Agricultural chemical composition

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a method for enhancing the effectiveness of an agricultural chemical, a novel agricultural chemical composition containing a specific enhancer and a use of an enhancer for the preparation of the agricultural chemical composition.
2. Description of the Related Art
Agricultural chemicals including fungicides (or bactericides), insecticides, herbicides, acaricides (or miticides) and plant growth regulators have been used in the forms of, for example, emulsions, wettable powders, granules, powders and flowables. In the properties of these agricultural chemical preparations, various attempts have been made to achieve the maximum effectiveness of the agricultural chemicals. However, it has been difficult to enhance the effectiveness of agricultural chemicals through adjustments in formulations. It is further difficult to develop novel agricultural chemicals. Therefore, further enhancement of existing agricultural chemicals would highly contribute to the industry.
As substances capable of enhancing agricultural chemicals, surfactants comprising various nitrogen-containing compounds such as quaternary ammonium salts, betaines and amine oxides have been known (see European Patent Publication-A No. 274369, published on Jul. 13, 1988). It is known that quaternized or further polyoxyethylenated long-chain amines, among the above-mentioned compounds, are effective for this purpose. These compounds capable of enhancing agricultural chemicals each contains a halogen ion as a counter ion. Namely, these compounds are halide compounds. However, these compounds are irritative.
DISCLOSURE OF THE INVENTION
SUMMARY OF THE INVENTION
From the viewpoint that agricultural chemicals can be enhanced by the combined use of agricultural chemicals with quaternary ammonium salt compounds, the present inventors have conducted extensive studies. As a result, they have found that specific compounds, among quaternary ammonium salt compounds, are particularly effective in enhancing the effectiveness of various agricultural chemicals, thus completing the present invention.
Thus, the present invention provides an agricultural chemical composition comprising an agricultural chemical and an effective amount for enhancing the effectiveness of the agricultural chemical of an enhancer compound selected from the group consisting of compounds represented by the following general formulae (I) to (III): ##STR1## wherein
A represents a hydrogen atom, --CH.sub.2 CH.sub.2 CN, --CH.sub.2 CH.sub.2 COOH, ##STR2## (wherein n is 2 to 9, p is 0 to 30, R or each of the plural R's is a hydrogen atom or a methyl group and R.sup.2 is an alkyl or alkenyl group having 4 to 30 carbon atoms), --C.sub.m H.sub.2m NH--COR.sup.2 (wherein m is 2 to 9 and R.sup.2 is as described above) or ##STR3## (wherein r is 2 to 6 and m, p, R and R.sup.2 are described above);
B, C and D are either the same or different from one another and each represents a hydrogen atom, a methyl group, an ethyl group --(C.sub.i H.sub.2i O).sub.j --COR.sup.3 (wherein i is 2 to 6, j is 1 to 10 and R.sup.3 is an alkyl or alkenyl group having 4 to 30 carbon atoms), --CH.sub.2 COO.sup..crclbar., --CH.sub.2 COOH, --(C.sub.i H.sub.2i O).sub.j --H (wherein i and j are as described above), --CH.sub.2 CH(OH)CH.sub.2 SO.sub.3.sup..crclbar. or ##STR4## with the proviso that only one of B, C and D represents either --CH.sub.2 COO.sup..crclbar. or --CH.sub.2 CH(OH)CH.sub.2 SO.sub.3.sup..crclbar. or B, C and D are other than --CH.sub.2 COO.sup..crclbar. and --CH.sub.2 CH(OH)CH.sub.2 SO.sub.3.sup..crclbar. ;
R.sup.1 represents an alkyl or alkenyl group having 4 to 30 carbon atoms; and
X.sup..crclbar. represents a counter ion;
with the proviso that when one of B, C and D represents either --CH.sub.2 COO.sup..crclbar. or --CH.sub.2 CH(OH)CH.sub.2 SO.sub.3.sup..crclbar., X.sup..crclbar. should be, deleted from the formula (I), ##STR5## wherein
Y and Z are either the same or different from each other and each represents an alkyl or alkenyl group having 6 to 30 carbon atoms, ##STR6## (wherein p is 0 to 30, R.sup.5 or each of the plural R.sup.5 's is a hydrogen atom or a methyl group and R.sup.6 is an alkyl or alkenyl group having 5 to 29 carbon atoms), --C.sub.3 H.sub.6 NHCOR.sup.6 (wherein R.sup.6 is as described above), --C.sub.3 H.sub.6 OR.sup.6 (wherein R.sup.6 is as described above), --CH.sub.2 CH(OH)CH.sub.2 OR.sup.6 (wherein R.sup.6 is as described above) or ##STR7## (wherein m is 2 to 9,
n is 2 to 9 and p, R.sup.5 and R.sup.6 are described above), with the proviso that Y and Z do not simultaneously represent alkyl and/or alkenyl groups having 6 to 30 carbon atoms;
R.sup.4 represents an alkyl group having 1to 4 carbon atoms or ##STR8## (wherein q is 1 to 30 and R.sup.5 is as described above); and
X.sup..crclbar. represents a counter ion, and ##STR9## wherein
R.sup.7 and R.sup.8 are either the same or different from each other and each represents an alkyl group having 1 to 4 carbon atoms, an alkenyl group having 2 to 4 carbon atoms or ##STR10## (wherein q is 1 to 30 and R.sup.10 or each of the plural R.sup.10 's is a hydrogen atom or a methyl group);
R.sup.9 represents an alkyl group having 6 to 36 carbon atoms, ##STR11## (wherein n is 2 to 9,
p is 0 to 30, R.sup.11 is an alkyl group having 5 to 35 carbon atoms and R.sup.10 is as described above), --C.sub.m H.sub.2m NH--COR.sup.11 (wherein m is 2 to 9 and R.sup.11 is as described above) or ##STR12## (wherein r is 2 to 6 and m, p, R.sup.10 and R.sup.11 are described above);
W represents ##STR13## (wherein p, R.sup.10 and
R.sup.11 are as described above), --NH--COR.sup.11 (wherein R.sup.11 is as described above) or ##STR14## (wherein p, r, R.sup.10 and R.sup.11 are as described above);
n is 2 to 9; and
X.sup..crclbar. is a counter ion.
Examples of the counter ion include a halogen ion such as Cl.sup.-, Br.sup.- or I.sup.-, an alkylsulfate anion (RSO.sub.4.sup.-), an alkylbenzenesulfonic acid anion (R-benzene-(SO.sub.3.sup.-), an alkylnaphthalenesulfonic acid anion (R-naphthalene-(SO.sub.3.sup.-), a fatty acid anion (RCOO.sup.-), an alkylphosphate anion (ROPO.sub.3 H.sup.- !, an anionic oligomer and an anionic polymer. As described above, a counter ion against N.sup..sym. is X.sup..crclbar., or --CH.sub.2 COO.sup..crclbar. or --CH.sub.2 CH(OH)CH.sub.2 SO.sub.3.sup..crclbar. as the substituent B, C or D in the general formula (I).
Preferable examples of the compounds represented by the above general formula (I) include those represented by the following general formula (Ia): ##STR15## wherein
A represents H, --CH.sub.2 CH.sub.2 --CN, --CH.sub.2 CH.sub.2 COOH, ##STR16##
B, C and D are either the same or different from one another and each represents H, --CH.sub.3, --CH.sub.2 CH.sub.3, ##STR17## --CH.sub.2 COO.sup..crclbar., --CH.sub.2 COOH, --(C.sub.p H.sub.2p O).sub.q--H (p= 2.about.6, q=1.about.10), ##STR18##
R.sup.1 to R.sup.5 are either the same or different from one another and each represents an alkyl or alkenyl group having 4 to 30 carbon atoms; and
X.sup..crclbar. is a counter ion.
Preferable examples of the compounds represented by the above general formula (II) include those represented by the following general formula (IIa): ##STR19## wherein
Y and Z are either the same or different from each other and each represents an alkyl group having 6 to 30 carbon atoms or an alkenyl group having 6 to 30 carbon atoms, --C.sub.2 H.sub.4 OCOR, --C.sub.3 H.sub.6 NHCOR, --C.sub.3 H.sub.6 OR or --CH.sub.2 CH(OH)CH.sub.2 OR (provided that Y and Z do not simultaneously represent alkyl or alkenyl groups having 6 to 30 carbon atoms);
R represents an alkyl group having 5 to 29 carbon atoms or an alkenyl group having 5 to 29 carbon atoms;
R.sup.1 represents an alkyl group having 1 to 4 carbon atoms or a hydroxyalkyl group having 1 to 4 carbon atoms; and
X.sup..crclbar. is a counter ion.
Preferable examples of the compounds represented by the above general formula (III) include those represented by the following general formula (IIIa): ##STR20## wherein
R.sup.1 and R.sup.2 are either the same or different from each other and each represents an alkyl group having 1 to 4 carbon atoms or an alkenyl group having 1 to 4 carbon atoms;
R.sup.3 represents an alkyl group having 6 to 36 carbon atoms, --C.sub.m H.sub.2m OCOR.sup.4 or --C.sub.m H.sub.2m NHCOR.sup.4 (m=2.about.9);
R.sup.4 represents an alkyl group having 5 to 35 carbon atoms;
Y represents --OCOR.sup.5 or --NHCOR.sup.5 ;
R.sup.5 represents an alkyl group having 5 to 35 carbon atoms:
n is 2.about.9; and
X.sup..crclbar. is a counter ion.
Further, the present invention provides a method for enhancing the effectiveness of an agricultural chemical which comprises applying an enhancer compound selected from the group consisting of compounds represented by the above general formulae (I) to (III) with an agricultural chemical to a locus which would benefit from such treatment. In this method, the enhancer and the agricultural chemical are generally diluted with water or a liquid carrier.
Examples of the locus or the area to be treated include farm, plantaion, fruit garden, orchard, flower garden, lawn, wood and forest. Examples of the locus include, further, plants, crops such as cereals, vegetables and fruits, trees, fruit trees, grasses, weeds, seeds, fungi, bacteria, insects, acarids and mites.
Furthermore, the present invention provides a use of a compound selected from the group consisting of compounds represented by the above general formulae (I) to (III) for the preparation of an agricultural chemical composition, an enhancer (or an adjuvant) for agricultural chemicals comprising a compound selected from the group consisting of compounds represented by the above general formulae (I) to (III); and a use of the enhancer for enhancing the efficacy of an agricultural chemical.
In addition, the present invention provides an agricultural chemical kit which comprises a container containing the enhancer described above and a container containing an agricultural chemical composition; another agricultural chemical kit which comprises a container containing the enhancer described above and a surfactant other than the compounds represented by the above formulae (I) to (III) and a container containing an agricultural chemical composition; and another agricultural chemical kit which comprises a container containing the enhancer described above, a container containing a surfactant other than the compounds represented by the above formulae (I) to (III) and a container containing an agricultural chemical composition.
In this specification, the term "agricultural chemical" means one which is employed as an active or principle ingredient in common agricultural chemical compositions or preparations, and examples thereof include a fungicide (or a bactericide), an insecticide, an acaricide (or a miticide), a herbicide, a plant growth regulator and the like.
Further the scope and the applicability of the present invention will become apparent from the detailed description given hereinafter. However, it should be understood that the detailed description and specific examples which follow, while indicating preferred embodiments of the invention, are given by way of illustration only, since various changes and modifications within the spirit and scope of the invention will become apparent to those skilled in the art from this detailed description.

