pat. No. 6,080,708 and WO 02/40627.
- the castor oils used herein are preferably not alkoxylated, especially not ethoxylated.
- Compounds of the formula (II) contain at least two stereocenters (configuration isomers) on the alpha carbon atom of the structural fragment of the compound of the formula (II) derived from the amino acid cysteine (see marking a and a ‘)
- Each of these stereocenters can independently represent the L or D stereoisomer. It is preferred according to the invention if a compound of the formula (II) is derived from the L-stereoisomer of cysteine.
- X + each independently represents a hydrogen atom or an equivalent of a cation
- R 1 , R 2 , R 3 and R 4 each independently of one another, represent a hydrogen atom, a halogen atom, a Ci-C 4 -alkyl group, a Ci-C 4 -alkoxy group, a C2-C4-hydroxyalkyl group, a hydroxyl group , an amino group, an N- (Ci-C 4 -alkyl) amino group, an N, N-di (Ci-C 4 -alkyl) amino group, an N- (C 2 -C 4 -hydroxyalkyl) amino group, or an N.
- N, N'-dibenzoyl-L-cystine is particularly preferred.
- Such compounds are, in various embodiments, selected in particular from the group of compounds represented by the following formula (III) where, in the compounds of the formula (III),
- R 1 represents a linear or branched, substituted or unsubstituted C 4 -Ci 2 -alkyl group, the substituents each being independently selected from the group consisting of F, CI, Br and I; and
- R 2 represents a hydrogen atom or a substituted or unsubstituted benzoyl group, the substituents each being independently selected from the group consisting of F, CI, Br, I, Ci-C3-alkyl and Ci-C3-alkoxy.
- those compounds D) are particularly preferred in which, according to formula (III), R 1 denotes a linear, unsubstituted C6-Ci2-alkyl group, preferably Cs-Cio-alkyl group, most preferably Cs-alkyl group.
- R 2 represents a hydrogen atom.
- those compounds D) are particularly preferred in which, according to formula (III), R 1 denotes a linear, unsubstituted C 8 -alkyl group and R 2 stands for a hydrogen atom.
- Compounds E), which are also suitable as low molecular weight gel formers according to the present invention, are, in various embodiments, those compounds which correspond to the following formula (IV): where, in the compounds of formula (IV),
- R 1 , R 2 , R 3 and R 4 each independently of one another, for a hydrogen atom, a hydroxyl group, a (Ci-C6) -alkyl group, a (C2-C6) -alkenyl group, a (C2-C6) -acyl group, a (C2-C6) - acyloxy group, a (Ci-C6) -alkoxy group, an amino group, a (C2-C6) -acylamino group, a (Ci-C6) -alkylaminocarbonyl group, an aryl group, an aroyl group, an aroyloxy group, an aryloxy group , an aryl (Ci-C 4 ) alkyloxy group, an aryl (Ci-C3) alkyl group, a heteroaryl group, a heteroaryl (Ci-C3) alkyl group, a (Ci-C 4 ) hydroxyalkyl group, a ( C1-C
- a radical different from a hydrogen atom is preferably understood to mean all radicals defined under the definitions of R 5 and R 1 according to formula (I) which are from a hydrogen atom are different, in particular a hydroxy group, an amino group, a (Ci-C6) alkyl group, a (C 2 -C 6) - alkenyl, (C 2 -C 6) acyl group, a (C 2 -C 6) acyloxy group , a (Ci-C6) alkoxy group, an amino group, a (C 2 -C6) acylamino group, a (Ci-C6) alkylaminocarbonyl group, an aryl group, an aroyl group, an aroyloxy group, an aryloxy group, an aryl (Ci- C 4 ) alkyloxy group, an aryl (Ci-C3) alkyl group, a heteroaryl group, a heteroaryl (Ci-C3) alkyl group,
- an alkyl group (or an alkyl structure fragment of a more complex group) is understood according to the invention to mean a group selected from a linear alkyl group, a branched alkyl group and a cyclic alkyl group (also: cycloalkyl group).
- Linear or branched (C 1 -C6) alkyl groups preferred in this context are selected from methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, n-pentyl, neo-pentyl, n-hexyl.
- Preferred branched (C3-Cio) -alkyl groups in this connection are selected from iso-propyl, sec-butyl, iso-butyl, tert-butyl, neo-pentyl, iso-octyl, 2-ethylhexyl, 2-ethylheptyl.
- Preferred cyclic alkyl groups ((C3-C6) -cycloalkyl groups) are selected in this connection from cyclopentyl and cyclohexyl.
- Preferred (C 2 -C 6) -alkenyl groups in this connection are selected from vinyl, allyl and 2-butenyl.
- Preferred (C 2 -C 6) -alkynyl groups in this connection are selected from ethynyl, propargyl, but-2-ynyl and hex-3-ynyl.
- acyl groups in this context are selected from acetyl, propanoyl, butanoyl, pentanoyl, hexanoyl, in particular acetyl.
- acyloxy groups in this context are selected from acetyloxy, propanoyloxy, butanoyloxy, pentanoyloxy and hexanoyloxy, in particular acetyloxy.
- an alkoxy group is understood to mean an alkyl group which is bonded via an oxygen atom and selected from a linear alkyl group, a branched alkyl group or a cyclic alkyl group (also: cycloalkyl group).
- Preferred (Ci-C6) -alkoxy groups in this context are methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, sec-butoxy, iso-butoxy and tert-butoxy.
- C2-C6 acylamino groups in this context are acetylamino, propanoylamino, butanoylamino, pentanoylamino and hexanoylamino, in particular acetylamino.
- Hexanoylamino especially acetylamino.
- Preferred aryl groups in this connection are phenyl, naphthyl, anthracenyl, these being substituted or unsubstituted.
- aroyl groups denote arene carbonyl groups in which a carbonyl group binds directly to the aromatic ring system.
- Preferred aroyl groups in this connection are benzoyl, naphthoyl and anthracenoyl, these being substituted or unsubstituted.
- aroyloxy groups denote aroyl groups which attach via an additional oxygen atom binding to the carbonyl radical.
- Preferred aroyloxy groups in this context are selected from benzoyloxy, naphthoyloxy and anthracenoyloxy, these being substituted or unsubstituted.
- a preferred aryloxy group is the phenoxy group or the naphthoxy group, these being substituted or unsubstituted.
- Preferred aryl (Ci-C3) alkyl groups are selected from benzyl, 2-phenylethyl, naphthylmethyl, 2-naphthylethyl, these being substituted or unsubstituted.
- Preferred heteroaryl groups are pyridyl, pyrimidinyl, imidazolyl, indolyl, furyl, thiophenyl, 1,3,5-triazolyl.
- Preferred heteroaryl (Ci-C3) -alkyl groups are selected from furfuryl, 2-indol-3-ylethyl, indol-3-ylmethyl, pyridylmethyl, these being substituted or unsubstituted.
- those 2,5-diketopiperazine compounds E) according to formula (IV) are particularly preferred in which R 5 represents a (C 1 -C 4 ) hydrocarbon group substituted with an aromatic radical, in particular a radical of the formulas below (IV) or (VI) as defined below.
- those 2,5-diketopiperazine compounds E) according to formula (IV) are also preferred in which R 3 and R 4 according to formula (IV) represent a hydrogen atom.
- particularly preferred compounds E) are those in which R 2 , R 3 and R 4 according to formula (I) represent a hydrogen atom. Therefore, in some embodiments, a compound E) corresponds in particular to a 2,5-diketopiperazine compound according to formula (IV-a): where, in formula (IV-a), R 1 and R 5 are as defined under formula (IV).
- the radical R 1 binds according to formula (I) and according to formula (Ia) in the para position of the phenyl ring. Therefore, in the context of the present invention, in some embodiments those compounds E) are preferred which contain at least one 2,5-diketopiperazine compound according to formula (Ib): (IV-b) where, according to formula (IV-b), R 1 and R 5 are defined as above under formula (IV).
