WO1994016559A1 - Solid bird aversion compositions - Google Patents
Solid bird aversion compositions Download PDFInfo
- Publication number
- WO1994016559A1 WO1994016559A1 PCT/US1994/000493 US9400493W WO9416559A1 WO 1994016559 A1 WO1994016559 A1 WO 1994016559A1 US 9400493 W US9400493 W US 9400493W WO 9416559 A1 WO9416559 A1 WO 9416559A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- weight
- total weight
- emulsion
- amount
- solution
- Prior art date
Links
- 206010063659 Aversion Diseases 0.000 title claims abstract description 52
- 239000007787 solid Substances 0.000 title claims abstract description 14
- 239000000203 mixture Substances 0.000 title claims description 22
- 239000000839 emulsion Substances 0.000 claims abstract description 39
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 36
- 150000001875 compounds Chemical class 0.000 claims abstract description 30
- VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 claims abstract description 28
- -1 terpene hydrocarbon Chemical class 0.000 claims abstract description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 24
- 235000007586 terpenes Nutrition 0.000 claims abstract description 23
- AROCNZZBLCAOPH-UHFFFAOYSA-N 1-methyl-4-prop-2-enoxybenzene Chemical compound CC1=CC=C(OCC=C)C=C1 AROCNZZBLCAOPH-UHFFFAOYSA-N 0.000 claims abstract description 19
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 19
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 17
- 229940102398 methyl anthranilate Drugs 0.000 claims abstract description 14
- AXMVYSVVTMKQSL-UHFFFAOYSA-N UNPD142122 Natural products OC1=CC=C(C=CC=O)C=C1O AXMVYSVVTMKQSL-UHFFFAOYSA-N 0.000 claims abstract description 13
- KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 claims abstract description 13
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Natural products CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims abstract description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 12
- KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 claims abstract description 11
- 229940117916 cinnamic aldehyde Drugs 0.000 claims abstract description 11
- 150000001412 amines Chemical class 0.000 claims abstract description 9
- GTDQGKWDWVUKTI-UHFFFAOYSA-N o-aminoacetophenone Chemical compound CC(=O)C1=CC=CC=C1N GTDQGKWDWVUKTI-UHFFFAOYSA-N 0.000 claims abstract description 9
- 229920001285 xanthan gum Chemical class 0.000 claims abstract description 7
- 150000004676 glycans Chemical class 0.000 claims abstract description 6
- 229920001282 polysaccharide Polymers 0.000 claims abstract description 6
- 239000005017 polysaccharide Substances 0.000 claims abstract description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 5
- 235000010443 alginic acid Nutrition 0.000 claims abstract description 5
- 229920000615 alginic acid Polymers 0.000 claims abstract description 5
- 125000005907 alkyl ester group Chemical group 0.000 claims abstract description 5
- 235000021122 unsaturated fatty acids Nutrition 0.000 claims abstract description 5
- 150000004670 unsaturated fatty acids Chemical class 0.000 claims abstract description 5
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 claims abstract description 4
- 108010010803 Gelatin Chemical class 0.000 claims abstract description 4
- 229940072056 alginate Drugs 0.000 claims abstract description 4
- 239000001913 cellulose Chemical class 0.000 claims abstract description 4
- 229920002678 cellulose Chemical class 0.000 claims abstract description 4
- 229920000159 gelatin Chemical class 0.000 claims abstract description 4
- 235000019322 gelatine Nutrition 0.000 claims abstract description 4
- 235000011852 gelatine desserts Nutrition 0.000 claims abstract description 4
- 229920001277 pectin Chemical class 0.000 claims abstract description 4
- 239000001814 pectin Chemical class 0.000 claims abstract description 4
- 235000010987 pectin Nutrition 0.000 claims abstract description 4
- 235000003441 saturated fatty acids Nutrition 0.000 claims abstract description 4
- 150000004671 saturated fatty acids Chemical class 0.000 claims abstract description 4
- APEJMQOBVMLION-UHFFFAOYSA-N cinnamamide Chemical compound NC(=O)C=CC1=CC=CC=C1 APEJMQOBVMLION-UHFFFAOYSA-N 0.000 claims description 22
- CRZQGDNQQAALAY-UHFFFAOYSA-N Methyl benzeneacetate Chemical compound COC(=O)CC1=CC=CC=C1 CRZQGDNQQAALAY-UHFFFAOYSA-N 0.000 claims description 18
