DD145695A5 - Herbizide mittel - Google Patents

Herbizide mittel Download PDF

Info

Publication number: DD145695A5
Authority: DD; German Democratic Republic
Prior art keywords: chloro; triazine; iii; case; herbicidal
Prior art date: 1978-09-08

Application number

DD79215385A

Other languages

German (de)

English (en)

Inventor

Hermann Bieringer

Friedhelm Schwerdtle

Original Assignee

Hoechst 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.)

1978-09-08

Filing date

1979-09-06

Publication date

1981-01-07

1979-09-06 Application filed by Hoechst Ag filed Critical Hoechst Ag

1981-01-07 Publication of DD145695A5 publication Critical patent/DD145695A5/de

Links

239000004009 herbicide Substances 0.000 title claims description 18
230000002363 herbicidal effect Effects 0.000 title claims description 17
239000000203 mixture Substances 0.000 claims description 25
241000196324 Embryophyta Species 0.000 claims description 18
150000001875 compounds Chemical class 0.000 claims description 16
239000004480 active ingredient Substances 0.000 claims description 6
238000009472 formulation Methods 0.000 claims description 4
229940126062 Compound A Drugs 0.000 claims description 3
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims description 3
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 3
150000003918 triazines Chemical class 0.000 claims description 3
YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 claims description 2
MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 claims description 2
238000000034 method Methods 0.000 claims description 2
BMLIZLVNXIYGCK-UHFFFAOYSA-N monuron Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C=C1 BMLIZLVNXIYGCK-UHFFFAOYSA-N 0.000 claims description 2
150000003672 ureas Chemical class 0.000 claims description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
PPKPKFIWDXDAGC-IHWYPQMZSA-N (z)-1,2-dichloroprop-1-ene Chemical compound C\C(Cl)=C\Cl PPKPKFIWDXDAGC-IHWYPQMZSA-N 0.000 claims 1
UMPSXRYVXUPCOS-UHFFFAOYSA-N 2,3-dichlorophenol Chemical compound OC1=CC=CC(Cl)=C1Cl UMPSXRYVXUPCOS-UHFFFAOYSA-N 0.000 claims 1
125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims 1
XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 claims 1
XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical group CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 claims 1
239000005510 Diuron Substances 0.000 claims 1
239000005573 Linuron Substances 0.000 claims 1
239000005574 MCPA Substances 0.000 claims 1
LKJPSUCKSLORMF-UHFFFAOYSA-N Monolinuron Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C=C1 LKJPSUCKSLORMF-UHFFFAOYSA-N 0.000 claims 1
XGEGHDBEHXKFPX-UHFFFAOYSA-N N-methyl urea Chemical compound CNC(N)=O XGEGHDBEHXKFPX-UHFFFAOYSA-N 0.000 claims 1
WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims 1
RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical group CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 claims 1
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 claims 1
STAPBGVGYWCRTF-UHFFFAOYSA-M sodium;2-(4-chloro-2-methylphenoxy)acetate Chemical compound [Na+].CC1=CC(Cl)=CC=C1OCC([O-])=O STAPBGVGYWCRTF-UHFFFAOYSA-M 0.000 claims 1
FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical group CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 claims 1
230000000694 effects Effects 0.000 description 13
229910052708 sodium Inorganic materials 0.000 description 10
239000011734 sodium Substances 0.000 description 10
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 8
239000000843 powder Substances 0.000 description 7
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
241000508725 Elymus repens Species 0.000 description 6
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
239000013543 active substance Substances 0.000 description 5
239000004495 emulsifiable concentrate Substances 0.000 description 5
239000000126 substance Substances 0.000 description 5
239000002253 acid Substances 0.000 description 4
239000000243 solution Substances 0.000 description 4
230000002195 synergetic effect Effects 0.000 description 4
