NO792544L - Insekticide komposisjoner og fremstilling av disse - Google Patents

Insekticide komposisjoner og fremstilling av disse

Info

Publication number: NO792544L
Authority: NO; Norway
Prior art keywords: microcapsules; methomyl; diisocyanate; insecticide; polyisocyanate
Prior art date: 1978-08-03

Application number

NO792544A

Other languages

English (en)

Norwegian (no)

Inventor

Robert Thomas Roche

Original Assignee

Du Pont

Priority date (The priority date 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 date listed.)

1978-08-03

Filing date

1979-08-02

Publication date

1980-02-05

1979-08-02 Application filed by Du Pont filed Critical Du Pont

1980-02-05 Publication of NO792544L publication Critical patent/NO792544L/no

Links

239000000203 mixture Substances 0.000 title claims description 44
239000002917 insecticide Substances 0.000 title claims description 28
238000004519 manufacturing process Methods 0.000 title claims description 4
239000003094 microcapsule Substances 0.000 claims description 55
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 51
239000005916 Methomyl Substances 0.000 claims description 38
UHXUZOCRWCRNSJ-QPJJXVBHSA-N methomyl Chemical compound CNC(=O)O\N=C(/C)SC UHXUZOCRWCRNSJ-QPJJXVBHSA-N 0.000 claims description 38
239000005950 Oxamyl Substances 0.000 claims description 19
KZAUOCCYDRDERY-UHFFFAOYSA-N oxamyl Chemical compound CNC(=O)ON=C(SC)C(=O)N(C)C KZAUOCCYDRDERY-UHFFFAOYSA-N 0.000 claims description 19
125000005442 diisocyanate group Chemical group 0.000 claims description 16
238000000034 method Methods 0.000 claims description 16
239000005056 polyisocyanate Substances 0.000 claims description 16
229920001228 polyisocyanate Polymers 0.000 claims description 16
239000004094 surface-active agent Substances 0.000 claims description 15
229920002396 Polyurea Polymers 0.000 claims description 14
150000001412 amines Chemical class 0.000 claims description 14
239000002245 particle Substances 0.000 claims description 12
229920000768 polyamine Polymers 0.000 claims description 11
229920000642 polymer Polymers 0.000 claims description 11
238000005538 encapsulation Methods 0.000 claims description 10
NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 claims description 10
150000004985 diamines Chemical class 0.000 claims description 9
230000000749 insecticidal effect Effects 0.000 claims description 9
239000000839 emulsion Substances 0.000 claims description 7
239000012948 isocyanate Substances 0.000 claims description 7
-1 diflubehzuron Chemical compound 0.000 claims description 6
STUSTWKEFDQFFZ-UHFFFAOYSA-N Chlordimeform Chemical compound CN(C)C=NC1=CC=C(Cl)C=C1C STUSTWKEFDQFFZ-UHFFFAOYSA-N 0.000 claims description 5
239000005946 Cypermethrin Substances 0.000 claims description 5
KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 claims description 5
229960005424 cypermethrin Drugs 0.000 claims description 5
229960002483 decamethrin Drugs 0.000 claims description 5
OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 claims description 5
LCCNCVORNKJIRZ-UHFFFAOYSA-N parathion Chemical compound CCOP(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 LCCNCVORNKJIRZ-UHFFFAOYSA-N 0.000 claims description 5
RLBIQVVOMOPOHC-UHFFFAOYSA-N parathion-methyl Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C=C1 RLBIQVVOMOPOHC-UHFFFAOYSA-N 0.000 claims description 5
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 claims description 5
229960000490 permethrin Drugs 0.000 claims description 5
239000005893 Diflubenzuron Substances 0.000 claims description 4
QGLZXHRNAYXIBU-WEVVVXLNSA-N aldicarb Chemical compound CNC(=O)O\N=C\C(C)(C)SC QGLZXHRNAYXIBU-WEVVVXLNSA-N 0.000 claims description 4
CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 claims description 4
229960005286 carbaryl Drugs 0.000 claims description 4
229940019503 diflubenzuron Drugs 0.000 claims description 4
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical group NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims description 3
239000004793 Polystyrene Substances 0.000 claims description 3
229920003229 poly(methyl methacrylate) Polymers 0.000 claims description 3
239000004926 polymethyl methacrylate Substances 0.000 claims description 3
229920002223 polystyrene Polymers 0.000 claims description 3
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical group CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 3
229920000538 Poly[(phenyl isocyanate)-co-formaldehyde] Polymers 0.000 claims description 2
238000006243 chemical reaction Methods 0.000 claims description 2
QQQYTWIFVNKMRW-UHFFFAOYSA-N diflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC=C(Cl)C=C1 QQQYTWIFVNKMRW-UHFFFAOYSA-N 0.000 claims 1
125000003916 ethylene diamine group Chemical group 0.000 claims 1
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 1
239000000243 solution Substances 0.000 description 26
238000009472 formulation Methods 0.000 description 14
241000196324 Embryophyta Species 0.000 description 10
239000012074 organic phase Substances 0.000 description 10
238000003756 stirring Methods 0.000 description 10
239000004480 active ingredient Substances 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
241000238631 Hexapoda Species 0.000 description 7
239000008346 aqueous phase Substances 0.000 description 7
230000000694 effects Effects 0.000 description 7
239000000047 product Substances 0.000 description 7
238000004458 analytical method Methods 0.000 description 6
150000002513 isocyanates Chemical class 0.000 description 6
239000007788 liquid Substances 0.000 description 6
229920002451 polyvinyl alcohol Polymers 0.000 description 6
239000000843 powder Substances 0.000 description 6
239000002002 slurry Substances 0.000 description 6
150000001875 compounds Chemical class 0.000 description 5
239000003085 diluting agent Substances 0.000 description 5
230000001976 improved effect Effects 0.000 description 5
230000002829 reductive effect Effects 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
239000004372 Polyvinyl alcohol Substances 0.000 description 4
239000006185 dispersion Substances 0.000 description 4
239000000575 pesticide Substances 0.000 description 4
