NO822090L - Nytt akaricid preparat, fremgangsmaate for dets fremstilling og bruk. - Google Patents
Nytt akaricid preparat, fremgangsmaate for dets fremstilling og bruk.Info
- Publication number
- NO822090L NO822090L NO822090A NO822090A NO822090L NO 822090 L NO822090 L NO 822090L NO 822090 A NO822090 A NO 822090A NO 822090 A NO822090 A NO 822090A NO 822090 L NO822090 L NO 822090L
- Authority
- NO
- Norway
- Prior art keywords
- acaricidal
- solvent
- dissolved
- acaricides
- phospholipids
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 8
- 238000002360 preparation method Methods 0.000 title claims description 26
- 238000004519 manufacturing process Methods 0.000 title abstract description 3
- 230000000895 acaricidal effect Effects 0.000 claims abstract description 42
- 239000000642 acaricide Substances 0.000 claims abstract description 27
- 239000000203 mixture Substances 0.000 claims abstract description 19
- 239000002904 solvent Substances 0.000 claims abstract description 9
- 239000003085 diluting agent Substances 0.000 claims abstract description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 27
- 150000003904 phospholipids Chemical class 0.000 claims description 22
- 150000001875 compounds Chemical class 0.000 claims description 14
- 241000239223 Arachnida Species 0.000 claims description 12
- -1 R 2 is H Chemical group 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 239000000654 additive Substances 0.000 claims description 7
- 241000238876 Acari Species 0.000 claims description 6
- 239000005948 Formetanate Substances 0.000 claims description 5
- RMFNNCGOSPBBAD-MDWZMJQESA-N formetanate Chemical compound CNC(=O)OC1=CC=CC(\N=C\N(C)C)=C1 RMFNNCGOSPBBAD-MDWZMJQESA-N 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- UOAMTSKGCBMZTC-UHFFFAOYSA-N dicofol Chemical compound C=1C=C(Cl)C=CC=1C(C(Cl)(Cl)Cl)(O)C1=CC=C(Cl)C=C1 UOAMTSKGCBMZTC-UHFFFAOYSA-N 0.000 claims description 4
- 239000000945 filler Substances 0.000 claims description 4
- WTJKGGKOPKCXLL-RRHRGVEJSA-N phosphatidylcholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCCC=CCCCCCCCC WTJKGGKOPKCXLL-RRHRGVEJSA-N 0.000 claims description 4
- 150000008105 phosphatidylcholines Chemical class 0.000 claims description 4
- 239000011877 solvent mixture Substances 0.000 claims description 4
- 238000003756 stirring Methods 0.000 claims description 4
- ZHLKXBJTJHRTTE-UHFFFAOYSA-N Chlorobenside Chemical compound C1=CC(Cl)=CC=C1CSC1=CC=C(Cl)C=C1 ZHLKXBJTJHRTTE-UHFFFAOYSA-N 0.000 claims description 3
- RAPBNVDSDCTNRC-UHFFFAOYSA-N Chlorobenzilate Chemical compound C=1C=C(Cl)C=CC=1C(O)(C(=O)OCC)C1=CC=C(Cl)C=C1 RAPBNVDSDCTNRC-UHFFFAOYSA-N 0.000 claims description 3
- QUWSDLYBOVGOCW-UHFFFAOYSA-N Tetrasul Chemical compound C1=CC(Cl)=CC=C1SC1=CC(Cl)=C(Cl)C=C1Cl QUWSDLYBOVGOCW-UHFFFAOYSA-N 0.000 claims description 3
- 239000000969 carrier Substances 0.000 claims description 3
- AXGUBXVWZBFQGA-UHFFFAOYSA-N chloropropylate Chemical compound C=1C=C(Cl)C=CC=1C(O)(C(=O)OC(C)C)C1=CC=C(Cl)C=C1 AXGUBXVWZBFQGA-UHFFFAOYSA-N 0.000 claims description 3
- YFBPRJGDJKVWAH-UHFFFAOYSA-N methiocarb Chemical compound CNC(=O)OC1=CC(C)=C(SC)C(C)=C1 YFBPRJGDJKVWAH-UHFFFAOYSA-N 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 claims description 3
