JP2010511037A5 - - Google Patents
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- Publication number
- JP2010511037A5 JP2010511037A5 JP2009538841A JP2009538841A JP2010511037A5 JP 2010511037 A5 JP2010511037 A5 JP 2010511037A5 JP 2009538841 A JP2009538841 A JP 2009538841A JP 2009538841 A JP2009538841 A JP 2009538841A JP 2010511037 A5 JP2010511037 A5 JP 2010511037A5
- Authority
- JP
- Japan
- Prior art keywords
- composition according
- methyl
- antibacterial
- flavoring
- flavor imparting
- 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.)
- Granted
Links
- YCOXTKKNXUZSKD-UHFFFAOYSA-N 3,4-xylenol Chemical compound CC1=CC=C(O)C=C1C YCOXTKKNXUZSKD-UHFFFAOYSA-N 0.000 claims description 10
- OSOIQJGOYGSIMF-UHFFFAOYSA-N cyclopentadecanone Chemical compound O=C1CCCCCCCCCCCCCC1 OSOIQJGOYGSIMF-UHFFFAOYSA-N 0.000 claims description 8
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 claims description 8
- -1 2-methyl-4- (2,2,3-trimethyl-3-cyclopentene -1-yl) -2-butanol Chemical compound 0.000 claims description 7
- RUVINXPYWBROJD-ONEGZZNKSA-N trans-anethole Chemical compound COC1=CC=C(\C=C\C)C=C1 RUVINXPYWBROJD-ONEGZZNKSA-N 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- SPEUIVXLLWOEMJ-UHFFFAOYSA-N 1,1-dimethoxyethane Chemical compound COC(C)OC SPEUIVXLLWOEMJ-UHFFFAOYSA-N 0.000 claims description 4
- YBUIAJZFOGJGLJ-SWRJLBSHSA-N 1-cedr-8-en-9-ylethanone Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1C(C)=C(C(C)=O)C2 YBUIAJZFOGJGLJ-SWRJLBSHSA-N 0.000 claims description 4
- CVKMFSAVYPAZTQ-UHFFFAOYSA-N 2-methylhexanoic acid Chemical compound CCCCC(C)C(O)=O CVKMFSAVYPAZTQ-UHFFFAOYSA-N 0.000 claims description 4
- FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 claims description 4
- BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 claims description 4
- BJIOGJUNALELMI-ARJAWSKDSA-N cis-isoeugenol Chemical compound COC1=CC(\C=C/C)=CC=C1O BJIOGJUNALELMI-ARJAWSKDSA-N 0.000 claims description 4
- HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 claims description 4
- NDTYTMIUWGWIMO-UHFFFAOYSA-N perillyl alcohol Chemical compound CC(=C)C1CCC(CO)=CC1 NDTYTMIUWGWIMO-UHFFFAOYSA-N 0.000 claims description 4
- DTUQWGWMVIHBKE-UHFFFAOYSA-N phenylacetaldehyde Chemical compound O=CCC1=CC=CC=C1 DTUQWGWMVIHBKE-UHFFFAOYSA-N 0.000 claims description 4
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 claims description 4
- KMPQYAYAQWNLME-UHFFFAOYSA-N undecanal Chemical compound CCCCCCCCCCC=O KMPQYAYAQWNLME-UHFFFAOYSA-N 0.000 claims description 4
- NGYMOTOXXHCHOC-UHFFFAOYSA-N 3-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pentan-2-ol Chemical compound CC(O)C(C)CCC1CC=C(C)C1(C)C NGYMOTOXXHCHOC-UHFFFAOYSA-N 0.000 claims description 3
- 229940011037 anethole Drugs 0.000 claims description 3
- 239000004615 ingredient Substances 0.000 claims description 3
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 claims description 3
- FQTLCLSUCSAZDY-UHFFFAOYSA-N (+) E(S) nerolidol Natural products CC(C)=CCCC(C)=CCCC(C)(O)C=C FQTLCLSUCSAZDY-UHFFFAOYSA-N 0.000 claims description 2
