IL29613A - Insecticidal baits and process for their production - Google Patents
Insecticidal baits and process for their productionInfo
- Publication number
- IL29613A IL29613A IL29613A IL2961368A IL29613A IL 29613 A IL29613 A IL 29613A IL 29613 A IL29613 A IL 29613A IL 2961368 A IL2961368 A IL 2961368A IL 29613 A IL29613 A IL 29613A
- Authority
- IL
- Israel
- Prior art keywords
- baits
- insecticidal
- carbamate
- methyl
- insect
- Prior art date
Links
- 230000000749 insecticidal effect Effects 0.000 title claims description 44
- 238000004519 manufacturing process Methods 0.000 title claims description 34
- 238000000034 method Methods 0.000 title claims description 21
- 239000000126 substance Substances 0.000 claims description 35
- 239000006260 foam Substances 0.000 claims description 19
- 150000003014 phosphoric acid esters Chemical class 0.000 claims description 19
- 239000011496 polyurethane foam Substances 0.000 claims description 16
- 229920005830 Polyurethane Foam Polymers 0.000 claims description 15
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 12
- 239000000654 additive Substances 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 11
- 229920005862 polyol Polymers 0.000 claims description 11
- 150000003077 polyols Chemical class 0.000 claims description 11
- 235000000346 sugar Nutrition 0.000 claims description 11
- 238000004040 coloring Methods 0.000 claims description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 9
- 241000238631 Hexapoda Species 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 239000012190 activator Substances 0.000 claims description 7
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- 229910019142 PO4 Inorganic materials 0.000 claims description 4
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 4
- JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical group O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 claims description 4
- 239000010452 phosphate Substances 0.000 claims description 4
- 229920001228 polyisocyanate Polymers 0.000 claims description 4
- 239000005056 polyisocyanate Substances 0.000 claims description 4
- 230000000996 additive effect Effects 0.000 claims description 3
- 238000005187 foaming Methods 0.000 claims description 3
- 239000004615 ingredient Substances 0.000 claims description 3
- BJKAYAOLECUCOJ-UHFFFAOYSA-N methyl-(2-methyl-2,3-dihydro-1-benzofuran-7-yl)carbamic acid Chemical compound C1=CC(N(C)C(O)=O)=C2OC(C)CC2=C1 BJKAYAOLECUCOJ-UHFFFAOYSA-N 0.000 claims description 3
- 108090000623 proteins and genes Proteins 0.000 claims description 3
- 102000004169 proteins and genes Human genes 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 239000005864 Sulphur Substances 0.000 claims description 2
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 229920001577 copolymer Polymers 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 229920001169 thermoplastic Polymers 0.000 claims description 2
- 239000004416 thermosoftening plastic Substances 0.000 claims description 2
- 241000607479 Yersinia pestis Species 0.000 claims 2
- CCLLNDNOXJTSFT-UHFFFAOYSA-N methyl-(2-prop-2-ynoxyphenyl)carbamic acid Chemical compound CN(C1=CC=CC=C1OCC#C)C(=O)O CCLLNDNOXJTSFT-UHFFFAOYSA-N 0.000 claims 2
- SASWHAXCWDSVBC-UHFFFAOYSA-N CC1(C)OC2=C(CC(N(C)C(O)=O)=O)C=CC=C2C1 Chemical compound CC1(C)OC2=C(CC(N(C)C(O)=O)=O)C=CC=C2C1 SASWHAXCWDSVBC-UHFFFAOYSA-N 0.000 claims 1
- 230000001419 dependent effect Effects 0.000 claims 1
- ZJUGAXARPHQZMX-UHFFFAOYSA-N dihydroxy-(3-methyl-4-nitrophenoxy)-sulfanylidene-$l^{5}-phosphane Chemical compound CC1=CC(OP(O)(O)=S)=CC=C1[N+]([O-])=O ZJUGAXARPHQZMX-UHFFFAOYSA-N 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 35
- 241000255925 Diptera Species 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 10
- 239000012876 carrier material Substances 0.000 description 10
- 239000000123 paper Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- 239000002904 solvent Substances 0.000 description 7
- 229920001131 Pulp (paper) Polymers 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 229920000570 polyether Polymers 0.000 description 4
- 241000257159 Musca domestica Species 0.000 description 3
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 239000004872 foam stabilizing agent Substances 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- -1 yeast Chemical compound 0.000 description 3
- ALKYHXVLJMQRLQ-UHFFFAOYSA-N 3-Hydroxy-2-naphthoate Chemical compound C1=CC=C2C=C(O)C(C(=O)O)=CC2=C1 ALKYHXVLJMQRLQ-UHFFFAOYSA-N 0.000 description 2
- 229930091371 Fructose Natural products 0.000 description 2
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 2
- 239000005715 Fructose Substances 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000011111 cardboard Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000002360 explosive Substances 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 239000004088 foaming agent Substances 0.000 description 2
- 229930182830 galactose Natural products 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 230000002045 lasting effect Effects 0.000 description 2
- 150000002772 monosaccharides Chemical class 0.000 description 2
- 235000008476 powdered milk Nutrition 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000001054 red pigment Substances 0.000 description 2
- 150000008163 sugars Chemical class 0.000 description 2
- GGPLWEZGITVTJX-UHFFFAOYSA-N 2,2,4-trimethyl-1,4,2-oxazasilinane Chemical compound CN1CCO[Si](C)(C)C1 GGPLWEZGITVTJX-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
- SHIILERBXRETDI-UHFFFAOYSA-N 3-amino-n-[2-[(3-amino-4-methoxyphenyl)sulfonylamino]ethyl]-4-methoxybenzenesulfonamide Chemical compound C1=C(N)C(OC)=CC=C1S(=O)(=O)NCCNS(=O)(=O)C1=CC=C(OC)C(N)=C1 SHIILERBXRETDI-UHFFFAOYSA-N 0.000 description 1
