WO1989010693A1 - Enhanced activity arthropodicidal solution - Google Patents
Enhanced activity arthropodicidal solution Download PDFInfo
- Publication number
- WO1989010693A1 WO1989010693A1 PCT/US1989/001197 US8901197W WO8910693A1 WO 1989010693 A1 WO1989010693 A1 WO 1989010693A1 US 8901197 W US8901197 W US 8901197W WO 8910693 A1 WO8910693 A1 WO 8910693A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- agent
- solution
- active ingredient
- fatty acid
- chelating agent
- Prior art date
Links
- 230000000694 effects Effects 0.000 title claims abstract description 22
- 239000000203 mixture Substances 0.000 claims abstract description 53
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 44
- 239000000194 fatty acid Substances 0.000 claims abstract description 44
- 229930195729 fatty acid Natural products 0.000 claims abstract description 44
- 150000003839 salts Chemical class 0.000 claims abstract description 32
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 23
- 239000002738 chelating agent Substances 0.000 claims abstract description 22
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 20
- 239000004480 active ingredient Substances 0.000 claims abstract description 16
- 229910021645 metal ion Inorganic materials 0.000 claims abstract description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 11
- 229910052751 metal Inorganic materials 0.000 claims abstract description 10
- 239000002184 metal Substances 0.000 claims abstract description 10
- 230000014759 maintenance of location Effects 0.000 claims abstract description 7
- 239000004094 surface-active agent Substances 0.000 claims abstract description 5
- 229930195733 hydrocarbon Natural products 0.000 claims abstract 3
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract 3
- -1 unsaturated fatty acid salt Chemical class 0.000 claims description 40
- 239000000243 solution Substances 0.000 claims description 25
- 241000238421 Arthropoda Species 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 12
- 239000002253 acid Substances 0.000 claims description 11
- 229910019142 PO4 Inorganic materials 0.000 claims description 7
- 239000010452 phosphate Substances 0.000 claims description 7
- 150000002500 ions Chemical class 0.000 claims description 6
- 235000019832 sodium triphosphate Nutrition 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 229910001424 calcium ion Inorganic materials 0.000 claims description 4
- 239000008139 complexing agent Substances 0.000 claims description 3
- 235000011180 diphosphates Nutrition 0.000 claims description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical class [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 3
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 claims description 3
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical class [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 claims description 3
- 235000021122 unsaturated fatty acids Nutrition 0.000 claims description 3
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 claims 3
- 239000004215 Carbon black (E152) Substances 0.000 claims 2
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical class [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 claims 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 2
- 235000021317 phosphate Nutrition 0.000 claims 2
- 101100366942 Mus musculus Ston1 gene Proteins 0.000 claims 1
- 239000003352 sequestering agent Substances 0.000 abstract description 26
- 150000001735 carboxylic acids Chemical class 0.000 abstract 1
- 239000008233 hard water Substances 0.000 description 15
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 12
- 239000011734 sodium Substances 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 230000000749 insecticidal effect Effects 0.000 description 10
- 239000000344 soap Substances 0.000 description 10
- 239000004615 ingredient Substances 0.000 description 9
- RGHNJXZEOKUKBD-SQOUGZDYSA-M D-gluconate Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O RGHNJXZEOKUKBD-SQOUGZDYSA-M 0.000 description 8
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 8
- 229940050410 gluconate Drugs 0.000 description 8
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 7
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 7
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 7
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 7
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 7
- 241000196324 Embryophyta Species 0.000 description 6
- 239000005642 Oleic acid Substances 0.000 description 6
- 125000000129 anionic group Chemical group 0.000 description 6
- 230000007613 environmental effect Effects 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 6
- 230000003389 potentiating effect Effects 0.000 description 6
- 241000238631 Hexapoda Species 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 231100000419 toxicity Toxicity 0.000 description 5
- 230000001988 toxicity Effects 0.000 description 5
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 239000000174 gluconic acid Substances 0.000 description 4
- 235000012208 gluconic acid Nutrition 0.000 description 4
- 239000002917 insecticide Substances 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 241000238876 Acari Species 0.000 description 3
- 241000982105 Brevicoryne brassicae Species 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 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 3
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical class CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 239000008367 deionised water Substances 0.000 description 3
- 229910021641 deionized water Inorganic materials 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 3
- 230000007774 longterm Effects 0.000 description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 241000894007 species Species 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 241001454293 Tetranychus urticae Species 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 235000010323 ascorbic acid Nutrition 0.000 description 2
- 239000011668 ascorbic acid Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 239000013043 chemical agent Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 229940070765 laurate Drugs 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 231100000208 phytotoxic Toxicity 0.000 description 2
- 230000000885 phytotoxic effect Effects 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 230000021148 sequestering of metal ion Effects 0.000 description 2
- 239000008234 soft water Substances 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
- FDMXADMEKAUMIV-NSCUHMNNSA-N (e)-prop-1-ene-1,2-diamine Chemical compound C\C(N)=C/N FDMXADMEKAUMIV-NSCUHMNNSA-N 0.000 description 1
- QBIAZVPERXOGAL-OWOJBTEDSA-N (e)-prop-1-ene-1,3-diamine Chemical compound NC\C=C\N QBIAZVPERXOGAL-OWOJBTEDSA-N 0.000 description 1
