US2793154A - Pyrethrum pesticide synergized with lower alkyl aryl ketone - Google Patents
Pyrethrum pesticide synergized with lower alkyl aryl ketone Download PDFInfo
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- US2793154A US2793154A US514782A US51478255A US2793154A US 2793154 A US2793154 A US 2793154A US 514782 A US514782 A US 514782A US 51478255 A US51478255 A US 51478255A US 2793154 A US2793154 A US 2793154A
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- Prior art keywords
- pyrethrins
- pyrethrum
- ketone
- pyrethrin
- pesticide
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- ROVGZAWFACYCSP-MQBLHHJJSA-N [2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-MQBLHHJJSA-N 0.000 title description 7
- 229940015367 pyrethrum Drugs 0.000 title description 7
- 239000000575 pesticide Substances 0.000 title description 3
- 150000004983 alkyl aryl ketones Chemical class 0.000 title description 2
- 241000250966 Tanacetum cinerariifolium Species 0.000 title 1
- HYJYGLGUBUDSLJ-UHFFFAOYSA-N pyrethrin Natural products CCC(=O)OC1CC(=C)C2CC3OC3(C)C2C2OC(=O)C(=C)C12 HYJYGLGUBUDSLJ-UHFFFAOYSA-N 0.000 claims description 36
- VQXSOUPNOZTNAI-UHFFFAOYSA-N Pyrethrin I Natural products CC(=CC1CC1C(=O)OC2CC(=O)C(=C2C)CC=C/C=C)C VQXSOUPNOZTNAI-UHFFFAOYSA-N 0.000 claims description 11
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 claims description 11
- 239000003208 petroleum Substances 0.000 claims description 10
- 150000002576 ketones Chemical class 0.000 claims description 9
- 239000007788 liquid Substances 0.000 claims description 7
- 239000004215 Carbon black (E152) Substances 0.000 claims description 4
- 229930195733 hydrocarbon Natural products 0.000 claims description 4
- 150000002430 hydrocarbons Chemical class 0.000 claims description 4
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 37
- 229940070846 pyrethrins Drugs 0.000 description 25
- 239000002728 pyrethroid Substances 0.000 description 25
- VXSIXFKKSNGRRO-MXOVTSAMSA-N [(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate;[(1s)-2-methyl-4-oxo-3-[(2z)-penta-2,4-dienyl]cyclopent-2-en-1-yl] (1r,3r)-3-[(e)-3-methoxy-2-methyl-3-oxoprop-1-enyl Chemical class CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1.CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VXSIXFKKSNGRRO-MXOVTSAMSA-N 0.000 description 24
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 18
- -1 aryl alkyl ketones Chemical class 0.000 description 9
- 239000002917 insecticide Substances 0.000 description 9
- 239000003350 kerosene Substances 0.000 description 9
- 241000607479 Yersinia pestis Species 0.000 description 7
- 239000007921 spray Substances 0.000 description 7
- 240000004460 Tanacetum coccineum Species 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 description 5
- 229950006824 dieldrin Drugs 0.000 description 5
- NGPMUTDCEIKKFM-UHFFFAOYSA-N dieldrin Natural products CC1=C(Cl)C2(Cl)C3C4CC(C5OC45)C3C1(Cl)C2(Cl)Cl NGPMUTDCEIKKFM-UHFFFAOYSA-N 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 5
- YVGGHNCTFXOJCH-UHFFFAOYSA-N DDT Chemical compound C1=CC(Cl)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(Cl)C=C1 YVGGHNCTFXOJCH-UHFFFAOYSA-N 0.000 description 4
- 230000000749 insecticidal effect Effects 0.000 description 4
- 238000011084 recovery Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 230000002195 synergetic effect Effects 0.000 description 4
- 231100000419 toxicity Toxicity 0.000 description 4
- 230000001988 toxicity Effects 0.000 description 4
- 241000238631 Hexapoda Species 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000000284 extract Substances 0.000 description 3
- GNKZMNRKLCTJAY-UHFFFAOYSA-N 4'-Methylacetophenone Chemical compound CC(=O)C1=CC=C(C)C=C1 GNKZMNRKLCTJAY-UHFFFAOYSA-N 0.000 description 2