- the numbers 3 and 6 positioned on the ring atoms in formula (IV-b) only mark positions 3 and 6 of the diketopiperazine ring as they are generally used in the context of the invention for the naming of all 2,5-diketopiperazines.
- Particularly preferred compounds E) according to the formula (IV-b) have the following radicals:
- radicals R 1 to R 5 apply to compounds of the formula (IV), but also to compounds of the formulas (IV-a) and (IV-b), with the proviso that for the formulas (IV-a) and (IV-b) the radicals R 2 , R 3 and R 4 necessarily represent a hydrogen atom.
- the radicals R 1 , R 2 , R 3 and R 4 each independently of one another, for a hydrogen atom, a hydroxyl group, a methyl group, an ethyl group, a / so -Propyl group, an n-propyl group, an n-butyl group, a / so-butyl group, a sec-butyl group, a fe / f-butyl group, a phenyl group, a benzyl group, a methoxy group, a (C2-C6) -acyloxy group, a Aryloxy group, a tosyloxy group, a triflyloxy group, a benzyloxy group or a benzoyloxy group.
- those compounds E) according to formula (IV) are particularly suitable in which R 5 is a hydrogen atom, a methyl group, an isopropyl group, a so-butyl group, a fe / f-butyl group, a 2- (methylsulfanyl) ethyl -Group, a hydroxymethyl group, a (Ci-C3) -alkoxymethyl group, a benzyloxymethyl group, an acetyloxymethyl group, a benzoyloxymethyl group, a tosyloxymethyl group, a 1-hydroxyethyl group, a 1 - ((Ci-C3) -alkoxy) ethyl group, a 1- ( Acetyloxy) ethyl group, a 1- (benzoyloxy) ethyl group, a 1- (tosyloxy) ethyl group, a mercaptomethyl group, a (C1-C3) -
- R 'according to formula (VI) stands for a hydrogen atom, a methyl group, an ethyl group, an iso-propyl group, an n-propyl group, an allyl group, a benzyl group or a phenyl group.
- R ′ according to formula (VII) stands for a hydrogen atom, a methyl group, an ethyl group, an iso-propyl group, a benzyl group, a benzoyloxy group or a phenyl group.
- R ‘according to formula (VIII) represents a hydrogen atom, a methyl group, an ethyl group, an iso-propyl group, a benzyl group, a benzoyloxy group or a phenyl group.
- R “and R“ 'according to formula (IX) independently of one another represent a hydrogen atom, a methyl group, an ethyl group, an n-propyl group, an iso-propyl group, a benzyl group, a benzoyl group, acetyl group, an aminoiminomethyl group or a tosyl group.
- R according to formula (X) is a hydrogen atom, a hydroxyl group, a methyl group, an ethyl group, an n-propyl group, an iso-propyl group, a tert-butyl group, a phenyl group, a methoxy group, an acetyloxy group, represents a tosyloxy group, a triflyloxy group, a benzyloxy group or a benzoyloxy group.
- radical R 1 When selecting the aforementioned preferred radicals R 1 to R 5, it is again preferred if, according to formula (IV) and according to formulas (IV-a) and (IV-b), the radical R 1 binds in the para position of the phenyl ring.
- the 2,5-diketopiperazine compounds of the formula (IV) have centers of chirality at least on the carbon atoms in positions 3 and 6 of the 2,5-diketopiperazine ring.
- the numbering of ring positions 3 and 6 was illustrated by way of example in formula (IV-b).
- the 2,5-diketopiperazine compound E) of the formula (IV) is preferred, based on the stereochemistry of the carbon atoms at the 3- and 6-positions of the 2,5-diketopiperazine ring, the configuration isomer 3S, 6S; 3R, 6S; 3S, 6R; 3R, 6R or mixtures thereof, particularly preferably 3S, 6S.
- a compound E) according to formula (IV) is selected in particular from the group consisting of: 3-benzyl-6-carboxyethyl-2,5-diketopiperazine (also: 3- (5-benzyl-3,6-dioxopiperazine- 2-yl) propanoic acid), 3-benzyl-6-carboxymethyl-2,5-diketopiperazine, 3-benzyl-6- (p-hydroxybenzyl) -2,5-diketopiperazine, 3-benzyl-6-iso-propyl-2 , 5-diketopiperazine, 3-benzyl-6- (4-aminobutyl) -2,5-diketopiperazine, 3,6-di (benzyl) -2,5-diketopiperazine, 3,6-di (4-hydroxybenzyl) -2 , 5-diketopiperazine, 3,6-di (4- (benzyloxy) benzyl) -2,5-diketopiperazine,
- a compound E) according to formula (IV) is in particular selected from the group consisting of: 3,6-bis (4-hydroxybenzyl) piperazine-2,5-dione, 3-benzyl-6-isopropylpiperazine-2, 5-dione, 3,6-bis (4- (benzyloxy) benzyl) piperazine-2,5-dione, 3-benzyl-piperazine-
- a compound E) according to formula (IV) is particularly preferably selected from the group consisting of: (3S, 6S) -3,6-bis (4-hydroxybenzyl) piperazine-
- 2,5-diketopiperazine compounds which can be contained in the compositions according to the invention can be prepared by means of known synthesis methods (cf. Suzuki et al., Chem. Pharm. Bull. 1981, 29 (1), 233-237).
- Compounds F) from the group of glucosamines are also suitable as low molecular weight gel formers according to the present invention.
- glucosamine compounds F correspond to the following formula (V): where, according to formula (V),
- R 1 is a radical which contains a vinyl group, preferably a radical which contains a (meth) acrylate group
- R 2 is hydrogen or a substituted or unsubstituted CMO hydrocarbon radical, preferably hydrogen or a substituted or unsubstituted CMO alkyl radical, more preferably hydrogen, ethyl or methyl.
- R 1 in formula (V) denotes an optionally halogen-substituted C1 alkyl radical, which is preferably selected from the group consisting of pentyl, hexyl, heptyl, octyl, 4-chlorobutyl and 5-bromopentyl; an optionally substituted phenyl, naphthyl, or anthracenyl radical; a C2-6 alkenyl radical, preferably selected from the group consisting of vinyl, allyl and 2-butenyl; or a C2-11 alkynyl radical, preferably selected from the group consisting of 4-pentynyl, 5-hexynyl, 6-heptynyl and 10-undecynyl; wherein all radicals are substituted with a vinyl group or a (meth) acrylate group.
- C1 alkyl radical which is preferably selected from the group consisting of pentyl, hexyl, heptyl,
- compounds F) have the formula (Va): where, in the compounds according to formula (Va),
- R 3 is a radical which contains a vinyl group, preferably a radical which contains a (meth) acrylate group
- R 2 is hydrogen or a substituted or unsubstituted CMO hydrocarbon radical, preferably hydrogen or a substituted or unsubstituted CMO alkyl radical, more preferably hydrogen, ethyl or methyl.
- R 3 is an optionally halogen-substituted C1-8 alkyl radical, preferably selected from the group consisting of pentyl, hexyl, heptyl, 2-chloroethyl and 2-bromoethyl; a substituted or unsubstituted phenyl, naphthyl or anthracenyl radical; a C2-7 alkynyl radical, preferably selected from 4-pentynyl and 5-hexynyl; a cyclopentyl radical; a cyclohexyl radical or a C hydroxyalkyl radical, all radicals being substituted by a vinyl group or a (meth) acrylate group.
- C1-8 alkyl radical preferably selected from the group consisting of pentyl, hexyl, heptyl, 2-chloroethyl and 2-bromoethyl
- the compounds F) have the formula (Vb): where, in the compounds according to formula (Vb),
- R 4 is hydrogen or a substituted or unsubstituted CMO hydrocarbon radical, preferably hydrogen or a substituted or unsubstituted CMO alkyl radical, more preferably hydrogen, ethyl or methyl;
- R 2 is hydrogen or a substituted or unsubstituted CMO hydrocarbon radical, preferably hydrogen or a substituted or unsubstituted CMO alkyl radical, more preferably hydrogen, ethyl or methyl.