- AEQDJSLRWYMAQI-UHFFFAOYSA-N 2,3,9,10-tetramethoxy-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinoline Chemical compound C1CN2CC(C(=C(OC)C=C3)OC)=C3CC2C2=C1C=C(OC)C(OC)=C2 AEQDJSLRWYMAQI-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 241001124076 Aphididae Species 0.000 description 1
- 241000239223 Arachnida Species 0.000 description 1
- 206010060969 Arthropod infestation Diseases 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- 241000258937 Hemiptera Species 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 239000004117 Lignosulphonate Substances 0.000 description 1
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 1
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 1
- 229910017677 NH4H2 Inorganic materials 0.000 description 1
- 239000003568 Sodium, potassium and calcium salts of fatty acids Substances 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 241000255993 Trichoplusia ni Species 0.000 description 1
- KFRFCPCUEHXWTN-UHFFFAOYSA-N [Na].[Na].[Na].[Na].NCCN Chemical compound [Na].[Na].[Na].[Na].NCCN KFRFCPCUEHXWTN-UHFFFAOYSA-N 0.000 description 1
- NHPKMFIBLXEDBI-UHFFFAOYSA-N acetic acid butane-1,4-diamine Chemical class CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O.NCCCCN NHPKMFIBLXEDBI-UHFFFAOYSA-N 0.000 description 1
- JTPLPDIKCDKODU-UHFFFAOYSA-N acetic acid;2-(2-aminoethylamino)ethanol Chemical compound CC(O)=O.CC(O)=O.CC(O)=O.NCCNCCO JTPLPDIKCDKODU-UHFFFAOYSA-N 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 229940072107 ascorbate Drugs 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- XMRUJYGYYCLRGJ-UHFFFAOYSA-N azanium;2-[2-[2-[2-(4-nonylphenoxy)ethoxy]ethoxy]ethoxy]ethyl sulfate Chemical compound [NH4+].CCCCCCCCCC1=CC=C(OCCOCCOCCOCCOS([O-])(=O)=O)C=C1 XMRUJYGYYCLRGJ-UHFFFAOYSA-N 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000001055 chewing effect Effects 0.000 description 1
- 229940001468 citrate Drugs 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- GHVNFZFCNZKVNT-UHFFFAOYSA-M decanoate Chemical compound CCCCCCCCCC([O-])=O GHVNFZFCNZKVNT-UHFFFAOYSA-M 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl group Chemical class [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 238000003898 horticulture Methods 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 1
- 235000019357 lignosulphonate Nutrition 0.000 description 1
- 229940049918 linoleate Drugs 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 229910001425 magnesium ion Inorganic materials 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- 150000002763 monocarboxylic acids Chemical group 0.000 description 1
- 229940105132 myristate Drugs 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- FBUKVWPVBMHYJY-UHFFFAOYSA-M nonanoate Chemical compound CCCCCCCCC([O-])=O FBUKVWPVBMHYJY-UHFFFAOYSA-M 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- 150000002889 oleic acids Chemical class 0.000 description 1
- 125000001477 organic nitrogen group Chemical group 0.000 description 1
- RECVMTHOQWMYFX-UHFFFAOYSA-N oxygen(1+) dihydride Chemical compound [OH2+] RECVMTHOQWMYFX-UHFFFAOYSA-N 0.000 description 1
- 229960003330 pentetic acid Drugs 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000003348 petrochemical agent Substances 0.000 description 1
- 230000008654 plant damage Effects 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 235000013966 potassium salts of fatty acid Nutrition 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical class C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 1
- 239000000176 sodium gluconate Substances 0.000 description 1
- 235000012207 sodium gluconate Nutrition 0.000 description 1
- 229940005574 sodium gluconate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- PWWJJDVDTKXWOF-UHFFFAOYSA-M sodium;2-[hexadecanoyl(methyl)amino]ethanesulfonate Chemical compound [Na+].CCCCCCCCCCCCCCCC(=O)N(C)CCS([O-])(=O)=O PWWJJDVDTKXWOF-UHFFFAOYSA-M 0.000 description 1
- IZWPGJFSBABFGL-GMFCBQQYSA-M sodium;2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS([O-])(=O)=O IZWPGJFSBABFGL-GMFCBQQYSA-M 0.000 description 1
- 238000007614 solvation Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 238000012956 testing procedure Methods 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- 239000002699 waste material Substances 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/06—Unsaturated carboxylic acids or thio analogues thereof; Derivatives thereof
Definitions
- This invention relates to arthropodicidal solutions and more particularly to aqueous solutions effective in controlling phytophagous insects and arachnids characterized by enhanced arthropodicidal effectiveness and improved environmental compatability.
- insecticides has greatly enhanced agricultural productivity, but it has become apparent that there are limits to the amount of petrochemical base materials that safely can be absorbed into the environment. Catastrophic, unanticipated, relatively long term effects experienced with materials such as DDT have increased awareness of the potentially dangerous environmental impact of widespread use of synthetics, contributed to the creation of regulatory agencies charged with protecting the environment, and promoted the development of potent, but apparently less dangerous insecticidal materials made from petrochemicals. These new insecticides are nevertheless far from ideal from the point of view of environmental safety, and sometimes collect in food and fresh water resources.
- Salts of fatty acids primarily sodium or potassium fatty acid soaps, recently have been used as an insecticide.
- Compositions having excellent insecticidal properties which exploit these salts are available commercially under the trademark SAFER INSECTICIDAL SOAP.
- SAFER INSECTICIDAL SOAP These fatty acid soaps are naturally occurring materials having no known long-term environmental effects. They are effective against mites and soft bodied insects such as aphids and whiteflies, but less effective against other types of arthropods.
- the invention comprises a method of protecting a plant from phytophagous arthropod infestation, e.g., from damage caused by sucking or chewing hard or soft bodied insects, and a composition used by direct application to the plant and the infesting arthropods by, for example, conventional spray application.
- the composition comprises an aqueous solution of an arthropodicidally effective amount of a composition comprising an arthropodicidally active monocarboxylic fatty acid and/or its monovalent metal salt and a sequestering agent for metal ions present together with the active components in solution in an amount sufficient to increase the arthropodicidal effect of the fatty acid active ingredients.
- the active ingredient comprises a mixture of monovalent metal salts, e.g., potassium or sodium salts, of fatty acids having eight to twenty carbon atoms.
- Monocarboxylic acid salts having eight to twelve carbon atoms work well.
