WO1994018836A1 - Composition herbicide synergique a base de thidiazimine - Google Patents
Composition herbicide synergique a base de thidiazimine Download PDFInfo
- Publication number
- WO1994018836A1 WO1994018836A1 PCT/EP1994/000451 EP9400451W WO9418836A1 WO 1994018836 A1 WO1994018836 A1 WO 1994018836A1 EP 9400451 W EP9400451 W EP 9400451W WO 9418836 A1 WO9418836 A1 WO 9418836A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- thidiazimin
- activity
- herbicidal composition
- glyphosate
- basis
- Prior art date
Links
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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
Definitions
- Th is invention relates to a new herbicidal composition
- a herbicidal composition which comprises , as active components , a mixture of a) thidiazimin and b) a non selective herbicide selected from a salt of glyphosate, glufosinate and paraquat, shows synergistic activity.
- Glyphosate is usually present as the isopropylammoniu salt but can also be present for example as the tri esium (trimethylsulfoniu ) salt.
- Glufosinate is usually present as the ammonium salt and paraquat as the dichloride.
- the combination of active ingredients of the invention can be used for example against the following plant species:
- the combinations are applied post-emergently.
- the total amount of active ingredients used in the mixture lies between 10 and 4000 g/ha.
- the weight ratio of component a) to b) is generally between 2:1 and 1:100, preferably between 1:1 and 50:1.
- An improvement in the intensity and speed of action can be obtained, for example, by addition of suitable adjuvants, such as organic solvents, wetting agents and oils.
- suitable adjuvants such as organic solvents, wetting agents and oils.
- Such additives may allow a decrease in the dose.
- active ingredients or their mixtures can suitably be used, for example, as powders, dusts, granules, solutions, emulsions or suspensions, with the addition of liquid and/or solid carriers and/or diluents and, optionally, binding, wetting, emulsifying and/or dispersing adjuvants.
- Suitable liquid carriers are, for example aliphatic and aromatic hydrocarbons, such as benzene, toluene, xylene, cyclohexanone, isophorone, dimethyl sulfoxide, dimethylformamide and other mineral-oil fractions and plant oils.
- Suitable solid carriers include mineral earths, e.g. bentonite, silica gel, talc, kaolin, attapulgite, limestone, silicic acid and plant products, e.g. flours.
- surface-active agents there can be used for example calcium lignosulfonate, polyoxyethylenealkylphenyl ethers, naphthalenesulfonic acids and their salts, phenolsulfonic acids and their salts, formaldehyde condensates, fatty alcohol sulfates, as well as substituted benzenesulfonic acids and their salts.
- compositions can contain about 10 to 90 percent by weight active ingredients, and about 90 to 10 percent by weight liquid or solid carriers, as well as, optionally up to 20 percent by weight of surfactant.
- the agents can be applied in customary fashion, for example with water as the carrier in spray mixture volumes of approximately 100 to 1,000 1/ha.
- the agents can be applied using low-volume or ultra-low-volume techniques or in the form of so-called microgranules.
- compositions can be carried out in known manner, for example by milling or mixing processes.
- individual components can be mixed just before use for example by the so-called commonly used tank-mixing method.
- X the herbicidal activity (%) of substance A at a rate of p g/ha.
- Y the herbicidal activity (%) of substance B at a rate of q g/ha.
- E the expected additive activity of the herbicide (%) of the substances A + B at a rate of p + q g/ha. If the observed value is greater than the value of E calculated according to Colby, the combination shows synergistic activity.
- Galium aparine GALAP.
- Matricaria chamomilla MATCH
- Stellaria media STEM
- the active ingredients thidiazimin (a) and glyphosate-isopropylammonium (bl) were tested alone and in combination with one another, post-emergently in winter cereals, winter wheat (TRZAW) and winter barley (HORVW) in test areas of a size of 10m 2 .
- Combinations of (a) with lower amounts of (bl) lead to a herbicidal effect that is greater than the additive activities calculated by Colby (synergism) without the cereal selectivity of (a) being negatively influenced.
- Galium aparine was treated post- emergently with the named amounts of (a) and glyphosate- isopropylammonium (bl) and their mixtures.
- Example 2 was repeated using Matricaria chamomillaand and glufosinate-ammonium (b2) instead of glyphosate- isopropylammonium.
- the results are as follows.
- Example 2 was repeated using paraquat- dichloride (b3) instead of glyphosate-isopropylammonium. The results are as follows.
