NL8603273A - PLANT GROWTH CONTROLLING PREPARATION AND METHOD FOR CONTROLLING PLANT GROWTH. - Google Patents
PLANT GROWTH CONTROLLING PREPARATION AND METHOD FOR CONTROLLING PLANT GROWTH. Download PDFInfo
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- NL8603273A NL8603273A NL8603273A NL8603273A NL8603273A NL 8603273 A NL8603273 A NL 8603273A NL 8603273 A NL8603273 A NL 8603273A NL 8603273 A NL8603273 A NL 8603273A NL 8603273 A NL8603273 A NL 8603273A
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- plant growth
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- controlling
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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
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/04—Nitrogen directly attached to aliphatic or cycloaliphatic carbon atoms
-
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/08—Amines; Quaternary ammonium compounds containing oxygen or sulfur
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- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05B—PHOSPHATIC FERTILISERS
- C05B15/00—Organic phosphatic fertilisers
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- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pretreatment Of Seeds And Plants (AREA)
Description
- 1 -- 1 -
Plantengroeiregelend preparaat en werkwijze voor het regelen van de plantengroei.Plant growth regulating preparation and method for controlling plant growth.
Deze uitvinding betreft een plantengroeiregelend en de rijping versnellend preparaat dat als werkzaam bestanddeel 0,2 tot 99,5 gew.% ammoniumfosfiet volgens formule 1 bevat, in welke formule een C^-alkyl-groep, R2 een (C^-alkoxy) -5 C^-alkyl- of een Cg_2Q-alkylgroep en waterstof of een C^j.-alkyl-groep voorstelt. Dat preparaat bestaat voor de rest uit vaste of vloeibare vulstof of drager en eventuele andere toeslagen, bij voorkeur oppervlak-actieve en/of de hechting bevorderende stoffen.This invention relates to a plant growth regulating and maturing accelerating composition containing as active ingredient 0.2 to 99.5 wt.% Ammonium phosphite according to formula 1, in which formula a C 1 -alkyl group, R 2 a (C 1 -alkoxy) - 5 represents C 1 -alkyl or a C 2-12 alkyl group and hydrogen or a C 1-20 alkyl group. The rest of the composition consists of solid or liquid filler or carrier and any other additives, preferably surfactants and / or adhesion promoters.
10 De bereiding van de werkzame stoffen volgens formule 1 en hun toepassing als fungiciden is beschreven in het Hongaarse octrooischrift 184.319, maar het plantengroeiregelende effect daarvan is in dat octrooischrift niet genoemd.The preparation of the active substances of formula 1 and their use as fungicides is described in Hungarian patent 184,319, but the plant growth regulating effect thereof is not mentioned in that patent.
Gevonden werd dat bij toepassing in geëigen-15 de doses de bovengenoemde verbindingen volgens de algemene formule 1 gebruikt kunnen worden voor het regelen van de wortelontwikke-ling, de groei, de vorming van bladoppervlak en van de vrucht-zetting, knopzetting en oogstrijping van te velde staande gewassen zoals tarwe, mais, suikerbieten, zonnebloemen en van tuingewassen 20 zoals paprika, tomaten, radijs, en aardappel, en verder van vruchtbomen zoals appels en bessendragende planten zoals druiven en krenten.It has been found that when used in appropriate doses the above compounds of general formula 1 can be used to control root development, growth, leaf surface formation and fruit set, bud setting and harvest maturation. standing crops such as wheat, corn, sugar beets, sunflowers and garden crops such as peppers, tomatoes, radishes and potatoes, and further from fruit trees such as apples and currant plants such as grapes and currants.
Voor het regelen van de plantengroei of voor het versnellen van de vruchtzetting kan het preparaat volgens de 25 uitvinding gebruikt worden met een concentratie aan werkzaam bestanddeel tussen 1 en 2000 dpm. De dosis is afhankelijk van de te behandelen plant, het doel van de behandeling, de fase waarin de plant verkeert en van de vorm van het preparaat.For controlling plant growth or for accelerating fruit set, the composition according to the invention can be used with a concentration of active ingredient between 1 and 2000 ppm. The dose depends on the plant to be treated, the purpose of the treatment, the phase of the plant and the form of the preparation.