- WRJZDDJYWWJLIS-UHFFFAOYSA-N 4-methyl-1-phenylpentan-1-one Chemical compound CC(C)CCC(=O)C1=CC=CC=C1 WRJZDDJYWWJLIS-UHFFFAOYSA-N 0.000 description 2
- DQFBYFPFKXHELB-UHFFFAOYSA-N Chalcone Natural products C=1C=CC=CC=1C(=O)C=CC1=CC=CC=C1 DQFBYFPFKXHELB-UHFFFAOYSA-N 0.000 description 2
- 241000257226 Muscidae Species 0.000 description 2
- 238000003556 assay Methods 0.000 description 2
- FFSAXUULYPJSKH-UHFFFAOYSA-N butyrophenone Chemical compound CCCC(=O)C1=CC=CC=C1 FFSAXUULYPJSKH-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- KRIOVPPHQSLHCZ-UHFFFAOYSA-N propiophenone Chemical class CCC(=O)C1=CC=CC=C1 KRIOVPPHQSLHCZ-UHFFFAOYSA-N 0.000 description 2
- 229940048383 pyrethrum extract Drugs 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- XKGLSKVNOSHTAD-UHFFFAOYSA-N valerophenone Chemical compound CCCCC(=O)C1=CC=CC=C1 XKGLSKVNOSHTAD-UHFFFAOYSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- UXUFNYMYKPYEFL-UHFFFAOYSA-N 2,4,5,7,8,9-hexachloro-3-oxapentacyclo[6.5.0.02,4.05,7.09,11]tridec-1(13)-ene Chemical compound ClC12C3(C4(C(C5(C(C3=CCC1C2)(O5)Cl)Cl)(C4)Cl)Cl)Cl UXUFNYMYKPYEFL-UHFFFAOYSA-N 0.000 description 1
- JQMFQLVAJGZSQS-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-N-(2-oxo-3H-1,3-benzoxazol-6-yl)acetamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)NC1=CC2=C(NC(O2)=O)C=C1 JQMFQLVAJGZSQS-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000257159 Musca domestica Species 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 235000005513 chalcones Nutrition 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 150000003997 cyclic ketones Chemical class 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000003197 gene knockdown Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 231100000171 higher toxicity Toxicity 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- DQFBYFPFKXHELB-VAWYXSNFSA-N trans-chalcone Chemical compound C=1C=CC=CC=1C(=O)\C=C\C1=CC=CC=C1 DQFBYFPFKXHELB-VAWYXSNFSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
Definitions
- compositions comprising pyrethrins for combating pests.
- pyrethrins are employed in the form of an extract of the active principle of a plant of the genus Pyrethrum and conveniently may be applied, as solutions in petroleum distillate fractions, in the form of liquid sprays.
- the pyrethrins While it is recognised that the pyrethrins have a degree of toxicity for many insect pests, they are of particular value in providing the means of rapidly immobilising the pests and it is common practice to include in the pyrethrin containing composition at least one other component which although slower acting is of higher toxicity. By the use of such compositions it is possible to ensure that the pests are rapidly immobilised until the slower acting component has had time to be effective. Thus, in the application of insecticidal containing sprays to the killing of house flies it is considered desirable to include in the composition a component such as pyrethrin which provides a high knock down rate.
- a compound, which in admixture with another component gives a composition having a toxicity greater than equivalent amounts of the compound or the component when used alone, is known as a synergist.
- synergists which have been used in sprays for combating house-flies are iso-butyl undecylenarnide and sesame oil.
- chalcone alpha-benzalacetophenone
- compositions containing pyrethrins are employed in the form of sprays and the technical literature contains a description of a wide variety of solvents which may be employed for producing a solution of suitable characteristics for application in this manner.