DETAILED DESCRIPTION OF THE INVENTION
In the present invention, compounds represented by the above general formulae (I), (II) or (III) are used as enhancers for agricultural chemicals.
Among the compounds represented by the above general formula (I), those wherein A represents --C.sub.n H.sub.2n O--COR.sup.2 or --C.sub.m H.sub.2m NH--COR.sup.2 (wherein R.sup.2 is an alkyl or alkenyl group having 10 to 30 carbon atoms) and B, C and D are each a hydrogen atom or a methyl group may be cited as particularly suitable.
The compound of the general formula (I) according to the present invention can be obtained by, for example, reacting an N,N-dialkylaminoalkylamine with a nitrile compound, hydrogenating the obtained product to give a triamine, reacting the triamine thus obtained with a fatty acid to thereby give a diamide amine and then quaternizing this diamide amine with, for example, an alkyl chloride. Needless to say, the method for the preparation of the compound of the general formula (I) according to the present invention is not restricted thereto.
Among the compounds represented by the general formula (II), those wherein R.sup.4 is an alkyl group having 1 to 4 carbon atoms, and either Y or Z is a group having an ester bond or an amido group and another is an alkyl group may be cited as particularly suitable.
The compound of the general formula (II) according to the present invention can be obtained by, for example, reacting the corresponding secondary amine with an epoxy compound or a halo alcohol to thereby give an amino alcohol and esterifying this amino alcohol with a fatty acid or a fatty acid ester to thereby give the ester amine of the present invention. Alternatively, the amide amine of the present invention can be obtained by allowing the corresponding secondary amine and acrylonitrile to undergo an addition reaction and hydrogenating, followed by the amidation of the amine thus obtained with a fatty acid or a fatty acid ester. Needless to say, the method for the preparation of the compound of the general formula (II) according to the present invention is not restricted thereto.
Among the compounds represented by the general formula (III), the compound represented by the following formula is particularly preferable: ##STR21##
The compound of the general formula (III) according to the present invention is prepared by, for example, cyanoethylating an N-(lower alkyl)alkanolamine, hydrogenating the reaction produce, condensing the corresponding tertiary amine thus obtained with a fatty acid and quaternizing it in a conventional manner. Alternatively, the compound of the general formula (III) can be prepared by condensing N,N-dimethylpropanediamine with a fatty acid and then quaternizing it with an alkyl halide. Needless to say, the method for the preparation of the compound of the general formula (III) according to the present invention is not restricted thereto.
When used together with an agricultural chemical, the enhancer for agricultural chemicals according to the present invention, i.e., the compound represented by the above general formulae (I), (II) or (III), can enhance the effectiveness of the agricultural chemical twice or thrice without causing any chemical injury. Namely, the enhancer for agricultural chemicals of the present invention can be safely applied to various crops without causing any chemical injury.
It has nor necessarily been clarified why the enhancer for agricultural chemicals comprising the compound of the general formula (I), (II) or (III) according to the present invention exerts a remarkable enhancement effect regardless of the type of the structure of the agricultural chemical. One of the reasons therefor seemingly resides in that the enhancer of the present invention exerts a very strong solubilizing power on an agricultural chemical and, therefore, promotes the penetration of the agricultural chemical into the surfaces of plants, insects, fungi or bacteria.
The combined use of at least one compound selected from the group consisting of the compounds represented by the general formulae (I) to (III) according to the present invention with surfactant(s) other than these compounds makes it possible to reduce the dose of the compound(s) represented by the general formulae (I) to (III) while maintaining their enhancement effect on agricultural chemicals. Namely, the present invention also relates to an enhancer (or an enhancer composition) comprising a compound represented by the general formulae (I), (II) or (III) and a surfactant other than compounds represented by the general formulae (I), (II) or (III).
As surfactants other than the compounds represented by the general formulae (I) to (III), nonionic surfactants, anionic surfactants, cationic surfactants, ampholytic surfactants and mixtures of two or more surfactants described above are useful.
Examples of the nonionic surfactants include polyoxyethylene alkyl ethers, polyoxyethylene alkylaryl ethers, polyoxyethylene alkylaryl ether/formaldehyde condensates, polyoxyalkylene aryl ethers, polyoxyalkylene alkyl esters, polyoxyalkylene alkylsorbitol esters, polyoxyalkylene sorbitan esters, polyoxyalkylene alkylglycerol esters, polyoxyalkylene block copolymers, polyoxyalkylene block copolymer/alkylglycerol esters, polyoxyalkylene alkylsulfonamides, polyoxyalkylene rosin esters, polyoxypropylene block copolymers, polyoxyethylene oleyl ether, polyoxyalkylene alkylphenols and mixtures comprising two or more of these surfactants.
Examples of the cationic surfactants include alkylamine/ethylene oxide adducts and alkylamine/propylene oxide adducts such as tallow amine/ethylene oxide adduct, oleylamine/ethylene oxide adduct, soy amine/ethylene oxide adduct, coco amine/ethylene oxide adduct, synthetic alkylamine/ethylene oxide adducts, octylamine/ethylene oxide adduct and mixtures thereof.
Among anionic surfactants, typical ones are available in the form of an aqueous solution or a solid. Examples thereof include sodium mono- and di-alkylnaphthalenesulfonates, sodium .alpha.-olefinsulfonate, sodium alkanesulfonates, alkyl-sulfates, polyoxyalkylene alkyl ether sulfates, polyoxyalkylene alkyl aryl ether sulfates, polyoxyalkylene styryl phenyl ether sulfates, mono- and dialkylbenzenesulfates, alkylnaphthalenesulfates, alkylnaphthalenesulfonate/formaldehyde condensates, alkyl diphenyl ether sulfonates, olefinic sulfonates, alkylphosphates, polyoxyalkylene alkylphosphates, polyoxyalkylene phenyl ether phosphates, polyoxyalkyl phenol phosphates, polycarboxylic acid salts, fatty acid salts, stearic acid and its salts, oleic acid and its salts, N-methyl fatty acid taurides and mixtures comprising two or more of these surfactants (including sodium, potassium, ammonium and amine salts).
Examples of suitable ampholytic surfactants include lauryldimethylamine oxide, Armox C/12, amine oxides, Monaterics, Miranols, betaine, Lonzaines, other amine oxides and mixtures thereof.
Among these surfactants, nonionic surfactants are particularly preferable. Still preferable surfactants include those of the ester type, such as polyoxyalkylene sorbitan esters and polyoxyalkylene alkyl glycerol esters, polyoxyalkylene alkyl ethers and polyoxyalkylene alkylnonyl phenols.
In an enhancer (or an enhancer composition) for agricultural chemicals comprising the compound(s) represented by the general formulae (I) to (III) and surfactant(s) other than said compounds, The weight ratio of the content of the compound(s) of the general formulae (I) to (III) to the content of the surfactant(s), i.e., �the (total) content of the compound(s) of the general formulae (I) to (III)/the (total) content of the surfactant(s) other than said compounds!, preferably ranges from 1/10 to 50/1, still preferably from 1/1 to 10/1.
The agricultural chemical composition of the present invention comprises the above-mentioned enhancer and an agricultural chemical.
In the agricultural chemical composition comprising the enhancer and an agricultural chemical according to the present invention, it is necessary to use the compound(s) represented by the general formulae (I) to (III), i.e., the enhancer, in an amount wherein the ratio of the (total) content of the compound(s) of the general formulae (I) to (III)/the (total) content of the agricultural chemical(s) is from 0.05 to 50, preferably from 0.05 to 20 and still preferably from 0.1 to 10. When this ratio is below 0.05, any desired effect of enhancing the effectiveness of the agricultural chemical(s) can be fully achieved. When this ratio exceeds 50, on the other hand, the enhancing effect is no longer improved.
Next, examples of the agricultural chemicals to be used in the agricultural chemical composition of the present invention will be cited, though the present invention is not restricted thereto.
In the case of fungicides (or bactericides), included are Dithane or Dipher �zinc ethylenebis(dithiocarbamate)!, Magneb or Maneb-dithane �manganese ethylenebis(dithiocarbamate)!, Thiram or Thiram 80 �bis(dimehtylthiocarbamoyl)disulfide!, Mancozeb �complex of zinc and manganese ethylenebis(dithiocarbamate)!, Bis-Dithane �dizinc bis(dimethyldithiocarbamate)ethylenebis(dithiocarbamate)!, Propineb or Antracol �polymeric zinc propylenebis(dithiocarbamate)!, benzimidazole fungicides such as Benomyl or Benlate �methyl 1-(butylcarbamoyl)-2-benzimidazolecarbamate! and Thiophanate-methyl or Topsin M �1,2-bis(3-methoxycarbonyl-2-thioureido)benzene!, Vinclozolin or Ronilan �3-(3,5-dichlorophenyl)-5-methyl-5-vinyl-1,3-oxazolidine-2,4-dione!, Iprodione or Rovral �3-(3,5-dichlorophenyl)-N-isopropyl-2,4-dioxoimidazolidine-1-carboxamide!, Procymidone or Sumilex �N-(3,5-dichlorophenyl)-1,2-dimethylcyclopropane-1,2-dicarboximide!, Triazine �2,4-dichloro-6-(2-chloroanilino)-1,3,5-triazine!, Triflumizole or Trifmine �(E)-4-chloro-.alpha.,.alpha.,.alpha.-trifluoro-N-(1-imidazol-1-yl-2-propoxyethylidene)-o-toluidine!, Metalaxyl or Ridomil �methyl-N-(2-methoxyacetyl)-N-(2,6-xylyl)-D,L-alaninate!, Bitertanol or Baycoral �all-rac-1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)-2-butan-2-ol!, Triadimefon or Bayleton �1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)-2-butanone!, Isoprothiolane or Fuji-one (diisopropyl 1,3-dithiolan-2-ylidenemalonate), Daconil (tetrachloroisophthalonitrile), Pansoil (5-ethoxy-3-trichloromethyl-1,2,4-thiadiazole), Rabcide (4,5,6,7-tetrachlorophthalide), Kitazin P (O,O-diisopropyl S-benzyl thiophosphate), Hinosan (O-ethyl S,S-diphenyl dithiophosphate), Probenazol or Oryzemate (3-allyloxy-1,2-benzisothiazole 1,1-dioxide) and Captan or Orthocide (N-trichloromethylthiotetrahydrophthalimide).
In the case of insecticides, included are pyrethroid insecticides such as Fenvalerate or Vegiphon �.alpha.-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanoate! and Baythroid �.alpha.-cyano-4-fluoro-3-phenoxyphenylmethyl 3-(2,2-dichloroethenyl)-2,2-dimethylcyclcopropanecarboxylate!, organophosphorus insecticides such as DDVP or Des (dimethyl 2,2-dichlorovinyl phosphate), Sumithion �O,O-dimethyl O-(3-methyl-4-nitrophenyl)thiophosphate!, Malathon or Malathion (S-�1,2-bis(ethoxycarbonyl)ethyl!dimethyl phosphorothionate), Dimethoate �dimethyl S-(N-methylcarbamoylmethyl)dithiophosphate!, Elsan or Papthion (S-�.alpha.-(ethoxycarbonyl)benzyl!dimethyl phosphorothiolthionate) and Baycid �O,O-dimethyl O-(3-methyl-4-methylthiophenyl)thiophosphate!, carbamate insecticides such as Bassa (o-sec-butylphenyl methylcarbamate), MTMC or Tsumacide (m-tolyl methylcarbamate), Meobal (3,4-dimethylphenyl N-methylcarbamate) and NAC or Papnac (1-naphthyl N-methylcarbamate), Methomyl or Lannate (S-methyl-N-�(methylcarbamoyl)oxy!thioacetimidate) and Cartap or Padan �1,3-bis(carbamoylthio)-2-(N,N-dimethylamino)propane hydrochloride!.
