US3102070A - Miticidal compositions - Google Patents
Miticidal compositions Download PDFInfo
- Publication number
- US3102070A US3102070A US109505A US10950561A US3102070A US 3102070 A US3102070 A US 3102070A US 109505 A US109505 A US 109505A US 10950561 A US10950561 A US 10950561A US 3102070 A US3102070 A US 3102070A
- Authority
- US
- United States
- Prior art keywords
- bis
- alkyl
- weight
- oleate
- ethylene oxide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 239000000203 mixture Substances 0.000 title claims description 38
- 230000003129 miticidal effect Effects 0.000 title claims description 13
- 239000003995 emulsifying agent Substances 0.000 claims description 24
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 16
- 229940049964 oleate Drugs 0.000 claims description 15
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical group CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 1
- -1 alkyl oleate Chemical compound 0.000 description 20
- 239000012141 concentrate Substances 0.000 description 20
- 239000000839 emulsion Substances 0.000 description 19
- 125000004432 carbon atom Chemical group C* 0.000 description 16
- 125000000217 alkyl group Chemical group 0.000 description 15
- 229940117927 ethylene oxide Drugs 0.000 description 13
- 239000007921 spray Substances 0.000 description 12
- 239000011575 calcium Substances 0.000 description 11
- 229910052791 calcium Inorganic materials 0.000 description 11
- 125000001033 ether group Chemical group 0.000 description 11
- 239000000843 powder Substances 0.000 description 11
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 10
- QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 9
- 238000009472 formulation Methods 0.000 description 9
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 9
- 229940073769 methyl oleate Drugs 0.000 description 9
- 230000000361 pesticidal effect Effects 0.000 description 9
- 239000000575 pesticide Substances 0.000 description 8
- 239000004563 wettable powder Substances 0.000 description 8
- ZWBANJRSWNLUEP-UHFFFAOYSA-N 2,2,2-trichloro-1,1-bis(2-chlorophenyl)ethanol Chemical compound C=1C=CC=C(Cl)C=1C(C(Cl)(Cl)Cl)(O)C1=CC=CC=C1Cl ZWBANJRSWNLUEP-UHFFFAOYSA-N 0.000 description 7
- 239000002270 dispersing agent Substances 0.000 description 6
- 239000000642 acaricide Substances 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical group CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 4
- 241000238876 Acari Species 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- LRCFXGAMWKDGLA-UHFFFAOYSA-N dioxosilane;hydrate Chemical compound O.O=[Si]=O LRCFXGAMWKDGLA-UHFFFAOYSA-N 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 229960004029 silicic acid Drugs 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- LVGKNOAMLMIIKO-UHFFFAOYSA-N Elaidinsaeure-aethylester Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC LVGKNOAMLMIIKO-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- JYIMWRSJCRRYNK-UHFFFAOYSA-N dialuminum;disodium;oxygen(2-);silicon(4+);hydrate Chemical compound O.[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Na+].[Na+].[Al+3].[Al+3].[Si+4] JYIMWRSJCRRYNK-UHFFFAOYSA-N 0.000 description 2
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 2
- LVGKNOAMLMIIKO-QXMHVHEDSA-N ethyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC LVGKNOAMLMIIKO-QXMHVHEDSA-N 0.000 description 2
- 229940093471 ethyl oleate Drugs 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 229910000286 fullers earth Inorganic materials 0.000 description 2
- 239000002917 insecticide Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- 150000003871 sulfonates Chemical class 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- KPWDGTGXUYRARH-UHFFFAOYSA-N 2,2,2-trichloroethanol Chemical compound OCC(Cl)(Cl)Cl KPWDGTGXUYRARH-UHFFFAOYSA-N 0.000 description 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-M 2-methylbenzenesulfonate Chemical compound CC1=CC=CC=C1S([O-])(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-M 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- AHJKRLASYNVKDZ-UHFFFAOYSA-N DDD Chemical compound C=1C=C(Cl)C=CC=1C(C(Cl)Cl)C1=CC=C(Cl)C=C1 AHJKRLASYNVKDZ-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000005909 Kieselgur Substances 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
- 231100000674 Phytotoxicity Toxicity 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- QQDCEHGSQINTLX-UHFFFAOYSA-N [Ca].CCCCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 Chemical compound [Ca].CCCCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 QQDCEHGSQINTLX-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 239000011717 all-trans-retinol Substances 0.000 description 1
- 235000019169 all-trans-retinol Nutrition 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 1
- 229940077388 benzenesulfonate Drugs 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000004799 bromophenyl group Chemical group 0.000 description 1
- 229920005551 calcium lignosulfonate Polymers 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid ester group Chemical class C(CCCCCCCCCCC)(=O)O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- WHDGWKAJBYRJJL-UHFFFAOYSA-K ferbam Chemical compound [Fe+3].CN(C)C([S-])=S.CN(C)C([S-])=S.CN(C)C([S-])=S WHDGWKAJBYRJJL-UHFFFAOYSA-K 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- 125000001207 fluorophenyl group Chemical group 0.000 description 1
- NVVZQXQBYZPMLJ-UHFFFAOYSA-N formaldehyde;naphthalene-1-sulfonic acid Chemical compound O=C.C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 NVVZQXQBYZPMLJ-UHFFFAOYSA-N 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000008233 hard water Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000004434 industrial solvent Substances 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 1
- 229920000940 maneb Polymers 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- UFEJKYYYVXYMMS-UHFFFAOYSA-N methylcarbamic acid Chemical compound CNC(O)=O UFEJKYYYVXYMMS-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 231100001184 nonphytotoxic Toxicity 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- YIYBQIKDCADOSF-UHFFFAOYSA-N pentenoic acid group Chemical class C(C=CCC)(=O)O YIYBQIKDCADOSF-UHFFFAOYSA-N 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 244000062645 predators Species 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229920005552 sodium lignosulfonate Polymers 0.000 description 1
- HLPHHOLZSKWDAK-UHFFFAOYSA-M sodium;formaldehyde;naphthalene-1-sulfonate Chemical compound [Na+].O=C.C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HLPHHOLZSKWDAK-UHFFFAOYSA-M 0.000 description 1
- 235000010356 sorbitol Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 239000003643 water by type Substances 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/04—Oxygen or sulfur attached to an aliphatic side-chain of a carbocyclic ring system
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S516/00—Colloid systems and wetting agents; subcombinations thereof; processes of
- Y10S516/01—Wetting, emulsifying, dispersing, or stabilizing agents
- Y10S516/03—Organic sulfoxy compound containing
Definitions
- Pesticides such as insecticides and miticides
- emulsion concentrates and wettable powders for spray purposes, as dusts, and as aerosols.
