CH608692A5 - Pesticide comprising an N,N'-dicarbamic acid sulphide derivative as active ingredient - Google Patents

Pesticide comprising an N,N'-dicarbamic acid sulphide derivative as active ingredient

Info

Publication number: CH608692A5
Authority: CH; Switzerland
Prior art keywords: sep; parts; formula; active ingredient; compound
Prior art date: 1976-06-22

Application number

CH767936A

Other languages

German (de)

English (en)

Inventor

Manfred Boeger

Jozef Dr Drabek

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.)

1976-06-22

Filing date

1976-06-22

Publication date

1979-01-31

1976-06-22 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1976-06-22 Priority to CH767936A priority Critical patent/CH608692A5/de

1977-05-21 Priority to IT24907/77A priority patent/IT1082108B/it

1977-06-20 Priority to DE19772727614 priority patent/DE2727614A1/de

1977-06-20 Priority to FR7718846A priority patent/FR2355818A1/fr

1977-06-20 Priority to TR19827A priority patent/TR19827A/xx

1977-06-20 Priority to CA280,873A priority patent/CA1080738A/fr

1977-06-20 Priority to NL7706779A priority patent/NL7706779A/xx

1977-06-21 Priority to AU26284/77A priority patent/AU512647B2/en

1977-06-21 Priority to ZA00773700A priority patent/ZA773700B/xx

1977-06-21 Priority to GB25871/77A priority patent/GB1579635A/en

1977-06-21 Priority to IL52362A priority patent/IL52362A/xx

1977-06-21 Priority to BR7704031A priority patent/BR7704031A/pt

1977-06-21 Priority to BE178628A priority patent/BE855928A/fr

1977-06-21 Priority to MX775830U priority patent/MX4690E/es

1977-06-21 Priority to AT436077A priority patent/AT353051B/de

1977-06-21 Priority to EG365/77A priority patent/EG12927A/xx

1977-06-22 Priority to SU772498355A priority patent/SU659064A3/ru

1979-01-31 Publication of CH608692A5 publication Critical patent/CH608692A5/de

Links

239000000575 pesticide Substances 0.000 title claims abstract 3
239000004480 active ingredient Substances 0.000 title abstract description 20
229910052757 nitrogen Inorganic materials 0.000 title description 6
239000002253 acid Substances 0.000 title description 3
150000003568 thioethers Chemical class 0.000 title description 3
150000001875 compounds Chemical class 0.000 claims abstract description 26
239000000203 mixture Substances 0.000 claims abstract description 14
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims abstract description 6
241000238631 Hexapoda Species 0.000 claims abstract description 6
125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 5
125000006527 (C1-C5) alkyl group Chemical group 0.000 claims abstract description 3
125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims abstract 2
125000004209 (C1-C8) alkyl group Chemical group 0.000 claims abstract 2
239000003795 chemical substances by application Substances 0.000 claims description 11
241000607479 Yersinia pestis Species 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 3
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 3
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 abstract 1
239000001257 hydrogen Substances 0.000 abstract 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 13
241000196324 Embryophyta Species 0.000 description 8
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
239000008187 granular material Substances 0.000 description 6
239000000243 solution Substances 0.000 description 6
239000000126 substance Substances 0.000 description 6
239000005995 Aluminium silicate Substances 0.000 description 5
235000012211 aluminium silicate Nutrition 0.000 description 5
230000000694 effects Effects 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
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
239000000654 additive Substances 0.000 description 4
239000000969 carrier Substances 0.000 description 4
239000000839 emulsion Substances 0.000 description 4
-1 n-octyl group Chemical group 0.000 description 4
239000002904 solvent Substances 0.000 description 4
239000007921 spray Substances 0.000 description 4
239000008096 xylene Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
241001425390 Aphis fabae Species 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 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
241000256244 Heliothis virescens Species 0.000 description 3
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
241000256250 Spodoptera littoralis Species 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
235000019993 champagne Nutrition 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
239000004495 emulsifiable concentrate Substances 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
230000000749 insecticidal effect Effects 0.000 description 3
238000000034 method Methods 0.000 description 3
239000000377 silicon dioxide Substances 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
240000007594 Oryza sativa Species 0.000 description 2
235000007164 Oryza sativa Nutrition 0.000 description 2
239000002202 Polyethylene glycol Substances 0.000 description 2
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
230000000895 acaricidal effect Effects 0.000 description 2
239000000642 acaricide Substances 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
239000002585 base Substances 0.000 description 2
150000004657 carbamic acid derivatives Chemical class 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 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
239000003085 diluting agent Substances 0.000 description 2
239000002270 dispersing agent Substances 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