- ASWBNKHCZGQVJV-UHFFFAOYSA-N (3-hexadecanoyloxy-2-hydroxypropyl) 2-(trimethylazaniumyl)ethyl phosphate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(O)COP([O-])(=O)OCC[N+](C)(C)C ASWBNKHCZGQVJV-UHFFFAOYSA-N 0.000 claims description 2
- TZCPCKNHXULUIY-RGULYWFUSA-N 1,2-distearoyl-sn-glycero-3-phosphoserine Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@H](COP(O)(=O)OC[C@H](N)C(O)=O)OC(=O)CCCCCCCCCCCCCCCCC TZCPCKNHXULUIY-RGULYWFUSA-N 0.000 claims description 2
- IRYSAAMKXPLGAM-UHFFFAOYSA-N 1-chloro-2-ethoxybenzene Chemical compound CCOC1=CC=CC=C1Cl IRYSAAMKXPLGAM-UHFFFAOYSA-N 0.000 claims description 2
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 claims description 2
- STUSTWKEFDQFFZ-UHFFFAOYSA-N Chlordimeform Chemical compound CN(C)C=NC1=CC=C(Cl)C=C1C STUSTWKEFDQFFZ-UHFFFAOYSA-N 0.000 claims description 2
- HDWLUGYOLUHEMN-UHFFFAOYSA-N Dinobuton Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)OC(C)C HDWLUGYOLUHEMN-UHFFFAOYSA-N 0.000 claims description 2
- JZNWSCPGTDBMEW-UHFFFAOYSA-N Glycerophosphorylethanolamin Natural products NCCOP(O)(=O)OCC(O)CO JZNWSCPGTDBMEW-UHFFFAOYSA-N 0.000 claims description 2
- ZWZWYGMENQVNFU-UHFFFAOYSA-N Glycerophosphorylserin Natural products OC(=O)C(N)COP(O)(=O)OCC(O)CO ZWZWYGMENQVNFU-UHFFFAOYSA-N 0.000 claims description 2
- 239000005951 Methiocarb Substances 0.000 claims description 2
- ATBOMIWRCZXYSZ-XZBBILGWSA-N [1-[2,3-dihydroxypropoxy(hydroxy)phosphoryl]oxy-3-hexadecanoyloxypropan-2-yl] (9e,12e)-octadeca-9,12-dienoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(COP(O)(=O)OCC(O)CO)OC(=O)CCCCCCC\C=C\C\C=C\CCCCC ATBOMIWRCZXYSZ-XZBBILGWSA-N 0.000 claims description 2
- 125000005090 alkenylcarbonyl group Chemical group 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 125000004849 alkoxymethyl group Chemical group 0.000 claims description 2
- 125000000304 alkynyl group Chemical group 0.000 claims description 2
- AWUCVROLDVIAJX-UHFFFAOYSA-N alpha-glycerophosphate Natural products OCC(O)COP(O)(O)=O AWUCVROLDVIAJX-UHFFFAOYSA-N 0.000 claims description 2
- FOANIXZHAMJWOI-UHFFFAOYSA-N bromopropylate Chemical compound C=1C=C(Br)C=CC=1C(O)(C(=O)OC(C)C)C1=CC=C(Br)C=C1 FOANIXZHAMJWOI-UHFFFAOYSA-N 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 239000008350 hydrogenated phosphatidyl choline Substances 0.000 claims description 2
- 150000008104 phosphatidylethanolamines Chemical class 0.000 claims description 2
- 150000003905 phosphatidylinositols Chemical class 0.000 claims description 2
- ZYHMJXZULPZUED-UHFFFAOYSA-N propargite Chemical compound C1=CC(C(C)(C)C)=CC=C1OC1C(OS(=O)OCC#C)CCCC1 ZYHMJXZULPZUED-UHFFFAOYSA-N 0.000 claims description 2
- ILERPRJWJPJZDN-UHFFFAOYSA-N thioquinox Chemical compound C1=CC=C2N=C(SC(=S)S3)C3=NC2=C1 ILERPRJWJPJZDN-UHFFFAOYSA-N 0.000 claims description 2
- 238000002604 ultrasonography Methods 0.000 claims description 2
- 239000003791 organic solvent mixture Substances 0.000 claims 2
- 239000003380 propellant Substances 0.000 claims 1
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- 239000003981 vehicle Substances 0.000 abstract 1