- XMGQYMWWDOXHJM-JTQLQIEISA-N (+)-α-limonene Chemical compound CC(=C)[C@@H]1CCC(C)=CC1 XMGQYMWWDOXHJM-JTQLQIEISA-N 0.000 claims description 12
- NPNUFJAVOOONJE-ZIAGYGMSSA-N β-(E)-Caryophyllene Chemical compound C1CC(C)=CCCC(=C)[C@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-ZIAGYGMSSA-N 0.000 claims description 12
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims description 11
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 claims description 11
- 229930016911 cinnamic acid Natural products 0.000 claims description 11
- 235000013985 cinnamic acid Nutrition 0.000 claims description 11
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims description 11
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 9
- JLIDRDJNLAWIKT-UHFFFAOYSA-N 1,2-dimethyl-3h-benzo[e]indole Chemical compound C1=CC=CC2=C(C(=C(C)N3)C)C3=CC=C21 JLIDRDJNLAWIKT-UHFFFAOYSA-N 0.000 claims description 8
- DULCUDSUACXJJC-UHFFFAOYSA-N benzeneacetic acid ethyl ester Natural products CCOC(=O)CC1=CC=CC=C1 DULCUDSUACXJJC-UHFFFAOYSA-N 0.000 claims description 8
- HFPZCAJZSCWRBC-UHFFFAOYSA-N p-cymene Chemical compound CC(C)C1=CC=C(C)C=C1 HFPZCAJZSCWRBC-UHFFFAOYSA-N 0.000 claims description 8
- GRWFGVWFFZKLTI-UHFFFAOYSA-N α-pinene Chemical compound CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 claims description 8
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 6
- 239000003963 antioxidant agent Substances 0.000 claims description 6
- NPNUFJAVOOONJE-UHFFFAOYSA-N beta-cariophyllene Natural products C1CC(C)=CCCC(=C)C2CC(C)(C)C21 NPNUFJAVOOONJE-UHFFFAOYSA-N 0.000 claims description 6
- NPNUFJAVOOONJE-UONOGXRCSA-N caryophyllene Natural products C1CC(C)=CCCC(=C)[C@@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-UONOGXRCSA-N 0.000 claims description 6
- 229940117948 caryophyllene Drugs 0.000 claims description 6
- 239000003086 colorant Substances 0.000 claims description 6
- WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 claims description 4
- WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 claims description 4
- GRWFGVWFFZKLTI-IUCAKERBSA-N 1S,5S-(-)-alpha-Pinene Natural products CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 claims description 4
- KUXGUCNZFCVULO-UHFFFAOYSA-N 2-(4-nonylphenoxy)ethanol Chemical class CCCCCCCCCC1=CC=C(OCCO)C=C1 KUXGUCNZFCVULO-UHFFFAOYSA-N 0.000 claims description 4
- WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 claims description 4
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 claims description 4
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 claims description 4
- 229930006722 beta-pinene Natural products 0.000 claims description 4
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 4
- LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 claims description 4
- 235000001510 limonene Nutrition 0.000 claims description 4
- 229940087305 limonene Drugs 0.000 claims description 4
- 238000004040 coloring Methods 0.000 claims description 3
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 claims description 3
- 239000004299 sodium benzoate Substances 0.000 claims description 3
- 235000010234 sodium benzoate Nutrition 0.000 claims description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 2
- 241000416162 Astragalus gummifer Species 0.000 claims description 2
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 claims description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 2
- 240000001058 Sterculia urens Species 0.000 claims description 2
- 235000015125 Sterculia urens Nutrition 0.000 claims description 2
- 229920001615 Tragacanth Polymers 0.000 claims description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 2
- 235000020778 linoleic acid Nutrition 0.000 claims description 2
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 claims description 2
- 229920000847 nonoxynol Polymers 0.000 claims description 2
- 229920002113 octoxynol Polymers 0.000 claims description 2
- 150000002888 oleic acid derivatives Chemical class 0.000 claims description 2
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 claims description 2
- 229960003656 ricinoleic acid Drugs 0.000 claims description 2
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 claims description 2
- 235000010487 tragacanth Nutrition 0.000 claims description 2
- 239000000326 ultraviolet stabilizing agent Substances 0.000 claims description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 2