- solvents such as ketones.
- compositions have been described containing an extract of pyrethin in kerosene or a heavy petroleum oil together with a phenol and as solvent a cyclic ketone such as cyclohexanone.
- aryl alkyl ketones have the unexpected property of acting as a synergist for pyrethrins.
- an improved pest combating composition comprising at least one pyrethrin and at least one aryl alkyl ketone.
- the composition consists of a solution of pyrethrum extract and an aryl alkyl ketone in a hydrocarbon distillate fraction.
- the distillate fraction is a kerosene or white spirit fraction of petroleum.
- the ketone is an aryl alkyl ketone in which the aryl group consists of an unsubstituted or alkyl substituted phenyl group.
- the ketone is an aryl alkyl ketone in which the alkyl group comprises 1-4 carbon atoms.
- ketones are acetophenone and the methyl acetophenones.
- Other ketones which may be employed include butyro phenone (propyl phenyl ketone) valero phenone (butyl phenyl ketone) and iso-capro phenone (iso amyl phenyl ketone).
- Suitable insecticides include the gamma isomer of benzene hexachloride, p,p dichlorodiphenyl trichloroethane and dieldrin.
- insecticidal compositions according to this invention contain 0.020.075% wt./vol. of total pyrethrins.
- the ratio of aryl alkyl ketone/total pyrethrins is not greater than 15/ 1 wt./Wt. It is particularly preferred that the ratio lies in the range 5/1 to 15/1 wt./Wt.
- the insecticidal composition contains up to 0.5% wt./vol. of a highly toxic insecticide, for example, benzene hexachloride.
- a highly toxic insecticide for example, benzene hexachloride.
- compositions according to the present invention it is possible to obtain a satisfactorily short insect knock-d-own time, while effecting an economy in the use of the relatively expensive pyrethrum extract.
- the kerosene employed in the examples was a premium grade commercial petroleum kerosene fraction having the following characteristics Specific Gravity F./60 F. A. S. T. M. Distillation BP Cc 172 2% recovered C.
- EXAMPLE 1 The essence of synergism is that pyrethrum plus synergist has a greater toxicity than either material alone, the toxicity of the mixture being greater than the sum of its parts. It has been found that if the synergist is sprayed before the Pyrethrum, the synergistic effect is just as strong and this is used to distinguish true synergism from pseudo synergism such as that exhibited by lubricating oils and oleic acid which have the physical effect of stabilizing the droplet size. To establish the true synergistic action of acetophone, the following tests were made in triplicate.
- the volume of the chamber was 18.7 cu. ft. (i. e. approx. A of the vol. of the standard Feet-Grady chamber).
- the dosage used was man cases 1 ml. (i. e. A of the dosage employed in the standard method).
- a pest-combating liquid composition comprising pyrethrin and phenyl alkyl ketone in which the alkyl group comprises 14 carbon atoms, the ratio of the total weight of phenyl alkyl ketone to total weight of the pyrethrin being in the range of from about 5:1 to about 15:1, said pyrethrin and phenyl alkyl ketone being in solution with a liquid hydrocarbon distillate fraction derived from petroleum.
- fraction is a kerosene fraction of petroleum.
- composition as specified in claim 1 in which the fraction is a white spirit fraction of petroleum is a white spirit fraction of petroleum.
- composition as specified in claim 1 and having included therein, the gamma isomer of benzene hexachloride.
- composition as specified in claim 1 and having included therein, pp dichlorodiphenyl trichloro ethane.
- composition as specified in claim 1 in which the total amount of pyrethrins present is 0.02-0.075 wt./vo1.
- a pest-combating liquid composition comprising 0.02-0.07 5% wt./vol. of pyrethrin; acetophenone, the ratio of the weight of acetophenone to the total weight of pyrethrin lying in the range of from about 5:1 to about 15: 1; a pesticide selected from the group consisting of the gamma isomer of benzene hexachloride, p,p'-dich1orodiphenyl trichloro-ethane, and dieldrin, the foregoing being in solution with a liquid hydrocarbon distillate fraction derived from petroleum.
