DE2355882B2 - FlieBbares, wäßriges Schädlingsbekämpfungsmittel Diamond Shamrock Corp, Cleveland, Ohio (VStA.) - Google Patents
FlieBbares, wäßriges Schädlingsbekämpfungsmittel Diamond Shamrock Corp, Cleveland, Ohio (VStA.)Info
- Publication number
- DE2355882B2 DE2355882B2 DE2355882A DE2355882A DE2355882B2 DE 2355882 B2 DE2355882 B2 DE 2355882B2 DE 2355882 A DE2355882 A DE 2355882A DE 2355882 A DE2355882 A DE 2355882A DE 2355882 B2 DE2355882 B2 DE 2355882B2
- Authority
- DE
- Germany
- Prior art keywords
- pesticide
- agent
- weight
- water
- composition according
- Prior art date
- Legal status (The legal status 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 status listed.)
- Granted
Links
- 239000000575 pesticide Substances 0.000 title claims description 53
- 230000009969 flowable effect Effects 0.000 title claims description 15
- 240000007930 Oxalis acetosella Species 0.000 title description 3
- 235000008098 Oxalis acetosella Nutrition 0.000 title description 3
- 229910003460 diamond Inorganic materials 0.000 title description 3
- 239000010432 diamond Substances 0.000 title description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 49
- 239000000203 mixture Substances 0.000 claims description 49
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 40
- 239000004094 surface-active agent Substances 0.000 claims description 21
- 239000000417 fungicide Substances 0.000 claims description 9
- 239000002518 antifoaming agent Substances 0.000 claims description 8
- 239000002736 nonionic surfactant Substances 0.000 claims description 7
- 230000000855 fungicidal effect Effects 0.000 claims description 6
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical group ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 claims description 5
- 239000002917 insecticide Substances 0.000 claims description 5
- 239000004009 herbicide Substances 0.000 claims description 4
- 239000000375 suspending agent Substances 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 3
- 230000008014 freezing Effects 0.000 claims description 3
- 238000007710 freezing Methods 0.000 claims description 3
- 230000002363 herbicidal effect Effects 0.000 claims description 3
- KZCBXHSWMMIEQU-UHFFFAOYSA-N Chlorthal Chemical compound OC(=O)C1=C(Cl)C(Cl)=C(C(O)=O)C(Cl)=C1Cl KZCBXHSWMMIEQU-UHFFFAOYSA-N 0.000 claims description 2
- 230000000994 depressogenic effect Effects 0.000 claims 2
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 claims 1
- 238000009472 formulation Methods 0.000 description 31
- 239000007787 solid Substances 0.000 description 20
- 238000003860 storage Methods 0.000 description 16
- 239000004615 ingredient Substances 0.000 description 15
- -1 methoxy- Chemical class 0.000 description 15
- 239000000725 suspension Substances 0.000 description 14
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 230000000361 pesticidal effect Effects 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 7
- 239000012071 phase Substances 0.000 description 7
- 239000007921 spray Substances 0.000 description 7
- 239000004721 Polyphenylene oxide Substances 0.000 description 6
- 229920000570 polyether Polymers 0.000 description 6
- 239000004480 active ingredient Substances 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 125000002877 alkyl aryl group Chemical group 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 241000589634 Xanthomonas Species 0.000 description 3
- 238000005054 agglomeration Methods 0.000 description 3
- 230000002776 aggregation Effects 0.000 description 3
- 239000007900 aqueous suspension Substances 0.000 description 3
- 150000001720 carbohydrates Chemical class 0.000 description 3
