DD151254A5 - Kristalline,insektizide zusammensetzung - Google Patents
Kristalline,insektizide zusammensetzung Download PDFInfo
- Publication number
- DD151254A5 DD151254A5 DD80221618A DD22161880A DD151254A5 DD 151254 A5 DD151254 A5 DD 151254A5 DD 80221618 A DD80221618 A DD 80221618A DD 22161880 A DD22161880 A DD 22161880A DD 151254 A5 DD151254 A5 DD 151254A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- cyano
- phenoxyphenyl
- methyl
- dichloroethenyl
- cis
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 57
- 239000002917 insecticide Substances 0.000 title description 2
- 230000000749 insecticidal effect Effects 0.000 claims abstract description 16
- 239000002728 pyrethroid Substances 0.000 claims abstract description 4
- 239000000546 pharmaceutical excipient Substances 0.000 claims abstract 2
- -1 2,2-dichloroethenyl Chemical group 0.000 claims description 21
- 241000238631 Hexapoda Species 0.000 claims description 14
- 150000001875 compounds Chemical class 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 8
- 239000013078 crystal Substances 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 5
- 239000000654 additive Substances 0.000 abstract description 3
- 239000000969 carrier Substances 0.000 abstract description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 21
- 239000000243 solution Substances 0.000 description 13
- 239000013543 active substance Substances 0.000 description 11
- 238000009472 formulation Methods 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
- 238000002425 crystallisation Methods 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000008025 crystallization Effects 0.000 description 6
- 241000196324 Embryophyta Species 0.000 description 5
- 241000462639 Epilachna varivestis Species 0.000 description 5
- 241001521235 Spodoptera eridania Species 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000002474 experimental method Methods 0.000 description 4
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 4
- 229960000490 permethrin Drugs 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- GXUQMKBQDGPMKZ-UHFFFAOYSA-N 2-hydroxy-2-(3-phenoxyphenyl)acetonitrile Chemical compound N#CC(O)C1=CC=CC(OC=2C=CC=CC=2)=C1 GXUQMKBQDGPMKZ-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 125000004093 cyano group Chemical group *C#N 0.000 description 3
- 238000011067 equilibration Methods 0.000 description 3
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 3
- 235000019341 magnesium sulphate Nutrition 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 241000253994 Acyrthosiphon pisum Species 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 241001674044 Blattodea Species 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 241000256244 Heliothis virescens Species 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- JSPIZDHQQLEUMP-BDZCPYMJSA-N OA-PS Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@H](COP(O)(=O)OC[C@H](N)C(O)=O)OC(=O)CCCCCCCC(O)=O JSPIZDHQQLEUMP-BDZCPYMJSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 2
- 241000256247 Spodoptera exigua Species 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 241000209149 Zea Species 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical class OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 description 2
- 125000000950 dibromo group Chemical group Br* 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 238000006345 epimerization reaction Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000012452 mother liquor Substances 0.000 description 2
- 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 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000005303 weighing Methods 0.000 description 2
