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Publication numberUS2572946 A
Publication typeGrant
Publication dateOct 30, 1951
Filing dateNov 19, 1949
Priority dateNov 19, 1949
Publication numberUS 2572946 A, US 2572946A, US-A-2572946, US2572946 A, US2572946A
InventorsPaulshock Marvin
Original AssigneeDu Pont
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Composition comprising 2-aliphatic-3-hydroxy-1, 4 napthoquinone and method for controlling mites and aphids
US 2572946 A
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Description  (OCR text may contain errors)

Patented Oct. 30, 1951 COMPOSITION COMPRISING Z-ALIPHATIC- 3-HYDROXY- 1,4 NAPTHOQUINONE AND METHOD FOR CONTROLLING MITES AND APHIDS Marvin Paulshock, Wilmington, Del., assignor to E. I. du Pont de Nemours and Company, Wilmington, Del., a corporation of Delaware No Drawing. Application November 19, 1949, Serial No. 128,491

Claims. 1

This invention relates to insecticidal compositions and more especially to compositions adapted for the control of mites and aphids. The compositions of the invention employ as an essential active ingredient a compound represented by the formula where R is a radical, containing from 6 thru 15 carbon atoms, selected from the group con sisting of alkyl, cyclohexyl, and cyclohexylalkyl; and the salts of said compounds. These compounds will be referred to hereafter more briefly as 2-aliphatic-3-hydroxy-1,4-naphthoquinones, it being understood that the term aliphatic so used is intended to include not only alkyl radicals, but also cyclohexyl, and cyclohexylalkyl radicals.

It is an object of this invention to provide compositions and methods for the control of insects and particularly for the control of mites and aphids. It is a further object to provide solutions, water-dispersible liquids, dusts and water-dispersible powders which are effective in killing mites and aphids in all stages of their development. A still further object is to provide compositions which may be used for protecting growing plants against mite and aphid nfestation without injuring the plants. Still other objects will become apparent hereinafter.

The foregoing and other objects of the invention are attained by means of compositions containing a 2-aliphatic-3-hydroxy-1,4-naphthoquinone responding to the formula and definition set out above in admixture with an adjuvant having dispersing properties. The compositions of the invention are characterized by the admixture of a dispersing agent with a 2-aliphatic- 3-hydroxy-1,4-naphthoquinone and these compositions may also be formulated with other appropriate adjuvants to give mite killing and aphid killing compositions in the form of solutions, water-dispersible liquids, dusts and water-dispersible powders.

The 2-aliphatic-3-hydroxy 1,4-naphthoquinones are prepared by alkylation of lawsone, 2- hydroxy-l,4-naphthoquinone, with a diacyl peroxide. The compounds are water insoluble yellow to orange colored solids having melting points in the range of about 50-150 C. The salts of the compounds are readily prepared by reaction, for example with an amine or a metal hydroxide. The salts are slightly water soluble red colored solids which decompose on heating.

Illustrative of the 2-aliphatic-3-hydroxy-l,4- naphthoquinones employed in the compositions of the invention are compounds represented by the formula given above in which: R is n-alkyl, such as hexyl, octyl, nonyl, decyl. hendecyl, dodecyl, tridecyl, tetradecyl, pentadecyl; R is branched chain such as 2-methyloctyl, isononyl, 2,4-dimethylpentyl, and l-isopropyl-Z-methylbutyl; R is cyclohexyl; R is cyclohexylalkyl such as cyclohexylmethyl, 3-cyclohexylpropyl, 4-cyclohexylbutyl, fi-cyclohexylhexyl, 8-cyclohexyloctyl, 9-cyclohexylnonyl; and the salts of any of the foregoing compounds, such as the sodium or other alkaline earth or alkaline metal salts and dimethylamine or similar amine salts.

The preferred 2-aliphatic-3-hydroxy-1,4-naphthoquinones employed in the compositions of the invention are those in which R is normal alkyl and still more preferably those in which R is n-alkyl containing from 11 thru 14 carbon atoms specifically the n-hendecyl-, n-dodecyl-, n-tridecyl-, and n-tetradecyl-3-hydroxy-1,4-naphthoquinones.