De uitvinding betreft dan ook een werkwijze 30 voor het regelen van de plantengroei en voor het bevorderen van de knopzetting, vruchtzetting en oogstrijping, waarbij men de zaden, beginnende planten en bloemen behandelt met 1 tot 2000 dpm 8603273 ί - 2 - werkzaam bestanddeel, of de grond voor de planten voor het zaaien met 0,001 tot 5,0 g/m2 werkzame stof of na het planten door besprenkelen met 1 tot 2000 dpm werkzame stof, waarbij het preparaat voor 0,2 tot 99,5 gew.% uit verbinding volgens formule 1 bestaat, waar-5 bij R^, R^ en R^ de hierboven gegeven definities hebben en voor de rest uit vast of vloeibare drager of vulstof en eventuele andere toeslagen, bij voorkeur een oppervlak-actieve en/of de hechting bevorderende stof.The invention therefore relates to a method for controlling plant growth and for promoting budding, fruiting and harvest ripening, whereby the seeds, starting plants and flowers are treated with 1 to 2000 ppm of active ingredient, or the soil for the plants before sowing with 0.001 to 5.0 g / m2 of active substance or after planting by sprinkling with 1 to 2000 ppm of active substance, the preparation being 0.2 to 99.5% by weight of compound according to formula 1, where R5, R5 and R5 have the definitions given above and the remainder consists of solid or liquid carrier or filler and any other additives, preferably a surfactant and / or adhesion promoting substance .
Voor de praktische toepassing wordt het werk-10 zame bestanddeel volgens de uitvinding tot een preparaat geformuleerd met behulp van vaste of vloeibare dragers en. eventuele andere toeslagen, bij· voorkeur oppervlak-actieve en de hechting bevorderende stoffen.For practical application, the active ingredient of the invention is formulated into a composition using solid or liquid carriers and. any other additives, preferably surfactants and adhesion promoters.
Tot de geschikte dragers behoren organische 15 en anorganische, natuurlijke of synthetische stoffen die de adsorptie of absorptie van het werkzame bestanddeel bevorderen (bijv. water, methanol, glycerol, wassen, harsen,, talk, enz.),.Suitable carriers include organic and inorganic, natural or synthetic substances which promote the adsorption or absorption of the active ingredient (eg water, methanol, glycerol, waxes, resins, talc, etc.).
Tot de geschikte oppervlak-actieve stoffen behoren de ionogene en/of niet-ionogene emulgatoren, dispersie-20 middelen en bevochtigers, bij voorkeur alkylaryl-polyglycol-ethers en vetzuur-polyglycol-esters; geschikte stoffen die de hechting bevorderen zijn polyvinylpyrrolidon, polyethyleenglycol en carboxymethylcellulose.Suitable surfactants include the ionic and / or nonionic emulsifiers, dispersants and wetting agents, preferably alkylaryl polyglycol ethers and fatty acid polyglycol esters; suitable adhesion promoters are polyvinylpyrrolidone, polyethylene glycol and carboxymethyl cellulose.
De preparaten volgens de uitvinding kunnen 25 geformuleerd worden als in water oplosbare concentraten (WSC), bevochtigbare poeders (WP), stuifpoeders, emulgeerbare concentraten (EC) en als granulaten (G).The compositions of the invention can be formulated as water-soluble concentrates (WSC), wettable powders (WP), dusting powders, emulsifiable concentrates (EC) and as granules (G).
