ES2235412T3 - Derivados de oxima de acido carboxilico. - Google Patents
Derivados de oxima de acido carboxilico.Info
- Publication number
- ES2235412T3 ES2235412T3 ES99115880T ES99115880T ES2235412T3 ES 2235412 T3 ES2235412 T3 ES 2235412T3 ES 99115880 T ES99115880 T ES 99115880T ES 99115880 T ES99115880 T ES 99115880T ES 2235412 T3 ES2235412 T3 ES 2235412T3
- Authority
- ES
- Spain
- Prior art keywords
- precursor
- formula
- oxime
- delm
- compound
- 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.)
- Expired - Lifetime
Links
- -1 CARBOXYL Chemical class 0.000 title abstract description 10
- 239000002253 acid Substances 0.000 title description 5
- 239000002243 precursor Substances 0.000 claims abstract description 39
- 239000003205 fragrance Substances 0.000 claims abstract description 29
- 150000001875 compounds Chemical class 0.000 claims abstract description 26
- 150000002923 oximes Chemical class 0.000 claims abstract description 13
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 12
- 230000000873 masking effect Effects 0.000 claims abstract description 10
- 230000000845 anti-microbial effect Effects 0.000 claims abstract description 5
- RMPKHUJAYKUKPH-ZKXNXJMVSA-N (e,2s)-2,6-dimethyloct-5-enal Chemical compound CC\C(C)=C\CC[C@H](C)C=O RMPKHUJAYKUKPH-ZKXNXJMVSA-N 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 10
- 239000004615 ingredient Substances 0.000 claims description 4
- 239000012634 fragment Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 101000996032 Xenopus laevis Nodal homolog Proteins 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000004171 alkoxy aryl group Chemical group 0.000 abstract 1
- 125000005160 aryl oxy alkyl group Chemical group 0.000 abstract 1
- 125000005325 aryloxy aryl group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000000796 flavoring agent Substances 0.000 abstract 1
- 235000019634 flavors Nutrition 0.000 abstract 1
- 239000000047 product Substances 0.000 description 26
- 239000000203 mixture Substances 0.000 description 15
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- 239000000243 solution Substances 0.000 description 7
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 6
- 150000001299 aldehydes Chemical group 0.000 description 6
- 239000004599 antimicrobial Substances 0.000 description 6
- 230000003111 delayed effect Effects 0.000 description 6
- 239000003599 detergent Substances 0.000 description 6
- 239000002979 fabric softener Substances 0.000 description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 5
- 238000000354 decomposition reaction Methods 0.000 description 5
- 239000002781 deodorant agent Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 239000004744 fabric Substances 0.000 description 5
- 235000019645 odor Nutrition 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- YGFGZTXGYTUXBA-UHFFFAOYSA-N (±)-2,6-dimethyl-5-heptenal Chemical compound O=CC(C)CCC=C(C)C YGFGZTXGYTUXBA-UHFFFAOYSA-N 0.000 description 4
- PSBKJPTZCVYXSD-UHFFFAOYSA-N 5-methylheptan-3-one Chemical compound CCC(C)CC(=O)CC PSBKJPTZCVYXSD-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 102000004882 Lipase Human genes 0.000 description 4
- 239000004367 Lipase Substances 0.000 description 4
- 108090001060 Lipase Proteins 0.000 description 4
- 235000019421 lipase Nutrition 0.000 description 4
- 239000002304 perfume Substances 0.000 description 4
- 239000003016 pheromone Substances 0.000 description 4
- GTVITUZSWANKRK-UHFFFAOYSA-N propan-2-yloxycyclododecane Chemical compound CC(C)OC1CCCCCCCCCCC1 GTVITUZSWANKRK-UHFFFAOYSA-N 0.000 description 4
- 241000894006 Bacteria Species 0.000 description 3
- 241000254173 Coleoptera Species 0.000 description 3
- 230000004913 activation Effects 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 238000004587 chromatography analysis Methods 0.000 description 3
- 239000012230 colorless oil Substances 0.000 description 3
- 238000013467 fragmentation Methods 0.000 description 3
- 238000006062 fragmentation reaction Methods 0.000 description 3
- 239000006210 lotion Substances 0.000 description 3
- 239000012074 organic phase Substances 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 239000012047 saturated solution Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 229940029225 2,6-dimethyl-5-heptenal Drugs 0.000 description 2
- SPUWOYCLMKSXKU-UHFFFAOYSA-N 4-oxo capric acid Chemical compound CCCCCCC(=O)CCC(O)=O SPUWOYCLMKSXKU-UHFFFAOYSA-N 0.000 description 2