In the case of acaricides (or miticides), included are Sunmite �2-tert-butyl-5-(4-tert-butylbenzylthio)-4-chloropyridazin-8(2H)-one!, Acricid (2,4-dinitro-6-sec-butylphenyldimethylacrylate!, Chloromite (isopropyl 4,4-dichlorobenzylate), Akar (ethyl 4,4-dichlorobenzilate), Kelthane �1,1-bis-(p-chlorophenyl)-2,2,2-trichloroethanol!, Citrazon (ethyl O-benzoyl-3-chloro-2,6-dimethoxybenzohydroximate), Omite �2-(p-tert-butylphenoxy)cyclohexyl 2-propynyl sulfite!, Osadan �hexakis(.beta.,.beta.-dimethylphenylethyl)distannoxane!, Hexythiazox or Nissorun �trans-5-(4-chlorophenyl)-N-cyclohexyl-4-methyl-2-oxo-thiazolidine-3-carboxamide! and Amitraz or Dani-Cut �3-methyl-1,5-bis(2,4-xylyl)-1,3,5-triazapenta-1,4-diene!.
In the case of herbicides, included are acid amide herbicides such as Stam (3',4'-dichloropropionanilide, DCPA) and Dacklone (3-chloro-2-methyl-p-valerotoluidide, CMMP), urea herbicides such as DCMU or Karmex �3-(3,4-dichlorophenyl)-1,1-dimethylurea! and Linuron �3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea), dipyridyl herbicides such as Paraquat (1,1'-dimethyl 4,4'-bipyridinium dichloride) and Diquat (6,7-dihydrodipyrido�1,2-a:2',1'-c!pyrazindiium dibromide), diazine herbicides such as Bromacil (5-bromo-3-sec-butyl-6-methyluracil), S-triazine herbicides such as Simazine �2-chloro-4,6-bis(ethylamino)-1,3,5-triazine! and Simetryne �2,4-bis(ethylamino)-6-methylthio-1,3,5-triazine!, nitrile herbicides such as DBN (2,6-dichlorobenzonitrile), dinitroaniline herbicides such as Trifluralin (.alpha.,.alpha.,.alpha.-trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine), carbamate herbicides such as Benthiocarb or Saturn �S-(p-chlorobenzyl) N,N-diethylthiolcarbamate! and MCC (methyl 3,4-dichlorocarbanilate), diphenylether herbicides such as NIP (2,4-dichlorophenyl-p-nitrophenylether), phenol herbicides such as PCP (sodium pentachloro-phenoxide), benzoic acid herbicides such as MDBA (dimethylamine-3,6-dichloro-o-anisate), phenoxy herbicides such as sodium 2,4-D (sodium 2,4-dichlorophenoxyacetate) and Mapica (�(4-chloro-o-toluyl)oxy!-aceto-o-chloroanilide), organic phosphorus herbicides such as Glyphosate �N-(phosphonomethyl)-glycine! and salts thereof, Bialaphos or Herbiace (sodium sale of L-2-amino-4-�(hydroxy)(methyl)=(phosphinoyl)!butyryl-L-alanyl-L-alanine) and Glufosinate or Basra �ammonium DL-homoalanin-4-yl (methyl)phosphinate!, and aliphatic herbicides such as sodium TCA (sodium trichloroacetate).
In the case of plant growth regulators, included are MH (maleic hydrazide), Ethrel (2-chloroethylphosphonic acid), UASTA and Bialaphos or Herbiace.
The agricultural chemical composition of the present invention may be formulated into any preparation such as emulsions, wettable powders, granules powders or flowables without any limitation. Accordingly, said composition may contain other additives which are selected depending on the formulation, for example, emulsifiers, dispersing agents and carriers.
The agricultural chemical composition according to the present invention may further contain a chelating agent, a pH regulator, an inorganic salt or a thickener, if required.
Examples of chelating agents include aminopolycarboxylic acid type chelating agents, aromatic or aliphatic carboxylic acid type chelating agents, amino acid type chelating agents, ether polycarboxylic acid type chelating agents, iminodimethylphosphonic acid (IDP), dimethylglyoxime (DG) and alkyldiphosphonic acids (ADPA). These chelating agents are as such or in the form of salts (sodium, potassium or ammonium salt) thereof.
Examples of the aminopolycarboxylic acid type chelating agents include a) compounds represented by the chemical formula of RNX.sub.2, b) compounds represented by the chemical formula of NX.sub.3, c) compounds represented by the chemical formula of R--NX--CH.sub.2 CH.sub.2 --NX--R, d) compounds represented by the chemical formula of R--NX--CH.sub.2 CH.sub.2 --NX.sub.2, e) compounds represented by the chemical formula of X.sub.2 N--R'--NX.sub.2 and f) compounds similar to compounds of e) and containing four or more X's, for example, a compound represented by the formula: ##STR22##
In the above formulae, X represents --CH.sub.2 COOH or --CH.sub.2 CH.sub.2 COOH, R represents a group to be contained in these type, known chelating agents such as a hydrogen atom, an alkyl group, a hydroxy group and a hydroxyalkyl group, and R' represents a group to be contained in these type, known chelating agents such as an alkylene group and a cycloalkylene group.
Representative examples of the aminopolycarboxylic acid type chelating agents include ethylenediaminetetraacetic acid (EDTA), cyclohexanediaminetetraacetic acid (CDTA), nitrilotriacetic acid (NTA), iminodiacetic acid (IDA), N-(2-hydroxyethyl)iminodiacetic acid (HIMDA), diethylenetriaminepentaacetic acid (DTPA), N-(2-hydroxyethyl)ethylenediaminetriacetic acid (EDTA-OH) and glycoletherdiaminetetraacetic acid (GEDTA), and salts thereof.
Examples of the aromatic or aliphatic carboxylic acid type chelating agents to be used in the present invention include citric acid, oxalic acid, glycolic acid, pyruvic acid and anthranilic acid, and salts thereof. Further, examples of the amino acid type chelating agents to be used in the present invention include glycine, serine, alanine, lysine, cystine, cysteine, ethionine, tyrosine and methionine, and salts and derivatives thereof.
Furthermore, examples of the ether polycarboxylic acid type chelating agents include compounds represented by the following formula, compounds similar to the compounds represented by the following formula and salts (e.g., sodium salt) thereof: ##STR23## wherein Y represents a hydrogen atom, --CH.sub.2 COOH or --COOH, and Z represents a hydrogen atom, --CH.sub.2 COOH or ##STR24##
Examples of the pH regulators to be used in the present invention include citric acid, phosphoric acid (e.g., pyrophosphoric acid) and gluconic acid, and salts thereof.
Examples of the inorganic acid salts to be used in the present invention include inorganic mineral salts such as inorganic salts of clay, talc, bentonite, zeolite, calcium carbonate, diatomaceous earth and white carbon, and inorganic ammonium salts such as ammonium sulfate, ammonium nitrate, ammonium phosphate, ammonium thiocyanate, ammonium chloride and ammonium sulfamate.
In addition, examples of thickeners to be used in the present invention include natural, semisynthetic and synthetic, water-soluble thickeners. As natural mucilaginous matters, xanthane gum and zanflow, which are derived from microorganism, and pectine, gum arabic and guar gum, which are derived from plant, are cited. As semisynthetic mucilaginous matters, methylated, carboxyalkylated and hydroxyalkylated products of cellulose such as methylcellulose, carboxymethylcellulose and hydroxymethylcellulose, methylated, carboxyalkylated and hydroxyalkylated products of starch derivatives, and sorbitol are cited. Furthermore, polyacrylates, polymaleates, polyvinylpyrrolidone and pentaerythritol/ethyleneoxide adducts are cited as synthetic mucilaginous matters.
The agricultural chemical composition of the present invention may further contain one or more ingredients such as plant growth regulators other than those cited above, fertilizers and preservatives.
The agricultural chemical composition of the present invention is used in order to control fungi (or bacteria), insects, acarids (or mites) and herbs or to regulate the growth of plants.
The agricultural chemical kit according to the present invention comprises a container containing the enhancer according to the present invention and another container containing an agricultural chemical composition. In this case, the enhancer may comprise at least one compound represented by the above general formulae (I) to (III), or a mixture of at least one compound represented by the above general formulae (I) to (III) and at lease one surfactant other than the compounds represented by the above general formulae (I) to (III). Alternatively, another agricultural chemical kit according to the present invention comprises a container containing at least one compound represented by the above general formulae (I) to (III), a container containing at least one surfactant other than the compounds represented by the above general formulae (I) to (III) and a container containing an agricultural chemical composition.
The "agricultural chemical composition" which is a constituent of the kit is a composition which comprises an agricultural chemical(s), is free from the compounds represented by the above general formulae (I) to (III) and is in the form of, for example, an emulsion or a wettable powder.
In the agricultural chemical kit according to the present invention, a composition comprising an agricultural chemical is separated from the compounds represented by the above general formulae (I) to (III). Namely, the kit differs from an agricultural chemical composition comprising the enhancer for agricultural chemicals and an agricultural chemical(s) in admixture.
Each of contents in these containers is not restricted in their form but appropriately prepared depending on the use and purpose. The material of the container is not restricted so long as it is not react with or affect the content. Examples of the material include plastics, glass, foil, etc.
The enhancer according to the present invention is applied with an agricultural chemical to a locus which would benefit from such treatment, i.e., the application of the enhancer and the agricultural chemical. In general, the enhancer and the agricultural chemical are used with water or a liquid carrier. As means for applying the enhancer for agricultural chemicals according to the present invention, (1) one wherein an agricultural chemical composition of the present invention containing the enhancer and having a preparation form is used (if necessary, the agricultural chemical composition is diluted with, for example, tap water), (2) another one wherein an enhancer is added to an agricultural chemical composition, which has been diluted with water, and (3) another one wherein an enhancer is diluted with water and then an agricultural chemical composition is diluted with the resultant diluted enhancer solution, are useful. The desired enhancement effect can be achieved by either means.
The agricultural chemical composition of the present invention includes one containing the agricultural chemical in high concentration and the enhancer in high concentration, and another one containing the agricultural chemical in an appropriate concentration for application and the enhancer in an appropriate concentration for application. When the former is used, the agricultural chemical composition is diluted with water, etc., for example, just before applying. On the other hand, the agricultural chemical compositions used in the above cases (2) and (3) include those containing the agricultural chemical in high concentration and being free from the enhancer of the present invention.
The contents of the agricultural chemical and the enhancer in their diluted solution are not limited. The content of the agricultural chemical in its diluted solution depends on, for example, the kind of the agricultural chemical and its use. While the content of the enhancer in its diluted solution depends on, for example, the kind of the agricultural chemical to be mixed.
The diluted liquid comprising an appropriate amount of an agricultural chemical and an appropriate amount of an enhancer of the present invention is applied to, for example, plants, crops, vegetables, fruits, trees, fruit trees, grasses, weeds or seeds, and, at the same time, to fungi, bacteria, insects, acarids or mites. In other words, the diluted liquid is applied to a farm, a plantain, a fruit garden, an orchard, a flower garden, a lawn, a wood and a forest.