- 235000014633 carbohydrates Nutrition 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 229920001451 polypropylene glycol Polymers 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 description 2
- 241000238876 Acari Species 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- 241000195493 Cryptophyta Species 0.000 description 2
- 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 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 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 2
- XGEGHDBEHXKFPX-UHFFFAOYSA-N N-methyl urea Chemical compound CNC(N)=O XGEGHDBEHXKFPX-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 241000589636 Xanthomonas campestris Species 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 230000014509 gene expression Effects 0.000 description 2
- 150000004676 glycans Chemical class 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000001069 nematicidal effect Effects 0.000 description 2
- 239000005645 nematicide Substances 0.000 description 2
- 239000012053 oil suspension Substances 0.000 description 2
- 239000003090 pesticide formulation Substances 0.000 description 2
- 229920001282 polysaccharide Polymers 0.000 description 2
- 239000005017 polysaccharide Substances 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 description 2
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 2
- 241000894007 species Species 0.000 description 2
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 2
- 229960002447 thiram Drugs 0.000 description 2
- 231100000167 toxic agent Toxicity 0.000 description 2
- 239000003440 toxic substance Substances 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- 229920001285 xanthan gum Polymers 0.000 description 2
- 239000000230 xanthan gum Substances 0.000 description 2
- 229940082509 xanthan gum Drugs 0.000 description 2
- 235000010493 xanthan gum Nutrition 0.000 description 2
- DNXHEGUUPJUMQT-UHFFFAOYSA-N (+)-estrone Natural products OC1=CC=C2C3CCC(C)(C(CC4)=O)C4C3CCC2=C1 DNXHEGUUPJUMQT-UHFFFAOYSA-N 0.000 description 1
- DSVOTYIOPGIVPP-UHFFFAOYSA-N (3,4-dichlorophenyl)methyl n-methylcarbamate Chemical compound CNC(=O)OCC1=CC=C(Cl)C(Cl)=C1 DSVOTYIOPGIVPP-UHFFFAOYSA-N 0.000 description 1
- JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical compound C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 description 1
- OWEGMIWEEQEYGQ-UHFFFAOYSA-N 100676-05-9 Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC2C(OC(O)C(O)C2O)CO)O1 OWEGMIWEEQEYGQ-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- UENGBOCGGKLVJJ-UHFFFAOYSA-N 2-chloro-1-(2,4-difluorophenyl)ethanone Chemical compound FC1=CC=C(C(=O)CCl)C(F)=C1 UENGBOCGGKLVJJ-UHFFFAOYSA-N 0.000 description 1
- XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 description 1
- XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 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
- 241000605281 Anaplasma phagocytophilum Species 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- RZXLPPRPEOUENN-UHFFFAOYSA-N Chlorfenson Chemical compound C1=CC(Cl)=CC=C1OS(=O)(=O)C1=CC=C(Cl)C=C1 RZXLPPRPEOUENN-UHFFFAOYSA-N 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- 125000002353 D-glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical group OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 1
- NPOJQCVWMSKXDN-UHFFFAOYSA-N Dacthal Chemical compound COC(=O)C1=C(Cl)C(Cl)=C(C(=O)OC)C(Cl)=C1Cl NPOJQCVWMSKXDN-UHFFFAOYSA-N 0.000 description 1
- 239000005510 Diuron Substances 0.000 description 1
- 239000001692 EU approved anti-caking agent Substances 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 229930091371 Fructose Natural products 0.000 description 1
- 239000005715 Fructose Substances 0.000 description 1
