FI65531C - Medel foer tillvaextreglering eller i synnerhet foer avloevande av vaexter - Google Patents
Medel foer tillvaextreglering eller i synnerhet foer avloevande av vaexter Download PDFInfo
- Publication number
- FI65531C FI65531C FI813262A FI813262A FI65531C FI 65531 C FI65531 C FI 65531C FI 813262 A FI813262 A FI 813262A FI 813262 A FI813262 A FI 813262A FI 65531 C FI65531 C FI 65531C
- Authority
- FI
- Finland
- Prior art keywords
- preparation according
- thiadiazol
- urea
- thiadiazolin
- weight
- Prior art date
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- -1 C 1 -C 4 alkylphenyl Chemical group 0.000 claims description 49
- 238000002360 preparation method Methods 0.000 claims description 40
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 24
- 241000196324 Embryophyta Species 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 22
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 13
- 239000000126 substance Substances 0.000 claims description 12
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 9
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 7
- 239000000376 reactant Substances 0.000 claims description 7
- HQYZTGGAEAFKIO-UHFFFAOYSA-N thiadiazol-5-ylurea Chemical class NC(=O)NC1=CN=NS1 HQYZTGGAEAFKIO-UHFFFAOYSA-N 0.000 claims description 6
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 claims description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 5
- 239000000969 carrier Substances 0.000 claims description 5
- 239000011734 sodium Substances 0.000 claims description 5
- 239000004094 surface-active agent Substances 0.000 claims description 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 4
- 239000011575 calcium Substances 0.000 claims description 4
- 159000000007 calcium salts Chemical class 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 239000011777 magnesium Substances 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 125000006501 nitrophenyl group Chemical group 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- 239000001301 oxygen Substances 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 125000004076 pyridyl group Chemical group 0.000 claims description 4
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 4
- 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 229910052717 sulfur Chemical group 0.000 claims description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- 229910000404 tripotassium phosphate Inorganic materials 0.000 claims description 4
- 235000019798 tripotassium phosphate Nutrition 0.000 claims description 4
- VJXKPMICAFCWKC-UHFFFAOYSA-N 1-pyridin-2-yl-3-(thiadiazol-5-yl)urea Chemical compound C=1C=CC=NC=1NC(=O)NC1=CN=NS1 VJXKPMICAFCWKC-UHFFFAOYSA-N 0.000 claims description 3
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 claims description 3
- 229910019142 PO4 Inorganic materials 0.000 claims description 3
- HFCYZXMHUIHAQI-UHFFFAOYSA-N Thidiazuron Chemical compound C=1C=CC=CC=1NC(=O)NC1=CN=NS1 HFCYZXMHUIHAQI-UHFFFAOYSA-N 0.000 claims description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 3
- 239000001099 ammonium carbonate Substances 0.000 claims description 3
- 235000012501 ammonium carbonate Nutrition 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 125000005059 halophenyl group Chemical group 0.000 claims description 3
- 230000008635 plant growth Effects 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- 239000011701 zinc Substances 0.000 claims description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 claims description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 2
- 150000001340 alkali metals Chemical group 0.000 claims description 2
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical group [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims description 2
- 229910052791 calcium Inorganic materials 0.000 claims description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 2
- 229910052744 lithium Inorganic materials 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 2
- FQENQNTWSFEDLI-UHFFFAOYSA-J sodium diphosphate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]P([O-])(=O)OP([O-])([O-])=O FQENQNTWSFEDLI-UHFFFAOYSA-J 0.000 claims description 2
- 239000001488 sodium phosphate Substances 0.000 claims description 2
- 239000011593 sulfur Chemical group 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- 235000019818 tetrasodium diphosphate Nutrition 0.000 claims description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 claims description 2
- 229910000406 trisodium phosphate Inorganic materials 0.000 claims description 2
- 235000019801 trisodium phosphate Nutrition 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 claims 2