- mites In the control of mites on agricultural and horticultural crops, it is common to apply emulsion concentrates or wettable powders in aqueous sprays.
- a particularly effective miticide for use in such sprays is l,l-bis (p -chlorophenyl) -2,2,2-trichloroetlranol. It is usual practice to use this agent in conjunction with other types of pesticidal agents.
- emulsion concentrates or wettable powders of these other agents are used in the same aqueous mixture as this miticide.
- the l,l-bis(halophenyl)-2,2,2-trichloroethanols are miticidal agents, the preparation of which is described in US. Patents No. 2,812,280 and 2,812,362.
- the product, 1,1-bis(chlorophenyl)-2,2,2 trichloroethanol is a wellknown commercial miticide and there are various pesticidal compositions which utilize it as an active miticide.
- emulsion concentrates and wettable powder formulations containing a l,l-bis(halophenyl)-2,2,2-trichloroethanol as an active mirticidal agent have been evolved which show excellent compatibility when admixed in a spray tank with other formulated pesticides, which promise favorable miticidal effectiveness under adverse .climatic conditions, and which have acceptable phytotoxic properties.
- the emulsion concentrates of this invention comprise 1,l-bis(halophenyl)-2,2,2-tnichloroethanol dissolved in an alkyl oleate with the incorporation of emulsifying agent.
- Emusifying agents are used in the concentration range of about 9 to about 20% by weight based on the emulsifialble concentrate and preferably 10% to 15%.
- dinitroallcylphenyl especially the dinitro(2- methylheptyl)-phenyl, esters of crotonic, acrylic, methacrylic, 5,,8-dimethylacrylic, and 4 pentenoic acids which have been shown to have miticidal, insecticidal, and fungicidal properties may be advantageously added to these concentrates, and likewise such insecticidal agents as 1,1,1- trichloro-2,2bis (p-chlorophen-yl) ethane, 1, 1-dichloro-2,2- bis(p-chlorophenyl)ethane, or 1,1-dichloro-2,2-bis(ethy1- phenyl)-ethane, phosphatic pesticides such as 0,0-dimethyl S-(LZ-diCBIbdthOXYCt-hfl) dithicphosphate, and l-na-phthyl N-
- 1,1-bis(halophenyl)-2,2,2-trichloroethanol with pesticidal agents which kill mite predators and which, when used alone, thus cause a build-up of the mite population.
- pesticidal agents which kill mite predators and which, when used alone, thus cause a build-up of the mite population.
- pesticidal agents of the above type may be added to an emulsion concentrate. The percentage depends in part on the solubility of the particular pesticidal agent being incorporated.
- the wettable powder formulations of this invention are made by mixing an inert, finely-divided, solid carrier with the emulsion concentrate.
- the emulsion concentrate There may be used from 5% to 25% by weight of 1,l bishalophenyl)-2,2,2-trichl0roethanol in such compositions, this compound being dissolved in alkyl oleate together with emulsifiers.
- the amount of the emulsion concentrate added to the inert solid will vary with the capacity of each individual carrier or combination of carriers to hold the liquid and still maintain the product as a powder of loose texture.
- the preferred 1,l bis(halophenyl)-2,2,2-trichloroethan- 01 used in this invention is 1,1-bis(p-chlorophenyl)-2,2,2- 'trichloroethanol. It may be used in a pure form or as a technical grade containing isomers having bis(orthochlorophenyl) groups and the p, o dichlorc-dip henyl groups as minor components. Also, the corresponding bromophenyl and fluorophenyl analogs may be used alone or admixed with 1,l-bis(chloropheny1) -2,2,2-trich1oroethanol.
- the solvent for the preparation of the emulsion concentrates there is used methyl oleate, ethyl oleate, or mixtures of these two.
- One purpose of the solvent is to act as a plasticizer for the l,l-bis(-halophenyl)-2,2,2-trichloroethanol and thus keep the active ingredient in a fluid condition at low temperatures. It is also desirable to have the emulsion concentrates flowable after prolonged storage at ambient temperatures in cold weather. 'For these reasons the oleic acid ester or mixture of esters used must have a low setting point; i.e., the temperature range wherein a solid forms. This point will vary with purity of the oleates and should be no more than 60 (about 16 C.). There may be used relatively pure alkyl oleates or commercially available technical products.
- emulsifying agents there may be used surface active ethylene oxide adducts of alkyl mercaptans, long-chained carboxylic acids, higher alcohols, and alkylphenols wherein the ethylene oxide content of the resulting product is about 15 to 100 ether units, preferably 20 to units.
- the alkyl mercaptans and higher alcohols should have 10 to 20 carbon atoms in their alkyl groups, while the acids should contain 12 to 24 carbon atoms in their carboxylic portion, which may be a straight or branched chain or a cycle, as in abietic acid.
