JP2013535464A - 製剤 - Google Patents
製剤 Download PDFInfo
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- JP2013535464A JP2013535464A JP2013521273A JP2013521273A JP2013535464A JP 2013535464 A JP2013535464 A JP 2013535464A JP 2013521273 A JP2013521273 A JP 2013521273A JP 2013521273 A JP2013521273 A JP 2013521273A JP 2013535464 A JP2013535464 A JP 2013535464A
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- 239000000203 mixture Substances 0.000 title claims abstract description 23
- 238000009472 formulation Methods 0.000 title claims abstract description 21
- 150000001875 compounds Chemical class 0.000 claims abstract description 34
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 14
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 12
- 239000001257 hydrogen Substances 0.000 claims abstract description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 12
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 5
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 5
- 239000000575 pesticide Substances 0.000 claims description 10
- -1 2-hydroxypropyl Chemical group 0.000 claims description 6
- 229930182692 Strobilurin Natural products 0.000 claims description 5
- 150000003852 triazoles Chemical class 0.000 claims description 5
- 102000019259 Succinate Dehydrogenase Human genes 0.000 claims description 4
- 108010012901 Succinate Dehydrogenase Proteins 0.000 claims description 4
- 239000003905 agrochemical Substances 0.000 claims description 4
- XTDZGXBTXBEZDN-UHFFFAOYSA-N 3-(difluoromethyl)-N-(9-isopropyl-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl)-1-methylpyrazole-4-carboxamide Chemical compound CC(C)C1C2CCC1C1=C2C=CC=C1NC(=O)C1=CN(C)N=C1C(F)F XTDZGXBTXBEZDN-UHFFFAOYSA-N 0.000 claims description 3
- 239000005730 Azoxystrobin Substances 0.000 claims description 3
- 239000005799 Isopyrazam Substances 0.000 claims description 3
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical group CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 claims description 3
- 239000000839 emulsion Substances 0.000 claims description 3
- CWSLAZMJENUWPG-UHFFFAOYSA-N 1-hydroxybutan-2-yl benzoate Chemical compound CCC(CO)OC(=O)C1=CC=CC=C1 CWSLAZMJENUWPG-UHFFFAOYSA-N 0.000 claims description 2
- LBPLLQWWWCNJBE-UHFFFAOYSA-N 1-hydroxypropan-2-yl benzoate Chemical compound OCC(C)OC(=O)C1=CC=CC=C1 LBPLLQWWWCNJBE-UHFFFAOYSA-N 0.000 claims description 2
- ZUGADGDFODHNMC-UHFFFAOYSA-N 2-hydroxybutyl benzoate Chemical compound CCC(O)COC(=O)C1=CC=CC=C1 ZUGADGDFODHNMC-UHFFFAOYSA-N 0.000 claims description 2
- SCYRDAWUOAHQIE-UHFFFAOYSA-N 2-hydroxypropyl benzoate Chemical compound CC(O)COC(=O)C1=CC=CC=C1 SCYRDAWUOAHQIE-UHFFFAOYSA-N 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 229940124186 Dehydrogenase inhibitor Drugs 0.000 claims 1
- 239000005760 Difenoconazole Substances 0.000 claims 1
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 claims 1
- 239000002904 solvent Substances 0.000 abstract description 21
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract description 4
- 239000004480 active ingredient Substances 0.000 description 7
