CN108057125A - Smelly eliminating composition or masking composition and their application method - Google Patents
Smelly eliminating composition or masking composition and their application method Download PDFInfo
- Publication number
- CN108057125A CN108057125A CN201711090588.4A CN201711090588A CN108057125A CN 108057125 A CN108057125 A CN 108057125A CN 201711090588 A CN201711090588 A CN 201711090588A CN 108057125 A CN108057125 A CN 108057125A
- Authority
- CN
- China
- Prior art keywords
- smelly eliminating
- composition
- formula
- compound
- peculiar smell
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 109
- 230000000873 masking effect Effects 0.000 title claims abstract description 31
- 238000000034 method Methods 0.000 title claims abstract description 19
- 150000001875 compounds Chemical class 0.000 claims abstract description 69
- ZFMSMUAANRJZFM-UHFFFAOYSA-N Estragole Chemical compound COC1=CC=C(CC=C)C=C1 ZFMSMUAANRJZFM-UHFFFAOYSA-N 0.000 claims description 54
- 125000000217 alkyl group Chemical group 0.000 claims description 27
- 125000001424 substituent group Chemical group 0.000 claims description 19
- 125000003545 alkoxy group Chemical group 0.000 claims description 18
- 235000013305 food Nutrition 0.000 claims description 18
- 125000005843 halogen group Chemical group 0.000 claims description 18
- 239000002781 deodorant agent Substances 0.000 claims description 17
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 14
- 235000013361 beverage Nutrition 0.000 claims description 13
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 claims description 11
- OHBQPCCCRFSCAX-UHFFFAOYSA-N 1,4-Dimethoxybenzene Chemical compound COC1=CC=C(OC)C=C1 OHBQPCCCRFSCAX-UHFFFAOYSA-N 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
- ABDKAPXRBAPSQN-UHFFFAOYSA-N veratrole Chemical compound COC1=CC=CC=C1OC ABDKAPXRBAPSQN-UHFFFAOYSA-N 0.000 claims description 8
- 239000004566 building material Substances 0.000 claims description 7
- 239000011347 resin Substances 0.000 claims description 7
- 229920005989 resin Polymers 0.000 claims description 7
- CHWNEIVBYREQRF-UHFFFAOYSA-N 4-Ethyl-2-methoxyphenol Chemical group CCC1=CC=C(O)C(OC)=C1 CHWNEIVBYREQRF-UHFFFAOYSA-N 0.000 claims description 6
- 235000013373 food additive Nutrition 0.000 claims description 6
- 239000002778 food additive Substances 0.000 claims description 6
- CHLICZRVGGXEOD-UHFFFAOYSA-N 1-Methoxy-4-methylbenzene Chemical group COC1=CC=C(C)C=C1 CHLICZRVGGXEOD-UHFFFAOYSA-N 0.000 claims description 5
- 240000006927 Foeniculum vulgare Species 0.000 claims description 5
- 235000004204 Foeniculum vulgare Nutrition 0.000 claims description 5
- 210000004556 brain Anatomy 0.000 claims description 5
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 claims description 5
- DPZNOMCNRMUKPS-UHFFFAOYSA-N resorcinol dimethyl ether Natural products COC1=CC=CC(OC)=C1 DPZNOMCNRMUKPS-UHFFFAOYSA-N 0.000 claims description 5
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 claims description 4
- WCVOGSZTONGSQY-UHFFFAOYSA-N 2,4,6-trichloroanisole Chemical class COC1=C(Cl)C=C(Cl)C=C1Cl WCVOGSZTONGSQY-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- YXTRCOAFNXQTKL-UHFFFAOYSA-N 2,4,6-tribromoanisole Chemical class COC1=C(Br)C=C(Br)C=C1Br YXTRCOAFNXQTKL-UHFFFAOYSA-N 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 abstract description 26
- 230000001877 deodorizing effect Effects 0.000 abstract description 11
- 239000000126 substance Substances 0.000 abstract description 10
- 230000035943 smell Effects 0.000 description 104
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 32
- 229910052799 carbon Inorganic materials 0.000 description 32
- 230000000694 effects Effects 0.000 description 24
- RUVINXPYWBROJD-ONEGZZNKSA-N trans-anethole Chemical compound COC1=CC=C(\C=C\C)C=C1 RUVINXPYWBROJD-ONEGZZNKSA-N 0.000 description 24
- 239000003205 fragrance Substances 0.000 description 17
- 235000019645 odor Nutrition 0.000 description 17
- -1 suberyl Chemical group 0.000 description 15
- 229940011037 anethole Drugs 0.000 description 12
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 12
- 125000003118 aryl group Chemical group 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 125000000753 cycloalkyl group Chemical group 0.000 description 10
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 description 10
- 206010040904 Skin odour abnormal Diseases 0.000 description 9
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 8
- 239000000443 aerosol Substances 0.000 description 8
- 229910052801 chlorine Inorganic materials 0.000 description 8
- 229910052731 fluorine Inorganic materials 0.000 description 8
- 150000002430 hydrocarbons Chemical class 0.000 description 8
- 229910052740 iodine Inorganic materials 0.000 description 8
- 125000003710 aryl alkyl group Chemical group 0.000 description 7
- 125000001246 bromo group Chemical group Br* 0.000 description 7
- 125000001309 chloro group Chemical group Cl* 0.000 description 7
- 125000001153 fluoro group Chemical group F* 0.000 description 7
- 239000000341 volatile oil Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 description 6
- 235000019441 ethanol Nutrition 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 108091008707 osmoreceptors Proteins 0.000 description 6
- 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 5
- 239000007789 gas Substances 0.000 description 5
- 229960001867 guaiacol Drugs 0.000 description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
- 240000001851 Artemisia dracunculus Species 0.000 description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 241001062472 Stokellia anisodon Species 0.000 description 4
- 125000000304 alkynyl group Chemical group 0.000 description 4
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 4
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
- 235000019504 cigarettes Nutrition 0.000 description 3
- 235000013399 edible fruits Nutrition 0.000 description 3
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- CXWGKAYMVASWDQ-UHFFFAOYSA-N 1,2-dithiane Chemical group C1CCSSC1 CXWGKAYMVASWDQ-UHFFFAOYSA-N 0.000 description 2
- MUZIZEZCKKMZRT-UHFFFAOYSA-N 1,2-dithiolane Chemical group C1CSSC1 MUZIZEZCKKMZRT-UHFFFAOYSA-N 0.000 description 2
- 125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 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 2
- 125000006201 3-phenylpropyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 235000003092 Artemisia dracunculus Nutrition 0.000 description 2
- 206010003497 Asphyxia Diseases 0.000 description 2
- 240000007124 Brassica oleracea Species 0.000 description 2
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 2
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 2
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 2
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 235000002722 Dioscorea batatas Nutrition 0.000 description 2
- 235000006536 Dioscorea esculenta Nutrition 0.000 description 2
- 240000001811 Dioscorea oppositifolia Species 0.000 description 2
- 235000003416 Dioscorea oppositifolia Nutrition 0.000 description 2
- WEEGYLXZBRQIMU-UHFFFAOYSA-N Eucalyptol Chemical compound C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 235000010676 Ocimum basilicum Nutrition 0.000 description 2
- 240000007926 Ocimum gratissimum Species 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical group C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 description 2
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 2
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical group C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical group C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 2
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 2
- MBMBGCFOFBJSGT-KUBAVDMBSA-N all-cis-docosa-4,7,10,13,16,19-hexaenoic acid Chemical compound CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCC(O)=O MBMBGCFOFBJSGT-KUBAVDMBSA-N 0.000 description 2
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical group 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- 125000004850 cyclobutylmethyl group Chemical group C1(CCC1)C* 0.000 description 2
- 125000001162 cycloheptenyl group Chemical group C1(=CCCCCC1)* 0.000 description 2
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 2
- 125000000522 cyclooctenyl group Chemical group C1(=CCCCCCC1)* 0.000 description 2
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 2
- 125000004851 cyclopentylmethyl group Chemical group C1(CCCC1)C* 0.000 description 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 150000004862 dioxolanes Chemical class 0.000 description 2