- the fatty acid salt component of the solution is rich in unsaturated fatty acid salts having eighteen carbon atoms in the hydrocarbon chain, e.g., contains a substantial content of oleic and linoleic acid esters. The potentiating effect has been observed both with active salts and active acids.
- the active ingredients are referred to collectively herein as fatty acid salts.
- the nature of the sequestering agent used in the potentiated composition determines the optimal concentration of sequestering agent in a given preparation.
- the ratio of fatty acid salts to sequestering agent, on a weight basis can vary between 1:0.05 to 1:5, but usually the agent is present in amounts no greater than the fatty acid salt content. Ratios outside these ranges may be used, but result generally in barely significant improvement at the lower amounts of sequestering agent or reagent waste at the higher amounts.
- Useful sequestering agents include chelating agents, for example, organic nitrogen-containing and/or carboxylic acid-containing chelating agents, hard water ion complexing agents, particularly those comprising phosphate groups such as water-soluble phosphate salts, pyrophosphates, and tripolyphosphates, and dispersing agents having a high affinity for hard water ions, preferably anionic or nonionic dispersing agents. While the reasons why such sequestering agents have the ability to increase toxicity of fatty acid salts to arthropods is unknown, it is clear that the observed effect is not simply a matter of preventing formation of lime soap and resulting precipitation in the presence of hardness ions because the enhanced effect is observed in both hard and soft waters, including deionized water.
- chelating agents for example, organic nitrogen-containing and/or carboxylic acid-containing chelating agents, hard water ion complexing agents, particularly those comprising phosphate groups such as water-soluble phosphate salts, pyrophosphates, and trip
- the arthropodicide of the invention employs an- arthropodicide comprising monocarboxylic fatty acid monovalent metal salts or acids and a metal ion sequestering agent. Either one, or preferably, a mixture of fatty acid salts are normally employed. Preferred fatty acid salts are those having between eight, and twenty carbon atoms in a straight chain structure with the alpha carbon comprising a monocarboxylic acid moiety esterified, preferably completely, with a monovalent metal such as sodium or potassium. This group of fatty acids are known to have insecticidal activity, and have been used for many years in the control of pestiferous arthropods. These materials are widely commercially available.
- coconut oils comprising predominantly a mixture of laurate (C-12) and myristate (C-14) . They are also derived from various plant and animal sources.
- the preferred fatty acids are those having eight to eighteen carbon atoms including caprylate and stearate. Most preferred are unsaturated, eighteen carbon atom salts such as alkali metal oleate and linoleate, and saturated eight to twelve carbon atom salts such as mixtures of alkali metal caprylate, pelargonate, caprate, undecylinate and laurate.
- a preferred composition comprises the fatty acid salt component of solutions available from Safer, Inc. of Wellesley, Mass. under the trademarks SAFER INSECTICIDAL SOAP.
- the composition of this product varies slightly from batch to batch, but always includes at least about 35% salt, or acid form, oleic acid, and at least about 6% salt, or acid form, linoleic acid.
- the remainder of the solutes comprise other fatty acids or salts having between 12 and 20 carbon atoms.
- the soap component is present in the commercial concentrate at levels in the range of 50% by weight.
- the toxicity of the composition has been greater than the sum of the toxicities of the individual ingredients in all cases tested to date.
- the result-effective chemical property of the sequestering agents useful in the composition of the invention appears to be their ability to reduce the chemical activity of metal ions, and particularly divalent metal ions. This is a known property of many chelating agents and sequestering agents. It also is a property of strong anionic, as well as some non-ionic and amphoteric surface active agents. In general, any composition useful in significantly "softening" water may be used in admixture with the fatty acid salts to improve their arthropodicidal activity.
- chelating agents which may be used are carboxylic acid chelating agents such as citrate, gluconate, and ascorbate, and alkylenepolyamine polyacetic acids such as nitrilotriacetic acid, N-2-hydroxyethylaminodiacetic acid, ethylenediamine tetraacetic acid (EDTA) , diethylene triamine penta acetic acid, N-2-hydroxyethyl ethylenediamine triacetic acid, propylene-1, 2-diamine tetracetic acid, propylene-1, 3-diamine tetracetic acid, and the isomeric butylenediamine tetraacetic acids. Either an alkali metal salt or alkanolamine salt of these chelating agents may be used.
- sequestering agents useful in the composition of the invention are water-soluble phosphate-containing sequestering agents such as tripolyphosphates and phosphate salts. Excellent results have been observed using NH.H-PO..
- anionic surfactants such as alkali metal or ammonium salts of lauryl alkanolamide sulphosuccinate, alkylarylpolyether sulphates and sulfonates, coco-isethionate and lignosulphonates.
- amphoteric surfactants such as the water soluble salts of coco-betaine, coco-amphocarboxlyglycinate, coco-sulphobetaine, and imidazoline.
- Non-ionic surfactants such as alkylphenolethoxylate, and compounds known to be useful to sequester hard metal ions, such as alkylphenolethoxylated phosphate, ci:tx-ate.> or fatty acid esters.
- alkylphenolethoxylated phosphate ci:tx-ate.> or fatty acid esters.
- compatible mixtures and blends of any of the foregoing may also be used.
- sequestering agents which may be used to formulate insecticidal compositions embodying the invention.
- non-insectidically active fatty acids and other ingredients such as alcohol
- minor amounts of non-insectidically active fatty acids and other ingredients may be included to function as carriers, solvation aids, adjuvants, emulsifiers, spreaders, stabilizers, preservatives, etc.
- compositions may be manufactured simply by mixing the ingredients together in water.
- the compositions are supplied to the trade as a concentrate which is diluted, either with hard or soft water, and applied directly to the leaves and fruit of plants and the arthropods present thereon as a spray using conventional spraying equipment.
- a preferred ready-to-use solution has a fatty acid salt concentration on the order of 1% by weight.