LUBJCRLGQSPQNN-UHFFFAOYSA-N 1-Phenylurea Chemical compound NC(=O)NC1=CC=CC=C1 LUBJCRLGQSPQNN-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
244000025254 Cannabis sativa Species 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
241000555745 Sciuridae Species 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
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
230000000996 additive effect Effects 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
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 2
238000002360 preparation method Methods 0.000 description 2
239000000377 silicon dioxide Substances 0.000 description 2
239000007921 spray Substances 0.000 description 2
230000000007 visual effect Effects 0.000 description 2
239000004563 wettable powder Substances 0.000 description 2
SMYMJHWAQXWPDB-UHFFFAOYSA-N (2,4,5-trichlorophenoxy)acetic acid Chemical compound OC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl SMYMJHWAQXWPDB-UHFFFAOYSA-N 0.000 description 1
125000000008 (C1-C10) alkyl group Chemical group 0.000 description 1
JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical class C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 description 1
ZMESHQOXZMOOQQ-UHFFFAOYSA-N 1-(naphthalen-1-ylmethyl)naphthalene Chemical compound C1=CC=C2C(CC=3C4=CC=CC=C4C=CC=3)=CC=CC2=C1 ZMESHQOXZMOOQQ-UHFFFAOYSA-N 0.000 description 1
239000003559 2,4,5-trichlorophenoxyacetic acid Substances 0.000 description 1
MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 description 1
FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical compound COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
241000283690 Bos taurus Species 0.000 description 1
241000339490 Brachyachne Species 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
241000252095 Congridae Species 0.000 description 1
206010011878 Deafness Diseases 0.000 description 1
101100310856 Drosophila melanogaster spri gene Proteins 0.000 description 1
241000380130 Ehrharta erecta Species 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
241001473279 Liatris Species 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
241000209082 Lolium Species 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
OMBMFTUITNFNAW-UHFFFAOYSA-N OCC(CO)(CO)N(P)CC(O)=O Chemical class OCC(CO)(CO)N(P)CC(O)=O OMBMFTUITNFNAW-UHFFFAOYSA-N 0.000 description 1
REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical class CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
241001268782 Paspalum dilatatum Species 0.000 description 1
241001148683 Zostera marina Species 0.000 description 1
230000001133 acceleration Effects 0.000 description 1
239000000654 additive Substances 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
-1 alkylphenyl sulfonates Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
238000009835 boiling Methods 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
235000013339 cereals Nutrition 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
QNICMVJKCYAMIK-UHFFFAOYSA-L disodium octadecanoate Chemical compound [Na+].[Na+].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O QNICMVJKCYAMIK-UHFFFAOYSA-L 0.000 description 1
YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
239000000890 drug combination Substances 0.000 description 1
238000004049 embossing Methods 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
210000003608 fece Anatomy 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
230000012010 growth Effects 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
230000002045 lasting effect Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
210000001699 lower leg Anatomy 0.000 description 1
NKUXJZGXSINEMP-UHFFFAOYSA-N n-propan-2-yl-1,3,5-triazin-2-amine Chemical compound CC(C)NC1=NC=NC=N1 NKUXJZGXSINEMP-UHFFFAOYSA-N 0.000 description 1
238000010899 nucleation Methods 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
229920005552 sodium lignosulfonate Polymers 0.000 description 1
RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000011885 synergistic combination Substances 0.000 description 1
239000000080 wetting agent Substances 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