- 125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- 125000001207 fluorophenyl group Chemical group 0.000 description 2
- 125000001072 heteroaryl group Chemical group 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 125000003707 hexyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 2
- 125000002883 imidazolyl group Chemical group 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 125000000842 isoxazolyl group Chemical group 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 229940043265 methyl isobutyl ketone Drugs 0.000 description 2
- OOFGXDQWDNJDIS-UHFFFAOYSA-N oxathiolane Chemical group C1COSC1 OOFGXDQWDNJDIS-UHFFFAOYSA-N 0.000 description 2
- 125000002971 oxazolyl group Chemical group 0.000 description 2
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 2
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 2
- 125000005561 phenanthryl group Chemical group 0.000 description 2
- 125000004193 piperazinyl group Chemical group 0.000 description 2
- 125000003386 piperidinyl group Chemical group 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 125000003226 pyrazolyl group Chemical group 0.000 description 2
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical group C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 2
- 125000000714 pyrimidinyl group Chemical group 0.000 description 2
- 125000000168 pyrrolyl group Chemical group 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 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 2
- RAOIDOHSFRTOEL-UHFFFAOYSA-N tetrahydrothiophene Chemical group C1CCSC1 RAOIDOHSFRTOEL-UHFFFAOYSA-N 0.000 description 2
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical group C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 description 2
- WHLUQAYNVOGZST-UHFFFAOYSA-N tifenamil Chemical group C=1C=CC=CC=1C(C(=O)SCCN(CC)CC)C1=CC=CC=C1 WHLUQAYNVOGZST-UHFFFAOYSA-N 0.000 description 2
- CLYZNABPUKUSDX-UHFFFAOYSA-N trichloromethoxybenzene Chemical compound ClC(Cl)(Cl)OC1=CC=CC=C1 CLYZNABPUKUSDX-UHFFFAOYSA-N 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- NHOWDZOIZKMVAI-UHFFFAOYSA-N (2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(Cl)C=C1 NHOWDZOIZKMVAI-UHFFFAOYSA-N 0.000 description 1
- 125000004972 1-butynyl group Chemical group [H]C([H])([H])C([H])([H])C#C* 0.000 description 1
- OMONCKYJLBVWOQ-UHFFFAOYSA-N 1-ethoxy-2-methoxybenzene Chemical compound CCOC1=CC=CC=C1OC OMONCKYJLBVWOQ-UHFFFAOYSA-N 0.000 description 1
- XYHKNCXZYYTLRG-UHFFFAOYSA-N 1h-imidazole-2-carbaldehyde Chemical compound O=CC1=NC=CN1 XYHKNCXZYYTLRG-UHFFFAOYSA-N 0.000 description 1
- 125000000069 2-butynyl group Chemical group [H]C([H])([H])C#CC([H])([H])* 0.000 description 1
- MOEFFSWKSMRFRQ-UHFFFAOYSA-N 2-ethoxyphenol Chemical compound CCOC1=CC=CC=C1O MOEFFSWKSMRFRQ-UHFFFAOYSA-N 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-M 3-Methylbutanoic acid Natural products CC(C)CC([O-])=O GWYFCOCPABKNJV-UHFFFAOYSA-M 0.000 description 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 244000291564 Allium cepa Species 0.000 description 1
- 235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 1
- 229920002752 Konjac Polymers 0.000 description 1
- 240000004760 Pimpinella anisum Species 0.000 description 1
- 235000012550 Pimpinella anisum Nutrition 0.000 description 1
- 244000223014 Syzygium aromaticum Species 0.000 description 1
- 235000016639 Syzygium aromaticum Nutrition 0.000 description 1
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical group C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- 244000290333 Vanilla fragrans Species 0.000 description 1
- 235000009499 Vanilla fragrans Nutrition 0.000 description 1
- 235000012036 Vanilla tahitensis Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001335 aliphatic alkanes Chemical group 0.000 description 1
- 125000005120 alkyl cycloalkyl alkyl group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 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
- 125000004429 atom Chemical group 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- GWYFCOCPABKNJV-UHFFFAOYSA-N beta-methyl-butyric acid Natural products CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- 125000001047 cyclobutenyl group Chemical group C1(=CCC1)* 0.000 description 1
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 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 1
- 125000000532 dioxanyl group Chemical group 0.000 description 1
- 208000002173 dizziness Diseases 0.000 description 1
- 229940090949 docosahexaenoic acid Drugs 0.000 description 1
- 235000020669 docosahexaenoic acid Nutrition 0.000 description 1
- 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 1
- 239000003814 drug Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 235000011194 food seasoning agent Nutrition 0.000 description 1
- 150000002240 furans Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 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 1
- 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 1
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
- 150000002475 indoles Chemical class 0.000 description 1
- 235000019562 intensity of smell Nutrition 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000000555 isopropenyl group Chemical group [H]\C([H])=C(\*)C([H])([H])[H] 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229940040511 liver extract Drugs 0.000 description 1
- 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 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 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
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000007923 nasal drop Substances 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000007830 nerve conduction Effects 0.000 description 1
- 230000036403 neuro physiology Effects 0.000 description 1
- 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 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
- 235000014571 nuts Nutrition 0.000 description 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 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
- 239000003921 oil Substances 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 210000000956 olfactory bulb Anatomy 0.000 description 1
- 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 1
- 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 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N pentanal Chemical compound CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 1
- 235000021110 pickles Nutrition 0.000 description 1
- 235000013324 preserved food Nutrition 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- ZFRKQXVRDFCRJG-UHFFFAOYSA-N skatole Natural products C1=CC=C2C(C)=CNC2=C1 ZFRKQXVRDFCRJG-UHFFFAOYSA-N 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 235000012976 tarts Nutrition 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
- 125000003944 tolyl group Chemical group 0.000 description 1
- 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 1
- 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 1
- 210000002700 urine Anatomy 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/01—Deodorant compositions
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L5/00—Preparation or treatment of foods or foodstuffs, in general; Food or foodstuffs obtained thereby; Materials therefor
- A23L5/20—Removal of unwanted matter, e.g. deodorisation or detoxification
- A23L5/27—Removal of unwanted matter, e.g. deodorisation or detoxification by chemical treatment, by adsorption or by absorption
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Nutrition Science (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- General Preparation And Processing Of Foods (AREA)
- Fats And Perfumes (AREA)
Abstract
The present invention is a kind of smelly eliminating composition or masking composition and their application method.It is an object of the present invention to improve the foreign odor of specific deodorizing ingredient, useful smelly eliminating composition is provided.The foreign odor of foregoing deodorizing ingredient can be sheltered or reduced with the specific compound that foregoing deodorizing ingredient has similar chemical constitution.
Description
Technical field
It is used the present invention relates to the smelly eliminating that the foreign odor of deodorizing ingredient is minimized with composition and using foregoing smelly eliminating
Composition, the method for reducing object peculiar smell.Moreover, it relates to the masking composition of the foreign odor of deodorizing ingredient,
And the covering method of the foreign odor of the deodorizing ingredient of foregoing masking composition is used.