- RYCLIXPGLDDLTM-UHFFFAOYSA-J tetrapotassium;phosphonato phosphate Chemical compound [K+].[K+].[K+].[K+].[O-]P([O-])(=O)OP([O-])([O-])=O RYCLIXPGLDDLTM-UHFFFAOYSA-J 0.000 claims 2
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 claims 1
- GIQXLBILFSQJRG-UHFFFAOYSA-N 1-methyl-1-phenyl-3-(thiadiazol-5-yl)urea Chemical compound C=1C=CC=CC=1N(C)C(=O)NC1=CN=NS1 GIQXLBILFSQJRG-UHFFFAOYSA-N 0.000 claims 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
- 240000002024 Gossypium herbaceum Species 0.000 claims 1
- 235000004341 Gossypium herbaceum Nutrition 0.000 claims 1
- 150000001447 alkali salts Chemical class 0.000 claims 1
- 125000005036 alkoxyphenyl group Chemical group 0.000 claims 1
- 125000005037 alkyl phenyl group Chemical group 0.000 claims 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 claims 1
- 239000004312 hexamethylene tetramine Substances 0.000 claims 1
- 159000000003 magnesium salts Chemical class 0.000 claims 1
- 150000002696 manganese Chemical class 0.000 claims 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 claims 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 1
- 239000010452 phosphate Substances 0.000 claims 1
- 150000003672 ureas Chemical class 0.000 claims 1
- 150000003839 salts Chemical class 0.000 description 16
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 15
- 229920000742 Cotton Polymers 0.000 description 13
- 241000219146 Gossypium Species 0.000 description 13
- 230000000694 effects Effects 0.000 description 10
- 239000004202 carbamide Substances 0.000 description 9
- 238000002474 experimental method Methods 0.000 description 9
- 235000015320 potassium carbonate Nutrition 0.000 description 7
- 239000004480 active ingredient Substances 0.000 description 5
- 239000013543 active substance Substances 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 230000012010 growth Effects 0.000 description 5
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-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
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000440 bentonite Substances 0.000 description 3
- 229910000278 bentonite Inorganic materials 0.000 description 3
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 3
- 230000002363 herbicidal effect Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 230000002195 synergetic effect Effects 0.000 description 3
- UGUHFDPGDQDVGX-UHFFFAOYSA-N 1,2,3-thiadiazole Chemical compound C1=CSN=N1 UGUHFDPGDQDVGX-UHFFFAOYSA-N 0.000 description 2
- LUBJCRLGQSPQNN-UHFFFAOYSA-N 1-Phenylurea Chemical compound NC(=O)NC1=CC=CC=C1 LUBJCRLGQSPQNN-UHFFFAOYSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 235000005206 Hibiscus Nutrition 0.000 description 2
- 235000007185 Hibiscus lunariifolius Nutrition 0.000 description 2
- 244000284380 Hibiscus rosa sinensis Species 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 235000020289 caffè mocha Nutrition 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000005202 decontamination Methods 0.000 description 2
- 230000003588 decontaminative effect Effects 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 238000003306 harvesting Methods 0.000 description 2
- 239000004009 herbicide Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 229920005610 lignin Polymers 0.000 description 2
- 239000011572 manganese Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- MBDQPNKRJDWOGF-UHFFFAOYSA-N 1-(4-methylpyrimidin-2-yl)-3-(thiadiazol-5-yl)urea Chemical compound CC1=CC=NC(NC(=O)NC=2SN=NC=2)=N1 MBDQPNKRJDWOGF-UHFFFAOYSA-N 0.000 description 1
- VOWZCUPCCYEQIN-UHFFFAOYSA-N 1-phenyl-1-(thiadiazol-5-yl)urea Chemical compound C=1C=CC=CC=1N(C(=O)N)C1=CN=NS1 VOWZCUPCCYEQIN-UHFFFAOYSA-N 0.000 description 1
- VZJJFYKWJUQLLH-UHFFFAOYSA-N 1-pyridin-4-yl-3-(thiadiazol-5-yl)urea Chemical compound C=1C=NC=CC=1NC(=O)NC1=CN=NS1 VZJJFYKWJUQLLH-UHFFFAOYSA-N 0.000 description 1
- DPWOISJOHBVMNF-UHFFFAOYSA-N 2,3-dihydrothiadiazole Chemical class N1NC=CS1 DPWOISJOHBVMNF-UHFFFAOYSA-N 0.000 description 1
- JACPTQMMZGZAOL-KHPPLWFESA-N 2-[methyl-[(z)-octadec-9-enyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCN(C)CCS(O)(=O)=O JACPTQMMZGZAOL-KHPPLWFESA-N 0.000 description 1
- IBTXNXRRUSMJKO-UHFFFAOYSA-N CC1=CC(=NC=C1)NC(=O)NC1=CN=NS1.NC(=O)N Chemical compound CC1=CC(=NC=C1)NC(=O)NC1=CN=NS1.NC(=O)N IBTXNXRRUSMJKO-UHFFFAOYSA-N 0.000 description 1
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- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
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- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
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- 235000010446 mineral oil Nutrition 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