- 244000007835 Cyamopsis tetragonoloba Species 0.000 claims 1
- 150000002148 esters Chemical class 0.000 abstract description 2
- 238000009472 formulation Methods 0.000 description 16
- 229920001577 copolymer Polymers 0.000 description 10
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 8
- LRCFXGAMWKDGLA-UHFFFAOYSA-N dioxosilane;hydrate Chemical compound O.O=[Si]=O LRCFXGAMWKDGLA-UHFFFAOYSA-N 0.000 description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- 241000271566 Aves Species 0.000 description 6
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000012467 final product Substances 0.000 description 5
- 229940074928 isopropyl myristate Drugs 0.000 description 5
- 244000215068 Acacia senegal Species 0.000 description 4
- SGHZXLIDFTYFHQ-UHFFFAOYSA-L Brilliant Blue Chemical compound [Na+].[Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C(=CC=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 SGHZXLIDFTYFHQ-UHFFFAOYSA-L 0.000 description 4
- 229920000084 Gum arabic Polymers 0.000 description 4
- 235000010489 acacia gum Nutrition 0.000 description 4
- 239000000205 acacia gum Substances 0.000 description 4
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 4
- 229910000019 calcium carbonate Inorganic materials 0.000 description 4
- 239000004927 clay Substances 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- 150000003505 terpenes Chemical class 0.000 description 4
- NVEQFIOZRFFVFW-UHFFFAOYSA-N 9-epi-beta-caryophyllene oxide Natural products C=C1CCC2OC2(C)CCC2C(C)(C)CC21 NVEQFIOZRFFVFW-UHFFFAOYSA-N 0.000 description 3
- PHYFQTYBJUILEZ-UHFFFAOYSA-N Trioleoylglycerol Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCCCCCCCC)COC(=O)CCCCCCCC=CCCCCCCCC PHYFQTYBJUILEZ-UHFFFAOYSA-N 0.000 description 3
- 238000013019 agitation Methods 0.000 description 3
- FAMPSKZZVDUYOS-UHFFFAOYSA-N alpha-Caryophyllene Natural products CC1=CCC(C)(C)C=CCC(C)=CCC1 FAMPSKZZVDUYOS-UHFFFAOYSA-N 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000012669 liquid formulation Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 3
- 229940117972 triolein Drugs 0.000 description 3
- 125000000545 (4R)-limonene group Chemical group 0.000 description 2
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 2
- 241000272517 Anseriformes Species 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 239000004258 Ethoxyquin Substances 0.000 description 2
- PVNIQBQSYATKKL-UHFFFAOYSA-N Glycerol trihexadecanoate Natural products CCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCC PVNIQBQSYATKKL-UHFFFAOYSA-N 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 150000001386 alpha-pinene derivatives Chemical class 0.000 description 2
- 150000001591 beta-pinene derivatives Chemical class 0.000 description 2
- 150000001720 carbohydrates Chemical class 0.000 description 2
- 235000014633 carbohydrates Nutrition 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- DECIPOUIJURFOJ-UHFFFAOYSA-N ethoxyquin Chemical compound N1C(C)(C)C=C(C)C2=CC(OCC)=CC=C21 DECIPOUIJURFOJ-UHFFFAOYSA-N 0.000 description 2
- 229940093500 ethoxyquin Drugs 0.000 description 2
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- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
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- 230000001846 repelling effect Effects 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000003981 vehicle Substances 0.000 description 2
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 1
- QHZLMUACJMDIAE-UHFFFAOYSA-N 1-monopalmitoylglycerol Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(O)CO QHZLMUACJMDIAE-UHFFFAOYSA-N 0.000 description 1
- HNLXNOZHXNSSPN-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[4-(2,4,4-trimethylpentan-2-yl)phenoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCOCCOCCOCCO)C=C1 HNLXNOZHXNSSPN-UHFFFAOYSA-N 0.000 description 1
- WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 244000303965 Cyamopsis psoralioides Species 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- 229920000569 Gum karaya Polymers 0.000 description 1
- 229920000161 Locust bean gum Polymers 0.000 description 1
- 239000004368 Modified starch Substances 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 239000004264 Petrolatum Substances 0.000 description 1
- 241000287182 Sturnidae Species 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000003674 animal food additive Substances 0.000 description 1