- the fatty acid salt component of the composition comprise naturally occurring substances which have no known long-term environmental effects. Sequestering agent are ubiquitous in commerce. Many are approved as food additives, and the environmental effect of their use in insecticidal compositions is minimal.
- the composition provides an effective arthropodicide useful in controlling plant damage caused by phytophagous insect and other arthropod species which is environmentally preferred over petrochemical based insecticides currently used in agriculture and horticulture.
- the composition is appropriate for use in enclosed environments such as living space and greenhouses.
- the amount of fatty acid salts required to obtain a given level of insect kill is substantially reduced. Since fatty acid salts can be phytotoxic when used at higher concentration, the addition of the potentiating agent to such compositions provides a more economical and less phytotoxic solution permitting use of lower concentrations of active ingredients.
- compositions were made by mixing together in soft or deionized water (excepting where use of hard water is specifically set forth) a potentiating agent and a fatty acid salt or mixture in the various absolute concentrations and weight ratios indicated.
- a potentiating agent and a fatty acid salt or mixture in the various absolute concentrations and weight ratios indicated.
- statistically significant data were collected on the effects of compositions embodying the invention, and on the various individual components used separately, on various target species, using established, controlled, testing procedures.
- the examples illustrate the invention but should not be regarded as limiting.
- Pesticidal potassium salts of fatty acids obtained commercially and derived from botanical and animal sources rich in saturated and unsaturated eighteen carbon monocarboxylic fatty acids (K salts) were mixed with tetrasodium ethylenediamine tetracidic acid (EDTA) in a ratio of fatty acid salt to chelator ranging from 1:0.25 to 1:1.
- EDTA tetrasodium ethylenediamine tetracidic acid
- potassium salts of coconut oil fatty acids (approximately 45% C-12, lesser amounts of C-14, unsaturated C-18, and other fatty acids) are mixed with sodium gluconate at a 1:1.5 ratio of salt to sequestering agent and sprayed on cabbage aphids.
- the percent mortalities observed when the spray contained the components individually andi in admixture at two different absolute concentrations (1:1.5 ratio) are set forth in Table 3 below.
- Lime soap dispersing agents useful in water softening applications also behave as potentiating agents.
- Several commercially available anionic and nonionic surfactant materials having insignificant arthropodicidal activity alone were tested in admixture with SIS in both hard and deionized water in controlled experiments on cabbage aphids and mites. Results are set forth below.
- Oleic acid 0.05%) 16 Oleic acid (0.2%) 60 Gluconic acid (0.15%) 3
- the invention may be embodied in other specific forms.
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Abstract
Disclosed are arthropodicidal solutions for application to plants comprising, as an active ingredient, arthropodicidally active mono alpha carboxylic acids, of hydrocarbons having 8 to 20 carbon atoms, and/or monovalent metal salts thereof. The arthropodicidal activity of these fatty acids is potentiated by including in the solution an agent capable of sequestering metal ions such as one or a mixture of chelating agents, sequestering agents, and surfactants.
Description
ENHANCED ACTIVITY ARTHROPODICIDAL SOLUTION
Background of the Invention
This invention relates to arthropodicidal solutions and more particularly to aqueous solutions effective in controlling phytophagous insects and arachnids characterized by enhanced arthropodicidal effectiveness and improved environmental compatability.
The use of insecticides has greatly enhanced agricultural productivity, but it has become apparent that there are limits to the amount of petrochemical base materials that safely can be absorbed into the environment. Catastrophic, unanticipated, relatively long term effects experienced with materials such as DDT have increased awareness of the potentially dangerous environmental impact of widespread use of synthetics, contributed to the creation of regulatory agencies charged with protecting the environment, and promoted the development of potent, but apparently less dangerous insecticidal materials made from petrochemicals. These new insecticides are nevertheless far from ideal from the point of view of environmental safety, and sometimes collect in food and fresh water resources.
Salts of fatty acids, primarily sodium or potassium fatty acid soaps, recently have been used as an insecticide. Compositions having excellent insecticidal properties which exploit these salts are available commercially under the trademark SAFER
INSECTICIDAL SOAP. These fatty acid soaps are naturally occurring materials having no known long-term environmental effects. They are effective against mites and soft bodied insects such as aphids and whiteflies, but less effective against other types of arthropods.
While the mode of activity of monovalent metal salts of monocarboxylic fatty acids has not been elucidated, it is apparent that this type of active compound must be dissolved in water in order to exhibit its arthropodicidal activity. When concentrates of SAFER INSECTICIDAL SOAP are diluted with hard water, i.e., water containing significant quantities of calcium and/or magnesium ions, the monocarboxylic acid anions tend to precipitate leading to reduced arthropodicidal activity.
It is an object of this invention to provide an arthropodicidally active solution of monovalent metal salts of fatty acids which have potentiated arthropodicidal activity and which can be diluted with water from various sources, having various concentrations of hardness ions, without reducing the arthropodicidal activity of the solution per unit weight of active salt. Another object is to provide a method of protecting plants from phytophagous arthropods comprising applying to the plant a potentiated solution of monocarboxylic fatty acids or their monovalent metal salts.
These and other objects of the invention will be apparent from the following.
Summary of the Invention
It has now been discovered that known chemical agents capable of sequestering metal ions can act as potentiators or synergists for arthropodicidally active aqueous solutions of monocarboxylic fatty acids and their monovalent metal salts. The enhanced activity has been observed with a wide variety of known chemical agents useful for sequestering metal ions, including various chelating agents, other substances which complex metal ions or otherwise mask the chemical activity of such ions in other than classical polydentate chelate structures, and surface active agents capable of sequestering metal ions in solution by micelle formation or otherwise.
