CH626875A5 - A pesticide which contains, as active ingredient, a carbonylaminocarbonylphenylformamidine - Google Patents

A pesticide which contains, as active ingredient, a carbonylaminocarbonylphenylformamidine Download PDF

Info

Publication number: CH626875A5
Authority: CH; Switzerland
Prior art keywords: formula; compound; parts; active component; chlorine
Prior art date: 1977-01-12

Application number

CH34077A

Other languages

German (de)

English (en)

Inventor

Jozef Dr Drabek

Ernst Dr Beriger

Dieter Dr Duerr

Kurt Dr Ruefenacht

Manfred Boeger

Original Assignee

Ciba Geigy Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1977-01-12

Filing date

1977-01-12

Publication date

1981-12-15

1977-01-11 Priority to ES465882A priority Critical patent/ES465882A1/es

1977-01-12 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1977-01-12 Priority to CH34077A priority patent/CH626875A5/de

1978-01-06 Priority to US05/867,651 priority patent/US4150160A/en

1978-01-09 Priority to DE19782800786 priority patent/DE2800786A1/de

1978-01-09 Priority to FI780058A priority patent/FI780058A7/fi

1978-01-10 Priority to TR19835A priority patent/TR19835A/xx

1978-01-10 Priority to IL53772A priority patent/IL53772A/xx

1978-01-10 Priority to FR7800519A priority patent/FR2377378A1/fr

1978-01-10 Priority to CA294,696A priority patent/CA1090820A/fr

1978-01-11 Priority to AU32349/78A priority patent/AU511793B2/en

1978-01-11 Priority to AT18778A priority patent/AT356456B/de

1978-01-11 Priority to BR7800151A priority patent/BR7800151A/pt

1978-01-11 Priority to EG19/78A priority patent/EG12962A/xx

1978-01-11 Priority to ZA00780167A priority patent/ZA78167B/xx

1978-01-11 Priority to NO780104A priority patent/NO780104L/no

1978-01-11 Priority to JP183778A priority patent/JPS5387335A/ja

1978-01-11 Priority to IT7819168A priority patent/IT7819168A0/it

1978-01-11 Priority to MX786766U priority patent/MX5268E/es

1978-01-11 Priority to GB1074/78A priority patent/GB1588062A/en

1978-01-11 Priority to SE7800305A priority patent/SE7800305L/xx

1978-01-11 Priority to DK13078A priority patent/DK13078A/da

1978-01-11 Priority to BE184238A priority patent/BE862814A/fr

1978-01-12 Priority to NL7800384A priority patent/NL7800384A/xx

1978-01-12 Priority to GR55140A priority patent/GR72110B/el

1981-12-15 Publication of CH626875A5 publication Critical patent/CH626875A5/de

Links

239000000575 pesticide Substances 0.000 title claims abstract description 8
239000004480 active ingredient Substances 0.000 title abstract description 30
ARLLRBGXKHIHEI-UHFFFAOYSA-N 1-(benzenecarboximidoyl)-3-(oxomethylidene)urea Chemical compound C(=O)=NC(=O)N=C(N)C1=CC=CC=C1 ARLLRBGXKHIHEI-UHFFFAOYSA-N 0.000 title abstract 2
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 9
239000001257 hydrogen Substances 0.000 claims abstract description 9
229910052736 halogen Inorganic materials 0.000 claims abstract description 7
150000002367 halogens Chemical class 0.000 claims abstract description 7
241000607479 Yersinia pestis Species 0.000 claims abstract description 6
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 5
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 5
150000002431 hydrogen Chemical class 0.000 claims abstract description 5
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 5
125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims abstract description 3
150000001875 compounds Chemical class 0.000 claims description 38
-1 carbonylaminocarbonylphenylformamide Chemical compound 0.000 claims description 20
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 16
239000003795 chemical substances by application Substances 0.000 claims description 13
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 12
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 12
239000000460 chlorine Substances 0.000 claims description 12
229910052801 chlorine Inorganic materials 0.000 claims description 12
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 8
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 6
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
241000238631 Hexapoda Species 0.000 claims description 6
241000244206 Nematoda Species 0.000 claims description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 5
238000000034 method Methods 0.000 claims description 5
239000008096 xylene Substances 0.000 claims description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 4
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 4
241000233866 Fungi Species 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 4
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 claims description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 4
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
229910052794 bromium Inorganic materials 0.000 claims description 4
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 4
230000003032 phytopathogenic effect Effects 0.000 claims description 4
239000002904 solvent Substances 0.000 claims description 4
239000011230 binding agent Substances 0.000 claims description 3
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 2
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 2
BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 claims description 2