- the respective radicals can be substituted one or more times.
- a particularly preferred glucosamine derivative F) is: Suitable compounds from the group of glucosamines, as defined above, are commercially available. In addition, they can, for example, as described by N. Goyal et al. in Tetrahedron 2010, 66, edition 32, pages 5962-5971 described.
- the at least one low molecular weight gel former is preferably in an amount of about 0.1 to about 20% by weight, preferably in an amount of 0.5 to 10% by weight, for example in an amount of 0.5; 0.6; 0.7; 0.8; 0.9; 1, 0; 1, 1; 1, 5; 2.0; 2.5; 3; 4; 5; 6; 7; 8th; 9; or 10% by weight, based in each case on the total weight of the composition or based on the total weight of the dispersed / oil phase, contained in the perfume oil storage composition according to the invention.
- the gel former is used to form stable droplets or particles that enclose the perfume oil in the form of a matrix or a capsule shell.
- the gelling agent can be used in liquid form to form the dispersed phase, so that an oil-in-water emulsion is formed in a first step, the oil phase including the gelling agent and the perfume oil.
- the gel former can solidify and form a solid or gel, which the perfume oil then in the form of solid or gel particles.
- the at least one low molecular weight gel former is present in the compositions of the invention as a dispersed phase, i.e. preferably in the form of particles dispersed in the aqueous phase, which additionally also comprise the at least one perfume oil.
- the corresponding particles formed are defined more precisely below.
- Another component of the perfume oil storage composition according to the invention is a perfume oil.
- fragrances or fragrances or perfume oils can be used as fragrances or fragrances or perfume oils.
- perfume oils for the purposes of this invention, the terms “fragrance (s)”, “fragrances” and “perfume oil (s)” are used synonymously. This means in particular all those substances or their mixtures which are perceived as odor by humans and animals, in particular are perceived by humans as a fragrance.
- perfume oils or perfume oil constituents can be used as fragrance components.
- perfume oils or fragrances can contain individual fragrance compounds, e.g. B. the synthetic products of the type of esters, ethers, aldehydes, ketones, alcohols and hydrocarbons.
- Fragrance compounds of the aldehyde type are for example adoxal (2,6,10-trimethyl-9-undecenal), anisaldehyde (4-methoxybenzaldehyde), cymal (3- (4-isopropyl-phenyl) -2-methylpropanal), ethylvanillin, florhydral ( 3- (3-isopropylphenyl) butanal), helional (3- (3,4-methylenedioxyphenyl) -2-methylpropanal), heliotropin, hydroxycitronellal, lauraldehyde, lyral (3- and 4- (4-hydroxy-4-methylpentyl) - 3- cyclohexene-1-carboxaldehyde), methylnonylacetaldehyde, Lilial (3- (4- tert-butylphenyl) -2-methylpropanal), phenylacetaldehyde, undecylenealdehyde, vanillin,
- Methyl octanal alpha-methyl-4- (1-methylethyl) benzene acetaldehyde, 6,6-dimethyl-2-norpinene-2-propionaldehyde, para-methylphenoxyacetaldehyde, 2-methyl-3-phenyl-2-propen-1-al, 3 , 5,5-trimethylhexanal, hexahydro-8,8-dimethyl-2-naphthaldehyde, 3-propyl-bicyclo- [2.2.1] -hept-5-en-2-carbaldehyde, 9-decenal, 3-methyl-5 -phenyl-1-pentanal, methylnonylacetaldehyde, hexanal and trans-2-hexenal.
- Fragrance compounds of the ketone type are, for example, methyl-beta-naphthyl ketone, musk indanone (1, 2, 3,5,6, 7-hexahydro-1, 1, 2,3,3-pentamethyl-4H-inden-4-one), Tonalid (6-acetyl-1, 1, 2,4,4, 7-hexamethyltetralin), alpha-damascone, beta-damascone, delta-damascone, iso-damascone, damascenone, methyl dihydrojasmonate, menthone, carvone, camphor, coavone (3 , 4, 5,6,6-pentamethylhept-3-en-2-one), fenchone, alpha-ionone, betalonone, gamma-methyl-ionone, fleuramone (2-heptylcyclopen-tanone), dihydrojasmone, cis-jasmone , iso-E-Super
- Fragrance compounds of the alcohol type are, for example, 10-undecen-1-ol, 2,6-dimethylheptan-2-ol, 2-methyl-butanol, 2-methylpentanol, 2-phenoxyethanol, 2-phenylpropanol, 2-tert.-butycyclohexanol, 3,5,5-trimethylcyclohexanol, 3-hexanol, 3-methyl-5-phenyl-pentanol, 3-octanol, 3-phenyl-propanol, 4-heptenol, 4-isopropyl-cyclohexanol, 4-tert.-butycyclohexanol, 6 , 8-dimethyl-2-nona-nol, 6-nonen-1-ol, 9-decen-1-ol, a-methylbenzyl alcohol, a-terpineol, amyl salicylate, benzyl alcohol, benzyl salicylate, ß-terpine
- Fragrance compounds of the ester type are, for example, benzyl acetate, phenoxyethyl isobutyrate, p-tert-butylcyclohexyl acetate, linalyl acetate, dimethylbenzylcarbinylacetate (DMBCA), phenylethyl acetate, benzyl acetate, ethylmethylphenylglycinate, allylcyclohexylpropionate, allylcyclohexylpropionate, allylcyclohexylpropionate, allylcyclohexylpropionate, allylcyclohexylpropionate, benzylcyclohexylpropionate, benzacylate, benzacylpropionate, florallyamallylpropionate, benzacylate and jasacyl propionylate, butylcyclohexyl acetate, linalyl acetate, styrofoy
- fragrances are preferably used, which together produce an appealing fragrance note.
- a mixture of fragrances can also be referred to as perfume or perfume oil.
- perfume oils can also contain natural fragrance mixtures, such as are available from vegetable sources.
- the fragrances of vegetable origin include essential oils such as angelica root oil, anise oil, arnica flower oil, basil oil, bay oil, champaca flower oil, citrus oil, noble fir oil, noble fir cone oil, elemi oil, eucalyptus oil, fennel oil, spruce needle oil, guajun oil, gourd oil, gherkin oil, galbanum oil, gherkin oil, gjajun oil , Ginger oil, iris oil, jasmine oil, kajeput oil, calamus oil, chamomile oil, camphor oil, kanaga oil, cardamom oil, cassia oil, pine needle oil, copai balsam oil, coriander oil, spearmint oil, caraway oil, cumin oil, labdanum oil, lavender oil, lemon blossom oil, lemongrass oil , Muscatel oil, myrrh oil, clove oil, neroli oil, niaouli oil, olibanum oil, orange blossom oil, orange peel oil,
- an odoriferous substance In order to be perceptible, an odoriferous substance must be volatile, with the molecular weight also playing an important role in addition to the nature of the functional groups and the structure of the chemical compound.
- Most fragrances for example, have molar masses of up to about 200 Dalton, while molar masses of 300 Dalton and above are more of an exception. Due to the different volatility of odorous substances, the odor of a perfume or fragrance composed of several odorous substances changes during evaporation, the odor impressions being classified as "top note”, “middle note” or “body”. and "base note” (end note or dry out).