Broadly, the invention comprises a method of protecting a plant from phytophagous arthropod infestation, e.g., from damage caused by sucking or chewing hard or soft bodied insects, and a composition used by direct application to the plant and the infesting arthropods by, for example, conventional spray application. The composition comprises an aqueous solution of an arthropodicidally effective amount of a composition comprising an arthropodicidally active monocarboxylic fatty acid and/or its monovalent metal salt and a sequestering agent for metal ions present together with the active components in solution in an amount sufficient to increase the arthropodicidal effect of the fatty acid active ingredients. Preferably, the active ingredient comprises a mixture of monovalent metal
salts, e.g., potassium or sodium salts, of fatty acids having eight to twenty carbon atoms. Monocarboxylic acid salts having eight to twelve carbon atoms work well. Most preferably, the fatty acid salt component of the solution is rich in unsaturated fatty acid salts having eighteen carbon atoms in the hydrocarbon chain, e.g., contains a substantial content of oleic and linoleic acid esters. The potentiating effect has been observed both with active salts and active acids. The active ingredients are referred to collectively herein as fatty acid salts.
Broadly, the nature of the sequestering agent used in the potentiated composition determines the optimal concentration of sequestering agent in a given preparation. Generally, the ratio of fatty acid salts to sequestering agent, on a weight basis, can vary between 1:0.05 to 1:5, but usually the agent is present in amounts no greater than the fatty acid salt content. Ratios outside these ranges may be used, but result generally in barely significant improvement at the lower amounts of sequestering agent or reagent waste at the higher amounts. Useful sequestering agents include chelating agents, for example, organic nitrogen-containing and/or carboxylic acid-containing chelating agents, hard water ion complexing agents, particularly those comprising phosphate groups such as water-soluble phosphate salts, pyrophosphates, and tripolyphosphates, and dispersing agents having a high affinity for hard water ions, preferably anionic or nonionic dispersing agents.
While the reasons why such sequestering agents have the ability to increase toxicity of fatty acid salts to arthropods is unknown, it is clear that the observed effect is not simply a matter of preventing formation of lime soap and resulting precipitation in the presence of hardness ions because the enhanced effect is observed in both hard and soft waters, including deionized water.
The foregoing and other features of the invention will be apparent from the description and claims which follow.
Detailed Description
The arthropodicide of the invention employs an- arthropodicide comprising monocarboxylic fatty acid monovalent metal salts or acids and a metal ion sequestering agent. Either one, or preferably, a mixture of fatty acid salts are normally employed. Preferred fatty acid salts are those having between eight, and twenty carbon atoms in a straight chain structure with the alpha carbon comprising a monocarboxylic acid moiety esterified, preferably completely, with a monovalent metal such as sodium or potassium. This group of fatty acids are known to have insecticidal activity, and have been used for many years in the control of pestiferous arthropods. These materials are widely commercially available. They are produced from coconut oils, comprising predominantly a mixture of laurate (C-12) and myristate (C-14) . They are also derived from various plant and animal sources. The preferred fatty acids are those having eight to eighteen carbon atoms including caprylate and stearate. Most preferred are unsaturated, eighteen carbon atom salts such as alkali metal oleate and linoleate, and saturated eight to twelve carbon atom salts such as mixtures of alkali metal caprylate, pelargonate, caprate, undecylinate and laurate.
A preferred composition comprises the fatty acid salt component of solutions available from Safer, Inc. of Wellesley, Mass. under the trademarks SAFER INSECTICIDAL SOAP. The composition of this
product varies slightly from batch to batch, but always includes at least about 35% salt, or acid form, oleic acid, and at least about 6% salt, or acid form, linoleic acid. The remainder of the solutes comprise other fatty acids or salts having between 12 and 20 carbon atoms. The soap component is present in the commercial concentrate at levels in the range of 50% by weight.
When a metal ion sequestering agent is added to. these aqueous mixtures of fatty acid salts, they exhibit an unanticipated increase in mortality of pestiferous arthropods. The enhanced toxicity is evident even when the absolute concentration and relative amounts of active ingredients are varied. Optimal composition is dependent on the arthropod target species, the stage of arthropod growth, and anticipated temperature at application. Concentration ratios and absolute concentrations of ingredients of specific compositions readily can be optimized empirically. Some species of sequestering agents have been observed to be very mildly toxic to phytophagous arthropods. However, generally, even sequestering agents which are not themselves toxic to arthropods to any significant extent nevertheless may be used in accordance with the invention. In those instances where a sequestering agent intended for use in an experimental composition has been found to have some toxicity, the toxicity of the composition has been greater than the sum of the toxicities of the individual ingredients in all cases tested to date.
The result-effective chemical property of the sequestering agents useful in the composition of the invention appears to be their ability to reduce the chemical activity of metal ions, and particularly divalent metal ions. This is a known property of many chelating agents and sequestering agents. It also is a property of strong anionic, as well as some non-ionic and amphoteric surface active agents. In general, any composition useful in significantly "softening" water may be used in admixture with the fatty acid salts to improve their arthropodicidal activity.
Among the chelating agents which may be used are carboxylic acid chelating agents such as citrate, gluconate, and ascorbate, and alkylenepolyamine polyacetic acids such as nitrilotriacetic acid, N-2-hydroxyethylaminodiacetic acid, ethylenediamine tetraacetic acid (EDTA) , diethylene triamine penta acetic acid, N-2-hydroxyethyl ethylenediamine triacetic acid, propylene-1, 2-diamine tetracetic acid, propylene-1, 3-diamine tetracetic acid, and the isomeric butylenediamine tetraacetic acids. Either an alkali metal salt or alkanolamine salt of these chelating agents may be used.
Another class of sequestering agents useful in the composition of the invention are water-soluble phosphate-containing sequestering agents such as tripolyphosphates and phosphate salts. Excellent results have been observed using NH.H-PO..
