FR2648316A1 - HERBICIDE COMPOSITIONS BASED ON N-PHOSPHONOMETHYLGLYCIN AND THEIR USE - Google Patents
HERBICIDE COMPOSITIONS BASED ON N-PHOSPHONOMETHYLGLYCIN AND THEIR USE Download PDFInfo
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- FR2648316A1 FR2648316A1 FR8908433A FR8908433A FR2648316A1 FR 2648316 A1 FR2648316 A1 FR 2648316A1 FR 8908433 A FR8908433 A FR 8908433A FR 8908433 A FR8908433 A FR 8908433A FR 2648316 A1 FR2648316 A1 FR 2648316A1
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- surfactant
- phosphonomethylglycine
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- ammonium salt
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- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
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- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Dispersion Chemistry (AREA)
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Abstract
Compositions herbicides liquides caractérisées en ce qu'elles sont constituées de solutions aqueuses contenant : a) de la N-phosphonométhylcine et/ou l'un de ses dérivés à raison d'au moins 40 g/l d'équivalent glyphosate; et b) un tensioactif de formule : (CF DESSIN DANS BOPI) dans laquelle : R est une chaîne linéaire ou ramifiée, alkyle ou alkényle, A représente un groupe alkylène, n, n' et n'' sont des nombres entiers tels que n + n' + n'' est compris entre 1 et 15, R**1 est l'atome d'hydrogène ou un radical acyle.Liquid herbicidal compositions characterized in that they consist of aqueous solutions containing: a) N-phosphonomethylcine and / or one of its derivatives in an amount of at least 40 g / l of glyphosate equivalent; and b) a surfactant of formula: (CF DRAWING IN BOPI) in which: R is a straight or branched chain, alkyl or alkenyl, A represents an alkylene group, n, n 'and n' 'are integers such as n + n '+ n' 'is between 1 and 15, R ** 1 is the hydrogen atom or an acyl radical.
Description
La présente invention concerne de nouvellesThe present invention relates to new
formulations concentrées à base de N- concentrated formulations based on N-
phosphonométhylglycine ou de composés à groupe N- phosphonomethylglycine or N-group compounds
phosphonométhylglycyle. D5 La N-phosphonométhylglycine (appelée quelque fois glyphosate), ainsi que les composés analogues, leurs propriétés herbicides et les formulations les contenant, sont décrites en particulier dans le brevet US 3 799 758. Bien que de nombreux dérivés du glyphosate, solubles ou insolubles dans l'eau soient connus, en fait on préfère très généralement utiliser les dérivés solubles dans l'eau, et c'est pour cela que ce sont les sels de N-phosphonométhylglycine qui ont été généralement développés ou commercialisés, phosphonométhylglycyle. D5 N-phosphonomethylglycine (sometimes called glyphosate), as well as analogous compounds, their herbicidal properties and formulations containing them, are described in particular in US Pat. No. 3,799,758. Although many glyphosate derivatives, soluble or insoluble in water are known, in fact it is very generally preferred to use the water-soluble derivatives, and it is for this reason that it is the N-phosphonomethylglycine salts which have generally been developed or marketed,
spécialement le sel d'isopropylammonium. especially the isopropylammonium salt.
Plus récemment (demande de brevet européen n'290416) on a cherché à développer des concentrats à base de sels de N-phosphonométhylcine, pouvant contenir de la N-phosphonométhylglycine sous forme acide, mais More recently (European Patent Application No. 2,90416) attempts have been made to develop concentrates based on N-phosphonomethylcine salts, which may contain N-phosphonomethylglycine in acid form, but
contenant de toute manière cette N- containing anyway this N-
phosphonométhylglycine et/ou ses dérivés sous des formes solubles ou solubilisées, ces concentrats étant caractérisés par la présence d'amine alcoxylée d'un type particulier. Cette amine alcoxylée doit avoir au plus 12 groupes alcoxy par molécule, et elle doit avoir un caractère d'agent tensioactif et elle phosphonomethylglycine and / or its derivatives in soluble or solubilized forms, these concentrates being characterized by the presence of alkoxylated amine of a particular type. This alkoxylated amine must have at most 12 alkoxy groups per molecule, and must be a surfactant and
doit favoriser l'activité herbicide des dérivés de N- must promote the herbicidal activity of N-derivatives
phosphonométhylglycine. Elle peut être utilisée en quantité moindre que les tensioactifs connus des formulations connues de la Nphosphonométhylglycine, au moins en ce qui concerne la réalisation de concentrats destinés à être appliqués en plein air, sous forme de bouillies diluées, à raison de 100 à phosphonomethylglycine. It can be used in a smaller quantity than the known surfactants of the known formulations of N-phosphonomethylglycine, at least as regards the production of concentrates intended to be applied in the open air, in the form of diluted slurries, in a proportion of 100 to
600 1/ha.600 1 / ha.