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- 239000007921 spray Substances 0.000 description 8
- 239000013065 commercial product Substances 0.000 description 7
- 239000000843 powder Substances 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 5
- ZRDUSMYWDRPZRM-UHFFFAOYSA-N 2-sec-butyl-4,6-dinitrophenyl 3-methylbut-2-enoate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)C=C(C)C ZRDUSMYWDRPZRM-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000000440 bentonite Substances 0.000 description 4
- 229910000278 bentonite Inorganic materials 0.000 description 4
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- 229910002012 Aerosil® Inorganic materials 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000002917 insecticide Substances 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 2
- LWLJUMBEZJHXHV-UHFFFAOYSA-N Dienochlor Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C1(Cl)C1(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LWLJUMBEZJHXHV-UHFFFAOYSA-N 0.000 description 2
- QJYHUJAGJUHXJN-UHFFFAOYSA-N Dinex Chemical compound C1=C([N+]([O-])=O)C=C([N+]([O-])=O)C(O)=C1C1CCCCC1 QJYHUJAGJUHXJN-UHFFFAOYSA-N 0.000 description 2
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- 229940018556 chloropropylate Drugs 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- KZTYYGOKRVBIMI-UHFFFAOYSA-N diphenyl sulfone Chemical compound C=1C=CC=CC=1S(=O)(=O)C1=CC=CC=C1 KZTYYGOKRVBIMI-UHFFFAOYSA-N 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 230000008029 eradication Effects 0.000 description 2
- 235000012055 fruits and vegetables Nutrition 0.000 description 2
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- 150000002632 lipids Chemical class 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
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- 235000021122 unsaturated fatty acids Nutrition 0.000 description 2
- 238000009369 viticulture Methods 0.000 description 2
- BXVKYLAYDKWDPI-LHHJGKSTSA-N (e)-2-(2,4-dinitro-6-octan-2-ylphenyl)but-2-enoic acid Chemical compound CCCCCCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1\C(=C/C)C(O)=O BXVKYLAYDKWDPI-LHHJGKSTSA-N 0.000 description 1
- CPZLRDXKLHKMQX-UHFFFAOYSA-N 1,1-bis(4-chlorophenyl)-2-ethoxyethanol Chemical compound C=1C=C(Cl)C=CC=1C(O)(COCC)C1=CC=C(Cl)C=C1 CPZLRDXKLHKMQX-UHFFFAOYSA-N 0.000 description 1
- OFCFYWOKHPOXKF-UHFFFAOYSA-N 1-(benzenesulfonyl)-4-chlorobenzene Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC=CC=C1 OFCFYWOKHPOXKF-UHFFFAOYSA-N 0.000 description 1
- GBZXOIUBLKUSJR-UHFFFAOYSA-N 1-chloro-4-[(4-fluorophenyl)sulfanylmethyl]benzene Chemical compound C1=CC(F)=CC=C1SCC1=CC=C(Cl)C=C1 GBZXOIUBLKUSJR-UHFFFAOYSA-N 0.000 description 1
- FJSRPVWDOJSWBX-UHFFFAOYSA-N 1-chloro-4-[1-(4-chlorophenyl)-2,2,2-trifluoroethyl]benzene Chemical compound C=1C=C(Cl)C=CC=1C(C(F)(F)F)C1=CC=C(Cl)C=C1 FJSRPVWDOJSWBX-UHFFFAOYSA-N 0.000 description 1
- KTEARTXATWOYDB-UHFFFAOYSA-N 1-chloro-4-[1-(4-chlorophenyl)ethyl]benzene Chemical compound C=1C=C(Cl)C=CC=1C(C)C1=CC=C(Cl)C=C1 KTEARTXATWOYDB-UHFFFAOYSA-N 0.000 description 1