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- 229940096898 glyceryl palmitate Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
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- 238000010348 incorporation Methods 0.000 description 1
- 235000010494 karaya gum Nutrition 0.000 description 1
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- 238000012986 modification Methods 0.000 description 1
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- 229920002114 octoxynol-9 Polymers 0.000 description 1
- 229940098514 octoxynol-9 Drugs 0.000 description 1
- UYDLBVPAAFVANX-UHFFFAOYSA-N octylphenoxy polyethoxyethanol Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCOCCO)C=C1 UYDLBVPAAFVANX-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
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- 238000004806 packaging method and process Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000009304 pastoral farming Methods 0.000 description 1
- 235000020030 perry Nutrition 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 229940066842 petrolatum Drugs 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 230000021317 sensory perception Effects 0.000 description 1
- XJKVPKYVPCWHFO-UHFFFAOYSA-N silicon;hydrate Chemical compound O.[Si] XJKVPKYVPCWHFO-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
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- 229940116362 tragacanth Drugs 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
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- 239000000230 xanthan gum Substances 0.000 description 1
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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
- A01N37/10—Aromatic or araliphatic carboxylic acids, or thio analogues thereof; Derivatives thereof
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/24—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients to enhance the sticking of the active ingredients
-
- 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing aliphatically bound aldehyde or keto groups, or thio analogues thereof; Derivatives thereof, e.g. acetals
-
- 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/04—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing aldehyde or keto groups, or thio analogues thereof, directly attached to an aromatic ring system, e.g. acetophenone; Derivatives thereof, e.g. acetals
-
- 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
- A01N37/18—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 containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
-
- 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
- A01N37/44—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 containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
Definitions
- the present invention relates generally to new formulations of bird aversion compounds.
- Methyl and dimethyl anthranilate are ester derivatives of anthranilic acid (also known as ortho-amino-benzoic acid) .
- MA, DMA and other derivatives of anthranilic acid as well as esters of phenylacetic acid are known to be bird aversion agents with preferred embodiments as feed additives to deter feed loss (U.S. Patent 2,967,128 and 4,790,990), and as an anti-grazing compound for geese and swans (Mason, J.R.
- Cinnamamide has also been shown to be a bird aversion agent. (Crocker & Perry, PLANT CHEMISTRY AND BIRD REPELLENTS, 132:300-308 (1990)).
- U.S. Patent 2,967,128 discloses the incorporation of MA and other ester derivatives of anthranilic acid as bird aversion agents into feed or pesticide additives, or into liquids to be sprayed on material.
- U.S. Patent 4,790,990 teaches that the aversion agent can be at least partially trapped in a solid vehicle to improve its persistency.
- the solid vehicle can be a modified starch, oil or polymer which microencapsulates the aversion agent.
- prior art bird aversion formulations cannot be used for all conditions.
- these prior art bird repellents are heavier than water, e.g. methyl anthranilate has a density of 1.16.
- the prior art bird aversion compounds sink in water and as a consequence, they are not capable of repelling birds.
- Other mixtures of vegetable oils and bird aversion agents clump or coagulate in messy globs on the surface of water, which are not capable of repelling birds.
