LU82602A1 - HERBICIDE COMPOSITION BASED ON BIPYRIDILIUM SALT - Google Patents
HERBICIDE COMPOSITION BASED ON BIPYRIDILIUM SALT Download PDFInfo
- Publication number
- LU82602A1 LU82602A1 LU82602A LU82602A LU82602A1 LU 82602 A1 LU82602 A1 LU 82602A1 LU 82602 A LU82602 A LU 82602A LU 82602 A LU82602 A LU 82602A LU 82602 A1 LU82602 A1 LU 82602A1
- Authority
- LU
- Luxembourg
- Prior art keywords
- bipyridilium
- composition
- compositions
- solutions
- herbicide
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 36
- 150000003839 salts Chemical class 0.000 title claims description 14
- 239000004009 herbicide Substances 0.000 title claims description 12
- 230000002363 herbicidal effect Effects 0.000 title claims description 10
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 claims description 15
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- WMXCDAVJEZZYLT-UHFFFAOYSA-N tert-butylthiol Chemical compound CC(C)(C)S WMXCDAVJEZZYLT-UHFFFAOYSA-N 0.000 claims description 6
- 229940125898 compound 5 Drugs 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 230000002688 persistence Effects 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical class CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- BUOSLGZEBFSUDD-BGPZCGNYSA-N bis[(1s,3s,4r,5r)-4-methoxycarbonyl-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 2,4-diphenylcyclobutane-1,3-dicarboxylate Chemical group O([C@H]1C[C@@H]2CC[C@@H](N2C)[C@H]1C(=O)OC)C(=O)C1C(C=2C=CC=CC=2)C(C(=O)O[C@@H]2[C@@H]([C@H]3CC[C@H](N3C)C2)C(=O)OC)C1C1=CC=CC=C1 BUOSLGZEBFSUDD-BGPZCGNYSA-N 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 235000013311 vegetables Nutrition 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
- 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
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
-
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
F' COMPOSITION HERBICIDE A BASE DE SEL DE BIPYRIDILIUM.F 'HERBICIDE COMPOSITION BASED ON BIPYRIDILIUM SALT.
**
La présente invention a pour objet une composition herbicide à base deThe subject of the present invention is a herbicidal composition based on
1 * I1 * I
~ , sel de bipyridilium contenant un agent susceptible de conférer une mauvaise odeur à la composition elle-même. Plus particulièrement, elle a pour objet une composition à base de sels de bipyridilium et une substance capable de. ; :>5 conférer à cette composition une odeur nauséabonde permettant de reconnaître ' i aisément que cette composition ne peut être consommée. ;~, bipyridilium salt containing an agent capable of imparting a bad odor to the composition itself. More particularly, it relates to a composition based on bipyridilium salts and a substance capable of. ; :> 5 give this composition a foul odor making it easy to recognize that this composition cannot be consumed. ;
Il est connu que ceux qui souvent manipulent de petites quantités d*herbicides destinés aux jardins potagers, vergers ou plus généralement aux jardins, transfèrent les compositions liquides de leur récipient original i 10 dans des bouteilles qui sont quelquefois utilisées pour conserver des boissons rafraîchissantes et peuvent donner lieu à des risques d'empoisonnements.It is known that those who often handle small quantities of herbicides intended for vegetable gardens, orchards or more generally in gardens, transfer the liquid compositions from their original container to 10 in bottles which are sometimes used to keep refreshing drinks and can give rise to risks of poisoning.
Afin d'éviter un tel risque, il est courant d'ajouter aux compositions à base de sel de bipyridilium formant un herbicide liquide, une substance conférant à la composition une odeur nauséabonde qui décourage quiconque de la 15 consommer par erreur.In order to avoid such a risk, it is common to add to the liquid herbicide forming bipyridilium salt compositions, a substance which gives the composition a foul odor which discourages anyone from consuming it by mistake.
Le choix de la substance conférant une odeur nauséabonde n'est pas aisé comme il aurait pu le sembler. Il est bien sûr évident que de nombreuses substances, par exemple, ne sont pas suffisamment solubles dans l'eau ou dans les solutions aqueuses de sels de bipyridilum, et donc donnent lieu, 20 soit à des précipités que l'on retrouve au fond des compositions liquides, soit à des dépôts à la surface de la composition liquide qui ne sont pas répartis de façon convenable même au cours des opérations de décantation.The choice of the substance conferring a foul odor is not as easy as it might have seemed. It is of course obvious that many substances, for example, are not sufficiently soluble in water or in aqueous solutions of bipyridilum salts, and therefore give rise either to precipitates which are found at the bottom of liquid compositions, or to deposits on the surface of the liquid composition which are not distributed in a suitable manner even during the settling operations.