- JATXLCWZFQHYGQ-UHFFFAOYSA-N benzoic acid;propane-1,2-diol Chemical compound CC(O)CO.OC(=O)C1=CC=CC=C1 JATXLCWZFQHYGQ-UHFFFAOYSA-N 0.000 description 5
- 239000003112 inhibitor Substances 0.000 description 3
- 230000000361 pesticidal effect Effects 0.000 description 3
- 150000003217 pyrazoles Chemical class 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- AIAYSXFWIUNXRC-PHIMTYICSA-N (1r,5s)-3-[hydroxy-[2-(2-methoxyethoxymethyl)-6-(trifluoromethyl)pyridin-3-yl]methylidene]bicyclo[3.2.1]octane-2,4-dione Chemical compound COCCOCC1=NC(C(F)(F)F)=CC=C1C(O)=C1C(=O)[C@@H](C2)CC[C@@H]2C1=O AIAYSXFWIUNXRC-PHIMTYICSA-N 0.000 description 2
- 239000005747 Chlorothalonil Substances 0.000 description 2
- 239000005758 Cyprodinil Substances 0.000 description 2
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 description 2
- HAORKNGNJCEJBX-UHFFFAOYSA-N cyprodinil Chemical compound N=1C(C)=CC(C2CC2)=NC=1NC1=CC=CC=C1 HAORKNGNJCEJBX-UHFFFAOYSA-N 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- QDBFCZCIBRFQBR-UHFFFAOYSA-N 4-hydroxybutyl benzoate Chemical compound OCCCCOC(=O)C1=CC=CC=C1 QDBFCZCIBRFQBR-UHFFFAOYSA-N 0.000 description 1
- 241000238578 Daphnia Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 206010040880 Skin irritation Diseases 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 238000003915 air pollution Methods 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 231100000584 environmental toxicity Toxicity 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000011499 joint compound Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [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
- 239000005645 nematicide Substances 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring
- C07C69/78—Benzoic acid esters
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/10—Esters; Ether-esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L101/00—Compositions of unspecified macromolecular compounds
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dispersion Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicinal Preparation (AREA)
Abstract
Description
この実施例は、本発明の溶剤中での複数の農薬有効成分のそれぞれ(表1の化合物1および2)の高い溶解度を例示する。
この実施例は、本発明の溶剤が、ストロビルリン類、トリアゾール類、およびコハク酸デヒドロゲナーゼ阻害剤(SDHI)の系列に属する有害生物防除剤を可溶化(具体的にはピラゾール類、好適にはピラザムに対する化学作用)する場合に特に効果的であることを示す。表3aおよび3bは、溶剤プロピレングリコールベンゾアート(表1の化合物1)中での有害生物防除剤アゾキシストロビン、ジフェノコナゾール、イソピラザム、シプロジニル、クロロタロニル、およびビシクロピロンの溶解度を示す。比較のために、一般的に利用されている溶剤一覧の溶解度も表中に示されている。データは、ほとんどの場合、プロピレングリコールベンゾアートが、最初の3種類の農薬(それぞれトリアゾール、SDHI、およびストロビルリン)に対してその他の一般の溶剤よりもより優れた溶媒であることを示す。溶解度は、20℃におけるw/w百分率として示す。
Claims (13)
- R1が水素である、請求項1に記載の製剤。
- R3が水素である、請求項1または2に記載の製剤。
- nが1である、請求項1、2、または3に記載の製剤。
- 前記製剤が乳剤またはエマルション製剤である、請求項1、2、3、または4に記載の製剤。
- 前記製剤がさらに農薬を含む、請求項1、2、3、4、または5に記載の製剤。
- 前記農薬が、ストロビルリン、トリアゾール、またはコハク酸デヒドロゲナーゼ阻害剤である、請求項6に記載の製剤。
- 前記農薬が、アゾキシストロビン、ジフェノコナゾール、またはイソピラザムである、請求項7に記載の製剤。
- R1が水素である、請求項9に記載の式(I)の化合物。
- R3が水素である、請求項9または10に記載の式(I)の化合物。
- nが1である、請求項9、10、または11に記載の式(I)の化合物。
- R2がメチルである、請求項9、10、11、または12に記載の式(I)の化合物。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB1012586.2A GB201012586D0 (en) | 2010-07-27 | 2010-07-27 | Formulations |
GB1012586.2 | 2010-07-27 | ||
PCT/IB2011/053325 WO2012014152A2 (en) | 2010-07-27 | 2011-07-26 | Formulations |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2013535464A true JP2013535464A (ja) | 2013-09-12 |
