CY1265A - Compounds and compositions containing them for use in the treatment of mammals for controlling parasitic diptera larvae - Google Patents

Compounds and compositions containing them for use in the treatment of mammals for controlling parasitic diptera larvae Download PDF

Info

Publication number: CY1265A
Authority: CY; Cyprus
Prior art keywords: formula; compound; composition; hydrogen; ofthe
Prior art date: 1978-02-17

Application number

CY1265A

Other languages

English (en)

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.)

1978-02-17

Filing date

1979-02-14

Publication date

1984-11-23

1979-02-14 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1984-11-23 Publication of CY1265A publication Critical patent/CY1265A/en

Links

239000000203 mixture Substances 0.000 title claims description 33
150000001875 compounds Chemical class 0.000 title claims description 31
241000255925 Diptera Species 0.000 title claims description 18
241000124008 Mammalia Species 0.000 title claims description 9
230000003071 parasitic effect Effects 0.000 title description 6
241001465754 Metazoa Species 0.000 claims description 27
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 15
150000003839 salts Chemical class 0.000 claims description 13
239000002253 acid Chemical group 0.000 claims description 11
239000001257 hydrogen Substances 0.000 claims description 11
229910052739 hydrogen Inorganic materials 0.000 claims description 11
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
229910021529 ammonia Inorganic materials 0.000 claims description 7
238000000034 method Methods 0.000 claims description 7
229910052736 halogen Inorganic materials 0.000 claims description 6
231100000252 nontoxic Toxicity 0.000 claims description 6
230000003000 nontoxic effect Effects 0.000 claims description 6
210000004767 rumen Anatomy 0.000 claims description 5
241001414987 Strepsiptera Species 0.000 claims description 4
239000000460 chlorine Substances 0.000 claims description 4
229910052801 chlorine Inorganic materials 0.000 claims description 4
125000005843 halogen group Chemical group 0.000 claims description 4
150000002431 hydrogen Chemical class 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
244000144972 livestock Species 0.000 claims description 4
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
HTJDQJBWANPRPF-UHFFFAOYSA-N Cyclopropylamine Chemical compound NC1CC1 HTJDQJBWANPRPF-UHFFFAOYSA-N 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
238000005507 spraying Methods 0.000 claims description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 claims 2
OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 claims 1
125000001309 chloro group Chemical group Cl* 0.000 claims 1
239000013543 active substance Substances 0.000 description 30
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 10
239000000243 solution Substances 0.000 description 9
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 7
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
238000009472 formulation Methods 0.000 description 7
239000002904 solvent Substances 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
238000002844 melting Methods 0.000 description 6
230000008018 melting Effects 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
LVQDKIWDGQRHTE-UHFFFAOYSA-N cyromazine Chemical compound NC1=NC(N)=NC(NC2CC2)=N1 LVQDKIWDGQRHTE-UHFFFAOYSA-N 0.000 description 4
230000000694 effects Effects 0.000 description 4
235000013601 eggs Nutrition 0.000 description 4
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 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
239000005995 Aluminium silicate Substances 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
241000283690 Bos taurus Species 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
208000006123 Myiasis Diseases 0.000 description 3
241001494479 Pecora Species 0.000 description 3
235000012211 aluminium silicate Nutrition 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
239000000470 constituent Substances 0.000 description 3
239000013078 crystal Substances 0.000 description 3
150000002367 halogens Chemical group 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
244000045947 parasite Species 0.000 description 3
150000003335 secondary amines Chemical class 0.000 description 3
239000000126 substance Substances 0.000 description 3
KCZIUKYAJJEIQG-UHFFFAOYSA-N 1,3,5-triazin-2-amine Chemical compound NC1=NC=NC=N1 KCZIUKYAJJEIQG-UHFFFAOYSA-N 0.000 description 2
JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical compound C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 description 2
YBXAUCWDTLINED-UHFFFAOYSA-N 2-n-cyclopropyl-4-n-methyl-1,3,5-triazine-2,4,6-triamine Chemical compound CNC1=NC(N)=NC(NC2CC2)=N1 YBXAUCWDTLINED-UHFFFAOYSA-N 0.000 description 2
229910002012 Aerosil® Inorganic materials 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
235000008733 Citrus aurantifolia Nutrition 0.000 description 2
241000238631 Hexapoda Species 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
206010042674 Swelling Diseases 0.000 description 2
235000011941 Tilia x europaea Nutrition 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
239000002671 adjuvant Substances 0.000 description 2
230000037396 body weight Effects 0.000 description 2
239000000969 carrier Substances 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
238000001914 filtration Methods 0.000 description 2
239000008187 granular material Substances 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
230000000974 larvacidal effect Effects 0.000 description 2
239000004571 lime Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
239000011707 mineral Substances 0.000 description 2
210000003800 pharynx Anatomy 0.000 description 2
229920001223 polyethylene glycol Polymers 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