De plus, cette substance ne doit pas réagir avec les constituants de la composition et doivent, en outre, se conserver aisément et ne pas se détériorer.In addition, this substance must not react with the constituents of the composition and must, moreover, be easily stored and not deteriorate.
25 Selon le brevet des Etats-Unis d'Amérique No. 4 075 005, de bons résul tats sont susceptibles d'être obtenus lorsque les compositions de sels de bipyridilium sont additionnées d'acide alkyl-carboxyTiques tels que acides valërianique ou butyrique, en quantités comprises entre 0,5 et 5¾. A des valeurs de pH proches de la neutralité, cependant, l'odeur nauséabonde a 30 tendance à disparaître.According to United States Patent No. 4,075,005, good results are likely to be obtained when the bipyridilium salt compositions are added with alkylcarboxylic acids such as valerianic or butyric acids, in particular quantities between 0.5 and 5¾. At pH values close to neutral, however, the offensive odor tends to disappear.
-L-L
............—......s r* -·— —............ — ...... s r * - · - -
Selon le brevet britannique NO. 1 406 881, il est possible d'employer une pyrîdîne basique, c'est-à-dire un mélange d'alkyl-pyridine; cette dernière a, cependant, un inconvénient qui réside dans son coût, attendu que la pyridine basique varie en fonction de son origine et qu'il est nécessaire de surveil-5 1er étroitement sa composition pour qu'elle satisfasse aux exigences requises.According to the British patent NO. 1 406 881, it is possible to use a basic pyridine, that is to say a mixture of alkyl-pyridine; the latter has, however, a drawback which lies in its cost, since basic pyridine varies according to its origin and it is necessary to closely monitor its composition so that it meets the required requirements.
On a constaté, et cela forme l'objet de la présente invention que,aux compositions herbicides à base de sel de bipyridilium, liquides,on peut ajouter du tert-butylmercaptan ou phënylmercaptan, en quantités comprises entre ... 0,025¾ et 0,1% de la composition, à des valeurs de pH comprises entre 3 et 8, 10 et de préférence de Tordre de 0,075% de Tun desdits mercaptans ou de leur mélange.It has been found, and this forms the object of the present invention, that, to the herbicidal compositions based on bipyridilium salt, liquids, tert-butylmercaptan or phenylmercaptan can be added, in amounts between ... 0.025¾ and 0, 1% of the composition, at pH values of between 3 and 8, 10 and preferably of the order of 0.075% of a Tun of said mercaptans or of their mixture.
- Dans de telles conditions, l'odeur doit être encore suffisamment percep tible même après deux années de stockage.- Under such conditions, the odor must still be sufficiently perceptible even after two years of storage.
Les avantages de ces additifs sont les suivants: 15 —faible coût de l'agent susceptible de conférer Todeur nauséabonde; — quantités minima d'agent requises pour obtenir l'effet recherché (jusqu'à 25 fois moins que les quantités d'acidesalkylcarboxyliques); — une longue persistance de Todeur nauséabonde de la composition durant son stockage; 20 — l'agent confère une odeur nauséabonde qui découragerait quiconque voudrait consommer la solution.The advantages of these additives are as follows: low cost of the agent capable of imparting nauseating odor; - minimum quantities of agent required to obtain the desired effect (up to 25 times less than the quantities of alkylcarboxylic acids); - a long persistence of foul smell of the composition during storage; 20 - the agent imparts a foul odor which would discourage anyone who wants to consume the solution.
L'agent qui confère la mauvaise odeur s'avère être compatible avec les additifs'généralement employés tels agents tensio-actîfs, diluants utilisés dans la formulation des herbicides à base de bipyridilium 25 . Les compositions à base de sel de bipyridilium contiennent en général de 200 à 500 g/1 d'herbicide. Dans ces conditions, les compositions peuvent être " additionnées des quantités indiquées d'agents conférant une odeur nauséabonde sans donner lieu aux inconvénients précités.The agent which imparts the bad odor appears to be compatible with the additives' generally employed such surfactants, diluents used in the formulation of herbicides based on bipyridilium 25. The bipyridilium salt compositions generally contain from 200 to 500 g / l of herbicide. Under these conditions, the compositions can be "added to the indicated quantities of agents conferring a foul odor without giving rise to the abovementioned drawbacks.