- top, heart and base notes can be determined on the basis of their vapor pressure (using the test method described in WO 2016/200761 ) are classified as follows: Top note: Vapor pressure at 25 ° C:> 0.0133 kPa Heart note: Vapor pressure at 25 ° C: 0.0133 to 0.000133 kPa Base note: Vapor pressure at 25 ° C: ⁇ 0.000133 kPa
- the firmly adhering fragrances that can be used in the context of the present invention include, for example, the essential oils such as angelica root oil, anise oil, arnica flower oil, basil oil, bay oil, bergamot oil, champaca flower oil, noble fir oil, noble fir cone oil, elemi oil, eucalyptus oil, fennel oil, spruce needle oil, Ginger grass oil, guaiac oil, gurjun balsam oil, helichrysum oil, Ho oil, ginger oil, iris oil, kajeput oil, calamus oil, chamomile oil, camphor oil, kanaga oil, cardamom oil, cassia oil, pine needle oil, copalva balsam oil, coriander oil, lime, lavender oil, almond oil, caraway seed oil, lime oil, cumin oil, almond oil Melissa oil, musk seed oil, myrrh oil, clove oil, neroli oil, niaouli oil, olibanum oil, orange
- High-boiling or solid odoriferous substances of natural or synthetic origin include, for example: ambrettolide, ⁇ -amylcinnamaldehyde, anethole, anisaldehyde, anisalcohol, anisole, anthranilic acid methyl ester, acetophenone, benzylacetone, benzaldehyde, benzoic acid ethyl ester, benzophenone, benzyl alcohol, benzyl acetate, benzyl formianzoate, Bornyl acetate, a-bromostyrene, n-decylaldehyde, n-dodecyl aldehyde, eugenol, eugenol methyl ether, eucalyptol, farnesol, fenchone, fenchyl acetate, geranyl acetate, geranyl formate, heliotropine, hept
- the more volatile fragrances include, in particular, the lower-boiling fragrances of natural or synthetic origin, which can be used alone or in mixtures.
- Examples of more volatile fragrances are alkyl isothiocyanates (alkyl mustard oils), butanedione, limonene, linalool, linaylacetate and propionate, menthol, menthone, methyl-n-heptenone, phellandrene, phenylacetaldehyde, terpinylacetate, citral, citronellal.
- Fragrance compounds of the aldehyde type that can be used with preference are hydroxycitronellal (CAS 107-75-5), helional (CAS 1205-17-0), citral (5392-40-5), bourgeonal (18127-01-0), triplal (CAS 27939 -60-2), Ligustral (CAS 68039-48-5), Vertocitral (CAS 68039-49-6), Florhydral (CAS 125109- 85-5), Citronellal (CAS 106-23-0), Citronellyloxyacetaldehyde (CAS 7492 -67-3).
- fragrances described in WO 2016/200761 A2 in particular the fragrances mentioned in Tables 1, 2 and 3, and the modulators listed in Tables 4a and 4b. This publication is incorporated herein by reference in its entirety.
- the at least one perfume oil which is part of the composition according to the invention as component b) can also be contained in the form of a perfume oil preparation and, for example, comprise at least one further active ingredient in oil form.
- suitable active ingredients in oil form are those which are suitable for washing, cleaning, care and / or finishing purposes, in particular
- Textile care materials such as preferably silicone oils, and / or
- Skin care active ingredients are all those active ingredients which give the skin a sensory and / or cosmetic advantage.
- Skin care active ingredients are preferably selected from the following substances: a) Waxes such as, for example, carnauba, spermaceti, beeswax, lanolin and / or derivatives thereof and others.
- Hydrophobic plant extracts c) Hydrocarbons such as squalene and / or squalane d) Higher fatty acids, preferably those with at least 12 carbon atoms, for example lauric acid, stearic acid, behenic acid, myristic acid, palmitic acid, oleic acid, linoleic acid, linolenic acid, isostearic acid and / or polyunsaturated fatty acids and others.
- Higher fatty alcohols preferably those with at least 12 carbon atoms, for example lauryl alcohol, cetyl alcohol, stearyl alcohol, oleyl alcohol, behenyl alcohol, cholesterol and / or 2-hexadecanol and others.
- Esters preferably those such as cetyloctanoate, lauryl lactate, myristyl lactate, cetyl lactate, isopropyl myristate, myristyl myristate, isopropyl palmitate, isopropyl adipate, butyl stearate, decyl oleate, cholesterol isostearate, glycerol monostearate and other, glycerol monostearate and other, glycerol monostearate, glycerol, glycerol, and other glycerol monostearate, glycerol, glycerol, and other glycerol monostearate, glycerol, glycerol, and other glycerol, glycerol, or glycerol, glycerol, or glycerol, glycerol, glycerol, glycerol, glycerol, glycerol,
- lipids such as cholesterol, ceramides and / or sucrose esters and others.
- Vitamins such as vitamins A, C and E, vitamin alkyl esters, including vitamin C alkyl esters and others.
- Sunscreens j) Phospholipids k) Derivatives of alpha-hydroxy acids
- Germicides for cosmetic use both synthetic, such as salicylic acid and / or others, and natural, such as neem oil and / or others.
- n) Natural oils e.g. almond oil as well as mixtures of any of the aforementioned components.
- the at least one perfume oil is contained in the composition according to the invention in an amount of approximately 1 to 50% by weight, preferably in an amount of 3 to 35% by weight, for example in an amount of 3; 3.1; 3.2; 3.3; 3.4; 3.5; 3.6; 3.7; 3, 8; 3, 9; 4; 4, 5; 5; 6; 7; 8th; 9; 10; 11; 12; 13; 14; 15; 16; 17; 18; 19; 20; 21; 22; 23; 24; 25; 30; or 35% by weight, based in each case on the total weight of the perfume oil storage composition.
- the perfume oil storage composition is a dispersion, for example an oil-in-water emulsion.
- the term “oil-in-water emulsion” is used herein to also encompass dispersions of gel particles, which are formed from the gelling agent and which include perfume oil, in a continuous, aqueous phase. Dispersions of the gel particles described herein are therefore included under the term “emulsion” for the purposes of the invention.
- the dispersed phase comprises the at least one low molecular weight gel former, as defined above, and the at least one perfume oil, as defined above.
- the dispersed phase consists of solid or gel-like particles, the gel former forming the particle matrix which encloses the perfume oil.
- the perfume oil can be in the matrix material, which of the gel former is formed, are present in dispersed form or are enclosed by this in the form of a shell.
- the particles can have a core-shell morphology.
- the matrix material ie the gelling agent
- the matrix material can enclose the perfume oil, which can be present in the form of one or more droplets, the gelling agent here forming a shell which encloses one or more cores of perfume oil.
- the particles are typically substantially spherical. Regardless of the type and shape of the particles, the gel former forms a matrix or shell that encloses the perfume oil and largely shields it from the continuous phase.
- the individual droplets / particles of the dispersed phase have an average diameter in the micrometer range, i.e. are microparticles.
- Such particles can have mean diameters d 50 from approximately 1 ⁇ m to approximately 400 ⁇ m, preferably from approximately 1 ⁇ m to approximately 200 ⁇ m, for example from approximately 1; 1, 5; 2; 2.5; 3; 3.5; 4; 4.5; 5; 5.5; 10; 10.5; 11; 15; 20; 25; 30; 35; 40; 45; 50; 70; 75; 80; 85; 90; 95; 100; 105; 110; 115; 120; 125; 150; 155; 160; 170; 180; 190; 195; 199; or 200 pm.
- the dgo value can be, for example, 500 pm, preferably in the range of 300-400 pm.
- 90% of the particles have a diameter in the range from 2 to 100 ⁇ m, for example 3 to 80 ⁇ m or 3 to 20 ⁇ m or 10 to 80 ⁇ m or 20 to 80 ⁇ m.
- the d 50 value indicates the diameter that results when 50% by weight of the droplets / particles have a smaller diameter and 50% by weight of the droplets have a larger diameter than the determined d 50 value.
- the dgo value of the droplet / particle size distribution is the value at which 90% of all droplets / particles are smaller and 10% of the particles are larger than this value.
- the diameter of the droplets / particles can be determined using customary methods. It can be determined, for example, with the aid of dynamic light scattering (DLS) or light diffraction, for example in accordance with DIN ISO 22412. It can also be carried out by evaluating light microscopic or electron microscopic recordings of the droplets / particles of the emulsion.
- DLS dynamic light scattering
- DIN ISO 22412 DIN ISO 22412. It can also be carried out by evaluating light microscopic or electron microscopic recordings of the droplets / particles of the emulsion.
- Another component of the perfume oil storage composition according to the invention is, in some embodiments of the present invention, at least one additional ingredient selected from the group of surfactants, thickeners, dyes and rheology modifiers.