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- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
United States Patent PYRETHRUM PESTICIDE SYNERGIZED WITH LOWER ALKYL ARYL KETONE George Stuart Shillitoe, London, and Arthur Douglas Harford, Sunbury-on-Thames, England, assignors to The British Petroleum Company Limited, London, England, a joint-stock corporation of England No Drawing. Application June 10, 1955, Serial No. 514,782
Claims priority, application Great Britain June 15, 1954 9 Claims. (Cl. 167-24) This invention'relates to improved pest combating compositions.
It is known to use compositions comprising pyrethrins for combating pests. Usually the pyrethrins are employed in the form of an extract of the active principle of a plant of the genus Pyrethrum and conveniently may be applied, as solutions in petroleum distillate fractions, in the form of liquid sprays.
While it is recognised that the pyrethrins have a degree of toxicity for many insect pests, they are of particular value in providing the means of rapidly immobilising the pests and it is common practice to include in the pyrethrin containing composition at least one other component which although slower acting is of higher toxicity. By the use of such compositions it is possible to ensure that the pests are rapidly immobilised until the slower acting component has had time to be effective. Thus, in the application of insecticidal containing sprays to the killing of house flies it is considered desirable to include in the composition a component such as pyrethrin which provides a high knock down rate.
Pyrethrins and extracts containing pyrethrins are expensive and it is therefore desirable to reduce as far as possible the quantities of these materials employed in the compositions.
It has been shown that the addition of certain compounds, which are not necessarily insecticidal, to these compositions leads to an increase in the efficiency of the compositions and thus, by their inclusion, permits a reduction in the amount of pyrethrins employed.
A compound, which in admixture with another component gives a composition having a toxicity greater than equivalent amounts of the compound or the component when used alone, is known as a synergist.
Examples of synergists which have been used in sprays for combating house-flies are iso-butyl undecylenarnide and sesame oil. Among the compounds which have been tried and found to lack synergistic products is included chalcone (alpha-benzalacetophenone) Usually the compositions containing pyrethrins are employed in the form of sprays and the technical literature contains a description of a wide variety of solvents which may be employed for producing a solution of suitable characteristics for application in this manner. Thus a number of compositions are described containing petroleum fractions together with an oxygenated solvent, such as ketones. Thus compositions have been described containing an extract of pyrethin in kerosene or a heavy petroleum oil together with a phenol and as solvent a cyclic ketone such as cyclohexanone.
It has now been found that in addition to their properties as solvents, aryl alkyl ketones have the unexpected property of acting as a synergist for pyrethrins.
It is an object of the present invention. to provide improved pest-combating compositions. It is a further object to provide pest-combating compositions containing pyrethrins in the presence of an economically attractive synergist therefor.
According to the present invention there is provided an improved pest combating composition comprising at least one pyrethrin and at least one aryl alkyl ketone.
Preferably the composition consists of a solution of pyrethrum extract and an aryl alkyl ketone in a hydrocarbon distillate fraction.
Suitably, the distillate fraction is a kerosene or white spirit fraction of petroleum.
Preferably the ketone is an aryl alkyl ketone in which the aryl group consists of an unsubstituted or alkyl substituted phenyl group.
Preferably, also, the ketone is an aryl alkyl ketone in which the alkyl group comprises 1-4 carbon atoms.
Particularly preferred ketones are acetophenone and the methyl acetophenones. Other ketones which may be employed include butyro phenone (propyl phenyl ketone) valero phenone (butyl phenyl ketone) and iso-capro phenone (iso amyl phenyl ketone).
In general it is found convenient to include in the pest combating compositions a proportion of a highly toxic insecticide to increase the percentage kill obtained by the insecticide. Suitable insecticides include the gamma isomer of benzene hexachloride, p,p dichlorodiphenyl trichloroethane and dieldrin.