Verdere details volgens de uitvinding worden toegelicht door de volgende, niet beperkende voorbeelden, waarin 30 de werkzame stoffen als volgt aangegeven zijn: • 3-butyloxypropylammoniummethylfosfiet BF-53 2-methoxyethylammoniumethylfosfiet BF-76Further details according to the invention are illustrated by the following, non-limiting examples, in which the active substances are indicated as follows: • 3-butyloxypropylammoniummethylphosphite BF-53 2-methoxyethylammoniumethylphosphite BF-76
Tetradecylammoniumethylfosfiet BF-96Tetradecylammonium ethylphosphite BF-96
Hexadecylammoniumethylfosfiet BF-97 35 Decylammoniumethylfosfiet BF-100 bis-(2-ethylhexyl)ammoniumethylfosfiet BF-105 8603273 ¢- ί» -3-Hexadecylammoniumethylphosphite BF-97 35 Decylammoniumethylphosphite BF-100 bis- (2-ethylhexyl) ammoniumethylphosphite BF-105 8603273 ¢ - ί »-3-
Dodecylammoniumethylfosfiet BP-120 2-methoxyethylammoniumisopropylfosfiet BF-195 2-methoxyethylammoniumbutylfosfiet BP-196 2-methoxyethylaxnmoniummethylfosfiet BF-197 5 Voorbeeld 1Dodecylammoniumethylphosphite BP-120 2-methoxyethylammonium isopropylphosphite BF-195 2-methoxyethylammoniumbutylphosphite BP-196 2-methoxyethyl-ammoniummethylphosphite BF-197 5 Example 1
Een in water oplosbaar, vloeibaar preparaat heeft de volgende samenstelling:A water-soluble liquid preparation has the following composition:
Gew.%Wt%
Decylammoniumethylf o sfiet 95 10 Nonylfenolpolyglycolether (bijv. Arkopal NO80) 5Decylammonium ethylphosphite 95 10 Nonylphenol polyglycol ether (eg Arkopal NO80) 5
Voorbeeld 2Example 2
Een vloeibaar, emulgeerbaar preparaat voor vernevelen heeft de volgende samenstelling:A liquid, emulsifiable preparation for nebulizing has the following composition:
Gew.% .Wt%.
15 Dodecylanrooniume thylf osf iet 40Dodecylanroonium thylphosphite 40
Atlox 4857B (een mengsel van anion- actieve niet-ionogene oppervlak-actieve stoffen) 10Atlox 4857B (a mixture of anionic nonionic surfactants) 10
Chloorbenzeen 50Chlorobenzene 50
Voorbeeld 3 20 Een vloeibaar, emulgeerbaar, te vernevelen preparaat heeft de volgende samenstelling:Example 3 A liquid, emulsifiable, atomizable preparation has the following composition:
Gew.%Wt%
Tetradecylanmoniumethylfosfiet 20Tetradecylanmonium ethylphosphite 20
Arkopal N 130 (nonylfenol-polyglycolether) 5 25 Chloorbenzeen 75Arkopal N 130 (nonylphenol polyglycol ether) 5 25 Chlorobenzene 75
Voorbeeld 4Example 4
Een vloeibaar, emulgeerbaar te verspuiten preparaat maakt men uit de volgende bestanddelen:A liquid, emulsifiable sprayable preparation is made from the following ingredients:
Gew.% 30 bis(2-ethylhexyl)aDHHoniumethylfosfiet 30Wt% 30 bis (2-ethylhexyl) aDHHoniumethylphosphite 30
Genapol PF 10 (een polyadduct van propy- leenoxyde en ethyleenoxyde) 3Genapol PF 10 (a polyadduct of propylene oxide and ethylene oxide) 3
Genapol PF 40 (een polyadduct van propyleen- oxyde en ethyleenoxyde) 3Genapol PF 40 (a polyadduct of propylene oxide and ethylene oxide) 3
Ethyleenglycol 15 35Ethylene glycol 15 35
Cyclohexanon 50 8603273 «<. ï - 4 -Cyclohexanone 50 8603273 «<. ï - 4 -
Voorbeeld 5Example 5
Een in oplossing nuttig preparaat heeft de volgende samenstelling:A preparation useful in solution has the following composition:
Gew.% 5 3-butoxypropylammonium-methylfosfiet 1Wt% 5 3-butoxypropylammonium methylphosphite 1
Glycerol 99Glycerol 99
Voorbeeld 6Example 6
Een preparaat dat nuttig is als stuif-poeder heeft de volgende samenstelling: 10 Gew.% 2- methoxyethylammoniumethylfosfiet 0,55A formulation useful as a dusting powder has the following composition: 10% by weight of 2-methoxyethylammoniumethylphosphite 0.55
Talk 99,5Talk 99.5
Voorbeeld 7Example 7
Tarwekorrels (MV-4) werden ondergedom-15 peld in oplossingen met diverse concentraties aan proefstoffen. Na opdrogen werden de zaden in kweekflessen uitgezet.Wheat grains (MV-4) were immersed in solutions with various concentrations of test substances. After drying, the seeds were seeded in culture bottles.