- Suitable surfactants which according to some embodiments can be part of the perfume oil storage composition according to the invention, are known in the prior art and include anionic surfactants, cationic surfactants, nonionic surfactants, zwitterionic, amphoteric surfactants and mixtures thereof.
- Suitable compounds from the class of anionic surfactants are those of the formula (I) R-SO - X + (I)
- R stands for a linear or branched unsubstituted alkylaryl radical.
- X stands for a monovalent cation or the nth part of an n-valent cation, preferred are the alkali metal ions, including Na + or K + , Na + being extremely preferred. Further cations X + can be selected from NH 4 + , Zn Mn 2+ , and their mixtures.
- Alkylaryl refers to organic radicals consisting of an alkyl radical and an aromatic radical. Typical examples of such groups include, but are not limited to, alkylbenzene groups such as benzyl, butylbenzene groups, nonylbenzene groups, decylbenzene groups, undecylbenzene groups, dodecylbenzene groups, tridecylbenzene groups, and the like.
- such surfactants are selected from linear or branched alkylbenzenesulfonates of the formula A-1:
- A-1 in which R ' and R " together contain 9 to 19, preferably 11 to 15 and in particular 11 to 13 carbon atoms.
- a very particularly preferred representative can be described by the formula A-1a:
- the compound of the formula (I) is preferably the sodium salt of a linear alkylbenzenesulfonate.
- Preferred anionic surfactants are those of the formula (II):
- R 1 represents a linear or branched, substituted or unsubstituted alkyl radical, preferably a linear, unsubstituted alkyl radical, particularly preferably a fatty alcohol radical.
- Preferred radicals R 1 are selected from decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl radicals and mixtures thereof, the representatives with an even number of C- Atoms are preferred.
- Particularly preferred radicals R 1 are derived from Ci2-Ci8-fatty alcohols, for example from coconut fatty alcohol, tallow fatty alcohol, lauryl, myristyl, cetyl or stearyl alcohol or from Cio-C2o-oxo alcohols.
- X stands for a monovalent cation or the nth part of an n-valent cation, preferred are the alkali metal ions, including Na + or K + , Na + being extremely preferred. Further cations X + can be selected from NH4 + , 14 Zn 2+ , 14 Mg 2+ , 14 Ca 2+ , 14 Mn 2+ , and mixtures thereof.
- AO stands for an ethylene oxide (EO) or propylene oxide (PO) group, preferably an ethylene oxide group.
- the index n stands for an integer from 1 to 50, preferably from 1 to 20 and in particular from 2 to 10. Very particularly preferably n stands for the numbers 2, 3, 4, 5, 6, 7 or 8.
- X stands for a monovalent cation or the n-th part of an n-valent cation, preferred are the alkali metal ions, including Na + or K + , Na + being extremely preferred. Further cations X + can be selected from NH4 + , 1 Zn 2+ , 14 Mg 2+ , 14 Ca 2+ , 1 Mn 2+ , and mixtures thereof.
- compositions can contain at least one anionic surfactant selected from fatty alcohol ether sulfates of the formula (11-1)
- R 2 represents a linear or branched, substituted or unsubstituted alkyl radical, preferably a linear, unsubstituted alkyl radical, particularly preferably a fatty alcohol radical.
- Preferred radicals R 2 are selected from decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl radicals and mixtures thereof, the representatives with an even number of C- Atoms are preferred.
- Especially preferred radicals R 2 are derived from Ci2-Ci8-fatty alcohols, for example from coconut fatty alcohol, tallow fatty alcohol, lauryl, myristyl, cetyl or stearyl alcohol or from Cio-C2o-oxo alcohols.
- X stands for a monovalent cation or the nth part of an n-valent cation, preferred are the alkali metal ions, including Na + or K + , Na + being extremely preferred. Further cations X + can be selected from NH4 + , 14 Zn 2+ , 14 Mg 2+ , 14 Ca 2+ , 14 Mn 2+ , and mixtures thereof.
- Suitable surfactants can be selected, for example, from fatty alcohol sulfates of the formula (III- 1)
- alkyl ester sulfonates in particular those of the formula (IV):
- R 1 represents a linear or branched, substituted or unsubstituted alkyl radical, preferably a linear, unsubstituted alkyl radical.
- Preferred radicals R 1 are selected from nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl, heneicosyl radicals and mixtures thereof, the representatives with an odd number of carbon atoms are preferred.
- radicals R 1 -CH are derived from Ci2-Ci8 fatty acids, for example from lauric, myristyl, cetyl or stearic acid.
- R 2 represents a linear or branched, substituted or unsubstituted alkyl radical, preferably a linear, unsubstituted alkyl radical.
- X stands for a monovalent cation or the nth part of an n-valent cation, preferred are the alkali metal ions, including Na + or K + , Na + being extremely preferred. Further cations X + can be selected from NH4 + , 1 Zn 2+ , 14 Mg 2+ , 14 Ca 2+ , 1 / Mn 2+ , and mixtures thereof.
- the secondary alkane sulfonates are also suitable as anionic surfactants. These have, for example, the formula (V)
- each R 1 and R 2 is independently a linear or branched alkyl having 1 to 20 carbon atoms and with the carbon atom to which they are attached form a linear or branched alkyl, preferably with 10 up to 30 carbon atoms, preferably with 10 to 20 carbon atoms and
- X + is selected from the group Na + , K + , NH 4 + , 14 Zn 2+ , 14 Mg 2+ , 14 Ca 2+ , 14 Mn 2+ and mixtures thereof , preferably Na + .
- the at least one secondary alkanesulfonate has the following formula (V-1)
- m + n is an integer between 7 and 17, preferably 10 to 14 and X + is selected from the group Na + , K + , NH4 + , 1 Zn 2+ , 14 Mg 2+ , 14 Ca 2+ , 14 Mn 2+ and mixtures thereof, preferably Na + .
- the at least one secondary alkanesulfonate is secondary C14-17 sodium alkanesulfonate.
- Such a secondary C14-17 sodium alkanesulfonate is sold, for example, by the Clariant company under the trade name “Hostapur SAS60”.
- nonionic surfactants are fatty alcohol alkoxylates.
- Suitable nonionic surfactants have the following formula in particular:
- R 3 stands for a linear or branched, substituted or unsubstituted alkyl radical
- AO stands for an ethylene oxide (EO) or propylene oxide (PO) grouping
- m stands for integers from 1 to 50.
- R 3 represents a linear or branched, substituted or unsubstituted alkyl radical, preferably a linear, unsubstituted alkyl radical, particularly preferably a fatty alcohol radical.
- Preferred radicals R 2 are selected from decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl radicals and mixtures thereof, the representatives with an even number of C- Atoms are preferred.
- radicals R 3 are derived from Ci2-Ci8-fatty alcohols, for example from coconut fatty alcohol, tallow fatty alcohol, lauryl, myristyl, cetyl or stearyl alcohol or from Cio-C2o-oxo alcohols.
- AO stands for an ethylene oxide (EO) or propylene oxide (PO) group, preferably an ethylene oxide group.
- the index m stands for an integer from 1 to 50, preferably from 1 to 20 and in particular from 2 to 10. m is very particularly preferably the numbers 2, 3, 4, 5, 6, 7 or 8.
- fatty alcohol alkoxylates to be used with preference are compounds of the formula
- Amine oxides are also suitable as nonionic surfactants.
- all amine oxides established in the prior art for these purposes i.e. compounds which have the formula R 1 R 2 R 3 NO, in which each R 1 , R 2 and R 3 independently of the others is an optionally substituted, for example hydroxy- substituted, C1-C30 hydrocarbon chain can be used.
- Particularly preferably used amine oxides are those in which R 1 is C12-C18 alkyl and R 2 and R 3 are each independently C1-C4 alkyl, in particular C12-C18 alkyldimethylamine oxides.
- Suitable amine oxides are N-cocoalkyl-N, N-dimethylamine oxide, N-tallowalkyl-N, N-dihydroxyethylamine oxide, myristyl / cetyldimethylamine oxide or lauryldimethylamine oxide.
