HUE028200T2 - Továbbfejlesztések szerves vegyületekre vonatkozóan - Google Patents
Továbbfejlesztések szerves vegyületekre vonatkozóan Download PDFInfo
- Publication number
- HUE028200T2 HUE028200T2 HUE08788307A HUE08788307A HUE028200T2 HU E028200 T2 HUE028200 T2 HU E028200T2 HU E08788307 A HUE08788307 A HU E08788307A HU E08788307 A HUE08788307 A HU E08788307A HU E028200 T2 HUE028200 T2 HU E028200T2
- Authority
- HU
- Hungary
- Prior art keywords
- preparation
- chemical
- composition
- rti
- formula
- Prior art date
Links
- 150000002894 organic compounds Chemical class 0.000 title 1
- 239000000203 mixture Substances 0.000 claims description 77
- -1 alkyl dichlorohexanones Chemical class 0.000 claims description 59
- 239000002904 solvent Substances 0.000 claims description 34
- 150000001875 compounds Chemical class 0.000 claims description 29
- 239000000126 substance Substances 0.000 claims description 18
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 9
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims description 8
- 241000607479 Yersinia pestis Species 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 125000004122 cyclic group Chemical group 0.000 claims description 5
- 150000003893 lactate salts Chemical class 0.000 claims description 5
- 150000001298 alcohols Chemical class 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 3
- 150000002170 ethers Chemical class 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 2
- 239000007921 spray Substances 0.000 claims description 2
- 150000003505 terpenes Chemical class 0.000 claims description 2
- 235000007586 terpenes Nutrition 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims 2
- 241000251468 Actinopterygii Species 0.000 claims 1
- 238000003723 Smelting Methods 0.000 claims 1
- 150000001413 amino acids Chemical class 0.000 claims 1
- 230000003444 anaesthetic effect Effects 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 230000002996 emotional effect Effects 0.000 claims 1
- 210000003743 erythrocyte Anatomy 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 235000014655 lactic acid Nutrition 0.000 claims 1
- 239000004310 lactic acid Substances 0.000 claims 1
- 235000020131 mattha Nutrition 0.000 claims 1
- 230000001172 regenerating effect Effects 0.000 claims 1
- 239000002002 slurry Substances 0.000 claims 1
- 235000011888 snacks Nutrition 0.000 claims 1
- 239000004575 stone Substances 0.000 claims 1
- 238000009941 weaving Methods 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 19
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 18
- 239000003905 agrochemical Substances 0.000 description 17
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 17
- 125000000217 alkyl group Chemical group 0.000 description 16
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 12
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 11
- 125000002757 morpholinyl group Chemical group 0.000 description 11
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 10
- 238000009472 formulation Methods 0.000 description 10
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical class CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 9
- 125000001424 substituent group Chemical group 0.000 description 9
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 8
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 7