Background technology
In recent years, as from deodorant be able to it is widely available and be appreciated that, cleaning purpose improve, take notice of life it is different
The people of taste or body odour etc. is more.In addition, newly-built building, new car compartment in, because can result in dizzy building syndrome etc.
Volatile materials and generate unique peculiar smell, the people not felt well to this peculiar smell is also more, has carried out largely related with peculiar smell grind
Study carefully.
For each glomerulus (yarn sphere) of olfactory bulb probably there are a kind of osmoreceptor, glomerulus can be by with common
A variety of smell substances of characterization of molecules activate (non-patent literature 1).With the similar region for experiencing molecule, (molecule is held
Ke Neng Collar domains) glomerulus be present in each other nearby and form cluster and sub- cluster (non-patent literature 1).In addition, patent is literary
1 is offered to describe:The compounds such as 2,4,6- Trichloroanisoles (TCA) and 2,4,6- tribromos anisole (TBA) are by hindering smell thin
Cationic channel on born of the same parents and make the sensitivity decrease of smell, thus given play to smelly eliminating effect.
Prior art literature
Patent document
Patent document 1:Japanese Unexamined Patent Publication 2013-147475 publications
Non-patent literature
Non-patent literature 1:Takahashi YK etc., Journal of Neurophysiology (2004), Vol.92,
pp.2413-2427
The content of the invention
Problems to be solved by the invention
However, the deodorizing ingredients itself such as TCA and TBA have fustiness, therefore not yet it is fully applicable to smelly eliminating composition.This
The purpose of invention is, improves the foreign odor of foregoing deodorizing ingredient, provides useful smelly eliminating composition.
The method for solving problem
The inventors of the present invention have made intensive studies in order to solve the above problems, it turns out that:With the smelly eliminatings such as TCA and TBA
Ingredient has the foreign odor that deodorizing ingredient can be sheltered or reduced to the specific compound of similar chemical constitution, so as to complete this
Invention.
That is, the present invention provides smelly eliminating composition described below or masking composition and their application method.
(1) a kind of smelly eliminating composition, it includes:At least one kind of compound and following formula (2) shown in following formula (1)
Shown at least one kind of compound.
(in formula, R1~R5It is same or different to each other, represents hydrogen atom, halogen atom or the hydrocarbon optionally with substituent group
Base, R1~R5In at least one be halogen atom)
(in formula, R6~R10It is same or different to each other, represents hydrogen atom, hydroxyl, alkoxy or alkyl)
(2) the smelly eliminating composition according to foregoing (1), wherein, at least one kind of compound shown in previously described formula (1) is
2,4,6- Trichloroanisoles and/or 2,4,6- tribromo anisoles.
(3) the smelly eliminating composition according to foregoing (1) or (2), wherein, in previously described formula (2), R6And R9For hydrogen atom,
R7、R8And R10For hydroxyl, alkoxy or alkyl.
(4) the smelly eliminating composition according to any one of foregoing (1)~(3), wherein, shown in previously described formula (2) extremely
Few a kind of compound is selected from by anisole, veratrole (ベ ラ ト ロ ー Le), estragole (エ ス ト ラ ゴ ー Le), guaiacol (グ
ア ヤ コ ー Le), 4-ethyl guaiacol, hydroquinone dimethyl ether, anethole, resorcin dimethyl ether, methyl phenol (Network レ
オ ゾ ー Le) and p-tolyl methyl ether composition one or more of group.
(5) the smelly eliminating composition according to any one of foregoing (1)~(4), wherein, shown in previously described formula (2) extremely
The content of few a kind of compound is 1 times or more of the content of at least one kind of compound shown in previously described formula (1).
(6) the smelly eliminating composition according to any one of foregoing (1)~(5), wherein, shown in previously described formula (1) extremely
The mass concentration of few a kind of compound is more than 1ppq.
(7) a kind of deodorant accommodates the smelly eliminating composition any one of foregoing (1)~(6).
(8) a kind of resin or building materials, it includes the smelly eliminating compositions any one of foregoing (1)~(6).
(9) a kind of beverage/food additive or beverage/food, it includes the smelly eliminatings any one of foregoing (1)~(6)
Use composition.
(10) a kind of peculiar smell is prevented and kill off with product, and it includes the smelly eliminating compositions any one of foregoing (1)~(6).
(11) a kind of method for reducing object peculiar smell, which is characterized in that it includes:Make aforementioned object or including aforementioned object
Space or composition in the process containing the smelly eliminating composition any one of foregoing (1)~(6).
(12) a kind of masking composition, which is characterized in that it is at least one kind ofization for sheltering shown in following formula (1)
The composition of the foreign odor of object is closed, it includes at least one kind of compound shown in following formula (2),
(in formula, R1~R5It is same or different to each other, represents hydrogen atom, halogen atom or the hydrocarbon optionally with substituent group
Base, R1~R5In at least one be halogen atom)
(in formula, R6~R10It is same or different to each other, represents hydrogen atom, hydroxyl, alkoxy or alkyl)
(13) the masking combination described in the smelly eliminating composition or foregoing (12) any one of foregoing (1)~(6)
Object is prevented and kill off in manufacture deodorant, resin, building materials, beverage/food additive, beverage/food or peculiar smell with the application in product.
(14) masking composition described in foregoing (12) for sheltering or reduce formula (1) institute defined in foregoing (12)
The application of the foreign odor at least one kind of compound shown.
The effect of invention
According to the present invention, by using the compound of previously described formula (2), it can shelter or reduce the compound of previously described formula (1)
Foreign odor.Therefore, it is possible to develop deodorant of the smelly eliminating for the compound for applying previously described formula (1) effect etc..
Specific embodiment
Hereinafter, the present invention is described in more detail.
The smelly eliminating of the present invention includes at least one kind of compound shown in following formula (1) with composition.
(in formula, R1~R5It is same or different to each other, represents hydrogen atom, halogen atom or the hydrocarbon optionally with substituent group
Base, R1~R5In at least one be halogen atom).The compound of previously described formula (1) can hinder the cationic channel of olfactory cell, as
Deodorizing ingredient and play a role (in short, with reference to Japanese Unexamined Patent Publication 2003-147475 publications).
R1~R5Shown halogen atom can be such as fluorine atom, chlorine atom, bromine atoms or iodine atom.
R1~R5Shown alkyl is not particularly limited, and can be such as alkyl, cycloalkyl, cycloalkyl-alkyl, aryl or virtue
Alkyl.Foregoing alkyl can have 1~5 identical or different substituent group.
R1~R5Shown aforesaid alkyl can be such as carbon number 1~20, be preferably carbon number 1~10, be more preferably carbon number 1
~6 straight-chain or the alkyl of branched.
Specifically, aforesaid alkyl can be methyl, ethyl, propyl, isopropyl, butyl, isobutyl group, sec-butyl, tertiary fourth
Base, amyl, isopentyl, neopentyl, hexyl, heptyl, octyl group, nonyl, decyl, undecyl, dodecyl, tridecyl, ten
The straight chains such as tetraalkyl, pentadecyl, cetyl, octadecyl, heptadecyl, octadecyl, nonadecyl and eicosyl
The alkyl of shape or branched.When aforesaid alkyl has substituent group, as its substituent group, it is former that such as alkoxy or halogen may be employed
One or more in sub (fluorine atom, chlorine atom, bromine atoms or iodine atom) etc..
R1~R5Shown foregoing cycloalkyl can be the cycloalkyl of such as carbon number 3~12, can be ring third specifically
Base, cyclobutyl, cyclopenta, cyclohexyl, suberyl, cyclooctyl or adamantyl etc..When foregoing cycloalkyl has substituent group, as
Its substituent group, a kind in may be employed such as alkoxy or halogen atom (fluorine atom, chlorine atom, bromine atoms or iodine atom)
It is or a variety of.