- Typical of these are t-tetradecylthiopolyethoxyethanol, tall-oil-acid polyethoxyethanol, dodecyloxypolyethoxyethanol, and alkylphenoxypolyethoxyethanol, wherein the alkyl group or groups contain 8 to 12 carbon atoms and the main group occurs preferably in the para position but that position is immaterial.
- alkyl group or groups contain 8 to 12 carbon atoms and the main group occurs preferably in the para position but that position is immaterial.
- ethylene oxide adducts -dodecylbenzenesulfonate There may also be used.
- esters are formed with such long-chained acids as oleic or lauric acids.
- alkylarenesulfonic aoids wherein the alkyl group or groups contain from 8 to 18 carbon atoms in admixtures with the above described ethylene 'oxide adducts.
- the preferred sulfonates are salts of alkylbenzenesulfonic acid, such as calcium p-t-dodecylbenzenesulfonate.
- alkylbenzenesulfonic acid such as calcium p-t-dodecylbenzenesulfonate.
- similar'alkyl 'naphthalenesulfonic acid salts such as oalcium'octylnaphthalenesulfonates.
- the ratio of weights of the ethylene oxide adduct to the sulfonate may vary from about 3 :1 to about 1:1.
- finely dispersed solid carriers for the preparation of these wettable powders are the finely particled clays such as fullers earth and kaolins,
- silica diatomaceous earth, and alkaline earth silicates
- dispersing agents I into the wettable powders.
- these are the salts of polymers formed from maleic anhydride and olefinically unsaturated hydrocarbons such as styrene, alkylstyrenes, or diisobutylene.
- styrene styrene
- alkylstyrenes alkylstyrenes
- diisobutylene diisobutylene.
- ammonia or some amines are used to form salts, some amide orimide formation also occurs.
- the amount of the added dispersit has good suspendibility in waters of varying hardness, and its application properties to foliage are entirely acceptable from its aqueous sprays.
- dispersing agent is a salt of a condensed formaldehyde-naphthalene sulfonate such as sodium formaldehyde-naphthalene sulfonate as sold under the trade names of Daxad or Tamol.
- ingagent is desirably 1% to 10% of the weight of the powderto which it is added.
- the resulting emulsion concentrate may be diluted with water to provide an efficient spray for protection against mites. It is compatible Wtih wettable powders containing fungicides such as wettable sulfur, ferbam, zineb, and
- Example 3 There are mixed 20 pants of technical 1,1-bis(cl1'lorophenyl)-2,2,2-trichloroethanol, 65' parts of methyl oleate (set point about 0 C.), and 15 parts of anemulsifier from 10 parts of long-chained fatty acid-ethylene oxide adduct, having'about ether groups perjmolecule and 5 parts of calcium tetradecylbenzenesulfonate.
- the resulting emulsion concentrate is stable on storage and is readily dispersed in even hard water to give effective aqueous sprays.
- the emulsion concentrates of this invention can be readily formulated so as to he acceptably low in phytotoxicity on plants, even on flush citrus growth. Thisis also true of properly formulated wettable powders. 1 Since the alkyl oleates :are very high boiling and havehigh flash points, they can be used in grinding-machinery without hazard. Because of thelow volatility of the alkyl oleates the active agents remain in a fluid and active state. Most important of all, however, is the unusual degree .ofcom- I patibility of compositions of this invention with man common formulations of other pesticides.
- a miticid-al composition comprising asian active miticidal agent a 1,1-bis(halophenyl)-2,2,2 trichloroethanol dissolved in an alkyl oleate'in which the alkyl group contains one to two carbon atoms together with emulsify- 'ing agents consisting of a surface active ethyleneoxide adduct having 15 to 100 ether units and a-surfaceactive oil-soluble alkylarenesulfon-ate, the ratio of the ethylene oxide adduct to the alkylarenesulfonate varying' from about 3:1 to about 1:1 by weight.
- a miticidal composition comprising'asian active miticidal agent 1,1-bis(chlorophenyl)-2,2,2-triohloroethanol and emulsifying agents dissolved in an alkyl oleate in which the alkyl group contains one to two carbon atoms, the ratio of said 1,1- bis(chlorophenyl)-2,2,2-trichloroethanol to said alkyl oleate 'being from 1:4 to 1.25 :1 and the emulsifying agents consisting of a surface active ethylene oxide adduct having 15 to 100 ether units and a surface active oil-soluble alkylarenesulfonate, theratio of the ethylene oxide adduct to the ialkylarenesulfonate I varying from about 3:1 to about 1:1 by weight.
- a miticidal composition in the form of a wettable powder comprising a finely divided inert solidcarrying a solution of 1,1-bis(-chlorophenyl)-2,2,2-trichloroethanol and emulsifying agents in an alkyl oleate in which the arenas/o alkyl group contains one to two carbon atoms, the ratio of said 1,1-bis (chlorophenyl)-2,2,2-trichloroethanol to said alkyl oleate being from 1 :4 to 1.25:1 and the emulsifying agents consisting of a surface active ethylene oxide adduct having to 100 ether units and a surface active oil-soluble alkylarenesu-lfonate, the ratio of the ethylene oxide adduct to the alkylarenesulfonate varying from about 3:1 to about 1:1 by Weight.
- a rniticidal composition comprising a solution of 1,1-bis(chlorophenyl)-2,2,2-trichloroethancl and emulsifying agents in at least one alkyl oleate in which the alkyl group contains one to two carbon atoms, the ratio of said l,l-bis(chlorophenyl)-2,2,2-trichloroethanol to said alkyl oleate being from 1:4 to 1.25:1 and the emulsifying agents consisting of a surface active ethylene oxide adduct having 15 to 100 ether units and a surf-ace active, oil-soluble alkylbenzenesulfonate wherein the alkyl group contains from 8 to 18 carbon atoms, the ratio of the ethylene oxide adduct to the alkylbenzenesulfonate varying from about 3:1 to about 1:1 by weight, the said emulsifying agents providing about 9% to of the weight of the solution.