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 7
- IBSREHMXUMOFBB-JFUDTMANSA-N 5u8924t11h Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C(C)C)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 IBSREHMXUMOFBB-JFUDTMANSA-N 0.000 description 7
- 239000005660 Abamectin Substances 0.000 description 7
- 239000005894 Emamectin Substances 0.000 description 7
- 229950008167 abamectin Drugs 0.000 description 7
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 7
- GCKZANITAMOIAR-XWVCPFKXSA-N dsstox_cid_14566 Chemical compound [O-]C(=O)C1=CC=CC=C1.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H]([NH2+]C)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 GCKZANITAMOIAR-XWVCPFKXSA-N 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 125000004433 nitrogen atom Chemical group N* 0.000 description 7
- 125000001931 aliphatic group Chemical group 0.000 description 6
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 6
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 6
- SXQFCVDSOLSHOQ-UHFFFAOYSA-N lactamide Chemical class CC(O)C(N)=O SXQFCVDSOLSHOQ-UHFFFAOYSA-N 0.000 description 6
- UUFQTNFCRMXOAE-UHFFFAOYSA-N 1-methylmethylene Chemical compound C[CH] UUFQTNFCRMXOAE-UHFFFAOYSA-N 0.000 description 5
- KWLVWJPJKJMCSH-UHFFFAOYSA-N 2-(4-chlorophenyl)-N-{2-[3-methoxy-4-(prop-2-yn-1-yloxy)phenyl]ethyl}-2-(prop-2-yn-1-yloxy)acetamide Chemical compound C1=C(OCC#C)C(OC)=CC(CCNC(=O)C(OCC#C)C=2C=CC(Cl)=CC=2)=C1 KWLVWJPJKJMCSH-UHFFFAOYSA-N 0.000 description 5
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 5
- 125000000753 cycloalkyl group Chemical group 0.000 description 5
- 150000005690 diesters Chemical class 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 5
- JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 description 5
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- LHXDLQBQYFFVNW-UHFFFAOYSA-N Fenchone Chemical compound C1CC2(C)C(=O)C(C)(C)C1C2 LHXDLQBQYFFVNW-UHFFFAOYSA-N 0.000 description 4
- 239000005804 Mandipropamid Substances 0.000 description 4
- 150000004729 acetoacetic acid derivatives Chemical class 0.000 description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 4
- 239000003607 modifier Substances 0.000 description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 235000013772 propylene glycol Nutrition 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
- DUFKCOQISQKSAV-UHFFFAOYSA-N Polypropylene glycol (m w 1,200-3,000) Chemical compound CC(O)COC(C)CO DUFKCOQISQKSAV-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 239000002671 adjuvant Substances 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 150000001408 amides Chemical class 0.000 description 3
- RRZXIRBKKLTSOM-XPNPUAGNSA-N avermectin B1a Chemical compound C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 RRZXIRBKKLTSOM-XPNPUAGNSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 3
- 239000003599 detergent Substances 0.000 description 3
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-L fumarate(2-) Chemical class [O-]C(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-L 0.000 description 3
- 230000000855 fungicidal effect Effects 0.000 description 3
- 239000003906 humectant Substances 0.000 description 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 150000002780 morpholines Chemical class 0.000 description 3