EXAMPLES
The present invention will now be described in more detail with reference to the following Examples which should not be considered to limit the scope of the present invention.
Production Example 1
(a) A four-neck flask provided with a stirrer, a thermometer and a dropping funnel was charged with 204 g of N,N-dimethylaminopropylamine and 106 g of acrylonitrile was added dropwise therein over 1 hour while maintaining the liquid temperature at 60.degree. C. After the completion of the addition, the mixture was aged, i.e., maintained, at the same temperature for 5 hours. After the completion of the aging, the reaction mixture was transferred into an autoclave equipped with a stirrer, a thermometer and a pressure gauge. Next, 30 g of Raney nickel was added thereto and hydrogenation was effected over 6 hours while maintaining the hydrogen pressure at 20 kg/cm.sup.2. G. After the completion of the reaction, the Raney nickel was filtered off and the reaction mixture was distilled to thereby give 180 g of a triamine. The boiling point of this product was 86.degree. C./0.2 mmHg.
(b) A four-neck flask provided with a stirrer, a thermometer and a dropping funnel was charged with 78 g of the triamine obtained above and 285 g of octadecanoic acid and heated to 150.degree. C. Then amidation was effected at the same temperature for 12 hours while distilling off the water thus formed to thereby give 350 g of the target diamide amine. Based on the NMR and IR spectra, it was confirmed that this diamide amine had the following structure: ##STR25## (c) Subsequently, the diamide amine obtained above was quaternized with methyl chloride in a conventional manner and thus the following compound (hereinafter referred to as "enhancer 1") was obtained. ##STR26##
Example 1
The enhancer 1 obtained in the above Production Example 1 was dissolved in deionized water so as to give a 0.2% by weight solution. By using this 0.2% by weight solution, commercially available herbicides, i.e., a Roundup liquid formulation (content of the active ingredient, i.e., isopropylamine salt of Glyphosate: 41% by weight), a Karmex wettable powder (content of the active ingredient. i.e., DCMU: 78.5% by weight) and a Herbiace water-soluble powder (content of the active ingredient, i.e., Bialaphos: 20% by weight) were each diluted 300-fold. Thus, three agricultural chemical compositions of the present invention which contain the same enhancer were obtained.
Rich soil obtained from a paddy field, gravels and a culture soil available on the market were mixed one another at the weight ratio of 7:2:1. Pots having an inside diameter of 12 cm were filled with the soil thus obtained. In order to conduct a glasshouse-test, the seeds of crabgrass were sowed in the pots and germinated. The pots wherein the growth of the crabgrass was abnormal were abandoned to reduce the irregularity among pots. The pots wherein crabgrasses had been grown at a height of about 18 cm were used in the test. Spray gun (mf. by Iwata Tosoki Kogyo K.K., type RG) was used for the application of the agricultural chemical compositions to the crabgrasses. The crabgrasses in the pots were uniformly sprayed with each of the agricultural chemical compositions at a ratio corresponding to 10 l/a (liter per are) to evaluate the herbicidal efficacy.
On the tenth day after the application, the above-ground part of the fresh plant was weighed and the result was expressed in a herbicidal percentage on the basis of the fresh weight of the above-ground part in the untreated lot (see the following formula). ##EQU1##
The above procedure was repeated except that the enhancer 1 was replaced by the following enhancers 2 to 24 to thereby give agricultural chemical compositions and the herbicidal efficacy of each composition was evaluated. Further, each agricultural chemical was used alone without adding any enhancer and the herbicidal efficacy was evaluated in the same manner. Namely, 3 agricultural chemical compositions which were prepared by diluting one of the above-described commercially available herbicides 300-fold with deionized water were also evaluated. Table 1 summarizes the results.
Enhancer 2; enhancer 1/Emulgen 909 �POE(9) nonyl phenol ether!=80/20.
Enhancer 3; enhancer 1/Emulgen 103 �POE(3) C.sub.12 H.sub.25 OH!=80/20.
Enhancer 4; enhancer 1/Emanon 4110 �POE(10) C.sub.17 H.sub.35 COOH!=80/20.
Enhancer 5; enhancer 1/Rheodol TWL-120 �POE(20) C.sub.11 H.sub.23 COO sorbitan ester!=80/20.
Enhancer 6; a compound represented by the following formula was used: ##STR27## Enhancer 7: enhancer 8/Emulgen 703 �a mixture of POE(3) C.sub.12 H.sub.25 OH and POE(3) C.sub.13 H.sub.27 OH!=75/25 .
Enhancer 8; enhancer 6/Emanon 1112 �POE(12) C.sub.11 H.sub.23 COOH!=75/25.
Enhancer 9; enhancer 6/Rheodol TWL-120 �POE(20) C.sub.17 H.sub.33 COO sorbitan ester!=75/25.
Enhancer 10; didecyldimethylammonium chloride.
Enhancer 11; monolauryltrimethylammonium chloride.
Enhancer 12; dilauryldihydroxyethylammonium chloride.
Enhancer 13; trimethylcocoammonium chloride.
Enhancer 14; a compound represented by the following formula was used: ##STR28## Enhancer 15; enhancer 14/Emulgen 909=80/20. Enhancer 16; enhancer 14/Emulgen 103=80/20.
Enhancer 17; enhancer 14/Emanon 4110=80/20.
Enhancer 18; enhancer 14/Rheodol TWO-120=80/20.
Enhancer 19; a compound represented by the following formula was used: ##STR29## Enhancer 20; enhancer 19/Emulgen 703=75/25. Enhancer 21; enhancer 19/Emanon 1112=75/25.
Enhancer 22; enhancer 19/Rheodol TWO-120=75/25.
Enhancer 23; a compound represented by the following formula was used: ##STR30## Enhancer 24; enhancer 23/Rheodol TWO-120=80/20.
The express on "POE" as used herein is an abbreviation of "polyoxyethylene" and each value given in the parentheses is an average addition mole number of oxyethylene. In the above-described enhancers, the composition ratio is by weight.
TABLE 1______________________________________ Herbicidal ratio (%) Herbiace Karmex water- RoundupNo. of wettable soluble liquidenhancer powder powder formulation______________________________________Inventionproduct 1 98.5 98.3 99.4 2 99.3 98.3 99.5 3 98.0 97.9 98.1 4 97.8 98.9 99.2 5 97.8 99.1 98.2 6 98.6 98.8 98.8 7 99.4 99.4 99.0 8 99.0 99.3 99.2 9 98.9 98.2 99.3Comparativeproduct10 63.5 70.0 73.511 44.5 72.2 76.112 60.3 70.1 71.113 50.3 65.8 75.3Inventionproduct14 98.5 98.7 98.715 98.5 99.3 98.716 98.5 99.0 99.317 96.7 99.2 99.418 98.5 98.3 98.319 98.2 98.3 98.520 99.5 98.5 99.321 99.3 98.7 98.322 99.2 99.0 98.323 98.3 99.0 98.124 97.8 97.2 98.3none 18.4 67.5 68.5______________________________________
Example 2
Female imagines of Tetranychus kanzawai Kishida were planted onto kidney bean leaf disks at a ratio of 30 imagines/lot in triplicate runs and incubated at 25.degree. C. for 24 hours. Next, the whole leaf disk was dipped in a test solution for 5 seconds and then taken out of the test solution. After being left to stand at 25.degree. C. for 48 hours, the leaf disk was observed and the acaricidal ratio was determined on the basis of the result in the untreated lot (see the following formula). ##EQU2##
As an acaricide, a Nissorun V emulsion �content of the active ingredient as an agricultural chemical: 55% by weight (50% by weight of hexythiazox+5% by weight of DDVP)! and an Osadan wettable powder-25 (content of the active ingredient, i.e., fenbutatin oxide: 25% by weight) were each diluted 2,000-fold and used. The same enhancers for agricultural chemicals as those employed in Example 1 were used. Each agricultural chemical composition was prepared in such a manner as to adjust the concentration of the enhancer for agricultural chemicals in the diluted solution to 0.1% by weight. Further, the same procedure was repeated without using any enhancer for agricultural chemicals. Namely, two agricultural chemical compositions which were prepared by diluting one of the above-described commercially available acaricides 2000-fold with deionized water were also evaluated. Table 2 shows the results.
TABLE 2______________________________________ Acaricidal ratio (%) Osadan Nissorun V wettableNo. of enhancer emulsion powder______________________________________Inventionproduct 1 98.8 98.8 2 97.8 97.8 3 97.8 100 4 97.8 98.8 5 98.8 100 6 100 98.8 7 98.8 97.8 8 100 100 9 100 99.2Comparativeproduct10 50.0 52.211 50.0 46.512 48.9 52.213 50.0 74.4Inventionproduct14 97.8 97.815 97.8 98.816 100 10017 98.8 99.218 92.2 10019 100 10020 100 99.221 100 10022 92.2 10023 98.9 95.624 96.7 97.8none 44.4 38.9______________________________________
Example 3
Rice insect larvae at the third instar were incubated and used in an efficacy test on insecticides in triplicate runs by the dipping method (each lot having 10 larvae). The insecticidal ratio was determined in the same manner as the one employed for the determination of the acaricidal ratio. Marketed insecticides, namely, a Sumithion emulsion (content of the active ingredient, i.e., MEP: 50% by weight) and a Malathion (or Malathon) emulsion (content of the active ingredient, i.e., Malathion: 50% by weight) were each diluted 2,000-fold and used. As enhancers for agricultural chemicals, those employed in Example 1 were used in such a manner as to adjust their concentration in the diluted solution to 0.1% by weight. Table 3 shows the results.
