PL63861B1 - - Google Patents

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Info

Publication number: PL63861B1
Authority: PL; Poland
Prior art keywords: formula; compound; weeds; methyl; parts
Prior art date: 1967-10-18

Application number

PL123083A

Other languages

English (en)

Polish (pl)

Original Assignee

Ciba Socicte Anonyme

Filing date

1967-10-18

Publication date

1971-08-31

1967-10-18 Application filed by Ciba Socicte Anonyme filed Critical Ciba Socicte Anonyme

1971-08-31 Publication of PL63861B1 publication Critical patent/PL63861B1/pl

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150000001875 compounds Chemical class 0.000 claims description 35
241000196324 Embryophyta Species 0.000 claims description 25
239000003795 chemical substances by application Substances 0.000 claims description 11
239000004480 active ingredient Substances 0.000 claims description 9
239000000203 mixture Substances 0.000 claims description 9
-1 4-bromo-3-chlorophenyl Chemical group 0.000 claims description 8
240000008042 Zea mays Species 0.000 claims description 7
235000002017 Zea mays subsp mays Nutrition 0.000 claims description 7
239000004009 herbicide Substances 0.000 claims description 7
244000068988 Glycine max Species 0.000 claims description 6
235000010469 Glycine max Nutrition 0.000 claims description 6
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 claims description 6
235000009973 maize Nutrition 0.000 claims description 6
235000013339 cereals Nutrition 0.000 claims description 5
239000002270 dispersing agent Substances 0.000 claims description 4
239000003995 emulsifying agent Substances 0.000 claims description 4
NLYNUTMZTCLNOO-UHFFFAOYSA-N Chlorbromuron Chemical compound CON(C)C(=O)NC1=CC=C(Br)C(Cl)=C1 NLYNUTMZTCLNOO-UHFFFAOYSA-N 0.000 claims description 3
239000002904 solvent Substances 0.000 claims description 3
241000238876 Acari Species 0.000 claims description 2
241000233866 Fungi Species 0.000 claims description 2
241000238631 Hexapoda Species 0.000 claims description 2
241000244206 Nematoda Species 0.000 claims description 2
241000607479 Yersinia pestis Species 0.000 claims description 2
239000000654 additive Substances 0.000 claims description 2
239000011230 binding agent Substances 0.000 claims description 2
239000000969 carrier Substances 0.000 claims description 2
239000003085 diluting agent Substances 0.000 claims description 2
239000003337 fertilizer Substances 0.000 claims description 2
239000002562 thickening agent Substances 0.000 claims description 2
239000002318 adhesion promoter Substances 0.000 claims 1
RZILCCPWPBTYDO-UHFFFAOYSA-N fluometuron Chemical compound CN(C)C(=O)NC1=CC=CC(C(F)(F)F)=C1 RZILCCPWPBTYDO-UHFFFAOYSA-N 0.000 claims 1
229940125904 compound 1 Drugs 0.000 description 16
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235000021307 Triticum Nutrition 0.000 description 9
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235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 3
235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
239000012141 concentrate Substances 0.000 description 3
238000003306 harvesting Methods 0.000 description 3
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 3
150000003672 ureas Chemical class 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
241001621841 Alopecurus myosuroides Species 0.000 description 2
239000005995 Aluminium silicate Substances 0.000 description 2
240000005979 Hordeum vulgare Species 0.000 description 2
235000007340 Hordeum vulgare Nutrition 0.000 description 2
244000042664 Matricaria chamomilla Species 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
235000005775 Setaria Nutrition 0.000 description 2
241000232088 Setaria <nematode> Species 0.000 description 2
241000220261 Sinapis Species 0.000 description 2
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 2
241001148683 Zostera marina Species 0.000 description 2
235000012211 aluminium silicate Nutrition 0.000 description 2
239000013068 control sample Substances 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
230000008029 eradication Effects 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
235000013312 flour Nutrition 0.000 description 2
239000008187 granular material Substances 0.000 description 2
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
235000019198 oils Nutrition 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
238000009331 sowing Methods 0.000 description 2
239000007921 spray Substances 0.000 description 2
230000002195 synergetic effect Effects 0.000 description 2
235000013311 vegetables Nutrition 0.000 description 2
239000008096 xylene Substances 0.000 description 2
MWAQUCGIDKZDEQ-UHFFFAOYSA-N 1,1-dimethyl-3-[2-(trifluoromethyl)phenyl]urea Chemical compound CN(C)C(=O)NC1=CC=CC=C1C(F)(F)F MWAQUCGIDKZDEQ-UHFFFAOYSA-N 0.000 description 1
GBDZXPJXOMHESU-UHFFFAOYSA-N 1,2,3,4-tetrachlorobenzene Chemical class ClC1=CC=C(Cl)C(Cl)=C1Cl GBDZXPJXOMHESU-UHFFFAOYSA-N 0.000 description 1
PIGINCCGZHXGRB-UHFFFAOYSA-N 3-(3-chlorophenyl)-1-methoxy-1-methylurea Chemical compound CON(C)C(=O)NC1=CC=CC(Cl)=C1 PIGINCCGZHXGRB-UHFFFAOYSA-N 0.000 description 1