- 125000005498 phthalate group Chemical class 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 125000003386 piperidinyl group Chemical group 0.000 description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000000719 pyrrolidinyl group Chemical group 0.000 description 3
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 239000002453 shampoo Substances 0.000 description 3
- 150000003890 succinate salts Chemical class 0.000 description 3
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 3
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 3
- 229940093635 tributyl phosphate Drugs 0.000 description 3
- 150000005691 triesters Chemical class 0.000 description 3
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 3
- LHXDLQBQYFFVNW-XCBNKYQSSA-N (+)-Fenchone Natural products C1C[C@]2(C)C(=O)C(C)(C)[C@H]1C2 LHXDLQBQYFFVNW-XCBNKYQSSA-N 0.000 description 2
- MEJYDZQQVZJMPP-ULAWRXDQSA-N (3s,3ar,6r,6ar)-3,6-dimethoxy-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan Chemical compound CO[C@H]1CO[C@@H]2[C@H](OC)CO[C@@H]21 MEJYDZQQVZJMPP-ULAWRXDQSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- ZZXUZKXVROWEIF-UHFFFAOYSA-N 1,2-butylene carbonate Chemical compound CCC1COC(=O)O1 ZZXUZKXVROWEIF-UHFFFAOYSA-N 0.000 description 2
- YFKBXYGUSOXJGS-UHFFFAOYSA-N 1,3-Diphenyl-2-propanone Chemical class C=1C=CC=CC=1CC(=O)CC1=CC=CC=C1 YFKBXYGUSOXJGS-UHFFFAOYSA-N 0.000 description 2
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 2
- FLPPEMNGWYFRSK-UHFFFAOYSA-N 2-(2-acetyloxypropoxy)propyl acetate Chemical compound CC(=O)OCC(C)OCC(C)OC(C)=O FLPPEMNGWYFRSK-UHFFFAOYSA-N 0.000 description 2
- JDSQBDGCMUXRBM-UHFFFAOYSA-N 2-[2-(2-butoxypropoxy)propoxy]propan-1-ol Chemical compound CCCCOC(C)COC(C)COC(C)CO JDSQBDGCMUXRBM-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 2
- 239000004129 EU approved improving agent Substances 0.000 description 2
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 2
- 241001465754 Metazoa Species 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 206010040880 Skin irritation Diseases 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- 239000004141 Sodium laurylsulphate Substances 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- 239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical class OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000001348 alkyl chlorides Chemical class 0.000 description 2
- 239000003242 anti bacterial agent Substances 0.000 description 2
- 150000008365 aromatic ketones Chemical class 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 150000001555 benzenes Chemical class 0.000 description 2
- 235000019445 benzyl alcohol Nutrition 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 235000013877 carbamide Nutrition 0.000 description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical class OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 2
- QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 2
- 229930006735 fenchone Natural products 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 150000002431 hydrogen Chemical group 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 235000020778 linoleic acid Nutrition 0.000 description 2
- 229960004232 linoleic acid Drugs 0.000 description 2
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 2
- 150000002688 maleic acid derivatives Chemical class 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 2