- nonionic surfactants which can be contained in the compositions described for the purposes of the present invention include, but are not limited to, alkyl glycosides, alkoxylated fatty acid alkyl esters, fatty acid alkanolamides, hydroxy mixed ethers, sorbitan fatty acid esters, polyhydroxy fatty acid amides and alkoxylated alcohols. Such surfactants are known in the prior art.
- Suitable alkyl (poly) glycosides are, for example, those of the formula R 2 0- [G] P , in which R 2 is a branched or branched alkyl with 12 to 16 carbon atoms, G is a sugar residue with 5 or 6 carbon atoms, in particular glucose, and the index p is 1 to 10.
- Suitable amphoteric surfactants are, for example, betaines of the formula (R iN ) (R iv ) (R v ) N + CH2COO-, in which R iN is an alkyl radical with 8 to 25, preferably 10 to 21 carbon atoms, and R iv and optionally interrupted by heteroatoms or heteroatom groups R v denote identical or different alkyl radicals with 1 to 3 carbon atoms, in particular Cio-Cis-alkyl-dimethylcarboxymethylbetaine and Cn-Ci7-alkylamidopropyl-dimethylcarboxymethylbetaine.
- Suitable cationic surfactants include the quaternary ammonium compounds of the formula (R vi ) (R vii ) (R viii ) (R ix ) N + X, in which R vi to R ix represent four identical or different types, in particular two long-chain and two short-chain , Alkyl radicals and X- stand for an anion, in particular a halide ion, for example didecyldimethylammonium chloride, alkylbenzyldidecylammonium chloride and mixtures thereof.
- quaternary surface-active compounds in particular with a sulfonium, phosphonium, iodonium or arsonium group, which are also known as antimicrobial agents.
- quaternary surface-active compounds with an antimicrobial effect, the composition can be designed with an antimicrobial effect or its antimicrobial effect, which may already be present due to other ingredients, can be improved.
- suitable surfactants in this context are selected in particular from the group consisting of sodium dodecyl sulfate (SDS), cetyltrimethylammonium bromide (CTAB), cetyltrimethylammonium chloride (CTAC), 1-acetoxy-2-stearoyloxyethane (AGS), sodium taurocholate, polysorbate 80 (Tween 80) and sorbitan monolaurate (Span 20).
- SDS sodium dodecyl sulfate
- CTAB cetyltrimethylammonium bromide
- CTAC cetyltrimethylammonium chloride
- AVS 1-acetoxy-2-stearoyloxyethane
- sodium taurocholate sodium taurocholate
- polysorbate 80 Teween 80
- sorbitan monolaurate sorbitan monolaurate
- the perfume oil storage composition according to the invention comprises at least one surfactant as a further component, this is, in some embodiments, preferably in an amount of 0 to 15% by weight, preferably in an amount of 0.01 to 5% by weight, for example in an amount of 0.01; 0.02; 0.03; 0.04; 0.05; 0.1; 0.2; 0.3; 0.4; 0.5; 1, 0; 1, 1; 1, 2; 1, 3; 1, 4; 1, 5; 2.0; 2.5; 3.0; 3.5; 4.0; 4.5; or 5.0% by weight, based in each case on the total weight of the perfume oil storage composition according to the invention, contained therein.
- Thickeners which are also suitable as an additional component of the perfume oil storage composition according to the invention, include all thickeners known in the prior art, in particular those which are suitable for washing, cleaning, care and / or finishing purposes.
- suitable thickeners include, for example, but are not limited to, low molecular weight gel formers, as defined above, which have a molar mass of ⁇ 1000 g / mol, and gel-forming macromolecules which have a molar mass of> 1000 g / mol exhibit.
- exemplary groups of suitable thickening agents include, but are not limited to, polysaccharides such as starch, glycosaminoglycans, for example hyaluronic acid, glucomannans or hydroxymethyl cellulose; Phospholipids such as lecithin; as well as proteins and protein mixtures, such as casein or gelatin.
- suitable thickeners are particularly preferably selected from the group consisting of xanthan, sodium hyaluronate, polyvinyl alcohol (PVA 80), lecithin, guar, alginate, starch and polyquaternium-10 (is also called “cellulose 2-hydroxyethyl 2- [2- hydroxy -3- (trimethylammonio) - propoxyjethyl 2-hydroxy-3- (trimethylammonio) propyl ether Chloride "and has the CAS number 81859-24-7.
- the compound is available, for example, under the trade name Antistatic 10 from 3V Sigma) .
- the perfume oil storage composition according to the invention comprises at least one thickener as a further component, this is, in some embodiments, preferably in an amount of 0 to 5% by weight, preferably in an amount of 0.2 to 3% by weight, for example in an amount of 0.2; 0.3; 0.4; 0.5; 1, 0; 1, 1; 1, 2; 1, 3; 1, 4; 1, 5; 2.0; 2.5; or 3.0 each based on the total weight of the perfume oil storage composition contained therein.
- the thickeners can be used, for example, to set a viscosity or flow limit in the compositions according to the invention, the viscosity and / or flow limit ensuring that the dispersed phase remains stably dispersed over long periods of time, i.e. neither sediments nor creams.
- Dyes which are suitable for use in the perfume oil storage composition according to the invention include all water-soluble and / or hydrophilic and water-insoluble and / or lipophilic dyes known in the prior art, in particular those used for washing, cleaning, care and maintenance / or refinement purposes as defined herein are suitable.
- Rheology modifiers which can also be a further component of the perfume oil storage composition described herein, include all rheology modifiers known in the art, in particular those which are suitable for washing, cleaning, care and / or finishing purposes.
- Exemplary rheology modifiers include, but are not limited to, alginate, carageenan, cellulose derivatives, succinoglucans, and acrylates. In the context of the present invention, however, those rheology modifiers are particularly preferred which do not fall under the term “microplastics” as defined above, such as, for example, polysaccharide-based rheology modifiers.
- the above-mentioned thickeners such as, for example, xanthan, can also be used / understood as rheology modifiers.
- the perfume oil storage composition comprises at least one further component which is selected from the group consisting of surfactants, Thickeners, dyes and rheology modifiers, as defined above, the additional components mentioned are incorporated into a composition according to the invention, as explained below with reference to the production process according to the invention.
- a method for producing a perfume oil storage composition defined and described above is a further subject matter of the present invention.
- the method according to the invention comprises the steps of a) providing a mixture comprising at least one low molecular weight gel former, as defined above, and at least one perfume oil; b) dispersing the mixture from step a) in water or an aqueous solution in order to obtain a dispersion, optionally an oil-in-water emulsion, the dispersed phase of which comprises the at least one low molecular weight gel former and the at least one perfume oil.
- step a) of a production method according to the invention comprises in some embodiments the heating of one or more components to a temperature of approximately 30 ° C. to approximately 130 ° C., preferably to a temperature of approximately 60 ° C.
- step a) The heating of individual or all components of the mixture according to step a) can simplify and / or accelerate the production of such a homogeneous mixture.
- the dispersing according to step b) of the production method comprises heating the mixture from step a) and / or the water or the aqueous solution to a temperature of approximately 30 ° C. to approximately 130 ° C., preferably to a Temperature from about 60 ° C to about 100 ° C, for example to a temperature of about 60, 61, 62, 63, 64, 65, 70, 75, 80, 85, 90, 95 or 100 ° C.
- the heating of individual or all of the components used in step b) can simplify and / or accelerate the production of a stable dispersion according to the invention.
- a perfume oil storage composition according to the invention is to contain one or more dyes, they can be part of the dispersed phase and / or the continuous phase and are accordingly added to the corresponding phase in step a) of the process according to the invention or step b) of the process according to the invention.
- Lipophilic and / or water-insoluble dyes are preferably chosen as a component of the oil phase and hydrophilic and / or water-soluble dyes as a component of the aqueous phase.
