DD227875A5 - Mittel zur bekaempfung von bienenparasitaeren milben - Google Patents

Mittel zur bekaempfung von bienenparasitaeren milben Download PDF

Info

Publication number: DD227875A5
Authority: DD; German Democratic Republic
Prior art keywords: acid; bees; mites; bee; compound
Prior art date: 1983-04-14

Application number

DD84261907A

Other languages

German (de)

English (en)

Inventor

Wolfgang Schmid

Original Assignee

Ciba Geigy Ag

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.)

1983-04-14

Filing date

1984-04-12

Publication date

1985-10-02

1984-04-12 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1985-10-02 Publication of DD227875A5 publication Critical patent/DD227875A5/de

Links

244000045947 parasite Species 0.000 title claims description 5
241000257303 Hymenoptera Species 0.000 claims abstract description 41
239000004480 active ingredient Substances 0.000 claims abstract description 37
241000238876 Acari Species 0.000 claims abstract description 27
239000000203 mixture Substances 0.000 claims abstract description 16
238000000034 method Methods 0.000 claims abstract description 12
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 abstract description 11
150000003839 salts Chemical class 0.000 claims abstract description 11
239000002253 acid Substances 0.000 claims abstract description 6
239000003795 chemical substances by application Substances 0.000 claims abstract description 5
241000895650 Varroa jacobsoni Species 0.000 claims abstract 4
241001580838 Acarapis woodi Species 0.000 claims abstract 3
241001245280 Tropilaelaps Species 0.000 claims abstract 3
230000003071 parasitic effect Effects 0.000 claims abstract 2
150000001875 compounds Chemical class 0.000 claims description 17
235000000346 sugar Nutrition 0.000 claims description 10
239000013543 active substance Substances 0.000 claims description 6
239000002904 solvent Substances 0.000 claims description 6
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
241000895647 Varroa Species 0.000 claims description 4
235000013305 food Nutrition 0.000 claims description 3
210000000087 hemolymph Anatomy 0.000 claims description 3
239000000126 substance Substances 0.000 claims description 3
238000009826 distribution Methods 0.000 claims description 2
239000012530 fluid Substances 0.000 claims description 2
235000012907 honey Nutrition 0.000 claims description 2
201000002266 mite infestation Diseases 0.000 claims description 2
239000000546 pharmaceutical excipient Substances 0.000 claims description 2
238000002360 preparation method Methods 0.000 claims description 2
241000894007 species Species 0.000 claims description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 3
230000000895 acaricidal effect Effects 0.000 claims 3
201000010099 disease Diseases 0.000 claims 3
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 3
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims 2
KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims 2
AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims 2
241000124008 Mammalia Species 0.000 claims 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 2
241001481703 Rhipicephalus <genus> Species 0.000 claims 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 2
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims 2
JXTHNDFMNIQAHM-UHFFFAOYSA-N dichloroacetic acid Chemical compound OC(=O)C(Cl)Cl JXTHNDFMNIQAHM-UHFFFAOYSA-N 0.000 claims 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 2
JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims 2
150000007522 mineralic acids Chemical class 0.000 claims 2
150000007524 organic acids Chemical class 0.000 claims 2
235000005985 organic acids Nutrition 0.000 claims 2
ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims 2
HFVMEOPYDLEHBR-UHFFFAOYSA-N (2-fluorophenyl)-phenylmethanol Chemical compound C=1C=CC=C(F)C=1C(O)C1=CC=CC=C1 HFVMEOPYDLEHBR-UHFFFAOYSA-N 0.000 claims 1
QXQAPNSHUJORMC-UHFFFAOYSA-N 1-chloro-4-propylbenzene Chemical compound CCCC1=CC=C(Cl)C=C1 QXQAPNSHUJORMC-UHFFFAOYSA-N 0.000 claims 1
PKRSYEPBQPFNRB-UHFFFAOYSA-N 2-phenoxybenzoic acid Chemical compound OC(=O)C1=CC=CC=C1OC1=CC=CC=C1 PKRSYEPBQPFNRB-UHFFFAOYSA-N 0.000 claims 1
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 claims 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims 1
WUBBRNOQWQTFEX-UHFFFAOYSA-N 4-aminosalicylic acid Chemical compound NC1=CC=C(C(O)=O)C(O)=C1 WUBBRNOQWQTFEX-UHFFFAOYSA-N 0.000 claims 1
PXRKCOCTEMYUEG-UHFFFAOYSA-N 5-aminoisoindole-1,3-dione Chemical compound NC1=CC=C2C(=O)NC(=O)C2=C1 PXRKCOCTEMYUEG-UHFFFAOYSA-N 0.000 claims 1
241000238679 Amblyomma Species 0.000 claims 1
BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 claims 1
241000283690 Bos taurus Species 0.000 claims 1
COVZYZSDYWQREU-UHFFFAOYSA-N Busulfan Chemical compound CS(=O)(=O)OCCCCOS(C)(=O)=O COVZYZSDYWQREU-UHFFFAOYSA-N 0.000 claims 1
WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 claims 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims 1
241000238631 Hexapoda Species 0.000 claims 1
GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims 1
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims 1
241001494479 Pecora Species 0.000 claims 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims 1
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims 1
239000000642 acaricide Substances 0.000 claims 1
229910000147 aluminium phosphate Inorganic materials 0.000 claims 1