- 229940073769 methyl oleate Drugs 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 229960002969 oleic acid Drugs 0.000 description 2
- 235000021313 oleic acid Nutrition 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- 230000036556 skin irritation Effects 0.000 description 2
- 231100000475 skin irritation Toxicity 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 229940124543 ultraviolet light absorber Drugs 0.000 description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- FOLPKOWCPVGUCA-UHFFFAOYSA-N 1-(2-methoxypropoxy)propan-2-ol Chemical compound COC(C)COCC(C)O FOLPKOWCPVGUCA-UHFFFAOYSA-N 0.000 description 1
- VCVWNAWLJLMCBE-UHFFFAOYSA-N 2,2-dimethyldecanamide Chemical compound CCCCCCCCC(C)(C)C(N)=O VCVWNAWLJLMCBE-UHFFFAOYSA-N 0.000 description 1
- IEORSVTYLWZQJQ-UHFFFAOYSA-N 2-(2-nonylphenoxy)ethanol Chemical compound CCCCCCCCCC1=CC=CC=C1OCCO IEORSVTYLWZQJQ-UHFFFAOYSA-N 0.000 description 1
- LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 1
- ZFUKERYTFURFGA-UHFFFAOYSA-N Avermectin B1b Natural products O1C(C)C(O)C(OC)CC1OC1C(OC)CC(OC2C(=CCC3CC(CC4(O3)C=CC(C)C(C(C)C)O4)OC(=O)C3C=C(C)C(O)C4OCC(C34O)=CC=CC2C)C)OC1C ZFUKERYTFURFGA-UHFFFAOYSA-N 0.000 description 1
- 239000005730 Azoxystrobin Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 241000238578 Daphnia Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241000447437 Gerreidae Species 0.000 description 1
- 101100071588 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) HSP12 gene Proteins 0.000 description 1
- WDJHALXBUFZDSR-UHFFFAOYSA-N acetoacetic acid Chemical class CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000005233 alkylalcohol group Chemical group 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- RRZXIRBKKLTSOM-UHFFFAOYSA-N avermectin B1a Natural products C1=CC(C)C(C(C)CC)OC11OC(CC=C(C)C(OC2OC(C)C(OC3OC(C)C(O)C(OC)C3)C(OC)C2)C(C)C=CC=C2C3(C(C(=O)O4)C=C(C)C(O)C3OC2)O)CC4C1 RRZXIRBKKLTSOM-UHFFFAOYSA-N 0.000 description 1
- ZFUKERYTFURFGA-PVVXTEPVSA-N avermectin B1b Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C(C)C)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C ZFUKERYTFURFGA-PVVXTEPVSA-N 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- 125000003725 azepanyl group Chemical group 0.000 description 1
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- HCWYXKWQOMTBKY-UHFFFAOYSA-N calcium;dodecyl benzenesulfonate Chemical compound [Ca].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 HCWYXKWQOMTBKY-UHFFFAOYSA-N 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 231100000584 environmental toxicity Toxicity 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 125000005468 isobutylenyl group Chemical group 0.000 description 1
- 229960002479 isosorbide Drugs 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 230000019612 pigmentation Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- 150000003873 salicylate salts Chemical class 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- 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
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Toxicology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Organic Chemistry (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Claims (5)