Un but de la présente invention est de fournir des compositions, ou formulations, concentrées (appelées aussi concentrats) à base de Nphosphonométhylcine, et spécialement à base de ses An object of the present invention is to provide compositions, or formulations, concentrated (also called concentrates) based on Nphosphonométhylcine, and especially based on its
sels solubles dans l'eau.soluble salts in water.
Un autre but de la présente invention est Another object of the present invention is
de fournir des concentrats à base de N- to supply N-based concentrates
phosphonométhylglycine ou de ses dérivés donnant naissance à des bouillies diluées ayant une bonne phosphonomethylglycine or its derivatives giving rise to dilute
activité herbicide.herbicidal activity.
Un autre but de l'invention est de fournir Another object of the invention is to provide
des concentrats à base de sels de N- concentrates based on N-salts
phosphonométhylglycine mettant en oeuvre de nouveaux types d'agents tensioactifs favorisant l'activité biologique Un autre but de l'invention est de fournir Another object of the invention is to provide phosphonomethylglycine using new types of surfactants which promote biological activity.
des concentrats à base de sels de N- concentrates based on N-salts
O20 phosphonométhylglycine mettant en oeuvre des tensioactifs ayant une aptitude à la solubilisation améliorée Un autre but de l'invention est de fournir O20 phosphonomethylglycine using surfactants having an improved solubilization ability Another object of the invention is to provide
des concentrats à base de sels de S- concentrates based on salts of S-
phosphonométhylglycine mettant en oeuvre de nouveaux types d'agents tensioactifs compatibles en solutions concentrées avec certains sels minéraux et spécialement avec le sulfate d'ammonium Il a maintenant été trouvé que ces buts pouvaient être atteints en tout ou partie grâce aux compositions selon l'invention. Dans ce qui suit les pourcentages sont, sauf indication spécifiques, des pourcentages pondéraux. Par ailleurs on appelle équivalent glyphosate la quantité correspondante de phosphonomethylglycine using new types of surfactants compatible in concentrated solutions with certain inorganic salts and especially with ammonium sulfate It has now been found that these goals could be achieved in whole or in part with the compositions according to the invention. In the following the percentages are, unless otherwise indicated, percentages by weight. Moreover, the equivalent quantity of glyphosate is called
produit si tout le dérivé de la N- product if all the derivative of the N-
phosphonométhylglycine était sous forme de N- phosphonomethylglycine was in the form of N-
phosphonométhylglycine ordinaire.ordinary phosphonomethylglycine.
Ces compositions sont des compositions liquides constituées de solutions aqueuses contenant: a) de la N-phosphonométhylcine et/ou l'un de ses dérivés à raison d'au moins 40 g/l d'équivalent glyphosate, b) un tensioactif (ayant le caractère d'actixvateur) de formule (AO)n R' / R - N <(AO)n' R' These compositions are liquid compositions consisting of aqueous solutions containing: a) N-phosphonomethylcine and / or one of its derivatives in a proportion of at least 40 g / l of glyphosate equivalent, b) a surfactant (having the activator character) of formula (AO) n R '/ R - N <(AO) n' R '
\ /\ /
CH2 -CH2 -CH2 -NCH2 -CH2 -CH2 -N
(A)n" R' dans laquelle R est une chaine linéaire ou ramifiée, alkyle ou alkényle, ayant de 8 à 22 atomes de carbone A représente un groupe alkylène, de préférence éthylène ou propylène n, n' et n" sont des nombres entiers tels que n + n'+ n" est compris entre 1 et 15 de préférence (A) n "R 'wherein R is a linear or branched chain, alkyl or alkenyl, having 8 to 22 carbon atoms A is alkylene, preferably ethylene or propylene n, n' and n" are numbers integers such that n + n '+ n "is preferably between 1 and 15
entre 3 et 12.between 3 and 12.