- ZMQDHPCRIFFYAV-UHFFFAOYSA-N (3-phenoxyphenyl)methanesulfonic acid Chemical compound O(C1=CC=CC=C1)C=1C=C(C=CC=1)CS(=O)(=O)O ZMQDHPCRIFFYAV-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- OHAMOQALFCXZBV-UHFFFAOYSA-N 2,2-dichloroethenyl 2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)CC1C(=O)OC=C(Cl)Cl OHAMOQALFCXZBV-UHFFFAOYSA-N 0.000 description 1
- ZQDDFKMLOJICSL-UHFFFAOYSA-N 2,2-dichloroethenyl cyclopropanecarboxylate Chemical compound ClC(Cl)=COC(=O)C1CC1 ZQDDFKMLOJICSL-UHFFFAOYSA-N 0.000 description 1
- QQNQOWHUBGUGQI-UHFFFAOYSA-N 2,2-dimethylcyclopropane-1-carbonyl chloride Chemical compound CC1(C)CC1C(Cl)=O QQNQOWHUBGUGQI-UHFFFAOYSA-N 0.000 description 1
- BFNMOMYTTGHNGJ-UHFFFAOYSA-N 2,2-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)CC1C(O)=O BFNMOMYTTGHNGJ-UHFFFAOYSA-N 0.000 description 1
- LLMLSUSAKZVFOA-UHFFFAOYSA-N 3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylic acid Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(O)=O LLMLSUSAKZVFOA-UHFFFAOYSA-N 0.000 description 1
- 241000253988 Acyrthosiphon Species 0.000 description 1
- 240000007124 Brassica oleracea Species 0.000 description 1
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 241001301805 Epilachna Species 0.000 description 1
- 241000258914 Oncopeltus Species 0.000 description 1
- 241000258913 Oncopeltus fasciatus Species 0.000 description 1
- 241001674048 Phthiraptera Species 0.000 description 1
- 241000256248 Spodoptera Species 0.000 description 1
- 241000255985 Trichoplusia Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000013375 chromatographic separation Methods 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 238000013270 controlled release Methods 0.000 description 1
- 239000000599 controlled substance Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- AYJZNWVARKKPFW-UHFFFAOYSA-N cyano 2-(2,2-dichloroethenyl)-1,3,3-trimethyl-2-(3-phenoxyphenyl)cyclopropane-1-carboxylate Chemical compound CC1(C)C(C)(C(=O)OC#N)C1(C=C(Cl)Cl)C1=CC=CC(OC=2C=CC=CC=2)=C1 AYJZNWVARKKPFW-UHFFFAOYSA-N 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000012377 drug delivery Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 244000013123 dwarf bean Species 0.000 description 1
- 210000005069 ears Anatomy 0.000 description 1
- 239000004495 emulsifiable concentrate Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 230000006911 nucleation Effects 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000004557 technical material Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 231100000167 toxic agent Toxicity 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/08—Oxygen or sulfur directly attached to an aromatic ring system
- A01N31/14—Ethers
-
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- 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
- A01N37/36—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 containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—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 containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/046,147 US4261921A (en) | 1979-06-06 | 1979-06-06 | Process for preparation of a crystalline insecticidal pyrethroid enantiomer pair |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD151254A5 true DD151254A5 (de) | 1981-10-14 |
Family
ID=21941871
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD80221618A DD151254A5 (de) | 1979-06-06 | 1980-06-05 | Kristalline,insektizide zusammensetzung |