Another class of agents which are capable of sequestering metal ions and may be used in compositions of the invention are anionic surfactants
such as alkali metal or ammonium salts of lauryl alkanolamide sulphosuccinate, alkylarylpolyether sulphates and sulfonates, coco-isethionate and lignosulphonates. Also useful are amphoteric surfactants such as the water soluble salts of coco-betaine, coco-amphocarboxlyglycinate, coco-sulphobetaine, and imidazoline. Non-ionic surfactants such as alkylphenolethoxylate, and compounds known to be useful to sequester hard metal ions, such as alkylphenolethoxylated phosphate, ci:tx-ate.> or fatty acid esters. Of course, compatible mixtures and blends of any of the foregoing may also be used. In summary, there is a wide variety of commercially available sequestering agents which may be used to formulate insecticidal compositions embodying the invention.
In addition to the foregoing, minor amounts of non-insectidically active fatty acids and other ingredients such as alcohol, may be included to function as carriers, solvation aids, adjuvants, emulsifiers, spreaders, stabilizers, preservatives, etc.
The compositions may be manufactured simply by mixing the ingredients together in water. Preferably, the compositions are supplied to the trade as a concentrate which is diluted, either with hard or soft water, and applied directly to the leaves and fruit of plants and the arthropods present thereon as a spray using conventional spraying equipment. A preferred ready-to-use solution has a fatty acid salt concentration on the order of 1% by weight.
The fatty acid salt component of the composition comprise naturally occurring substances which have no known long-term environmental effects. Sequestering agent are ubiquitous in commerce. Many are approved as food additives, and the environmental effect of their use in insecticidal compositions is minimal. Accordingly, the composition provides an effective arthropodicide useful in controlling plant damage caused by phytophagous insect and other arthropod species which is environmentally preferred over petrochemical based insecticides currently used in agriculture and horticulture. The composition is appropriate for use in enclosed environments such as living space and greenhouses.
Because of the potentiating effect of the chelating or sequestering agent, the amount of fatty acid salts required to obtain a given level of insect kill is substantially reduced. Since fatty acid salts can be phytotoxic when used at higher concentration, the addition of the potentiating agent to such compositions provides a more economical and less phytotoxic solution permitting use of lower concentrations of active ingredients.
In the examples which follow, all of the compositions were made by mixing together in soft or deionized water (excepting where use of hard water is specifically set forth) a potentiating agent and a fatty acid salt or mixture in the various absolute concentrations and weight ratios indicated. In each test, statistically significant data were collected on the effects of compositions embodying the invention, and on the various individual components
used separately, on various target species, using established, controlled, testing procedures. The examples illustrate the invention but should not be regarded as limiting.
Example 1
The effectiveness of various compositions embodying the invention was tested together with SAFER INSECTICIDAL SOAP (SIS) at various levels on two spotted spider mites. The tests were conducted by spraying the soap alone, the chelating agent alone, and then a mixture of the two for each test run. Percent kill was assessed for the components of the composition used individually, and these were added together to obtain the expected mortality. The data are set forth in Table 1 below.
Table 1
Ingredient % Mortaliity % Mortality (weight %) Observed Expected
A. SIS (0.05) 16.2
Na gluconate (0.075) 2.2 mix 50.2 18.4
B. SIS (0.05) 8.6
Na gluconate (0.12) 0 mix 92.2 8.6
C. SIS (0.05) 8.6
Na gluconate (0.15) 0 mix 100 8.6
D. SIS (0.05) 2.5, 6.3 ascorbic acid (0.15) 0, 5 mix 83.8, 72.5 2.5, 11
E. SIS (0.05) 21.4 Na EDTA (0.12) 4.3 mix 82.9 25 . 7
G. SIS (0.05) 3.8 Cheelox B-131 (0. ,15) 2.5 mix 63.8 6.3
H. SIS (0.2) 32.8 Na4 EDTA (0.12) 1.4 mix 84.3 34 .2
I. SIS (0.05) 10
Na tripolyphosphate (0. 12) 1 mix 64 11
J. 1000 ppm hard water 1.3
NH4H2P0 (0.12) in 500 ppm hard water 3.8
NH4H2PO4 (0.12) in 1000 ppm hard water 3.8
SIS (0.4) in 500 ppm hard water 17.5
SIS (0.4) in 1000 ppm hard water 11.3 mix in 500 ppm hard water 90.0 21.3 mix in 1000 ppm hard water 88.8 15 . 1
1. mixed sodium and alkanolamine salt of alkyldiamine polyacetic acid - G.A.F. corp.
As illustrated by the data, the presence of a chelating or sequestering agent uniformly increases the percent mortality of the fatty acid salts over that which could be expected based on the additive effects of the salt plus the sequestering agent. Furthermore, the effect is observed in hard water as well as tap water having a very low hardness ion content.
Example 2
Pesticidal potassium salts of fatty acids obtained commercially and derived from botanical and animal sources rich in saturated and unsaturated eighteen carbon monocarboxylic fatty acids (K salts) were mixed with tetrasodium ethylenediamine tetracidic acid (EDTA) in a ratio of fatty acid salt to chelator ranging from 1:0.25 to 1:1. The percent mortality induced by the individual components and by the mix was assessed in a standard test on cabbage loopers. The results are set forth in Table 2.
Table 2
Ingredient % Mortality % Mortality
(% bv weight) observed Expected
K salts (0.2) 37.5
EDTA (0.05) 25
EDTA (0.1) 10
EDTA (0.2) 27.5
K salt (0.2) + EDTA (0.05) 82.5 62.5
K salt (0.2) + EDTA (0.1) 77.5 47.5
K salt (0.2) + EDTA (0.2) 85.0 65.0
As is evident from the data, compositions ranging in fatty acid to sequestering agent ratio from 1:0.25 to 1:1 uniformly exhibit enhanced activity greater than could be expected from the additive effect of the sequestering agent and potassium fatty acid salts alone.
Example 3
In this example, potassium salts of coconut oil fatty acids (approximately 45% C-12, lesser amounts of C-14, unsaturated C-18, and other fatty acids) are mixed with sodium gluconate at a 1:1.5 ratio of salt to sequestering agent and sprayed on cabbage aphids. The percent mortalities observed when the spray contained the components individually andi in admixture at two different absolute concentrations (1:1.5 ratio) are set forth in Table 3 below.