- the present invention is a formulation of a solid free flowing compound consisting essentially of a bird aversion agent in an amount of from 10 to 80%, preferably from 30 to 75%, by weight of a total weight of the compound; and an inorganic or organic carrier in an amount of from 20 to 90%, preferably from 25 to 70%, by weight of a total weight of the compound.
- UV stabilizers, antioxidants and "lakes" or colors can be added in s all concentrations, usually below 1% by weight of the total weight of the final product.
- the present invention concerns a bird aversion solution which is lighter than water.
- the liquid formulation comprises a bird aversion agent in an amount of from 5 to 50% by weight of a total weight of the solution; a terpene hydrocarbon and oxygenated derivative thereof in an amount of from 10 to 50% by weight of a total weight of the solution; and alkylesters selected from the group consisting of saturated fatty acids having from 4-20 carbon atoms and unsaturated fatty acids having from 10-18 carbon atoms esterified with an alcohol having from 1-8 carbon atoms in an amount of from 10 to 50% by weight of a total weight of the solution.
- the bird aversion compound is an emulsion, consisting essentially of a bird aversion agent in an amount of from 5 to 30% by weight of a total weight of the emulsion; a terpene hydrocarbon and oxygenated derivative thereof in an amount of from 5 to 10% by weight of a total weight of the emulsion; gums selected from the group consisting of storage polysaccharides, pectins, gelatins, xanthans, cellulose derivatives and alginate in an amount of from 0.5 to 10% by weight of a total weight of the emulsion; and water in an amount of from 70 to 80% by weight of a total weight of the emulsion.
- the bird aversion agent is selected from the group consisting of methyl anthranilate, methyl phenyl acetate, ethyl phenyl acetate, ortho-amino acetophenone, 2-amino-4,5-dimethyl acetophenone, veratroyl amine, dimethyl anthranilate, cinnamic aldehyde, cinnamamide, cinnamic acid and combinations thereof.
- birds refers to members of the class "Aves”.
- a formulation in a solid free flowing form consists essential of from 10-80%, or preferably from 30-75%, by weight of the total weight of the solid form of a bird aversion agent; and 20-90%, preferably from 25-70%, by weight of the total weight of the solid form of a carrier.
- the bird aversion agent is selected from the group consisting of as methyl anthranilate, ortho-amino acetophenone, methyl phenyl acetate, ethyl phenyl acetate, veratroyl amine, 2-amino-4,5-dimethyl acetophenone, dimethyl anthranilate, cinnamamide, cinnamic acid, cinnamic aldehyde and combinations thereof.
- the carrier may be inorganic, organic or combinations of both.
- acceptable inorganic carriers are precipitated silica, such as silicon dioxide hydrate, e.g. SIPERNAT 22 HR from the North American Silica Company and talc.
- acceptable organic carriers are methacrylate ester copolymer, e.g. POLYTRAP Q5-6603 polymer powder from Dow Corning Corporation and calcium carbonate. When calcium carbonate and talc are used in the solid formulation either together or separately, they are added in amounts of from 40%-65% by weight of the total weight of the compound together with 1-10% silicon hydrate.
- “lakes” or colors, ultra violet stabilizers and antioxidants can each be added in amounts of from 0 to 1% by weight of the total weight of the compound. In this amount, they do not affect the formulation.
- antioxidants are BHA, BHT and ethoxyquin, and some examples of colors are D&C violet #2 and FD&C blue #1.
- the solid free flowing form may be prepared by first charging the "carrier” into a mixer or ribbon blender.
- the bird aversion agent e.g. dimethyl anthranilate
- the final product may be sifted through a 20-80 mesh screen to ensure uniform particle size.
- Optional "lakes" or colors may be added during the blending operation if so desired.
- the final product is analyzed for the bird aversion agent.
- EXAMPLE la EXAMPLE la:
- the present invention relates to a liquid formulation that is lighter than water and forms a thin liquid film on the water surface.
- the present invention formulation is made lighter than water by dissolving the bird aversion agent in a mixture of terpene hydrocarbons and oxygenated derivatives together with aliphatic mono-esters.