R1~R5Shown foregoing cycloalkyl-alkyl can be the cycloalkyl and carbon number 1~20 for example comprising carbon number 3~12
The cycloalkyl-alkyl of alkyl can be Cvclopropvlmethvl, cyclobutylmethyl, cyclopentyl-methyl or cyclohexyl methyl specifically
Deng.When foregoing cycloalkyl-alkyl has substituent group, as its substituent group, such as alkoxy or halogen atom may be employed, and (fluorine is former
Son, chlorine atom, bromine atoms or iodine atom) etc. in one or more.
R1~R5Shown aforesaid aryl can be the aryl of such as carbon number 6~18, can be phenyl, naphthalene specifically
Base, anthryl, phenanthryl or xenyl etc..When aforesaid aryl has substituent group, as its substituent group, may be employed such as straight-chain or
Alkoxy (the methoxy of the carbon number 1~6 of the alkyl (methyl and tertiary butyl etc.) of the carbon number 1~6 of branched, straight-chain or branched
Base and tert-butoxy etc.) or halogen atom (fluorine atom, chlorine atom, bromine atoms or iodine atom) etc. in one or more.Tool
The aryl of substituted base can be such as p-methylphenyl, tolyl, o-tolyl, 3,5- xylyls, 3,5- di-t-butyls
Phenyl, to tert-butyl-phenyl, p-methoxyphenyl, 3,5- di-t-butyl -4- methoxyphenyls, rubigan, chlorphenyl, right
Fluorophenyl or fluorophenyl etc..
R1~R5Shown foregoing aralkyl can be such as carbon number 7~16 aralkyl, specifically, can be benzyl,
1- phenylethyls, 2- phenylethyls, 1- phenyl propyls, 2- phenyl propyls, 3- phenyl propyls or diphenyl methyl etc..It is foregoing
When aralkyl has substituent group, as its substituent group, such as alkoxy or halogen atom (fluorine atom, chlorine atom, bromine may be employed
Atom or iodine atom) etc. in one or more.
R1~R5The alcoxyl substituted on shown aforesaid alkyl, foregoing cycloalkyl, foregoing cycloalkyl-alkyl and foregoing aralkyl
Base can be such as carbon number 1~15, be preferably carbon number 1~10, the alkoxy of more preferably carbon number 1~6, specifically, can be with
For such as methoxyl group, ethyoxyl, positive propoxy, isopropoxy, n-butoxy, sec-butoxy, isobutoxy, tert-butoxy, penta
Oxygroup or hexyloxy etc..These alkoxies can further have such as halogen atom (fluorine atom, chlorine atom, bromine atoms or iodine
Atom) and carbon number 6~18 the substituent groups such as aryl.
R1~R5Ring can be formed by being selected from arbitrary 2 among them.Foregoing ring can be the yuan of rings of such as 3 yuan of rings~8
Non-aromatic hydrocarbon ring, non-aromatic heterocyclic, aromatic series hydrocarbon ring or heteroaromatic.Foregoing non-aromatic hydrocarbon ring can be such as ring
Alkane ring (cyclopropane ring, cyclobutane ring, pentamethylene ring, cyclohexane ring, cycloheptane ring and cyclooctane ring etc.) or cyclenes hydrocarbon ring
(cyclopentene ring, cyclohexene ring, cycloheptene ring and cyclo-octene ring etc.) etc..Foregoing non-aromatic heterocyclic can be such as tetrahydrochysene -2H-
Pyranoid ring, tetrahydrochysene -2H- thio-pyryliums ring, piperidine ring, dioxanes ring, thioxane ring (オ キ サ チ ア ン Ring), morpholine
Ring, thiomorpholine ring, dithiane ring (ジ チ ア ン Ring), piperazine ring, pyrrolidine ring, thiophane ring, tetrahydrofuran ring, 1,3-
Oxazolidine ring (オ キ サ ゾ ラ ン Ring), dithiolane ring (ジ チ オ ラ ン Ring), oxathiolane ring (オ キ サ チ オ ラ
ン Ring) or dioxolanes etc..Aforementioned fragrance race hydrocarbon ring can be such as phenyl ring.Aforementioned fragrance race heterocycle can be such as furan
Mutter ring, thiphene ring, pyrrole ring, pyridine ring, pyridine ring, pyrimidine ring, pyridazine ring, imidazole ring, pyrazole ring, thiazole ring, oxazole rings or
Isoxazole ring etc..When foregoing ring has substituent group, as its substituent group, such as halogen atom may be employed, and (fluorine atom, chlorine are former
Son, bromine atoms or iodine atom) or the alkyl etc. of carbon number 1~20 in one or more.
On R1~R5, it is preferred that R1、R3And R5For halogen atom, and R2And R4For hydrogen atom.If R1~R5For this
Combination, then the effect of the obstruction cationic channel of the compound of previously described formula (1) is more excellent.
At least one kind of compound shown in previously described formula (1) is preferably halogenated anisole, further preferably 2,4,6- trichlorine fennels
Fragrant ether (TCA) and/or 2,4,6- tribromos anisole (TBA).
The present invention smelly eliminating composition in previously described formula (1) as long as shown at least one kind of compound mass concentration
The effective concentration for playing smelly eliminating effect, is just not particularly limited, can be such as more than 1ppq, be preferably 1ppt with
Upper, more preferably more than 0.1ppb.The upper limit value of the mass concentration of at least one kind of compound shown in previously described formula (1) is not special
It limits, such as can also effectively play a role even if for below 10ppm or below 0.1ppm.
It should be noted that " ppq " (parts per quadrillion described in this specification;1000 parts per trillions 1),
“ppt”(parts per trillion;1 parts per trillion 1), " ppb " (parts per billion;1/1000000000th) and
“ppm”(parts per million;1/1000000th) quality ppq, quality ppt, quality ppb and quality ppm are referred respectively to.
The smelly eliminating composition of the present invention also includes on the basis of comprising at least one kind of compound shown in previously described formula (1)
At least one kind of compound shown in following formula (2).
(in formula, R6~R10It is same or different to each other, represents hydrogen atom, hydroxyl, alkoxy or alkyl)
The compound of previously described formula (2) can play work as the masking ingredient of the foreign odor of the compound of previously described formula (1)
With.
R6~R10Shown alkoxy is saturations or undersaturated straight chain shape or the alkoxy of branched, can be such as carbon
The alkoxy of number 1~20, preferably carbon number 1~10, more preferably carbon number 1~6, can be such as methoxyl group, second specifically
Oxygroup, positive propoxy, isopropoxy, n-butoxy, sec-butoxy, isobutoxy, tert-butoxy, amoxy or hexyloxy etc..
R6~R10Shown alkyl is not particularly limited, and can be such as alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkyl alkane
Base, aryl or aralkyl.
R6~R10Shown aforesaid alkyl can be such as carbon number 1~20, be preferably carbon number 1~10, be more preferably carbon number 1
~6 straight-chain or the alkyl of branched can be methyl, ethyl, n-propyl, isopropyl, sec-butyl or tertiary fourth specifically
Base etc..
R6~R10Shown foregoing alkenyl can be such as carbon number 2~20, be preferably carbon number 2~10, be more preferably carbon number 2
~6 straight-chain or the alkenyl of branched can be vinyl, 1- acrylic, 2- acrylic, isopropenyl, 1- specifically
Cyclobutenyl, 2- cyclobutenyls, 3- cyclobutenyls, 1- methyl-1-propylenes base, 2- methyl-1-propylenes base, 1- methyl -2- acrylic, 2- first
Base -2- acrylic or 1- ethyl-vinyls etc..