- 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 1
- 241000233866 Fungi Species 0.000 description 1
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Chemical group O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 1
- 241000238631 Hexapoda 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
- 239000005573 Linuron Substances 0.000 description 1
- GUBGYTABKSRVRQ-PICCSMPSSA-N Maltose Natural products O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@@H]1[C@@H](CO)OC(O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-PICCSMPSSA-N 0.000 description 1
- CCGPUGMWYLICGL-UHFFFAOYSA-N Neburon Chemical compound CCCCN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 CCGPUGMWYLICGL-UHFFFAOYSA-N 0.000 description 1
- 229920002059 Pluronic® P 104 Polymers 0.000 description 1
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
- JXVIIQLNUPXOII-UHFFFAOYSA-N Siduron Chemical compound CC1CCCCC1NC(=O)NC1=CC=CC=C1 JXVIIQLNUPXOII-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 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
- 229930006000 Sucrose Natural products 0.000 description 1
- 239000005843 Thiram Substances 0.000 description 1
- 241001517672 Xanthomonas axonopodis pv. begoniae Species 0.000 description 1
- 241001677365 Xanthomonas axonopodis pv. vasculorum Species 0.000 description 1
- 241000589643 Xanthomonas translucens Species 0.000 description 1
- 241000567019 Xanthomonas vesicatoria Species 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 229960001413 acetanilide Drugs 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 1
- 206010000496 acne Diseases 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 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 1
- AEMOLEFTQBMNLQ-WAXACMCWSA-N alpha-D-glucuronic acid Chemical group O[C@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-WAXACMCWSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000002528 anti-freeze Effects 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- SMDHCQAYESWHAE-UHFFFAOYSA-N benfluralin Chemical compound CCCCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O SMDHCQAYESWHAE-UHFFFAOYSA-N 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
- GUBGYTABKSRVRQ-QUYVBRFLSA-N beta-maltose Chemical compound OC[C@H]1O[C@H](O[C@H]2[C@H](O)[C@@H](O)[C@H](O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@@H]1O GUBGYTABKSRVRQ-QUYVBRFLSA-N 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 231100000481 chemical toxicant Toxicity 0.000 description 1
- PFIADAMVCJPXSF-UHFFFAOYSA-N chloroneb Chemical compound COC1=CC(Cl)=C(OC)C=C1Cl PFIADAMVCJPXSF-UHFFFAOYSA-N 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 description 1
- 229950006824 dieldrin Drugs 0.000 description 1
- NGPMUTDCEIKKFM-UHFFFAOYSA-N dieldrin Natural products CC1=C(Cl)C2(Cl)C3C4CC(C5OC45)C3C1(Cl)C2(Cl)Cl NGPMUTDCEIKKFM-UHFFFAOYSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229930182830 galactose Natural products 0.000 description 1
- JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 1
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 229960002809 lindane Drugs 0.000 description 1
- 239000006194 liquid suspension Substances 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N monoethanolamine hydrochloride Natural products NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- BMLIZLVNXIYGCK-UHFFFAOYSA-N monuron Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C=C1 BMLIZLVNXIYGCK-UHFFFAOYSA-N 0.000 description 1
- AGKHYRYULQFGQA-UHFFFAOYSA-N n-(4-methylphenyl)nitramide Chemical compound CC1=CC=C(N[N+]([O-])=O)C=C1 AGKHYRYULQFGQA-UHFFFAOYSA-N 0.000 description 1