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 claims description 2
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
239000002253 acid Substances 0.000 claims description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
239000003513 alkali Substances 0.000 claims description 2
229910052783 alkali metal Inorganic materials 0.000 claims description 2
150000001340 alkali metals Chemical class 0.000 claims description 2
150000001342 alkaline earth metals Chemical class 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims description 2
150000001408 amides Chemical class 0.000 claims description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
150000004649 carbonic acid derivatives Chemical class 0.000 claims description 2
150000003857 carboxamides Chemical class 0.000 claims description 2
239000003085 diluting agent Substances 0.000 claims description 2
POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 claims description 2
229910052731 fluorine Inorganic materials 0.000 claims description 2
239000011737 fluorine Substances 0.000 claims description 2
150000008282 halocarbons Chemical class 0.000 claims description 2
150000004679 hydroxides Chemical class 0.000 claims description 2
239000003701 inert diluent Substances 0.000 claims description 2
239000012442 inert solvent Substances 0.000 claims description 2
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 2
150000002576 ketones Chemical class 0.000 claims description 2
150000002825 nitriles Chemical class 0.000 claims description 2
229910052757 nitrogen Inorganic materials 0.000 claims description 2
229910052700 potassium Inorganic materials 0.000 claims description 2
239000011591 potassium Substances 0.000 claims description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 2
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
150000003512 tertiary amines Chemical class 0.000 claims description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 2
125000005270 trialkylamine group Chemical group 0.000 claims description 2
239000000203 mixture Substances 0.000 abstract description 9
238000012360 testing method Methods 0.000 description 15
239000008187 granular material Substances 0.000 description 8
239000007921 spray Substances 0.000 description 8
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
230000000694 effects Effects 0.000 description 7
239000000126 substance Substances 0.000 description 7
241000196324 Embryophyta Species 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
239000000839 emulsion Substances 0.000 description 6
230000000749 insecticidal effect Effects 0.000 description 6
239000000243 solution Substances 0.000 description 6
235000015112 vegetable and seed oil Nutrition 0.000 description 6
239000008158 vegetable oil Substances 0.000 description 6
239000005995 Aluminium silicate Substances 0.000 description 5
235000012211 aluminium silicate Nutrition 0.000 description 5
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 5
229920000151 polyglycol Polymers 0.000 description 5
239000010695 polyglycol Substances 0.000 description 5
230000000895 acaricidal effect Effects 0.000 description 4
239000000654 additive Substances 0.000 description 4
239000004495 emulsifiable concentrate Substances 0.000 description 4
239000002689 soil Substances 0.000 description 4
241000238876 Acari Species 0.000 description 3
241000426497 Chilo suppressalis Species 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
240000005979 Hordeum vulgare Species 0.000 description 3
239000000969 carrier Substances 0.000 description 3
235000019993 champagne Nutrition 0.000 description 3
238000010790 dilution Methods 0.000 description 3
239000012895 dilution Substances 0.000 description 3
239000000843 powder Substances 0.000 description 3
238000012545 processing Methods 0.000 description 3
239000000377 silicon dioxide Substances 0.000 description 3
230000009885 systemic effect Effects 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
241001124076 Aphididae Species 0.000 description 2
241001425390 Aphis fabae Species 0.000 description 2
241001480061 Blumeria graminis Species 0.000 description 2
229920000742 Cotton Polymers 0.000 description 2
240000002024 Gossypium herbaceum Species 0.000 description 2
235000004341 Gossypium herbaceum Nutrition 0.000 description 2
241000256244 Heliothis virescens Species 0.000 description 2
239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
241000243784 Meloidogyne arenaria Species 0.000 description 2
244000046052 Phaseolus vulgaris Species 0.000 description 2
239000002202 Polyethylene glycol Substances 0.000 description 2
241000949016 Rhipicephalus bursa Species 0.000 description 2
241000238680 Rhipicephalus microplus Species 0.000 description 2
241000256250 Spodoptera littoralis Species 0.000 description 2
241001454293 Tetranychus urticae Species 0.000 description 2
239000013543 active substance Substances 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
239000000470 constituent Substances 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
235000013601 eggs Nutrition 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
238000009472 formulation Methods 0.000 description 2