- WTOYNNBCKUYIKC-JMSVASOKSA-N (+)-nootkatone Chemical compound C1C[C@@H](C(C)=C)C[C@@]2(C)[C@H](C)CC(=O)C=C21 WTOYNNBCKUYIKC-JMSVASOKSA-N 0.000 claims description 2
- PANBRUWVURLWGY-MDZDMXLPSA-N (E)-2-undecenal Chemical compound CCCCCCCC\C=C\C=O PANBRUWVURLWGY-MDZDMXLPSA-N 0.000 claims description 2
- KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 claims description 2
- HBBONAOKVLYWBI-MDZDMXLPSA-N (e)-dodec-3-enal Chemical group CCCCCCCC\C=C\CC=O HBBONAOKVLYWBI-MDZDMXLPSA-N 0.000 claims description 2
- GJJSUPSPZIZYPM-UHFFFAOYSA-N 1,4-dioxacyclohexadecane-5,16-dione Chemical compound O=C1CCCCCCCCCCC(=O)OCCO1 GJJSUPSPZIZYPM-UHFFFAOYSA-N 0.000 claims description 2
- VDBHOHJWUDKDRW-UHFFFAOYSA-N 1-(1,1,2,3,3,6-hexamethyl-2h-inden-5-yl)ethanone Chemical compound CC1=C(C(C)=O)C=C2C(C)(C)C(C)C(C)(C)C2=C1 VDBHOHJWUDKDRW-UHFFFAOYSA-N 0.000 claims description 2
- ZKCZHZHXSQGGDC-UHFFFAOYSA-N 1-(5-methyl-2-propan-2-ylcyclohexyl)oxypropane-1,2-diol Chemical compound CC(C)C1CCC(C)CC1OC(O)C(C)O ZKCZHZHXSQGGDC-UHFFFAOYSA-N 0.000 claims description 2
- NFAVNWJJYQAGNB-UHFFFAOYSA-N 2-methylundecanal Chemical compound CCCCCCCCCC(C)C=O NFAVNWJJYQAGNB-UHFFFAOYSA-N 0.000 claims description 2
- OOOOFOPLSIWRAR-NTEUORMPSA-N 3,7,11-Trimethyl-6E,10-dodecadien-1-ol Chemical compound OCCC(C)CC\C=C(/C)CCC=C(C)C OOOOFOPLSIWRAR-NTEUORMPSA-N 0.000 claims description 2
- AUBLFWWZTFFBNU-UHFFFAOYSA-N 6-butan-2-ylquinoline Chemical compound N1=CC=CC2=CC(C(C)CC)=CC=C21 AUBLFWWZTFFBNU-UHFFFAOYSA-N 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
- KKVZAVRSVHUSPL-GQCTYLIASA-N Cassiastearoptene Chemical compound COC1=CC=CC=C1\C=C\C=O KKVZAVRSVHUSPL-GQCTYLIASA-N 0.000 claims description 2
- FQTLCLSUCSAZDY-ATGUSINASA-N Nerolidol Chemical compound CC(C)=CCC\C(C)=C\CC[C@](C)(O)C=C FQTLCLSUCSAZDY-ATGUSINASA-N 0.000 claims description 2
- 230000000845 anti-microbial effect Effects 0.000 claims description 2
- SVURIXNDRWRAFU-OGMFBOKVSA-N cedrol Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1[C@@](O)(C)CC2 SVURIXNDRWRAFU-OGMFBOKVSA-N 0.000 claims description 2
- 229940026455 cedrol Drugs 0.000 claims description 2
- PCROEXHGMUJCDB-UHFFFAOYSA-N cedrol Natural products CC1CCC2C(C)(C)C3CC(C)(O)CC12C3 PCROEXHGMUJCDB-UHFFFAOYSA-N 0.000 claims description 2
- 229940117916 cinnamic aldehyde Drugs 0.000 claims description 2
- KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 claims description 2
- DAZYFPVYDAKNQJ-UHFFFAOYSA-N cyclohexadec-2-en-1-one Chemical compound O=C1CCCCCCCCCCCCCC=C1 DAZYFPVYDAKNQJ-UHFFFAOYSA-N 0.000 claims description 2
- WTOYNNBCKUYIKC-UHFFFAOYSA-N dl-nootkatone Natural products C1CC(C(C)=C)CC2(C)C(C)CC(=O)C=C21 WTOYNNBCKUYIKC-UHFFFAOYSA-N 0.000 claims description 2
- SVURIXNDRWRAFU-UHFFFAOYSA-N juniperanol Natural products C1C23C(C)CCC3C(C)(C)C1C(O)(C)CC2 SVURIXNDRWRAFU-UHFFFAOYSA-N 0.000 claims description 2
- WASNIKZYIWZQIP-AWEZNQCLSA-N nerolidol Natural products CC(=CCCC(=CCC[C@@H](O)C=C)C)C WASNIKZYIWZQIP-AWEZNQCLSA-N 0.000 claims description 2