TABLE 3______________________________________ Insecticidal ratio (%) Sumithion MalathionNo. of enhancer emulsion emulsion______________________________________Inventionproduct 1 100 90.0 2 100 93.3 3 93.3 100 4 90.0 96.7 5 90.0 98.7 6 100 100 7 100 96.7 8 100 96.7 9 100 100Comparativeproduct10 60.0 50.011 50.0 53.312 53.3 60.013 40.0 43.3Inventionproduct14 100 10015 93.3 96.716 93.3 93.317 100 10018 96.7 96.719 100 93.320 100 10021 93.3 93.322 93.3 10023 96.7 96.724 93.3 100control lot 40.0 50.0______________________________________
Examples 1, 2 and 3 show the tests wherein the efficacies of the enhancers for agricultural chemicals according to the present invention were compared with those of common cationic surfactants (comparative products) as enhancers for agricultural chemicals. As Tables 1 to 3 clearly indicate, the enhancers for agricultural chemicals of the present invention exerted remarkable effects and thus were usable on a practical level. In contrast, the comparative products somewhat enhanced the efficacies of the agricultural chemicals but were not effective on a practical level. Accordingly, it is observed that the enhancers for agricultural chemicals of the present invention would specifically enhance the efficacies of agricultural chemicals as compared with common cationic surfactants.
Example 4
The same test as the one effected in Example 1 was carried out by using a Roundup liquid formulation as a herbicide and the enhancers 1 and 14 listed in Example 1 each in a dose as specified in Table 4. Table 4 shows the results.
TABLE 4______________________________________ Herbicide/ Herbicide Enhancer enhancer HerbicidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 2000 200 1/0.1 82.3 2 1 2000 1000 1/0.5 97.5 3 2000 2000 1/1.0 99.1 4 2000 10000 1/5 99.2 5 2000 24000 1/12 99.1 6 2000 30000 1/15 99.3 7 2000 60000 1/30 99.1 8 2000 0 56.5 9 0 010 Enhancer 2000 200 1/0.1 78.511 14 2000 1000 1/0.5 88.512 2000 2000 1/1.0 92.613 2000 10000 1/5 96.014 2000 24000 1/12 99.215 2000 30000 1/15 99.116 2000 60000 1/30 99.317 2000 0 56.518 0 0______________________________________
Example 5
The same test as the one effected in Example 1 was carried out by using a Roundup liquid formulation as a herbicide and the enhancers 6 and 19 listed in Example 1 each in a dose as specified in Table 5. Table 5 shows the results.
TABLE 5______________________________________ Herbicide/ Herbicide Enhancer enhancer HerbicidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 2000 200 1/0.1 82.1 2 6 2000 1000 1/0.5 95.3 3 2000 2000 1/1.0 98.7 4 2000 10000 1/5 99.0 5 2000 24000 1/12.0 98.9 6 2000 60000 1/30 99.1 7 2000 80000 1/40 99.1 8 2000 0 56.5 9 0 010 Enhancer 2000 200 1/0.1 75.411 19 2000 1000 1/0.5 90.512 2000 2000 1/1.0 93.513 2000 10000 1/5 98.614 2000 24000 1/12.0 99.115 2000 60000 1/30 99.316 2000 80000 1/40 99.117 2000 0 56.518 0 0______________________________________
Example 6
The same test as the one effected in Example 1 was carried out by using a Roundup liquid formulation as a herbicide and the enhancers 2 and 15 listed in Example 1 each in a dose as specified in Table 6. Table 6 shows the results.
TABLE 6______________________________________ Herbicide/ Herbicide Enhancer enhancer HerbicidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 2000 200 1/0.1 81.8 2 2 2000 1000 1/0.5 95.4 3 2000 2000 1/1.0 99.1 4 2000 10000 1/5 98.9 5 2000 24000 1/12 99.1 6 2000 30000 1/15 99.2 7 2000 80000 1/40 99.1 8 2000 0 56.5 9 0 010 Enhancer 2000 200 1/0.1 85.211 15 2000 1000 1/0.5 96.512 2000 2000 1/1.0 99.413 2000 10000 1/5 99.214 2000 24000 1/12 98.715 2000 30000 1/15 99.316 2000 80000 1/40 99.217 2000 0 56.518 0 0______________________________________
Example 7
The same test as the one effected in Example 3 was carried out by using a Sumithion emulsion as an insecticide and the enhancers 1 and 14 listed in Example 1 each in a dose as specified in Table 7. Table 7 shows the results.
TABLE 7______________________________________ Insecticide Enhancer Insecticide/ InsecticidalTest content content enhancer rationo Enhancer (ppm) (ppm) weight ratio (%)______________________________________ 1 Enhancer 250 25 1/0.1 83.3 2 1 250 125 1/0.5 93.3 3 250 250 1/1.0 100 4 250 500 1/2.0 100 5 250 1000 1/4.0 100 6 250 2500 1/10 100 7 250 5000 1/20 100 8 250 0 46.7 9 0 010 Enhancer 250 25 1/0.1 83.311 14 250 125 1/0.5 90.012 250 250 1/1.0 10013 250 500 1/2.0 10014 250 1000 1/4.0 10015 250 2500 1/10 10016 250 5000 1/20 10017 250 0 46.718 0 0______________________________________
Example 8
The same test as the one effected in Example 2 was carried out by using an Osadan wettable powder as an acaricide and. the enhancers 5 and 18 listed in Example 1 each in a dose as specified in Table 8. Table 8 shows the results.
TABLE 8______________________________________ Acaricide/ Acaricide Enhancer enhancer AcaricidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 100 10 1/0.1 77.8 2 5 100 50 1/0.5 91.1 3 100 100 1/1.0 100 4 100 200 1/2.0 100 5 100 1000 1/10 100 6 100 1500 1/15 100 7 100 2000 1/20 100 8 100 0 52.3 9 0 0 2.210 Enhancer 100 10 1/0.1 77.811 18 100 50 1/0.5 91.112 100 100 1/1.0 10013 100 200 1/2.0 10014 100 1000 1/10 10015 100 1500 1/15 10016 100 2000 1/20 10017 100 0 52.318 0 0 2.2______________________________________
Example 9
The same test as the one effected in Example 2 was carried out by using an Osadan wettable powder as an acaricide and the enhancers 7 and 20 listed in Example 1 each in a dose as specified in Table 9. Table 9 shows the results.
TABLE 9______________________________________ Acaricide/ Acaricide Enhancer enhancer AcaricidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 100 10 1/0.1 72.2 2 7 100 50 1/0.5 91.1 3 100 100 1/1.0 100 4 100 200 1/2.0 100 5 100 1000 1/10 100 6 100 1500 1/15 100 7 100 2000 1/20 100 8 100 0 52.3 9 0 0 2.210 Enhancer 100 10 1/0.1 77.811 20 100 50 1/0.5 94.412 100 200 1/2.0 10013 100 1000 1/10 10014 100 0 52.315 0 0 2.2______________________________________
Example 10
The same test as the one effected in Example 1 was carried out by using a Roundup liquid formulation as a herbicide and the enhancers 23 and 24 listed in Example 1 each in a dose as specified in Table 10. Table 10 shows the results.
TABLE 10______________________________________ Herbicide/ Herbicide Enhancer enhancer HerbicidalTest content content weight rationo. Enhancer (ppm) (ppm) (ppm) (%)______________________________________ 1 Enhancer 2000 200 1/0.1 85.6 2 23 2000 1000 1/0.5 91.2 3 2000 2000 1/1.0 98.5 4 2000 10000 1/5 99.1 5 2000 24000 1/12 98.3 6 2000 30000 1/15 98.4 7 2000 60000 1/30 99.0 8 2000 0 56.5 9 0 010 Enhancer 2000 200 1/0.1 82.311 24 2000 1000 1/0.5 88.712 2000 2000 1/1.0 96.813 2000 10000 1/5 97.214 2000 24000 1/12 98.315 2000 30000 1/15 97.716 2000 60000 1/30 98.917 2000 0 56.518 0 0______________________________________
Example 11
The same test as the one effected in Example 2 was carried out by using an Osadan wettable powder as an acaricide and the enhancers 23 and 24 listed in Example 1 each in a dose as specified in Table 11. Table 11 shows the results.
TABLE 11______________________________________ Acaricide/ Acaricide Enhancer enhancer AcaricidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 100 10 1/0.1 90.0 2 23 100 50 1/0.5 92.2 3 100 100 1/1.0 100 4 100 200 1/2.0 100 5 100 1000 1/10 100 6 100 1500 1/15 100 7 100 2000 1/20 100 8 100 0 52.3 9 0 0 2.210 Enhancer 100 10 1/0.1 86.711 24 100 50 1/0.5 92.212 100 100 1/1.0 10013 100 200 1/2.0 10014 100 1000 1/10 10015 100 1500 1/15 10016 100 2000 1/20 10017 100 0 52.318 0 0 2.2______________________________________
Production Example 2
An autoclave provided with a stirrer, a thermometer, a pressure gauge and a pressure dropping funnel was charged with 250 g of N-methyloctadecylamine and heated to 160.degree. C. Then 45 g of ethylene oxide was occasionally added dropwise thereto under a pressure of 0 to 6 kg/cm.sup.2 G. Three hours were required for completing the addition. Next, the resulting mixture was aged, i.e., maintained, at 160.degree. C. for 2 hours and then cooled. The reaction mixture was taken out and distilled to thereby give 250 g of N-(2-hydroxyethyl)-N-methyloctadecylamine. This product had a boiling point of 185.degree. to 190.degree. C./0.2 mmHg.