- the bird aversion agent is selected from the group consisting of as methyl anthranilate, methyl phenyl acetate, ethyl phenyl acetate, ortho-amino acetophenone, 2-amino-4,5-dimethyl acetophenone, veratroyl amine, dimethyl anthranilate, cinnamic aldehyde, cinnamamide, cinnamic acid and combinations thereof.
- the bird aversion agent used in this formulation is in an amount of from 5 to 50%, preferably from 10 to 40%, and more preferably from 30 to 40% by weight of the total weight of the solution.
- the terpene hydrocarbon and oxygenated derivatives comprise from 10 to 50%, preferably 20-40%, and more preferably 25-35% by weight of a total weight of the solution.
- the terpene hydrocarbon and oxygenated derivatives are selected from limonene, di-pentene, alpha-pinene, beta-pinene, caryophyllene, and p-cymene.
- the preferred terpene hydrocarbon and oxygenated derivative is d-limonene.
- a terpene hydrocarbon and oxygenated derivative is used because it is inert and reduces specific gravity.
- the alkylesters which comprise from 10 to 50% by weight of a total weight of the solution are selected from saturated fatty acids having from 4 to 20 carbon atoms, unsaturated fatty acids having from 10 to 18 carbon atoms, including oleic, ricinoleic and linoleic acid esterified with an alcohol having from 1 to 8 carbon atoms, such as methyl to octyl alcohol, preferably isopropyl alcohol.
- Examples of some of the alkylesters are iso-propyl myristate, liquid petrolatum, castor oil, glyceryl trioleate and glyceryl palmitate.
- solubilizers such as ethoxy alkalated phenols
- ethoxy alkalated examples include octoxynols, such as octyl phenoxy polyethoxyethanol (octoxynol 9 or TRITON X-100) , and nonoxynols, such as nonoxynol 10.
- a coloring dye may be added in an amount of from 0 to 1% by weight of the total weight of the solution.
- An exemplary color is D&C violet #2.
- An antioxidant, such as BHT, BHA and ethoxyquin may also be added in an amount of from 0 to 0.5% by weight of the total weight of the solution.
- a liquid "lighter than water” formulation was prepared by adding to a clean container, 80 g methyl anthranilate, 60 g iso-propyl myristate, and 60 g d-limonene. Additional ingredients such as antioxidants may also be added.
- the present invention relates to an emulsion formulation miscible with water, containing terpene hydrocarbons and gums to form a polymeric film on plant leaves and fruits.
- the formulation consists essentially of a bird aversion agent in an amount of from 5 to 30%, preferably from 10 to 20%, and more preferably 12% by weight of the total weight of the emulsion, a terpene hydrocarbon from 5 to 10% by weight of the total weight of the emulsion, and gum from 0.5 to 10%, preferably from 3 to 4% by weight of the total weight of the emulsion, with the remaining portion of the emulsion being water.
- citric acid, sodium benzoate, colors may each be added in amounts of from 0 to 1% by weight of the total weight of the emulsion for stabilization and for appearance.
- the bird aversion agent is selected from the group consisting of as methyl anthranilate, methyl phenyl acetate, ethyl phenyl acetate, ortho-amino acetophenone, 2-amino-4,5-dimethyl acetophenone, veratroyl amine, dimethyl anthranilate, cinnamic aldehyde, cinnamamide, cinnamic acid and combinations thereof.
- the gums are selected from polysaccharides, such as arabic, karaya, guar, tragacanth or pectin (carbohydrates) , gelatins (proteins) , xanthans, cellulose derivative or alginate (carbohydrates) and combinations thereof.
- Some exemplary gums are KETROL (a xanthan) , EMUL (a gum arabic) , KELGIN F and KELCO-GEL (alginates) , locust bean gum and malto-dextrins.
- the terpene is selected from limonene, di-pentene, alpha-pinene, beta-pinene, caryophyllene, p-cymene and combinations thereof.