- Mixing / stirring in or dispersing the respective components, for example according to step a) or step b) of the method according to the invention, is not limited according to the invention to certain techniques and can include, for example, the use of vortex devices or stirrers, the use of spoons, spatulas or the like.
- step b) of the method consists of the following steps: b1) dispersing the mixture from step a) in an aqueous solution of at least one thickening agent; and b2) stirring the dispersion from step b1) into an aqueous solution of at least one surfactant and / or at least one rheology modifier.
- step b) of the method consists of the following steps: b1 .1) dispersing the mixture from step a) in an aqueous solution of at least one surfactant and / or at least one rheology modifier; and b2.1) stirring the dispersion from step b1 .1) into an aqueous solution of at least one thickening agent.
- step b) of the method consists of step b1) or of step b1 .1).
- Thickeners which according to some embodiments according to step b1) are incorporated into a perfume oil storage composition according to the invention, have been defined and described above.
- the at least one thickener is an additional component of the perfume oil storage composition according to the invention and is a component of the continuous phase and serves to thicken the same.
- the oil-in-water emulsion according to the invention can be additionally stabilized.
- Surfactants and / or rheology modifiers which in some embodiments according to step b2) are incorporated into a perfume oil storage composition according to the invention, have been defined and described above.
- this is at least one surfactant and / or the at least one rheology modifier as an additional component of the perfume oil storage composition according to the invention, component of the continuous phase and serves to sterically stabilize the dispersed phase.
- the oil-in-water emulsion according to the invention can accordingly be additionally stabilized.
- the dispersing according to step b1) or step b1.1) and / or the stirring in according to step b2) or step b2.1) the heating of the mixture from step a) and / or the respective aqueous Solution to a temperature of about 30 ° C to about 130 ° C, preferably to a temperature of about 60 ° C to about 100 ° C, for example to a temperature of about 60, 61, 62, 63, 64, 65, 70, 75, 80, 85, 90, 95 or 100 ° C.
- the production of a dispersion or oil-in-water emulsion according to the invention can be simplified and / or accelerated.
- a perfume oil storage composition according to the invention can be produced by means of a method as described above.
- the embodiments described as preferred at that point for low molecular weight gel formers, perfume oil, thickeners, surfactants, rheology modifiers and dyes also apply to the process according to the invention.
- Another object of the present invention is the use of a low molecular weight gel former for stabilizing at least one perfume oil in water or in an aqueous solution.
- a low molecular weight gel former as a component of the dispersed phase, as explained above, enables the production of stable oil-in-water emulsions in which the at least one low molecular gel former is a component of the dispersed phase and the at least one perfume oil is in the form of finely divided particles / Droplets are in the continuous phase.
- both the gelling agent and the perfume oil are preferably as defined above.
- the gelling agent preferably forms a matrix or shell which encloses the perfume oil, so that particles of gelling agent and perfume oil result accordingly.
- a detergent, cleaning agent or treatment agent such as a particulate detergent or cleaning agent, a liquid detergent or cleaning agent, a fabric softener or a scented product, such as scented lozenges for use in textile washing
- a perfume oil storage composition at different points / times of the packaging process of the respective agent, as well as to leave the final packaging of the finished agent to the consumer himself by giving him provides several perfume oil storage compositions with different beneficial agents as well as a washing, cleaning or treatment base agent and the consumer mixes the washing, cleaning or treatment agent required in each case himself, in accordance with the operation of a modular system.
- Another object of the present invention is an agent comprising a perfume oil storage composition as described herein, the agent being a detergent, cleaning agent or treatment agent, for example a cosmetic product, detergent, cleaning agent or textile treatment agent.
- Agents according to the invention are suitable for washing, cleaning, conditioning, caring for and / or dyeing hard or soft surfaces.
- the agents according to the invention can consequently be detergents, cleaning agents, aftertreatment agents and / or cosmetic agents.
- Hard surfaces in the sense of this application are windows, mirrors and other glass surfaces, surfaces made of ceramic, plastic, metal or wood as well as lacquered wood that can be found in households and businesses, such as bathroom ceramics, cookware and tableware, kitchen surfaces or floors.
- Soft surfaces in the context of this application are textile fabrics, skin and hair.
- Means for washing hard or soft surfaces in the context of this application are textile detergents, e.g. formulations in the form of powders, granules, pearls, tablets, pastes, gels, cloths, pieces or liquids.
- Means for cleaning hard or soft surfaces within the meaning of this application include all cleaners for hard or soft surfaces, in particular dishwashing detergents, all-purpose cleaners, toilet cleaners, sanitary cleaners and glass cleaners, toothpastes, skin washes such as shower gels or shampoos.
- Means for conditioning hard or soft surfaces in the context of this application are fabric softeners, fragrance rinsers, conditioning towels for use in the tumble dryer, hygiene rinsers, deodorants, antiperspirants, hair conditioning agents, styling agents and / or hair setting agents.
- Means for the care of hard or soft surfaces in the context of this application are textile care products, hair care products or skin treatment products such as creams, lotions or gels.
- Agents for coloring hard or soft surfaces in the context of this application are hair colorants and hair tinting agents and agents for lightening keratinic fibers.
- the surface is a textile surface. If the surface is a textile surface, it is particularly preferred if the agent for washing, cleaning, conditioning, caring for and / or dyeing hard or soft surfaces is a detergent, cleaning agent or aftertreatment agent.
- the surface is a part of the body, in particular skin and / or hair. If the surface is a part of the body, in particular skin and / or hair, it is preferred if the agent for washing, cleaning, conditioning, caring for and / or coloring hard or soft surfaces is a cosmetic composition.
- An agent according to the invention comprises at least one type of perfume oil storage composition as defined and described herein.
- such an agent contains at least one perfume oil storage composition according to the invention in an amount of up to about 20% by weight, preferably up to about 10% by weight, preferably up to about 7% by weight, even more preferably up to about 5% by weight, in particular up to about 2% by weight.
- an agent according to the invention can also contain other ingredients that are customary and known as such to the person skilled in the art, for example at least one or preferably several substances from the group of enzymes, surfactants, bleaching agents, complexing agents, builders, electrolytes, non-aqueous solvents, pH - Thickening agents, additional fragrances, additional fragrance carriers, fluorescent agents, dyes, hydrotropes, foam inhibitors, silicone oils, anti-redeposition agents, graying inhibitors, anti-enema agents, anti-crease agents, color transfer inhibitors, antimicrobial agents, germicides, fungicides, anticorrosive agents, bitter inhibitors, anti-corrosive agents, anti-oxidants, anticorrosive agents, anti-corrosive agents, antioxidants, anti-corrosive agents , Swelling and non-slip agents, plasticizing components and UV absorbers.
- enzymes for example at least one or preferably several substances from the group of enzymes, surfactants, bleaching agents, complexing agents, builders, electrolytes, non-aque
- the present invention furthermore relates to the use of a perfume oil storage composition according to the invention for treating surfaces and / or in textile washing and / or in textile care, as defined above, and a method for treating a surface or for washing and / or caring for of textiles, characterized in that an agent according to the invention is used in at least one process step, as described above.
- the low molecular weight gel former here: 12-HSA
- the mixture obtained in this way was dispersed with vigorous stirring (800 rpm) in an aqueous solution of the thickener (here: xanthan gum) which had previously been heated to 70.degree.
- the dispersion thus obtained was then added at 70 ° C. to an aqueous solution of the stabilizing agent (here: SDS), which had previously been heated to 70 ° C., with slow stirring. On cooling to room temperature, a stable dispersion was formed within about 2 hours.
- the low molecular weight gel former (12-HSA) was dissolved in perfume oil at 75 ° C.
- the mixture obtained in this way was dispersed with ultrasound (20 kHz, 100W) for a total of 6 minutes in an aqueous solution of the surfactant cetyltrimethylammonium bromide (CTAB) which had previously been heated to 70 ° C.