- RJMUSRYZPJIFPJ-UHFFFAOYSA-N niclosamide Chemical compound OC1=CC=C(Cl)C=C1C(=O)NC1=CC=C([N+]([O-])=O)C=C1Cl RJMUSRYZPJIFPJ-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- AAEVYOVXGOFMJO-UHFFFAOYSA-N prometryn Chemical compound CSC1=NC(NC(C)C)=NC(NC(C)C)=N1 AAEVYOVXGOFMJO-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- 231100000765 toxin Toxicity 0.000 description 1
- WHNYVDJJCTVMGO-UHFFFAOYSA-N tricyclo[5.2.1.02,6]dec-8-ene Chemical compound C1=CC2CC1C1C2CCC1 WHNYVDJJCTVMGO-UHFFFAOYSA-N 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 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
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Dispersion Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Plant Pathology (AREA)
- Toxicology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/305,064 US3948636A (en) | 1972-11-09 | 1972-11-09 | Flowable aqueous composition of water-insoluble pesticide |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2355882A1 DE2355882A1 (de) | 1974-05-16 |
| DE2355882B2 true DE2355882B2 (de) | 1979-03-15 |
| DE2355882C3 DE2355882C3 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1989-12-14 |
Family
ID=23179168
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2355882A Granted DE2355882B2 (de) | 1972-11-09 | 1973-11-08 | FlieBbares, wäßriges Schädlingsbekämpfungsmittel Diamond Shamrock Corp, Cleveland, Ohio (VStA.) |
Country Status (7)
Families Citing this family (66)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2547968A1 (de) * | 1975-10-27 | 1977-05-05 | Basf Ag | Herbizid |
| IE43966B1 (en) * | 1975-11-12 | 1981-07-15 | Fisons Ltd | Aqueous suspensions of substituted benzofuran herbicides |
| US4188202A (en) * | 1975-11-12 | 1980-02-12 | Fisons Limited | Composition |
| JPS5824401B2 (ja) * | 1975-11-27 | 1983-05-20 | ホクコウカガクコウギヨウ カブシキガイシヤ | アンテイナルケンダクジヨウノウヤク |
| US4094664A (en) * | 1976-02-04 | 1978-06-13 | Hoffmann-La Roche Inc. | Plant growth regulating agents |
| US4061770A (en) * | 1976-04-15 | 1977-12-06 | Diamond Shamrock Corporation | Flowable, aqueous pesticide compositions of improved activity |
| US4119537A (en) * | 1977-04-29 | 1978-10-10 | Hershel Finkelstein | Method for slime control |
| JPS545037A (en) * | 1977-06-13 | 1979-01-16 | Katayama Chemical Works Co | Gell state preparation for controlling harmful organism in sea water |
| US4313847A (en) * | 1978-06-15 | 1982-02-02 | Ici Americas Inc. | Surfactant compositions |
| CA1118226A (en) * | 1978-07-17 | 1982-02-16 | Harold A. Kaufman | Flowable ammonium thiocyanate defoliant and desiccant compositions |
| US4389238A (en) * | 1978-07-17 | 1983-06-21 | J. T. Baker Chemical Company | Flowable herbicide and pesticide formulation |
| EG13714A (en) * | 1978-11-03 | 1982-06-30 | Monsanto Co | Flow able herbicides |
| US4372777A (en) * | 1978-11-03 | 1983-02-08 | Monsanto Company | Flowable herbicides |
| US4371390A (en) * | 1978-11-03 | 1983-02-01 | Monsanto Company | Flowable herbicides |
| US4303793A (en) * | 1979-03-12 | 1981-12-01 | Ppg Industries, Inc. | Aqueous carbamate dispersions |
| JPS55129201A (en) * | 1979-03-28 | 1980-10-06 | Kao Corp | Fluid pesticidal composition |
| DE2914867A1 (de) * | 1979-04-12 | 1980-10-16 | Hoechst Ag | Herbizide mittel |
| US4379144A (en) * | 1979-08-30 | 1983-04-05 | Olin Corporation | Process for producing a flowable fungicide formulation |
| US4266965A (en) * | 1979-10-29 | 1981-05-12 | Stauffer Chemical Company | 2-(α-naphthoxy)-N,N-diethyl propionamide as an aqueous flowable concentrate |
| DE3062372D1 (en) * | 1979-11-23 | 1983-04-21 | Shell Int Research | Water-based pesticidal suspension and process for its manufacture |