Foregoing alkynyl can be such as carbon number 2~20, is preferably carbon number 2~10, be more preferably the straight-chain of carbon number 2~6
Or the alkynyl of branched, can be acetenyl, 1- propinyls, 2-propynyl, 1- butynyls, 2- butynyls, 3- fourths specifically
Alkynyl or 1- methyl -2-propynyl etc..
R6~R10Shown foregoing cycloalkyl can be the cycloalkyl of such as carbon number 3~12, can be ring third specifically
Base, cyclobutyl, cyclopenta, cyclohexyl, suberyl, cyclooctyl or adamantyl etc..
R6~R10Shown foregoing cycloalkyl-alkyl can be included for example by the cycloalkyl of carbon number 3~12 and carbon number 1~20
Alkyl cycloalkyl-alkyl, can be Cvclopropvlmethvl, cyclobutylmethyl, cyclopentyl-methyl or cyclohexyl specifically
Methyl etc..
R6~R10Shown aforesaid aryl can be the aryl of such as carbon number 6~18, can be phenyl, naphthalene specifically
Base, anthryl, phenanthryl or xenyl etc..
R6~R10Shown foregoing aralkyl can be the aralkyl of such as carbon number 7~16, can be benzyl specifically
Base, 1- phenylethyls, 2- phenylethyls, 1- phenyl propyls, 2- phenyl propyls, 3- phenyl propyls or diphenyl methyl etc..
R6~R10Ring can be formed by being selected from arbitrary 2 among them.Foregoing ring can be the yuan of rings of such as 3 yuan of rings~8
Non-aromatic hydrocarbon ring, non-aromatic heterocyclic, aromatic series hydrocarbon ring or heteroaromatic.Foregoing non-aromatic hydrocarbon ring can be for example
Cycloalkanes hydrocarbon ring (cyclopropane ring, cyclobutane ring, pentamethylene ring, cyclohexane ring, cycloheptane ring and cyclooctane ring etc.) or cycloolefin
Ring (cyclopentene ring, cyclohexene ring, cycloheptene ring and cyclo-octene ring etc.) etc..
Foregoing non-aromatic heterocyclic can be such as tetrahydrochysene -2H- pyranoid rings, tetrahydrochysene -2H- thio-pyryliums ring, piperidine ring, two
Oxane ring, thioxane ring, morpholine ring, thiomorpholine ring, dithiane ring, piperazine ring, pyrrolidine ring, thiophane ring,
Tetrahydrofuran ring, 1,3- oxazolidines ring, dithiolane ring, oxathiolane ring or dioxolanes etc..Aforementioned fragrance race hydrocarbon
Ring can be such as phenyl ring.Aforementioned fragrance race heterocycle can be for example furan nucleus, thiphene ring, pyrrole ring, pyridine ring, pyridine ring,
Pyrimidine ring, pyridazine ring, imidazole ring, pyrazole ring, thiazole ring, oxazole ring Huo isoxazole rings etc..
On R6~R10, it is preferred that R6And R9For hydrogen atom, and R7、R8And R10For hydroxyl, alkoxy or alkyl.If
R6~R10For the combination, then the effect of the foreign odor of the compound of previously described formula (1) is sheltered using the compound of previously described formula (2)
It is more excellent.
At least one kind of compound shown in previously described formula (2) be preferably selected from by anisole, veratrole, estragole, guaiacol,
4-ethyl guaiacol, hydroquinone dimethyl ether, anethole, resorcin dimethyl ether, methyl phenol and p-tolyl methyl ether
One or more of group of composition.It is illustrated below go out previously described formula (2) compound represented chemical constitution.
Made using the compound of previously described formula (2) to shelter or reduce the masking of the foreign odor of the compound of previously described formula (1)
With or reduction effect need not be bound to specific theory, it is believed that:Since the characterization of molecules of such as these compounds is total to
The general character, signal multilated that osmoreceptor is sent and given play to above-mentioned effect.It can think:On previously described formula (1)
Compound, each part-structure in chemical constitution are bonded to multiple osmoreceptors, according to the osmoreceptor of its bonding
Species and generate characteristic signal pattern for the bond strength of each osmoreceptor, but the chemical combination of previously described formula (2)
The chemical constitution of object and the offset of charge etc. divide the compound of subcharacter and previously described formula (1) be it is common, therefore, two kinds of compounds
It is competitively mutually bonded with a part of osmoreceptor, the characteristic signal image of previously described formula (1) is disturbed, and therefore, brain can not
The signal pattern is perceived as to the peculiar smell of the compound of previously described formula (1).
The present invention smelly eliminating composition in previously described formula (2) as long as shown at least one kind of compound mass concentration
The effective concentration for having given play to the uncomfortable effect of compound of masking previously described formula (1), is just not particularly limited, can be with
1 times or more for the quality of at least one kind of compound shown in such as previously described formula (1), be preferably more than 10 times, be more preferably 100
Times or more.Specifically, the mass concentration of at least one kind of compound shown in previously described formula (2) can be more than 1ppq, be preferably
More than 1ppt, more preferably more than 0.1ppb.The upper limit value of the mass concentration of at least one kind of compound shown in previously described formula (2) does not have
It is particularly limited to, is, for example, that below 1000ppm or below 10ppm also can effectively play a role.
The compound of previously described formula (2) is included in known essential oil or fragrance, accordingly it is also possible to which previously described formula (2) chemical combination will be included
The essential oil or fragrance of object are used for the smelly eliminating composition of the present invention as the supply source of the compound of previously described formula (2).Foregoing essence
It as long as oil or fragrance include the compound of previously described formula (2), is just not particularly limited, can be that the essential oil of such as fennel (includes wormwood artemisia
Brain), the essential oil of sweet basil (including estragole), the essential oil (including estragole) of tarragon, octagonal essential oil (including anethole), fennel seed
The leaf (including estragole) of (including estragole and anethole), sweet basil, leaf (including estragole), the octagonal fruit of tarragon (include
Anethole), the fruit of vanilla (including guaiacol), the bud (including guaiacol) of cloves or aniseed (include fennel
Brain) etc..In foregoing essential oil or fragrance, in addition to the compound comprising previously described formula (2), also comprising a variety of fragrance ingredients, therefore,
There is significantly high masking effect not only for the foreign odor of the compound of previously described formula (1), additionally it is possible to improve this tremendously
The smelly eliminating effect of the smelly eliminating composition of invention.
