PL122688B1 - Herbicide - Google Patents
Herbicide Download PDFInfo
- Publication number
- PL122688B1 PL122688B1 PL1980225113A PL22511380A PL122688B1 PL 122688 B1 PL122688 B1 PL 122688B1 PL 1980225113 A PL1980225113 A PL 1980225113A PL 22511380 A PL22511380 A PL 22511380A PL 122688 B1 PL122688 B1 PL 122688B1
- Authority
- PL
- Poland
- Prior art keywords
- denotes
- mixture
- atom
- active substance
- calculated difference
- Prior art date
Links
- 230000002363 herbicidal effect Effects 0.000 title claims description 8
- 239000004009 herbicide Substances 0.000 title claims description 3
- 239000013543 active substance Substances 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 claims description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
- 125000004432 carbon atom Chemical group C* 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 125000004434 sulfur atom Chemical group 0.000 claims 2
- ZRNOVONGMRDZEL-UHFFFAOYSA-N 4-hydroxy-octanoic acid Chemical compound CCCCC(O)CCC(O)=O ZRNOVONGMRDZEL-UHFFFAOYSA-N 0.000 claims 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 1
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 24
- 230000006378 damage Effects 0.000 description 10
- 230000000694 effects Effects 0.000 description 5
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 4
- 239000004148 curcumin Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 230000002195 synergetic effect Effects 0.000 description 3
- 240000005702 Galium aparine Species 0.000 description 2
- 235000014820 Galium aparine Nutrition 0.000 description 2
- 206010061217 Infestation Diseases 0.000 description 2
- QBEXFUOWUYCXNI-UHFFFAOYSA-N Ioxynil octanoate Chemical compound CCCCCCCC(=O)OC1=C(I)C=C(C#N)C=C1I QBEXFUOWUYCXNI-UHFFFAOYSA-N 0.000 description 2
- 241000125413 Lapsana Species 0.000 description 2
- 240000004674 Papaver rhoeas Species 0.000 description 2
- 235000007846 Papaver rhoeas Nutrition 0.000 description 2
- 244000292697 Polygonum aviculare Species 0.000 description 2
- 235000006386 Polygonum aviculare Nutrition 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- DQKWXTIYGWPGOO-UHFFFAOYSA-N (2,6-dibromo-4-cyanophenyl) octanoate Chemical class CCCCCCCC(=O)OC1=C(Br)C=C(C#N)C=C1Br DQKWXTIYGWPGOO-UHFFFAOYSA-N 0.000 description 1
- XWOAQACIQLBEPN-UHFFFAOYSA-N C(CCCCCCC)(=O)O.BrC1=C(C=CC=C1)C#N Chemical compound C(CCCCCCC)(=O)O.BrC1=C(C=CC=C1)C#N XWOAQACIQLBEPN-UHFFFAOYSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- 241000207892 Convolvulus Species 0.000 description 1
- 244000207543 Euphorbia heterophylla Species 0.000 description 1
- 241000816457 Galeopsis Species 0.000 description 1
- 240000006503 Lamium purpureum Species 0.000 description 1
- 235000009193 Lamium purpureum Nutrition 0.000 description 1
- 244000042664 Matricaria chamomilla Species 0.000 description 1
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 1
- 241000499917 Milla Species 0.000 description 1
- 241000205407 Polygonum Species 0.000 description 1
- 239000005606 Pyridate Substances 0.000 description 1
- JTZCTMAVMHRNTR-UHFFFAOYSA-N Pyridate Chemical compound CCCCCCCCSC(=O)OC1=CC(Cl)=NN=C1C1=CC=CC=C1 JTZCTMAVMHRNTR-UHFFFAOYSA-N 0.000 description 1
- 240000007641 Spergula rubra Species 0.000 description 1
- 244000297179 Syringa vulgaris Species 0.000 description 1
- 235000004338 Syringa vulgaris Nutrition 0.000 description 1
- 235000005545 Veronica americana Nutrition 0.000 description 1
- 240000005592 Veronica officinalis Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- OMOVVBIIQSXZSZ-UHFFFAOYSA-N [6-(4-acetyloxy-5,9a-dimethyl-2,7-dioxo-4,5a,6,9-tetrahydro-3h-pyrano[3,4-b]oxepin-5-yl)-5-formyloxy-3-(furan-3-yl)-3a-methyl-7-methylidene-1a,2,3,4,5,6-hexahydroindeno[1,7a-b]oxiren-4-yl] 2-hydroxy-3-methylpentanoate Chemical compound CC12C(OC(=O)C(O)C(C)CC)C(OC=O)C(C3(C)C(CC(=O)OC4(C)COC(=O)CC43)OC(C)=O)C(=C)C32OC3CC1C=1C=COC=1 OMOVVBIIQSXZSZ-UHFFFAOYSA-N 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 230000001186 cumulative effect Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000009940 knitting Methods 0.000 description 1