- NVUMAPVZONTQRR-UHFFFAOYSA-N 2,2-dichloro-1,1-bis(4-chlorophenyl)ethanol Chemical compound C=1C=C(Cl)C=CC=1C(C(Cl)Cl)(O)C1=CC=C(Cl)C=C1 NVUMAPVZONTQRR-UHFFFAOYSA-N 0.000 description 1
- PXEMTFAKVKRTPG-UHFFFAOYSA-N 2,4-dichloro-1-(2,4-dichlorophenyl)sulfanylbenzene Chemical compound ClC1=CC(Cl)=CC=C1SC1=CC=C(Cl)C=C1Cl PXEMTFAKVKRTPG-UHFFFAOYSA-N 0.000 description 1
- FCGKUUOTWLWJHE-UHFFFAOYSA-N 2,6-ditert-butyl-4-nitrophenol Chemical compound CC(C)(C)C1=CC([N+]([O-])=O)=CC(C(C)(C)C)=C1O FCGKUUOTWLWJHE-UHFFFAOYSA-N 0.000 description 1
- MEWWGGOSRILCKZ-UHFFFAOYSA-N 2-chloro-1,1-bis(4-chlorophenyl)ethanol Chemical compound C=1C=C(Cl)C=CC=1C(CCl)(O)C1=CC=C(Cl)C=C1 MEWWGGOSRILCKZ-UHFFFAOYSA-N 0.000 description 1
- LQGSWLJZAKVBJH-UHFFFAOYSA-N 4,4'-dichlorodiphenylmethane Chemical compound C1=CC(Cl)=CC=C1CC1=CC=C(Cl)C=C1 LQGSWLJZAKVBJH-UHFFFAOYSA-N 0.000 description 1
- RJWBTWIBUIGANW-UHFFFAOYSA-N 4-chlorobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(Cl)C=C1 RJWBTWIBUIGANW-UHFFFAOYSA-N 0.000 description 1
- 241001558864 Aceria Species 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241001643374 Brevipalpus Species 0.000 description 1
- 241000488564 Bryobia Species 0.000 description 1
- JOIQIUVYCDOANM-UHFFFAOYSA-N CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1C(=C(C)C)C(O)=O Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1C(=C(C)C)C(O)=O JOIQIUVYCDOANM-UHFFFAOYSA-N 0.000 description 1
- 108010076119 Caseins Proteins 0.000 description 1
- URYAFVKLYSEINW-UHFFFAOYSA-N Chlorfenethol Chemical compound C=1C=C(Cl)C=CC=1C(O)(C)C1=CC=C(Cl)C=C1 URYAFVKLYSEINW-UHFFFAOYSA-N 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- YVGGHNCTFXOJCH-UHFFFAOYSA-N DDT Chemical compound C1=CC(Cl)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(Cl)C=C1 YVGGHNCTFXOJCH-UHFFFAOYSA-N 0.000 description 1
- 241001558857 Eriophyes Species 0.000 description 1
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- 241000221785 Erysiphales Species 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 241000488581 Panonychus citri Species 0.000 description 1
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- 241001559006 Phyllocoptes Species 0.000 description 1
- 241000497192 Phyllocoptruta oleivora Species 0.000 description 1
- 241001396980 Phytonemus pallidus Species 0.000 description 1
- 229920001030 Polyethylene Glycol 4000 Polymers 0.000 description 1
- NWGKJDSIEKMTRX-AAZCQSIUSA-N Sorbitan monooleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O NWGKJDSIEKMTRX-AAZCQSIUSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 241000496694 Vasates Species 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
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- 230000000694 effects Effects 0.000 description 1
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- 239000003995 emulsifying agent Substances 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
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- 229930195729 fatty acid Natural products 0.000 description 1
- 238000004108 freeze drying Methods 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- DSWNRHCOGVRDOE-UHFFFAOYSA-N n,n-dimethylmethanimidamide Chemical compound CN(C)C=N DSWNRHCOGVRDOE-UHFFFAOYSA-N 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 231100000194 ovacidal Toxicity 0.000 description 1