239000002917 insecticide Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000004519 manufacturing process Methods 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
239000000843 powder Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 2
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
235000009566 rice Nutrition 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
235000015112 vegetable and seed oil Nutrition 0.000 description 2
239000008158 vegetable oil Substances 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
AIFGMSJANCWYBB-UHFFFAOYSA-N 1-methyl-3-(1-methylsulfanylethyl)urea Chemical compound CNC(O)=NC(C)SC AIFGMSJANCWYBB-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
OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical class CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 1
BSKHPKMHTQYZBB-UHFFFAOYSA-N 2-methylpyridine Chemical class CC1=CC=CC=N1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
241001124076 Aphididae Species 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
241000238660 Blattidae Species 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
241000907223 Bruchinae Species 0.000 description 1
BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 description 1
241000257161 Calliphoridae Species 0.000 description 1
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
241001124134 Chrysomelidae Species 0.000 description 1
241001414835 Cimicidae Species 0.000 description 1
241000255749 Coccinellidae Species 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
241000256113 Culicidae 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
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-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
240000002024 Gossypium herbaceum Species 0.000 description 1
235000004341 Gossypium herbaceum Nutrition 0.000 description 1
241000238816 Gryllidae Species 0.000 description 1
241001243087 Gryllotalpidae Species 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
241001124557 Lymantriidae Species 0.000 description 1
241000257226 Muscidae Species 0.000 description 1
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
241000256259 Noctuidae Species 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
241001415279 Pseudococcidae Species 0.000 description 1
241000258921 Pulicidae Species 0.000 description 1
241000255893 Pyralidae 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
241000254107 Tenebrionidae Species 0.000 description 1
241000255588 Tephritidae Species 0.000 description 1
241000896028 Tettigoniidae Species 0.000 description 1
241000130767 Tineidae Species 0.000 description 1
240000006677 Vicia faba Species 0.000 description 1
235000010749 Vicia faba Nutrition 0.000 description 1
239000008186 active pharmaceutical agent Substances 0.000 description 1
239000013543 active substance Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
125000001931 aliphatic group Chemical class 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
125000003545 alkoxy group Chemical group 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
150000001408 amides Chemical class 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
RTEXIPZMMDUXMR-UHFFFAOYSA-N benzene;ethyl acetate Chemical compound CCOC(C)=O.C1=CC=CC=C1 RTEXIPZMMDUXMR-UHFFFAOYSA-N 0.000 description 1
MDHYEMXUFSJLGV-UHFFFAOYSA-N beta-phenethyl acetate Natural products CC(=O)OCCC1=CC=CC=C1 MDHYEMXUFSJLGV-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
238000009835 boiling Methods 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
235000013877 carbamide Nutrition 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000003857 carboxamides Chemical class 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
239000007931 coated granule Substances 0.000 description 1
244000038559 crop plants Species 0.000 description 1
239000012043 crude product Substances 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 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
229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
239000013057 ectoparasiticide Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
235000013305 food Nutrition 0.000 description 1
235000012055 fruits and vegetables Nutrition 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
238000005470 impregnation Methods 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
UHXUZOCRWCRNSJ-UHFFFAOYSA-N methomyl Chemical compound CNC(=O)ON=C(C)SC UHXUZOCRWCRNSJ-UHFFFAOYSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 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
239000005645 nematicide Substances 0.000 description 1
150000002825 nitriles Chemical class 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
230000000361 pesticidal effect Effects 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
150000003018 phosphorus compounds Chemical class 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
230000008092 positive effect Effects 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000000741 silica gel Substances 0.000 description 1
229910002027 silica gel Inorganic materials 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
239000007858 starting material Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000000725 suspension Substances 0.000 description 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
150000003738 xylenes Chemical class 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
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)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CH767936A 1976-06-22 1976-06-22 Pesticide comprising an N,N'-dicarbamic acid sulphide derivative as active ingredient CH608692A5 (en)

Priority Applications (17)