239000000843 powder Substances 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
150000003141 primary amines Chemical class 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
229910052938 sodium sulfate Inorganic materials 0.000 description 2
235000011152 sodium sulphate Nutrition 0.000 description 2
239000007858 starting material Substances 0.000 description 2
230000008961 swelling Effects 0.000 description 2
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
KKVNELLMUOYULB-UHFFFAOYSA-N 1,3,5-triazine;dihydrochloride Chemical compound Cl.Cl.C1=NC=NC=N1 KKVNELLMUOYULB-UHFFFAOYSA-N 0.000 description 1
PSUUJJDPUSEFPD-UHFFFAOYSA-N 2-n,4-n,6-n-tricyclopropyl-1,3,5-triazine-2,4,6-triamine Chemical compound C1CC1NC1=NC(NC2CC2)=NC(NC2CC2)=N1 PSUUJJDPUSEFPD-UHFFFAOYSA-N 0.000 description 1
LYNMVQPJIKZMNY-UHFFFAOYSA-N 4-N-cyclopropyl-2-N,2-N,6-N-trimethyl-1,3,5-triazine-2,4,6-triamine dihydrochloride Chemical compound Cl.Cl.CN(C)C1=NC(NC)=NC(NC2CC2)=N1 LYNMVQPJIKZMNY-UHFFFAOYSA-N 0.000 description 1
OFMQRQUUPYBUND-UHFFFAOYSA-N 6-chloro-2-n-cyclopropyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(Cl)=NC(NC2CC2)=N1 OFMQRQUUPYBUND-UHFFFAOYSA-N 0.000 description 1
108010039224 Amidophosphoribosyltransferase Proteins 0.000 description 1
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
241000257161 Calliphoridae Species 0.000 description 1
241000282472 Canis lupus familiaris Species 0.000 description 1
241000692095 Cuterebra Species 0.000 description 1
241000531134 Cuterebrinae Species 0.000 description 1
241000202813 Dermatobia Species 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
241000283086 Equidae Species 0.000 description 1
241000283074 Equus asinus Species 0.000 description 1
241001331845 Equus asinus x caballus Species 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
241000282326 Felis catus Species 0.000 description 1
241001660203 Gasterophilus Species 0.000 description 1
241000257176 Hypoderma <fly> Species 0.000 description 1
241000543830 Hypoderma bovis Species 0.000 description 1
241001194722 Hypoderma tarandi Species 0.000 description 1
206010061217 Infestation Diseases 0.000 description 1
GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
241000257162 Lucilia <blowfly> Species 0.000 description 1
241000736227 Lucilia sericata Species 0.000 description 1
241000237536 Mytilus edulis Species 0.000 description 1
241000257191 Oestridae Species 0.000 description 1
241000543819 Oestrus ovis Species 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
241000282941 Rangifer tarandus Species 0.000 description 1
241001194723 Rhinoestrus Species 0.000 description 1
241000257185 Sarcophagidae Species 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
241000282887 Suidae Species 0.000 description 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 description 1
241000609107 Wohlfahrtia vigil Species 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
230000002411 adverse Effects 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
235000011114 ammonium hydroxide Nutrition 0.000 description 1
239000003674 animal food additive Substances 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
230000003115 biocidal effect Effects 0.000 description 1
-1 bolusses Substances 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
FUFJGUQYACFECW-UHFFFAOYSA-L calcium hydrogenphosphate Chemical compound [Ca+2].OP([O-])([O-])=O FUFJGUQYACFECW-UHFFFAOYSA-L 0.000 description 1
239000002775 capsule Substances 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
239000008119 colloidal silica Substances 0.000 description 1
235000012343 cottonseed oil Nutrition 0.000 description 1
239000012043 crude product Substances 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 1
239000003651 drinking water Substances 0.000 description 1
235000020188 drinking water Nutrition 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
210000001035 gastrointestinal tract Anatomy 0.000 description 1
244000144980 herd Species 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
230000001939 inductive effect Effects 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
239000008101 lactose Substances 0.000 description 1
239000012669 liquid formulation Substances 0.000 description 1
208000020442 loss of weight Diseases 0.000 description 1
235000012054 meals Nutrition 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
239000008267 milk Substances 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
235000020638 mussel Nutrition 0.000 description 1
210000003928 nasal cavity Anatomy 0.000 description 1
210000001331 nose Anatomy 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
230000024241 parasitism Effects 0.000 description 1
238000009304 pastoral farming Methods 0.000 description 1
239000008188 pellet Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
229940068886 polyethylene glycol 300 Drugs 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
239000000047 product Substances 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
230000019617 pupation Effects 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
239000007787 solid Substances 0.000 description 1
RNVYQYLELCKWAN-UHFFFAOYSA-N solketal Chemical compound CC1(C)OCC(CO)O1 RNVYQYLELCKWAN-UHFFFAOYSA-N 0.000 description 1
241000894007 species Species 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000009885 systemic effect Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
239000011782 vitamin Substances 0.000 description 1
229940088594 vitamin Drugs 0.000 description 1
229930003231 vitamin Natural products 0.000 description 1
235000013343 vitamin Nutrition 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
210000002268 wool Anatomy 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/54—Three nitrogen atoms
- C07D251/70—Other substituted melamines