239000003674 animal food additive Substances 0.000 claims 1
230000009286 beneficial effect Effects 0.000 claims 1
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 claims 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 1
230000004071 biological effect Effects 0.000 claims 1
244000144987 brood Species 0.000 claims 1
238000011109 contamination Methods 0.000 claims 1
229960005215 dichloroacetic acid Drugs 0.000 claims 1
230000002349 favourable effect Effects 0.000 claims 1
210000001035 gastrointestinal tract Anatomy 0.000 claims 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims 1
230000000749 insecticidal effect Effects 0.000 claims 1
239000004310 lactic acid Substances 0.000 claims 1
235000014655 lactic acid Nutrition 0.000 claims 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims 1
239000011976 maleic acid Substances 0.000 claims 1
230000000116 mitigating effect Effects 0.000 claims 1
229910017604 nitric acid Inorganic materials 0.000 claims 1
210000000056 organ Anatomy 0.000 claims 1
244000052769 pathogen Species 0.000 claims 1
230000001717 pathogenic effect Effects 0.000 claims 1
235000019260 propionic acid Nutrition 0.000 claims 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims 1
230000009885 systemic effect Effects 0.000 claims 1
239000011975 tartaric acid Substances 0.000 claims 1
235000002906 tartaric acid Nutrition 0.000 claims 1
ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 1
YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 claims 1
230000035899 viability Effects 0.000 claims 1
238000009472 formulation Methods 0.000 abstract description 7
239000000243 solution Substances 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
239000012141 concentrate Substances 0.000 description 7
235000008504 concentrate Nutrition 0.000 description 7
239000000839 emulsion Substances 0.000 description 7
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
239000003814 drug Substances 0.000 description 5
229940079593 drug Drugs 0.000 description 5
238000002474 experimental method Methods 0.000 description 5
238000009736 wetting Methods 0.000 description 5
FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
239000001361 adipic acid Substances 0.000 description 3
235000011037 adipic acid Nutrition 0.000 description 3
SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
239000000843 powder Substances 0.000 description 3
238000005507 spraying Methods 0.000 description 3
239000004552 water soluble powder Substances 0.000 description 3
HVXRCAWUNAOCTA-UHFFFAOYSA-N 4-(6-methylheptyl)phenol Chemical compound CC(C)CCCCCC1=CC=C(O)C=C1 HVXRCAWUNAOCTA-UHFFFAOYSA-N 0.000 description 2
LVGKNOAMLMIIKO-UHFFFAOYSA-N Elaidinsaeure-aethylester Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC LVGKNOAMLMIIKO-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
239000004495 emulsifiable concentrate Substances 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 2
LVGKNOAMLMIIKO-QXMHVHEDSA-N ethyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC LVGKNOAMLMIIKO-QXMHVHEDSA-N 0.000 description 2
229940093471 ethyl oleate Drugs 0.000 description 2
239000000155 melt Substances 0.000 description 2
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
235000010333 potassium nitrate Nutrition 0.000 description 2
239000004323 potassium nitrate Substances 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
239000000779 smoke Substances 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
HZAOAIZJMMTSFN-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)-3-methylthiourea Chemical compound CNC(=S)NC1=CC=C(C)C=C1C HZAOAIZJMMTSFN-UHFFFAOYSA-N 0.000 description 1
QSKPIOLLBIHNAC-UHFFFAOYSA-N 2-chloro-acetaldehyde Chemical compound ClCC=O QSKPIOLLBIHNAC-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
230000006399 behavior Effects 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
235000015165 citric acid Nutrition 0.000 description 1
238000001816 cooling Methods 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
239000002552 dosage form Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
DDLNJUKFVPHVHA-UHFFFAOYSA-N ethyl acetate;2-hydroxypropanoic acid Chemical compound CCOC(C)=O.CC(O)C(O)=O DDLNJUKFVPHVHA-UHFFFAOYSA-N 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
229910021485 fumed silica Inorganic materials 0.000 description 1
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 1
150000002334 glycols Chemical class 0.000 description 1
JAXFJECJQZDFJS-XHEPKHHKSA-N gtpl8555 Chemical group OC(=O)C[C@H](N)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@@H]1C(=O)N[C@H](B1O[C@@]2(C)[C@H]3C[C@H](C3(C)C)C[C@H]2O1)CCC1=CC=C(F)C=C1 JAXFJECJQZDFJS-XHEPKHHKSA-N 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
244000144972 livestock Species 0.000 description 1
230000007774 longterm Effects 0.000 description 1
239000000463 material Substances 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
230000000391 smoking effect Effects 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
235000017550 sodium carbonate Nutrition 0.000 description 1
-1 sodium potassium aluminum silicates Chemical class 0.000 description 1
235000020354 squash Nutrition 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
230000000699 topical effect Effects 0.000 description 1
150000003626 triacylglycerols Chemical class 0.000 description 1
238000009827 uniform distribution Methods 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles