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
239000007788 liquid Substances 0.000 description 2
230000001069 nematicidal effect Effects 0.000 description 2
125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
239000002574 poison Substances 0.000 description 2
231100000614 poison Toxicity 0.000 description 2
229920001223 polyethylene glycol Polymers 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
UXPPDBVMSPAPCL-UHFFFAOYSA-N 1-prop-1-ynoxyprop-1-yne Chemical compound CC#COC#CC UXPPDBVMSPAPCL-UHFFFAOYSA-N 0.000 description 1
QQGRFMIMXPWKPM-UHFFFAOYSA-N 2,3,4-tributylphenol Chemical compound CCCCC1=CC=C(O)C(CCCC)=C1CCCC QQGRFMIMXPWKPM-UHFFFAOYSA-N 0.000 description 1
241000894006 Bacteria Species 0.000 description 1
241000238660 Blattidae Species 0.000 description 1
241000283690 Bos taurus Species 0.000 description 1
FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 1
BNARGNJKJAZKNK-UHFFFAOYSA-N CC#COP(O)=O Chemical class CC#COP(O)=O BNARGNJKJAZKNK-UHFFFAOYSA-N 0.000 description 1
241000257161 Calliphoridae Species 0.000 description 1
241001414835 Cimicidae Species 0.000 description 1
241000255749 Coccinellidae Species 0.000 description 1
241001466044 Delphacidae Species 0.000 description 1
241000131287 Dermestidae Species 0.000 description 1
241001414830 Diaspididae Species 0.000 description 1
241000255925 Diptera Species 0.000 description 1
235000009161 Espostoa lanata Nutrition 0.000 description 1
240000001624 Espostoa lanata Species 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
PNKUSGQVOMIXLU-UHFFFAOYSA-N Formamidine Chemical class NC=N PNKUSGQVOMIXLU-UHFFFAOYSA-N 0.000 description 1
241000219146 Gossypium Species 0.000 description 1
241000238816 Gryllidae Species 0.000 description 1
241001243087 Gryllotalpidae Species 0.000 description 1
241000256257 Heliothis Species 0.000 description 1
235000007340 Hordeum vulgare Nutrition 0.000 description 1
206010061217 Infestation Diseases 0.000 description 1
241000238889 Ixodidae Species 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
241000258916 Leptinotarsa decemlineata Species 0.000 description 1
235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
241000257159 Musca domestica Species 0.000 description 1
241000257226 Muscidae Species 0.000 description 1
241000721621 Myzus persicae Species 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
241000488585 Panonychus Species 0.000 description 1
241001415279 Pseudococcidae Species 0.000 description 1
241000258921 Pulicidae Species 0.000 description 1
241001510071 Pyrrhocoridae Species 0.000 description 1
241001124072 Reduviidae Species 0.000 description 1
241000254062 Scarabaeidae Species 0.000 description 1
WABPPBHOPMUJHV-UHFFFAOYSA-N Sesamex Chemical compound CCOCCOCCOC(C)OC1=CC=C2OCOC2=C1 WABPPBHOPMUJHV-UHFFFAOYSA-N 0.000 description 1
240000003768 Solanum lycopersicum Species 0.000 description 1
241000256248 Spodoptera Species 0.000 description 1
241000254107 Tenebrionidae Species 0.000 description 1
241000255588 Tephritidae Species 0.000 description 1
241001454294 Tetranychus Species 0.000 description 1
241000896028 Tettigoniidae Species 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
240000006677 Vicia faba Species 0.000 description 1
235000010749 Vicia faba Nutrition 0.000 description 1
241000700605 Viruses Species 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
DNEHKUCSURWDGO-UHFFFAOYSA-N aluminum sodium Chemical compound [Na].[Al] DNEHKUCSURWDGO-UHFFFAOYSA-N 0.000 description 1
238000009835 boiling Methods 0.000 description 1
OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 1
YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
230000001418 larval effect Effects 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
238000002156 mixing Methods 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
RBXVOQPAMPBADW-UHFFFAOYSA-N nitrous acid;phenol Chemical class ON=O.OC1=CC=CC=C1 RBXVOQPAMPBADW-UHFFFAOYSA-N 0.000 description 1
239000006072 paste Substances 0.000 description 1
230000001717 pathogenic effect Effects 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
150000003018 phosphorus compounds Chemical class 0.000 description 1
229960005235 piperonyl butoxide Drugs 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
FHQKDLNFTINTBW-UHFFFAOYSA-N prop-1-ynyl carbamate Chemical class CC#COC(N)=O FHQKDLNFTINTBW-UHFFFAOYSA-N 0.000 description 1
230000003014 reinforcing effect Effects 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000002002 slurry Substances 0.000 description 1
KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
SRAWNDFHGTVUNZ-UHFFFAOYSA-M sodium;3,6-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(CCCC)=CC2=CC(CCCC)=CC=C21 SRAWNDFHGTVUNZ-UHFFFAOYSA-M 0.000 description 1
238000009331 sowing Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
ZOKXUAHZSKEQSS-UHFFFAOYSA-N tribufos Chemical compound CCCCSP(=O)(SCCCC)SCCCC ZOKXUAHZSKEQSS-UHFFFAOYSA-N 0.000 description 1
244000045561 useful plants Species 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/46—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylureas
- C07C275/48—Y being a hydrogen or a carbon atom
- C07C275/56—X being a nitrogen atom
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products