AJBZENLMTKDAEK-UHFFFAOYSA-N 3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-4,9-diol Chemical compound CC12CCC(O)C(C)(C)C1CCC(C1(C)CC3O)(C)C2CCC1C1C3(C)CCC1C(=C)C AJBZENLMTKDAEK-UHFFFAOYSA-N 0.000 description 1
BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
241000743985 Alopecurus Species 0.000 description 1
235000007639 Anthemis cotula Nutrition 0.000 description 1
241001666377 Apera Species 0.000 description 1
DJHGAFSJWGLOIV-UHFFFAOYSA-K Arsenate3- Chemical class [O-][As]([O-])([O-])=O DJHGAFSJWGLOIV-UHFFFAOYSA-K 0.000 description 1
241000219198 Brassica Species 0.000 description 1
235000011331 Brassica Nutrition 0.000 description 1
235000008427 Brassica arvensis Nutrition 0.000 description 1
244000024671 Brassica kaber Species 0.000 description 1
235000004977 Brassica sinapistrum Nutrition 0.000 description 1
235000003880 Calendula Nutrition 0.000 description 1
240000001432 Calendula officinalis Species 0.000 description 1
244000025254 Cannabis sativa Species 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
241000219312 Chenopodium Species 0.000 description 1
XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical class [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
235000007516 Chrysanthemum Nutrition 0.000 description 1
240000005250 Chrysanthemum indicum Species 0.000 description 1
235000002918 Fraxinus excelsior Nutrition 0.000 description 1
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 description 1
235000021506 Ipomoea Nutrition 0.000 description 1
241000207783 Ipomoea Species 0.000 description 1
235000017945 Matricaria Nutrition 0.000 description 1
235000007232 Matricaria chamomilla Nutrition 0.000 description 1
244000182930 Matricaria sp Species 0.000 description 1
235000008885 Matricaria sp Nutrition 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241000283973 Oryctolagus cuniculus Species 0.000 description 1
241000209504 Poaceae Species 0.000 description 1
241000205407 Polygonum Species 0.000 description 1
241000219295 Portulaca Species 0.000 description 1
DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
240000006394 Sorghum bicolor Species 0.000 description 1
235000011684 Sorghum saccharatum Nutrition 0.000 description 1
240000006694 Stellaria media Species 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
241000219422 Urtica Species 0.000 description 1
241000219873 Vicia Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
229960000583 acetic acid Drugs 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000003463 adsorbent Substances 0.000 description 1
229920000615 alginic acid Polymers 0.000 description 1
235000010443 alginic acid Nutrition 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
GCPXMJHSNVMWNM-UHFFFAOYSA-N arsenous acid Chemical class O[As](O)O GCPXMJHSNVMWNM-UHFFFAOYSA-N 0.000 description 1
239000002956 ash Substances 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
238000009835 boiling Methods 0.000 description 1
150000001642 boronic acid derivatives Chemical class 0.000 description 1
230000031709 bromination Effects 0.000 description 1
238000005893 bromination reaction Methods 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
229910000389 calcium phosphate Inorganic materials 0.000 description 1
235000011010 calcium phosphates Nutrition 0.000 description 1
OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000005018 casein Substances 0.000 description 1
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
235000021240 caseins Nutrition 0.000 description 1
229960001927 cetylpyridinium chloride Drugs 0.000 description 1
YMKDRGPMQRFJGP-UHFFFAOYSA-M cetylpyridinium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 YMKDRGPMQRFJGP-UHFFFAOYSA-M 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000011280 coal tar Substances 0.000 description 1
229940125810 compound 20 Drugs 0.000 description 1
239000007799 cork Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical class OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
230000006378 damage Effects 0.000 description 1
239000002283 diesel fuel Substances 0.000 description 1
FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 1
238000010410 dusting Methods 0.000 description 1
230000002500 effect on skin Effects 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000012362 glacial acetic acid Substances 0.000 description 1
239000003292 glue Substances 0.000 description 1
230000009931 harmful effect Effects 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
125000001183 hydrocarbyl group Chemical group 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
239000011707 mineral Substances 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
239000010742 number 1 fuel oil Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
150000004714 phosphonium salts Chemical class 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
239000000047 product Substances 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
239000002023 wood Substances 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1