Smelly eliminating as the present invention is smelt with the compound of the previously described formula (1) of the deodorizing ingredient included in composition by hindering
Feel the cationic channel of cell and give play to smelly eliminating effect (barrier effect of nerve conduction), therefore, no matter which kind of class peculiar smell is,
Various peculiar smell can be reduced.The smelly eliminating of the present invention can be applied to be not particularly limited with the odorant of composition, it can be exemplified by
As acetaldehyde (irritating green grass peculiar smell), ammonia (dung urine peculiar smell), isopentyl aldehyde (the sour-sweet peculiar smell being charred as asphyxia),
Isobutanol (irritating fermentation peculiar smell), isobutylaldehyde (irritating sour-sweet peculiar smell being charred), the isovaleric acid (socks of sultry humidity
Such peculiar smell), dimethylbenzene (peculiar smell as gasoline), styrene (peculiar smell as city gas), (rotten fish is such for trimethylamine
Peculiar smell), toluene (peculiar smell as gasoline), valeraldehyde (the sour-sweet peculiar smell being charred as asphyxia), n-butanal it is (irritating
The sour-sweet peculiar smell being charred), positive valeric acid (peculiar smell as the socks of sultry humidity), n-butyric acie (stink with perspiration), propionic aldehyde (irritating acid
The peculiar smell that sweet tea is charred), propionic acid (irritating tart flavour), methyl iso-butyl ketone (MIBK) (peculiar smell as irritating diluent), methyl
Mercaptan (peculiar smell as rotten onions), ethyl acetate (peculiar smell as irritating diluent (シ ン ナ ー)), curing
Methyl (curing メ チ Le) (rot peculiar smell as cabbage), methyl sulfide (rot peculiar smell as cabbage), hydrogen sulfide
(peculiar smell as rotten egg), acetic acid, butyric acid, caproic acid (stink with perspiration, body odour), nonenyl aldehyde (body odour of the elderly), scatol (excrement
Just stink) or indoles (stool odor) etc..Like this, smelly eliminating of the invention can be answered with composition for various odorants
With, therefore, can be applied to peculiar smell that clothes, room or automobile etc. distribute, be specially the peculiar smell of cigarette, the peculiar smell of food, body odour,
Body odour plus age peculiar smell, old peculiar smell, lavatory peculiar smell, the peculiar smell of aqueous rubbish, peculiar smell of pet, undried washings peculiar smell,
The peculiar smell of new building or the peculiar smell of new car etc..
The smelly eliminating effect or the effect of reduction peculiar smell realized by the smelly eliminating composition of the present invention can pass through this technology
The method of generally use is evaluated in field.For example, in six stage peculiar smell intensity representations, be divided into as follows 0~5 this
Six stages evaluate the intensity of smell.
0 free from extraneous odour
1 smell that can be perceived reluctantly
2 are difficult to be judged as the smell of which kind of smell
3 smells that can be perceived easily
4 stronger smells
5 strong smells
In addition, in nine stages comfortable immoderation representation, it was divided into for -4~4 this nine stages as follows to evaluate gas
The essence of taste.
- 4 is extreme uncomfortable
- 3 is very uncomfortable
- 2 is uncomfortable
- 1 is slightly uncomfortable
0 is non-comfortable nor uncomfortable
1 is slightly comfortable
2 is comfortable
3 as snug as a bug in a rug
4 is extreme comfortable
In some way, the present invention relates to the deodorants for accommodating foregoing smelly eliminating composition.The deodorant of the present invention
As long as form can give play to smelly eliminating effect, be just not particularly limited, can be for example aerosol type, aerial fog type, fixed or
Person's artificial tooth deodorant etc..The deodorant of the present invention can be applied to the peculiar smell that clothes, room or automobile etc. distribute, be specially cigarette
Peculiar smell, the peculiar smell of food, body odour, body odour plus age peculiar smell, old peculiar smell, lavatory peculiar smell, the peculiar smell of aqueous rubbish, peculiar smell of pet,
Peculiar smell of the peculiar smell of undried washings, the peculiar smell of new building or new car etc..
In some way, the present invention relates to the resins or building materials that include foregoing smelly eliminating composition.By by the present invention
Resin or building materials for manufacture such as furniture, the component (hood (ボ Application ネ ッ ト)) of automobile or apartment etc., can
It reduces in room or the peculiar smell of cigarette in automobile, the peculiar smell of food, body odour, body odour plus age peculiar smell, old age peculiar smell, lavatory is different
Taste, the peculiar smell of aqueous rubbish, peculiar smell of pet, the peculiar smell of undried washings, the peculiar smell of the peculiar smell of new building or new car
Deng.
It to be eaten in some way, the present invention relates to the beverage/food additives comprising foregoing smelly eliminating composition or beverage
Product.By by the beverage/food additive application of the present invention in the stronger food composition of such as peculiar smell or food materials (liver extract,
Docosahexaenoic acid, konjaku silk, dried food and nuts, pickle or alec when) or when being used in edible such food composition or food materials
Seasoning, the peculiar smell of foregoing food composition or food materials can be reduced.In addition, in the beverage/food of the present invention, eaten from the beverage
The food composition or the stronger peculiar smell of food materials used in product is minimized, and can compatibly be eaten.
In some way, the present invention relates to prevented and kill off to use product with the peculiar smell of composition comprising foregoing smelly eliminating.The present invention's
As long as peculiar smell is prevented and kill off can give play to peculiar smell preventive effect with the form of product, be just not particularly limited, can be such as mask,
Nasal drop, ointment or toilet cream (ク リ ー system) etc..By the way that the peculiar smell of the present invention is prevented and kill off the week equipped with product or applied to nose
It encloses or applied to the position as gas with foreign flavor, various peculiar smell can be reduced.
In some way, the present invention relates to the method for reducing object peculiar smell, this method includes:Make aforementioned object or including
The process that foregoing smelly eliminating composition is included in the space of aforementioned object or composition.As aforementioned object, may be employed has
The object of various peculiar smell, for example, can be using clothes, room, automobile, resin, building materials, food composition or food materials etc. as object
Implement the method for the present invention.
In some way, the masking use of the foreign odor the present invention relates at least one kind of compound shown in previously described formula (1)
Composition, said composition include at least one kind of compound shown in previously described formula (2).The masking composition of the present invention can incite somebody to action
At least one kind of compound shown in previously described formula (1) for smelly eliminating and before use, while use or after use, in order to shelter
Or it reduces the foreign odor of at least one kind of compound shown in the formula (1) and uses.
Hereinafter, the present invention is illustrated by embodiment, but the scope of the present invention is not limited to these embodiments.
Embodiment
(embodiment 1)
TCA (Kanto Kagaku K. K.'s system) is dissolved in the water, prepares the aqueous solution of the TCA comprising 1ppm.To the water
Various masking ingredients are added in solution, it is tested and is capable of the fustiness of no masking TCA.Evaluation by smelt by skilled estimator take it is molten
The function of liquid peculiar smell is tested to carry out.As foregoing masking ingredient, anethole (Kanto Kagaku K. K.'s system), estragole have been used
(Kanto Kagaku K. K.'s system), methyl phenol (rice Chinese yam product Industrial Co., Ltd system), veratrole, guaiacol (rice Chinese yam
Product Industrial Co., Ltd system), resorcin dimethyl ether, hydroquinone dimethyl ether (Wako Pure Chemical Industries, Ltd.'s system), ethyl
Guaiacol (Junsei Chemical Co., Ltd.'s system) and p-tolyl methyl ether.Show the result in table 1.
[table 1]
Table 1:For the effect of the masking ingredient of TCA fustiness
×:Feel fustiness strongly.
○:Fustiness is minimized.
◎:Imperceptible fustiness.
Fustiness, but the masking ingredient by coordinating the present invention, the fustiness of TCA are felt by the solution for only including TCA strongly
It is minimized.It should be noted that by guaiacol, resorcin dimethyl ether, hydroquinone dimethyl ether, guaethol or
When person's p-tolyl methyl ether is used as masking ingredient, although the fustiness of TCA is minimized, these masking ingredients are felt strongly certainly
The characteristic peculiar smell of body.
(embodiment 2)
For the peculiar smell comprising TCA and the smelly eliminating composition of estragole, further experiment in detail.Into the water of 80 mass parts
96% ethyl alcohol of 20 mass parts is mixed, and adds TCA and estragole thereto, prepares smelly eliminating composition.By prepared smelly eliminating
It is fitted into composition 0.1cc into commercially available polybag, stands after five minutes, opened the sack by skilled estimator and smelt and take
Peculiar smell.The peculiar smell of fustiness and estragole itself for TCA is evaluated by six stage odor strength representations, for smelly eliminating
With comfortable/immoderation of composition entirety, using nine stages, comfortably uncomfortable representation is evaluated.Show the result in table 2 below.