238000006116 polymerization reaction Methods 0.000 description 4
XUNYDVLIZWUPAW-UHFFFAOYSA-N (4-chlorophenyl) n-(4-methylphenyl)sulfonylcarbamate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(=O)OC1=CC=C(Cl)C=C1 XUNYDVLIZWUPAW-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
241000244206 Nematoda Species 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 3
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
241000607479 Yersinia pestis Species 0.000 description 3
239000007864 aqueous solution Substances 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
238000001816 cooling Methods 0.000 description 3
238000002955 isolation Methods 0.000 description 3
239000000463 material Substances 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000000178 monomer Substances 0.000 description 3
239000005645 nematicide Substances 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
239000007787 solid Substances 0.000 description 3
239000007921 spray Substances 0.000 description 3
229920000742 Cotton Polymers 0.000 description 2
AIGRXSNSLVJMEA-UHFFFAOYSA-N EPN Chemical compound C=1C=CC=CC=1P(=S)(OCC)OC1=CC=C([N+]([O-])=O)C=C1 AIGRXSNSLVJMEA-UHFFFAOYSA-N 0.000 description 2
IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 2
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
241000219146 Gossypium Species 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
241000124008 Mammalia Species 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
231100000674 Phytotoxicity Toxicity 0.000 description 2
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
125000000066 S-methyl group Chemical group [H]C([H])([H])S* 0.000 description 2
239000007900 aqueous suspension Substances 0.000 description 2
238000005119 centrifugation Methods 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
238000001035 drying Methods 0.000 description 2
230000001804 emulsifying effect Effects 0.000 description 2
238000001914 filtration Methods 0.000 description 2
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
230000001069 nematicidal effect Effects 0.000 description 2
238000012856 packing Methods 0.000 description 2
KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
239000002689 soil Substances 0.000 description 2
239000011343 solid material Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
241000894007 species Species 0.000 description 2
RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 2
AYCUWIWOZKQLMI-UHFFFAOYSA-N 1,2,3,5-tetrachloro-4,6-diisocyanatobenzene Chemical compound ClC1=C(Cl)C(N=C=O)=C(Cl)C(N=C=O)=C1Cl AYCUWIWOZKQLMI-UHFFFAOYSA-N 0.000 description 1
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 1
SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 1
ICLCCFKUSALICQ-UHFFFAOYSA-N 1-isocyanato-4-(4-isocyanato-3-methylphenyl)-2-methylbenzene Chemical compound C1=C(N=C=O)C(C)=CC(C=2C=C(C)C(N=C=O)=CC=2)=C1 ICLCCFKUSALICQ-UHFFFAOYSA-N 0.000 description 1
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 1
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
241000254171 Curculionidae Species 0.000 description 1
240000002024 Gossypium herbaceum Species 0.000 description 1
235000004341 Gossypium herbaceum Nutrition 0.000 description 1
239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
GQSIVKYXTYPKIX-UHFFFAOYSA-N N=C=O.N=C=O.C=1C=CC=CC=1C(Cl)(Cl)C1=CC=CC=C1 Chemical compound N=C=O.N=C=O.C=1C=CC=CC=1C(Cl)(Cl)C1=CC=CC=C1 GQSIVKYXTYPKIX-UHFFFAOYSA-N 0.000 description 1
WMTLVUCMBWBYSO-UHFFFAOYSA-N N=C=O.N=C=O.C=1C=CC=CC=1OC1=CC=CC=C1 Chemical class N=C=O.N=C=O.C=1C=CC=CC=1OC1=CC=CC=C1 WMTLVUCMBWBYSO-UHFFFAOYSA-N 0.000 description 1
241000341511 Nematodes Species 0.000 description 1
241000305186 Persectania ewingii Species 0.000 description 1
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
240000001417 Vigna umbellata Species 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000011149 active material Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
239000002775 capsule Substances 0.000 description 1
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 1
239000000969 carrier Substances 0.000 description 1
UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical compound [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 description 1
230000000295 complement effect Effects 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
239000003599 detergent Substances 0.000 description 1
238000007865 diluting Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000007613 environmental effect Effects 0.000 description 1
238000005187 foaming Methods 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000003701 inert diluent Substances 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
238000004811 liquid chromatography Methods 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
230000002906 microbiologic effect Effects 0.000 description 1
LSHROXHEILXKHM-UHFFFAOYSA-N n'-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCN LSHROXHEILXKHM-UHFFFAOYSA-N 0.000 description 1
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
239000007764 o/w emulsion Substances 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
231100000208 phytotoxic Toxicity 0.000 description 1
230000000885 phytotoxic effect Effects 0.000 description 1
231100000614 poison Toxicity 0.000 description 1
239000002574 poison Substances 0.000 description 1
238000012643 polycondensation polymerization Methods 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
150000003335 secondary amines Chemical group 0.000 description 1
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
239000002195 soluble material Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000006228 supernatant Substances 0.000 description 1
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000002023 wood Substances 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
- 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
- A01N25/26—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 in coated particulate form
- A01N25/28—Microcapsules or nanocapsules
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Agronomy & Crop Science (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