Preferably the insecticidal compositions according to this invention contain 0.020.075% wt./vol. of total pyrethrins.
Preferably the ratio of aryl alkyl ketone/total pyrethrins is not greater than 15/ 1 wt./Wt. It is particularly preferred that the ratio lies in the range 5/1 to 15/1 wt./Wt.
Preferably the insecticidal composition contains up to 0.5% wt./vol. of a highly toxic insecticide, for example, benzene hexachloride.
By the use of compositions according to the present invention it is possible to obtain a satisfactorily short insect knock-d-own time, while effecting an economy in the use of the relatively expensive pyrethrum extract.
The invention is illustrated but in no way limited by the following examples.
The kerosene employed in the examples was a premium grade commercial petroleum kerosene fraction having the following characteristics Specific Gravity F./60 F. A. S. T. M. Distillation BP Cc 172 2% recovered C.
5% recovered 10% recovered 20% recovered 30% recovered 40% recovered 50% recovered 60% recovered recovered recovered recovered FBP Recovery Residue- Loss Recovery C. Recovery 200C" Recovery 240C..-
EXAMPLE 1 The essence of synergism is that pyrethrum plus synergist has a greater toxicity than either material alone, the toxicity of the mixture being greater than the sum of its parts. It has been found that if the synergist is sprayed before the Pyrethrum, the synergistic effect is just as strong and this is used to distinguish true synergism from pseudo synergism such as that exhibited by lubricating oils and oleic acid which have the physical effect of stabilizing the droplet size. To establish the true synergistic action of acetophone, the following tests were made in triplicate.
with 1 ml. of kerosene and eing sprayed with 1 ml. of the 10 (a) the volume of the chamber was 18.7 cu. ft. (i. e. approx. A of the vol. of the standard Feet-Grady chamber).
(b) the dosage used was man cases 1 ml. (i. e. A of the dosage employed in the standard method).
a spraying pressure of 10 lb./sq. in. was employed employing as the spray gun Aerograph Artists Brush with a No. 2 nozzle. 7
(d) the number of test insects employed was 90-104 per test.
Table 2 0.05% w./v. Pyrethrins with Acetophenone 0.1% 0.05% percent W./V. as below Insecticide W./V. w./v.
Pyrcth- Pyrethrlns rins 0.05% 0.15% 0.25% 0.40% 0.50% 0.60% 0.75% w./v. w./v. W./v. w./v. w./v. w./v. w./v.
. Aeetophenone I Rntw wn/w "I "I n, 1/1 3/1 /1 8/1 10/1 12/1 I 15/1 Time for 50% K. D. (seconds) 88 120 92 107 103 100 103 92 89 Time for 90% K. D. (seccuds) 153 241 231 191 160 159 154 144 190 Time for 100% K. D. (seconds) 373 538 360 445 433 420 400 360 300 Percent K. D. in 600 seconds. 100 100 100 100 100 100 100 100 100 Percent Kill in 24 hours 39. 2 13. 6 14. 7 12. 6 13. 0 14. 0 22. 4 22. G 23. 0
(c) The flies were sprayed with 1 ml. of kerosene and EXAMPLE 3 the same airing procedure adopted as in the tests under (a) and (b) before being sprayed with a blend of 0.05% w./v. pyrethrins plus 0.5% w./v. acetophenone.
The mean results of these three sets of tests are recorded in Table l.
the nine assays for each blend were The experiment described in Example 2 was repeated carrying out three assays 011 each of three different generations of Musca domestica L. The mean results of as shown in Table 3.
Table 3 0.1% 0.05% 0.05% \v./v. Pyrethrins with Acetophenone percent wt. as below Insecticide W./V. W./v.