- IMPPGHMHELILKG-UHFFFAOYSA-N 4-ethoxyaniline Chemical compound CCOC1=CC=C(N)C=C1 IMPPGHMHELILKG-UHFFFAOYSA-N 0.000 description 1
- OLCMNCWEUMBNIS-UHFFFAOYSA-N 5-chloro-2,4-dimethoxyaniline Chemical compound COC1=CC(OC)=C(Cl)C=C1N OLCMNCWEUMBNIS-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 241000238818 Acheta domesticus Species 0.000 description 1
- 241000256111 Aedes <genus> Species 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 241000256186 Anopheles <genus> Species 0.000 description 1
- 241000238659 Blatta Species 0.000 description 1
- 241000238657 Blattella germanica Species 0.000 description 1
- 241001674044 Blattodea Species 0.000 description 1
- 241000257163 Calliphora vicina Species 0.000 description 1
- 241000256054 Culex <genus> Species 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- XTJFFFGAUHQWII-UHFFFAOYSA-N Dibutyl adipate Chemical compound CCCCOC(=O)CCCCC(=O)OCCCC XTJFFFGAUHQWII-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 241000953886 Fannia canicularis Species 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 241000257303 Hymenoptera Species 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 241000948337 Lasius niger Species 0.000 description 1
- 241000736227 Lucilia sericata Species 0.000 description 1
- 125000003047 N-acetyl group Chemical group 0.000 description 1
- 241000238814 Orthoptera Species 0.000 description 1
- 241000238675 Periplaneta americana Species 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- BPNJJCFBKGKZBP-UHFFFAOYSA-N [2-(dimethylamino)phenyl]-methylcarbamic acid Chemical compound CN(C)C1=CC=CC=C1N(C)C(O)=O BPNJJCFBKGKZBP-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000006193 alkinyl group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- JQZRVMZHTADUSY-UHFFFAOYSA-L di(octanoyloxy)tin Chemical compound [Sn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O JQZRVMZHTADUSY-UHFFFAOYSA-L 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- 150000002016 disaccharides Chemical class 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000005516 engineering process Methods 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
- 239000000835 fiber Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000012052 hydrophilic carrier Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 125000005394 methallyl group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000004080 punching Methods 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
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229960004793 sucrose Drugs 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 150000003580 thiophosphoric acid esters Chemical class 0.000 description 1
- 150000004072 triols Chemical class 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment 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
- 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
- A01N25/002—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 a foodstuff as carrier or diluent, i.e. baits
- A01N25/006—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 a foodstuff as carrier or diluent, i.e. baits insecticidal
-
- 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0058—Biocides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2375/00—Characterised by the use of polyureas or polyurethanes; Derivatives of such polymers
- C08J2375/04—Polyurethanes
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Pest Control & Pesticides (AREA)
- Polymers & Plastics (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Biodiversity & Conservation Biology (AREA)
- Dentistry (AREA)
- Toxicology (AREA)
- Plant Pathology (AREA)
- Food Science & Technology (AREA)
- Insects & Arthropods (AREA)
- Materials Engineering (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
Ineecticidal baits and process for their production FARBENFABRIK N BAYER AXTIENGESELLSCHAPT C: 28032 The present invention is concerned with new insecticidal baits, as well as a process foi the production of the baits, Insecticidal baits are already known which consist mainly of a carrier material, in which the insecticidal active compound, the luring substance and, when present, the attracting colour, are substantially on the surface (cf. for example German Gebrauohe-muster 1 708 559, German Patent Specification 818435).
As carrier materials for these baits there have been used, in the main, paper, cardboard, mechanical wood-pulp, fibre materials, textiles, synthetic substances, wool, wadding and rubber♦ As insecticidal active compounds, chlorinated hydrocarbons have mainly been used, as well as phosphoric acid esters and carbamates.
As luring substances there have been used monosaccharides and disaccharides such as cane sugar, fructose and galactose, and also proteins, such as yeast, powdered egg and powdered milk. Also known is the strong attracting effect of water. For this reason, hydrophilic carrier materials are particularly suitable and various methods have been developed for moistening them and keeping them moist (German Gebrauchsmuster 1708 559, 1 746, 283, 1 756 939). As attracting colours, in these baits, red and black have given particularly good results.
The production of these baits is, in principle, carried out in two steps. In the first step, the carrier material is produced; in the second step, the carrier material is soaked with solutions of the active compounds, the luring substances and the attracting colours, optionally in several individual operations, for example when the individual substances are not soluble in the same solvent.