Rl est l'atome d'hydrogène ou un radical acyle R1 is the hydrogen atom or an acyl radical
tel que formyl, acétyl propanoyl (c'est-à-dire CH3- such as formyl, acetyl propanoyl (i.e., CH3-
CH2- CO).CH2-CO).
Bien entendu, on peut remplacer ce surfactant unique par un mélange de surfactant dans lesquels, en moyenne, R, n, n' et n" répondent aux Of course, this single surfactant can be replaced by a surfactant mixture in which, on average, R, n, n 'and n "respond to
définitions données ci-avant.definitions given above.
De manière avantageuse la présente invention concerne des compositions concentrées telles que décrites ci-avant et concernant en outre l'une ou l'autre des caractéristiques suivantes: i a) la N-phosphonométhylglycine est en quantité ne dépassant pas la limite de solubilité dans le milieu considéré, de préférence comprise entre 60 et g/l, et encore plus préférentiellement entre 90 et 150 g/l, b) la solution concentrée comprend un sel d'ammonium (NH4) tel que le nitrate, le phosphate, le sulfamate, le thiocyanate ou de préférence le sulfate, à raison de 50 à 400 g/l, de préférence 100 Advantageously, the present invention relates to concentrated compositions as described above and furthermore relating to one or other of the following characteristics: ia) N-phosphonomethylglycine is in an amount not exceeding the limit of solubility in the medium considered, preferably between 60 and g / l, and even more preferably between 90 and 150 g / l, b) the concentrated solution comprises an ammonium salt (NH4) such as nitrate, phosphate, sulphamate, thiocyanate or preferably sulphate, at a rate of 50 to 400 g / l, preferably 100
à 300 g/il.at 300 g / il.
c) les compositions concentrées sont destinées à être diluées par les agriculteurs dans des conteneurs contenant de l'eau de manière à pouvoir épandre ces bouillies diluées à raison de 100 à 600 1/ha, la matière active étant, quant à elle, appliquée à raison de 0,125 à 4,5 kg/ha, d) le rapport pondéral éqouivalent "lvDhosate tensioactif est compris entre 0,6 et 6, de préférence entre 1 et 3. c) the concentrated compositions are intended to be diluted by the farmers in containers containing water so as to be able to spread these diluted slurries at a rate of 100 to 600 l / ha, the active ingredient being, for its part, applied to 0.125 to 4.5 kg / ha, d) the equivalent weight ratio of the surfactant is between 0.6 and 6, preferably between 1 and 3.
e) le solvant est l'eau.e) the solvent is water.
La quantité relativement élevée de tensioactif indiquée ci-dessus concerne ce tensioactif à caractère d'activateur biologique/herbicide, étant entendu que les compositions selon l'invention peuvent contenir en outre, comme cela va être précisé ci-après, toutes sortes d'autres composants, et notamment de tensioactifs ( ou surfactants) de natures les plus diverses à caractère mouillant; ces tensioactifs sont alors utilisés à des doses très The relatively high amount of surfactant indicated above relates to this surfactant with the character of biological activator / herbicide, it being understood that the compositions according to the invention may furthermore contain, as will be specified hereinafter, all sorts of other components, including surfactants (or surfactants) of various natures wetting nature; these surfactants are then used in very high doses
inférieures à la dose de l'activateur. less than the dose of the activator.
Les compositions liquides concentrées selon l'invention sont préparées habituellement par simple The concentrated liquid compositions according to the invention are usually prepared by simple
mélangeage des constituants.mixing of the constituents.
Les compositions selon l'invention contiennent habituellement de 5 à 25 % (de préférence de 7 à 20 %) de matières actives (herbicides), de 0,5 à 40 % (de préférence de 10 à 20 %) d'agent(s) tensioactif(s) à caractère activateur, de 10 à 50 % (de préférence de 20 à 30 %*é) d'un sel d'ammonium (adjuvant), de 0,1 à 10 % d'agent(s) tensioactifs à caractère mouillant, de 0 à 30 % d'additifs appropriés, comme des anti-mousses, des inhibiteurs de corrosion, des séquestrants, des stabilisants, des agents de pénétration, des adhésifs. Bien entendu les compositions selon l'invention peuvent contenir encore tous les additifs solides ou liquides correspondant aux techniques habituelles de la mise The compositions according to the invention usually contain from 5 to 25% (preferably from 7 to 20%) of active ingredients (herbicides), from 0.5 to 40% (preferably from 10 to 20%) of agent (s). surfactant (s) having an activating character, from 10 to 50% (preferably from 20 to 30%) of an ammonium salt (adjuvant), from 0.1 to 10% of surfactant (s) wetting agent, from 0 to 30% of suitable additives, such as antifoams, corrosion inhibitors, sequestering agents, stabilizers, penetrating agents, adhesives. Naturally, the compositions according to the invention may still contain all the solid or liquid additives corresponding to the usual techniques of setting
en formulation.in formulation.