Pyreth- Pyrethrins rins 0.125 0.025 0.05 0.15 0.25 0.35 0.40 0.50 0.60 0.75 1.0 Acctophcnone Y I RBtIO Pyrethrum w/w 0.25/1 05/1 1/1 t 3/1 5/1 7/1 8/1 10/1 12/1 15/1 20/1 Time for K. D. (8005.).... 82 133 106 110 114 100 101 82 90 101 101 103 90 Time or 90% K. D. (8005.) 149 276 259 275 253 268 179 174 177 173 173 201 230 Time for 100% K. D. (Secs.) 325 538 410 420 420 497 390 360 340 387 360 300 300 PercentILDJnGOO see0nds 100 100 100 100 100 100 100 100 100 100 100 100 100 Percent Ki1lin24 hours 44.7 13.4 13.0 13.1 14.7 17.0 17.3 18.3 18.3 17.3 19.8 10.0 22.0
Table 1 EXAMPLE 4 Method of Spraying Insecticide Method Method Method (a) (c) The elfect of adding chlorinated hydrocarbon contact *f insecticides to a Pyrethrum spray synergised with aceto- Time for 509 K. D. (Secs) 120 77 89 Time for K (SBCSLV J 218 140 140 phenone was studied by preparing, w1th kerosene as sol ITirne rot- 100 IQ DO. (secs r. 88 3 vent, three blends crcent .in O se-on 1 0 Percent 1311 in 24 hours 19.3 22.3 21.8 Contamlng O05% pyrethrins, 035% acetophone and 0.5 w./v. DDT (pp' dichlorodiphenyl trichloro ethane) I I (b) containing 0.05 w./v. pyrethrins 0.35% w./v. acctophenone and 0.1% w./v. pure B. H. C. (pure gamma isomer of benzene hexachloride).
(c) containing 0.05 w./v. pyrethrins 0.35% w./v. acetophenone and 0.1% w./v. dieldrin (hexachloroepoxy-octahydrodimethano naphthalene).
These blends were assayed in triplicate against a blend of 0.05 w./v. pyrethrins with 0.35 w./v. acetophenone using a 0.05 w./v. pyrethrins spray as control and the mean results of the tests are recorded in Table 4.
Table 4 0.05% w./v. Pyrethrins plus 0.05% w./v. 0.35% Ac ophenone With- 0.05% w./v. Pyrethrlns Insecticide Pyrethrins plus 0.35%
w./v.aceto- 0.5% 0.1% 0.1% phenone w. v. w./v. w.lv.
D T 3.11. C. Dieldrin Time for 50% K. D. 138 85 79 78 Time for 90% K. D. 277 135 135 157 234 Time for 100% K. 4, 455 260 358 570 570 Percent K. D. in 60 100 100 100 100 100 Percent K i 24 16. 7 19. 100 100 100 EXAMPLE 5 2. A compositlon as specified m cla1m 1 1n which the p-Methylacetophenone, propio-phenone and benzophenone were tested for synergistic activity by preparing three blends containing 0.05% w./v. pyrethrins with 0.35% w./v. of the appropriate compound under test in kerosene and assaying in triplicate each blend against a 0.05% w./v. pyrethrins blend. The mean results are recorded in Table 5.
We claim:
1. A pest-combating liquid composition comprising pyrethrin and phenyl alkyl ketone in which the alkyl group comprises 14 carbon atoms, the ratio of the total weight of phenyl alkyl ketone to total weight of the pyrethrin being in the range of from about 5:1 to about 15:1, said pyrethrin and phenyl alkyl ketone being in solution with a liquid hydrocarbon distillate fraction derived from petroleum.
fraction is a kerosene fraction of petroleum.