In preparing the compositions of the invention,

a 2-aliphatic-3-hydroxy-1,4-naphthoquinone is admixed with a surface active agent of the type used to impart dispersibility of an organic liquid composition or a powder in water. Such agents will be referred to herein as dispersing agents since they cause the compositions of the invention, whether in liquid or in powdered form, to be easily dispersed in water to give aqueous spray compositions. Such agents when used in admixture with an organic liquid composition are sometimes also referred to in the art as emulsifying agents since the dispersion of the organic liquid in water which they promote is an emulsion.

Where a water-dispersible organic liquid composition containing a 2-aliphatic-3-hydroxy-1,4- naphthoquinone is desired, the dispersing agent used is preferably one that is soluble in the organic liquid used as solvent for the insecticidal agent. Typical of such oil-soluble dispersing, or emulsifying, agents are the amine salts of oleic acid, the sulfonated animal and vegetable oils such as sulfonated fish and castor oils, sulfonated petroleum oils, glycerol monostearate, sorbitan tristearate, diglycol oleate, diethylene glycol laurate; pentaerythritol monostearate, phthalic glycerol alkyd resins, and polyethylene oxides.

In the preparation of water-dispersible pow- 3 dered compositions of the invention, the oil-soluble dispersing agents of the type illustrated above may be used and other dispersing agents which are not generally thought of as oil-soluble mayalso be employed. Examples of the latter .are the calcium or sodium salts of lignin sulfonic ,acid such as goulac, polyvinyl alcohols, and the sodium salts of sulfonated condensation products of naphthalene and formaldehyde.

Other dispersing agents are listed in detail in U. S. Department of Agriculture Bulletin 131-607 and in an article by McCutcheon in Chemical Industries, November 1947, page 811, entitled Synthetic Detergents.

The amount of dispersing agent used in the compositions of the invention will vary with the dispersing properties of the particular adjuvant used and will be varied too with the particular use for which the composition is intended. Generally the dispersing agent will not comprise more than about by weight of the composition and with the better adjuvant materials, the percentage will be 5% or less.

The compositions of the inventions consisting of a 2-aliphatic-3-hydroxy-1,4-naphthoquinone in admixture with a dispersing agent may be used as such in the preparation of aqueous spray compositions or, alternatively, they may be diluted with solvents to give solutions and water-dispersible liquids, or they may be diluted with finely-divided inert powders to give dusts and water-dispersible powders.

It is preferred to prepare the compositions of the invention in the form of concentrates, that is, solutions or dusts containing the toxicant in high concentration. These concentrates are then dispersed or diluted before actual application. Such dispersion or dilution is obtained by mixing the compositions with additional amounts of diluent, solvents or dusts, or more preferably by dispersing the compositions in water to give aqueous emulsions or suspensions which are readily applied by means of the conventional insecticidal spray equipment.

In preparing the water-dispersible dust compositions of the invention, the finely-divided inert powder used as a diluent is preferably selected from the class consisting of talcs, pyrophyllite, natural clays, and diatomaceous earths. Other powdered inert diluents which may be used in dust compositions include powders such as calcium phosphate, calcium carbonate, magnesium carbonate, sulfur, lime, and flours such as walnut shell, wheat, redwood, soya bean, and cottonseed.

Various solvents may be used if it is desired to prepare solutions containing a 2-aliphatic-3- hydroxy-1,4-naphthoquinone and a dispersing agent. Typical solvents are kerosene, trichloroethylene, tetrachloroethylene, alkylated naphthalene, xylene, toluene, cyclohexanone, and acetone. One should bet careful, however, in the selection of a solvent diluent if it is desired to apply a solution to growing crops since many of the common solvents tend to damage plants.

The concentration of the active ingredient in the concentrates may be varied widely. For example, compositions in the form of dusts or water-dispersible powders can be prepared containing from 1 to about 65% by weight of the active ingredient. The maximum concentrations obtained in the preparation of solutions will, of course, vary according to the solubility of the active toxicant in the particular solvent selected.