| FR2474278A1 (fr) * | 1980-01-29 | 1981-07-31 | Rhone Poulenc Agrochimie | Suspensions aqueuses d'insecticide, leur preparation et leur utilisation |
| US4323602A (en) * | 1980-05-14 | 1982-04-06 | Roberts Consolidated Industries, Inc. | Water repellent and preservative for wood products |
| DE3048021A1 (de) * | 1980-12-19 | 1982-07-15 | Bayer Ag, 5090 Leverkusen | Insektizide und akarizide mittel und ihre verwendung |
| US4411692A (en) * | 1981-03-26 | 1983-10-25 | Monsanto Company | Flowable herbicides |
| US4411693A (en) * | 1981-03-26 | 1983-10-25 | Monsanto Company | Flowable herbicides |
| FR2510870A1 (fr) * | 1981-08-10 | 1983-02-11 | Rhone Poulenc Agrochimie | Suspensions aqueuses concentrees a base de neburon |
| JPS58124702A (ja) * | 1982-01-21 | 1983-07-25 | Kumiai Chem Ind Co Ltd | 水中懸濁型農薬製剤 |
| US4461641A (en) * | 1982-02-25 | 1984-07-24 | Ciba-Geigy Corporation | Herbicidal mixtures |
| DE3240862A1 (de) * | 1982-11-05 | 1984-05-10 | Hoechst Ag, 6230 Frankfurt | Fluessige pestizide mittel in form von suspensionskonzentraten |
| GB2138798A (en) * | 1983-04-25 | 1984-10-31 | Dearborn Chemicals Ltd | Biocide |
| US4599192A (en) * | 1983-08-24 | 1986-07-08 | Mineral Research And Development Corp. | Wood-treating composition |
| JPH0759481B2 (ja) * | 1983-11-10 | 1995-06-28 | 日本農薬株式会社 | 安定なる水中懸濁状農薬製剤 |
| US5073189A (en) * | 1985-09-27 | 1991-12-17 | American Cyanamid Company | Pesticidal aqueous flowable compositions |
| US4874854A (en) * | 1985-10-08 | 1989-10-17 | Merck & Co., Inc. | Low viscosity heteropolysaccharides |
| FR2600862B1 (fr) * | 1986-03-10 | 1990-04-13 | Rhone Poulenc Chim Base | Compositions aqueuses contenant un compose cationique et de la gomme xanthane et procede de preparation. |
| CA1289065C (en) * | 1986-05-23 | 1991-09-17 | Leonard John Morgan | Aqueous suspension concentrate compositions |
| US4875929A (en) * | 1986-05-23 | 1989-10-24 | American Cyanamid Company | Aqueous suspension concentrate compositions |
| US5624884A (en) * | 1986-05-23 | 1997-04-29 | American Cyanamid Company | Aqueous suspension concentrate compositions of pendimethalin |
| US5679619A (en) * | 1986-05-23 | 1997-10-21 | American Cyanamid Company | Aqueous suspension concentrate compositions of pendimethalin |
| US4871392A (en) * | 1986-05-23 | 1989-10-03 | American Cyanamid Company | Aqueous suspension concentrate compositions of pendimethalin |
| FR2630885B1 (fr) * | 1988-05-09 | 1991-03-01 | Rhone Poulenc Agrochimie | Emulsion pesticide huile dans l'eau, procede de mise en oeuvre |
| US5254344A (en) * | 1988-05-09 | 1993-10-19 | Rhone-Poulenc Inc. | Oil-in-water pesticidal emulsion, process for application |
| US5206021A (en) * | 1988-05-09 | 1993-04-27 | Rhone-Poulenc Ag Company | Stabilized oil-in-water emulsions or suspoemulsions containing pesticidal substances in both oil and water phases |
| AU657493B2 (en) * | 1990-08-08 | 1995-03-16 | Carlton Lahey Chemicals, Inc. | Extender formulation imparting sustaining properties to agricultural products |
| DE4037504A1 (de) * | 1990-11-26 | 1992-05-27 | Henkel Kgaa | Fungizide wirkstoffloesung |
| CA2075920A1 (en) * | 1990-12-18 | 1992-06-19 | Jeffrey L. Jensen | Precipitated flowable concentrate formulations, their preparation and their agricultural uses |
| TR27743A (tr) * | 1992-05-28 | 1995-07-07 | Dowelanco | Sulu, akici fenazakin bilesimi. |
| WO1994009626A1 (en) * | 1992-11-03 | 1994-05-11 | Sil-Tech International Corporation | Insect control compositions |
| US5866153A (en) * | 1993-02-09 | 1999-02-02 | Novartis Corporation | Process for the preparation of microcapsules |
| DE4343856A1 (de) * | 1993-12-22 | 1995-06-29 | Hoechst Ag | Öl-in-Wasser-Emulsionen |
