AP222A - An animal pour-on pesticidal formulation. - Google Patents

An animal pour-on pesticidal formulation. Download PDF

Info

Publication number: AP222A
Authority: AP; ARIPO
Prior art keywords: formulation; group; pesticidal; cypermethrin; cattle
Prior art date: 1989-08-18

Application number

APAP/P/1990/000200A

Other languages

English (en)

Other versions

AP9000200A0 (en

Inventor

Tonder Stephanus Johannes Van

Original Assignee

Pfizer

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1989-08-18

Filing date

1990-08-17

Publication date

1992-10-29

1990-08-17 Application filed by Pfizer filed Critical Pfizer

1990-10-31 Publication of AP9000200A0 publication Critical patent/AP9000200A0/xx

1992-10-29 Application granted granted Critical

1992-10-29 Publication of AP222A publication Critical patent/AP222A/en

Links

239000000203 mixture Substances 0.000 title claims abstract description 101
238000009472 formulation Methods 0.000 title claims abstract description 92
241001465754 Metazoa Species 0.000 title claims abstract description 53
239000004540 pour-on Substances 0.000 title claims abstract description 24
230000000361 pesticidal effect Effects 0.000 title claims abstract description 12
239000002728 pyrethroid Substances 0.000 claims description 14
KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 claims description 13
239000000575 pesticide Substances 0.000 claims description 13
239000005946 Cypermethrin Substances 0.000 claims description 11
229960005424 cypermethrin Drugs 0.000 claims description 11
239000003921 oil Substances 0.000 claims description 11
235000019198 oils Nutrition 0.000 claims description 11
239000002904 solvent Substances 0.000 claims description 11
KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 claims description 9
239000005877 Alpha-Cypermethrin Substances 0.000 claims description 9
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 claims description 8
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 claims description 8
206010061217 Infestation Diseases 0.000 claims description 7
235000015112 vegetable and seed oil Nutrition 0.000 claims description 7
239000008158 vegetable oil Substances 0.000 claims description 7
239000002798 polar solvent Substances 0.000 claims description 6
VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 claims description 5
-1 cyhalothrln Chemical compound 0.000 claims description 5
235000020238 sunflower seed Nutrition 0.000 claims description 5
UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical group COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 claims description 5
FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 claims description 4
229960002380 dibutyl phthalate Drugs 0.000 claims description 4
NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 claims description 4
RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 claims description 4
229960005235 piperonyl butoxide Drugs 0.000 claims description 4
229960005199 tetramethrin Drugs 0.000 claims description 4
229960002587 amitraz Drugs 0.000 claims description 3
QXAITBQSYVNQDR-ZIOPAAQOSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1/N=C/N(C)\C=N\C1=CC=C(C)C=C1C QXAITBQSYVNQDR-ZIOPAAQOSA-N 0.000 claims description 3
239000006184 cosolvent Substances 0.000 claims description 3
YUAUPYJCVKNAEC-UHFFFAOYSA-N n-(2,4-dimethylphenyl)-3-methyl-1,3-thiazol-2-imine Chemical compound CC1=CC(C)=CC=C1N=C1N(C)C=CS1 YUAUPYJCVKNAEC-UHFFFAOYSA-N 0.000 claims description 3
229960003536 phenothrin Drugs 0.000 claims description 3
ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 claims description 2
CXBMCYHAMVGWJQ-CABCVRRESA-N (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-CABCVRRESA-N 0.000 claims description 2
FJDPATXIBIBRIM-QFMSAKRMSA-N (1R)-trans-cyphenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 FJDPATXIBIBRIM-QFMSAKRMSA-N 0.000 claims description 2
FHNKBSDJERHDHZ-UHFFFAOYSA-N (2,4-dimethylphenyl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC1=CC=C(C)C=C1C FHNKBSDJERHDHZ-UHFFFAOYSA-N 0.000 claims description 2
YJXNJQHBVKTWCC-UHFFFAOYSA-N (3-cyclopent-2-en-1-yl-2-methyl-4-oxocyclopent-2-en-1-yl) 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OC1C(C)=C(C2C=CCC2)C(=O)C1 YJXNJQHBVKTWCC-UHFFFAOYSA-N 0.000 claims description 2
RLLPVAHGXHCWKJ-MJGOQNOKSA-N (3-phenoxyphenyl)methyl (1r,3s)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-MJGOQNOKSA-N 0.000 claims description 2
VEMKTZHHVJILDY-PMACEKPBSA-N (5-benzylfuran-3-yl)methyl (1r,3s)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-PMACEKPBSA-N 0.000 claims description 2