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Fodder In General (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

CY1265A 1978-02-17 1979-02-14 Compounds and compositions containing them for use in the treatment of mammals for controlling parasitic diptera larvae CY1265A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH176278		1978-02-17

Publications (1)

Publication Number	Publication Date
CY1265A true CY1265A (en)	1984-11-23

Family

ID=4217965

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CY1265A CY1265A (en)	1978-02-17	1979-02-14	Compounds and compositions containing them for use in the treatment of mammals for controlling parasitic diptera larvae

Country Status (13)

Country	Link
US (1)	US4187305A (de)
AT (1)	AT363711B (de)
AU (1)	AU525516B2 (de)
CY (1)	CY1265A (de)
DE (1)	DE2905667A1 (de)
FR (1)	FR2417297A1 (de)
GB (1)	GB2014449B (de)
HK (1)	HK62083A (de)
IE (1)	IE47842B1 (de)
KE (1)	KE3280A (de)
MY (1)	MY8400211A (de)
NZ (1)	NZ189681A (de)
ZA (1)	ZA79719B (de)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4732899A (en) *	1985-12-02	1988-03-22	Ciba-Geigy Corporation	(Di)alkoxycarbonylamino-s-triazine derivatives and the use thereof against pests which are parasites of domestic animals and cultivated plants
NZ221262A (en) *	1986-08-06	1990-08-28	Ciba Geigy Ag	Preventing the reinfestation of dogs and cats by fleas by administering to the host a flea growth inhibiting substance orally, parenterally or by implant
US5104873A (en) *	1989-11-23	1992-04-14	Ciba-Geigy Corporation	Pesticide composition
US5439924A (en) *	1991-12-23	1995-08-08	Virbac, Inc.	Systemic control of parasites
CN1071321C (zh) *	1997-06-18	2001-09-19	吉林集团吉林市江南研究院有限责任公司	一种两步法合成灭虫嗪的工艺

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IL39385A (en) *	1971-06-01	1974-12-31	Ciba Geigy Ag	A method for combating insects by the use of 4-azido-2,6-diamino triazine derivatives,certain such novel derivatives and their manufacture
CH609835A5 (en) *	1976-08-19	1979-03-30	Ciba Geigy Ag	Pesticide

1979
- 1979-02-07 US US06/010,279 patent/US4187305A/en not_active Expired - Lifetime
- 1979-02-14 CY CY1265A patent/CY1265A/en unknown
- 1979-02-14 DE DE19792905667 patent/DE2905667A1/de not_active Ceased
- 1979-02-14 GB GB7905270A patent/GB2014449B/en not_active Expired
- 1979-02-15 FR FR7903856A patent/FR2417297A1/fr active Granted
- 1979-02-16 ZA ZA79719A patent/ZA79719B/xx unknown
- 1979-02-16 NZ NZ189681A patent/NZ189681A/xx unknown
- 1979-02-16 AU AU44316/79A patent/AU525516B2/en not_active Ceased
- 1979-02-16 IE IE303/79A patent/IE47842B1/en unknown
- 1979-02-16 AT AT0121579A patent/AT363711B/de not_active IP Right Cessation
1983
- 1983-04-19 KE KE3280A patent/KE3280A/xx unknown
- 1983-12-01 HK HK620/83A patent/HK62083A/xx unknown
1984
- 1984-12-30 MY MY211/84A patent/MY8400211A/xx unknown