Table 3
Ingredient % Mortality % Mortality (% by weight) observed Expected
K salt (0.2) 13
K salt (0.4) 26
Na gluconate (0.3) 8
Na gluconate (0.6) 9
K salt (0.2) + Na gluconate (0.3) 45 21
K salt (0.4) + Na gluconate (0.6) 78 35
This example again demonstrates the ability of sequestering agents to enhance insecticidal activity of fatty acid salts.
Example 4
Lime soap dispersing agents useful in water softening applications also behave as potentiating agents. Several commercially available anionic and nonionic surfactant materials having insignificant arthropodicidal activity alone were tested in admixture with SIS in both hard and deionized water in controlled experiments on cabbage aphids and mites. Results are set forth below.
Cabbage Aphids in Distilled Water
Ingredients Percent Mortality
(percent by weight)
SIS (0.4%) 73
SIS (0.4%) Agriwet T-F1 (0.1%) 89
SIS (0.4%) Stepfac 81702 (0.1%) 93
SIS (0.4%) Fenopon Co4363 (0.1%) 94
SIS (0.4%) Fenopon TN-744 (0.1%) 93
Mites in 1000 ppm Hard Water
SIS (0.4%) 4
Stepfac 81735 (0.06%) 31
Mix 63
1 sodium N-methyl-N-oleoyl taurate (anionic)
2 phosphate ester of alkyl phenoxy poly ethoxy ethanol (nonionic)
3 ammonium salt of sulfated nonyl phenoxy poly (ethyleneoxy) ethanol (anionic)
4 sodium-N-methyl-N-palmitoyl taurate (anionic)
5. phosphate ester of alkyl phenol polyethoxy ethanol (nonionic)
Example 5
In this experiment, oleic acid alone and in admixture with gluconic acid were assessed alone and together for arthropodicidal activity on two-spotted spider mites. The results are set forth below.
Ingredient Percent Mortality Percent Mortality (% by weight) Observed Expected
Oleic acid (0.05%) 16 Oleic acid (0.2%) 60 Gluconic acid (0.15%) 3
Oleic acid (0.05%) +
Gluconic acid (0.15%) 99 19
Oleic acid (0.2%) +
Gluconic acid (0.15%) 95 63
The invention may be embodied in other specific forms.
What is claimed is:
Claims
1. A method of protecting a plant from phytophagous arthropods comprising applying to the plant and arthropods thereon an aqueous solution of an arthropodicidally-effective amount of a composition comprising an arthropodically-active ingredient comprising a fatty acid comprising an alpha monocarboxylic hydrocarbon having 8 to 20 carbon atoms or a monovalent metal salt thereof, and an agent capable of sequestering metal ions, said agent being present in said solution in an amount sufficient to increase the arthropodicidal effect of said active ingredient.
2. The method of claim 1 wherein said active ingredient comprises an unsaturated fatty acid salt having 18 carbon atoms.
3. The method of claim 1 wherein said active ingredient is a mixture of said fatty acids.
4. The method of claim 1 wherein said agent is a chelating agent.
5. The method of claim 4 wherein said chelating agent is an organic, nitrogen-containing chelating agent.
6. The method of claim 4 wherein said chelating agent is an organic polycarboxylic acid chelating agent.
7. The method of claim 1 wherein said agent is a surfactant having the ability to sequester calcium ions.
8. The method of claim 1 wherein said agent is a phosphate-containing hardness ion complexing agent selected from the group consisting of salts of phosphate, pyrophosphate, and tripolyphosphate.
9. The method of claim 1 wherein the weight ratio in said solution of said active ingredient to said agent is within the range of 1:0.05 to 1:5.
10. The method of claim 1 wherein the weight ratio in said solution of said active ingredient to said agent is within the range of 1:0.05 to 1:1.
11. An aqueous arthropodicidal solution comprising an arthropodicidally active fatty acid comprising a monoalphacarboxylic hydrocarbon having 8 to 12 carbon atoms or a monovalent salf thereof, and an agent capable of sequestering metal ions, said agent being present in said solutions in an amount sufficient to increase the arthropodicidal effect of said fatty acid.
12. The solution of claim 13 wherein said active ingredient comprises an unsaturated fatty acid salt having 18 carbon atoms.
13. The solution of claim 11 wherein said active ingredient is a mixture of fatty acids.
14. The solution of claim 11 wherein said agent is a chelating agent.
IS**.. The solution of claim 14 wherein said chelating agent is an organic, nitrogen-containing chelating agent.
16. The solution of claim 14 wherein said chelating agent is an organic, polycarboxylic acid chelating agent.
17. The solution of claim 11 wherein said agent is a surfactant having the ability to sequester calcium ions.
18. The solution of claim 11 wherein said agent is a phosphate-containing calcium ion complexing agent selected from the group consisting of salts of phosphate, pyrophosphate, and tripolyphosphate.
19. The solution of claim 11 wherein the weight ratio therein of said active ingredient to said agent is within the range of 1:0.05 to 1:5.