Selon ce qui a déjà été dit, les compositions concentrées selon l'invention peuvent contenir un ou plusieurs agents tensioactifs, outre le tensioactif à caractère d'activateur défini plus haut. Comme agent tensioactif, on peut utiliser un agent mouillant de type ionique ou non ionique ou un mélange de tels agents tensioactifs. On peut citer par exemple, des polycondensats d'oxyde d'éthylène sur des alcools gras ou sur des acides gras ou sur des amines grasses, des phénols substitués (notamment des alkylphénols ou des arylphénols), des sels d'esters d'acides sulfosucciniques, des dérivés de la taurine (notamment des alkyltaurates), des esters phosphoriques d'alcools ou de phénols polyoxyéthylés, des esters d'acides gras et de polyols, les dérivés à fonction sulfates, sulfonates et phosphates des According to what has already been said, the concentrated compositions according to the invention may contain one or more surfactants, in addition to the activator surfactant defined above. As surface-active agent, it is possible to use an ionic or nonionic wetting agent or a mixture of such surfactants. There may be mentioned, for example, polycondensates of ethylene oxide with fatty alcohols or with fatty acids or with fatty amines, substituted phenols (in particular alkylphenols or arylphenols), salts of sulphosuccinic acid esters. , taurine derivatives (especially alkyltaurates), phosphoric esters of polyoxyethylated alcohols or phenols, esters of fatty acids and polyols, sulphonates, sulphonates and phosphates functional derivatives of
composés précédents.previous compounds.
A titre d'exemple donné à titre non limitatif on donne ci-après des exemples de solutions selon l'invention ainsi que des exemples d'utilisation de ces solutions. Dans ces exemples la matière active est de la N-phosphonométhylglycine By way of non-limiting example, examples of solutions according to the invention as well as examples of use of these solutions are given below. In these examples the active ingredient is N-phosphonomethylglycine
sous forme de sel d'isopropylammonium. in the form of isopropylammonium salt.
EXEMPLE 1EXAMPLE 1
- N-Phosphonomethylglycine sous forme de sel d'isopropylammonium 100 g/1 Sulfate d'anmonium 200 g/l - tensioactif de formule définie ci-après 100 g/l - eau quantité suffisante pour 1 1 Le tensioactif mis en oeuvre dans cet exemple était un produit de formule (CH2 -CHZ -O)n H / Cies H3s- N (CHz2-CH2-O)n' H N-Phosphonomethylglycine in the form of isopropylammonium salt 100 g / l ammonium sulphate 200 g / l - surfactant of formula defined below 100 g / l - water sufficient quantity for 1 1 The surfactant used in this example was a product of the formula (CH 2 -CH 2 -O) n H / C H 3 S-N (CH 2 2 -CH 2 -O) n 'H
\ /\ /
CH2 -CHz -CH2 -N \ (CH2-CH2 -O)n" H avec n + n' + n" = 3 CH 2 -CH 2 -CH 2 -N (CH 2 -CH 2 -O) n "H with n + n '+ n" = 3
EXEMPLE -2EXAMPLE -2
- N-Phosphonomethylglycine, sous forme de sel d'isopropylammonium 100 g/l - Sulfate d'anmonium 100 g/1 - tensioactif utilisé à l'exemple 1 200 g/l eau quantité suffisante pour 1 i - N-Phosphonomethylglycine, in the form of isopropylammonium salt 100 g / l - ammonium sulfate 100 g / 1 - surfactant used in Example 1 200 g / l water quantity sufficient for 1 i
EXEMPLE 3EXAMPLE 3
- N-phosphométhylglycine, sous forme de sel d'isopropylammonium 100 g/l Sulfate d'ammonium 150 g/l - Tensioactif utilisé à l'exemple 1 150 g/l Eau quantité suffisante pour 1 1 N-phosphomethylglycine, in the form of isopropylammonium salt 100 g / l ammonium sulphate 150 g / l - surfactant used in example 1 150 g / l Water sufficient quantity for 1 1
EXEMPLE 4EXAMPLE 4
- N-phosphométhylglycine, sous forme de sel d'isopropylammonium 100 g/l Sulfate d'ammonium 300 gl/1 - Tensioactif utilisé à l'exemple 1 100 g/1 Eau quantité suffisante pour 1 1 Ces solutions sont diluées dans l'eau à raison de 2,5 et 5 1 dans 300 1, les bouillies ainsi obtenues sont pulvérisées sur différentes plantes N-phosphomethylglycine, in the form of isopropylammonium salt 100 g / l ammonium sulphate 300 g / l-surfactant used in example 1 100 g / 1 water sufficient quantity for 1 1 These solutions are diluted in water at a rate of 2.5 and 5 liters in 300 liters, the slurries thus obtained are sprayed on different plants
adventices.weeds.