| DD80227655A DD156364A5 (de) | 1979-06-06 | 1980-06-05 | Verfahren zur herstellung eines kristallinen insektiziden pyrethroids |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD80227655A DD156364A5 (de) | 1979-06-06 | 1980-06-05 | Verfahren zur herstellung eines kristallinen insektiziden pyrethroids |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US4261921A (en:Method) |
| EP (1) | EP0022382B1 (en:Method) |
| JP (1) | JPS55164608A (en:Method) |
| KR (1) | KR840000184B1 (en:Method) |
| AR (1) | AR240800A1 (en:Method) |
| AU (1) | AU535625B2 (en:Method) |
| BR (2) | BR8003509A (en:Method) |
| CA (1) | CA1145255A (en:Method) |
| CY (1) | CY1289A (en:Method) |
| DD (2) | DD151254A5 (en:Method) |
| DE (1) | DE3066678D1 (en:Method) |
| DK (1) | DK170469B1 (en:Method) |
| EG (1) | EG14484A (en:Method) |
| HK (1) | HK50985A (en:Method) |
| HU (1) | HU184783B (en:Method) |
| IL (1) | IL60085A (en:Method) |
| IN (1) | IN154326B (en:Method) |
| MX (1) | MX6813E (en:Method) |
| OA (1) | OA06544A (en:Method) |
| SG (1) | SG15785G (en:Method) |
| SU (2) | SU1431661A3 (en:Method) |
| TR (1) | TR20425A (en:Method) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5657756A (en) * | 1979-10-15 | 1981-05-20 | Sumitomo Chem Co Ltd | Preparation of more highly active carboxylic ester |
| CA1150301A (en) * | 1979-11-27 | 1983-07-19 | Michael J. Bull | Cyclopropane carboxylic acid ester derivatives |
| CA1162560A (en) * | 1980-04-23 | 1984-02-21 | Ronald F. Mason | Process for preparing cyclopropane carboxylic acid ester derivatives |
| CA1150730A (en) * | 1980-04-23 | 1983-07-26 | Michael J. Bull | Process for preparing cyclopropane carboxylic acid ester derivatives |
| CA1206483A (en) * | 1982-11-11 | 1986-06-24 | Johannes Van Berkel | Process for preparing cyclopropane carboxylic acid ester derivatives |
| CA1275108A (en) * | 1985-01-16 | 1990-10-09 | Laszlo Pap | Insecticidal composition comprising more than one active ingredients |
| HU198373B (en) * | 1986-01-08 | 1989-10-30 | Chinoin Gyogyszer Es Vegyeszet | Artropodicide composition containing trans-cipermetrin isomeres and process for producing the active components |
| CA1314559C (en) * | 1987-06-15 | 1993-03-16 | John Winfrid Ager | Conversion of pyrethroid isomers to more active species |
| JPH0554208U (ja) * | 1991-12-24 | 1993-07-20 | ストラパック株式会社 | 梱包機のバンドリ−ルおよびバンドリ−ルのシャフト |
| US5439690A (en) * | 1993-05-21 | 1995-08-08 | Ecosmart, Inc. | Non-hazardous pest control |
| FR2713954B1 (fr) * | 1993-12-22 | 1996-01-12 | Roussel Uclaf | Nouveau procédé de préparation d'émulsion ou de suspoémulsion sèche ou extrudée sous forme de granulés et granulés obtenus. |
| US5840958A (en) * | 1996-10-17 | 1998-11-24 | Fmc Corporation | 1S to 1R Epimerizations of pyrethroid intermediates |
| RU2179805C1 (ru) * | 2000-11-30 | 2002-02-27 | Закрытое акционерное общество "Щелково Агрохим" | Масляный инсектицидный препарат на основе пиретроидов |
| RU2185061C1 (ru) * | 2000-11-30 | 2002-07-20 | Закрытое акционерное общество "Щелково Агрохим" | Инсектицидный препарат на основе циперметрина |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4024163A (en) * | 1972-05-25 | 1977-05-17 | National Research Development Corporation | Insecticides |
| IE41614B1 (en) * | 1973-08-15 | 1980-02-13 | Nat Res Dev | Substituted 2,2-dimethyl cylopropane carboxylic acid estersprocess for their preperation and their use as insecticides |
| FR2375161A1 (fr) * | 1976-04-23 | 1978-07-21 | Roussel Uclaf | Procede de transformation d'un ester d'acide chiral d'alcool secondaire a-cyane optiquement actif de structure (r) en ester d'acide chiral d'alcool secondaire a-cyane de structure (s) |