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- 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)
Abstract
Nouvelle composition herbicide à activité synergique comportant, à titre d'ingrédient actif, un mélange (a) de thidiazimine et (b) d'un herbicide non sélectif sélectionné dans le groupe constitué d'un sel de glyphosate, de glufosinate et de paraquat.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEP4305517.6 | 1993-02-17 | ||
DE4305517 | 1993-02-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1994018836A1 true WO1994018836A1 (fr) | 1994-09-01 |
Family
ID=6481120
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1994/000451 WO1994018836A1 (fr) | 1993-02-17 | 1994-02-17 | Composition herbicide synergique a base de thidiazimine |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO1994018836A1 (fr) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996015674A1 (fr) * | 1994-11-17 | 1996-05-30 | Basf Corporation | Effet securisant de combinaisons de glyphosate et d'acifluorfene |
US8530383B2 (en) * | 2008-11-24 | 2013-09-10 | Dow Agrosciences Llc | Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on cereal crops |
US8609586B2 (en) | 2008-11-24 | 2013-12-17 | Dow Agrosciences, Llc. | Safening composition of 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicides and cloquintocet-mexyl for cereal crops |
US8916498B2 (en) | 2008-11-24 | 2014-12-23 | Dow Agrosciences, Llc. | Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on direct seeded and transplanted paddy rice |
AU2015203090B2 (en) * | 2008-11-24 | 2016-06-16 | Corteva Agriscience Llc | Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on cereal crops |
JP2020530025A (ja) * | 2017-08-09 | 2020-10-15 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | L−グルホシネート又はその塩と少なくとも1種のプロトポルフィリノーゲン−ixオキシダーゼ阻害剤とを含む除草剤混合物 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0311135A2 (fr) * | 1987-10-09 | 1989-04-12 | Schering Aktiengesellschaft | Azoles et azines hétérocycliques substituées, procédé pour leur préparation et leur utilisation comme agents à activité herbicide |
EP0352508A1 (fr) * | 1988-07-05 | 1990-01-31 | Sumitomo Chemical Company, Limited | Composition herbicide |
EP0354346A1 (fr) * | 1988-07-08 | 1990-02-14 | Sumitomo Chemical Company, Limited | Composition herbicide |
WO1993005655A1 (fr) * | 1991-09-23 | 1993-04-01 | Schering Aktiengesellschaft | Compositions herbicides synergiques |
-
1994
- 1994-02-17 WO PCT/EP1994/000451 patent/WO1994018836A1/fr active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0311135A2 (fr) * | 1987-10-09 | 1989-04-12 | Schering Aktiengesellschaft | Azoles et azines hétérocycliques substituées, procédé pour leur préparation et leur utilisation comme agents à activité herbicide |
EP0352508A1 (fr) * | 1988-07-05 | 1990-01-31 | Sumitomo Chemical Company, Limited | Composition herbicide |
EP0354346A1 (fr) * | 1988-07-08 | 1990-02-14 | Sumitomo Chemical Company, Limited | Composition herbicide |
WO1993005655A1 (fr) * | 1991-09-23 | 1993-04-01 | Schering Aktiengesellschaft | Compositions herbicides synergiques |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996015674A1 (fr) * | 1994-11-17 | 1996-05-30 | Basf Corporation | Effet securisant de combinaisons de glyphosate et d'acifluorfene |
US8530383B2 (en) * | 2008-11-24 | 2013-09-10 | Dow Agrosciences Llc | Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on cereal crops |
US8609586B2 (en) | 2008-11-24 | 2013-12-17 | Dow Agrosciences, Llc. | Safening composition of 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicides and cloquintocet-mexyl for cereal crops |
US8916498B2 (en) | 2008-11-24 | 2014-12-23 | Dow Agrosciences, Llc. | Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on direct seeded and transplanted paddy rice |
US8921267B2 (en) | 2008-11-24 | 2014-12-30 | Dow Agrosciences, Llc. | Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on cereal crops |
US9040458B2 (en) | 2008-11-24 | 2015-05-26 | Dow Agrosciences Llc | Safening composition of 6-(trisubstituded phenyl)-4-amino-2-pyridinecarboxylate herbicides and cloquintocet-mexyl for cereal crops |
AU2015203090B2 (en) * | 2008-11-24 | 2016-06-16 | Corteva Agriscience Llc | Safening 6-(trisubstituted phenyl)-4-amino-2-pyridinecarboxylate herbicide injury on cereal crops |
JP2020530025A (ja) * | 2017-08-09 | 2020-10-15 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | L−グルホシネート又はその塩と少なくとも1種のプロトポルフィリノーゲン−ixオキシダーゼ阻害剤とを含む除草剤混合物 |
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