Landscapes

Life Sciences & Earth Sciences (AREA)
Environmental Sciences (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Agronomy & Crop Science (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Catching Or Destruction (AREA)
Feed For Specific Animals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Measuring Pulse, Heart Rate, Blood Pressure Or Blood Flow (AREA)
Control Of Electric Motors In General (AREA)
Absorbent Articles And Supports Therefor (AREA)
Organic Insulating Materials (AREA)
Materials For Medical Uses (AREA)
Medicinal Preparation (AREA)
Heterocyclic Compounds Containing Sulfur Atoms (AREA)

DD84261907A 1983-04-14 1984-04-12 Mittel zur bekaempfung von bienenparasitaeren milben DD227875A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH200283		1983-04-14

Publications (1)

Publication Number	Publication Date
DD227875A5 true DD227875A5 (de)	1985-10-02

Family

ID=4223598

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD84261907A DD227875A5 (de)	1983-04-14	1984-04-12	Mittel zur bekaempfung von bienenparasitaeren milben

Country Status (15)

Country	Link
US (1)	US4876265A (cs)
EP (1)	EP0126024B1 (cs)
JP (1)	JPS59199610A (cs)
AT (1)	ATE41585T1 (cs)
AU (2)	AU576493B2 (cs)
BG (1)	BG40956A3 (cs)
DD (1)	DD227875A5 (cs)
DE (1)	DE3477343D1 (cs)
FI (1)	FI73864C (cs)
GB (1)	GB2139497B (cs)
GR (1)	GR81978B (cs)
MY (1)	MY101437A (cs)
NZ (1)	NZ207851A (cs)
TR (1)	TR22078A (cs)
ZA (1)	ZA842784B (cs)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FI73864C (fi) *	1983-04-14	1987-12-10	Ciba Geigy Ag	Foerfarande och sockerhaltigt medel foer bekaempning av biparasitkvalster.
JPS6284005A (ja) *	1985-10-09	1987-04-17	Kenji Yoshida	蜜蜂寄生物の防除法
US6353006B1 (en)	1999-01-14	2002-03-05	Bayer Corporation	Substituted 2-arylimino heterocycles and compositions containing them, for use as progesterone receptor binding agents
US6468129B1 (en)	2000-03-03	2002-10-22	Granville Griffith	Beehive bottom board for reducing parasite infestation
US6620025B2 (en)	2001-04-12	2003-09-16	Theodore W. Scheuneman	Evaporator for the treatment of honey bee diseases and undesirable hive conditions
US20050095954A1 (en) *	2003-11-04	2005-05-05	Jose Castillo	Method of controlling pests
US20070026765A1 (en) *	2005-08-01	2007-02-01	Renn Richard M	Composition and method for the control of parasitic mites of honey bees
US7922559B2 (en) *	2006-07-27	2011-04-12	Cook Ernest C	Compositions and methods for the treatment and management of bee hives and the bees therein
RU2013157901A (ru)	2011-06-06	2015-07-20	Джон И. Хаас, Инк.	Композиции и способы борьбы с заражением пчел медоносных паразитическими клещами
AU2013271382A1 (en) *	2012-06-07	2015-01-15	John I. Haas, Inc.	Compositions and methods for controlling a Tropilaelaps parasitic mite