In actual application to vegetation or agricultural crops, the concentrates are diluted and the compositions applied in the form of a dust or an aqueous spray containing preferably from about 0.001 to 0.1% by weight of the 2-aliphatic-3- hydroxy-1,4-naphthoquinone.

In applying the compositions of the invention for the control of aphids and other insects and for the control of mites, the compositions are applied directly on the area or locus which is to be protected from the pest infestation in amount sumcient to exert an insecticidal or miticidal action. It is not necessary that the composition be applied directly to the pests.

While the compositions of the invention include as an essential active ingredient a Z-aliphatic-3-hydroxy-1,4-naphthoquinone in admixture with a dispersing agent, they may also include insect toxicants, bactericides, and fungicides such as those disclosed in U. S. Patent 2,426,417.

The invention is illustrated further by reference to the following examples:

Example I 2-cyclohexyl-3-hydroxy-1,4 naphthoquinone (yellow needles, M. P. 135 C.) is mixed with the dispersing agent glycerol monostearate in proportions to give by weight of the toxicant and 5% by weight of the dispersing agent.

The above concentrate is readily dispersible in water to provide aqueous spray compositions. A spray composition adapted for application to apple trees for the protection of the trees against infestation by mites and aphids is obtained by dispersing the composition of this example in water to give an aqueous suspension containing from 0.001 to 0.01% by weight of 2-cyclohexyl-, 3-hydroxy-1,4-naphthoquinone.

Example II The following is an example of a dust and water-dispersible powder composition of the invention. It is prepared by mixing the ingredients tabulated below to obtain a finely-divided solid.

10% 2 n dodecyl-B-hydroxy-1,4-naphthoquinone (yellow powder, M. P. 93.8-94.6 C.) 85% pyrophyllite (average particle size less than 40 microns) 5% pentaerythritol monostearate The composition of this example is applied as a dust or more preferably it is dispersed in water to form an aqueous suspension for application as a spray for the control of mites and aphids.

Example III Following is a solution or water-dispcrsible liquid composition of the invention:

1% 2- (9-cyclohexylnonyl) -3-hydroxy-1,4-naphthoquinone (yellow powder M. P. 97-98 C.)

96% alkylated naphthalene 3% diethyl cyclohexylamine dodecyl sulfate The composition of this example is readily dispersible in water. A spray composition well suited for the control of mites is obtained by dispersing a quart of the above formulation in 100 gallons of water.

Example IV pensions suitable for application by means of conventional agricultural spray equipment.

Example V A mixture of parts by weight of the dimethylamine salt of 2-methyioctyl-3-hydroxy-1,4-naphthoquinone, 90 parts by weight of talc, and 5 parts by weight of diglycol oleate is pulverized and mixed to give a composition adapted for application as a dust or in the form of an aqueous suspension for the control of mites and aphids.

Iclaim:

1. A composition adapted for the control of mites and aphids which comprises as an essential active ingredient in admixture with a surface active agent in amount effective for imparting water dispersability to the composition, a 2-aliphatic-3-hydroxy-1,4-naphthoquinone represented by the formula where R is a radical, containing from 6 thru 15 carbon atoms, selected from the group consisting of alkyl, cyclohexyl, and cyclohexylalkyl; and the salts thereof.

2. A composition for the control of mites and aphids which comprises as an essential active ingredient in admixture with a surface active agent in amount effective for imparting water dispersability to the composition a 2-n-alkyl-3- hydroxy-1,4-naphthoquinone, in which the n-alkyl radical contains 6 thru 15 carbon atoms.

3. A composition adapted for the control of mites and aphids which comprises as an essential active ingredient in admixture with a surface active agent in amount effective for imparting water dispersability to the composition a 2-n-al- 6 kyl-3-hydroxy-1,4-naphthoquinone, in which the 'n-alkyl radical contains 11 thru 14*carbon atoms.