[table 2]
Table 2:The peculiar smell of smelly eliminating composition comprising TCA and estragole
In the composition that TCA is only included without estragole, the fustiness from TCA is perceived, is evaluated as the gas of extreme discomfort
Taste.On the other hand, if coordinating estragole into the composition comprising TCA, the fustiness from TCA is masked, if improving wormwood artemisia
The concentration of brain, then its masking effect also improve.
(embodiment 3)
For the peculiar smell comprising TCA and the smelly eliminating composition of anethole, further experiment in detail.Except using anethole
It replaces outside estragole, prepares smelly eliminating composition according to the method for embodiment 2, and evaluate its peculiar smell.It shows the result in following
Table 3.
[table 3]
Table 3:The peculiar smell of smelly eliminating composition comprising TCA and anethole
In the composition that TCA is only included without anethole, the fustiness from TCA is perceived, is evaluated as extreme discomfort
Smell.On the other hand, if coordinating anethole into the composition comprising TCA, the fustiness from TCA is masked, if carried
The concentration of high anethole, then its masking effect also improve.
(embodiment 4)
Method according to embodiment 2 prepares the smelly eliminating comprising TCA 100ppb and comprising various masking ingredient 1000bp and uses
Composition, and evaluate its peculiar smell.As control, limonene (the key aroma ingredient of lemon) and 1,8- cineole (fan have been used
Repeatedly fragrant key aroma ingredient).Show the result in table 4 below.
[table 4]
Table 4:The peculiar smell of smelly eliminating composition comprising TCA and various masking ingredients
If combining the compound for coordinating previously described formula (2) with TCA, the fustiness from TCA is masked.On the other hand,
Fragrance ingredient without chemical constitution shown in previously described formula (2) can not shelter the fustiness from TCA.
(embodiment 5)
It is tested for the smelly eliminating comprising TBA and estragole with the peculiar smell of composition.Except using TBA (the pure medicine industry of woods
Co. Ltd. system) it replaces outside TCA, smelly eliminating composition is prepared according to the method for embodiment 2, and evaluates its peculiar smell.It will knot
Fruit is shown in table 5 below.
[table 5]
Table 5:The peculiar smell of smelly eliminating composition comprising TBA and estragole
In the composition that TBA is only included without estragole, the fustiness from TBA is perceived, is evaluated as the gas of extreme discomfort
Taste.On the other hand, if coordinating estragole into the composition comprising TBA, the fustiness from TBA is masked.As can be seen:
The compound of previously described formula (2) not only shelters the peculiar smell from TCA, is also played for being derived from the peculiar smell of compound of previously described formula (1)
Go out masking effect.
(embodiment 6)
It is tested for the smelly eliminating of the present invention with the smelly eliminating effect of composition.
Various odorants are added in water, prepare stench composition).In addition, 20 matter are mixed into the water of 80 mass parts
96% ethyl alcohol of part is measured, and adds TCA and estragole thereto, prepares smelly eliminating composition.By prepared stench composition) 1cc
It is fitted into commercially available polybag, stands after five minutes, prepared smelly eliminating with composition 1cc is packed into and is combined comprising foregoing stench
In the polybag of object, 5 minutes are stood.
Thereafter, opened the sack by skilled estimator and smelt and take peculiar smell.For comfortable/immoderation of peculiar smell, nine are utilized
Stage, comfortably uncomfortable representation was evaluated.Show the result in following tables 6.
[table 6]
Table 6:The smelly eliminating effect of smelly eliminating composition comprising TCA and estragole
The smelly eliminating of the present invention reduces the peculiar smell of various odorants with composition, does not also have the fustiness from TCA, therefore
Excellent smelly eliminating effect is given play to.On the other hand, only in the composition comprising TCA, the peculiar smell of odorant is minimized, but mould
Smelly relatively strong, as discomfort peculiar smell.In addition, not having for masking ingredient, the i.e. estragole of TCA fustiness reduces the different of odorant
The effect of taste.
(embodiment 7)
(1) example of aerosol type deodorant
Trichloroanisole (TCA), estragole, second alcohol and water are mixed with the ratio shown in table 7 below, preparation includes
The smelly eliminating composition of TCA 1ppb, estragole 10ppm and 19.2 mass % of ethyl alcohol.The smelly eliminating is accommodated with composition to spraying and is held
In device, aerosol type deodorant is manufactured.The aerosol type deodorant shows excellent smelly eliminating effect, but hardly feels and be derived from
The fustiness of TCA.
[table 7]
Table 7:The composition example of smelly eliminating composition
(2) example of aerosol type strength deodorant
Trichloroanisole (TCA), estragole, second alcohol and water are mixed with the ratio shown in table 8 below, preparation includes
The smelly eliminating composition of 19.2 mass % of TCA 10ppb, 0.1 mass % of estragole and ethyl alcohol.By the smelly eliminating with composition accommodate to
In automiser spray, aerosol type strength deodorant is manufactured.The aerosol type strength deodorant shows the aerosol type smelly eliminating than above-mentioned (1)
The stronger smelly eliminating effect of agent, but hardly feel the fustiness from TCA.
[table 8]
Table 8:The composition example of smelly eliminating composition
As can seen above:The foreign odor of the compound of previously described formula (1) can be sheltered or reduced to the compound of previously described formula (2), and
And compound comprising previously described formula (1) and the smelly eliminating of the compound of previously described formula (2) have given play to various odorants with composition
Smelly eliminating effect.Therefore, deodorant of smelly eliminating effect for the compound for applying previously described formula (1) etc. can be developed.
Claims (14)
1. a kind of smelly eliminating composition, it includes:Shown at least one kind of compound and following formula (2) shown in following formula (1)
At least one kind of compound,
In formula (1), R1~R5It is same or different to each other, represents hydrogen atom, halogen atom or the alkyl optionally with substituent group,
R1~R5In at least one be halogen atom;
In formula (2), R6~R10It is same or different to each other, represents hydrogen atom, hydroxyl, alkoxy or alkyl.
2. smelly eliminating composition according to claim 1, wherein, at least one kind of compound shown in the formula (1) is 2,4,
6- Trichloroanisoles and/or 2,4,6- tribromo anisoles.
3. smelly eliminating composition according to claim 1 or 2, wherein, in the formula (2), R6And R9For hydrogen atom, R7、R8
And R10For hydroxyl, alkoxy or alkyl.
4. smelly eliminating composition described in any one of claim 1 to 3, wherein, it is at least one kind of shown in the formula (2)
Compound is selected from by anisole, veratrole, estragole, guaiacol, 4-ethyl guaiacol, hydroquinone dimethyl ether, fennel
One or more of group that brain, resorcin dimethyl ether, methyl phenol and p-tolyl methyl ether form.
5. smelly eliminating composition according to any one of claims 1 to 4, wherein, it is at least one kind of shown in the formula (2)
The content of compound is 1 times or more of the content of at least one kind of compound shown in the formula (1).
6. according to smelly eliminating composition according to any one of claims 1 to 5, wherein, it is at least one kind of shown in the formula (1)
The mass concentration of compound is more than 1ppq.
7. a kind of deodorant accommodates smelly eliminating composition according to any one of claims 1 to 6.
8. a kind of resin or building materials, it includes smelly eliminating compositions according to any one of claims 1 to 6.
9. a kind of beverage/food additive or beverage/food, it includes smelly eliminating according to any one of claims 1 to 6 combinations
Object.
10. a kind of peculiar smell is prevented and kill off with product, it includes smelly eliminating compositions according to any one of claims 1 to 6.