- CTAB cetyltrimethylammonium bromide
- the low molecular weight gel former (DBS) was dissolved in propylene glycol (PG) and a 10% solution was prepared. This solution was dissolved in perfume oil at 80 ° C. The mixture obtained in this way was dispersed with ultrasound (20 kHz, 100W) for a total of 6 minutes in an aqueous solution of the surfactant (CTAB) which had previously been heated to 80 ° C. When cooling to room temperature, the sample was slowly stirred with a magnetic stirrer until it reached approx. 25 ° C.
- CTAB surfactant
- the low molecular weight gelling agent group E (diketopiperazine) (L-Phe-L-His) was dissolved in propylene glycol (PG) and a 10% solution was prepared. This solution was dissolved in perfume oil at 80 ° C. The mixture obtained in this way was dispersed with ultrasound (20 kHz, 100W) for a total of 6 minutes in an aqueous solution of the surfactant (CTAB) which had previously been heated to 80 ° C. When cooling to room temperature, the sample was slowly stirred with the magnetic stirrer for 12 hours.
- CTAB surfactant
- the diameters of the dispersed particles were determined with the aid of optical light microscopy or dynamic light scattering (DLS, Malvern Zetasizer).
- a lipophilic dye fat red
- the measurement took place approx. 2 hours after the emulsion had been produced.
- the diameter of the particles was between 30 ⁇ m and 80 ⁇ m and did not change significantly even after a renewed measurement after several weeks.
- analogous to composition E1 an emulsion without 12-HSA but with the same amount of 1,2-propylene glycol was produced. Without the addition of 12-HSA, the diameter of the particles is between 100 ⁇ m and 500 ⁇ m.
- the dispersion formed is only stable for a few days.
- the matrix encapsulation of perfume of composition E1 was made visible with the aid of scanning electron microscopy.
- the diameter of the matrix encapsulation was determined to be from 3 ⁇ m to 20 ⁇ m.
- TGA-IR measurements thermogravimetry combined with IR measurements
- the weight loss was determined during the isothermal heating run at 40 ° C. in a nitrogen atmosphere for 24 hours.
- the gas flow emerging from the TGA was examined by means of FTIR spectroscopy (Fourier transform infrared spectroscopy) with regard to released gas components.
- composition E1 composition E1 or composition analogous to E1 without 12-HSA but with the same amount of 1,2-propylene glycol
- composition E1 composition analogous to E1 without 12-HSA but with the same amount of 1,2-propylene glycol
- Fig. 1 The integrals of the corresponding peaks were plotted against time in order to determine the release of the perfume oil (Fig. 1). It can be seen from Fig. 1 that the encapsulated sample releases less and more slowly perfume oil than the non-encapsulated sample.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Dispersion Chemistry (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Textile Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cosmetics (AREA)
Abstract
Description
Claims
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP19218999 | 2019-12-20 | ||
PCT/EP2020/086238 WO2021122608A1 (en) | 2019-12-20 | 2020-12-15 | Low-molecular gelling agent as fragrant substance dispensing system |
Publications (1)
Publication Number | Publication Date |
---|---|
EP4076344A1 true EP4076344A1 (en) | 2022-10-26 |
Family
ID=69005403
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP20824935.9A Pending EP4076344A1 (en) | 2019-12-20 | 2020-12-15 | Low-molecular gelling agent as fragrant substance dispensing system |
Country Status (3)
Country | Link |
---|---|
US (1) | US20230066457A1 (en) |
EP (1) | EP4076344A1 (en) |
WO (1) | WO2021122608A1 (en) |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5340390A (en) | 1992-10-29 | 1994-08-23 | Rheox, Inc. | Rheological additive comprising derivatives of castor oil |
US6080708A (en) | 1995-02-15 | 2000-06-27 | The Procter & Gamble Company | Crystalline hydroxy waxes as oil in water stabilizers for skin cleansing liquid composition |
US6855680B2 (en) | 2000-10-27 | 2005-02-15 | The Procter & Gamble Company | Stabilized liquid compositions |
KR101481849B1 (en) * | 2007-02-13 | 2015-01-12 | 지보당 에스아 | Microcapsules |
DE102008061045A1 (en) * | 2008-12-11 | 2009-10-08 | Henkel Ag & Co. Kgaa | Use of epsilon-viniferin to combat skin aging, to protect the skin against the effects of UV and/or infrared radiations, to the repair of damage caused by extrinsic skin aging, and to improve the elasticity of the skin |
EP2932956B1 (en) * | 2014-04-14 | 2017-12-27 | Symrise AG | Capsules with high active load |
EP3103431A1 (en) | 2015-06-12 | 2016-12-14 | The Procter and Gamble Company | Fragrance compositions and uses thereof |
WO2017140336A1 (en) * | 2016-02-15 | 2017-08-24 | Symrise Ag | Fragrant mixtures containing esters and ketones |
-
2020
- 2020-12-15 US US17/781,381 patent/US20230066457A1/en active Pending
- 2020-12-15 EP EP20824935.9A patent/EP4076344A1/en active Pending
- 2020-12-15 WO PCT/EP2020/086238 patent/WO2021122608A1/en unknown
Also Published As
Publication number | Publication date |
---|---|
US20230066457A1 (en) | 2023-03-02 |
WO2021122608A1 (en) | 2021-06-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP3516029B1 (en) | Fragrance pellets composed of solids-containing melt dispersions | |
WO2018114056A1 (en) | Microcapsules | |
EP2809756B1 (en) | Combination of an amino alcohol, a fragrance and a silicic acid ester, and the use of same as a pro-fragrance | |
EP2809761B1 (en) | Combination of 1-aza-3,7-dioxabicyclo[3.3.0]octane compounds and silicic acid ester and use as fragrance precursor | |
DE102017218991A1 (en) | Solid perfumed composition | |
EP3630295B1 (en) | Microcapsule system for polysensory olfactory effects i | |
EP3701005B1 (en) | Solid fragrance-containing composition | |
EP4076344A1 (en) | Low-molecular gelling agent as fragrant substance dispensing system | |
EP3516033A1 (en) | Continuous method for producing perfume-containing melting bodies | |
DE102013226098A1 (en) | Silyl enol ethers of fragrance ketones or aldehydes | |
EP4106822B1 (en) | Composition comprising micro-encapsulated malodor control agents and their use for reducing malodors | |
EP3692047A1 (en) | Hydrolytically labile silyl enol ether fragrance ketones or aldehydes | |
EP3360951B1 (en) | Composition comprising perfumed oil and encapsulated perfumes | |
WO2018055115A1 (en) | Perfume-containing melting bodies which contain highly ethoxylated non-ionic surfactants | |
DE102020204509A1 (en) | Laundry detergent with pheromones | |
WO2020249707A1 (en) | Granular detergent-, cleaning agent- or treatment agent additive | |
DE102019111837A1 (en) | HEAT / DRYER STABLE PERFUME APPLICATION | |
WO2019076589A1 (en) | Hydrolysis-labile dienolsilyl ethers of odorant ketones or odorant aldehydes | |
WO2019120779A1 (en) | Producing a meltable object containing a perfume | |
DE102019129873A1 (en) | CONTROLLED ODOR RELEASE WITH CHITOSAN AS A CARRIER | |
WO2019101444A1 (en) | Hydrolytically labile heterocycles of odoriferous ketones or odoriferous aldehydes | |
EP3516034A1 (en) | Perfume-containing melting body containing eo/po block copolymers | |
DE102017203502A1 (en) | Perfume-containing enamel bodies containing highly ethoxylated, nonionic surfactants | |
DE102017203505A1 (en) | Perfume-containing enamel bodies containing EO / PO block copolymers | |
DE102012223423A1 (en) | Washing, cleaning or care products containing fragrance particles |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: UNKNOWN |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE |
|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE |
|
17P | Request for examination filed |
Effective date: 20220601 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |
|
DAV | Request for validation of the european patent (deleted) | ||
DAX | Request for extension of the european patent (deleted) | ||
P01 | Opt-out of the competence of the unified patent court (upc) registered |
Effective date: 20230530 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: EXAMINATION IS IN PROGRESS |
|
17Q | First examination report despatched |
Effective date: 20240403 |