PL123083A 1967-10-18 PL63861B1 (de)

Publications (1)

Publication Number	Publication Date
PL63861B1 true PL63861B1 (de)	1971-08-31

Publication	Publication Date	Title
UA71569C2 (en)	2004-12-15	Method of controlling weeds and a herbicidal agent
PL218214B1 (pl)	2014-10-31	Zastosowanie kompozycji herbicydów typu glufosynatu i chlopyralidu do zwalczania szkodliwych roślin w uprawach buraków cukrowych i sposób zwalczania szkodliwych roślin w tolerujących uprawach buraków cukrowych
PL175384B1 (pl)	1998-12-31	Kompozycja herbicydowa i sposób zwalczania chwastów
CH633260A5 (de)	1982-11-30	N'-(4-phenylaethyloxyphenyl)-n-methyl-n-methoxyharnstoffe, bei denen der phenylrest des phenylaethylrestes substituiert ist.
PL183859B1 (pl)	2002-07-31	Synergiczny środek chwastobójczy, sposób zwalczania kiełkowania i wzrostu niepożądanej roślinności oraz sposób selektywnego zwalczania wzrostu lub kiełkowania niepożądanych roślin
DE69329531T2 (de)	2001-02-08	Triazolinone enthaltende herbizide zusammensetzungen
RU2052932C1 (ru)	1996-01-27	Гербицидная синергитическая композиция и способ подавления нежелательной растительности
US11690377B2 (en)	2023-07-04	Herbicidal composition and method of use thereof
DE60027347T2 (de)	2007-02-08	Herbizide Zusammensetzungen
US4185993A (en)	1980-01-29	Herbicidal compositions and methods
DE1965134A1 (de)	1971-07-15	Schaedlingsbekaempfungsmittel
US4032324A (en)	1977-06-28	Synergistic herbicidal composition for the control of weeds
JPS5942306A (ja)	1984-03-08	移植した稲植物の作物または水中で種子から生長する稲作物中の雑草を選択的に防除するための組成物および方法
JPS5857404B2 (ja)	1983-12-20	除草剤組成物
PT99272A (pt)	1992-09-30	Processo para a preparacao de composicoes herbicidas contendo misturas sinergicas de (2r)-2-{4-(6-cloroquinoxalin-2-iloxi)-fenoxi}-propionato de (-+)-tetra-hidrofurfurilo com diversos outros agentes herbicidas selectivos
EP0110660B1 (de)	1987-04-08	Synergistische herbizide Kombination
SK93293A3 (en)	1994-06-08	Herbicidal composition
PL93788B1 (de)	1977-06-30
US4220467A (en)	1980-09-02	Composition and method for combatting weeds in cereals
US4042628A (en)	1977-08-16	2,6-Dinitro-4-trifluoromethylanilines
PL129327B1 (en)	1984-05-31	Herbicide and method of obtaining new sulfonamidic derivatives
DE2635967A1 (de)	1977-03-17	2-cyanacetamid-derivate und ihre herstellung und anwendung
EP0149268A2 (de)	1985-07-24	Verfahren zur Bekämpfung von Pflanzenwuchs
DE2633159C2 (de)	1982-05-27	Phosphorhaltige Verbindungen, Verfahren zu ihrer Herstellung, sowie diese Verbindungen enthaltende herbizide Mittel
US3933464A (en)	1976-01-20	Herbicide

PL63861B1 - - Google Patents

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