These methods of production have a number of disadvantages.
Much work is involved in undertaking the entire manufacture in two or more different operations. Solvents have to be used; after every impregnation, the baits have to be dried, for which purpose considerable drying energies are required and, moreover, the solvents have to be wholly removed and at least partially recovered. In addition, when working with combustible and explosive solvents, suitable safety precautions have to be taken.
The baits themselves also exhibit certain disadvantages.
They have only a relatively small surface. Their effectiveness rapidly wears and we have found that this is because the active compounds and luring substances are present chiefly on the surface of the carrier material, and are not uniformly distributed within it.
Insecticidal baits are also known which consist essentially of a carrier material in which the active compounds, the luring substances and the dyestuffs are uniformly embedded (cf. for example German Patent Specification 818435 and German Published Specification 1182 468). The carrier materials are, for example, paper and cardboard. In this case, the active compounds and other additives have to be added (possibly with the aid of solvents and emulsifiers) direct to the aqueous paper pulp from which the paper or board is made. This type of manufacture has the considerable disadvantage that sizable amounts of active compounds and additives are lost. Moreover, only active compounds which do not hydrolyse can be used. The water and the other organic solvents have to be removed or dried out.
Other baits use sugar as the carrier material. In this case, all the constituents are compressed into tablets under very high pressure. A disadvantage of this method of manufacture is that special compressing devices which work with very high pressure are required. Moreover, the tablets, when appreciably moistened, dissolve, smear and become unsightly· κ Independently of the method of manufacture, baits of these types have the disadvantage that their surface is relatively small in proportion to their weight.
Prom the multiplicity of previously known baits, those which have gained the greatest importance in practice are those in which the carrier material, in general cellulose or mechanical wood-pulp, is first produced and this is then soaked with the active compounds and, as the case may be, other additives. The baits are, in general, put on the market as spheres, circular plates or as strips.
The exploitation of the insecticidal potency of the active compounds used is by no means optimum in such baits.
The present invention provides insecticidal baits having a particularly good immediate activity and a particularly long lasting activity (and thus ensures particularly favourable utilisation of the insecticidal potency of the active compounds). These new baits consist essentially of a non-thermoplastic hydrophilic polyurethane foam and contain insecticidal carbamates and/or insecticidal phosphoric acid esters, as well as insect-luring substances (and, optionally, insect-attracting colouring matter), substantially uniformly embedded in the cell framework of the polyurethane foam.
It has further been found that the baits of the invention are obtained in a one-step process in particularly simple manner when (l) an insecticidal carbamate and/or insecticidal phosphoric acid ester and (2) an insect-luring substance, together with (3) either a hydrophilic polyol or a non-hydrophilic polyol and hydrophilic additive, (4) a polyisocyanate and (5) an activator mixture are foamed into a hydrophilic polyurethane foam and the poly-urethane foam so obtained is brought into a form suitable for baits. Further ingredients such as (6) an insect-attracting colouring matter and (7) other additives may if desired be included in the foaming step.
Surprisingly, the baits of the invention, compared with the best baits known from the prior art, show a better immediate activity and a longer lasting activity. It is, however^,, quite especially surprising that the insecticidal carbamates and phosphoric acid esters can wholly retain their insecticidal potency during the manufacture of the foams, although it is known on the one hand that carbamates and phosphoric acid esters hydrolyse readily, and on the other hand that the manufacture of foam is carried out in the presence of bases and basic catalysts at high temperatures, in general over 100°0.
As insecticidal carbamates, all carbamates can be used which have a sufficient insecticidal effect on the insects which are to be destroyed, that is, chiefly on Diptera, such as flies (for example Musca domestica, Fannia canicularis, Calliphora erythro-cephala, Lucilia sericata, Chrysomyia putoria), mosquitoes (for example Aedes, Culex and Anopheles species), cockroaches (for example Blattella germanica, Blatta orientails, Periplaneta ameri-cana), crickets (for example Acheta domesticus) and ants (for example Lasius niger).
Carbamates of the general formula have given particularly good results.
In this formula, R stands for hydrogen or an acyl radical, in particular acetyl or propionyl, A stands for phenyl or a phenyl radical with condensed hetero c clic rings which contain oxygen, nitrogen or sulphur, All these radicals may be substituted by 1 to 3 substituents of the following nature: alkyl with 1 to 6 carbon atoms, such as methyl, ethyl, isopropyl or sec-butyl; alkoxy with 1 to 6 carbon atoms, such as aethoxy, ethoxy, isopropoxy, or sec.-butoxy; alkenyl with 2 to 6 carbon atoms, such as allyl or methallyl; alkinyl with 2 - 6 carbon atoms, such as propargyl; dialkylamlno groups, such as dimethylamino; dialkenylamino groups, such as diallyl-amino; alkyl-alkenylamino groups, such as allyl methylamino, Insecticidal carbamates which can be used in the baits of the invention are mentioned for example in German Patent Specifications 1108202, 1159929, 1145 162, 1, 162 352 and 1153012 and in Belgian Patent Specifications 649 260 and 681442.