- a miticid al composition in the form of a wettable powder comprising a finely divided inert solid carrying a solution of 1,1-bis(chlorophenyl)-2,2,2-trichloroethanol and emulsifying agents in an alkyl oleate in which the a-llryl group contains one to two carbon atoms, the ratio of said 1,1-bis(chlorophenyl)-2,2,2-trichloroethanol to calcium alkylbenzenesu-lfonate is calcium dodecylbenzenesaid alkyl oleate being from 1:4 to 1.25 :1 land the emulsifying agents consisting of a surface active ethylene oxide adduct having 15 to 100 ether units and a surface active, oil-soluble ialkylbenzenesulfonate wherein the alkyl substituent contains from 8 to 18 carbon atoms, the ratio of the ethylene oxide adduct to the alkylbenzene sulfonate varying from
- composition according to claim 5 in which there is added to the Wettable powder 1% to 10% by weight of a dispersing agent.
- composition according to claim 6 in which the dispersing agent is a salt of a polymer of maleic anhydride and diisobutylene.
- a miticidal composition in the form of a Wettable powder comprising a finely divided hydrated silica carrying a solution of 1,1- bis(chlorophenyl)-2,2,2-trichloroethanol and emulsifying agents in methyl oleate, the ratio of said 1,1-bis-(ch1orophenyl)-2,2,2-trichloroethanol to said methyl oleate being from 1:4 to 1.25:1 and the emulsifying agents consisting of an alkylphenoxypolyethoxyethanol having 20 to 70 ether units and containing 8 to 12 carbon atoms in its alkyl substituent and a surface active, oil-soluble calcium alkylbenzenesulfonate wherein the alkyl substituent contains from 8 to 18 carbon atoms, the ratio of the alkylphenox'ypolyethoxyethanol to the calcium alkyl'benzenesulfonate being about 3:1 to
- the said emulsifying agents providing about 9% to 20% of the Weight of the solution, and the percentage of the said 1,1-bis(chlorophenyl)-2,2,2-
- a miticidal composition comprising a solution of 1, 'l-bis (chlorophenyl -2,2,2-t-richloroethanol and emulsifying agents in methyl oleate, the ratio of said 1,1-bis- (ch lorophenyl)-2,2,2-trichloroethanol to methyl oleate being from 1:2 to 1:1 and the emulsifying agents consisting of an alkylphenoxypo lyethoxyethanol having 20 to other units and containing 8 to 12 carbon atoms in its alltyl substituent and a surface active, oil-soluble calcium alkylbenzenesulfonate wherein the alkyl substituent contains from 8 to 18 carbon atoms, the ratio of the ialkylphenoxypolyethoxyethanol to the calcium aikylbenzenesulfonate being about 3:1 to about 1:1 byweight, the said emulsifying agent providing about 9% to 20% of the weight of the solution.
- composition according to claim 11 in which the a1kylphenoxypolyethoxyethanol is diisobutylphenoxypolyethoxyethanol.
- a composition according to claim 11 in which the calcium alkylbenzenesulfonate is calcium dodecylbenzenesu'lfonate.
- a miticid al composition comprising :a solution of about 50% by weight of 1,l-bis(chlorophenyl)-2,2,2-trichloroethanol and 10% by weight of emulsifying agents in methyloleate, the emulsifying agents consisting of pdiisobutylphenoxypolyethoxyethano1 containing about 30 ether groups and calcium dodecylbenzenesulfonate in about equal weights.
- a miticidal composition comprising about 50% by weight of a finely divided hydrated silica carrying about an equal weight of a solution of about 50 parts by weight of '1,l-bis(chlorophenyl)-2,2,24trichloroethano1 and 10 parts by weight of emulsifying agents dissolved in 40 parts by weight of methyl oleate, the emulsifying agents consisting of p-diisobutylphenoxypolyethoxyethanol containing about 30 ether groups and calcium dodecylbenzenesulfonate in about equal weights.
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Description
United States Patent 3,102,117 0 MITICIDAL (JGMPOSITIUNS Gerard C. Riley, Churchville, and Edward A. Nolan, Philadelphia, Pa., assignors to Rohm & Haas Company, Philadelphia, Pa, a corporation of Delaware N0 Drawing. Filed May 12, 1961, Ser. No. 109,505 15 Claims. (til. 167-390) This invention concerns pesticidal compositions which contain 1,1-bis(halophenyl)-2,2,2-trichloroethanol dissolved in an alkyl oleate in which the alkyl group contains one to two carbon atoms.
Pesticides, such as insecticides and miticides, are commonly formulated as emulsion concentrates and wettable powders for spray purposes, as dusts, and as aerosols. In the control of mites on agricultural and horticultural crops, it is common to apply emulsion concentrates or wettable powders in aqueous sprays. A particularly effective miticide for use in such sprays is l,l-bis (p -chlorophenyl) -2,2,2-trichloroetlranol. It is usual practice to use this agent in conjunction with other types of pesticidal agents. For this purpose emulsion concentrates or wettable powders of these other agents are used in the same aqueous mixture as this miticide.
Often when this is done there is incompatibility. This incompatibility usually manifests itself in the formation of agglomerates or curds. This phenomenon is commonly known as greasing out. The curdy or clabber-like material often accumulates at the surface of the spray mixture or on the sides of the spray tank and it may clog screens. Since it is not readily redispersed into the spray liquid, it is rendered unavailable for spray purposes. It
is also conceivable that this type of incompatibility could occur on a leaf surface :as well as in a spray tank when at least two pesticides are applied to leaf surfaces.
There are other situations wherein the pesticidal formulations of the art are reduced in effectiveness as when climatic conditions, such as low temperature, prevent the pesticidal formulations from acting in their optimum manner.
