RO82994B1 - Antidote-containing herbicidal composition - Google Patents
Antidote-containing herbicidal compositionInfo
- Publication number
- RO82994B1 RO82994B1 RO105811A RO10581181A RO82994B1 RO 82994 B1 RO82994 B1 RO 82994B1 RO 105811 A RO105811 A RO 105811A RO 10581181 A RO10581181 A RO 10581181A RO 82994 B1 RO82994 B1 RO 82994B1
- Authority
- RO
- Romania
- Prior art keywords
- carbon atoms
- atoms including
- phenyl
- antidote
- lower alkyl
- Prior art date
Links
- 239000000729 antidote Substances 0.000 title abstract 3
- 230000002363 herbicidal effect Effects 0.000 title abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 10
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 150000002431 hydrogen Chemical class 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical class [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical class C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methyl-N-phenylamine Natural products CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 abstract 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical class [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000000068 chlorophenyl group Chemical group 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 239000004009 herbicide Substances 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- -1 phenyl-substituted phenyl Chemical group 0.000 abstract 1
- 239000011591 potassium Chemical class 0.000 abstract 1
- 229910052700 potassium Inorganic materials 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 125000005504 styryl group Chemical group 0.000 abstract 1
- 229910052717 sulfur Chemical group 0.000 abstract 1
- 239000011593 sulfur Chemical group 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Inventia se refera la o compozitie erbicida cu antidot, constituita dintr-un derivat de arilsulfoniluree, în calitate de antidot, cu formula generala I: (vezi formula) în care X reprezinta oxigen sau sulf; n este un numar întreg de la 0 la 3 inclusiv; R reprezinta alchil inferior cu 1...4 atomi de carbon inclusiv, alcoxi inferior cu 1...4 atomi de carbon inclusiv, alchiltio inferior cu 1...4 atomi de carbon inclusiv, halogen, trifluormetil cian, nitro sau alchilsulfonil inferior; R4 reprezinta hidrogen, alchil inferior cu 1...4 atomi de carbon inclusiv, alcoxialchil inferior cu 2...6 atomi de carbon inclusiv, fenil sau clorfenil; R2 reprezinta hidrogen, alchil inferior cu 1...4 atomi de carbon inclusiv, alchenil cu 3...6 atomi de carbon inclusiv, halogenalchil cu 1...4 atomi de carbon inclusiv, alcoxialchil cu 2...6 atomi de carbon inclusiv, 1-fenil sau fenil substituit cu alchil, în care restul alchil are 1...4 atomi de carbon inclusiv; si Ar reprezinta fenil, benzil, naftil, piridil sau stiril; sarurile anorganice ale acestuia de sodiu, potasiu, amoniu si saruri organice ale acestuia, alese dintre sarurile de anilina, p-toluidina, benzilamina, alilamina...The invention relates to an antidote herbicide composition consisting of an arylsulfonylurea derivative as an antidote of the general formula I wherein X represents oxygen or sulfur; n is an integer from 0 to 3 inclusive; R represents lower alkyl of 1 to 4 carbon atoms including lower alkoxy of 1-4 carbon atoms including lower alkylthio of 1-4 carbon atoms including halogen, trifluoromethyl, cyano, nitro or lower alkylsulfonyl ; R 4 represents hydrogen, lower alkyl of 1-4 carbon atoms, lower alkoxy of 2-6 carbon atoms including phenyl or chlorophenyl; R2 represents hydrogen, lower alkyl of 1-4 carbon atoms including alkenyl of 3-6 carbon atoms including haloalkyl of 1-4 carbon atoms including alkoxyalkyl of 2-6 carbon atoms carbon, including 1-phenyl or phenyl-substituted phenyl, wherein the alkyl moiety has 1 to 4 carbon atoms inclusive; and Ar represents phenyl, benzyl, naphthyl, pyridyl or styryl; Inorganic salts of sodium, potassium, ammonium and organic salts thereof, chosen from the aniline, p-toluidine, benzylamine, alilamine salts ...
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| RO105811A RO82994B1 (en) | 1981-11-18 | 1981-11-18 | Antidote-containing herbicidal composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| RO105811A RO82994B1 (en) | 1981-11-18 | 1981-11-18 | Antidote-containing herbicidal composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RO82994B1 true RO82994B1 (en) | 1984-08-30 |
Family
ID=40903328
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RO105811A RO82994B1 (en) | 1981-11-18 | 1981-11-18 | Antidote-containing herbicidal composition |
Country Status (1)
| Country | Link |
|---|---|
| RO (1) | RO82994B1 (en) |
-
1981
- 1981-11-18 RO RO105811A patent/RO82994B1/en unknown
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