As particularly effective insecticidal carbamates there may be mentioned: 2-isopropoxyphenyl-N-methylcarbamate; 2-methyl-coumaran-7-yl-N-HDttethylcarbamate, 2^2-dimethyl-coumaran-7-yl-N-methylcarbamate as well as the N-acetyl derivatives of these two coumaranyl compounds and 2-dimethylaminophenyl-N-methylcarbamate» As insecticidal phosphoric acid esters, all phosphoric acid esters are suitable which have an adequate insecticidal effectiveness against the above-mentioned insects which are to be destroyed. The term "insecticidal phosphoric acid esters" is used here in the comprehensive meaning in which it is used in the hygiene-insecticide field. It therefore includes phosphoric acid esters in the narrower sense, thiophosphoric acid esters, thiophosphonic acid esters. There may be mentioned in particular: 0,0-dimethyl-2,2-dichlorovinylphospha e, 0,O-dimethyl-(l-hydroxy-2,2,2-tri-chloroethyl)-phosphonate, 0,O-dimethyl-3-methyl-4-nitrophenylthio-phosphate and 0,0-dimethyl-3-nitrophenylthiophosphate.
For the baits, individual carbamates as well as individual phosphoric acid esters are suitable, but mixtures of representatives of these two groups of active compounds are also suitable.
The concentration of active compound in the baits can vary within a wide range. In general, it is from 0.01 to 20, preferably from 0.1 to 5, per cent by weight.
As luring substances, the usual insect lures may be used (Wiesmann, Schweizer Archiv fur Tierheilkunde 102 I960, p. 134; Gebrauchsmusterschutz 1 708 559; Wiesmann, Z'. f. angew. Zool. 47. I960, p. 159)· Particularly favourable are sugars, such as di-saccharides and monosaccharides, for example cane sugars, glucose lactose, galactose and fructose. However, proteins can be used, in particular yeast, yeast hydrolysate, powdered egg and powdered milk.
The concentration of the luring substances in the bait may al30 vary within fairly wide ranges. In general, it is from 0.1 to 80, preferably from 1 to 50, per cent by weight.
A further increase of the attractiveness of the baits to insects may be achieved by attractive colouring matters (German Sebrauchsmuster 1 708 559). In particular, red, violet, and black colours have a significance in insect baits. As colouring matters there may be mentioned: the coupling product of 1,2-bis ( 3' -amino-4'-methoxybenzenesulphonamido)ethane on to the 2,4-di-methoxy-5-chlorophenylamide of β-hydroxynaphthoic acid, the coupling product of 1,2-bis(3 '-amino^'-methoxybenzenesulphonamido) ethane on to the 4-ethoxyphenyl-amide of β-hydroxynaphthoic acid, carbon black.
The concentration of the colouring matter in the bait can also vary within fairly wide ranges. In general, it is from 0.1 to 10, preferably from 0.5 to 5, per cent by weight.
As hydrophylic agents, the usual hydrophilic agents can be used which do not have any disturbing influence on the formation of polyurethane foam. These include, in the main, silica gel and polyhydroxy compounds, such as sugar.
The polyurethane foams may be produced in the usual manner. On this there exists a wide-ranging literature (compare for example J.J. Saunders, K.C. Frisch: Polyurethanes, Part I, Chemistry, Interscience-Wiley, New York (1962), Part II, Technology, Interscience-Wiley, New York (1964); ¾· Vieweg, A.Hoechtlen, Kunstetoff-Handbuch, Vol. VII, Polyurethane, Carl Hanser (1966)).
According to the usual process, polyols are mixed with the polyisocyanates, with the addition of catalysts, foam stabilisers and other additives. Foam formation sets in automatically with an exothermic reaction. The temperatures occurring during foam production generally lie between 50 and 170°C, preferably above 100°C.
The active compounds, luring substances and hydrophllic agents are expediently added to the polyols before foaming. However, it it is also possible to mix them with the other reaction components, in particular the activator mixtures.
During foam production the dyestuffs or other colouring matter are preferably used as dispersions in the usual plasticisers, such as polyadipates, polyphthalates, adipic acid di-n-butyl ester, triphenylphosphate or dioctylphthalate. However, addition in admixture with the additives customarily used in foam production, such as catalysts, emulsifiers or foam stabilisers, is also possible.
For the baits of the invention it has proved desirable to use hydrophilically adjusted polyurethane foams, because these are easy to moisten and, through the attraction of water from the atmosphere, always remain somewhat moist, whereby the insects are attracted to an increased extent.
For the production of these hydrophilic polyurethane foams, polyethers are used which are co-polymers of ethylene oxide and propylene oxide. The polyethers should possess a functionality of at least 2 and are preferably triols. The molecular weight varies between 1000 and 4000· The ethylene oxide content in the polyethers should be higher than 10% of the total amounts of alkylene oxide. The polyols possess a very high content of pri-mary hydroxyl groups.
For the production of the polyurethane foams the usual iso-cyanates, activators, foam stabilisers, foaming agents as well as other additives may be used.
As isocyanate, toluylenediisocyanate (80 2,4- and 20 2,6-isomer, or 65% 2,4- and 35% 2,6-isomer) is preferably used.