Application Number	Priority Date	Filing Date	Title
CH767936A CH608692A5 (en)	1976-06-22	1976-06-22	Pesticide comprising an N,N'-dicarbamic acid sulphide derivative as active ingredient
IT24907/77A IT1082108B (it)	1976-06-22	1977-05-21	Prodotti disinfestanti,procedimento per la loro preparazione e loro impiego
DE19772727614 DE2727614A1 (de)	1976-06-22	1977-06-20	N,n'-bis-carbaminsaeure-sulfid-derivate, verfahren zu ihrer herstellung sowie schaedlingsbekaempfungsmittel
FR7718846A FR2355818A1 (fr)	1976-06-22	1977-06-20	Nouveaux derives de sulfure d'acide n,n'biscarbamique, leur preparation et leur application en tant qu'agents de lutte contre les parasites
TR19827A TR19827A (tr)	1976-06-22	1977-06-20	Hasaratla muecadele maddesi
CA280,873A CA1080738A (fr)	1976-06-22	1977-06-20	Compositions pesticides
NL7706779A NL7706779A (nl)	1976-06-22	1977-06-20	Werkwijze voor het bereiden van preparaten voor het bestrijden van schadelijke organismen.
AU26284/77A AU512647B2 (en)	1976-06-22	1977-06-21	Solpenamide derivatives
ZA00773700A ZA773700B (en)	1976-06-22	1977-06-21	Pesticidal compositions
GB25871/77A GB1579635A (en)	1976-06-22	1977-06-21	Sulphenamides and their use in pesticidal compositions
IL52362A IL52362A (en)	1976-06-22	1977-06-21	N-(n-methylcarbamic-acid-1-methyl or ethyl-thioethylimide)-('n-(n'-alkyl or cycloalkyl-n'-alkoxycarbonyl-formyl-or cylopropylcarbonyl-amino)-sulphide derivatives,their production and pesticidal compsitions containing them
BR7704031A BR7704031A (pt)	1976-06-22	1977-06-21	Compostos organicos,processo para sua preparacao,composicoes praguicidas e seu emprego
BE178628A BE855928A (fr)	1976-06-22	1977-06-21	Nouveaux derives de sulfure d'acide n,n'-bis-carbamique, leur preparation et leur application en tant qu'agents de lutte contre les parasites
MX775830U MX4690E (es)	1976-06-22	1977-06-21	Procedimiento para la preparacion de derivados de sulfuro de acido n.n'-bis-carbamico
AT436077A AT353051B (de)	1976-06-22	1977-06-21	Insektizides mittel
EG365/77A EG12927A (en)	1976-06-22	1977-06-21	Process for preparing of novel n,n-bis-carbamic acid sulphide derivatives and their use as insecticide
SU772498355A SU659064A3 (ru)	1976-06-22	1977-06-22	Инсектицидное средство

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH767936A CH608692A5 (en)	1976-06-22	1976-06-22	Pesticide comprising an N,N'-dicarbamic acid sulphide derivative as active ingredient

Publications (1)

Publication Number	Publication Date
CH608692A5 true CH608692A5 (en)	1979-01-31

Family

ID=4332646

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH767936A CH608692A5 (en)	1976-06-22	1976-06-22	Pesticide comprising an N,N'-dicarbamic acid sulphide derivative as active ingredient

Country Status (3)

Country	Link
BE (1)	BE855928A (fr)
CH (1)	CH608692A5 (fr)
ZA (1)	ZA773700B (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4210668A (en) *	1979-02-23	1980-07-01	E. I. Du Pont De Nemours And Company	Insecticidal carbamates
US4316911A (en) *	1980-11-03	1982-02-23	E. I. Du Pont De Nemours And Company	Ureidosulfenyl carbamate nematicides

1976
- 1976-06-22 CH CH767936A patent/CH608692A5/de not_active IP Right Cessation
1977
- 1977-06-21 BE BE178628A patent/BE855928A/fr not_active IP Right Cessation
- 1977-06-21 ZA ZA00773700A patent/ZA773700B/xx unknown

Also Published As

Publication number	Publication date
ZA773700B (en)	1978-05-30
BE855928A (fr)	1977-12-21

Legal Events

Date	Code	Title	Description
1992-02-28	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
EP0001203B1 (fr)	1980-09-03	N-phényl-N'-benzoyl-urées, procédé pour leur préparation, produits les contenant, et leur utilisation comme pesticides
DE2418295C2 (de)	1986-04-03	Substituierte Benzyloxydiphenyläther, Verfahren zu ihrer Herstellung und diese enthaltende Schädlingsbekämpfungsmittel
DE2637395C2 (fr)	1987-12-03
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DE2727614A1 (de)	1978-01-05	N,n'-bis-carbaminsaeure-sulfid-derivate, verfahren zu ihrer herstellung sowie schaedlingsbekaempfungsmittel
DE2632692A1 (de)	1977-02-10	Schaedlingsbekaempfungsmittel
DE2643428A1 (de)	1977-04-07	Schaedlingsbekaempfungsmittel
DE2751028C2 (de)	1986-08-28	Thiosubstituierte Carbamidsäure-Derivate, Verfahren zu ihrer Herstellung sowie Schädlingsbekämpfungsmittel
DE2754287A1 (de)	1978-06-15	1,3,5-triazapenta-1,4-diene, verfahren zu iher herstellung und ihre verwendung in der schaedlingsbekaempfung
CH643563A5 (en)	1984-06-15	1,3-Diaza-2-phosphacyclohexane derivatives
DE2732811A1 (de)	1978-01-26	Neue cyclopropancarbonsaeurederivate
DE2616755A1 (de)	1976-10-28	Diaether, verfahren zu ihrer herstellung und ihre verwendung
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CH621922A5 (en)	1981-03-13	A pesticide
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CH616563A5 (en)	1980-04-15	Pesticide containing a 5-phenylcarbamoylbarbituric acid as active ingredient
CH602010A5 (en)	1978-07-14	Alkynyloxy-benzyl-cyclopropane-carboxylates
DE2654293A1 (de)	1977-06-08	Cyclopropancarbonsaeure-3-alkinyloxy- benzylester, verfahren zu ihrer herstellung und ihre verwendung