| US5629261A (en) * | 1995-08-08 | 1997-05-13 | Isp Investments Inc. | Free-flowing, non-dusting water dispersible granules of a water-insoluble, hydrophobic agriculturally active chemical having low friability and superior crush strength |
| US5629350A (en) * | 1996-03-20 | 1997-05-13 | The Dow Chemical Company | Suspension formulations of ortho-phenylphenol |
| US5627135A (en) * | 1996-03-20 | 1997-05-06 | The Dow Chemical Company | Suspension fomulations of 2,2-dibromo-3-nitrilopropionamide |
| US6156803A (en) * | 1997-10-14 | 2000-12-05 | Isp Investments Inc | Aqueous, flowable suspension concentrate of an agriculturally active chemical, and sprayable use formulation thereof |
| US6121197A (en) * | 1999-05-24 | 2000-09-19 | Creanova Inc. | Biocidal composition |
| US6121198A (en) * | 1999-05-24 | 2000-09-19 | Creanova Inc. | Synergistic composition of biocides |
| US7246717B2 (en) * | 2002-09-12 | 2007-07-24 | Power Generation & Engineering, Inc. | Fire resistant base tank for mounting a generator |
| US20060115506A1 (en) * | 2004-11-30 | 2006-06-01 | Harmer Mark A | Compositions and method of wood preservation |
| WO2007081965A2 (en) * | 2006-01-10 | 2007-07-19 | Innovaform Technologies, Llc | Pesticide delivery system |
| PE20131355A1 (es) | 2010-09-14 | 2013-12-06 | Basf Se | Composicion que contiene un insecticida de piripiropeno y un adyuvante |
| KR101938020B1 (ko) | 2010-09-14 | 2019-01-11 | 바스프 에스이 | 피리피로펜 살곤충제 및 염기를 함유하는 조성물 |
| MX360698B (es) * | 2012-03-12 | 2018-11-14 | Basf Se | Formulación concentrada líquida que contiene un insecticida de piripiropeno i. |
| CN104185421B (zh) | 2012-03-12 | 2016-06-01 | 巴斯夫欧洲公司 | 含有啶南平杀虫剂的液体浓缩物配制剂ii |
| EP2825043B1 (en) | 2012-03-12 | 2018-09-05 | Basf Se | Method for producing an aqueous suspension concentrate formulation of a pyripyropene insecticide |
| US20130331267A1 (en) * | 2012-06-06 | 2013-12-12 | Dow Agrosciences Llc | High strength herbicidal suspension concentrates |
| DE102015105841A1 (de) | 2015-04-16 | 2016-10-20 | Sanoviva Ag | Verfahren zum Herstellen eines Mittels zur Verbesserung des Pflanzenwachstums |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2786011A (en) * | 1954-06-18 | 1957-03-19 | Ohio Commw Eng Co | Stable concentrated aqueous dispersion of pesticides and the like |
| US3020206A (en) * | 1960-05-23 | 1962-02-06 | Jersey Prod Res Co | Process for synthesizing polysaccharides |
| US3244695A (en) * | 1963-10-11 | 1966-04-05 | Kelco Co | Cationic ethers of xanthomonas hydrophilic colloids |
| US3399991A (en) * | 1964-05-05 | 1968-09-03 | Du Pont | Freeze-resistant pesticidal composition |
| GB1047601A (en) * | 1964-06-16 | 1966-11-09 | Amchem Prod | Herbicidal compositions |
| US3484229A (en) * | 1966-03-28 | 1969-12-16 | Hercules Inc | Microbial polysaccharide gums as herbicide spray drift control agents |
| US3551133A (en) * | 1966-08-01 | 1970-12-29 | Diamond Shamrock Corp | Granular thickening agent and preparation |
| US3594151A (en) * | 1968-11-12 | 1971-07-20 | Diamond Shamrock Corp | Herbicidally active spray composition |
| US3659026A (en) * | 1969-12-08 | 1972-04-25 | Kelso Co | Mixture of xanthomonas hydrophylic colloid and locust bean gum as agricultural carrier |
| US3717452A (en) * | 1970-01-16 | 1973-02-20 | Kelco Co | Applying agricultural chemicals with xanthomones hydrophillic colloids |
-
1972
- 1972-11-09 US US05/305,064 patent/US3948636A/en not_active Expired - Lifetime
-
1973
- 1973-11-08 DE DE2355882A patent/DE2355882B2/de active Granted
- 1973-11-08 BR BR8749/73A patent/BR7308749D0/pt unknown
- 1973-11-08 CA CA185,369A patent/CA1022071A/en not_active Expired
- 1973-11-08 FR FR7339692A patent/FR2206049B1/fr not_active Expired