- 230000003151 ovacidal effect Effects 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
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- 235000019698 starch Nutrition 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
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- 239000000454 talc Substances 0.000 description 1
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- 239000002562 thickening agent Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
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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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Static Random-Access Memory (AREA)
- Manufacture, Treatment Of Glass Fibers (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Electrical Discharge Machining, Electrochemical Machining, And Combined Machining (AREA)
- Moulds, Cores, Or Mandrels (AREA)
- Inorganic Insulating Materials (AREA)
- Prostheses (AREA)
- Medicinal Preparation (AREA)
- Seasonings (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Medicines Containing Plant Substances (AREA)
- Treatment And Processing Of Natural Fur Or Leather (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19813125448 DE3125448A1 (de) | 1981-06-27 | 1981-06-27 | "neue acarizid-zusammensetzung, verfahren zur herstellung und deren verwendung" |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO822090L true NO822090L (no) | 1982-12-28 |
Family
ID=6135587
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO822090A NO822090L (no) | 1981-06-27 | 1982-06-22 | Nytt akaricid preparat, fremgangsmaate for dets fremstilling og bruk. |
Country Status (17)
| Country | Link |
|---|---|
| EP (1) | EP0068294B1 (es) |
| AT (1) | ATE16971T1 (es) |
| AU (1) | AU8444282A (es) |
| BR (1) | BR8203746A (es) |
| CA (1) | CA1173744A (es) |
| CS (1) | CS229687B2 (es) |
| DD (1) | DD202379A5 (es) |
| DE (2) | DE3125448A1 (es) |
| DK (1) | DK285082A (es) |
| ES (1) | ES513430A0 (es) |
| FI (1) | FI822250L (es) |
| GR (1) | GR76145B (es) |
| IE (1) | IE53079B1 (es) |
| NO (1) | NO822090L (es) |
| PL (1) | PL130616B1 (es) |
| PT (1) | PT75133B (es) |
| ZA (1) | ZA823834B (es) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3225705A1 (de) * | 1982-07-09 | 1984-01-12 | A. Nattermann & Cie GmbH, 5000 Köln | Verfahren zum ausbringen von pflanzenschutzmittelspritzbruehen durch verspruehen und verpackungseinheit fuer konzentrate |
| GB8321913D0 (en) * | 1983-08-15 | 1983-09-14 | Acacia Chem Ltd | Spray method |
| EP0604806A3 (de) * | 1992-12-18 | 2000-07-19 | Rhone-Poulenc Rorer Gmbh | Phospholipidische Zusammensetzung |
| CA2269631C (en) * | 1996-10-25 | 2008-03-25 | Monsanto Company | Composition and method for treating plants with exogenous chemicals |
| AU4998997A (en) * | 1996-10-25 | 1998-05-15 | Monsanto Company | Composition and method for treating plants with exogenous chemicals |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3298820A (en) * | 1967-01-17 | Herbicidal concentrate containing monosodium acid methanearsonate | ||