- the preferred terpene is d-limonene. In this formulation, the terpene is used as an organic solvent.
- an emulsion was prepared by mixing the "gums”, e.g. 6 g of gum arabic (such as EMUL BV IRX 2900), with 150.2 g of water, and heating to about 50 ⁇ C. Using a homogenizer, the "gums" are dispersed in water free of lumps. At this point 1.0 g of another gum such as a xanthan (for example KELTROL polysaccharide gum) is added under continued agitation until homogenized.
- a xanthan for example KELTROL polysaccharide gum
- a premix consisting of a blend of 16.8 g of a terpene, for example caryophyllene, and 25.4 g of a bird aversion agent, such as cinnamamide, is slowly added under continued agitation until a stable emulsion is obtained. Additional ingredients such as 0.2 g citric acid and 0.4 g sodium benzoate may be added for stability. The final product is analyzed for the content of bird aversion agent.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU60884/94A AU6088494A (en) | 1993-01-25 | 1994-01-14 | Solid bird aversion compositions |
CA002154564A CA2154564C (en) | 1993-01-25 | 1994-01-14 | Solid bird aversion compositions |
EP94907215A EP0680256A1 (en) | 1993-01-25 | 1994-01-14 | Solid bird aversion compositions |
JP6517109A JPH08509463A (en) | 1993-01-25 | 1994-01-14 | Bird dislike solid composition |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US867593A | 1993-01-25 | 1993-01-25 | |
US08/008,675 | 1993-01-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1994016559A1 true WO1994016559A1 (en) | 1994-08-04 |
Family
ID=21733022
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1994/000493 WO1994016559A1 (en) | 1993-01-25 | 1994-01-14 | Solid bird aversion compositions |
Country Status (7)
Country | Link |
---|---|
US (3) | US5466674A (en) |
EP (1) | EP0680256A1 (en) |
JP (1) | JPH08509463A (en) |
AU (1) | AU6088494A (en) |
CA (1) | CA2154564C (en) |
IL (1) | IL108365A0 (en) |
WO (1) | WO1994016559A1 (en) |
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Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
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WO1997005776A1 (en) * | 1995-08-03 | 1997-02-20 | New Waste Concepts, Inc. | Water fog for repelling birds |
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2967128A (en) * | 1957-06-06 | 1961-01-03 | S B Penick And Company Inc | Bird repellent |
US4542162A (en) * | 1983-02-09 | 1985-09-17 | International Flavors & Fragrances Inc. | Process for forming insect, animal or bird repellent fluid and solid-containing thermoplastic films and pellets, uses thereof and process for producing same |
US4626274A (en) * | 1982-12-20 | 1986-12-02 | Bayer Aktiengesellschaft | Herbicidal agents |
US4735803A (en) * | 1986-02-14 | 1988-04-05 | International Flavors & Fragrances Inc. | Repelling animals with compositions comprising lemon oil and alpha-terpinyl methyl ether |
US5187196A (en) * | 1989-03-13 | 1993-02-16 | The United States Of America As Represented By The Secretary Of Agriculture | Grazing repellent for geese and swans |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3627878A (en) * | 1967-11-06 | 1971-12-14 | Wilson Pharm & Chem Corp | Herbivore repellent and method |
JPS6355481B2 (en) * | 1979-10-13 | 1988-11-02 | Mikaeru Jeimuzu Sanpuson | |
US4956129A (en) * | 1984-03-30 | 1990-09-11 | Ici Americas Inc. | Microencapsulation process |
US4511579A (en) * | 1981-03-27 | 1985-04-16 | Union Carbide Corporation | Pest repellant |
JPS58189115A (en) * | 1982-04-30 | 1983-11-04 | Kowa Co | Drug for external use |