Les compositions des exemples 1 à 4, utilisées à la dose de 250 g/1 de matière active comptée sous forme de N-phosphonométhyl-glycine, présentent sur diverses mauvaises herbes, notamment Ipomée, pourpier et abutilon, une efficacité nettement supérieure à celle de produits commerciaux, et notamment du produit commercialisé sous la marque Round- up et qui contient le même matière active associée à des agents The compositions of Examples 1 to 4, used at the dose of 250 g / l of active ingredient counted in the form of N-phosphonomethyl-glycine, have on a variety of weeds, especially Ipomea, purslane and velvetleaf, an efficiency significantly higher than that of commercial products, and in particular of the product marketed under the trademark Round-up and which contains the same active ingredient associated with agents
tensioactifs banaux.ordinary surfactants.
Claims (10)
Priority Applications (18)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8908433A FR2648316A1 (en) | 1989-06-20 | 1989-06-20 | HERBICIDE COMPOSITIONS BASED ON N-PHOSPHONOMETHYLGLYCIN AND THEIR USE |
IE213090A IE902130A1 (en) | 1989-06-20 | 1990-06-13 | Herbicidal compositions based on n-phosphonomethylglycine¹and their use |
CA002019087A CA2019087A1 (en) | 1989-06-20 | 1990-06-15 | Herbicidal compositions based on n-phosphonomethylglycine, and their uses |
SE9002166A SE9002166L (en) | 1989-06-20 | 1990-06-18 | HERBICID COMPOSITIONS BASED ON N-PHOSPHONOMETHYLGYLINE AND THEIR USE |
DE4019362A DE4019362A1 (en) | 1989-06-20 | 1990-06-18 | HERBICIDE COMPOSITIONS BASED ON N-PHOSPHONOMETHYL GLYCIN AND THEIR USE |
PT94414A PT94414A (en) | 1989-06-20 | 1990-06-19 | PROCESS FOR THE PREPARATION OF HERBICIDAL COMPOSITIONS CONTAINING N-PHOSPHONOMETILGLYCIN |
GR900100459A GR900100459A (en) | 1989-06-20 | 1990-06-19 | N-phosphonomethyloglycine insecticide compositions and use thereof |
DK149390A DK149390A (en) | 1989-06-20 | 1990-06-19 | LIQUID HERBICIDE PREPARATION AND ITS USE |
AU57565/90A AU5756590A (en) | 1989-06-20 | 1990-06-19 | Herbical compositions based on n-phosphonomethylglycine and their use |
LU87747A LU87747A1 (en) | 1989-06-20 | 1990-06-19 | N-PHOSPHONOMETHYLGLYCIN HERBICIDE COMPOSITIONS AND THEIR USE |
GB9013692A GB2233229B (en) | 1989-06-20 | 1990-06-20 | Herbicidal compositions based on n-phosphonomethylglycine |
NL9001407A NL9001407A (en) | 1989-06-20 | 1990-06-20 | HERBICIDE COMPOSITIONS BASED ON N-PHOSPHONOMETHYLGLYCIN AND ITS USE. |
IT02070190A IT1248734B (en) | 1989-06-20 | 1990-06-20 | HERBICIDE COMPOSITIONS BASED ON N-PHOSPHONOMETHYLGLYCIN AND THEIR USE |
JP2162548A JPH0334901A (en) | 1989-06-20 | 1990-06-20 | Herbicide compound based on n-phosphonomethyl glycine and its usage |
BR909002986A BR9002986A (en) | 1989-06-20 | 1990-06-20 | LIQUID HERBICIDAL COMPOSITIONS AND WEED FIGHTING PROCESS |
KR1019900009081A KR910000016A (en) | 1989-06-20 | 1990-06-20 | Herbicide compositions based on N-phosphonomethylglycine and uses thereof |
ZA904785A ZA904785B (en) | 1989-06-20 | 1990-06-20 | Herbicidal compositions based on n-phosphonomethylglycine and their use |