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 238000004220 aggregation Methods 0.000 description 2
- 230000002776 aggregation Effects 0.000 description 2
- 239000002386 air freshener Substances 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000001815 facial effect Effects 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229960005480 sodium caprylate Drugs 0.000 description 2
- BYKRNSHANADUFY-UHFFFAOYSA-M sodium octanoate Chemical compound [Na+].CCCCCCCC([O-])=O BYKRNSHANADUFY-UHFFFAOYSA-M 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- NIMLCWCLVJRPFY-UHFFFAOYSA-N 1-(5-bicyclo[2.2.1]hept-2-enyl)ethanone Chemical compound C1C2C(C(=O)C)CC1C=C2 NIMLCWCLVJRPFY-UHFFFAOYSA-N 0.000 description 1
- AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 1
- RGUKYNXWOWSRET-UHFFFAOYSA-N 4-pyrrolidin-1-ylpyridine Chemical compound C1CCCN1C1=CC=NC=C1 RGUKYNXWOWSRET-UHFFFAOYSA-N 0.000 description 1
- XVMSFILGAMDHEY-UHFFFAOYSA-N 6-(4-aminophenyl)sulfonylpyridin-3-amine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=N1 XVMSFILGAMDHEY-UHFFFAOYSA-N 0.000 description 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- 102100037486 Reverse transcriptase/ribonuclease H Human genes 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000001166 anti-perspirative effect Effects 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000003213 antiperspirant Substances 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 235000019568 aromas Nutrition 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- JYYOBHFYCIDXHH-UHFFFAOYSA-N carbonic acid;hydrate Chemical compound O.OC(O)=O JYYOBHFYCIDXHH-UHFFFAOYSA-N 0.000 description 1
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- BKMAIDRLVDHVHD-UHFFFAOYSA-N n-[1-(5-bicyclo[2.2.1]hept-2-enyl)ethylidene]hydroxylamine Chemical compound C1C2C(C(=NO)C)CC1C=C2 BKMAIDRLVDHVHD-UHFFFAOYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 238000010419 pet care Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000012549 training Methods 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q15/00—Anti-perspirants or body deodorants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/005—Antimicrobial preparations
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/62—Oximes having oxygen atoms of oxyimino groups esterified
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/62—Oximes having oxygen atoms of oxyimino groups esterified
- C07C251/64—Oximes having oxygen atoms of oxyimino groups esterified by carboxylic acids
- C07C251/66—Oximes having oxygen atoms of oxyimino groups esterified by carboxylic acids with the esterifying carboxyl groups bound to hydrogen atoms, to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/32—Oximes
- C07C251/62—Oximes having oxygen atoms of oxyimino groups esterified
- C07C251/64—Oximes having oxygen atoms of oxyimino groups esterified by carboxylic acids
- C07C251/68—Oximes having oxygen atoms of oxyimino groups esterified by carboxylic acids with at least one of the esterifying carboxyl groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/36—Systems containing two condensed rings the rings having more than two atoms in common
- C07C2602/42—Systems containing two condensed rings the rings having more than two atoms in common the bicyclo ring system containing seven carbon atoms
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Dermatology (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
- Detergent Compositions (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- General Preparation And Processing Of Foods (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP98115403 | 1998-08-17 | ||
| EP98115403 | 1998-08-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2235412T3 true ES2235412T3 (es) | 2005-07-01 |
Family
ID=8232466
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES99115880T Expired - Lifetime ES2235412T3 (es) | 1998-08-17 | 1999-08-12 | Derivados de oxima de acido carboxilico. |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US6521797B1 (enExample) |
| JP (1) | JP2000109457A (enExample) |
| AT (1) | ATE288418T1 (enExample) |
| AU (1) | AU4453399A (enExample) |
| BR (1) | BR9903629A (enExample) |
| CA (1) | CA2280374A1 (enExample) |
| DE (1) | DE69923505T2 (enExample) |
| ES (1) | ES2235412T3 (enExample) |