3. A composition as specified in claim 1 in which the fraction is a white spirit fraction of petroleum.
4. A composition as specified in claim 1 in which the ketone is acetophenone.
5. A composition as specified in claim 1, and having included therein, the gamma isomer of benzene hexachloride.
6. A composition as specified in claim 1, and having included therein, pp dichlorodiphenyl trichloro ethane.
7. A composition as specified in claim 1, and having included therein, dieldrin.
8. A composition as specified in claim 1 in which the total amount of pyrethrins present is 0.02-0.075 wt./vo1.
9. A pest-combating liquid composition comprising 0.02-0.07 5% wt./vol. of pyrethrin; acetophenone, the ratio of the weight of acetophenone to the total weight of pyrethrin lying in the range of from about 5:1 to about 15: 1; a pesticide selected from the group consisting of the gamma isomer of benzene hexachloride, p,p'-dich1orodiphenyl trichloro-ethane, and dieldrin, the foregoing being in solution with a liquid hydrocarbon distillate fraction derived from petroleum.
References Cited in the file of this patent FOREIGN PATENTS 494,463 Germany Mar. 24, 1930 350,897 Great Britain June 15, 1931 126,959 Australia Feb. 25, 1948 OTHER REFERENCES J. Econ. Entomology, vol. 44, December 1951, p. 896.
Claims (1)
1. A PEST-COMBATING LIQUID COMPOSITIO COMPRISING PYRETHRIN AND PHENYL ALKYL KETONE IN WHICH THE ALKYL GROUP COMPRISES 1-4 CARBON ATOMS, THE RATIO OF THE TOTAL WEIGHT OF PHENYL ALKYL KETONE TO TOTAL WEIGHT OF THE PYRETHRIN BEING IN THE RANGE OF FROM ABOUT 5:1 TO ABOUT 15:1, SAID PYRETHRIN AND PHENYL ALKYL KETONE BEING IN SOLUTION WITH A LIQUID HYDROCARBON DISTILLATE FRACTION DERIVED FROM PETROLEUM.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2793154X | 1954-06-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2793154A true US2793154A (en) | 1957-05-21 |
Family
ID=10915437
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US514782A Expired - Lifetime US2793154A (en) | 1954-06-15 | 1955-06-10 | Pyrethrum pesticide synergized with lower alkyl aryl ketone |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2793154A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9999218B2 (en) | 2011-10-04 | 2018-06-19 | 0903608 B.C. Ltd. | Pest control formulations and methods of making and using same |
| US9999227B2 (en) | 2011-10-04 | 2018-06-19 | 0903608 B.C. Ltd. | Pest control formulations and methods of making and using same |
| US12342808B2 (en) | 2013-11-18 | 2025-07-01 | 0903608 B.C. Ltd. | Compositions, devices and methods for control of pests using vapor activity |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE494463C (en) * | 1928-05-10 | 1930-03-24 | I G Farbenindustrie Akt Ges | Means for combating muscids |
| GB350897A (en) * | 1930-02-15 | 1931-06-15 | Standard Oil Dev Co | Improved insecticidal, insect-repelling and fungicidal compositions |
-
1955
- 1955-06-10 US US514782A patent/US2793154A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE494463C (en) * | 1928-05-10 | 1930-03-24 | I G Farbenindustrie Akt Ges | Means for combating muscids |
| GB350897A (en) * | 1930-02-15 | 1931-06-15 | Standard Oil Dev Co | Improved insecticidal, insect-repelling and fungicidal compositions |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9999218B2 (en) | 2011-10-04 | 2018-06-19 | 0903608 B.C. Ltd. | Pest control formulations and methods of making and using same |
| US9999227B2 (en) | 2011-10-04 | 2018-06-19 | 0903608 B.C. Ltd. | Pest control formulations and methods of making and using same |
| US10791744B2 (en) | 2011-10-04 | 2020-10-06 | 0903608 B.C. Ltd. | Pest control formulations and methods of making and using same |
| US10905114B2 (en) | 2011-10-04 | 2021-02-02 | 0903608 B.C. Ltd. | Pest control formulations and methods of making and using same |
| US12342808B2 (en) | 2013-11-18 | 2025-07-01 | 0903608 B.C. Ltd. | Compositions, devices and methods for control of pests using vapor activity |
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