Also Published As

Publication number	Publication date
IE790303L (en)	1979-08-17
FR2417297B1 (de)	1982-04-30
US4187305A (en)	1980-02-05
HK62083A (en)	1983-12-09
ATA121579A (de)	1981-01-15
MY8400211A (en)	1984-12-31
AT363711B (de)	1981-08-25
ZA79719B (en)	1980-03-26
FR2417297A1 (fr)	1979-09-14
GB2014449A (en)	1979-08-30
GB2014449B (en)	1982-07-28
DE2905667A1 (de)	1979-08-30
KE3280A (en)	1983-05-13
AU525516B2 (en)	1982-11-11
AU4431679A (en)	1979-08-23
IE47842B1 (en)	1984-06-27
NZ189681A (en)	1982-03-16

Publication	Publication Date	Title
AU599313B2 (en)	1990-07-19	Acyl ureas for controlling endoparasites and ectoparasites
US4089975A (en)	1978-05-16	Method of controlling manure-breeding insects
DE3151685C2 (de)	1987-08-13
JPH01305070A (ja)	1989-12-08	トリアジン除草剤
JPS5928535B2 (ja)	1984-07-13	原虫類防除用医薬組成物及び薬剤添加動物用飼料
TWI383748B (zh)	2013-02-01	有機化合物
JPS6052705B2 (ja)	1985-11-20	２−シクロプロピルアミノ−４，６−ジアミノ−ｓ−トリアジン類及びその製法並びに該化合物を有効成分とする有害昆虫防除剤
EP0215354B1 (de)	1991-04-24	Substituierte 2-Phenyl-hexahydro-1,2,4-triazin-3,5-dione, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung
US4187304A (en)	1980-02-05	Procedure for treating mammals to control parasitic diptera larvae
CY1265A (en)	1984-11-23	Compounds and compositions containing them for use in the treatment of mammals for controlling parasitic diptera larvae
CA2000234A1 (en)	1990-04-08	Substituted 1,3,5-triazinetriones, processes for their preparation and their use against parasitic protozoa
HU196767B (en)	1989-01-30	Process for production of derivatives of 2-/acyl-amin/-4-amin-2,4-bis /acyl-amin/-6-/alkyl-amin/-and-cycloalkyl-amin/-1,3,5-triasinine and agrochemical larvicides containg these compounds as active substance
DE2532363A1 (de)	1977-02-03	Substituierte 2-phenyl-1,2,4- triazin-3,5(2h,4h)-dione, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel
DE2229248B2 (de)	1979-07-26	5-IminomethyI-2-nitroimidazol-Derivate und Verfahren zu deren Herstellung
DE2509037A1 (de)	1976-09-02	1-aryluracile, verfahren zu ihrer herstellung sowie ihre verwendung als arzneimittel
US4160832A (en)	1979-07-10	Novel insecticides
US3484451A (en)	1969-12-16	2,3-dialkyl-n((haloalkyl)thio)bicarbamimides
US3781290A (en)	1973-12-25	Phenoxyphenyl phenylthiophenyl and phenylaminophenyl piperazinylthio-ureas
NL7905724A (nl)	1981-01-27	Werkwijze voor de behandeling van zoogdieren ter be- strijding van parasitische larven van de orde diptera.
DE2105112A1 (de)	1971-08-12	Chinoxahn di Noxide und ihre Verwendung in einem pharmazeutischen Gemisch
EP0084758B1 (de)	1986-02-12	Als Schädlingsbekämpfungsmittel wirksame Pyrimidin Derivate
GB2057262A (en)	1981-04-01	Veterinary depot preparation with prolonged release of insecticide
NL7905723A (nl)	1981-01-27	Werkwijze voor de bereiding van antiparasitisch werk- zame aminotriazinen en de preparaten daarvan voor de behandeling van zoogdieren ter bestrijding van para- sitische diptera-larven.
US3555152A (en)	1971-01-12	Controlling fungi and bacteria with 2,3-dialkyl -n((haloalkyl)thio)bicarbaminides
IL37336A (en)	1975-10-15	Parasiticidal compositions containing substituted 2-trifluoromethyl benzimidazole-4-sulphonamides,their use,certain new compounds of this class and their preparation