In the cold, for example, the 1,1-bis(halophenyl)-2,2,2- trichloroethanols as heretofore applied tend to become somewhat horny and thus become less active against mites. Yet these same compounds have been found highly effective under warmer conditions. It is, therefore, desired to so formulate them as to increase their activity under a wide range of climatic conditions. Of course, such formulations should not only be compatible with other common pesticidal formulations so as. to permit their conjoint application, but also they must be relatively nonphytotoxic to the host plants.
The l,l-bis(halophenyl)-2,2,2-trichloroethanols are miticidal agents, the preparation of which is described in US. Patents No. 2,812,280 and 2,812,362. The product, 1,1-bis(chlorophenyl)-2,2,2 trichloroethanol is a wellknown commercial miticide and there are various pesticidal compositions which utilize it as an active miticide.
In accordance with the present invention, emulsion concentrates and wettable powder formulations containing a l,l-bis(halophenyl)-2,2,2-trichloroethanol as an active mirticidal agent have been evolved which show excellent compatibility when admixed in a spray tank with other formulated pesticides, which promise favorable miticidal effectiveness under adverse .climatic conditions, and which have acceptable phytotoxic properties.
The emulsion concentrates of this invention comprise 1,l-bis(halophenyl)-2,2,2-tnichloroethanol dissolved in an alkyl oleate with the incorporation of emulsifying agent.
. The ratio of the 1,1=bis(halophenyl)-2,2,2-trich1oroethanol to alkyl oleate may be varied from one part of such compound to four parts of the alkyl oleate to 1.25 parts to one part. Preferably, the ratios are from 1:2 to 1:1.
Emusifying agents are used in the concentration range of about 9 to about 20% by weight based on the emulsifialble concentrate and preferably 10% to 15%.
If desired, other pesticides may be incorporated. For example, dinitroallcylphenyl, especially the dinitro(2- methylheptyl)-phenyl, esters of crotonic, acrylic, methacrylic, 5,,8-dimethylacrylic, and 4 pentenoic acids which have been shown to have miticidal, insecticidal, and fungicidal properties may be advantageously added to these concentrates, and likewise such insecticidal agents as 1,1,1- trichloro-2,2bis (p-chlorophen-yl) ethane, 1, 1-dichloro-2,2- bis(p-chlorophenyl)ethane, or 1,1-dichloro-2,2-bis(ethy1- phenyl)-ethane, phosphatic pesticides such as 0,0-dimethyl S-(LZ-diCBIbdthOXYCt-hfl) dithicphosphate, and l-na-phthyl N-methylcarbamate. It is often desirable to blend 1,1-bis(halophenyl)-2,2,2-trichloroethanol with pesticidal agents which kill mite predators and which, when used alone, thus cause a build-up of the mite population. In general from 5 to 25% of pesticidal agents of the above type may be added to an emulsion concentrate. The percentage depends in part on the solubility of the particular pesticidal agent being incorporated.
The wettable powder formulations of this invention are made by mixing an inert, finely-divided, solid carrier with the emulsion concentrate. There may be used from 5% to 25% by weight of 1,l bishalophenyl)-2,2,2-trichl0roethanol in such compositions, this compound being dissolved in alkyl oleate together with emulsifiers. The amount of the emulsion concentrate added to the inert solid will vary with the capacity of each individual carrier or combination of carriers to hold the liquid and still maintain the product as a powder of loose texture.
The preferred 1,l bis(halophenyl)-2,2,2-trichloroethan- 01 used in this invention is 1,1-bis(p-chlorophenyl)-2,2,2- 'trichloroethanol. It may be used in a pure form or as a technical grade containing isomers having bis(orthochlorophenyl) groups and the p, o dichlorc-dip henyl groups as minor components. Also, the corresponding bromophenyl and fluorophenyl analogs may be used alone or admixed with 1,l-bis(chloropheny1) -2,2,2-trich1oroethanol.
As the solvent for the preparation of the emulsion concentrates there is used methyl oleate, ethyl oleate, or mixtures of these two. One purpose of the solvent is to act as a plasticizer for the l,l-bis(-halophenyl)-2,2,2-trichloroethanol and thus keep the active ingredient in a fluid condition at low temperatures. It is also desirable to have the emulsion concentrates flowable after prolonged storage at ambient temperatures in cold weather. 'For these reasons the oleic acid ester or mixture of esters used must have a low setting point; i.e., the temperature range wherein a solid forms. This point will vary with purity of the oleates and should be no more than 60 (about 16 C.). There may be used relatively pure alkyl oleates or commercially available technical products.
As emulsifying agents there may be used surface active ethylene oxide adducts of alkyl mercaptans, long-chained carboxylic acids, higher alcohols, and alkylphenols wherein the ethylene oxide content of the resulting product is about 15 to 100 ether units, preferably 20 to units. In general the alkyl mercaptans and higher alcohols should have 10 to 20 carbon atoms in their alkyl groups, while the acids should contain 12 to 24 carbon atoms in their carboxylic portion, which may be a straight or branched chain or a cycle, as in abietic acid. Typical of these are t-tetradecylthiopolyethoxyethanol, tall-oil-acid polyethoxyethanol, dodecyloxypolyethoxyethanol, and alkylphenoxypolyethoxyethanol, wherein the alkyl group or groups contain 8 to 12 carbon atoms and the main group occurs preferably in the para position but that position is immaterial. There may also be used ethylene oxide adducts -dodecylbenzenesulfonate.
pesticides.
"of'partia'l-ly esterified sorbitols and similar polyhydric alcohols, the esters being formed with such long-chained acids as oleic or lauric acids.
Also, there are used surface active, oil-soluble calcium and magnesium salts of alkylarenesulfonic aoids wherein the alkyl group or groups contain from 8 to 18 carbon atoms in admixtures with the above described ethylene 'oxide adducts. The preferred sulfonates are salts of alkylbenzenesulfonic acid, such as calcium p-t-dodecylbenzenesulfonate. There may also be used similar'alkyl 'naphthalenesulfonic acid salts, such as oalcium'octylnaphthalenesulfonates.