A four-neck flask provided with a stirrer, a thermometer and a dehydrating tube was charged with 200 g of the N-(2-hydroxyethyl)-N-methyloctadecylamine and 174 g of octadecanoic acid. The mixture was heated to 180.degree. C. and maintained at this temperature for 12 hours while distilling off the water thus formed. Thus 350 g of N-(2-octadecanoyloxyethyl)-N-methyloctadecylamine was obtained. Based on the NMR and IR spectra, it was confirmed that this product had the following structure. This compound will be referred to as the enhancer 25 hereinafter. ##STR31##
Example 12
The same test as the one effected in Example 1 was carried out, except that the enhancer 25 prepared in Production Example 2 and, the following enhancers 26 to 46 were used to prepare agricultural chemical compositions. Table 12 summarizes the results.
Enhancer 26; enhancer 25/Emulgen 909 �POE(9) nonylphenol ether!=80/20.
Enhancer 27; enhancer 25/Emulgen 103 �POE(3) C.sub.12 H.sub.25 OH!=80/20.
Enhancer 28; enhancer 25/Emanon 4110 �POE(10) C.sub.17 H.sub.35 COOH!=80/20.
Enhancer 29; enhancer 25/Rheodol TWL-120 �POE(20) C.sub.11 H.sub.23 COO sorbitan ester!=80/20.
Enhancer 30; a compound represented by the following formula was used: ##STR32## Enhancer 31; enhancer 30/Emulgen 703 �a mixture of POE(3) C.sub.12 H.sub.25 OH and POE(3) C.sub.13 H.sub.27 OH!=75/25.
Enhancer 32; enhancer 30/Emanon 1112 �POE(12) C.sub.11 H.sub.23 COOH!=75/25.
Enhancer 33; enhancer 30/Rheodol TWO-120 �POE(20) C.sub.17 H.sub.33 COO sorbitan ester!=75/25.
Enhancer 34; didecyldimethylammonium chloride.
Enhancer 35; monolauryltrimethylammonium chloride.
Enhancer 36; dilauryldihydroxyethylammonium chloride.
Enhancer 37; trimethylcocoammonium chloride.
Enhancer 38; a compound represented by the following formula was used: ##STR33## Enhancer 39; enhancer 38/Emulgen 909=80/20. Enhancer 40; enhancer 38/Emulgen 103=80/20.
Enhancer 41; enhancer 38/Emanon 4110=80/20.
Enhancer 42; enhancer 38/Rheodol TWO-120=80/20.
Enhancer 43; a compound represented by the following formula was used: ##STR34## Enhancer 44; enhancer 43/Emulgen 703=75/25. Enhancer 45; enhancer 43/Emanon 1112=75/25.
Enhancer 46; enhancer 43/Rheodol TWO-120=75/25.
The express on "POE" as used herein is an abbreviation of "polyoxyethylene" and each value given in the parentheses is an average addition mole number of oxyethylene. In the above-described enhancers, the composition ratio is by weight.
TABLE 12______________________________________ Herbicidal ratio (%) Karmex Herbiace RoundupNo. of wettable water-soluble liquidenhancer powder powder formulation______________________________________Inventionproduct25 98.0 98.9 99.226 98.0 98.9 99.127 99.3 99.0 99.128 99.4 99.2 97.529 99.4 99.1 99.330 98.9 98.9 99.031 99.3 99.3 97.832 99.1 99.3 99.033 99.0 99.1 99.1Comparativeproduct34 63.5 70.0 73.535 44.5 72.2 76.136 60.3 70.1 71.137 50.3 65.8 75.3Inventionproduct38 98.5 98.7 99.239 98.5 99.3 99.140 98.5 99.4 98.741 96.7 99.5 98.342 98.5 98.3 98.543 99.3 98.3 99.444 99.2 98.5 99.345 99.0 99.0 99.346 99.4 99.1 99.0none 18.4 67.5 68.5______________________________________
Example 18
The same test as the one effected in Example 2 was carried out, except that the enhancers 25 to 46, which were employed in Example 12, were used to prepare agricultural chemical compositions. Table 13 shows the results.
TABLE 13______________________________________ Acaricidal ratio (%) OsadanNo. of Nissorun V wettableenhancer emulsion powder______________________________________Inventionproduct25 98.8 98.826 97.8 97.827 100 97.828 100 98.829 100 10030 98.8 10031 98.8 10032 98.8 99.233 98.8 100Comparativeproduct34 50.0 52.235 50.0 46.536 48.9 52.237 50.0 74.4Inventionproduct38 97.8 97.839 97.8 98.840 97.8 97.841 100 10042 98.8 10043 92.2 92.244 100 92.245 100 10046 100 100none 44.4 38.9______________________________________
Example 14
The same test as the one effected in Example 3 was carried out, except that the enhancers 25 to 46, which were employed in Example 12, were used to prepare agricultural chemical compositions. Table 14 shows the results.
TABLE 14______________________________________ Insecticidal ratio (%) Sumithion MalathionNo. of enhancer emulsion emulsion______________________________________Inventionproduct25 90.0 10026 90.0 10027 93.3 93.328 93.3 90.029 100 10030 100 93.331 93.3 10032 100 96.733 93.3 96.7Comparativeproduct34 60.0 50.035 50.0 53.336 60.0 53.337 43.3 40.0Inventionproduct38 100 96.739 93.3 93.340 96.7 10041 100 10042 96.7 10043 96.7 96.744 100 96.745 100 93.346 93.3 93.3control lot 40.0 50.0______________________________________
Examples 12, 13 and 14 show the tests wherein the efficacies of the enhancers for agricultural chemicals according to the present invention were compared with those of common cationic surfactants (comparative products) as enhancers for agricultural chemicals. As Tables 12 to 14 clearly indicate, the enhancers for agricultural chemicals of the present invention exerted remarkable effects and thus were usable on a practical level. In contrast, the comparative products somewhat enhanced the efficacies of the agricultural chemicals but were not effective on a practical level. Accordingly, it is observed that the enhancers for agricultural chemicals of the present invention would specifically enhance the efficacies of agricultural chemicals as compared with common cationic surfactants.
Example 15
The same test as the one effected in Example 12 was carried out by using a Roundup liquid formulation as a herbicide and the enhancers 25 and 38 listed in Example 12 each in a dose as specified in Table 15. Table 15 shows the results.
TABLE 15______________________________________ Herbicide/ Herbicide Enhancer enhancer HerbicidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 2000 200 1/0.1 82.3 2 25 2000 1000 1/0.5 95.6 3 2000 2000 1/1.0 97.8 4 2000 10000 1/5 99.0 5 2000 24000 1/12 98.7 6 2000 30000 1/15 99.1 7 2000 60000 1/30 99.0 8 2000 0 56.5 9 0 0 010 Enhancer 2000 200 1/0.1 78.511 38 2000 1000 1/0.5 90.212 2000 2000 1/1.0 95.613 2000 10000 1/5 98.814 2000 24000 1/12 99.115 2000 30000 1/15 99.016 2000 60000 1/30 99.117 2000 0 56.518 0 0 0______________________________________
Example 16
The same test as the one effected in Example 12 was carried out by using a Roundup liquid formulation as a herbicide and the enhancers 30 and 43 listed in Example 12 each in a dose as specified in Table 16. Table 16 shows the results.
TABLE 16______________________________________ Herbicide/ Herbicide Enhancer enhancer HerbicidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 2000 200 1/0.1 75.6 2 30 2000 1000 1/0.5 88.4 3 2000 2000 1/1.0 93.8 4 2000 10000 1/5 97.7 5 2000 24000 1/12.0 99.1 6 2000 60000 1/30 99.3 7 2000 80000 1/40 99.2 8 2000 0 56.5 9 0 0 010 Enhancer 2000 200 1/0.1 78.511 43 2000 1000 1/0.5 93.412 2000 2000 1/1.0 99.113 2000 10000 1/5 98.914 2000 24000 1/12.0 99.215 2000 60000 1/30 99.116 2000 80000 1/40 98.117 2000 0 56.518 0 0 0______________________________________
Example 17
The same test as the one effected in Example 12 was carried out by using a Roundup liquid formulation as a herbicide and the enhancers 26 and 39 listed in Example 12 each in a dose as specified in Table 17. Table 17 shows the results.
TABLE 17______________________________________ Herbicide/ Herbicide Enhancer enhancer HerbicidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 2000 200 1/0.1 81.5 2 26 2000 1000 1/0.5 94.3 3 2000 2000 1/1.0 98.2 4 2000 10000 1/5 98.9 5 2000 24000 1/12 99.2 6 2000 30000 1/15 99.0 7 2000 80000 1/40 99.1 8 2000 0 56.5 9 0 0 010 Enhancer 2000 200 1/0.1 83.211 39 2000 1000 1/0.5 95.512 2000 2000 1/1.0 99.113 2000 10000 1/5 99.014 2000 24000 1/12 89.915 2000 30000 1/15 99.016 2000 80000 1/40 99.117 2000 0 56.518 0 0 0______________________________________
Example 18
The same test as the one effected in Example 14 was carried out by using a Sumithion emulsion as an insecticide and the enhancers 25 and 38 listed in Example 12 each in a dose as specified in Table 18. Table 18 shows the results.
TABLE 18______________________________________ Insecticide Enhancer Insecticide/ InsecticidalTest content content enhancer rationo. Enhancer (ppm) (ppm) weight ratio (%)______________________________________ 1 Enhancer 250 25 1/0.1 83.3 2 25 250 125 1/0.5 93.3 3 250 250 1/1.0 93.3 4 250 500 1/2.0 100 5 250 1000 1/4.0 100 6 250 2500 1/10 100 7 250 5000 1/20 100 8 250 0 46.7 9 0 0 010 Enhancer 250 25 1/0.1 83.311 38 250 125 1/0.5 93.312 250 250 1/1.0 10013 250 500 1/2.0 10014 250 1000 1/4.0 10015 250 2500 1/10 10016 250 5000 1/20 10017 250 0 46.718 0 0 0______________________________________
Example 19
The same test as the one effected in Example 13 was carried out by using an Osadan wettable powder as an acaricide and the enhancers 29 and 42 listed in Example 12 each in a dose as specified in Table 19. Table 19 shows the results.
TABLE 19______________________________________ Acaricide/ Acaricide Enhancer enhancer AcaricidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 100 10 1/0.1 77.8 2 29 100 50 1/0.5 91.1 3 100 100 1/1.0 91.1 4 100 200 1/2.0 100 5 100 1000 1/10 100 6 100 1500 1/15 100 7 100 2000 1/20 100 8 100 0 52.3 9 0 0 2.210 Enhancer 100 10 1/0.1 77.811 42 100 50 1/0.5 94.412 100 100 1/1.0 94.413 100 200 1/2.0 10014 100 1000 1/10 10015 100 1500 1/15 10016 100 2000 1/20 10017 100 0 52.318 0 0 2.2______________________________________