20. The solution of claim 11 wherein the weight ratio therein of said active ingredient to said agent is within the range of 1:0.05 to 1:1.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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US19014688A | 1988-05-04 | 1988-05-04 | |
US190,146 | 1988-05-04 |
Publications (1)
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---|---|
WO1989010693A1 true WO1989010693A1 (en) | 1989-11-16 |
Family
ID=22700188
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1989/001197 WO1989010693A1 (en) | 1988-05-04 | 1989-03-23 | Enhanced activity arthropodicidal solution |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0413765A4 (en) |
JP (1) | JPH03505091A (en) |
AU (1) | AU620885B2 (en) |
WO (1) | WO1989010693A1 (en) |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1991018508A1 (en) * | 1990-05-28 | 1991-12-12 | Sostra S.R.L. | Composition against ozone damages to cultivations and method for its application |
EP0617888A1 (en) * | 1993-02-18 | 1994-10-05 | W.Neudorff Gmbh Kg | Fatty acid salt pesticidal composition |
WO1995002961A1 (en) * | 1993-07-22 | 1995-02-02 | Japan Tobacco Inc. | Fatty acid insecticide and insecticidal method using the same |
WO2001091555A3 (en) * | 2000-05-26 | 2002-04-04 | Procter & Gamble | Soap based pesticides |
NL1020693C2 (en) * | 2002-05-28 | 2003-12-01 | J & J Beheer B V | Use of a composition comprising an aqueous soap solution to control pests on animals or plants, especially poultry mites |
WO2006076761A1 (en) * | 2005-01-20 | 2006-07-27 | Hatchtech Pty Ltd | Methods and compositions for controlling ectoparasites |
BE1018399A3 (en) * | 2009-05-06 | 2010-10-05 | Globachem | USE OF BICARBONATE, CARBONATE AND PHOSPHATE SALTS AS INSECTICIDE FOR AGRICULTURAL AND HORTICULTURAL CROPS. |
US8212038B2 (en) | 2003-07-16 | 2012-07-03 | Hatchtech Pty Ltd. | Methods and compositions for controlling ectoparasites |
CN105638657A (en) * | 2015-01-30 | 2016-06-08 | 中国烟草总公司湖南省公司 | Insect and bacterium killing agent, preparation method and application method thereof |
US9980479B2 (en) | 2004-06-07 | 2018-05-29 | Syngenta Crop Protection, Llc | Method of reducing nematode damage |
US10292389B2 (en) | 2013-12-17 | 2019-05-21 | Dr. Reddy's Laboratories, S.A. | Pediculicidal composition |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP7370272B2 (en) * | 2020-02-13 | 2023-10-27 | 日本曹達株式会社 | Pest control agent |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3954967A (en) * | 1971-08-05 | 1976-05-04 | Vanguard Chemical Company, Inc. | Method of producing microcolloidal aqueous emulsions of unsaturated organic insecticidal compounds |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5624500A (en) * | 1979-08-08 | 1981-03-09 | Kogyo Gijutsuin | Metal soap composition |
CA1187409A (en) * | 1983-02-09 | 1985-05-21 | George S. Puritch | Insecticide mixtures containing fatty acids |
-
1989
- 1989-03-23 JP JP1506794A patent/JPH03505091A/en active Pending
- 1989-03-23 EP EP19890907399 patent/EP0413765A4/en not_active Withdrawn
- 1989-03-23 AU AU37494/89A patent/AU620885B2/en not_active Ceased
- 1989-03-23 WO PCT/US1989/001197 patent/WO1989010693A1/en not_active Application Discontinuation
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3954967A (en) * | 1971-08-05 | 1976-05-04 | Vanguard Chemical Company, Inc. | Method of producing microcolloidal aqueous emulsions of unsaturated organic insecticidal compounds |
Non-Patent Citations (2)
Title |
---|
Puritch "Pesticidal Soaps and Adjuvants - what are they and how do they work?", Proceedings of the 23rd Annual Lower Mainland Horticultural Improvement Association Growers' Short Course - Feb. 11, 12 and 13, 1981 - ABBOTSFORD. B.C. see pages 54 and 56-66. * |
See also references of EP0413765A4 * |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1991018508A1 (en) * | 1990-05-28 | 1991-12-12 | Sostra S.R.L. | Composition against ozone damages to cultivations and method for its application |
EP0617888A1 (en) * | 1993-02-18 | 1994-10-05 | W.Neudorff Gmbh Kg | Fatty acid salt pesticidal composition |
WO1995002961A1 (en) * | 1993-07-22 | 1995-02-02 | Japan Tobacco Inc. | Fatty acid insecticide and insecticidal method using the same |
WO2001091555A3 (en) * | 2000-05-26 | 2002-04-04 | Procter & Gamble | Soap based pesticides |
NL1020693C2 (en) * | 2002-05-28 | 2003-12-01 | J & J Beheer B V | Use of a composition comprising an aqueous soap solution to control pests on animals or plants, especially poultry mites |
US9839631B2 (en) | 2003-07-16 | 2017-12-12 | Dr. Reddy's Laboratories, S.A. | Methods and compositions for controlling ectoparasites |
US8212038B2 (en) | 2003-07-16 | 2012-07-03 | Hatchtech Pty Ltd. | Methods and compositions for controlling ectoparasites |
US9980479B2 (en) | 2004-06-07 | 2018-05-29 | Syngenta Crop Protection, Llc | Method of reducing nematode damage |
WO2006076761A1 (en) * | 2005-01-20 | 2006-07-27 | Hatchtech Pty Ltd | Methods and compositions for controlling ectoparasites |
BE1018399A3 (en) * | 2009-05-06 | 2010-10-05 | Globachem | USE OF BICARBONATE, CARBONATE AND PHOSPHATE SALTS AS INSECTICIDE FOR AGRICULTURAL AND HORTICULTURAL CROPS. |
US10292389B2 (en) | 2013-12-17 | 2019-05-21 | Dr. Reddy's Laboratories, S.A. | Pediculicidal composition |
US11510410B2 (en) | 2013-12-17 | 2022-11-29 | Hatchtech Pty Limited | Pediculicidal composition |
CN105638657A (en) * | 2015-01-30 | 2016-06-08 | 中国烟草总公司湖南省公司 | Insect and bacterium killing agent, preparation method and application method thereof |
Also Published As
Publication number | Publication date |
---|---|
AU3749489A (en) | 1989-11-29 |
JPH03505091A (en) | 1991-11-07 |
EP0413765A4 (en) | 1992-05-13 |
EP0413765A1 (en) | 1991-02-27 |
AU620885B2 (en) | 1992-02-27 |
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