NO844828L - Synergistisk herbicid blanding - Google Patents
Synergistisk herbicid blandingInfo
- Publication number
- NO844828L NO844828L NO844828A NO844828A NO844828L NO 844828 L NO844828 L NO 844828L NO 844828 A NO844828 A NO 844828A NO 844828 A NO844828 A NO 844828A NO 844828 L NO844828 L NO 844828L
- Authority
- NO
- Norway
- Prior art keywords
- approx
- chlorine
- hydrogen
- chloro
- composition according
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 27
- 230000002195 synergetic effect Effects 0.000 title claims description 8
- -1 thiol carbamate Chemical class 0.000 claims description 21
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 18
- 229910052801 chlorine Inorganic materials 0.000 claims description 18
- 239000000460 chlorine Chemical group 0.000 claims description 18
- 229910052739 hydrogen Inorganic materials 0.000 claims description 18
- 239000001257 hydrogen Substances 0.000 claims description 18
- 230000002363 herbicidal effect Effects 0.000 claims description 17
- 150000002431 hydrogen Chemical group 0.000 claims description 15
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 12
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 12
- 229910052794 bromium Chemical group 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 11
- NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 claims description 5
- QHTQREMOGMZHJV-UHFFFAOYSA-N Thiobencarb Chemical compound CCN(CC)C(=O)SCC1=CC=C(Cl)C=C1 QHTQREMOGMZHJV-UHFFFAOYSA-N 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- LLLFASISUZUJEQ-UHFFFAOYSA-N orbencarb Chemical compound CCN(CC)C(=O)SCC1=CC=CC=C1Cl LLLFASISUZUJEQ-UHFFFAOYSA-N 0.000 claims description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- BXEHUCNTIZGSOJ-UHFFFAOYSA-N Esprocarb Chemical compound CC(C)C(C)N(CC)C(=O)SCC1=CC=CC=C1 BXEHUCNTIZGSOJ-UHFFFAOYSA-N 0.000 claims description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 3
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 3
- 125000004414 alkyl thio group Chemical group 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims description 3
- KQTOYEUYHXUEDB-UHFFFAOYSA-N 2,2,3,3,3-pentafluoropropanamide Chemical compound NC(=O)C(F)(F)C(F)(F)F KQTOYEUYHXUEDB-UHFFFAOYSA-N 0.000 claims 1
- 239000003701 inert diluent Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 16
- 239000004009 herbicide Substances 0.000 description 15
- 241000196324 Embryophyta Species 0.000 description 11
- 230000012010 growth Effects 0.000 description 9
- 230000004044 response Effects 0.000 description 9
- 239000000126 substance Substances 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 6
- 230000036515 potency Effects 0.000 description 5
- 239000002689 soil Substances 0.000 description 5
- 229940125904 compound 1 Drugs 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000004495 emulsifiable concentrate Substances 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229940125782 compound 2 Drugs 0.000 description 3
- MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 description 2
- 229940126214 compound 3 Drugs 0.000 description 2
- 229940125898 compound 5 Drugs 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 230000008635 plant growth Effects 0.000 description 2
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 2
- 150000004040 pyrrolidinones Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- JMVIVASFFKKFQK-UHFFFAOYSA-N 1-phenylpyrrolidin-2-one Chemical compound O=C1CCCN1C1=CC=CC=C1 JMVIVASFFKKFQK-UHFFFAOYSA-N 0.000 description 1
- KKYIAOSXVVCZKM-UHFFFAOYSA-N 2,2-diphenoxypentanoic acid Chemical class C=1C=CC=CC=1OC(C(O)=O)(CCC)OC1=CC=CC=C1 KKYIAOSXVVCZKM-UHFFFAOYSA-N 0.000 description 1
- HKROQOWBHZLRCU-UHFFFAOYSA-N 2,2-diphenoxypropanoic acid Chemical class C=1C=CC=CC=1OC(C(O)=O)(C)OC1=CC=CC=C1 HKROQOWBHZLRCU-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical class OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 239000005496 Chlorsulfuron Substances 0.000 description 1
- 241000209510 Liliopsida Species 0.000 description 1
- UKIOGKJGGBIFCN-UHFFFAOYSA-N NC([O-])=[S+]CC1=CC=CC=C1 Chemical class NC([O-])=[S+]CC1=CC=CC=C1 UKIOGKJGGBIFCN-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000008029 eradication Effects 0.000 description 1
- VOMHMJILNADLNM-UHFFFAOYSA-N ethyl 4-[4-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxyphenoxy]-3-hydroxypentanoate Chemical compound C1=CC(OC(C)C(O)CC(=O)OCC)=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl VOMHMJILNADLNM-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 241001233957 eudicotyledons Species 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 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