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- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical compound C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-UHFFFAOYSA-N 0.000 description 1
- 230000002485 urinary effect Effects 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 239000008096 xylene 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3040902 | 1980-10-27 | ||
| DE19803040902 DE3040902A1 (de) | 1980-10-27 | 1980-10-27 | Mittel insbesondere zur entblaetterung von pflanzen |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI813262L FI813262L (fi) | 1982-04-28 |
| FI65531B FI65531B (fi) | 1984-02-29 |
| FI65531C true FI65531C (fi) | 1984-06-11 |
Family
ID=6115564
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI813262A FI65531C (fi) | 1980-10-27 | 1981-10-19 | Medel foer tillvaextreglering eller i synnerhet foer avloevande av vaexter |
Country Status (35)
| Country | Link |
|---|---|
| JP (1) | JPS5799504A (cs) |
| KR (1) | KR830007606A (cs) |
| AT (1) | AT380624B (cs) |
| AU (1) | AU550920B2 (cs) |
| BE (1) | BE890871A (cs) |
| BG (1) | BG37071A3 (cs) |
| BR (1) | BR8106908A (cs) |
| CA (1) | CA1165580A (cs) |
| CH (1) | CH647928A5 (cs) |
| CS (1) | CS221995B2 (cs) |
| DD (1) | DD201560A5 (cs) |
| DE (1) | DE3040902A1 (cs) |
| DK (1) | DK440481A (cs) |
| EG (1) | EG15216A (cs) |
| FI (1) | FI65531C (cs) |
| FR (1) | FR2492632B1 (cs) |
| GB (1) | GB2086228B (cs) |
| GR (1) | GR74697B (cs) |
| HU (1) | HU188555B (cs) |
| IE (1) | IE51687B1 (cs) |
| IL (1) | IL64096A (cs) |
| IN (1) | IN157368B (cs) |
| IT (1) | IT1139268B (cs) |
| LU (1) | LU83705A1 (cs) |
| MA (1) | MA19312A1 (cs) |
| NL (1) | NL8104620A (cs) |
| NZ (1) | NZ198660A (cs) |
| PH (1) | PH18494A (cs) |
| PL (1) | PL127943B1 (cs) |
| RO (1) | RO84304B (cs) |
| SE (1) | SE448143B (cs) |
| SU (1) | SU1245252A3 (cs) |
| TR (1) | TR21352A (cs) |
| ZA (1) | ZA817446B (cs) |
| ZW (1) | ZW25981A1 (cs) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2522065B (en) | 2014-01-14 | 2015-12-02 | Crop Intellect Ltd | Agrochemical composition |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2506690A1 (de) * | 1975-02-14 | 1976-09-02 | Schering Ag | Mittel zur entblaetterung von pflanzen |
| DE2719810A1 (de) * | 1977-04-28 | 1978-11-02 | Schering Ag | 1,2,3-thiadiazolin-2-id-derivate, verfahren zur herstellung dieser verbindungen sowie diese enthaltende mittel mit wachstumsregulatorischer wirkung fuer pflanzen |
-
1980
- 1980-10-27 DE DE19803040902 patent/DE3040902A1/de not_active Withdrawn
-
1981
- 1981-09-28 SU SU813360509A patent/SU1245252A3/ru active
- 1981-10-05 DK DK440481A patent/DK440481A/da not_active Application Discontinuation
- 1981-10-09 NL NL8104620A patent/NL8104620A/nl not_active Application Discontinuation
- 1981-10-12 IN IN653/DEL/81A patent/IN157368B/en unknown
- 1981-10-15 NZ NZ198660A patent/NZ198660A/en unknown
- 1981-10-19 FI FI813262A patent/FI65531C/fi not_active IP Right Cessation
- 1981-10-21 IT IT24600/81A patent/IT1139268B/it active
- 1981-10-21 DD DD81234265A patent/DD201560A5/de unknown
- 1981-10-22 CA CA000388500A patent/CA1165580A/en not_active Expired
- 1981-10-22 CS CS817744A patent/CS221995B2/cs unknown
- 1981-10-22 IL IL64096A patent/IL64096A/xx unknown
- 1981-10-22 LU LU83705A patent/LU83705A1/de unknown
- 1981-10-22 FR FR8119817A patent/FR2492632B1/fr not_active Expired
- 1981-10-23 AT AT0454481A patent/AT380624B/de not_active IP Right Cessation
- 1981-10-23 GR GR66348A patent/GR74697B/el unknown
- 1981-10-23 CH CH6799/81A patent/CH647928A5/de not_active IP Right Cessation
- 1981-10-23 PL PL1981233556A patent/PL127943B1/pl unknown
- 1981-10-23 JP JP56168862A patent/JPS5799504A/ja active Pending
- 1981-10-23 IE IE2485/81A patent/IE51687B1/en unknown
- 1981-10-26 TR TR21352A patent/TR21352A/xx unknown
- 1981-10-26 BR BR8106908A patent/BR8106908A/pt unknown
- 1981-10-26 SE SE8106300A patent/SE448143B/sv not_active IP Right Cessation
- 1981-10-26 GB GB8132217A patent/GB2086228B/en not_active Expired
- 1981-10-26 BE BE0/206350A patent/BE890871A/fr not_active IP Right Cessation
- 1981-10-26 HU HU813141A patent/HU188555B/hu unknown
- 1981-10-26 BG BG053942A patent/BG37071A3/xx unknown
- 1981-10-27 AU AU76849/81A patent/AU550920B2/en not_active Ceased
- 1981-10-27 ZW ZW259/81A patent/ZW25981A1/xx unknown
- 1981-10-27 MA MA19514A patent/MA19312A1/fr unknown
- 1981-10-27 PH PH26406A patent/PH18494A/en unknown
- 1981-10-27 ZA ZA817446A patent/ZA817446B/xx unknown
- 1981-10-27 KR KR1019810004089A patent/KR830007606A/ko not_active Ceased
- 1981-10-27 EG EG624/81A patent/EG15216A/xx active
- 1981-10-27 RO RO105654A patent/RO84304B/ro unknown
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed |
Owner name: SCHERING AKTIENGESELLSCHAFT |