- 230000002101 lytic effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- YZHUMGUJCQRKBT-UHFFFAOYSA-M sodium chlorate Chemical compound [Na+].[O-]Cl(=O)=O YZHUMGUJCQRKBT-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 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
- A01N47/02—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 no bond to a nitrogen atom
- A01N47/06—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 no bond to a nitrogen atom containing —O—CO—O— groups; 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)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19792925335 DE2925335A1 (de) | 1979-06-22 | 1979-06-22 | Herbizides mittel |
Publications (2)
Publication Number | Publication Date |
---|---|
PL225113A1 PL225113A1 (pt) | 1981-05-22 |
PL122688B1 true PL122688B1 (en) | 1982-08-31 |
Family
ID=6073947
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL1980225113A PL122688B1 (en) | 1979-06-22 | 1980-06-20 | Herbicide |
Country Status (19)
Country | Link |
---|---|
AR (1) | AR225044A1 (pt) |
AU (1) | AU526903B2 (pt) |
BR (1) | BR8003872A (pt) |
CA (1) | CA1139121A (pt) |
CS (1) | CS220778B2 (pt) |
DD (1) | DD151405A1 (pt) |
DE (1) | DE2925335A1 (pt) |
DK (1) | DK156982C (pt) |
FR (1) | FR2459617A1 (pt) |
GB (1) | GB2051578B (pt) |
HU (1) | HU185893B (pt) |
IT (1) | IT1129226B (pt) |
KE (1) | KE3301A (pt) |
PL (1) | PL122688B1 (pt) |
SE (1) | SE446928B (pt) |
SU (1) | SU934897A3 (pt) |
TR (1) | TR20588A (pt) |
UA (1) | UA6316A1 (pt) |
ZA (1) | ZA803236B (pt) |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE636416A (pt) * | 1962-08-30 | |||
DE2331398C3 (de) * | 1973-06-20 | 1979-10-11 | Lentia Gmbh | Ester von S-PhenyM-hydroxy-e-halogenpyridazinverbindungen, ihre Herstellung und sie enthaltende herbizide Mittel |
DE2351553A1 (de) * | 1973-10-13 | 1975-04-24 | Basf Ag | Herbizid |
-
1979
- 1979-06-22 DE DE19792925335 patent/DE2925335A1/de not_active Ceased
-
1980
- 1980-05-29 CA CA000353054A patent/CA1139121A/en not_active Expired
- 1980-05-30 ZA ZA00803236A patent/ZA803236B/xx unknown
- 1980-06-06 DK DK244280A patent/DK156982C/da not_active IP Right Cessation
- 1980-06-11 GB GB8019037A patent/GB2051578B/en not_active Expired
- 1980-06-12 SE SE8004382A patent/SE446928B/sv not_active IP Right Cessation
- 1980-06-16 CS CS435580A patent/CS220778B2/cs unknown
- 1980-06-17 SU SU802936199A patent/SU934897A3/ru active
- 1980-06-17 UA UA2936199A patent/UA6316A1/uk unknown
- 1980-06-17 DD DD80221891A patent/DD151405A1/de active Protection Beyond IP Right Term
- 1980-06-18 AU AU59394/80A patent/AU526903B2/en not_active Ceased
- 1980-06-18 AR AR281438A patent/AR225044A1/es active
- 1980-06-19 FR FR8013600A patent/FR2459617A1/fr active Granted
- 1980-06-20 PL PL1980225113A patent/PL122688B1/pl unknown
- 1980-06-20 HU HU801537A patent/HU185893B/hu not_active IP Right Cessation
- 1980-06-20 IT IT67972/80A patent/IT1129226B/it active Protection Beyond IP Right Term
- 1980-06-20 BR BR8003872A patent/BR8003872A/pt not_active IP Right Cessation
- 1980-06-23 TR TR20588A patent/TR20588A/xx unknown
-
1983
- 1983-06-27 KE KE3301A patent/KE3301A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
KE3301A (en) | 1983-08-05 |
DD151405A1 (de) | 1981-10-21 |
BR8003872A (pt) | 1981-01-21 |
AR225044A1 (es) | 1982-02-15 |
GB2051578B (en) | 1983-06-02 |
SU934897A3 (ru) | 1982-06-07 |
PL225113A1 (pt) | 1981-05-22 |
AU5939480A (en) | 1981-01-08 |
CS220778B2 (en) | 1983-04-29 |
GB2051578A (en) | 1981-01-21 |
DK244280A (da) | 1980-12-23 |
SE446928B (sv) | 1986-10-20 |
DE2925335A1 (de) | 1981-01-08 |
ZA803236B (en) | 1981-05-27 |
FR2459617A1 (fr) | 1981-01-16 |
IT8067972A0 (it) | 1980-06-20 |
HU185893B (en) | 1985-04-28 |
DK156982B (da) | 1989-10-30 |
FR2459617B1 (pt) | 1982-04-16 |
CA1139121A (en) | 1983-01-11 |
TR20588A (tr) | 1982-02-01 |
AU526903B2 (en) | 1983-02-03 |
UA6316A1 (uk) | 1994-12-29 |
DK156982C (da) | 1990-03-26 |
IT1129226B (it) | 1986-06-04 |
SE8004382L (sv) | 1980-12-23 |
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