The ratio of weights of the ethylene oxide adduct to the sulfonate may vary from about 3 :1 to about 1:1.
' To prepare the wettable powders from the emulsion concentrates, a variety of finely dispersed solid carriers for the preparation of these wettable powders are the finely particled clays such as fullers earth and kaolins,
silica, diatomaceous earth, and alkaline earth silicates,
particularly those silicates which have been carbonated to'neutralize any basic impurities.
It is often desirable to incorporate dispersing agents I into the wettable powders. Typical of these are the salts of polymers formed from maleic anhydride and olefinically unsaturated hydrocarbons such as styrene, alkylstyrenes, or diisobutylene. When ammonia or some amines are used to form salts, some amide orimide formation also occurs. The amount of the added dispersit has good suspendibility in waters of varying hardness, and its application properties to foliage are entirely acceptable from its aqueous sprays.
In place of the above sodium salt used as a dispersant there may be used other common dispersing agents such as sodium or calcium lignosulfonates. These serve to provide good suspendibility, but it has been observed that compositions utilizing these sulfonates tend to deteriorate on extended storage. This improvement in suspendabili-ty in recently prepared mixtures is also observed when the dispersing agent is a salt of a condensed formaldehyde-naphthalene sulfonate such as sodium formaldehyde-naphthalene sulfonate as sold under the trade names of Daxad or Tamol.
ingagent is desirably 1% to 10% of the weight of the powderto which it is added.
Typical formulations and products of this invention are illustrated by the following examples. Parts are by weight unless otherwise designated.
'added 5' parts of p-diisobutylphenoxypolyethoxyethanol containing about 30 ether groups and 5 parts of calcium The mixture is stirred and warmed until homogeneous.
The resulting emulsion concentrate may be diluted with water to provide an efficient spray for protection against mites. It is compatible Wtih wettable powders containing fungicides such as wettable sulfur, ferbam, zineb, and
" maneb, with DDT, and with phosphatics.
(b) There are taken 50 parts of the above emulsion This powder is compatible with preparations of other Example 2 methylbenzenesulfonate. The product is useful and effecfive as an emulsion concentrate and can be diluted with water for spraying. It is compatible with the usual preparations of other pesticides.
(b) There are mixed 40 parts of the above emulsion concentrate, 50 parts of hydrated silica, and 10 parts of fullers earth. The mixture is then blended with five parts of 'the sodium salt formed from the copolymer from equal moles of maleic anhydride and diisobutylene. The resulting wettable powder is readily dispersed in water,
Example 3 (a) There are mixed 20 pants of technical 1,1-bis(cl1'lorophenyl)-2,2,2-trichloroethanol, 65' parts of methyl oleate (set point about 0 C.), and 15 parts of anemulsifier from 10 parts of long-chained fatty acid-ethylene oxide adduct, having'about ether groups perjmolecule and 5 parts of calcium tetradecylbenzenesulfonate. The resulting emulsion concentrate is stable on storage and is readily dispersed in even hard water to give effective aqueous sprays.
(b) There are mixed 50 parts of the above emulsion concentrate and 50 parts of finely divided sodium silicoaluminate (Zeolex 23) to form a useful wettable powder. The initial suspendibility is very good for this product, but storage characteristics are improved lay lblending therewith 3 to 10% of the ammonium salt of the copolymer from maleic anhydride, diisobutylene, and styrene.
The above formulation, repeatedwith substitution of an equal weight of ethyl oleate for the methyl oleate, provides another eflicient emulsion concentrate which, when blended with finely divided carriers, gives useful wettable powders. There may likewise be'used mixtures of methyl and ethyl oleates with like outcomes.
The emulsion concentrates of this invention can be readily formulated so as to he acceptably low in phytotoxicity on plants, even on flush citrus growth. Thisis also true of properly formulated wettable powders. 1 Since the alkyl oleates :are very high boiling and havehigh flash points, they can be used in grinding-machinery without hazard. Because of thelow volatility of the alkyl oleates the active agents remain in a fluid and active state. Most important of all, however, is the unusual degree .ofcom- I patibility of compositions of this invention with man common formulations of other pesticides.
We claim: 1. A miticid-al composition comprising asian active miticidal agent a 1,1-bis(halophenyl)-2,2,2 trichloroethanol dissolved in an alkyl oleate'in which the alkyl group contains one to two carbon atoms together with emulsify- 'ing agents consisting of a surface active ethyleneoxide adduct having 15 to 100 ether units and a-surfaceactive oil-soluble alkylarenesulfon-ate, the ratio of the ethylene oxide adduct to the alkylarenesulfonate varying' from about 3:1 to about 1:1 by weight.
2. A miticidal composition comprising'asian active miticidal agent 1,1-bis(chlorophenyl)-2,2,2-triohloroethanol and emulsifying agents dissolved in an alkyl oleate in which the alkyl group contains one to two carbon atoms, the ratio of said 1,1- bis(chlorophenyl)-2,2,2-trichloroethanol to said alkyl oleate 'being from 1:4 to 1.25 :1 and the emulsifying agents consisting of a surface active ethylene oxide adduct having 15 to 100 ether units and a surface active oil-soluble alkylarenesulfonate, theratio of the ethylene oxide adduct to the ialkylarenesulfonate I varying from about 3:1 to about 1:1 by weight.