4. A composition adapted for the control of mites and aphids comprising 2-n-dodecy1-3-hydroxy-1,4-naphthoquinone as an essential active ingredient in admixture with a surface active agent in amount effective for imparting water dispersability to the composition,

5. The method of protecting plants from infestation by mites and aphids which comprises applying to the plants a composition containing as an essential active ingredient a 2-aliphatic-3- hydroxy-1,4-naphthoquinone represented by the formula REFERENCES CITED The following references are of record in the file of this patent:

UNITED STATES PATENTS Number Name Date 1,752,293 Brodersen et a1. c Apr. 1, 1930 2,348,976 Hyman May 16, 1944 2,398,418 Fieser Apr. 16, 1946 2,435,500 Ladd Feb. 3, 1948 OTHER REFERENCES Anfinsen et al.: Chemical Abstracts, vol. 41, page 7539f (1947).

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US1752293 *Sep 27, 1926Apr 1, 1930By Mesne AssignmentsKarl brodebsen and werner ext
US2348976 *Jan 29, 1943May 16, 1944Velsicol CorpInsecticide
US2398418 *Aug 27, 1943Apr 16, 1946Louis F FieserIntroduction of organic radicals into quinones
US2435500 *Aug 5, 1944Feb 3, 1948Us Rubber Co2, 3-epoxy-1, 2, 3, 4-tetrahydronaphthalenedione-1, 4 as parasiticidal preparations
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US2802769 *Mar 22, 1955Aug 13, 1957Us Rubber CoInsecticides
US3673222 *Nov 26, 1969Jun 27, 1972Sydney Archer2-(8-cyclohexyloctyl or 7-cyclohexylheptyl)-1,4-naphthoquinone and process for preparation and use thereof
US4053634 *Sep 13, 1976Oct 11, 1977E. I. Du Pont De Nemours And CompanyMiticidal and aphicidal method utilizing 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters
US4055661 *Sep 15, 1975Oct 25, 1977E. I. Du Pont De Nemours And CompanyMiticidal and aphicidal method utilizing 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters
US4070481 *Mar 29, 1976Jan 24, 1978E. I. Du Pont De Nemours And CompanySubstituted 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters and their use as miticides
US4082848 *Apr 29, 1976Apr 4, 1978E. I. Du Pont De Nemours And Company2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters
US4107325 *Aug 25, 1977Aug 15, 1978E. I. Du Pont De Nemours And CompanyPesticides
US4110473 *Jul 14, 1977Aug 29, 1978E. I. Du Pont De Nemours And CompanyMiticidal ethers
US4115584 *Oct 12, 1977Sep 19, 1978E. I. Du Pont De Nemours And CompanySubstituted 2-higher alkyl-3-hydroxy-1,4-naphthoquinone carboxylic acid esters and their use as miticides
US4143157 *May 9, 1978Mar 6, 1979E. I. Du Pont De Nemours And CompanyMiticidal and aphicidal method utilizing 2-higher alkyl-3-hydroxy-1'4-naphthoquinone carboxylic acid esters
US4148918 *Jul 31, 1978Apr 10, 1979E. I. Du Pont De Nemours And CompanyAphicides
US5849793 *Aug 15, 1997Dec 15, 1998The Picower Institute For Medical ResearchHIV matrix protein tyrosine position 29 pocket binders
US6043286 *Jul 10, 1997Mar 28, 2000Btg International LimitedPesticidal compounds
DE2520739A1 *May 9, 1975Nov 20, 1975Du PontPestizid
EP0036502A1 *Feb 25, 1981Sep 30, 1981Zyma Gmbh2-Alkyl-5-hydroxy-1,4-naphthoquinones, process for their manufacture and pharmaceutical preparations containing these compounds
WO1996021354A1 *Jan 10, 1996Jul 18, 1996Duncan BattyPesticidal compounds
WO2012038945A2 *Sep 9, 2011Mar 29, 2012Bimeda International Pharmaceutical LimitedControl of mites
Classifications
U.S. Classification514/681, 552/298
International ClassificationA01N35/06
Cooperative ClassificationA01N35/06
European ClassificationA01N35/06