GR82163B (en) * | 1984-01-31 | 1984-12-13 | Earth Chemical Co | |
EP0173410A1 (en) * | 1984-05-09 | 1986-03-05 | Michael James Sampson | Repellent for birds and other creatures |
US4790990A (en) * | 1984-08-27 | 1988-12-13 | Monell Chemistry Senses Center | Mammalian livestock feed, Mammalian livestock feed additive, and methods for using same |
US4616036A (en) * | 1985-09-12 | 1986-10-07 | Byron Hodgin | Formulation for the control of nematodes |
US4891222A (en) * | 1987-02-24 | 1990-01-02 | Eichhoefer Gerald W | Pine oil fire ant insecticide |
US4853413A (en) * | 1987-04-03 | 1989-08-01 | International Flavors & Fragrances Inc. | Repelling animals with compositions comprising citronellyl nitrile, citronellol and, optionally methyl terpenyl ether, lemon oil, caryophyllene, isopulegol, isopulegyl acetate and quinine or one or more of its salts |
JPH01110602A (en) * | 1987-10-22 | 1989-04-27 | Ezaki Glyco Kk | Cat repellent |
JPH01139515A (en) * | 1987-11-27 | 1989-06-01 | Fumakilla Ltd | Repellent composition for dog, cat and birds |
US5196451A (en) * | 1987-12-14 | 1993-03-23 | National Research Development Corporation | Avian control |
US4965070A (en) * | 1988-07-07 | 1990-10-23 | Messina James J | Deer repellent formulation |
DE3824211A1 (en) * | 1988-07-16 | 1990-01-18 | Basf Ag | 2-TERT.-BUTYL-4-CHLORINE-5- (4-TERT.-BUTYLBENZYLTHIO) -3 (2H) -PYRIDAZINONE FOR CONTROLLING SNAILS |
US5364626A (en) * | 1990-11-29 | 1994-11-15 | Osaka Gas Company Ltd. | Repelling material for animals |
US5296226A (en) * | 1991-02-12 | 1994-03-22 | Dolphin Trust | Bird repellent compositions |
-
1994
- 1994-01-14 EP EP94907215A patent/EP0680256A1/en not_active Withdrawn
- 1994-01-14 AU AU60884/94A patent/AU6088494A/en not_active Abandoned
- 1994-01-14 JP JP6517109A patent/JPH08509463A/en active Pending
- 1994-01-14 CA CA002154564A patent/CA2154564C/en not_active Expired - Fee Related
- 1994-01-14 WO PCT/US1994/000493 patent/WO1994016559A1/en not_active Application Discontinuation
- 1994-01-18 IL IL10836594A patent/IL108365A0/en unknown
- 1994-07-13 US US08/274,408 patent/US5466674A/en not_active Expired - Lifetime
- 1994-12-19 US US08/358,462 patent/US5549902A/en not_active Expired - Lifetime
-
1996
- 1996-09-19 US US08/710,774 patent/US5700474A/en not_active Expired - Lifetime
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2967128A (en) * | 1957-06-06 | 1961-01-03 | S B Penick And Company Inc | Bird repellent |
US4626274A (en) * | 1982-12-20 | 1986-12-02 | Bayer Aktiengesellschaft | Herbicidal agents |
US4542162A (en) * | 1983-02-09 | 1985-09-17 | International Flavors & Fragrances Inc. | Process for forming insect, animal or bird repellent fluid and solid-containing thermoplastic films and pellets, uses thereof and process for producing same |
US4735803A (en) * | 1986-02-14 | 1988-04-05 | International Flavors & Fragrances Inc. | Repelling animals with compositions comprising lemon oil and alpha-terpinyl methyl ether |
US5187196A (en) * | 1989-03-13 | 1993-02-16 | The United States Of America As Represented By The Secretary Of Agriculture | Grazing repellent for geese and swans |
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Also Published As
Publication number | Publication date |
---|---|
AU6088494A (en) | 1994-08-15 |
US5549902A (en) | 1996-08-27 |
US5466674A (en) | 1995-11-14 |
IL108365A0 (en) | 1994-04-12 |
US5700474A (en) | 1997-12-23 |
CA2154564C (en) | 2004-10-12 |
CA2154564A1 (en) | 1994-08-04 |
JPH08509463A (en) | 1996-10-08 |
EP0680256A1 (en) | 1995-11-08 |
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