| FR2348901A1 (fr) * | 1976-04-23 | 1977-11-18 | Roussel Uclaf | Procede de transformation d'un ester d'acide chiral d'alcool secondaire alpha-cyane optiquement actif en ester d'acide chiral d'alcool secondaire alpha-cyane racemique |
| FR2382422A2 (fr) * | 1977-03-02 | 1978-09-29 | Roussel Uclaf | Procede de transformation d'un ester d'acide chiral d'alcool secondaire a-cyane optiquement actif de structure r en ester d'acide chiral d'alcool secondaire a-cyane de structure s |
| FR2383147A2 (fr) * | 1977-03-09 | 1978-10-06 | Roussel Uclaf | Procede de transformation d'un ester d'acide chiral d'alcool secondaire a-cyane optiquement actif en ester d'acide chiral d'alcool secondaire a-cyane racemique |
| DE2713538A1 (de) * | 1977-03-26 | 1978-09-28 | Bayer Ag | Verfahren zur trennung stereoisomerer cyclischer carbonsaeuren |
| GB1599876A (en) | 1977-06-13 | 1981-10-07 | Shell Int Research | Conversion of a stereoisomer into its diastereoisomer |
| US4308279A (en) * | 1979-06-06 | 1981-12-29 | Fmc Corporation | Crystalline, insecticidal pyrethroid |
-
1979
- 1979-06-06 US US06/046,147 patent/US4261921A/en not_active Expired - Lifetime
-
1980
- 1980-05-12 IN IN345/DEL/80A patent/IN154326B/en unknown
- 1980-05-13 CA CA000351832A patent/CA1145255A/en not_active Expired
- 1980-05-15 IL IL60085A patent/IL60085A/xx unknown
- 1980-05-26 MX MX808844U patent/MX6813E/es unknown
- 1980-06-03 CY CY1289A patent/CY1289A/xx unknown
- 1980-06-03 AR AR281283A patent/AR240800A1/es active
- 1980-06-03 EP EP80400793A patent/EP0022382B1/en not_active Expired
- 1980-06-03 DE DE8080400793T patent/DE3066678D1/de not_active Expired
- 1980-06-04 EG EG80343A patent/EG14484A/xx active
- 1980-06-04 BR BR8003509A patent/BR8003509A/pt not_active IP Right Cessation
- 1980-06-04 TR TR20425A patent/TR20425A/xx unknown
- 1980-06-04 BR BR8003522A patent/BR8003522A/pt not_active IP Right Cessation
- 1980-06-04 DK DK241380A patent/DK170469B1/da not_active IP Right Cessation
- 1980-06-05 KR KR1019800002223A patent/KR840000184B1/ko not_active Expired
- 1980-06-05 JP JP7498980A patent/JPS55164608A/ja active Granted
- 1980-06-05 DD DD80221618A patent/DD151254A5/de unknown
- 1980-06-05 SU SU802931801A patent/SU1431661A3/ru active
- 1980-06-05 DD DD80227655A patent/DD156364A5/de unknown
- 1980-06-05 AU AU59075/80A patent/AU535625B2/en not_active Expired
- 1980-06-06 HU HU801433A patent/HU184783B/hu unknown
- 1980-06-06 OA OA57128A patent/OA06544A/xx unknown
- 1980-12-15 SU SU803217248A patent/SU1169529A3/ru active
-
1985
- 1985-02-27 SG SG157/85A patent/SG15785G/en unknown
- 1985-07-04 HK HK509/85A patent/HK50985A/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| IL60085A (en) | 1983-07-31 |
| TR20425A (tr) | 1981-07-02 |
| KR840000184B1 (ko) | 1984-02-28 |
| HU184783B (en) | 1984-10-29 |
| DK170469B1 (da) | 1995-09-11 |
| EG14484A (en) | 1985-03-31 |
| CY1289A (en) | 1985-10-18 |
| DK241380A (da) | 1980-12-07 |
| HK50985A (en) | 1985-07-12 |
| SU1169529A3 (ru) | 1985-07-23 |
| MX6813E (es) | 1986-08-04 |
| AU5907580A (en) | 1980-12-11 |
| IL60085A0 (en) | 1980-07-31 |
| JPS55164608A (en) | 1980-12-22 |
| EP0022382A1 (en) | 1981-01-14 |
| CA1145255A (en) | 1983-04-26 |
| US4261921A (en) | 1981-04-14 |
| BR8003509A (pt) | 1981-01-05 |
| DE3066678D1 (en) | 1984-03-29 |
| JPH0231708B2 (en:Method) | 1990-07-16 |
| DD156364A5 (de) | 1982-08-18 |
| IN154326B (en:Method) | 1984-10-20 |
| AR240800A2 (es) | 1991-02-28 |
| AR240800A1 (es) | 1991-02-28 |
| AU535625B2 (en) | 1984-03-29 |
| SU1431661A3 (ru) | 1988-10-15 |
| BR8003522A (pt) | 1981-01-05 |
| KR830002321A (ko) | 1983-05-28 |
| OA06544A (fr) | 1981-07-31 |
| EP0022382B1 (en) | 1984-02-22 |
| SG15785G (en) | 1985-08-16 |
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