| DE476293C (de) * | 1927-12-08 | 1929-05-13 | Bruno Rewald Dr | Verfahren zur Herstellung von Schaedlingsbekaempfungsmitteln |
| US1938864A (en) * | 1929-10-21 | 1933-12-12 | Firm Hanseatische Muhlenwerke | Insecticidal emulsion |
| GB431759A (en) * | 1933-10-09 | 1935-07-15 | Grasselli Chemical Co | Insecticidal compositions |
| US2006227A (en) * | 1932-10-19 | 1935-06-25 | Grasselli Chemical Co | Contact insecticide |
| US2465335A (en) * | 1944-03-29 | 1949-03-29 | Socony Vacuum Oil Co Inc | Insecticidal spray oil containing lecithin |
| US3052599A (en) * | 1960-06-15 | 1962-09-04 | American Cyanamid Co | Stabilized organic phosphate pesticidal compositions in fuel oil |
| DE1792687A1 (de) * | 1967-05-03 | 1971-11-25 | Du Pont | Fungicides Mittel |
| US3983214A (en) * | 1972-12-08 | 1976-09-28 | Ajinomoto Co., Inc. | Fungicidal compositions and method for protecting plants by the use thereof |
| US4007258A (en) * | 1973-09-10 | 1977-02-08 | Union Corporation | Sustained release pesticidal composition |
| US4183740A (en) * | 1978-01-05 | 1980-01-15 | American Cyanamid Company | Solid compositions of a liquid surfactant and a pyrazolium herbicide |
-
1981
- 1981-06-27 DE DE19813125448 patent/DE3125448A1/de not_active Withdrawn
-
1982
- 1982-05-31 IE IE1300/82A patent/IE53079B1/en unknown
- 1982-06-02 ZA ZA823834A patent/ZA823834B/xx unknown
- 1982-06-03 AU AU84442/82A patent/AU8444282A/en not_active Abandoned
- 1982-06-11 GR GR68422A patent/GR76145B/el unknown
- 1982-06-16 AT AT82105253T patent/ATE16971T1/de not_active IP Right Cessation
- 1982-06-16 CA CA000405252A patent/CA1173744A/en not_active Expired
- 1982-06-16 DE DE8282105253T patent/DE3268008D1/de not_active Expired
- 1982-06-16 EP EP82105253A patent/EP0068294B1/en not_active Expired
- 1982-06-22 FI FI822250A patent/FI822250L/fi not_active Application Discontinuation
- 1982-06-22 NO NO822090A patent/NO822090L/no unknown
- 1982-06-23 DD DD82241008A patent/DD202379A5/de unknown
- 1982-06-24 DK DK285082A patent/DK285082A/da not_active Application Discontinuation
- 1982-06-25 PT PT75133A patent/PT75133B/pt unknown
- 1982-06-25 PL PL1982237105A patent/PL130616B1/pl unknown
- 1982-06-25 CS CS824792A patent/CS229687B2/cs unknown
- 1982-06-25 ES ES513430A patent/ES513430A0/es active Granted
- 1982-06-25 BR BR8203746A patent/BR8203746A/pt unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE3125448A1 (de) | 1983-01-13 |
| GR76145B (es) | 1984-08-03 |
| DD202379A5 (de) | 1983-09-14 |
| ES8308471A1 (es) | 1983-09-01 |
| CS229687B2 (en) | 1984-06-18 |
| EP0068294B1 (en) | 1985-12-18 |
| ATE16971T1 (de) | 1986-01-15 |
| PL130616B1 (en) | 1984-08-31 |
| DE3268008D1 (en) | 1986-01-30 |
| IE821300L (en) | 1982-12-27 |
| ZA823834B (en) | 1983-03-30 |
| FI822250A0 (fi) | 1982-06-22 |
| PT75133A (en) | 1982-07-01 |
| IE53079B1 (en) | 1988-06-08 |
| DK285082A (da) | 1982-12-28 |
| FI822250L (fi) | 1982-12-28 |
| EP0068294A1 (en) | 1983-01-05 |
| AU8444282A (en) | 1983-01-06 |
| PT75133B (en) | 1985-07-26 |
| CA1173744A (en) | 1984-09-04 |
| BR8203746A (pt) | 1983-06-21 |
| PL237105A1 (en) | 1983-02-28 |
| ES513430A0 (es) | 1983-09-01 |
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