- KKVZAVRSVHUSPL-UHFFFAOYSA-N o-methoxycinnamic aldehyde Natural products COC1=CC=CC=C1C=CC=O KKVZAVRSVHUSPL-UHFFFAOYSA-N 0.000 claims description 2
- 229940100595 phenylacetaldehyde Drugs 0.000 claims description 2
- 230000000844 anti-bacterial effect Effects 0.000 claims 9
- 239000000796 flavoring agent Substances 0.000 claims 9
- 235000019634 flavors Nutrition 0.000 claims 9
- 241000959640 Fusobacterium sp. Species 0.000 claims 2
- 241000194019 Streptococcus mutans Species 0.000 claims 2
- 235000009508 confectionery Nutrition 0.000 claims 2
- 230000002401 inhibitory effect Effects 0.000 claims 2
- KHQDWCKZXLWDNM-KPKJPENVSA-N (e)-2-ethyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-en-1-ol Chemical compound CC\C(CO)=C/CC1CC=C(C)C1(C)C KHQDWCKZXLWDNM-KPKJPENVSA-N 0.000 claims 1
- GIEMHYCMBGELGY-UHFFFAOYSA-N 10-undecen-1-ol Chemical compound OCCCCCCCCCC=C GIEMHYCMBGELGY-UHFFFAOYSA-N 0.000 claims 1
- BTANRVKWQNVYAZ-UHFFFAOYSA-N 2-butanol Substances CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 claims 1
- SJMDLCVBSNYMMJ-UHFFFAOYSA-N 3-(4-tert-butylphenyl)-2-methylpropan-1-ol Chemical compound OCC(C)CC1=CC=C(C(C)(C)C)C=C1 SJMDLCVBSNYMMJ-UHFFFAOYSA-N 0.000 claims 1
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 claims 1
- 241000606125 Bacteroides Species 0.000 claims 1
- 241000605986 Fusobacterium nucleatum Species 0.000 claims 1
- 241000588747 Klebsiella pneumoniae Species 0.000 claims 1
- 241001135213 Porphyromonas endodontalis Species 0.000 claims 1
- 241001135221 Prevotella intermedia Species 0.000 claims 1
- 241001135223 Prevotella melaninogenica Species 0.000 claims 1
- 241000605036 Selenomonas Species 0.000 claims 1
- 241001148135 Veillonella parvula Species 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 235000013361 beverage Nutrition 0.000 claims 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 claims 1
- BOPPSUHPZARXTH-UHFFFAOYSA-N ocean propanal Chemical compound O=CC(C)CC1=CC=C2OCOC2=C1 BOPPSUHPZARXTH-UHFFFAOYSA-N 0.000 claims 1
- 230000001717 pathogenic effect Effects 0.000 claims 1
- CYVGAJHMMVDTDZ-JQWIXIFHSA-N (2s)-2-methyl-4-[(1s)-2,2,3-trimethylcyclopent-3-en-1-yl]butan-1-ol Chemical compound OC[C@@H](C)CC[C@H]1CC=C(C)C1(C)C CYVGAJHMMVDTDZ-JQWIXIFHSA-N 0.000 description 3
- UUQHKWMIDYRWHH-UHFFFAOYSA-N Methyl beta-orcinolcarboxylate Chemical compound COC(=O)C1=C(C)C=C(O)C(C)=C1O UUQHKWMIDYRWHH-UHFFFAOYSA-N 0.000 description 2
- WTOYNNBCKUYIKC-XIKARTHZSA-N (4r)-4,4a-dimethyl-6-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one Chemical compound C1CC(C(C)=C)CC2(C)[C@H](C)CC(=O)C=C21 WTOYNNBCKUYIKC-XIKARTHZSA-N 0.000 description 1
- KHQDWCKZXLWDNM-BWODNOAJSA-N (e)-2-ethyl-4-[(1r)-2,2,3-trimethylcyclopent-3-en-1-yl]but-2-en-1-ol Chemical compound CC\C(CO)=C/C[C@H]1CC=C(C)C1(C)C KHQDWCKZXLWDNM-BWODNOAJSA-N 0.000 description 1
- VDBHOHJWUDKDRW-GFCCVEGCSA-N 1-[(2r)-1,1,2,3,3,6-hexamethyl-2h-inden-5-yl]ethanone Chemical compound CC1=C(C(C)=O)C=C2C(C)(C)[C@H](C)C(C)(C)C2=C1 VDBHOHJWUDKDRW-GFCCVEGCSA-N 0.000 description 1