3. A miticidal composition in the form of a wettable powder comprising a finely divided inert solidcarrying a solution of 1,1-bis(-chlorophenyl)-2,2,2-trichloroethanol and emulsifying agents in an alkyl oleate in which the arenas/o alkyl group contains one to two carbon atoms, the ratio of said 1,1-bis (chlorophenyl)-2,2,2-trichloroethanol to said alkyl oleate being from 1 :4 to 1.25:1 and the emulsifying agents consisting of a surface active ethylene oxide adduct having to 100 ether units and a surface active oil-soluble alkylarenesu-lfonate, the ratio of the ethylene oxide adduct to the alkylarenesulfonate varying from about 3:1 to about 1:1 by Weight.
4. A rniticidal composition comprising a solution of 1,1-bis(chlorophenyl)-2,2,2-trichloroethancl and emulsifying agents in at least one alkyl oleate in which the alkyl group contains one to two carbon atoms, the ratio of said l,l-bis(chlorophenyl)-2,2,2-trichloroethanol to said alkyl oleate being from 1:4 to 1.25:1 and the emulsifying agents consisting of a surface active ethylene oxide adduct having 15 to 100 ether units and a surf-ace active, oil-soluble alkylbenzenesulfonate wherein the alkyl group contains from 8 to 18 carbon atoms, the ratio of the ethylene oxide adduct to the alkylbenzenesulfonate varying from about 3:1 to about 1:1 by weight, the said emulsifying agents providing about 9% to of the weight of the solution.
5. A miticid al composition in the form of a wettable powder comprising a finely divided inert solid carrying a solution of 1,1-bis(chlorophenyl)-2,2,2-trichloroethanol and emulsifying agents in an alkyl oleate in which the a-llryl group contains one to two carbon atoms, the ratio of said 1,1-bis(chlorophenyl)-2,2,2-trichloroethanol to calcium alkylbenzenesu-lfonate is calcium dodecylbenzenesaid alkyl oleate being from 1:4 to 1.25 :1 land the emulsifying agents consisting of a surface active ethylene oxide adduct having 15 to 100 ether units and a surface active, oil-soluble ialkylbenzenesulfonate wherein the alkyl substituent contains from 8 to 18 carbon atoms, the ratio of the ethylene oxide adduct to the alkylbenzene sulfonate varying from about 3:1 to about 1:1 by Weight, the said emulsifying agents providing about 9% to 20% of the weight of the solution, and the percentage of the said 1,1-bis(chlorophenyl)-2,2,2-t1ich1oroethano=l being from 5% to 25% of the Weight of the composition.
6. A composition according to claim 5 in which there is added to the Wettable powder 1% to 10% by weight of a dispersing agent.
7. A composition according to claim 6 in which the dispersing agent is a salt of a polymer of maleic anhydride and =diisobutylene. i
8. A miticidal composition in the form of a Wettable powder comprising a finely divided hydrated silica carrying a solution of 1,1- bis(chlorophenyl)-2,2,2-trichloroethanol and emulsifying agents in methyl oleate, the ratio of said 1,1-bis-(ch1orophenyl)-2,2,2-trichloroethanol to said methyl oleate being from 1:4 to 1.25:1 and the emulsifying agents consisting of an alkylphenoxypolyethoxyethanol having 20 to 70 ether units and containing 8 to 12 carbon atoms in its alkyl substituent and a surface active, oil-soluble calcium alkylbenzenesulfonate wherein the alkyl substituent contains from 8 to 18 carbon atoms, the ratio of the alkylphenox'ypolyethoxyethanol to the calcium alkyl'benzenesulfonate being about 3:1 to
about 1:1 by weight, the said emulsifying agents providing about 9% to 20% of the Weight of the solution, and the percentage of the said 1,1-bis(chlorophenyl)-2,2,2-
sulfonate.
11. A miticidal composition comprising a solution of 1, 'l-bis (chlorophenyl -2,2,2-t-richloroethanol and emulsifying agents in methyl oleate, the ratio of said 1,1-bis- (ch lorophenyl)-2,2,2-trichloroethanol to methyl oleate being from 1:2 to 1:1 and the emulsifying agents consisting of an alkylphenoxypo lyethoxyethanol having 20 to other units and containing 8 to 12 carbon atoms in its alltyl substituent and a surface active, oil-soluble calcium alkylbenzenesulfonate wherein the alkyl substituent contains from 8 to 18 carbon atoms, the ratio of the ialkylphenoxypolyethoxyethanol to the calcium aikylbenzenesulfonate being about 3:1 to about 1:1 byweight, the said emulsifying agent providing about 9% to 20% of the weight of the solution.
12. A composition according to claim 11 in which the a1kylphenoxypolyethoxyethanol is diisobutylphenoxypolyethoxyethanol.
13. A composition according to claim 11 in which the calcium alkylbenzenesulfonate is calcium dodecylbenzenesu'lfonate.
14. A miticid al composition comprising :a solution of about 50% by weight of 1,l-bis(chlorophenyl)-2,2,2-trichloroethanol and 10% by weight of emulsifying agents in methyloleate, the emulsifying agents consisting of pdiisobutylphenoxypolyethoxyethano1 containing about 30 ether groups and calcium dodecylbenzenesulfonate in about equal weights.
15. A miticidal composition comprising about 50% by weight of a finely divided hydrated silica carrying about an equal weight of a solution of about 50 parts by weight of '1,l-bis(chlorophenyl)-2,2,24trichloroethano1 and 10 parts by weight of emulsifying agents dissolved in 40 parts by weight of methyl oleate, the emulsifying agents consisting of p-diisobutylphenoxypolyethoxyethanol containing about 30 ether groups and calcium dodecylbenzenesulfonate in about equal weights.
References Cited in the file of this patent UNITED STATES PATENTS? OTHER REFERENCES Mellan: Industrial Solvents, 2nd Ed., 19.50, published by Reinhold Publishing Corp, 330 West Forty-Second St, New York, New York, pages 166 (particularly page 16 2).