As activators, tertiary amines, such as dimethylbenzylamine , N-methyl- · -dimethylaminoethylpiperazine and 2,2, 4-trimethyl-2-silamorpholine, are particularly suitable.
The polyurethane foams containing the active compounds, luring substances and other additives are, in general, obtained (as in the production of polyurethane foams according to the prior art) in the form of blocks or thick slabs. From these, the baits of the invention can be produced by cutting up, sawing up or punching out.
The form of the baits according to the invention is entirely optional. They can be produced as small plates, ribbons, foils, films, spheres, cubes, rectangular parallelepipeds, cylinders or small, barrel-shaped bodies.
The baits of the invention may be used in the usual manner; it is particularly advantageous if they are moistened with water, since in this condition they exercise a particularly great attracting action.
Some of the advantages of the baits of the invention and their production as compared with the previously known baits (especially those which have hitherto been important in practice) may be summarised as follows: (1) The active compounds- are uniformly distributed in the bait material. (2) The hydrophilic polyurethane foam ensures high hydrophilia and water absorbency. (3) The active compounds are, through being embedded in the polyurethane foam structure, protected against too rapid a washing out, rapid hydrolysis and rapid mechanical wearing off. (4) When used with smaller amounts of active compound, the baits show more rapid and longer lasting effectiveness than other baits and therefore exploit particularly well the insecticidal potency of the insecticidal active compounds. (5) The production of the carrier material, the introduction of the insecticidal active compound, the introduction of the luring substance as well as the introduction of any colouring matter are achieved in one single operation. Production can therefore be particularly simple and rapid. Solvents and drying energies are saved. Moreover, safety precautions which would be necessary with the use of combustible and explosive solvents are not required. Finally, no problems arise when readily volatile active compounds are used which would evaporate during the usual drying.
The production of baits of the invention is illustrated by the following Production Examples 1 and 2.
Production Example 1 Production of foam: 100 parts by weight of a trifunctional hydrophilic poly-ether (hydroxyl number 6,averagemolecular weight 3000) which was obtained by addition of 5 ethylene oxide and 55 propylene oxide to glycerol as starting component are mixed with 40 parts by weight of powdered sugar (luring substance), 10 parts by weight of a red paste (dispersion of an azo red pigment in a conventional plasticiser (attracting colour)), 0.05 part by weight of 2,2,4- triraethyl-2-silamorpholine, 0.25 part by weight of tin-(II)-octoate (both as activators), 3 parts by weight of water (foaming agent), 1.0 part by weight of a water-soluble polyethersiloxane (stabiliser) as well as 2 parts by weight of 0,0-dimethyl-(l-hydroxy-2,2, 2-trichloroethyl)-phosphonate are intimately mixed. The mixture is then thoroughly stirred together with 39 parts by weight toluy-lene-diisocyanate (65 2,4- and 3 2,6-isomer). After about 5 seconds the mixture becomes turbid, and a foam forms which after a further 60 seconds has reached its final height. The red foam obtained is elastic, possesses a fine cell structure and is very hydrophilic; by gravimetric determination, after immersion in water the foam absorbs 1100 per cent by weight of water. Production of the bait: Prom the foam so produced, 0.5 cm thick slabs are produced by means of a rotating knife (commercial polyurethane foam slitting installation) . These slabs are cut into slabs with an edge length of 6.3 and 9 cm. with the same equipment. These slabs can be used directly as bait.
In the same manner, baits in any other desired shape can be produced from the foam.
Production Example 2 Production of foam: 100 parts by weight of a trifunctional hydrophilic polyether (hydroxyl number 56,averagemolecular weight 3000) which was ob-tained as starting component by addition of 4 ethylene oxide and 55% propylene oxide to glycerol, are thoroughly mixed with 80 parts by weight of powdered sugar, 20 parts by weight of powdered egg, 2.175 parts by weight of 2-methylcoumaran-7-yl-N-methyl-carbamate, 2.175 parts by weight of 0,0-dimethyl-2 , 2-dichlorovinyl-phosphate and 10.0 parts by weight of a red paste (dispersion of an azo red pigment in a usual plasticiser) . To this polyol mix- ture is added an activator solution of 0.05 part by weight 2,2,4-trimethyl-2-eilamorpholine , 0.6 part by weight tin-(Il)-octoate, 3 parts by weight of water and 1.75 parts by weight of a water-soluble polyethersiloxane. The mixture is then thoroughly stirred together with 43 parts by weight toluylenediisocyanate (65% 2,4-and 35 2,6-isomer) and the polyurethane foam forming after about 5 seconds is filled into moulds, in which it reaches its maximum height after a further 60 seconds. The red coloured foam obtained is elastic and possesses a fine cell structure. The hydro-philia is measured by water absorption; the foam (with the air squeezed out) was immersed in water. The water absorption is 1480 per cent by weight.
Production of bait: In the same manner as stated in Production Example 1, baits in the form of slabs or any other form desired can be produced from the foam.
The effectiveness of the baits of the invention is illustrated by the following Use Examples A-F.
Use Example A A bait according to the invention was compared with a bait of a previously known type. The bait according to the invention was a foam slab with edge lengths of 0.5 x 6.3 x 9 cm and a weight of 2.1 g.