Het percentage dat ontkiemde, de lengte der planten, het groene gewicht en het wortelgewicht werden bepaald toen de blanco planten in het stadium van vier bladeren 20 waren.. Ter vergelijking werden ook Gibberellazuur (GA) en 3- indoolazijnzuur gebruikt.Germination percentage, plant length, green weight and root weight were determined when the blank plants were at the stage of four leaves 20. Gibberella acid (GA) and 3-indole acetic acid were also used for comparison.
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Voorbeeld 8Example 8
Mais werd uitgezaaid in kweekflessen (5 plantjes per fles) en na opkomen besproeid met oplossingen die de proefstoffen op Gibberallazuur of 3-indoolazijnzuur be-5 vatten, en wel in concentraties van 250 en 500 dpm. De plant-lengte, groene massa en wortelmassa werden gemeten toen de onbehandelde planten in het stadium van 4 bladeren waren; deze uitkomsten staan in tabel II. Van elk tweede blad (van de top af gerekend) werden de chlorophylgehalten bepaald; deze uitkom-10 sten staan in tabel III.Corn was sown in culture bottles (5 plants per bottle) and, after emergence, sprayed with solutions containing the test substances on Gibberalic acid or 3-indole acetic acid, at concentrations of 250 and 500 ppm. Plant length, green mass and root mass were measured when the untreated plants were at the 4-leaf stage; these results are shown in Table II. The chlorophyll contents of each second leaf (counted from the top) were determined; these results are shown in table III.
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8603273 - 10 - ~ "5 üit de uitkomsten is duidelijk dat de ontwikkeling van de planten, vergeleken met de onbehandelde planten, significant bevorderd werd door elk der proefstoffen.From the results, it is clear that the development of the plants, compared to the untreated plants, was significantly enhanced by each of the test substances.
De verhouding tussen planthoogte en groene 5 massa geeft echter een duidelijker aanwijzing van het effect der BF-stoffen vergeleken met die der vergelijkingsstoffen. Zo bleek de habites van de mais niet nadelig beïnvloed te zijn door BF-12Q of FR-96, terwijl onder invloed van gibberellazuur betrekkelijk lang doorgeschoten planten met nadelige habites 10 ontstonden.However, the ratio between plant height and green mass gives a clearer indication of the effect of the BF substances compared to that of the comparative substances. For example, the habites of the corn were found not to be adversely affected by BF-12Q or FR-96, while under the influence of gibberellic acid plants with detrimental habites were produced for a relatively long time.
üit de uitkomsten der chlorophyll-bepalingen blijkt dat BF-120 het gunstigste effect op de hoeveelheid chlorophyll per gram groene plant als wel in de totale plant had.From the results of the chlorophyll determinations it appears that BF-120 had the most favorable effect on the amount of chlorophyll per gram of green plant as in the total plant.
15 Voorbeeld 915 Example 9
Tomatenplanten die over kleine perceeltjes verdeeld war.en werden bij het begin, van de bloei tot afdruipens toe besproeid met oplossingen die 250 of 500 dpm BF-120 bevatten. Op één dag, vier dagen en dertien dagen na de 20 behandeling werden van hetzelfde bladlob op dezelfde blad- hoogte monsters genomen en daarin werd het chlorophyll bepaald. De uitkomsten staan in tabel IV.Tomato plants distributed in small plots were sprayed initially with solutions containing 250 or 500 ppm BF-120 from flowering to dripping. One day, four days and thirteen days after the treatment, samples were taken from the same leaf lobe at the same leaf height and the chlorophyll was determined therein. The results are shown in Table IV.
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Voorbeeld 10 * - 12 -Example 10 * - 12 -
Hoogte en massa van maisplaten die met BF- 120 behandeld waren.Height and mass of corn plates treated with BF-120.
Maïs werd op 25 april 1985 gezaaid en de op-5 gekomen planten werden op 17 mei besproeid, toen ze in het stadium van 4 bladeren waren. De dosis was 2 liter per hectare, de werkzame stof was BF-120. De metingen gebeurden op 4 juli 1985; de uitkomsten staan in tabel V.Corn was sown on April 25, 1985, and the plants raised on 5 were sprayed on May 17, when they were at the 4-leaf stage. The dose was 2 liters per hectare, the active substance was BF-120. The measurements were taken on July 4, 1985; the results are shown in table V.