- Szabadalmi igénypontok1, Készítmény, amely tartalmaz Ï ké|>tetű vegyhleíei: CíMíCO^cr-OildR1!" (i) óból Rf és Bejelentése egymástól íllggellerul! horogéig: vagy G*.,,: áltól, alkotni: vagy €5.4 slkloaíkii,. asjelyék tniodegyiks iáéi ésethea skhhsxmtiált legíellebb Iámig ». kovetkesök: kiMtl ilggetlerhíl Masztól :S^teáísmssöl: :febí| Mdrmiil %* Äoxi» iMÄl Is 1¾ didi R'! és R* jeiiíniése egymástól Ríggetlstibl Cj.3 áltól; vagy feli »égi esetbéa szubs.2iUuálvs: Íeg|é|«bb lÄR. a következik ikhztl tógpttestó választót; smlsztltóenssel: Ej.j ÄS; vagy R* és R? a Brtpgóitótóimmd «gy«|. helyhez kapcsolódjak, piof&itóil“, ihrralidMi-, pipritiimE vagy azepnMgyMR képnek, »melyek tóiMegyike adod eseílsp spbsziimák legfeljebb három, » kössössaök. közöl feggeífeató vijavtóoh sattbszSíiieMsel: (½ »Ikjl; és legalább egy, » köptkeztók atköítá ospgpíb#! válaszolt mezbgazdaságí vegyszert: Iriasxepse-eíi, Maadsp'öpHaid* Abampitó és Emämeetm, apai a fbliiellel, bogy a tpzögazdasági vegysasr sem: afoameeím vagy emameetm, ha az oldószer NRB-hldroxieíSHakíamid
- 2. Az elő# Igénypont szerkó i készimsétiy, ahol az I kőplató vegyijeiben R5 jeleatósc a<mcb|drógea, mohi, e-d, propll, zt-huíil, xaec-httiil, feo-btiîil, o-axolî, izo-atm), feo-bntikisil, «-hex 11, 1 -d-dlmetilbtsiil., allil, CHíCMjÖH, Rdódrosipropi, 3>lldyp3~í»Rjaí:ll,: í:,3-dtóídíóxE2mmtM-2^píoplk trlax-bi^xEmarrbíaefil, Cí-RCMjÖOMí, dklohexlí RoS, bentól;, «pfeilltólzS, fvfenlleíil, 3-lvi#oxipïg5ïl vagy 1-hidmxi-2-feató, la :R" Jelentése hidrogén; S! jelentésé: hei» metí| álli! vagy Um!; há .$t?‘ jelentése mehl; R*jÄÄ'd8ä5 eil; b»:R;3 jelentése e!i:!;: Rs jelentése aem «'batik ha R* jelentése onbníi R R* jefeniese hem fembatik ha R; jelentése &o-buiil; Rs jelentése «am a-amil, ha R.Ä jelentése o-amd; R^jeiestíése wem Ro-amti, ha 8* jelentés». ^ö-amiR R* jelentése nenï «-lexll, ha R” jelentése phexti; R* jelentése wem allil, ha RJ jelentése all!!; Rä jelentése sem haul vagy fenti, ha R: jelentése Rail; R1 jelentése .nem henzál, ha R*’ jelentése benxik &' jelentése oe«v O^O^Oll y^y':ei|f|i8 Rj jeletttéss CIREBjOM:; ,R: jelentéi!# nem 2-hidtoxiptopii, la R: jelentése a-hklroxzpropii:. és R: Is B;'' a mtrogénatomroal: fegylhk »tplylez kapcsolódnák, óém képeznek szuhszthuslatlan. morfatól·, pi.íTOlídithi- vágy pipendiml-gyónit. :k Bátanelyik előzd igénypont aaeétófl Ms/thncny, amely kwéhM íatlálmaz a következők alkótós esnprtből választól oldóas:e:rt: allas oldósáésvk, egyenes vagy elágázh lÉRú: páívlliok; ciklusos saénhidrógóöefc;: atétals óldósaesek; fbsxfhrtailalmú oldószerek; kétharlálídi (ïldèszerek; íhoktgóntarralmö. oldószerek: alliai; mono··, dt·· vagy tnesztarek. aromás HORör-ás·díét^erek; éikíasns észterek; ciklasos, altiâs: es áríéöás: betonok; alkil-dJklohexanonok, dímühkeamok, aeeíoaeeíáíök, heázibkeítmök; acetefeon; alkoholok; cifclntdkohoiok. glikölök; glifed-éetcsk és ástok. pollteetPfe prefilés-'glikölok;: giikokéletvaeeíáíök; aromás alkoholok; karbonátok; éterek és halogénézeií oldószerek, A. Az előző igénypont szer&*| készítmény, .étel afc olőöseer » MvstteÄ alkote csopottbêl vàfesz fehér olaj, dekáim; mono-* dk vagy triálklíálí gazolok; Solvesste i* vagy 3ÂÔ (íj; ixibmll-feszlSi vagy írisz-2-eii!hex!Slb»zfâi; m«ü~aieÉ:;: iftófeávk intoteasav; oiajssty; dimetíl-dekánamkl; teíramelimzol&Sí; Őitíréöb szdlibsdd; aíkil-kstrbamldok; alkatmiatiunok; -morfoHnok; atbiildk; ídkil-alkanoások, laktátok és ssetoaeetiiok; ímmMók, szakeMtok; zdlpátok; maisatok; glicerin és dírontsav-észterek; alkil-banzoátokj ÄdiylkdäÄbk; alkilmzalk'ííáiok; Éal&ok és dibetszöáíek; garnsna-busiroíaklo«; kaproiakton; terpén feakon; ciklobaxaSiM; älksb CifeIohe\ano!a>k; 2-eíS:Ui«xa8öl; elklbhezano!; íeírahidsss&tmtrsbalkohed;: etiléi?