It contained as active compound 0,0-dimethyl-(l-hydroxy-2, 2, 2-trichloroethyl)-phosphate in an amount of 1.0$, as luring substance powdered sugar in an amount of 20.4 , and as attracting colour a red azo pigment dyestuff.
The bait was produced by a method according to Example 1.
The previously known bait had the same dimensions as the bait according to the invention, but weighed 6.8 g. It contained the same active compound and the same luring substance in the same concentration. The attracting colour was also red. This bait was produced from a mechanical wood-pulp board by impregnation with the individual substances.
In the comparison of the two baits, account must be taken of the fact that the previously known bait was more than 3 times as heavy as the bait according to the invention and therefore, in absolute terms, contained more than 3 times as much active compound and luring substance.
The biological test was carried out as follows: To test the bait activity, each bait was laid on a saucer, moistened with water up to the limit of the absorption time and then placed on the floor of a room of 3.7 x 3.8 metres lateral dimensions and a height of 2.9 metres, each in the middle of a sheet of white filter paper of 52 cm x 52 cm size and at the same distance from the walls of the room. About 2000 flies of the species Musca domestica were then released into this room. The flies were able to choose completely freely between the two baits.
After 4 hours there was determined the number of dead flies which, in the case of each bait, lay on the saucer and on the sheet of filter paper. The other dead flies lying scattered around, the room were not counted, since in their cases it was not certain by which of the two baits they were killed.
The flies on the two saucers, as well as the flies on the sheets of filter paper, were counted separately. There was then ascertained what percentage of the total of flies counted had been killed by one bait and what percentage had been killed by the other. These percentage figures represent the effectiveness index.
The results are stated in the following Table. It can be seen that the bait according to the invention has a much higher effectiveness index and, in addition, exercises a much more rapid action on the flies than does the previously known bait.
In the case of the bait according to the invention, a higher percentage of the flies lay on the saucer than in the case of the previously known baits, with reference respectively to the total number of flies evaluated.
TABLE Number of flies killed; Bait Saucer Paper Saucer and paper Effectiveness index According to 548 739 1287 73 the invention Previo sly known 98 384 482 27 Use Example B A bait according to the invention was compared with a previously known bait. The bait according to the invention was a slab with dimensions 0.5 x 6.3 x 9.0 cm. It weighed 2.5 g. As active compound it contained 2-methyl-coumaran-7-yl-N-methyl-carbamate in an amount of 0.83 and 0,0-dimethyl-2,2-dichloro-vinyl phosphate in an amount of 0.83 . As luring substance it contained powdered sugar in an amount of 30.4 and powdered egg in an amount of 7.6 and, as attracting colour, a red azo pigment dyestuff.
The bait had been prepared according to Production Example 2.
The previously known bait had the same dimensions as the bait according to the invention but weighed 7.5 g. It contained the same active compounds and the same luring substances in the same concentration. Its attracting colour was also red.
The bait was produced from a board of mechanical wood-pulp, and which was impregnated with the individual substances.
In the comparison of the two baits, account must be taken of the fact that the previously known bait, in absolute terms, contained 3 times the amount of active compounds and luring substances.
The activity of the two baits was compared according to the test stated in Use Example A. About 3000 flies of the species Musca domestica were used. After 4 hours, 2710 flies had been killed by the two baits.
TABLE Bait Effectiveness index According to the invention 64 .Previously known 36 Use Example C Two baits were compared. The bait according to the invention was a slab with the dimensions of 0.5 x 6.3 x 9 cm. It weighed 2.3 g.
As active compound, it contained 2-raethyl-coumaran-7-yl-N-methylcarbamate in an amount of 1.0 , as luring substance powdered sugar in an amount of 20.4 and as attracting colour a red azo pigment dyestuff.
The bait had been produced according to Production Example 1.
The previously known bait had the same dimensions as the bait according to the invention. However, it weighed 6.9 g. It contained the same active compounds and luring substances in the same concentration. The attracting colour was also red.
It had been produced in the usual manner from a board of mechanical wood-pulp by impregnation with the individual substances.
In the comparison of the two baits, account must be taken of the fact that the previously known bait, in absolute terms, contained 3 times more active compounds and luring substances than the bait according to the invention.
The activity of the two baits was determined according to the test described in Use Example A.
Of about 1500 flies, 1399 were killed in 4 hours. The results are listed in the following Table. In this connection it is particularly to be taken into account that the bait according to the invention has a higher immediate activity. Comparatively many flies lay on the saucer and relatively few on the paper.
TABLE Number of flies killed on: Effectiveness index Bait Saucer Paper Saucer and paper According to 737 229 966 69 the invention Previously known 261 172 433 31 Use Example D Two baits were compared with each other. The bait according to the invention corresponded exactly to the bait described in Example C, The previously known bait corresponded generally to the previously known bait described in Example C but its size was reduced to one third, so that the weights of the two baits were equal.
The two baits therefore contained the same amounts of active and luring substances, not only in percentage terms but also in absolute terms.
The activity of the two baits was determined according to the test stated in Use Example A. The effectiveness indexes are given in the following Table.