Example 20
The same test as the one effected in Example 13 was carried out by using an Osadan wettable powder as an acaricide and the enhancers 31 and 44 listed in Example 12 each in a dose as specified in Table 20. Table 20 shows the results.
TABLE 20______________________________________ Acaricide/ Acaricide Enhancer enhancer AcaricidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 100 10 1/0.1 66.7 2 31 100 50 1/0.5 83.3 3 100 100 1/1.0 97.8 4 100 200 1/2.0 100 5 100 1000 1/10 100 6 100 1500 1/15 100 7 100 2000 1/20 100 8 100 0 52.3 9 0 0 010 Enhancer 100 10 1/0.1 75.611 44 100 50 1/0.5 88.912 100 200 1/2.0 94.413 100 1000 1/10 10014 100 0 52.315 0 0 0______________________________________
Production Example 3
A four-neck flask provided with a stirrer, a thermometer and a dehydrating tube was charged with 66 g of N-(2-hydroxyethyl)-N-methyl-1,3-propylenediamine, which had been synthesized from an adduct of N-methylethanolamine with acrylonitrile in accordance with a known method �see J. Org. Chem., 26, 3409 (1960)!, and 284 g of stearic acid. The mixture was heated to 180.degree. C. and maintained at this temperature for about 10 hours while distilling off the water thus formed. Then 300 g of the product thus obtained was dissolved in 60 g of isopropyl alcohol and fed into an autoclave provided with a stirrer, a thermometer and a pressure gauge. After injecting 28 g of methyl chloride thereinto, the mixture was reacted at 100.degree. C. for about 8 hours. After distilling off the isopropyl alcohol under reduced pressure, 320 g of the target compound was obtained. Based on the NMR and IR spectra, it was confirmed that this product had the following chemical structure. This compound will be referred to as the enhancer 47 hereinafter. ##STR35##
Example 21
The same test as the one effected in Example 1 was carried out, except that the enhancer 47 obtained in Production Example 3 and, the following enhancers 48 to 74 were used to prepare agricultural chemical compositions. Table 21 summarizes the results.
Enhancer 48; enhancer 47/Emulgen 909 �POE(9) nonyl phenol ether!=80/20.
Enhancer 49; enhancer 47/Emulgen 103 �POE(3) C.sub.12 H25OH!=80/20.
Enhancer 50; enhancer 47/Emanon 4110 �POE(10) C.sub.17 H.sub.35 COO H!=80/20.
Enhancer 51; enhancer 47/Rheodol TWL-120 �POE(20) C.sub.11 H.sub.23 COO sorbitan ester!=80/20 .
Enhancer 52; a compound represented by the following formula was used: ##STR36## Enhancer 53; enhancer 52/Emulgen 703 �a mixture of POE(3) C.sub.12 H.sub.25 OH and POE(3) C.sub.13 H.sub.27 OH!=75/25.
Enhancer 54; enhancer 52/Emanon 1112 �POE(12) C.sub.11 H.sub.23 COOH!=75/25.
Enhancer 55; enhancer 52/Rheodol TWO-120 �POE(20) C.sub.17 H.sub.33 COO sorbitan ester!=75/25.
Enhancer 56; didecyldimethylammonium chloride.
Enhancer 57; monolauryltrimethylammonium chloride.
Enhancer 58; dilauryldihydroxyethylammonium chloride.
Enhancer 59; trimethylcocoammonium chloride.
Enhancer 60; a compound represented by the following formula was used: ##STR37## Enhancer 61; enhancer 80/Emulgen 909=80/20. Enhancer 62;enhancer 80/Emulgen 103=80/20.
Enhancer 63;enhancer 80/Emanon 4110=80/20.
Enhancer 64; enhancer 60/Rheodol TWO-120=80/20.
Enhancer 65; a compound represented by the following formula was used: ##STR38## Enhancer 66; enhancer 65/Emulgen 703=75/25. Enhancer 67; enhancer 65/Emanon 1112=75/25.
Enhancer 68; enhancer 65/Rheodol TWO-120=75/25.
Enhancer 69; a compound represented by the following formula was used: ##STR39## Enhancer 70; enhancer 69/Emulgen 707 �POE(7) sec-C.sub.12,C.sub.13 ether!=75/25.
Enhancer 71; enhancer 69/Rheodol TWO-120=75/25.
Enhancer 72; a compound represented by the following formula was used: ##STR40## Enhancer 73; enhancer 72/Emulgen 909=80/20. Enhancer 74; enhancer 72/Rheodol TWO-120=80/20.
The expression "POE" as used herein is an abbreviation of "polyoxyethylene" and each value given in the parentheses is an average addition mole number of oxyethylene. In enhancer compositions, the composition ratio is by weight.
TABLE 21______________________________________ Herbicidal ratio (%) Karmex Herbiace RoundupNo. of wettable water-soluble liquidenhancer powder powder formulation______________________________________Inventionproduct47 97.8 97.6 99.148 97.5 99.1 99.049 99.1 99.1 99.050 99.2 98.5 97.551 99.0 98.5 98.952 99.0 98.9 99.153 98.5 99.1 99.154 98.9 98.6 98.755 99.1 99.2 99.3Comparativeproduct56 63.5 70.0 69.557 44.5 72.2 70.058 60.3 70.1 71.159 50.3 67.8 70.5Inventionproduct60 99.3 98.7 98.761 98.5 99.3 98.761 98.5 99.1 99.063 98.9 99.0 99.064 98.9 98.7 98.865 99.3 98.3 98.866 99.2 98.5 98.867 99.4 98.2 99.368 98.9 98.5 99.269 99.7 99.5 99.370 99.1 99.2 99.071 99.2 99.1 99.172 98.2 97.3 98.973 99.1 97.8 99.274 97.6 98.5 97.9none 18.4 67.5 68.5______________________________________
Example 22
The same test as the one effected in Example 2 was carried out, except that the enhancers 47 to 74, which were employed in Example 21, were used to prepare agricultural chemical compositions. Table 22 shows the results.
TABLE 22______________________________________ Acaricidal ratio (%) Osadan No. of Nissorun V wettable enhancer emulsion powder______________________________________Invention 47 98.8 100product 48 97.8 100 49 98.8 100 50 100 98.8 51 100 98.8 52 100 98.8 53 100 97.8 54 100 99.2 55 97.8 100Comparative 56 50.0 52.2product 57 50.0 46.5 58 48.9 52.2 59 50.0 74.4Invention 60 97.8 97.8product 61 97.8 98.8 62 98.8 100 63 100 100 64 100 100 65 100 100 66 100 97.8 67 100 98.8 68 100 97.8 69 100 98.9 70 99.4 100 71 100 100 72 96.7 97.8 73 100 96.7 74 93.3 95.6none 44.4 38.9______________________________________
Example 23
The same test as the one effected in Example 3 was carried out, except that the enhancers 47 to 74, which were employed in Example 21, were used to prepare agricultural chemical compositions. Table 23 shows the results.
TABLE 23______________________________________ Insecticidal ratio (%) No. of Sumithion Malathion enhancer emulsion emulsion______________________________________Invention 47 90.0 90.0product 48 100 100 49 93.3 93.3 50 93.3 96.7 51 93.3 96.7 52 90.0 90.0 53 100 100 54 100 100 55 100 100Comparative 56 60.0 50.0product 57 50.0 53.3 58 53.3 60.0 59 40.0 43.3Invention 60 100 100product 61 93.3 100 62 93.3 96.7 63 96.7 93.3 64 100 100 65 100 96.7 66 100 100 67 93.3 100 68 93.3 93.3 69 95.5 97.8 70 100 100 71 100 100 72 93.3 100 73 100 96.7 74 93.3 93.3control lot 40.0 50.0______________________________________
Examples 21, 22 and 23 show the tests wherein the efficacies of the enhancers for agricultural chemicals according to the present invention were compared with those of common cationic surfactants (comparative products) as enhancers for agricultural chemicals. As Tables 21 to 23 clearly indicate, the enhancers for agricultural chemicals of the present invention exerted remarkable effects and thus were usable on a practical level. In contrast, the comparative products somewhat enhanced the efficacies of the agricultural chemicals but were not effective on a practical level. Accordingly, it is observed that the enhancers for agricultural chemicals of the present invention would specifically enhance the efficacies of agricultural chemicals as compared with common cationic surfactants.
Example 24
The same test as the one effected in Example 21 was carried out by using a Roundup liquid formulation as a herbicide and the enhancers 47 and 60 listed in Example 21 each in a dose as specified in Table 24. Table 24 shows the results.
TABLE 24______________________________________ Herbicide/ Herbicide Enhancer enhancer HerbicidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________1 Enhancer 2000 200 1/0.1 82.32 47 2000 1000 1/0.5 95.53 2000 2000 1/1.0 97.84 2000 10000 1/5 98.95 2000 24000 1/12 99.36 2000 30000 1/15 99.07 2000 60000 1/30 99.18 2000 0 50.69 0 0 010 Enhancer 2000 200 1/0.1 85.511 60 2000 1000 1/0.5 98.512 2000 2000 1/1.0 98.913 2000 10000 1/5 98.714 2000 24000 1/12 99.315 2000 30000 1/15 99.116 2000 60000 1/30 98.817 0 0 0______________________________________
Example 25
The same test as the one effected in Example 21 was carried out by using a Roundup liquid formulation as a herbicide and the enhancers 52 and 65 listed in Example 21 each in a dose as specified in Table 25. Table 25 shows the results.
TABLE 25______________________________________ Herbicide/ Herbicide Enhancer enhancer HerbicidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 2000 200 1/0.1 74.5 2 52 2000 1000 1/0.5 90.0 3 2000 2000 1/1.0 99.0 4 2000 10000 1/5 98.1 5 2000 24000 1/12.0 99.3 6 2000 60000 1/30 99.2 7 2000 80000 1/40 99.1 8 2000 0 56.5 9 0 0 010 Enhancer 2000 200 1/0.1 83.511 65 2000 1000 1/0.5 95.612 2000 2000 1/1.0 99.313 2000 10000 1/5 99.014 2000 24000 1/12.0 99.015 2000 60000 1/30 98.916 2000 80000 1/40 99.217 2000 0 56.518 0 0 0______________________________________