KPMWGGRSOPMANK-UHFFFAOYSA-N (6-chloro-1,3-benzodioxol-5-yl)methyl 2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC(C(=C1)Cl)=CC2=C1OCO2 KPMWGGRSOPMANK-UHFFFAOYSA-N 0.000 claims description 2
FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 claims description 2
ZYVTYOMVFLAPLX-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethyl 1,3-benzodioxole-5-carboxylate Chemical compound CCCCOCCOCCOC(=O)C1=CC=C2OCOC2=C1 ZYVTYOMVFLAPLX-UHFFFAOYSA-N 0.000 claims description 2
SYBKGANKGIGMCQ-UHFFFAOYSA-N 4-methyl-5-(4-octan-2-ylsulfinylphenyl)-1,3-dioxolane Chemical compound C1=CC(S(=O)C(C)CCCCCC)=CC=C1C1C(C)OCO1 SYBKGANKGIGMCQ-UHFFFAOYSA-N 0.000 claims description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
239000005892 Deltamethrin Substances 0.000 claims description 2
UEKQGZQLUMSLNW-UHFFFAOYSA-N Propyl isome Chemical compound C1=C2C(C(=O)OCCC)C(C(=O)OCCC)C(C)CC2=CC2=C1OCO2 UEKQGZQLUMSLNW-UHFFFAOYSA-N 0.000 claims description 2
WABPPBHOPMUJHV-UHFFFAOYSA-N Sesamex Chemical compound CCOCCOCCOC(C)OC1=CC=C2OCOC2=C1 WABPPBHOPMUJHV-UHFFFAOYSA-N 0.000 claims description 2
VQHJWDTTWVEXFE-UHFFFAOYSA-N [cyano-(3-phenoxyphenyl)methyl] 3-(1,2-dibromo-2,2-dichloroethyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C(Br)C(Cl)(Cl)Br)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 VQHJWDTTWVEXFE-UHFFFAOYSA-N 0.000 claims description 2
YXWCBRDRVXHABN-JCMHNJIXSA-N [cyano-(4-fluoro-3-phenoxyphenyl)methyl] 3-[(z)-2-chloro-2-(4-chlorophenyl)ethenyl]-2,2-dimethylcyclopropane-1-carboxylate Chemical compound C=1C=C(F)C(OC=2C=CC=CC=2)=CC=1C(C#N)OC(=O)C1C(C)(C)C1\C=C(/Cl)C1=CC=C(Cl)C=C1 YXWCBRDRVXHABN-JCMHNJIXSA-N 0.000 claims description 2
229940024113 allethrin Drugs 0.000 claims description 2
150000001409 amidines Chemical class 0.000 claims description 2
229950002373 bioresmethrin Drugs 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
150000001735 carboxylic acids Chemical class 0.000 claims description 2
229960001591 cyfluthrin Drugs 0.000 claims description 2
QQODLKZGRKWIFG-QSFXBCCZSA-N cyfluthrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@@H](C#N)C1=CC=C(F)C(OC=2C=CC=CC=2)=C1 QQODLKZGRKWIFG-QSFXBCCZSA-N 0.000 claims description 2
229960002483 decamethrin Drugs 0.000 claims description 2
OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 claims description 2
244000078703 ectoparasite Species 0.000 claims description 2
125000005456 glyceride group Chemical group 0.000 claims description 2
229960000490 permethrin Drugs 0.000 claims description 2
SBNFWQZLDJGRLK-UHFFFAOYSA-N phenothrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-UHFFFAOYSA-N 0.000 claims description 2
229940108410 resmethrin Drugs 0.000 claims description 2
VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 claims description 2
150000003462 sulfoxides Chemical class 0.000 claims description 2
CXBMCYHAMVGWJQ-UHFFFAOYSA-N tetramethrin Chemical compound CC1(C)C(C=C(C)C)C1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-UHFFFAOYSA-N 0.000 claims description 2
YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 claims description 2
239000004615 ingredient Substances 0.000 claims 2
SBNFWQZLDJGRLK-RTWAWAEBSA-N (1R)-trans-phenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-RTWAWAEBSA-N 0.000 claims 1
IBZZDPVVVSNQOY-UHFFFAOYSA-N Chloromethiuron Chemical compound CN(C)C(=S)NC1=CC=C(Cl)C=C1C IBZZDPVVVSNQOY-UHFFFAOYSA-N 0.000 claims 1
150000007942 carboxylates Chemical class 0.000 claims 1
150000001875 compounds Chemical class 0.000 claims 1
238000000034 method Methods 0.000 claims 1
241000283690 Bos taurus Species 0.000 description 36
238000011282 treatment Methods 0.000 description 25
241000985247 Ornithodoros savignyi Species 0.000 description 19
244000144980 herd Species 0.000 description 11
241000238876 Acari Species 0.000 description 9
241001674048 Phthiraptera Species 0.000 description 8
239000000047 product Substances 0.000 description 8
241001480736 Amblyomma hebraeum Species 0.000 description 7
241000257226 Muscidae Species 0.000 description 7
230000000694 effects Effects 0.000 description 7
244000309465 heifer Species 0.000 description 6
OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 5
235000013365 dairy product Nutrition 0.000 description 4
230000009467 reduction Effects 0.000 description 4
241000255925 Diptera Species 0.000 description 3
241000283086 Equidae Species 0.000 description 3
241000238745 Musca autumnalis Species 0.000 description 3
241000257159 Musca domestica Species 0.000 description 3