AU2014203897A1 (en)	2013-01-07	2015-07-23	John I. Haas, Inc.	Compositions and methods for controlling a honey bee parasitic mite infestation
WO2014192717A1 (ja) *	2013-05-27	2014-12-04	ＭｅｉｊｉＳｅｉｋａファルマ株式会社	ミツバチ寄生性害虫に対する防除剤及びそれらを使用したミツバチ寄生性害虫の防除方法
CA3043388A1 (en)	2018-05-14	2019-11-14	John I. Hass, Inc.	Compositions and methods for controlling a honey bee parasitic mite infestation
US20220338471A1 (en) *	2019-09-23	2022-10-27	Kansas State University Research Foundation	Honey bee-safe acaricidal compounds

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CH614946A5 (cs) *	1975-05-07	1979-12-28	Ciba Geigy Ag
DE2531606A1 (de) *	1975-07-15	1977-02-03	Bayer Ag	Substituierte 2-phenylimino-thiazoline, verfahren zu ihrer herstellung sowie ihre verwendung als ektoparasitizide
IL52927A (en) *	1976-09-17	1980-01-31	Ciba Geigy Ag	2-(n-methylcarbamoyloxyphenyl imino)-4-thiazoline derivatives their production and their use as pesticides
FI73864C (fi) *	1983-04-14	1987-12-10	Ciba Geigy Ag	Foerfarande och sockerhaltigt medel foer bekaempning av biparasitkvalster.

1984
- 1984-04-09 FI FI841401A patent/FI73864C/fi not_active IP Right Cessation
- 1984-04-09 DE DE8484810173T patent/DE3477343D1/de not_active Expired
- 1984-04-09 EP EP84810173A patent/EP0126024B1/de not_active Expired
- 1984-04-09 AT AT84810173T patent/ATE41585T1/de active
- 1984-04-10 GB GB08409277A patent/GB2139497B/en not_active Expired
- 1984-04-10 BG BG065015A patent/BG40956A3/xx unknown
- 1984-04-12 DD DD84261907A patent/DD227875A5/de not_active IP Right Cessation
- 1984-04-12 TR TR22078A patent/TR22078A/xx unknown
- 1984-04-12 GR GR74395A patent/GR81978B/el unknown
- 1984-04-13 AU AU26813/84A patent/AU576493B2/en not_active Ceased
- 1984-04-13 JP JP59073111A patent/JPS59199610A/ja active Granted
- 1984-04-13 ZA ZA842784A patent/ZA842784B/xx unknown
- 1984-04-13 NZ NZ207851A patent/NZ207851A/en unknown
1987
- 1987-09-23 MY MYPI87001883A patent/MY101437A/en unknown
1988
- 1988-11-23 AU AU25841/88A patent/AU610659B2/en not_active Ceased
- 1988-11-23 US US07/275,254 patent/US4876265A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
FI73864C (fi)	1987-12-10
NZ207851A (en)	1988-05-30
GB8409277D0 (en)	1984-05-23
MY101437A (en)	1991-11-18
JPS59199610A (ja)	1984-11-12
BG40956A3 (bg)	1987-03-14
ATE41585T1 (de)	1989-04-15
US4876265A (en)	1989-10-24
FI73864B (fi)	1987-08-31
GB2139497B (en)	1987-01-21
FI841401A0 (fi)	1984-04-09
TR22078A (tr)	1986-03-14
EP0126024B1 (de)	1989-03-22
DE3477343D1 (en)	1989-04-27
AU576493B2 (en)	1988-09-01
AU2681384A (en)	1984-10-18
ZA842784B (en)	1984-12-24
AU610659B2 (en)	1991-05-23
GB2139497A (en)	1984-11-14
AU2584188A (en)	1989-03-09
FI841401L (fi)	1984-10-15
GR81978B (cs)	1984-12-12
JPH0521881B2 (cs)	1993-03-25
EP0126024A1 (de)	1984-11-21