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Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pyridine Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CH34077A 1977-01-12 1977-01-12 A pesticide which contains, as active ingredient, a carbonylaminocarbonylphenylformamidine CH626875A5 (en)

Priority Applications (24)

Application Number	Priority Date	Filing Date	Title
ES465882A ES465882A1 (es)	1977-01-12	1977-01-11	Procedimiento para la preparacion de carbimido-carbonil fe- nil formamidinas
CH34077A CH626875A5 (en)	1977-01-12	1977-01-12	A pesticide which contains, as active ingredient, a carbonylaminocarbonylphenylformamidine
US05/867,651 US4150160A (en)	1977-01-12	1978-01-06	Pesticidal carbimidocarbonylphenylformamidines
DE19782800786 DE2800786A1 (de)	1977-01-12	1978-01-09	Carbimidocarbonylphenyl-formamidine, verfahren zu ihrer herstellung und ihre verwendung in der schaedlingsbekaempfung
FI780058A FI780058A7 (fi)	1977-01-12	1978-01-09	Nya amidiner och foerfarande foer deras framstaellning
TR19835A TR19835A (tr)	1977-01-12	1978-01-10	Yeni amidinler
IL53772A IL53772A (en)	1977-01-12	1978-01-10	N'-phenylcarbimidocarbonyl phenylformamidines,their manufacture and pesticidal compositions containing them
FR7800519A FR2377378A1 (fr)	1977-01-12	1978-01-10	Nouvelles amidines
CA294,696A CA1090820A (fr)	1977-01-12	1978-01-10	Amidines
BR7800151A BR7800151A (pt)	1977-01-12	1978-01-11	Composto organico,processo para sua preparacao,composicao praguicida e seu emprego
IT7819168A IT7819168A0 (it)	1977-01-12	1978-01-11	Ammidine procedimento per la loro preparazione e loro impiego.
AU32349/78A AU511793B2 (en)	1977-01-12	1978-01-11	Carbimidocarbonylphenylformamidines
EG19/78A EG12962A (en)	1977-01-12	1978-01-11	Process for preparing of carbimidocarbonylphenylformaidine compounds and their use in pest control
ZA00780167A ZA78167B (en)	1977-01-12	1978-01-11	Novel amidines
NO780104A NO780104L (no)	1977-01-12	1978-01-11	Nye amidiner.
JP183778A JPS5387335A (en)	1977-01-12	1978-01-11	Carbimidecarbonylphenylformamidin and method of its production and preventive agent for harmful organism containing said compound
AT18778A AT356456B (de)	1977-01-12	1978-01-11	Mittel zur bekaempfung von insekten und vertretern der ordnung akarina
MX786766U MX5268E (es)	1977-01-12	1978-01-11	Procedimiento para la preparacion de carbimidocarbonilfenil-formamidinas
GB1074/78A GB1588062A (en)	1977-01-12	1978-01-11	N-carbimidocarbonylphenyl formamidines and their pesticidal compositions
SE7800305A SE7800305L (sv)	1977-01-12	1978-01-11	Nya amidiner
DK13078A DK13078A (da)	1977-01-12	1978-01-11	Carbimidocarbonylphenylformmidiner fremgangsmaade til fremstilling heraf og anvedelse heraf til bekaeaapelse af skadelige arganismer
BE184238A BE862814A (fr)	1977-01-12	1978-01-11	Nouvelles amidines
NL7800384A NL7800384A (nl)	1977-01-12	1978-01-12	Amidinen.
GR55140A GR72110B (fr)	1977-01-12	1978-01-12

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH34077A CH626875A5 (en)	1977-01-12	1977-01-12	A pesticide which contains, as active ingredient, a carbonylaminocarbonylphenylformamidine

Publications (1)