TABLE Bait Effectiveness index According to the invention 75% Previously known 25% Use Example E Two baits were compared. The bait according to the invention corresponded generally to the bait of the invention according to Use Example A, but contained as active compound 0,0-di— methyl-2,2-dichlorovinyl phosphate in an amount of 0.85% and as luring substance powdered sugar in an amount of 34-%· The previously known bait corresponded in principle to the previously known bait according to Use Example A, but contained the same luring and active substances in the same amount as the bait according to the invention described in this Example. · For 5 weeks both baits were moistened daily with water to the limit of their absorbency and were, at intervals of one week, tested for their biological activity in the manner stated in Use Example A.
The results are listed in the following Table. From this Table it can be clearly seen that the bait according to the invention was, from the beginning of the experiment, distinctly superior to the comparative bait and became more and more superior in the course of time.
TABLE Test time in weeks Effectiveness index of the two baits According to the invention Previously known 0 60 40 1 62 38 2 65 35 3 70 30 4 84 16 91 9 Use Bxample F The comparative experiments according to Example C were repeated several times with baits which in each case contained, instead of 2-→nethyl-7-coumaranyl-N-methylcarbamatef the active compounds mentioned in the following Table. The effectiveness in dexes for the pairs of baits of the invention and of the prior art are stated in the following Table: TABLE Active compound Effectiveness indexes for the baits According to the Previously known invention CH-CH=CH, Active compound .Effectiveness indexes for the baits According to the Previously knoim invention For the production of the hydrophilic polyurethane foamsS' polyols with hydroxyl numbers below 250, especially below 100, are preferably used. When producing these polyols, more than 10 ethylene oxide, relative to the total amount of alkylene oxide, are used.
Claims (21)
1. What we claim is:- 1. Insecticidal baits which consist essentially of a non-thermoplastic hydrophilic polyurethane foam containing substantially uniformly embedded in the cell framework thereof an insecticidal carbamate and/or an insecticidal phosphoric acid ester as well as an insect-luring substance.
2. Insecticidal baits according to claim 1 which contain substantially uniformly embedded in the cell framework of the foam an insect-attracting colouring matter.
3. Insecticidal baits according to claim 1 or 2 containing an insecticidal carbamate of the formula:- in which R stands for hydrogen or an acyl radical,
4. A stands for phenyl or a phenyl radical with condensed heterocyclic rings which contain oxygen, nitrogen or sulphur, and these radicals may be substituted by 1 to 3 of the following substituents : alley1 radicals (each containing 1-6 carbon atoms), alkoxy radicals (each containing 1-6 carbon atoms), alkenyl radicals (each containing 2-6 carbon atoms), alkinyl radicals (each containing 2-6 carbon atoms), dialkylamino radicals, dialkenylamino radicals and alkyl-alkenylamino radicals. 4. Insecticidal baits according to claim 1 or 2 containing one or more of the following: 2-isopropoxy-phenyl-N-methyl-carbamate, 2-methyl-coumaran-7-yl-N-methyl-carbamate, 0,0-di-methyl-(l-hydroxy-2, 2, 2-trichloroethyl)-phosphonate, 3» 5-Li-methyl-4-allylmercaptophenyl-N-methyl-carbamate , 2-propargyl-oxyphenyl-N-methylcarbamate , 2-(methyl-allyl)-phenyl-N-meth l carbamate , 2 ,.2-dimethylcoumaran-7-yl-N-methyl-N-acetylcarbam- 0-(3-methyl-4-nitrophenyl)-thiophosphate, 0,O-dimethyl-0-3-nitrophenylthiophosphate and dimethyl-2,2-dichlorvinylphosphate.
5. Insecticidal baits according to any of claims 1-4 containing from 0.01 to 20 of the carbamate and/or phosphoric acid ester, by weight of the baits.
6. Insecticidal baits according to claim 5 containing from 0.1 to 5% of the carbamate and/or phosphoric acid ester, by weight of the baits.
7. Insecticidal baits according to any of claims 1-6 in which the insect-luring substance is sugar or protein.
8. Insecticidal baits according to any of claims 1-7 containing from 1 to 5 of the insect-luring substance, by weight of the baits.
9. Insecticidal baits according to claim 2 or any of claims 3-8 as dependent on claim 2 containing from 0.5 to 5% of the colouring matter, by weight of the baits.
10. Insecticidal baits according to claim 1, substantially as hereinbefore described in any of the Examples.
11. A process for the production of insecticidal baits which comprises forming a mixture of (l) an insecticidal carbamate and/or insecticidal phosphoric acid esters, (2) an insect-luring substance, (3) a hydrophilic polyol, or a non-hydro-philic polyol and hydrophilic additive, (4) a polyisocyanate and (5) an activator, and foaming the mixture to form a hydro- . philic po]yurethane foam containing embedded in the cell framework thereof the carbamate and/or phosphoric acid ester and the insect-luring substance.
12. A process according to claim 11 in which the mixture also contains an insect-attracting colouring matter.
13. A process according to claim 11 or 12 in which the carbamate and/or phosphoric acid ester, the insect-luring substance and the hydrophilic additive are first formed into a mixture
14. A process according to claim 11 or 12 in which the hydrophilic polyol is a copolymer of ethylene oxide, propylene oxide and glycerol.