Claims (1)
1. A MITICIDAL COMPOSITION COMPRISING AS AN ACTIVE MITICICAL AGENT A 1,1-BIS(HALOPHENYL)-2,2,2-TRICHLOROERTHAND DISSOLVED IN AN ALKYL OLEATE IN WHICH THE ALKYL GROUP CONTAINS ONE TO TWO CARBON ATOMS TOGETHER WITH EMULSIFYING AGENTS CONSISTING OF A SURFACE ACTIVE ETHYLENE OXIDE ADDUCT HAVING 15 TO 100 ETHER UNITS AND A SURFACE ACTIVE OIL SOLUBLE ALKYLARENSULFONATE, THE RATIO OF THE ETHYLENE OXIDE ADDUCT TO THE ALKYARENESULFONATE VARYING FROM ABOUT 3:1 TO ABOUT 1:1 BY WEIGHT.
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US109505A US3102070A (en) | 1961-05-12 | 1961-05-12 | Miticidal compositions |
| BR138794/62A BR6238794D0 (en) | 1961-05-12 | 1962-05-04 | MITICIDE COMPOSITES |
| GB17529/62A GB995383A (en) | 1961-05-12 | 1962-05-07 | Miticidal containing 1,1-bis(halophenyl)-2,2,2-tri-chloroethanols |
| ES277137A ES277137A1 (en) | 1961-05-12 | 1962-05-08 | A procedure for preparing a mitricide agent in the form of emulsion concentrate or hemectable powder (Machine-translation by Google Translate, not legally binding) |
| AT390062A AT246491B (en) | 1961-05-12 | 1962-05-11 | Anti-mite agents |
| CH572862A CH409513A (en) | 1961-05-12 | 1962-05-11 | New acaricidal composition |
| MY196984A MY6900084A (en) | 1961-05-12 | 1969-12-31 | Miticidal containing 1,1,-bis (halophenyl) -2,2,2-tri-chloro-ethanols |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US109505A US3102070A (en) | 1961-05-12 | 1961-05-12 | Miticidal compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3102070A true US3102070A (en) | 1963-08-27 |
Family
ID=22328022
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US109505A Expired - Lifetime US3102070A (en) | 1961-05-12 | 1961-05-12 | Miticidal compositions |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3102070A (en) |
| AT (1) | AT246491B (en) |
| BR (1) | BR6238794D0 (en) |
| CH (1) | CH409513A (en) |
| ES (1) | ES277137A1 (en) |
| GB (1) | GB995383A (en) |
| MY (1) | MY6900084A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3256201A (en) * | 1955-09-27 | 1966-06-14 | Armour & Co | Antiseptic detergent compositions |
| US3442818A (en) * | 1965-03-12 | 1969-05-06 | Swift & Co | Emulsifiers for agricultural pesticides |
| US4357350A (en) * | 1978-05-17 | 1982-11-02 | Roussel Uclaf | Novel acaricide compositions |
| US4705902A (en) * | 1985-10-03 | 1987-11-10 | Rohm And Haas Company | DDTR-free 1,1-bis(chlorophenyl)-2,2,2-trichloroethanol |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2677849B1 (en) * | 1991-06-20 | 1995-06-16 | Francais Prod Ind Cfpi | PHYTOPHARMACEUTICAL WETABLE POWDERS AND THEIR PREPARATION METHOD. |
| JP3855321B2 (en) * | 1996-11-01 | 2006-12-06 | 住友化学株式会社 | Agrochemical composition |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2696453A (en) * | 1952-05-27 | 1954-12-07 | Herbert L Sanders | Emulsifiers and toxicants containing the same |
| US2812280A (en) * | 1954-04-20 | 1957-11-05 | Rohm & Haas | Preparation of bis (halophenyl) trichloroethanol |
| US2819996A (en) * | 1955-11-23 | 1958-01-14 | Rohm & Haas | Stabilized pesticidal emulsifier composition |
-
1961
- 1961-05-12 US US109505A patent/US3102070A/en not_active Expired - Lifetime
-
1962
- 1962-05-04 BR BR138794/62A patent/BR6238794D0/en unknown
- 1962-05-07 GB GB17529/62A patent/GB995383A/en not_active Expired
- 1962-05-08 ES ES277137A patent/ES277137A1/en not_active Expired
- 1962-05-11 AT AT390062A patent/AT246491B/en active
- 1962-05-11 CH CH572862A patent/CH409513A/en unknown
-
1969
- 1969-12-31 MY MY196984A patent/MY6900084A/en unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2696453A (en) * | 1952-05-27 | 1954-12-07 | Herbert L Sanders | Emulsifiers and toxicants containing the same |
| US2812280A (en) * | 1954-04-20 | 1957-11-05 | Rohm & Haas | Preparation of bis (halophenyl) trichloroethanol |
| US2819996A (en) * | 1955-11-23 | 1958-01-14 | Rohm & Haas | Stabilized pesticidal emulsifier composition |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3256201A (en) * | 1955-09-27 | 1966-06-14 | Armour & Co | Antiseptic detergent compositions |
| US3442818A (en) * | 1965-03-12 | 1969-05-06 | Swift & Co | Emulsifiers for agricultural pesticides |
| US4357350A (en) * | 1978-05-17 | 1982-11-02 | Roussel Uclaf | Novel acaricide compositions |
| US4705902A (en) * | 1985-10-03 | 1987-11-10 | Rohm And Haas Company | DDTR-free 1,1-bis(chlorophenyl)-2,2,2-trichloroethanol |
Also Published As
| Publication number | Publication date |
|---|---|
| ES277137A1 (en) | 1962-09-16 |
| GB995383A (en) | 1965-06-16 |
| CH409513A (en) | 1966-03-15 |
| AT246491B (en) | 1966-04-25 |
| BR6238794D0 (en) | 1973-05-10 |
| MY6900084A (en) | 1969-12-31 |
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