·· es propíÍéo-:pkől Is ézek polmmr-ei; djprop«tee-gJlfc$& mohoméit!·· vagy ítionoktéil-éier; diprepiten-fllknl-diacmp vágy ttftteípiléo·· glikol-iaonobaiil'esc;; be?tz?imikôito!::; popíin vagy bnisten-katbonái; dpetii-lzoszsrfeid:;: alkoxialkannlok; dlfaikéier; klórbenzol ésm klóralkások, Báratelyik előzi? igénypont szsrioíi fcészlímétty, .amely továbbá: íariatetaz: legalább égy» a kOvetkpzdk alkotta ésoporíbói yalasztdi, vegyi! leid; adfeváosek, ióifileíaktiv aayagöl;, polimerek, sár&tesrefc, számzékek vagy pigmentek, i?ilmho|yáÉ*tyí sbszt>rhfeá!ő sgérek, bskdrimneiteaes aprók, sók, :$msség®MmM szagylastó ésiHaleslíó szerek, izméóosiíé sxesyk, íá?-sőSdőspeek és rssdipslíŐszeí^k.: 6.. iárrnt-iyík előző igénypemt: :gpmiá iteszitnteny, ahol az ! képleté ; vegyüíet íM-^9% met??ty!s%boo yao jelen a kë^itmény tömegére számiévá és m ípeaőpzdaságl: vegyszer metmyissgbsn vaa Jeteit, fcasonléfcéppen tömegre számítva. ?. á i-é. igénypontok barmely IP szerb?#: készítmény, «tel az 1 képlett? vegySM #,1-99¾¾ tsmtmyíségte van jelen: a készítmény tőjoegp® számítva, a s»ezőgazdasági vegyszer ö,i-?S% mmgi&gW® van: jelen, tömegre számítva és az óidőszer 0,1 OKA- inconytségteo V&« jelen, itasoihőképpen: lőrsegre számítva,
- 8. Az dőzö igénypont sp:iji?í? készítmény, ai?ol az 1 képied?: vegyidet mezőgazdaság! vegysptfsez «s oldószerhez vnzonyito» >«$$y« & kővetkező halárokos ibelkl í?mgbsipö®öií: 4(11-1 ; öJl-1 #,#1-1,
- 9. Az etóxö igénypont; .szerinti kfe&steay·* :«itel az ! képlet# vegyöiet tnezogazdasági vegyszerhez és oldószerhez vtszoayitoti arényá ! ;!.;! vagy 2:1 ; 1 vagy 2:1:2 vagy 3: t i vsgy J: 1:2 vagy 4,5:1:4,S vagy 6:1:3. 10. idrotelydi dózó !gény|508t sPrlhti készimény, amely emtskiós kímeeatrátmnkéstt ©éj Ibmnliázolt, ti;, Epráa; báríhelylk előz# Igénypont szerinti: készítmény slbáliítíbíása, amely tZPaiisazza áx 3, igénypont szemét 1 képiéi# vsgyület osszskeveréséi az 1, Igértypoth szerinti mezőgazdasági vegysxeäTek
- 12. Az i-lÖ, igpypotítok yrmélyiké szerisis kásziiméay aikateazása ntezőgazdaságs kártevőnek s készítmény kátsevőm, az azt lartabnazd éllbelyre vagy őtidtelrSj amèlÿéii: az: képes jeím lmm!: törtét?#: leiaszsàlàsàva! va tó visszaszoí késáite szolgáló készítmény előáilííásálm O, Az l-i#:. igénypontok bérí'Steiyiké szerinti készítmény alkaltnazása nbvéayi kártevő vissZaszodtássÉv
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0716593.9A GB0716593D0 (en) | 2007-08-24 | 2007-08-24 | Improvements in or relating to organic compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HUE028200T2 true HUE028200T2 (hu) | 2016-12-28 |
Family
ID=38599261
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HUE08788307A HUE028200T2 (hu) | 2007-08-24 | 2008-08-12 | Továbbfejlesztések szerves vegyületekre vonatkozóan |
Country Status (35)
| Country | Link |
|---|---|
| US (1) | US20110230437A1 (hu) |
| EP (1) | EP2194779B1 (hu) |
| JP (1) | JP5539874B2 (hu) |
| KR (1) | KR20100058502A (hu) |
| CN (1) | CN101784185A (hu) |
| AP (1) | AP2515A (hu) |
| AR (1) | AR068616A1 (hu) |
| AU (1) | AU2008292011B2 (hu) |
| BR (1) | BRPI0816146A2 (hu) |
| CA (1) | CA2695499C (hu) |
| CR (1) | CR11246A (hu) |
| CY (1) | CY1118177T1 (hu) |