NO792544A 1978-08-03 1979-08-02 Insekticide komposisjoner og fremstilling av disse NO792544L (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US93076078A	1978-08-03	1978-08-03
US4219179A	1979-05-29	1979-05-29

Publications (1)

Publication Number	Publication Date
NO792544L true NO792544L (no)	1980-02-05

Family

ID=26718967

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO792544A NO792544L (no)	1978-08-03	1979-08-02	Insekticide komposisjoner og fremstilling av disse

Country Status (23)

Country	Link
EP (1)	EP0008207B1 (da)
AU (1)	AU527286B2 (da)
BG (2)	BG31480A3 (da)
BR (1)	BR7904857A (da)
CA (1)	CA1131560A (da)
DE (1)	DE2961508D1 (da)
DK (1)	DK253779A (da)
EG (1)	EG14188A (da)
ES (1)	ES483119A1 (da)
GB (1)	GB2027346B (da)
GR (1)	GR69852B (da)
HU (1)	HU181870B (da)
IL (1)	IL57960A (da)
KE (1)	KE3263A (da)
MA (1)	MA18551A1 (da)
NO (1)	NO792544L (da)
NZ (1)	NZ191195A (da)
OA (1)	OA06309A (da)
PH (1)	PH15548A (da)
PT (1)	PT70017A (da)
RO (1)	RO77008A (da)
TR (1)	TR20266A (da)
ZM (1)	ZM6679A1 (da)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4280833A (en) *	1979-03-26	1981-07-28	Monsanto Company	Encapsulation by interfacial polycondensation, and aqueous herbicidal composition containing microcapsules produced thereby
DE3685920D1 (de) *	1985-09-13	1992-08-13	Ciba Geigy Ag	Verfahren zur herstellung von mikrokapseln.
GB8603061D0 (en) *	1986-02-07	1986-03-12	Wellcome Found	Pesticidal formulations
US5229122A (en) *	1986-02-07	1993-07-20	Burroughs Wellcome Co.	Pesticidal compositions
DE3789078T2 (de) *	1986-07-09	1994-08-11	Monsanto Co	Formulierungen von wasserdispergierbaren Granulaten und Verfahren zu deren Herstellung.
JPH0818937B2 (ja) *	1987-07-06	1996-02-28	住友化学工業株式会社	農園芸用有機燐系殺虫組成物
JP2524201B2 (ja) *	1988-08-22	1996-08-14	日本特殊陶業株式会社	窒化珪素質焼結体及びその製造方法
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1979
- 1979-06-18 DK DK253779A patent/DK253779A/da unknown
- 1979-07-30 BR BR7904857A patent/BR7904857A/pt unknown
- 1979-08-01 RO RO7998332A patent/RO77008A/ro unknown
- 1979-08-01 MA MA18749A patent/MA18551A1/fr unknown
- 1979-08-01 EG EG467/79A patent/EG14188A/xx active
- 1979-08-01 CA CA333,004A patent/CA1131560A/en not_active Expired
- 1979-08-02 IL IL57960A patent/IL57960A/xx unknown
- 1979-08-02 NZ NZ191195A patent/NZ191195A/xx unknown
- 1979-08-02 TR TR20266A patent/TR20266A/xx unknown
- 1979-08-02 AU AU49504/79A patent/AU527286B2/en not_active Ceased
- 1979-08-02 NO NO792544A patent/NO792544L/no unknown
- 1979-08-02 PT PT70017A patent/PT70017A/pt unknown
- 1979-08-02 OA OA56864A patent/OA06309A/xx unknown
- 1979-08-02 PH PH22843A patent/PH15548A/en unknown
- 1979-08-03 BG BG044550A patent/BG31480A3/xx unknown
- 1979-08-03 BG BG048676A patent/BG31481A3/xx unknown
- 1979-08-03 ES ES483119A patent/ES483119A1/es not_active Expired
- 1979-08-03 GB GB7927101A patent/GB2027346B/en not_active Expired
- 1979-08-03 HU HU79DU313A patent/HU181870B/hu unknown
- 1979-08-03 EP EP79301568A patent/EP0008207B1/en not_active Expired
- 1979-08-03 GR GR59768A patent/GR69852B/el unknown
- 1979-08-03 ZM ZM66/79A patent/ZM6679A1/xx unknown
- 1979-08-03 DE DE7979301568T patent/DE2961508D1/de not_active Expired
1983
- 1983-02-25 KE KE3263A patent/KE3263A/xx unknown