Example 26
The same test as the one effected in Example 21 was carried out by using a Roundup liquid formulation as a herbicide and the enhancers 48 and 61 listed in Example 21 each in a dose as specified in Table 26. Table 26 shows the results.
TABLE 26______________________________________ Herbicide/ Herbicide Enhancer enhancer HerbicidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 2000 200 1/0.1 78.6 2 48 2000 1000 1/0.5 94.5 3 2000 2000 1/1.0 98.0 4 2000 10000 1/5 99.1 5 2000 24000 1/12 99.0 6 2000 30000 1/15 99.3 7 2000 80000 1/40 99.1 8 2000 0 56.5 9 0 0 010 Enhancer 2000 200 1/0.1 83.211 61 2000 1000 1/0.5 95.112 2000 2000 1/1.0 99.313 2000 10000 1/5 99.014 2000 24000 1/12 99.115 2000 30000 1/15 99.216 2000 80000 1/40 98.817 2000 0 56.518 0 0 0______________________________________
Example 27
The same test as the one effected in Example 23 was carried out by using a Sumithion emulsion as an insecticide and the enhancers 47 and 60 listed in Example 21 each in a dose as specified in Table 27. Table 27 shows the results.
TABLE 27______________________________________ Insecti- Insecticide/ Insecti- cide Enhancer enhancer cidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 250 25 1/0.1 83.3 2 47 250 125 1/0.5 93.3 3 250 250 1/1.0 100 4 250 500 1/2.0 100 5 250 1000 1/4.0 100 6 250 2500 1/10 100 7 250 5000 1/20 100 8 250 0 53.3 9 0 0 010 Enhancer 250 25 1/0.1 80.011 60 250 125 1/0.5 90.012 250 250 1/1.0 10013 250 500 1/2.0 10014 250 1000 1/4.0 10015 250 2500 1/10 10016 250 5000 1/20 10017 250 0 53.318 0 0 0______________________________________
Example 28
The same test as the one effected in Example 22 was carried out by using an Osadan wettable powder as an acaricide and the enhancers 51 and 64 listed in Example 21 each in a dose as specified in Table 28. Table 28 shows the results.
TABLE 28______________________________________ Acaricide/ Acaricide Enhancer enhancer AcaricidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 100 10 1/0.1 83.3 2 51 100 50 1/0.5 91.1 3 100 100 1/1.0 100 4 100 200 1/2.0 100 5 100 1000 1/10 100 6 100 1500 1/15 100 7 100 2000 1/20 100 8 100 0 52.3 9 0 0 2.210 Enhancer 100 10 1/0.1 77.811 64 100 50 1/0.5 88.912 100 100 1/1.0 94.413 100 200 1/2.0 10014 100 1000 1/10 10015 100 1500 1/15 10016 100 2000 1/20 10017 100 0 52.318 0 0 2.2______________________________________
Example 29
The same test as the one effected in Example 22 was carried out by using an Osadan wettable powder as an acaricide and the enhancers 53 and 66 listed in Example 21 each in a dose as specified in Table 29. Table 29 shows the results.
TABLE 29______________________________________ Acaricide/ Acaricide Enhancer enhancer AcaricidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________1 Enhancer 100 10 1/0.1 68.92 53 100 50 1/0.5 83.33 100 100 1/1.0 94.44 100 200 1/2.0 1005 100 1000 1/10 1006 100 1500 1/15 1007 100 2000 1/20 1008 100 0 52.39 0 0 2.210 Enhancer 100 10 1/0.1 72.211 66 100 50 1/0.5 83.312 100 200 1/2.0 10013 100 1000 1/10 10014 100 0 52.315 0 0 2.2______________________________________
Example 30
The same test as the one effected in Example 21 was carried out by using a Roundup liquid formulation as a herbicide and the enhancers 69 and 71 listed in Example 21 each in a dose as specified in Table 30. Table 30 shows the results.
TABLE 30______________________________________ Herbicide/ Herbicide Enhancer enhancer HerbicidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________1 Enhancer 2000 200 1/0.1 88.22 69 2000 1000 1/0.5 95.63 2000 2000 1/1.0 99.34 2000 10000 1/5 99.25 2000 24000 1/12 99.26 2000 30000 1/15 99.37 2000 60000 1/30 99.08 2000 0 56.59 0 0 010 Enhancer 2000 200 1/0.1 90.411 71 2000 1000 1/0.5 97.612 2000 2000 1/1.0 98.513 2000 10000 1/5 99.214 2000 24000 1/12 99.015 2000 30000 1/15 98.916 2000 60000 1/30 99.017 0 0 0______________________________________
Example 31
The same test as the one effected in Example 21 was carried out by using a Roundup liquid formulation as a herbicide and the enhancers 72 and 73 listed in Example 21 each in a dose as specified in Table 31. Table 31 shows the results.
TABLE 31______________________________________ Herbicide/ Herbicide Enhancer enhancer HerbicidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________1 Enhancer 2000 200 1/0.1 87.62 72 2000 1000 1/0.5 89.23 2000 2000 1/1.0 99.14 2000 10000 1/5 98.65 2000 24000 1/12 98.86 2000 30000 1/15 97.57 2000 60000 1/30 97.98 2000 0 56.59 0 0 010 Enhancer 2000 200 1/0.1 85.611 73 2000 1000 1/0.5 88.312 2000 2000 1/1.0 97.613 2000 10000 1/5 98.614 2000 24000 1/12 99.015 2000 30000 1/15 98.216 2000 60000 1/30 98.817 0 0 0______________________________________
Example 32
The same test as the one effected in Example 22 was carried out by using an Osadan wettable powder as an acaricide and the enhancers 69 and 70 listed in Example 21 each in a dose as specified in Table 32. Table 32 shows the results.
TABLE 32______________________________________ Acaricide/ Acaricide Enhancer enhancer AcaricidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________1 Enhancer 100 10 1/0.1 85.32 69 100 50 1/0.5 92.43 100 100 1/1.0 1004 100 200 1/2.0 1005 100 1000 1/10 1006 100 1500 1/15 1007 100 2000 1/20 1008 100 0 52.39 0 0 2.210 Enhancer 100 10 1/0.1 80.611 70 100 50 1/0.5 89.912 100 100 1/1.0 95.513 100 200 1/2.0 10014 100 1000 1/10 10015 100 1500 1/15 10016 100 2000 1/20 10017 100 0 52.318 0 0 2.2______________________________________
Example 33
The same test as the one effected in Example 22 was carried out by using an Osadan wettable powder as an acaricide and the enhancers 72 and 73 listed in Example 21 each in a dose as specified in Table 33. Table 33 shows the results.
TABLE 33______________________________________ Acaricide/ Acaricide Enhancer enhancer AcaricidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________1 Enhancer 100 10 1/0.1 93.32 72 100 50 1/0.5 97.83 100 100 1/1.0 1004 100 200 1/2.0 1005 100 1000 1/10 1006 100 1500 1/15 1007 100 2000 1/20 1008 100 0 52.39 0 0 2.210 Enhancer 100 10 1/0.1 92.211 73 100 50 1/0.5 96.712 100 100 1/1.0 98.913 100 200 1/2.0 10014 100 1000 1/10 10015 100 1500 1/15 10016 100 2000 1/20 10017 100 0 52.318 0 0 2.2______________________________________
Example 34
The same test as the one effected in Example 23 was carried out by using a Sumithion emulsion as an insecticide and the enhancers 69 and 71 listed in Example 21 each in a dose as specified in Table 34. Table 34 shows the results.
TABLE 34______________________________________ Insecti- Insecticide/ Insecti- cide Enhancer enhancer cidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 250 25 1/0.1 82.5 2 69 250 125 1/0.5 96.1 3 250 250 1/1.0 100 4 250 500 1/2.0 100 5 250 1000 1/4.0 100 6 250 2500 1/10 100 7 250 5000 1/20 100 8 250 0 53.3 9 0 0 010 Enhancer 250 25 1/0.1 89.211 71 250 125 1/0.5 98.012 250 250 1/1.0 10013 250 500 1/2.0 10014 250 1000 1/4.0 10015 250 2500 1/10 10016 250 5000 1/20 10017 250 0 53.318 0 0 0______________________________________
Example 35
The same test as the one effected in Example 23 was carried out by using a Sumithion emulsion as an insecticide and the enhancers 72 and 78 listed in Example 21 each in a dose as specified in Table 35. Table 35 shows the results.
TABLE 35______________________________________ Insecti- Insecticide/ Insecti- cide Enhancer enhancer cidalTest content content weight rationo. Enhancer (ppm) (ppm) ratio (%)______________________________________ 1 Enhancer 250 25 1/0.1 86.7 2 72 250 125 1/0.5 93.3 3 250 250 1/1.0 100 4 250 500 1/2.0 100 5 250 1000 1/4.0 100 6 250 2500 1/10 100 7 250 5000 1/20 100 8 250 0 53.3 9 0 0 010 Enhancer 250 25 1/0.1 90.011 73 250 125 1/0.5 93.312 250 250 1/1.0 10013 250 500 1/2.0 10014 250 1000 1/4.0 10015 250 2500 1/10 10016 250 5000 1/20 10017 250 0 53.318 0 0 0______________________________________
The invention being thus described, it will be obvious that the same may be varied in many ways. Such variations are not to be regarded as a departure from the spirit and scope of the invention, and all such modifications as would be obvious to one skilled in the art are intended to be included within the scope of the following claims.

Number	Date	Country
4-303978	Nov 1992	JPX
4-303979	Nov 1992	JPX
4-303980	Nov 1992	JPX

Number	Name	Date	Kind
4228042	Letton	Oct 1980
4888049	Iwasaki et al.	Dec 1989

Number	Date	Country
0453086	Oct 1991	EPX
0509346	Oct 1992	EPX
2600494	Dec 1987	FRX
4105536	Aug 1992	DEX
428745	Jan 1992	JPX

Agricultural chemical composition

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

US Classifications

Field of Search

US

International Classifications

Abstract

Description

Claims

Priority Claims (3)

Parent Case Info

US Referenced Citations (2)

Foreign Referenced Citations (5)

Divisions (1)