| DK (1) | DK2194779T3 (hu) |
| DO (1) | DOP2010000063A (hu) |
| EA (1) | EA018635B1 (hu) |
| EG (1) | EG26192A (hu) |
| ES (1) | ES2557004T3 (hu) |
| GB (1) | GB0716593D0 (hu) |
| GE (1) | GEP20125660B (hu) |
| GT (1) | GT201000048A (hu) |
| HR (1) | HRP20151354T1 (hu) |
| HU (1) | HUE028200T2 (hu) |
| MA (1) | MA31620B1 (hu) |
| MX (1) | MX2010001673A (hu) |
| MY (1) | MY152092A (hu) |
| NI (1) | NI201000027A (hu) |
| NZ (1) | NZ583090A (hu) |
| PL (1) | PL2194779T3 (hu) |
| PT (1) | PT2194779E (hu) |
| SI (1) | SI2194779T1 (hu) |
| TN (1) | TN2010000085A1 (hu) |
| TW (1) | TW200913880A (hu) |
| UA (1) | UA102073C2 (hu) |
| WO (1) | WO2009027626A2 (hu) |
| ZA (1) | ZA201000995B (hu) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2951447B1 (fr) | 2009-10-19 | 2012-10-19 | Rhodia Operations | Composes de type ether-amide et utilisattions |
| GB2482299A (en) * | 2010-07-27 | 2012-02-01 | Syngenta Ltd | Use of a dialkylamide to reduce the phytotoxicity of an agrochemical |
| HRP20210721T1 (hr) * | 2012-04-04 | 2021-06-11 | Syngenta Participations Ag | Pesticidni pripravak |
| UA118214C2 (uk) | 2014-02-14 | 2018-12-10 | Басф Агро Б.В. | Здатний до емульгування концентрат, що включає пестицид, жирний амід і лактамід |
| CA2938806C (en) * | 2014-02-14 | 2022-05-10 | BASF Agro B.V. | Emulsifiable concentrate comprising pesticide, alkyl lactate, and lactamide |
| CN109468459B (zh) * | 2018-11-20 | 2020-09-29 | 清华大学 | 锂萃取剂以及从盐湖卤水中提取锂的方法 |
| PY2222107A (es) * | 2021-03-30 | 2022-10-06 | Syngenta Crop Protection Ag | Formulación |
| WO2024201452A1 (en) * | 2023-03-24 | 2024-10-03 | Adama Makhteshim Ltd. | Liquid homogeneous agrochemical composition of insecticides |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1083501B (de) * | 1959-03-26 | 1960-06-15 | Merck Ag E | Verfahren zur Herstellung von Loesungen in Wasser schwer- oder unloeslicher Arzneimittel |
| EP0179583A1 (en) * | 1984-10-04 | 1986-04-30 | Merck & Co. Inc. | A system for enhancing the water dissolution rate and solubility of poorly soluble drugs |
| DE4130189A1 (de) * | 1991-04-19 | 1993-03-18 | Sehring Richard H Dr | Neue emulsionskonzentrate fuer den einsatz im pflanzenschutz |
| DE4112873A1 (de) * | 1991-04-19 | 1992-10-22 | Richard H Dr Sehring | Fungicides pflanzenschutzmittel mit wirkung im zierpflanzen und obstbau sowie gegen echten mehltau an getreide, gurken, reben und hopfen |
| AUPQ875700A0 (en) * | 2000-07-13 | 2000-08-03 | Reflex Research Limited | Combination compositions |
| DE102004013527A1 (de) * | 2004-03-19 | 2005-10-06 | Bayer Healthcare Ag | Parasitizide Mittel |
| GB0605780D0 (en) * | 2006-03-22 | 2006-05-03 | Syngenta Ltd | Formulations |
-
2007
- 2007-08-24 GB GBGB0716593.9A patent/GB0716593D0/en not_active Ceased
-
2008
- 2008-08-12 AP AP2010005161A patent/AP2515A/xx active
- 2008-08-12 CA CA2695499A patent/CA2695499C/en active Active
- 2008-08-12 NZ NZ583090A patent/NZ583090A/en unknown
- 2008-08-12 MY MYPI20100744 patent/MY152092A/en unknown
- 2008-08-12 EA EA201070306A patent/EA018635B1/ru not_active IP Right Cessation
- 2008-08-12 WO PCT/GB2008/002738 patent/WO2009027626A2/en not_active Ceased
- 2008-08-12 JP JP2010521464A patent/JP5539874B2/ja active Active
- 2008-08-12 CN CN200880104184A patent/CN101784185A/zh active Pending
- 2008-08-12 DK DK08788307.0T patent/DK2194779T3/en active