HU903921A HUT54023A (en) | 1989-06-20 | 1990-06-20 | Process for producing liquide plant protecting composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR8908433A FR2648316A1 (en) | 1989-06-20 | 1989-06-20 | HERBICIDE COMPOSITIONS BASED ON N-PHOSPHONOMETHYLGLYCIN AND THEIR USE |
Publications (1)
Publication Number | Publication Date |
---|---|
FR2648316A1 true FR2648316A1 (en) | 1990-12-21 |
Family
ID=9383094
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR8908433A Withdrawn FR2648316A1 (en) | 1989-06-20 | 1989-06-20 | HERBICIDE COMPOSITIONS BASED ON N-PHOSPHONOMETHYLGLYCIN AND THEIR USE |
Country Status (18)
Country | Link |
---|---|
JP (1) | JPH0334901A (en) |
KR (1) | KR910000016A (en) |
AU (1) | AU5756590A (en) |
BR (1) | BR9002986A (en) |
CA (1) | CA2019087A1 (en) |
DE (1) | DE4019362A1 (en) |
DK (1) | DK149390A (en) |
FR (1) | FR2648316A1 (en) |
GB (1) | GB2233229B (en) |
GR (1) | GR900100459A (en) |
HU (1) | HUT54023A (en) |
IE (1) | IE902130A1 (en) |
IT (1) | IT1248734B (en) |
LU (1) | LU87747A1 (en) |
NL (1) | NL9001407A (en) |
PT (1) | PT94414A (en) |
SE (1) | SE9002166L (en) |
ZA (1) | ZA904785B (en) |
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FR2737390A1 (en) * | 1995-08-04 | 1997-02-07 | Rhone Poulenc Chimie | WATER-SOLUBLE PHYTOSANITARY COMPOSITION CONTAINING AT LEAST POLYACOXYLATED AMIDOAMINES |
FR2766669A1 (en) * | 1997-07-30 | 1999-02-05 | Flamel Tech Sa | Foliage treatment composition having enhanced effectiveness |
WO1999005914A1 (en) * | 1997-07-30 | 1999-02-11 | Monsanto Company | Process and compositions promoting biological effectiveness of exogenous chemical substances in plants |
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DK169734B1 (en) * | 1993-03-09 | 1995-01-30 | Kvk Agro As | Herbicide preparation, method of preparation thereof and activating additive for admixture with herbicide preparations |
FI933374A (en) * | 1993-07-28 | 1995-01-29 | Kemira Oy | Herbicidal composition, enhancer for improving the effectiveness of herbicide and method for treating crops |
DE69606855D1 (en) * | 1995-02-13 | 2000-04-06 | Novartis Ag | HERBICIDAL COMPOSITION AND METHOD FOR CONTROLLING AND WEEDS |
US6586367B2 (en) | 1996-09-05 | 2003-07-01 | Syngenta Crop Protection, Inc. | Process for the control of weeds |
AUPO405696A0 (en) * | 1996-12-06 | 1997-01-09 | Ici Australia Operations Proprietary Limited | Herbicidal compositions |
US6127317A (en) * | 1997-09-17 | 2000-10-03 | American Cyanamid Company | Concentrated, aqueous herbicidal compositions containing an imidazolinyl acid salt and a glyphosate salt |
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US4528023A (en) * | 1983-07-25 | 1985-07-09 | Stauffer Chemical Company | Enhancement of herbicidal activity of tetraaluminum salts of N-phosphonomethylglycine |
EP0290416A2 (en) * | 1987-04-29 | 1988-11-09 | Monsanto Europe S.A./N.V. | Improved glyphosate formulations |
-
1989
- 1989-06-20 FR FR8908433A patent/FR2648316A1/en not_active Withdrawn
-
1990
- 1990-06-13 IE IE213090A patent/IE902130A1/en unknown
- 1990-06-15 CA CA002019087A patent/CA2019087A1/en not_active Abandoned
- 1990-06-18 DE DE4019362A patent/DE4019362A1/en not_active Withdrawn