- CYVGAJHMMVDTDZ-UHFFFAOYSA-N 2-methyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)butan-1-ol Chemical compound OCC(C)CCC1CC=C(C)C1(C)C CYVGAJHMMVDTDZ-UHFFFAOYSA-N 0.000 description 1
- LBICMZLDYMBIGA-UHFFFAOYSA-N 2-methyldecanal Chemical compound CCCCCCCCC(C)C=O LBICMZLDYMBIGA-UHFFFAOYSA-N 0.000 description 1
- YGCZTXZTJXYWCO-UHFFFAOYSA-N 3-phenylpropanal Chemical compound O=CCCC1=CC=CC=C1 YGCZTXZTJXYWCO-UHFFFAOYSA-N 0.000 description 1
- SDQFDHOLCGWZPU-UHFFFAOYSA-N lilial Chemical compound O=CC(C)CC1=CC=C(C(C)(C)C)C=C1 SDQFDHOLCGWZPU-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06125259 | 2006-12-01 | ||
| EP06125259.9 | 2006-12-01 | ||
| PCT/IB2007/054844 WO2008068683A1 (en) | 2006-12-01 | 2007-11-29 | Antimicrobial flavouring composition |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010511037A JP2010511037A (ja) | 2010-04-08 |
| JP2010511037A5 true JP2010511037A5 (enExample) | 2011-01-20 |
| JP5661284B2 JP5661284B2 (ja) | 2015-01-28 |
Family
ID=37943617
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2009538841A Active JP5661284B2 (ja) | 2006-12-01 | 2007-11-29 | 抗菌フレーバー付与組成物 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US20090324515A1 (enExample) |
| EP (1) | EP2099421B1 (enExample) |
| JP (1) | JP5661284B2 (enExample) |
| CN (1) | CN101541297B (enExample) |
| AT (1) | ATE472314T1 (enExample) |
| BR (1) | BRPI0715422B1 (enExample) |
| CA (1) | CA2670283C (enExample) |
| DE (1) | DE602007007520D1 (enExample) |
| ES (1) | ES2346594T3 (enExample) |
| MX (1) | MX2009005362A (enExample) |
| WO (1) | WO2008068683A1 (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5507892B2 (ja) * | 2009-05-29 | 2014-05-28 | 曽田香料株式会社 | 活性酸素起因障害抑制剤 |
| KR101188581B1 (ko) | 2010-06-09 | 2012-10-05 | 동국대학교 경주캠퍼스 산학협력단 | 향부자 메탄올 추출물을 유효성분으로 함유하는 패혈증 예방 또는 치료용 조성물 |
| US20130310452A1 (en) * | 2011-02-07 | 2013-11-21 | Firmenich Sa | Antifungal flavouring ingredients and compositions |
| IN2014MN00808A (enExample) | 2011-11-03 | 2015-09-04 | Unilever Plc | |
| US9307761B2 (en) * | 2011-12-06 | 2016-04-12 | Dow Global Technologies Llc | Microbial composition |
| BR112014013615B1 (pt) * | 2011-12-06 | 2020-10-06 | Unilever N.V. | Composição microbicida sinérgica |
| EP2790533B1 (en) * | 2011-12-13 | 2018-04-04 | Firmenich SA | Antifungal flavoring compositions |
| JP2014140373A (ja) * | 2014-03-20 | 2014-08-07 | Soda Aromatic Co Ltd | 飲食品に活性酸素起因障害抑制機能を付加する方法並びに活性酸素起因障害抑制機能が付加された飲食品の製造方法 |
| EP2957283B1 (de) * | 2014-06-19 | 2022-12-21 | Symrise AG | Verfahren zur Identifizierung von Medikamenten zur Beschleunigung der Wundheilung |
| WO2016089347A1 (en) * | 2014-12-01 | 2016-06-09 | Colgate-Palmolive Company | Increasing micro-robustness |
| JP2023523290A (ja) * | 2020-05-01 | 2023-06-02 | ザ プロクター アンド ギャンブル カンパニー | ミント風味組成物 |
| WO2023222213A1 (en) | 2022-05-18 | 2023-11-23 | Symrise Ag | Antimicrobial mixtures |
| CN120535790A (zh) * | 2025-06-13 | 2025-08-26 | 山东天宸塑业有限公司 | 一种复合抗菌材料负载的bopp珠光膜及其制备方法与应用 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4537765A (en) * | 1982-03-24 | 1985-08-27 | Colgate-Palmolive Company | Peroxydiphosphate toothpaste composition |