- 2008-08-12 AU AU2008292011A patent/AU2008292011B2/en active Active
- 2008-08-12 BR BRPI0816146-1A2A patent/BRPI0816146A2/pt not_active Application Discontinuation
- 2008-08-12 ES ES08788307.0T patent/ES2557004T3/es active Active
- 2008-08-12 SI SI200831547T patent/SI2194779T1/sl unknown
- 2008-08-12 PT PT87883070T patent/PT2194779E/pt unknown
- 2008-08-12 HU HUE08788307A patent/HUE028200T2/hu unknown
- 2008-08-12 EP EP08788307.0A patent/EP2194779B1/en active Active
- 2008-08-12 MX MX2010001673A patent/MX2010001673A/es not_active Application Discontinuation
- 2008-08-12 UA UAA201003387A patent/UA102073C2/ru unknown
- 2008-08-12 HR HRP20151354TT patent/HRP20151354T1/hr unknown
- 2008-08-12 PL PL08788307T patent/PL2194779T3/pl unknown
- 2008-08-12 KR KR1020107003959A patent/KR20100058502A/ko not_active Ceased
- 2008-08-12 US US12/674,741 patent/US20110230437A1/en not_active Abandoned
- 2008-08-12 GE GEAP200811737A patent/GEP20125660B/en unknown
- 2008-08-15 TW TW097131099A patent/TW200913880A/zh unknown
- 2008-08-22 AR ARP080103674A patent/AR068616A1/es active IP Right Grant
-
2010
- 2010-01-29 CR CR11246A patent/CR11246A/es not_active Application Discontinuation
- 2010-02-10 ZA ZA201000995A patent/ZA201000995B/xx unknown
- 2010-02-16 NI NI201000027A patent/NI201000027A/es unknown
- 2010-02-19 MA MA32633A patent/MA31620B1/fr unknown
- 2010-02-19 TN TNP2010000085A patent/TN2010000085A1/fr unknown
- 2010-02-22 EG EG2010020293A patent/EG26192A/en active
- 2010-02-23 GT GT201000048A patent/GT201000048A/es unknown
- 2010-02-23 DO DO2010000063A patent/DOP2010000063A/es unknown
-
2015
- 2015-12-21 CY CY20151101164T patent/CY1118177T1/el unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| HUE028200T2 (hu) | Továbbfejlesztések szerves vegyületekre vonatkozóan | |
| JP2009534302A (ja) | 製剤 | |
| HUE031139T2 (hu) | Javítások szerves vegyületekben vagy azokra vonatkozóan | |
| WO2012068001A1 (en) | N-alkyl lactam ethers, and compositions and uses thereof | |
| EP2439188A1 (de) | p-Menthan-3,8-diolderivate und sie enthaltende Insektenschutzmittel | |
| NZ280982A (en) | Antimicrobial composition having low voc (volatile organic compound) comprising a microemulsion (concentrate) of 2-n-octyl-3-isothiazolone and surfactant mixture of ethoxylated oil non-ionic surfactant and sulphated or sulphonated oil anionic surfactant | |
| FR2957492A1 (fr) | Nouvelles utilisations de composes de type esteramide | |
| FR2957596A1 (fr) | Nouveaux composes de type esteramide, leurs procedes de preparation et leurs utilisations | |
| DE2265312B2 (de) | 2-Amino-4-hydroxy-pyrimidüi-sulfaminsäureester | |
| DE19652531C2 (de) | Verfahren zur Herstellung eines 3-Isothiazolongemisches und eine das Gemisch enthaltende Zusammensetzung | |
| EP0648416A1 (fr) | Associations fongicides à base d'un phénylbenzamide | |
| AU2011284344B2 (en) | Formulations | |
| CA2529689A1 (en) | Paint scenting additive mixtures | |
| EP0840549A1 (fr) | Associations insecticides d'un oxime carbamate avec un insecticide a groupe pyrazole, pyrrole ou phenylimidazole | |
| DD289531A5 (de) | Macrolidverbindungen | |
| FR2574626A1 (fr) | Compositions fongicides selectives contenant des sels d'acides benzenesulfoniques et leurs applications | |
| JPH03161405A (ja) | 有害雑草の防除方法 | |
| JPH03161406A (ja) | 有害雑草の防除方法 | |
| DE1205088B (de) | Verfahren zur Herstellung von Xanthogensaeureestern |