| ZA (1) | ZA995213B (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6949496B1 (en) * | 1999-08-10 | 2005-09-27 | The Procter & Gamble Company | Detergent compositions comprising hydrotropes |
| DE10326760A1 (de) * | 2003-06-13 | 2005-01-13 | Infineon Technologies Ag | Verfahren und Schaltung zur Crestfaktor-Reduzierung |
| WO2007013581A1 (ja) * | 2005-07-28 | 2007-02-01 | Kobayashi Pharmaceutical Co., Ltd. | 鎮静用組成物 |
| US20110028566A1 (en) * | 2009-05-15 | 2011-02-03 | Eastman Chemical Company | Compositions and products containing cycloaliphatic diol antimicrobial agents and methods of using the compositions and products |
| CN104093315B (zh) * | 2011-12-06 | 2018-04-03 | 荷兰联合利华有限公司 | 抗微生物组合物 |
| CA2894446C (en) * | 2012-12-14 | 2017-07-18 | The Procter & Gamble Company | Antiperspirant and deodorant compositions |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE451889C (de) * | 1928-03-20 | Anton Till | Verfahren zur Massenherstellung von Achat- u. dgl. Lagerpfannen | |
| US3259622A (en) | 1962-09-07 | 1966-07-05 | Merck & Co Inc | 1-benzyl-3-indolyl-alpha-haloalkyl and alkylidenyl acetic acids |
| DE1809385A1 (de) * | 1968-11-16 | 1970-06-11 | Bayer Ag | Oxim-O-kohlensaeure-phenylester sowie Verfahren zu ihrer Herstellung |
| DE2227921A1 (de) * | 1972-06-08 | 1973-12-20 | Bayer Ag | Benzimidazol-2-yl-carbaminsaeureketonoximester, verfahren zu ihrer herstellung und ihre gungizide verwendung |
| DE2429749A1 (de) * | 1974-06-21 | 1976-01-08 | Hoechst Ag | Substituierte o-acyl-acrylaldoxime |
| US4014915A (en) | 1975-04-22 | 1977-03-29 | Fujisawa Pharmaceutical Co., Ltd. | Oxime carbonates |
| JPS6051460B2 (ja) * | 1975-04-22 | 1985-11-14 | 藤沢薬品工業株式会社 | 炭酸エステル類、その製造方法およびその用途 |
| AT365410B (de) | 1978-08-31 | 1982-01-11 | Ciba Geigy Ag | Mittel zum schutz von kulturpflanzen vor aggressi-ven herbiziden |
| US4416686A (en) | 1978-08-31 | 1983-11-22 | Ciba-Geigy Corporation | 3,4-Dichlorophenylacetonitrile-N-tert.butylcarbamoyloxy ether for the protection of crops against injury by herbicides |
| DE3224787A1 (de) * | 1982-07-02 | 1984-01-05 | Bayer Ag, 5090 Leverkusen | Oximcarbamate, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel |
| JPS60108837A (ja) * | 1983-11-17 | 1985-06-14 | Fuji Photo Film Co Ltd | 酸プレカ−サ− |
| JPS62286961A (ja) * | 1986-06-05 | 1987-12-12 | Asahi Chem Ind Co Ltd | 新規なオキシムエステル化合物及びその製造方法 |
| AU604263B2 (en) * | 1986-11-06 | 1990-12-13 | Clorox Company, The | Acyloxynitrogen peracid precursors |
| JPH03232859A (ja) * | 1990-02-09 | 1991-10-16 | Ube Ind Ltd | ピラゾール誘導体、その製造方法及び殺菌剤 |
| JPH0687812A (ja) * | 1992-09-04 | 1994-03-29 | Chisso Corp | 生理活性を有するオキシム類およびそれらのｏ−アシル誘導体 |
| CN1046958C (zh) * | 1993-08-09 | 1999-12-01 | 弗门尼舍有限公司 | 纺织物的加香方法 |
| JP3396068B2 (ja) * | 1993-10-28 | 2003-04-14 | 株式会社トクヤマ | 保護された水酸基を有する複素環化合物の製造方法 |
| JP3295257B2 (ja) * | 1994-11-25 | 2002-06-24 | 株式会社トクヤマ | オキシムカーボネート化合物の製造方法 |
| GB2303789A (en) * | 1995-07-29 | 1997-03-05 | Procter & Gamble | Perfumed compositions containing formaldehyde generating preservatives |
| JPH1072595A (ja) * | 1996-07-01 | 1998-03-17 | Lion Corp | 液体酸素系漂白性組成物 |
| EP1223160B1 (en) * | 1997-06-23 | 2006-08-16 | Givaudan SA | Carbonates for the delivery of aldehydes and/or ketones |
| JP4279915B2 (ja) * | 1997-12-22 | 2009-06-17 | ダイセル化学工業株式会社 | α−シアンヒドリンエステル及びα−ヒドロキシ酸の製造方法 |
-
1999
- 1999-08-12 ES ES99115880T patent/ES2235412T3/es not_active Expired - Lifetime
- 1999-08-12 AT AT99115880T patent/ATE288418T1/de not_active IP Right Cessation
- 1999-08-12 DE DE69923505T patent/DE69923505T2/de not_active Expired - Fee Related
- 1999-08-16 CA CA002280374A patent/CA2280374A1/en not_active Abandoned
- 1999-08-16 BR BR9903629-0A patent/BR9903629A/pt not_active Application Discontinuation
- 1999-08-16 ZA ZA9905213A patent/ZA995213B/xx unknown
- 1999-08-17 US US09/376,776 patent/US6521797B1/en not_active Expired - Fee Related
- 1999-08-17 AU AU44533/99A patent/AU4453399A/en not_active Abandoned
- 1999-08-17 JP JP11267612A patent/JP2000109457A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| JP2000109457A (ja) | 2000-04-18 |
| DE69923505T2 (de) | 2006-01-12 |
| CA2280374A1 (en) | 2000-02-17 |
| ZA995213B (en) | 2000-04-03 |
| DE69923505D1 (de) | 2005-03-10 |
| US6521797B1 (en) | 2003-02-18 |
| ATE288418T1 (de) | 2005-02-15 |
| AU4453399A (en) | 2000-03-09 |
| BR9903629A (pt) | 2000-09-26 |
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