- 1990-06-18 SE SE9002166A patent/SE9002166L/en not_active Application Discontinuation
- 1990-06-19 AU AU57565/90A patent/AU5756590A/en not_active Abandoned
- 1990-06-19 LU LU87747A patent/LU87747A1/en unknown
- 1990-06-19 GR GR900100459A patent/GR900100459A/en unknown
- 1990-06-19 DK DK149390A patent/DK149390A/en not_active IP Right Cessation
- 1990-06-19 PT PT94414A patent/PT94414A/en not_active Application Discontinuation
- 1990-06-20 GB GB9013692A patent/GB2233229B/en not_active Expired - Lifetime
- 1990-06-20 BR BR909002986A patent/BR9002986A/en unknown
- 1990-06-20 IT IT02070190A patent/IT1248734B/en active IP Right Grant
- 1990-06-20 NL NL9001407A patent/NL9001407A/en not_active Application Discontinuation
- 1990-06-20 KR KR1019900009081A patent/KR910000016A/en not_active Application Discontinuation
- 1990-06-20 HU HU903921A patent/HUT54023A/en unknown
- 1990-06-20 ZA ZA904785A patent/ZA904785B/en unknown
- 1990-06-20 JP JP2162548A patent/JPH0334901A/en active Pending
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US4528023A (en) * | 1983-07-25 | 1985-07-09 | Stauffer Chemical Company | Enhancement of herbicidal activity of tetraaluminum salts of N-phosphonomethylglycine |
EP0290416A2 (en) * | 1987-04-29 | 1988-11-09 | Monsanto Europe S.A./N.V. | Improved glyphosate formulations |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2737390A1 (en) * | 1995-08-04 | 1997-02-07 | Rhone Poulenc Chimie | WATER-SOLUBLE PHYTOSANITARY COMPOSITION CONTAINING AT LEAST POLYACOXYLATED AMIDOAMINES |
WO1997005779A1 (en) * | 1995-08-04 | 1997-02-20 | Rhone-Poulenc Chimie | Plant protection composition containing one or more water soluble active materials and one or more polyalkoxylated amidoamines |
FR2766669A1 (en) * | 1997-07-30 | 1999-02-05 | Flamel Tech Sa | Foliage treatment composition having enhanced effectiveness |
WO1999005914A1 (en) * | 1997-07-30 | 1999-02-11 | Monsanto Company | Process and compositions promoting biological effectiveness of exogenous chemical substances in plants |
US6133199A (en) * | 1997-07-30 | 2000-10-17 | Monsanto Company | Process and compositions promoting biological effectiveness of exogenous chemical substances in plants |
Also Published As
Publication number | Publication date |
---|---|
AU5756590A (en) | 1991-01-03 |
GB2233229A (en) | 1991-01-09 |
GR900100459A (en) | 1991-11-15 |
SE9002166L (en) | 1990-12-21 |
ZA904785B (en) | 1991-04-24 |
LU87747A1 (en) | 1991-02-18 |
DK149390A (en) | 1990-12-21 |
HU903921D0 (en) | 1990-11-28 |
BR9002986A (en) | 1991-08-20 |
GB2233229B (en) | 1992-05-06 |
PT94414A (en) | 1991-02-08 |
IT9020701A1 (en) | 1991-12-20 |
KR910000016A (en) | 1991-01-29 |
JPH0334901A (en) | 1991-02-14 |
NL9001407A (en) | 1991-01-16 |
SE9002166D0 (en) | 1990-06-18 |
IE902130A1 (en) | 1991-01-02 |
IT9020701A0 (en) | 1990-06-20 |
DE4019362A1 (en) | 1991-01-03 |
IE902130L (en) | 1990-12-20 |
CA2019087A1 (en) | 1990-12-20 |
HUT54023A (en) | 1991-01-28 |
IT1248734B (en) | 1995-01-26 |
DK149390D0 (en) | 1990-06-19 |
GB9013692D0 (en) | 1990-08-08 |
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