241001480756 Otobius megnini Species 0.000 description 3
241001494115 Stomoxys calcitrans Species 0.000 description 3
244000309466 calf Species 0.000 description 3
230000001984 ectoparasiticidal effect Effects 0.000 description 3
230000001965 increasing effect Effects 0.000 description 3
241000322476 Bovicola bovis Species 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
241001608644 Hippoboscidae Species 0.000 description 2
230000000895 acaricidal effect Effects 0.000 description 2
239000004480 active ingredient Substances 0.000 description 2
235000011089 carbon dioxide Nutrition 0.000 description 2
FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 description 2
244000144993 groups of animals Species 0.000 description 2
238000000338 in vitro Methods 0.000 description 2
239000002917 insecticide Substances 0.000 description 2
230000002147 killing effect Effects 0.000 description 2
230000003287 optical effect Effects 0.000 description 2
230000035515 penetration Effects 0.000 description 2
239000004576 sand Substances 0.000 description 2
201000001064 tick infestation Diseases 0.000 description 2
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
241000283707 Capra Species 0.000 description 1
241000255930 Chironomidae Species 0.000 description 1
241000256135 Chironomus thummi Species 0.000 description 1
STUSTWKEFDQFFZ-UHFFFAOYSA-N Chlordimeform Chemical compound CN(C)C=NC1=CC=C(Cl)C=C1C STUSTWKEFDQFFZ-UHFFFAOYSA-N 0.000 description 1
LVZHCTADYVHHSN-UHFFFAOYSA-N ClC(Cl)=CC1(C(O)=O)C(C)(C)C1C(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 Chemical class ClC(Cl)=CC1(C(O)=O)C(C)(C)C1C(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 LVZHCTADYVHHSN-UHFFFAOYSA-N 0.000 description 1
241000238631 Hexapoda Species 0.000 description 1
241000771992 Hippobosca rufipes Species 0.000 description 1
101000795130 Homo sapiens Trehalase Proteins 0.000 description 1
241001113946 Linognathus vituli Species 0.000 description 1
241001494479 Pecora Species 0.000 description 1
206010040880 Skin irritation Diseases 0.000 description 1
241000282887 Suidae Species 0.000 description 1
102100029677 Trehalase Human genes 0.000 description 1
INISTDXBRIBGOC-CGAIIQECSA-N [cyano-(3-phenoxyphenyl)methyl] (2s)-2-[2-chloro-4-(trifluoromethyl)anilino]-3-methylbutanoate Chemical compound N([C@@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-CGAIIQECSA-N 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000008280 blood Substances 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000013066 combination product Substances 0.000 description 1
229940127555 combination product Drugs 0.000 description 1
239000013065 commercial product Substances 0.000 description 1
239000000470 constituent Substances 0.000 description 1
ZXQYGBMAQZUVMI-UNOMPAQXSA-N cyhalothrin Chemical compound CC1(C)C(\C=C(/Cl)C(F)(F)F)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-UNOMPAQXSA-N 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
210000005069 ears Anatomy 0.000 description 1
230000002708 enhancing effect Effects 0.000 description 1
230000008029 eradication Effects 0.000 description 1
JCLHQFUTFHUXNN-UHFFFAOYSA-N ethyl biscoumacetate Chemical compound C1=CC=C2OC(=O)C(C(C=3C(OC4=CC=CC=C4C=3O)=O)C(=O)OCC)=C(O)C2=C1 JCLHQFUTFHUXNN-UHFFFAOYSA-N 0.000 description 1
239000013020 final formulation Substances 0.000 description 1
238000003197 gene knockdown Methods 0.000 description 1
239000000077 insect repellent Substances 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
238000007689 inspection Methods 0.000 description 1
210000003734 kidney Anatomy 0.000 description 1
230000000974 larvacidal effect Effects 0.000 description 1
210000003205 muscle Anatomy 0.000 description 1
239000012454 non-polar solvent Substances 0.000 description 1
230000003151 ovacidal effect Effects 0.000 description 1
238000009304 pastoral farming Methods 0.000 description 1
239000000447 pesticide residue Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
230000036556 skin irritation Effects 0.000 description 1
231100000475 skin irritation Toxicity 0.000 description 1
241000894007 species Species 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
230000000638 stimulation Effects 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
230000003612 virological effect Effects 0.000 description 1
230000003442 weekly effect Effects 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
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Agronomy & Crop Science (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