Legal Events

Date	Code	Title	Description
1999-07-08	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
EP0126024B1 (de)	1989-03-22	Verfahren zur Schädlingsbekämpfung
EP0255803A1 (de)	1988-02-10	Verfahren zur Verhinderung des Wiederbefalls von Hunden und Katzen mit Flöhen
DE69210438T2 (de)	1996-11-28	Akarizides Mittel verwendbar gegen Varroatose der Bienen, und eine dieses enthaltende Vorrichtung
DE3141224C2 (de)	1995-11-30	Behandlung von Ectoparasiten bei Schweinen
DE69530913T2 (de)	2004-03-11	Mikroverkapselte zusammensetzung von chlorpyrifos und endosulfan
DE69803710T2 (de)	2002-11-21	Langwirkende, injezierbare, parasitizide Zubereitung und Verfahren zu ihrer Herstellung
CH678381A5 (cs)	1991-09-13
EP0265825B1 (de)	1992-06-17	Verwendung von Desinfectionsmitteln zur Bekämpfung und Abtötung von parasitären Dauerformen
DE3106426C2 (cs)	1993-08-26
EP1085805B1 (de)	2002-02-13	Verwendung mindestens einer säure des zitronensäure-kreislaufs in kombination mit glycerin als schädlingsbekämpfungsmittel
DE3407042A1 (de)	1985-09-05	Verfahren zur schaedlingsbekaempfung
WO2011103694A1 (de)	2011-09-01	Spot-on präparat mit parasiten- repellierender wirkung
DE3407072A1 (de)	1985-08-29	Verfahren zur schaedlingsbekaempfung
DE68910220T2 (de)	1994-05-05	Veterinäre Zusammensetzungen zur Verwendung gegen Endoparasiten und Verfahren zu ihrer Herstellung.
DE60214989T2 (de)	2007-05-10	Verwendung von vicinalen 1,2-Diole zur Bekämpfung von Anthropoden
EP0167710A1 (de)	1986-01-15	Verwendung von Benomyl zur Herstellung eines Arzneimittels gegen Ichthyophthyriasis
EP0756821B1 (de)	2001-03-14	Para-Hydroxyphenylessigsäure zur Reduktion der Repellenz von Insektiziden
DE2458464C2 (cs)	1988-02-04
DE69521996T2 (de)	2002-04-04	Verwendung mindestens einer fettsäure gegen die eiablage von lepidoptera tortricidae
DE69723274T2 (de)	2004-05-27	Verfahren zur systemischen verabreichung von insektiziden vom 2,4-diensäure-typ an terrestrische säugetiere
DE60011096T2 (de)	2005-06-16	Ester enthaltende zusammensetzungen zur behandlung von parasitischem befall in organismen
DE2558918C2 (de)	1983-09-22	Acaricide und ovicide Mittel auf Basis eines Thiobenzoats
DD260859A1 (de)	1988-10-12	Verfahren zur herstellung von neuen mitteln zur bekaempfung der milbe varroajacobsoni
EP0096656B1 (de)	1985-10-23	Schädlingsbekämpfungsmittel
DE1693183A1 (de)	1971-04-22	Schaedlingsbekaempfungsmittel