JP5847179B2 JP5847179B2 (ja) | 2016-01-20 |
Family
ID=42752855
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2013521273A Active JP5847179B2 (ja) | 2010-07-27 | 2011-07-26 | 製剤 |
Country Status (27)
Country | Link |
---|---|
US (1) | US9807999B2 (ja) |
EP (1) | EP2598472B1 (ja) |
JP (1) | JP5847179B2 (ja) |
KR (1) | KR101746806B1 (ja) |
CN (1) | CN103025704B (ja) |
AP (1) | AP2013006689A0 (ja) |
AR (1) | AR082394A1 (ja) |
AU (1) | AU2011284344B2 (ja) |
BR (1) | BR112013001956B1 (ja) |
CA (1) | CA2804730C (ja) |
CL (1) | CL2013000226A1 (ja) |
CO (1) | CO6680615A2 (ja) |
CR (1) | CR20130028A (ja) |
DK (1) | DK2598472T3 (ja) |
EA (1) | EA022772B1 (ja) |
ES (1) | ES2543029T3 (ja) |
GB (1) | GB201012586D0 (ja) |
MA (1) | MA34399B1 (ja) |
MX (1) | MX2013000740A (ja) |
MY (1) | MY161240A (ja) |
NI (1) | NI201300012A (ja) |
PL (1) | PL2598472T3 (ja) |
PT (1) | PT2598472E (ja) |
SG (1) | SG186858A1 (ja) |
UA (1) | UA112844C2 (ja) |
WO (1) | WO2012014152A2 (ja) |
ZA (1) | ZA201300196B (ja) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2017397235B2 (en) | 2017-01-31 | 2023-09-21 | Kimberly-Clark Worldwide, Inc. | Antibacterial composition including benzoic acid ester and methods of inhibiting bacterial growth utilizing the same |
Citations (2)
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JP2005501906A (ja) * | 2001-08-30 | 2005-01-20 | ヴェルシコル・ケミカル・コーポレイショーン | 液状安息香酸エステル組成物および可塑剤として当該エステルを含有する水性ポリマー組成物 |
JP2010513700A (ja) * | 2006-12-19 | 2010-04-30 | アリゾナ・ケミカル・カンパニー・エルエルシー | 架橋ポリマーマトリックス及び固定化された活性液を含有する組成物及び製品、並びにその製造法及び使用法 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
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US3649546A (en) * | 1967-05-15 | 1972-03-14 | Norac Co | Non-hazardous ketone peroxide polymerization initiators |
DE2443645A1 (de) * | 1974-09-12 | 1976-04-01 | Cassella Farbwerke Mainkur Ag | Modifizierter aminoplast, verfahren zu seiner herstellung und seine verwendung |
IL58111A (en) * | 1979-08-26 | 1984-04-30 | Yissum Res Dev Co | Emulsions of essential oils for citrus beverages |
EP0268927A3 (en) * | 1986-11-24 | 1990-01-10 | American Cyanamid Company | Resin-coated, non-sorptive granular, pesticidal compositions and method for the preparation thereof |
US5676742A (en) * | 1995-10-30 | 1997-10-14 | Velsicol Chemical Corporation | Mono and dibenzoate ester blends as caulk plasticizers that are bioresistant to fungal growth |
US6939551B2 (en) * | 2001-05-21 | 2005-09-06 | Coty Inc. | Cosmetic films |
ES2213467B1 (es) * | 2002-09-29 | 2005-06-01 | Condensia Quimica, S.A. | Mezcla de plastificantes para la dispersibilidad acuosa de resinas. |
GB0224316D0 (en) * | 2002-10-18 | 2002-11-27 | Syngenta Participations Ag | Chemical compounds |
CN101516966A (zh) * | 2006-02-10 | 2009-08-26 | 杜邦塔特和莱尔生物产品有限责任公司 | 包括生物学基1,3-丙二醇的单酯和二酯的组合物 |
EP2000485B1 (en) | 2007-05-29 | 2010-08-11 | Wacker Chemical Corporation | Formaldehyde-free emulsion polymer dispersion composition including fully hydrolyzed polyvinyl alcohol as colloidal stabilizer provding improved heat resistance |
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