APAP/P/1990/000200A 1989-08-18 1990-08-17 An animal pour-on pesticidal formulation. AP222A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
ZA896322		1989-08-18

Publications (2)

Publication Number	Publication Date
AP9000200A0 AP9000200A0 (en)	1990-10-31
AP222A true AP222A (en)	1992-10-29

Family

ID=25579792

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
APAP/P/1990/000200A AP222A (en)	1989-08-18	1990-08-17	An animal pour-on pesticidal formulation.

Country Status (8)

Country	Link
US (1)	US5130135A (de)
EP (1)	EP0413610A3 (de)
AP (1)	AP222A (de)
AU (1)	AU640677B2 (de)
BR (1)	BR9004190A (de)
MX (1)	MX174303B (de)
NZ (1)	NZ234970A (de)
OA (1)	OA09305A (de)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB9106365D0 (en) *	1991-03-26	1991-05-15	Bioglan Lab Ltd	An emollient for use with ultraviolet light
DE4216535A1 (de) *	1991-08-21	1993-02-25	Bayer Ag	Formkoerper zur bekaempfung von schaedlingen
ZA94170B (en) *	1993-01-20	1995-03-15	Soltec Res Pty Ltd	Ectoparasiticidal formulation
US5674829A (en) *	1993-01-29	1997-10-07	Antoinetta P. Martin	Stable aqueous glutaraldehyde solutions containing sodium acetate and a nonionic detergent
AU674100B2 (en) *	1993-10-25	1996-12-05	Monsanto Australia Limited	Adjuvant for sprayable mixes of plant or insect controlling agents
DE4417742A1 (de)	1994-05-20	1995-11-23	Bayer Ag	Nicht-systemische Bekämpfung von Parasiten
US5906983A (en) *	1997-08-20	1999-05-25	The Clorox Company	High fructose containing insecticide compositions and methods of using the same
US6117854A (en) *	1997-08-20	2000-09-12	The Clorox Company	Enhanced performance insecticide compositions containing plant derived oil carriers and methods of using the same
US6024972A (en) *	1998-07-21	2000-02-15	Isp Investments Inc.	Water-free concentrate of amitraz insecticide and clear pour-on formulations thereof
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Also Published As

Publication number	Publication date
AU640677B2 (en)	1993-09-02
OA09305A (en)	1992-09-15
AU6111390A (en)	1991-02-21
BR9004190A (pt)	1991-09-03
EP0413610A3 (en)	1992-08-26
NZ234970A (en)	1992-03-26
US5130135A (en)	1992-07-14
MX174303B (es)	1994-05-04
AP9000200A0 (en)	1990-10-31
EP0413610A2 (de)	1991-02-20

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