Λ La persistance de cette odeur nauséabonde est la même,que le produit soit 30 maintenu à un pH acide ou à un pH alcalin compris entre 3 et 8. Il est cependant courant que la valeur du pH soit maintenue aux environs de 8,5, car dans un milieu ou environnement alcalin les sels de bipyridilium sont stables.Λ The persistence of this foul odor is the same, whether the product is maintained at an acidic pH or at an alkaline pH between 3 and 8. It is however common that the pH value is maintained at around 8.5, because in an alkaline medium or environment the bipyridilium salts are stable.
D'autres avantages et caractéristiques de la présente invention apparai-tront à la lecture de la description suivante et des exemples donnés à titre 35 illustratif mais non limitatif.Other advantages and characteristics of the present invention will appear on reading the following description and examples given by way of illustration but not limitation.
—». -*> j*·-- ". - *> j * · -
"TV"TV
i / / r* ·. ' EXEMPLE 1i / / r * ·. '' EXAMPLE 1
On introduit dans un homogënéiseur: • chlorure de 1,1-dimêthyl-L ,1+ ’-bipyridilium L........... 250g • eau 700g.The following are introduced into a homogenizer: • 1,1-dimethyl-L chloride, 1 + ′ -bipyridilium L ........... 250g • water 700g.
5 Sous agitation, on ajoute alors: • nonylphénol-polyoxyéthylate 20g .5 With stirring, then: • nonylphenol-polyoxyethylate 20g is added.
• · dérivé quaternaire de cocoamine 30g • agent anti-moussage à base de silicium ............ 0,5g » • tert-butylmercaptan 0,5g·, 10 Le mélange est alors porté à un volume de 1000 ml par addition d'eau.• · quaternary cocoamine derivative 30g • silicon-based anti-foaming agent ............ 0.5g »• tert-butylmercaptan 0.5g ·, 10 The mixture is then brought to a volume 1000 ml by addition of water.
Après dissolution complète, les compositions sont versées dans une bou- * teille close et conservées à cette température durant deux ans. A l'ouverture de la bouteille, après cette période de stockage, la solution obtenue est claire et ne présente plus les caractéristiques d'odeur nauséabonde que con-15 fêre le tert-butylmercaptan.After complete dissolution, the compositions are poured into a closed bottle and kept at this temperature for two years. At the opening of the bottle, after this storage period, the solution obtained is clear and no longer exhibits the characteristics of foul odor than that of tert-butyl mercaptan.
EXEMPLE 2EXAMPLE 2
Dans Thomogënéiseur, on introduit: • chlorure de 1,1-dimethyl-L,U'-bipyridilrum ............ LûOg 20 · eau ............ 500g·In Thomogënéiseur, we introduce: • 1,1-dimethyl-L chloride, U'-bipyridilrum ............ LûOg 20 · water ............ 500g ·
Ensuite, sous agitation, on ajoute: • nonylphénol-polyoxyéthylate 32g • dérivé quaternaire de cocamine k8g • agent anti-moussage à base de silicium 0,5g 25 · phénylmercaptan ............ 1g.Then, with stirring, the following are added: • nonylphenol-polyoxyethylate 32g • quaternary cocamine derivative k8g • anti-foaming agent based on silicon 0.5g 25 · phenylmercaptan ............ 1g.
4 Le mélange est alors porté à 1000 ml par addition d'eau, puis il est agité jusqu'à l'obtention d'une totale homogénéisation.4 The mixture is then brought to 1000 ml by addition of water, then it is stirred until complete homogenization is obtained.
La composition est subdivisée en deux parties: « — une partie (formée de 500g) est mise dans un flacon telle quelle, 30 — une autre partie est diluée dans 300 cm3 d'eau.The composition is subdivided into two parts: “- one part (formed of 500g) is put in a bottle as it is, 30 - another part is diluted in 300 cm3 of water.
Les deux flacons sont alors conservés durant deux ans. Lorsqu'on les ouvre, on constate que les solutions ont conservé leur état limpide et leur odeur nauséabonde.The two bottles are then kept for two years. When opened, we see that the solutions have retained their clear state and their foul odor.