A kind of 11. method for reducing object peculiar smell, which is characterized in that it includes:Make the object or include the sky of the object
Between or composition in contain smelly eliminating composition according to any one of claims 1 to 6 process.
12. a kind of masking composition, which is characterized in that it is at least one kind of compound for sheltering shown in following formula (1)
The composition of foreign odor,
It includes at least one kind of compound shown in following formula (2),
In formula (1), R1~R5It is same or different to each other, represents hydrogen atom, halogen atom or the alkyl optionally with substituent group,
R1~R5In at least one be halogen atom;
In formula (2), R6~R10It is same or different to each other, represents hydrogen atom, hydroxyl, alkoxy or alkyl.
13. the masking composition described in smelly eliminating composition according to any one of claims 1 to 6 or claim 12 exists
Manufacture deodorant, resin, building materials, beverage/food additive, beverage/food or peculiar smell are prevented and kill off with the application in product.
14. masking composition described in claim 12 for sheltering or reduce formula defined in claim 12 (1) institute
The application of the foreign odor at least one kind of compound shown.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2016-218826 | 2016-11-09 | ||
| JP2016218826A JP6371817B2 (en) | 2016-11-09 | 2016-11-09 | Deodorant composition or masking composition and methods of use thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN108057125A true CN108057125A (en) | 2018-05-22 |
Family
ID=62134910
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201711090588.4A Pending CN108057125A (en) | 2016-11-09 | 2017-11-08 | Smelly eliminating composition or masking composition and their application method |
Country Status (2)
| Country | Link |
|---|---|
| JP (1) | JP6371817B2 (en) |
| CN (1) | CN108057125A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116602387A (en) * | 2022-02-15 | 2023-08-18 | 丘比株式会社 | Acidic liquid seasoning |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP7550523B2 (en) * | 2020-03-25 | 2024-09-13 | 日清食品ホールディングス株式会社 | Sea urchin flavoring agent |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1863653A (en) * | 2003-08-07 | 2006-11-15 | 电离卫生产品芯片中心有限公司 | Process for eliminating/reducing compounds with a musty taste/odour in materials that are to come into contact with foodstuffs and in foods or drinks |
| JP2013147475A (en) * | 2012-01-23 | 2013-08-01 | Osaka Univ | Cation channel inhibitor and olfactory desensitizer composition including the same |
| US20150110669A1 (en) * | 2013-10-22 | 2015-04-23 | Kao Corporation | Inhibitor of Odor Caused by Sotolone |
| JP2015211667A (en) * | 2014-04-14 | 2015-11-26 | 花王株式会社 | Search method for urine odor suppressor |
| CN105339509A (en) * | 2013-06-29 | 2016-02-17 | 弗门尼舍有限公司 | Methods of identifying, isolating and using odorant and aroma receptors |
| JP5982044B2 (en) * | 2015-07-09 | 2016-08-31 | 花王株式会社 | Odor control agent |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4755503A (en) * | 1987-10-21 | 1988-07-05 | Givaudan Corporation | Fragrance compositions containing 2,4,6-tribromo-3-methylanisole methylanisole |
-
2016
- 2016-11-09 JP JP2016218826A patent/JP6371817B2/en active Active
-
2017
- 2017-11-08 CN CN201711090588.4A patent/CN108057125A/en active Pending
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1863653A (en) * | 2003-08-07 | 2006-11-15 | 电离卫生产品芯片中心有限公司 | Process for eliminating/reducing compounds with a musty taste/odour in materials that are to come into contact with foodstuffs and in foods or drinks |
| JP2013147475A (en) * | 2012-01-23 | 2013-08-01 | Osaka Univ | Cation channel inhibitor and olfactory desensitizer composition including the same |
| CN105339509A (en) * | 2013-06-29 | 2016-02-17 | 弗门尼舍有限公司 | Methods of identifying, isolating and using odorant and aroma receptors |
| US20150110669A1 (en) * | 2013-10-22 | 2015-04-23 | Kao Corporation | Inhibitor of Odor Caused by Sotolone |
| JP2015211667A (en) * | 2014-04-14 | 2015-11-26 | 花王株式会社 | Search method for urine odor suppressor |
| JP5982044B2 (en) * | 2015-07-09 | 2016-08-31 | 花王株式会社 | Odor control agent |
Non-Patent Citations (1)
| Title |
|---|
| TAKAHASHI YK等: "Topographic Representation of Odorant Molecular Features in the Rat", 《JOURNAL OF NEUROPHYSIOLOGY》 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116602387A (en) * | 2022-02-15 | 2023-08-18 | 丘比株式会社 | Acidic liquid seasoning |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2018075172A (en) | 2018-05-17 |
| JP6371817B2 (en) | 2018-08-08 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Wypych | Handbook of odors in plastic materials | |
| Podduturi et al. | Potential contribution of fish feed and phytoplankton to the content of volatile terpenes in cultured pangasius (Pangasianodon hypophthalmus) and tilapia (Oreochromis niloticus) | |
| Li et al. | Essential oils as reagents in green chemistry | |
| Petrakis et al. | Responses of Myzus persicae (Sulzer) to three Lamiaceae essential oils obtained by microwave-assisted and conventional hydrodistillation | |
| US9877927B2 (en) | Inhibitor of odor caused by Furaneol | |
| AU2014250625B2 (en) | Inhibitor of odor caused by sotolone | |
| JP2008289899A (en) | Deodorant composition and method of using the same | |
| Ravit et al. | Organic compounds associated with microplastic pollutants in New Jersey, USA surface waters | |
| JP2018520779A (en) | Indane derivatives for odor neutralization | |
| CN108057125A (en) | Smelly eliminating composition or masking composition and their application method | |
| JP2002193723A (en) | Miticidal compound extracted from plant | |
| Balcerzak et al. | Minor constituents of essential oils and aromatic extracts. Oximes derived from natural flavor and fragrance raw materials–Sensory evaluation, spectral and gas chromatographic characteristics | |
| Wood et al. | The scent of the reticulated giraffe (Giraffa camelopardalis reticulata) | |
| Kroener et al. | Sensory-analytical comparison of the aroma of different horseradish varieties (Armoracia rusticana) | |
| Lorber et al. | Influence of the chemical structure on odor qualities and odor thresholds in homologous series of alka-1, 5-dien-3-ones, alk-1-en-3-ones, alka-1, 5-dien-3-ols, and alk-1-en-3-ols | |
| Sen | Esters, terpenes and flavours: Make the mood cheers by three musketeers | |
| Becher et al. | The scent of the fly | |
| CN114009459A (en) | Deodorizing aromatic and its preparation method | |
| US10064408B2 (en) | Bird repelling treatment composition | |
| JP6732842B2 (en) | Deodorant composition or masking composition and their use | |
| DE2737525A1 (en) | FRAGRANCES AND FLAVORS | |
| CN104651050B (en) | It is a kind of suitable for fragrant atmosphere essential oil of compressed air atomization type scent diffusion equipment and preparation method thereof | |
| Duman et al. | The Chemical composition of Achillea wilhelmsii, Leucanthemum vulgare and Thymus citriodorus essential oils | |
| WO2011125728A1 (en) | Volatile liquid to be volatilized using piece of rattan stem as volatilization member | |
| Chen et al. | Volatile compounds and sensory analysis of both harvests of double‐cut Yakima peppermint (Mentha piperita L.) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PB01 | Publication | ||
| PB01 | Publication | ||
| SE01 | Entry into force of request for substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| RJ01 | Rejection of invention patent application after publication |
Application publication date: 20180522 |
|
| RJ01 | Rejection of invention patent application after publication |