15. . A process according to any of claims 11-14 in which the polyisocyanate is toluylenediisocyanate .
16. A process according to any of claims 11-15 in which the carbamate and/or phosphoric acid ester is one or more of the following:- 2-isopropoxy-phenyl-N-methylcarbamate, 2-me hyl-coumaran-7-yl-N-methyl-carbamate, 0 , 0-dimeth 1- ( 1-hydroxy-2 , 2 , 2-trichloroethyl)-phosphonate, 3 , 5-dimethyl-4- allylmercaptophenyl-N-methyl-carbamate , 2-propargyl-oxyphenyl- N-methylcarbamate , 2-(B-methyl-allyl)-phenyl-N-methyl-carbamate, 2 , 2-dimethylcoumaran-7-yl-N-methyl-N-acetylcarbamate , 2-tri- methylaminophenyl-N-methyl-carbamate , 0 , 0-dimethyl-0-r ( 3-methyl- 4-nitrophenyl)-thiophosphate, 0 , 0-dimethyl-0-3-nitrophenylthio- phosphate and dimethyl-2 , 2-dichlorvinyl-phosphate.
17. A process according to any of claims 11-16 in which there is used an amount of the carbamate and/or phosphoric acid ester which is from 0.01 to 20 , by weight of the total ingredients.
18. A process according to claim 17 in which there is used an amount of the carbamate and/or phosphoric acid ester which is from 0.1 to 5%, by weight of the total ingredients.
19. A process for the production of insecticidal baits, substantially as hereinbefore described in Example 1 or 2 .
20. Insecticidal baits whenever produced by a process according to any of claims 11-19.
21. A method of controlling insect pests which comprises applying to an area in which insect pests are to be controlled an insecticidal bait according to any of claims 1-10 or 20 . Dated this 10th March 1968
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE1642261A DE1642261C3 (en) | 1967-05-24 | 1967-05-24 | Insecticidally effective baits and methods for their manufacture |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL29613A true IL29613A (en) | 1971-11-29 |
Family
ID=7105496
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL29613A IL29613A (en) | 1967-05-24 | 1968-03-11 | Insecticidal baits and process for their production |
Country Status (12)
| Country | Link |
|---|---|
| AT (1) | AT285242B (en) |
| BE (1) | BE704109A (en) |
| CH (1) | CH498560A (en) |
| CY (1) | CY504A (en) |
| DE (1) | DE1642261C3 (en) |
| DK (1) | DK118796B (en) |
| ES (1) | ES354261A1 (en) |
| GB (1) | GB1145433A (en) |
| IL (1) | IL29613A (en) |
| MY (1) | MY6900412A (en) |
| NL (1) | NL6807184A (en) |
| OA (1) | OA02514A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2537894C2 (en) * | 1975-08-26 | 1986-07-31 | Bayer Ag, 5090 Leverkusen | Elastomers with an insecticidal depot gas effect |
| DE2715595A1 (en) * | 1977-04-07 | 1978-10-12 | Bayer Ag | Insecticidal coating mass for animal collars - contg. an insecticide in a cold-hardening two-component system pref. polyurethane |
| DE3503608A1 (en) * | 1985-02-02 | 1986-08-07 | Bayer Ag, 5090 Leverkusen | LIGHT GRAIN LURE |
| MX393107B (en) * | 2016-07-29 | 2025-03-19 | Basf Se | A METHOD FOR CONTROLLING INSECTS WHERE AN ALKOXYLATED GLYCEROL IS APPLIED TO THE SOIL. |
-
1967
- 1967-05-24 DE DE1642261A patent/DE1642261C3/en not_active Expired
- 1967-09-20 BE BE704109D patent/BE704109A/xx unknown
- 1967-09-26 GB GB43790/67A patent/GB1145433A/en not_active Expired
- 1967-10-06 OA OA53070A patent/OA02514A/en unknown
-
1968
- 1968-03-08 CH CH347168A patent/CH498560A/en not_active IP Right Cessation
- 1968-03-11 IL IL29613A patent/IL29613A/en unknown
- 1968-05-21 NL NL6807184A patent/NL6807184A/xx unknown
- 1968-05-22 DK DK238968AA patent/DK118796B/en unknown
- 1968-05-24 ES ES354261A patent/ES354261A1/en not_active Expired
- 1968-05-24 AT AT498068A patent/AT285242B/en not_active IP Right Cessation
-
1969
- 1969-11-04 CY CY50469A patent/CY504A/en unknown
- 1969-12-31 MY MY1969412A patent/MY6900412A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE1642261C3 (en) | 1979-05-31 |
| CH498560A (en) | 1970-11-15 |
| DE1642261B2 (en) | 1978-10-05 |
| DK118796B (en) | 1970-10-05 |
| AT285242B (en) | 1970-10-27 |
| DE1642261A1 (en) | 1971-04-22 |
| OA02514A (en) | 1970-05-05 |
| NL6807184A (en) | 1968-11-25 |
| BE704109A (en) | 1968-03-20 |
| GB1145433A (en) | 1969-03-12 |
| MY6900412A (en) | 1969-12-31 |
| ES354261A1 (en) | 1969-11-01 |
| CY504A (en) | 1969-11-04 |
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