Bien entendu, la présente invention n'est nullement limitée aux exemples 35 et modes de mise en oeuvre mentionnés ci-dessus; elle est susceptible de nombreuses variantes accessibles à l'homme de l'art, suivant les applications envisagées et sans que l'on ne s'écarte de l'esprit de l'invention.Of course, the present invention is in no way limited to the examples and modes of implementation mentioned above; it is susceptible of numerous variants accessible to those skilled in the art, depending on the applications envisaged and without departing from the spirit of the invention.
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Claims (5)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT24226/79A IT1122094B (en) | 1979-07-10 | 1979-07-10 | HERBICIDE COMPOSITION BASED ON BIPYRIDYLUM SALTS CONTAINING A SUBSTANCE THAT LEAVES BAD ODOR |
| IT2422679 | 1979-07-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LU82602A1 true LU82602A1 (en) | 1981-02-02 |
Family
ID=11212651
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU82602A LU82602A1 (en) | 1979-07-10 | 1980-07-09 | HERBICIDE COMPOSITION BASED ON BIPYRIDILIUM SALT |
Country Status (15)
| Country | Link |
|---|---|
| AU (1) | AU6018880A (en) |
| BE (1) | BE884261A (en) |
| BR (1) | BR8004274A (en) |
| DE (1) | DE3026012A1 (en) |
| DK (1) | DK292380A (en) |
| EG (1) | EG14378A (en) |
| FR (1) | FR2460622A1 (en) |
| GB (1) | GB2053684B (en) |
| GR (1) | GR69333B (en) |
| IT (1) | IT1122094B (en) |
| KE (1) | KE3425A (en) |
| LU (1) | LU82602A1 (en) |
| NL (1) | NL8003909A (en) |
| NZ (1) | NZ194272A (en) |
| ZA (1) | ZA804133B (en) |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1406881A (en) * | 1972-04-13 | 1975-09-17 | Ici Ltd | Herbicidal compositions |
| GB1574600A (en) * | 1976-03-19 | 1980-09-10 | Ici Ltd | Herbicidal compositions |
| GB1570981A (en) * | 1976-01-20 | 1980-07-09 | Ici Ltd | Herbicidal compositions |
-
1979
- 1979-07-10 IT IT24226/79A patent/IT1122094B/en active
-
1980
- 1980-07-06 EG EG402/80A patent/EG14378A/en active
- 1980-07-07 NL NL8003909A patent/NL8003909A/en not_active Application Discontinuation
- 1980-07-07 DK DK292380A patent/DK292380A/en not_active Application Discontinuation
- 1980-07-08 GR GR62408A patent/GR69333B/el unknown
- 1980-07-08 AU AU60188/80A patent/AU6018880A/en not_active Abandoned
- 1980-07-08 FR FR8015129A patent/FR2460622A1/en active Granted
- 1980-07-08 NZ NZ194272A patent/NZ194272A/en unknown
- 1980-07-09 GB GB8022443A patent/GB2053684B/en not_active Expired
- 1980-07-09 ZA ZA00804133A patent/ZA804133B/en unknown
- 1980-07-09 DE DE19803026012 patent/DE3026012A1/en not_active Withdrawn
- 1980-07-09 LU LU82602A patent/LU82602A1/en unknown
- 1980-07-10 BE BE0/201362A patent/BE884261A/en not_active IP Right Cessation
- 1980-07-10 BR BR8004274A patent/BR8004274A/en unknown
-
1984
- 1984-07-20 KE KE3425A patent/KE3425A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EG14378A (en) | 1983-12-31 |
| DK292380A (en) | 1981-01-11 |
| IT1122094B (en) | 1986-04-23 |
| GB2053684B (en) | 1983-03-02 |
| DE3026012A1 (en) | 1981-02-19 |
| FR2460622A1 (en) | 1981-01-30 |
| ZA804133B (en) | 1981-07-29 |
| NL8003909A (en) | 1981-01-13 |
| GR69333B (en) | 1982-05-17 |
| GB2053684A (en) | 1981-02-11 |
| BE884261A (en) | 1981-01-12 |
| NZ194272A (en) | 1982-09-14 |
| KE3425A (en) | 1984-08-10 |
| FR2460622B1 (en) | 1983-03-11 |
| AU6018880A (en) | 1981-01-15 |
| IT7924226A0 (en) | 1979-07-10 |
| BR8004274A (en) | 1981-01-27 |
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