| US4610890A (en) * | 1984-07-16 | 1986-09-09 | Sunkist Growers, Inc. | Preparation of solid essential oil flavor composition |
| IN168400B (enExample) * | 1987-01-30 | 1991-03-23 | Colgate Palmolive Co | |
| US5236696A (en) * | 1992-03-27 | 1993-08-17 | Colgate-Palmolive Company | Continuous process for making a non-Newtonian paste or cream like material |
| US5474761A (en) * | 1993-04-08 | 1995-12-12 | The Procter & Gamble Company | Oral compositions for treating plaque and gingivitis |
| WO1995034222A1 (fr) * | 1994-06-16 | 1995-12-21 | Firmenich S.A. | Procede d'aromatisation et composition aromatisante |
| US6025326A (en) * | 1995-07-07 | 2000-02-15 | Intrabiotics Pharmaceuticals, Inc. | Compositions and methods for the prevention and treatment of oral mucositis |
| EP0996422A1 (en) * | 1997-06-04 | 2000-05-03 | The Procter & Gamble Company | Mild, rinse-off antimicrobial liquid cleansing compositions |
| US6596299B1 (en) * | 2000-05-19 | 2003-07-22 | Northern Research Laboratories, Inc. | Method of treating periodontal disease |
| JP3877537B2 (ja) * | 2001-03-07 | 2007-02-07 | 高砂香料工業株式会社 | 口腔用組成物用抗菌剤およびそれを含む口腔用組成物 |
| JP2004018470A (ja) * | 2002-06-18 | 2004-01-22 | Takasago Internatl Corp | 抗菌香料組成物および口臭抑制香料組成物ならびにそれらを含有する口腔用組成物 |
| US6689342B1 (en) * | 2002-07-29 | 2004-02-10 | Warner-Lambert Company | Oral care compositions comprising tropolone compounds and essential oils and methods of using the same |
| GB0303677D0 (en) * | 2003-02-18 | 2003-03-19 | Quest Int | Flavoured products |
| JP2005015684A (ja) * | 2003-06-27 | 2005-01-20 | Kiyomitsu Kawasaki | 野菜フレーバーの製造方法 |
| US20050042266A1 (en) * | 2003-08-21 | 2005-02-24 | Closure Medical Corporation | Cyanoacrylate compositions containing anti-microbial agent |
| GB2413563A (en) * | 2004-04-27 | 2005-11-02 | Micap Plc | Composition comprising a biocide encapsulated within a fungal cell |
| US20060115440A1 (en) * | 2004-09-07 | 2006-06-01 | Arata Andrew B | Silver dihydrogen citrate compositions |
| WO2006120135A1 (en) * | 2005-05-10 | 2006-11-16 | Ciba Specialty Chemicals Holding Inc. | Antimicrobial porous silicon oxide particles |
-
2007
- 2007-11-29 EP EP07849288A patent/EP2099421B1/en active Active
- 2007-11-29 US US12/514,786 patent/US20090324515A1/en not_active Abandoned
- 2007-11-29 CA CA2670283A patent/CA2670283C/en not_active Expired - Fee Related
- 2007-11-29 JP JP2009538841A patent/JP5661284B2/ja active Active
- 2007-11-29 BR BRPI0715422-4A patent/BRPI0715422B1/pt not_active IP Right Cessation
- 2007-11-29 WO PCT/IB2007/054844 patent/WO2008068683A1/en not_active Ceased
- 2007-11-29 MX MX2009005362A patent/MX2009005362A/es active IP Right Grant
- 2007-11-29 DE DE602007007520T patent/DE602007007520D1/de active Active
- 2007-11-29 ES ES07849288T patent/ES2346594T3/es active Active
- 2007-11-29 CN CN2007800441303A patent/CN101541297B/zh active Active
- 2007-11-29 AT AT07849288T patent/ATE472314T1/de not_active IP Right Cessation
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