Also Published As

Publication number	Publication date
BG31480A3 (en)	1982-01-15
DK253779A (da)	1980-02-04
GR69852B (da)	1982-07-19
ZM6679A1 (en)	1981-02-23
AU4950479A (en)	1980-02-07
ES483119A1 (es)	1980-09-01
EG14188A (en)	1983-12-31
MA18551A1 (fr)	1980-04-01
BR7904857A (pt)	1980-05-06
NZ191195A (en)	1981-12-15
EP0008207B1 (en)	1981-12-02
GB2027346A (en)	1980-02-20
EP0008207A2 (en)	1980-02-20
KE3263A (en)	1983-03-25
CA1131560A (en)	1982-09-14
IL57960A (en)	1982-04-30
IL57960A0 (en)	1979-12-30
AU527286B2 (en)	1983-02-24
PT70017A (en)	1979-09-01
DE2961508D1 (en)	1982-01-28
PH15548A (en)	1983-02-09
BG31481A3 (en)	1982-01-15
RO77008A (ro)	1981-08-30
GB2027346B (en)	1982-08-04
HU181870B (en)	1983-11-28
OA06309A (fr)	1981-06-30
EP0008207A3 (en)	1980-03-05
TR20266A (tr)	1980-12-08

Publication	Publication Date	Title
NO792544L (no)	1980-02-05	Insekticide komposisjoner og fremstilling av disse
US4235872A (en)	1980-11-25	Microencapsulated methomyl insecticide
CA2225052C (en)	2008-08-19	Herbicidal compositions
AU734072B2 (en)	2001-05-31	Microcapsules with readily adjustable release rates
AU711932B2 (en)	1999-10-21	Microencapsulated compositions
DK149341B (da)	1986-05-12	Fremgangsmaade til indkapsling af hydrofobe stoffer ved graensefladepolykondensation
US6133197A (en)	2000-10-17	Microencapsulated compositions
CN103298338B (zh)	2016-02-10	包含包封农药的农业化学配制剂
BG64638B1 (bg)	2005-10-31	Микрокапсули, отделящи под действието на киселина
EP0005302A2 (en)	1979-11-14	Impregnated porous granules with slow-release pore membranes, and process for the manufacture thereof
HU215771B (hu)	2000-09-28	2-Klór-N-(etoxi-metil)-6'-etil-o-aceto-toluidid herbicidet tartalmazó kapszulák és eljárás előállításukra
CN107529756B (zh)	2020-12-29	具有磺酸盐和共分散剂的微胶囊的农用配制剂
US20020068169A1 (en)	2002-06-06	Acid-triggered microcapsules
US20150373979A1 (en)	2015-12-31	Agrochemical composition, method for its preparation and use thereof
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EA018830B1 (ru)	2013-11-29	Стабилизированные препараты микрокапсул карбофоса
JP7692268B2 (ja)	2025-06-13	マイクロカプセル農薬組成物
KR830001488B1 (ko)	1983-08-03	살충제 조성물의 제조방법
CN109414015A (zh)	2019-03-01	囊化有λ-氯氟氰菊酯的微囊剂
KR100481932B1 (ko)	2005-07-18	마이크로캡슐화된조성물
KR930002952B1 (ko)	1993-04-16	마이크로 캡슐화된 아세토클로르
CS210682B2 (en)	1982-01-29	Herbicides in microcapsule form
JP2012017266A (ja)	2012-01-26	マイクロカプセル混合農薬組成物
MXPA00002307A (en)	2001-12-04	Microcapsules with readily adjustable release rates
CZ2000748A3 (cs)	2000-09-13	Mikrotobolky se snadno nastavitelnými poměry uvolňování