- 1973-11-09 JP JP12553973A patent/JPS5346889B2/ja not_active Expired
-
1978
- 1978-06-28 BE BE188897A patent/BE868530Q/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| CA1022071A (en) | 1977-12-06 |
| FR2206049B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1977-06-03 |
| JPS49133531A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1974-12-21 |
| JPS5346889B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1978-12-16 |
| DE2355882A1 (de) | 1974-05-16 |
| US3948636A (en) | 1976-04-06 |
| FR2206049A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1974-06-07 |
| US3948636B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1985-09-10 |
| BR7308749D0 (pt) | 1974-08-29 |
| BE868530Q (fr) | 1978-10-16 |
| DE2355882C3 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1989-12-14 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2355882B2 (de) | FlieBbares, wäßriges Schädlingsbekämpfungsmittel Diamond Shamrock Corp, Cleveland, Ohio (VStA.) | |
| EP0052313B1 (de) | Fliessfähige Pestizide | |
| EP0110174B1 (de) | Flüssige pestizide Mittel in Form von Suspensionskonzentraten | |
| DE69810900T2 (de) | Agrochemische zusammensetzungen von oberflächenaktiven verbindungen | |
| DE69517063T2 (de) | Pestizide Zusammensetzungen enthaltend Zinkoxid | |
| EP0117999B1 (de) | Pflanzenschutzmittel in Form von Mischdispersionen | |
| DE69015849T2 (de) | Agrochemische und biozide Suspensionen. | |
| DE69607743T2 (de) | Insektizide kombinationen enthaltend ein insektizid der chloronikotinyl-reihe und ein insektizid mit eine pyrazol-, pyrrol oder phenylimidazol-gruppe | |
| DE3875251T2 (de) | Agrochemische zusammensetzungen auf basis von latex. | |
| DE3786845T2 (de) | Wässrige Suspensionskonzentrate von Pendimethalin. | |
| EP0702896A1 (de) | Thixotrope wässrige Pflanzenschutzmittel-Suspension | |
| DE4013930A1 (de) | Fluessige konzentrierte zusammensetzungen auf der basis von n-phosphonomethylglycin | |
| DD207140A5 (de) | Herbizide emulsionen | |
| DD276023A5 (de) | Verfahren zur herstellung einer waessrigen suspensionskonzentratzusammensetzung von pendimethalin | |
| DE69903524T2 (de) | Pestizide hilfsmittel | |
| EP0499798A1 (de) | Flüssige Zubereitungen von Herbizidmischungen auf Basis Glufosinate | |
| DE68912942T2 (de) | Stabilisiertes wässriges Pestizidsuspensionskonzentrat. | |
| DE69826020T2 (de) | Wässriges, fließfähiges Suspensionskonzentrat einer Agrichemikalie und deren sprühbare Formulierung | |
| EP0074329B1 (de) | Wässrige Pestizidkonzentrate | |
| DD153755A5 (de) | Waessriges fliessfaehiges lagerungsstabiles herbizides konzentrat | |
| DE3005016A1 (de) | Insektizide hilfsmittelzusammensetzung | |
| DE69530146T2 (de) | Dispergierendes Mittel für feste Pflanzenschutzformulierungen | |
| EP0017879B1 (de) | Flüssige Formulierungen enthaltend 3-(3,4-Dichlorphenyl)-1-methyl-1-methoxy-harnstoff und ihre Verwendung zur Unkrautbekämpfung | |
| EP0975215B1 (de) | Pflanzenschutzmittel | |
| CH603055A5 (en) | Aq. formulations of insol. pesticides |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8227 | New person/name/address of the applicant |
Free format text: SDS BIOTECH CORP., PAINESVILLE, OHIO, US |
|
| 8228 | New agent |
Free format text: WEICKMANN, H., DIPL.-ING. FINCKE, K., DIPL.-PHYS. DR. WEICKMANN, F., DIPL.-ING. HUBER, B., DIPL.-CHEM. LISKA, H., DIPL.-ING. DR.-ING. PRECHTEL, J., DIPL.-PHYS. DR.RER.NAT., PAT.-ANW., 8000 MUENCHEN |
|
| C3 | Grant after two publication steps (3rd publication) | ||
| 8327 | Change in the person/name/address of the patent owner |
Owner name: FERMENTA ASC CORP., MENTOR, OHIO, US |
|
| 8327 | Change in the person/name/address of the patent owner |
Owner name: ISK BIOTECH CORP., MENTOR, OHIO, US |