- 239000003350 kerosene Substances 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- VRZKGXNOIKPXBW-UHFFFAOYSA-N methyl 4-[4-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxyphenoxy]-3-hydroxypentanoate Chemical compound C1=CC(OC(C)C(O)CC(=O)OC)=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl VRZKGXNOIKPXBW-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000000051 modifying effect Effects 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
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000005737 synergistic response Effects 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 239000000080 wetting agent Substances 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
- 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
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
-
- 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
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)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicines Containing Plant Substances (AREA)
- Degasification And Air Bubble Elimination (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US55799483A | 1983-12-05 | 1983-12-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO844828L true NO844828L (no) | 1985-06-06 |
Family
ID=24227718
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO844828A NO844828L (no) | 1983-12-05 | 1984-12-04 | Synergistisk herbicid blanding |
Country Status (19)
| Country | Link |
|---|---|
| EP (1) | EP0146835A3 (pt) |
| JP (1) | JPS60139604A (pt) |
| KR (1) | KR850004379A (pt) |
| AU (1) | AU559251B2 (pt) |
| CA (1) | CA1235919A (pt) |
| CS (1) | CS939084A2 (pt) |
| DD (1) | DD232187A5 (pt) |
| DK (1) | DK573784A (pt) |
| ES (1) | ES8604407A1 (pt) |
| FI (1) | FI74385C (pt) |
| HU (1) | HUT36801A (pt) |
| IL (1) | IL73720A (pt) |
| NO (1) | NO844828L (pt) |
| NZ (1) | NZ210424A (pt) |
| PL (1) | PL141435B1 (pt) |
| PT (1) | PT79607A (pt) |
| RO (1) | RO89784A (pt) |
| TR (1) | TR22091A (pt) |
| ZA (1) | ZA849421B (pt) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FI76671C (fi) * | 1983-12-05 | 1988-12-12 | Stauffer Chemical Co | Synergistisk herbicidblandning och foerfarande foer bekaempning av icke oenskvaerd vaextlighet. |
| ES2686621T3 (es) * | 2004-12-17 | 2018-10-18 | Syngenta Participations Ag | Composición herbicida que comprende prosulfocarb |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS49134839A (pt) * | 1973-05-10 | 1974-12-25 | ||
| JPS5036637A (pt) * | 1973-08-08 | 1975-04-05 | ||
| JPS5127734B2 (pt) * | 1973-11-16 | 1976-08-14 | ||
| HU179058B (en) * | 1975-03-28 | 1982-08-28 | Stauffer Chemical Co | Herbicide compositions containing n-substituted 2-pyrrolidinone derivatives and process for preparing the active substances thereof |
-
1984
- 1984-11-20 FI FI844548A patent/FI74385C/fi not_active IP Right Cessation
- 1984-12-03 PT PT79607A patent/PT79607A/pt unknown
- 1984-12-03 DK DK573784A patent/DK573784A/da not_active Application Discontinuation
- 1984-12-04 ZA ZA849421A patent/ZA849421B/xx unknown
- 1984-12-04 RO RO84116513A patent/RO89784A/ro unknown
- 1984-12-04 AU AU36262/84A patent/AU559251B2/en not_active Ceased
- 1984-12-04 IL IL73720A patent/IL73720A/xx unknown
- 1984-12-04 NO NO844828A patent/NO844828L/no unknown
- 1984-12-04 CA CA000469254A patent/CA1235919A/en not_active Expired
- 1984-12-04 EP EP84114739A patent/EP0146835A3/en not_active Ceased
- 1984-12-04 HU HU844478A patent/HUT36801A/hu unknown
- 1984-12-04 NZ NZ210424A patent/NZ210424A/en unknown
- 1984-12-04 KR KR1019840007639A patent/KR850004379A/ko not_active IP Right Cessation
- 1984-12-04 PL PL1984250712A patent/PL141435B1/pl unknown
- 1984-12-05 JP JP59257318A patent/JPS60139604A/ja active Pending
- 1984-12-05 ES ES538300A patent/ES8604407A1/es not_active Expired
- 1984-12-05 TR TR22091A patent/TR22091A/xx unknown
- 1984-12-05 DD DD84270327A patent/DD232187A5/de unknown
- 1984-12-05 CS CS849390A patent/CS939084A2/cs unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TR22091A (tr) | 1986-03-30 |
| IL73720A0 (en) | 1985-03-31 |
| HUT36801A (en) | 1985-10-28 |
| EP0146835A2 (en) | 1985-07-03 |
| PT79607A (en) | 1985-01-01 |
| FI844548L (fi) | 1985-06-06 |
| KR850004379A (ko) | 1985-07-15 |
| CS939084A2 (en) | 1988-08-16 |
| NZ210424A (en) | 1987-06-30 |
| FI74385B (fi) | 1987-10-30 |
| FI74385C (fi) | 1988-02-08 |
| PL250712A1 (en) | 1985-07-30 |
| AU3626284A (en) | 1985-06-13 |
| DK573784A (da) | 1985-06-06 |
| AU559251B2 (en) | 1987-03-05 |
| ZA849421B (en) | 1985-10-30 |
| ES538300A0 (es) | 1986-02-01 |
| FI844548A0 (fi) | 1984-11-20 |
| IL73720A (en) | 1988-06-30 |
| ES8604407A1 (es) | 1986-02-01 |
| JPS60139604A (ja) | 1985-07-24 |
| PL141435B1 (en) | 1987-07-31 |
| DK573784D0 (da) | 1984-12-03 |
| CA1235919A (en) | 1988-05-03 |
| DD232187A5 (de) | 1986-01-22 |
| RO89784A (ro) | 1986-07-30 |
| EP0146835A3 (en) | 1986-01-15 |
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