Publication Number	Publication Date
CH626875A5 true CH626875A5 (en)	1981-12-15

Family

ID=4184782

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH34077A CH626875A5 (en)	1977-01-12	1977-01-12	A pesticide which contains, as active ingredient, a carbonylaminocarbonylphenylformamidine

Country Status (4)

Country	Link
AT (1)	AT356456B (fr)
BE (1)	BE862814A (fr)
CH (1)	CH626875A5 (fr)
ZA (1)	ZA78167B (fr)

1977
- 1977-01-12 CH CH34077A patent/CH626875A5/de not_active IP Right Cessation
1978
- 1978-01-11 AT AT18778A patent/AT356456B/de not_active IP Right Cessation
- 1978-01-11 BE BE184238A patent/BE862814A/fr not_active IP Right Cessation
- 1978-01-11 ZA ZA00780167A patent/ZA78167B/xx unknown

Also Published As

Publication number	Publication date
ZA78167B (en)	1978-10-25
ATA18778A (de)	1979-09-15
AT356456B (de)	1980-04-25
BE862814A (fr)	1978-07-11

Legal Events

Date	Code	Title	Description
1984-09-28	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
DE2447095A1 (de)	1975-04-10	Harnstoffphosphonate, verfahren zu ihrer herstellung und ihre verwendung
DE2412564A1 (de)	1974-10-17	N,n-dimethylcarbamoyl-1,2,4-triazolyl(3)-ester, verfahren zu ihrer herstellung und ihre verwendung
DE2754287A1 (de)	1978-06-15	1,3,5-triazapenta-1,4-diene, verfahren zu iher herstellung und ihre verwendung in der schaedlingsbekaempfung
DE2719561A1 (de)	1977-11-17	Chrysanthemumsaeureester, verfahren zu ihrer herstellung und schaedlingsbekaempfungsmittel
DE2422324C2 (de)	1984-05-03	Diphenyläther-phosphorverbindungen, Verfahren zu ihrer Herstellung und diese enthaltende Schädlingsbekämpfungsmittel
CH580910A5 (fr)	1976-10-29
AT328795B (de)	1976-04-12	Schadlingsbekampfungsmittel
CH623992A5 (en)	1981-07-15	A pesticide
CH573206A5 (en)	1976-03-15	Pesticidal 5-halo-1,2,4-triazol-3-yl carbamates - e.g. 1-isopropyl-5-chloro-1,2,4-triazol-3-yl dimethylcarbamate
CH621235A5 (en)	1981-01-30	A pesticide.
DE2801072A1 (de)	1978-07-13	Carbamidosulfonylphenyl-formamidine, verfahren zu ihrer herstellung und ihre verwendung in der schaedlingsbekaempfung
CH623985A5 (en)	1981-07-15	A pesticide
CH622409A5 (en)	1981-04-15	A pesticide
DE2755481A1 (de)	1978-06-22	Phenyl-diformamidine und ihre salze mit anorganischen und organischen saeuren, verfahren zu ihrer herstellung und ihre verwendung in der schaedlingsbekaempfung
CH631867A5 (en)	1982-09-15	A pesticide
DE2354586A1 (de)	1974-05-16	Neue ester
CH623989A5 (en)	1981-07-15	A pesticide
CH583516A5 (en)	1977-01-14	O,S-dialkyl-S-(oxadiazolyl-methyl)-dithiophosphates - used as pesticides, prepd. from chloro-methyl-oxadiazole and dithiophosphate salt
CH570764A5 (en)	1975-12-31	Phosphoramidothiolic acid esters - insecticides, acaricides, nematocides, viricides, bactericides, fungicides and herbicides
CH620341A5 (en)	1980-11-28	Pesticides
DE2754310A1 (de)	1978-06-15	1,3,5-triazapenta-1,4-diene, verfahren zu ihrer herstellung und ihre verwendung in der schaedlingsbekaempfung
DE2356453A1 (de)	1974-05-16	Alkylendithiophosphorsaeureester, verfahren zu ihrer herstellung und ihre verwendung
CH581435A5 (en)	1976-11-15	Pesticidal 1,2,3-Triazol-4-yl-(thiono)phosph(on)ates - prepd. by reacting 4-hydroxy-1,2,4-triazoles with (thiono)phosphor(on)yl halides
CH625396A5 (en)	1981-09-30	Pesticides
DE2800086A1 (de)	1978-07-13	1,3,5-triazapenta-1,4-diene, verfahren zu ihrer herstellung und ihre verwendung in der schaedlingsbekaempfung