Tabel VTable V
10 -10 -
Blanco BehandeldBlank Treated
Hoogte (cm) Massa (g) Hoogte (cm) Massa (g) 15 Σ. x25=3844 £ x25=8888 £x'25=4212 £x25=s1Q646 x"2(-= 153$76 x25= 355,..52 X2g= ^-68>48 *84 5 = 9^64 s = 98,13 x = 10,24 s =119,0 20 Σ X2is3237 Gm ^x2l=7373 2X2l=354° - Σχ21=9093 *2la cm "*21~ 35^·)^· X21 * ^88r6 **2 Is 433*9 s = 7^52 s = 66,7 s = 7,3 s = 92,7 25 s = standaard deviatie 4 8603273 —r* -------— -—Height (cm) Mass (g) Height (cm) Mass (g) 15 Σ. x25 = 3844 £ x25 = 8888 £ x'25 = 4212 £ x25 = s1Q646 x "2 (- = 153 $ 76 x25 = 355, .. 52 X2g = ^ -68> 48 * 84 5 = 9 ^ 64 s = 98, 13 x = 10.24 s = 119.0 20 Σ X2is3237 Gm ^ x2l = 7373 2X2l = 354 ° - Σχ21 = 9093 * 2la cm "* 21 ~ 35 ^) ^ X21 * ^ 88r6 ** 2 Is 433 * 9 s = 7 ^ 52 s = 66.7 s = 7.3 s = 92.7 25 s = standard deviation 4 8603273 —r * -------— -—
Voorbeeld 11 - 13 -Example 11 - 13 -
Tomatenzaailingen (20 stuks) werden na knopvorming maar voor het begin van de bloei besproeid met oplossingen van diverse stoffen in twee verschillende concentra-5 ties. Alle planten kregen viermaal dezelfde besproeiing. De opbrengst van de eerste oogst werd gewogen; de uitkomsten staan in tabel VI.Tomato seedlings (20 pieces) were sprayed with solutions of various substances in two different concentrations after bud formation but before the beginning of flowering. All plants received the same watering four times. The yield of the first harvest was weighed; the results are shown in table VI.
Tabel VITable VI
Behandeling Dosis Oogst als % van de dpm_._blanco _______________Treatment Dose Harvest as% of ppm _._ blank _______________
Blanco - 100,00 BF-100 250 129,24 500 189,77 BF-105 250 143,96 15 500 122,70 BF-120 250 139,26 500 96,52 ETHREL 1 1/ha* 118,75 20 * De in de praktijk gebruikelijke dosis; de oplossing bevatte 40 % 2-chloorethylfosfiet.Blank - 100.00 BF-100 250 129.24 500 189.77 BF-105 250 143.96 15 500 122.70 BF-120 250 139.26 500 96.52 ETHREL 1 1 / ha * 118.75 20 * The usual dose in practice; the solution contained 40% 2-chloroethylphosphite.
Dat de beproefde stoffen het rijpen versnellen bleek ondubbelzinnig uit deze proeven.The tests proved that the tested substances accelerate ripening.
25 860327325 8603273
Claims (2)
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AR242482A1 (en) | 1993-04-30 |
CN86108565A (en) | 1987-09-16 |
HUT42294A (en) | 1987-07-28 |
HU197492B (en) | 1989-04-28 |
CS997386A2 (en) | 1987-12-17 |
CH669089A5 (en) | 1989-02-28 |
IT1198261B (en) | 1988-12-21 |
SU1593557A3 (en) | 1990-09-15 |
CA1276076C (en) | 1990-11-13 |
ATA330686A (en) | 1990-05-15 |
BE906023A (en) | 1987-04-16 |
ES2007598A6 (en) | 1989-07-01 |
TR23772A (en) | 1990-09-12 |
PT84021B (en) | 1989-01-17 |
PT84021A (en) | 1987-01-01 |
CS258496B2 (en) | 1988-08-16 |
DE3643102A1 (en) | 1987-07-02 |
IT8622875A1 (en) | 1988-06-24 |
JPS62190108A (en) | 1987-08-20 |
IT8622875A0 (en) | 1986-12-24 |
GR862928B (en) | 1987-04-27 |
LU86726A1 (en) | 1987-05-04 |
AT391588B (en) | 1990-10-25 |
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