DD79215385A 1978-09-08 1979-09-06 Herbizide mittel DD145695A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19782839087 DE2839087A1 (de)	1978-09-08	1978-09-08	Herbizide mittel

Publications (1)

Publication Number	Publication Date
DD145695A5 true DD145695A5 (de)	1981-01-07

Family

ID=6048939

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79215385A DD145695A5 (de)	1978-09-08	1979-09-06	Herbizide mittel

Country Status (15)

Country	Link
US (2)	US4692181A (fr)
EP (1)	EP0009620B1 (fr)
JP (1)	JPS5538379A (fr)
AR (1)	AR243057A1 (fr)
AT (1)	ATE127T1 (fr)
AU (1)	AU527466B2 (fr)
BR (1)	BR7905732A (fr)
CA (1)	CA1160468A (fr)
DD (1)	DD145695A5 (fr)
DE (2)	DE2839087A1 (fr)
ES (1)	ES483791A1 (fr)
IL (1)	IL58188A (fr)
MY (1)	MY8500552A (fr)
PH (3)	PH15592A (fr)
ZA (1)	ZA794748B (fr)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3139060A1 (de) *	1981-10-01	1983-04-21	Hoechst Ag, 6230 Frankfurt	Herbizide mittel
JPS58110510A (ja) *	1981-12-24	1983-07-01	Meiji Seika Kaisha Ltd	除草剤組成物
JPS60132790A (ja) *	1983-12-22	1985-07-15	Konishiroku Photo Ind Co Ltd	熱転写記録方法および感熱転写記録媒体
DE3416201A1 (de) *	1984-05-02	1985-11-07	Hoechst Ag, 6230 Frankfurt	Herbizide mittel
ATE64819T1 (de) *	1986-05-09	1991-07-15	Hoechst Ag	Herbizide mittel.
US4846872A (en) *	1986-08-11	1989-07-11	Fujisawa Pharmaceutical Co., Ltd.	Herbicide
US5173103A (en) *	1988-07-05	1992-12-22	Sumitomo Chemical Co., Ltd.	Herbicidal composition comprising2-[7-fluoro-3,4-dihydro-3-oxo-4-(2-pyropynyl)-2H-1,4-benzoxazin-6-yl]-4,5,6,7-tetrahydro-1H-isoindole-1,3(2H)-dione and either glufosinate or bialaphos
JP2727588B2 (ja) *	1988-10-05	1998-03-11	住友化学工業株式会社	除草組成物
DE3919036A1 (de) *	1989-06-10	1990-12-13	Hoechst Ag	Fluessige herbizide mischformulierungen
DE3919037A1 (de) *	1989-06-10	1990-12-13	Hoechst Ag	Fluessige herbizide mischformulierungen
DE3940573A1 (de) *	1989-12-08	1991-06-13	Hoechst Ag	Selektive herbizide mittel
US5818636A (en) *	1990-02-26	1998-10-06	Molecular Displays, Inc.	Complementary surface confined polmer electrochromic materials, systems, and methods of fabrication therefor
US5457564A (en) *	1990-02-26	1995-10-10	Molecular Displays, Inc.	Complementary surface confined polymer electrochromic materials, systems, and methods of fabrication therefor
US5599769A (en) *	1990-11-13	1997-02-04	Hoechst Aktiengesellschaft	Synergistic herbicidal compositions comprising glyphosate or glufosinate in combination with a sulfonylurea herbicide
US5238904A (en) *	1991-01-22	1993-08-24	Hoechst Aktiengesellschaft	Liquid preparations of herbicide mixture based on glufosinate
JPH0598109A (ja) *	1991-10-02	1993-04-20	Sanyo Chem Ind Ltd	制振鋼板用樹脂組成物、制振鋼板及びその製法
AR008158A1 (es) *	1996-09-05	1999-12-09	Syngenta Participations Ag	Proceso para el control de malas hierbas en cultivos de plantas utiles que son resistentes a un fosfo-herbicida y una composicion herbicida para dicho uso.
US6586367B2 (en)	1996-09-05	2003-07-01	Syngenta Crop Protection, Inc.	Process for the control of weeds
IL261271B2 (en)	2016-03-02	2025-03-01	Agrimetis Llc	Methods for preparing L-glucosinate
WO2019018406A1 (fr)	2017-07-18	2019-01-24	Agrimetis, Llc	Procédés de purification de l-glufosinate
BR122023020912A2 (pt)	2017-08-09	2024-01-09	Basf Se	Uso de uma mistura herbicida, mistura pesticida, composição pesticida e método para controlar a vegetação indesejável
WO2019030092A1 (fr) *	2017-08-09	2019-02-14	Basf Se	Mélanges herbicides comprenant du l-glufosinate ou son sel et au moins un inhibiteur de photosynthèse
US12559777B2 (en)	2018-09-05	2026-02-24	Basf Se	Methods for improving yields of L-glufosinate
CN113767107A (zh)	2019-04-16	2021-12-07	巴斯夫欧洲公司	生产结晶l-草铵膦铵盐一水合物的方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2717440C2 (de) *	1976-05-17	1984-04-05	Hoechst Ag, 6230 Frankfurt	Unkrautbekämpfung mit [(3-Amino-3-carboxy)-propyl-1]-methylphosphinsäure-Derivaten
GB2011416B (en) *	1977-12-28	1982-10-20	Meiji Seika Kaisha	Herbicidal compositions

1978
- 1978-09-08 DE DE19782839087 patent/DE2839087A1/de not_active Withdrawn
1979
- 1979-08-29 AT AT79103188T patent/ATE127T1/de not_active IP Right Cessation
- 1979-08-29 DE DE7979103188T patent/DE2960580D1/de not_active Expired
- 1979-08-29 EP EP79103188A patent/EP0009620B1/fr not_active Expired
- 1979-08-31 ES ES483791A patent/ES483791A1/es not_active Expired
- 1979-09-06 BR BR7905732A patent/BR7905732A/pt unknown
- 1979-09-06 PH PH23006A patent/PH15592A/en unknown
- 1979-09-06 AR AR79277979A patent/AR243057A1/es active
- 1979-09-06 DD DD79215385A patent/DD145695A5/de unknown
- 1979-09-06 IL IL58188A patent/IL58188A/xx unknown
- 1979-09-07 ZA ZA00794748A patent/ZA794748B/xx unknown
- 1979-09-07 JP JP11432579A patent/JPS5538379A/ja active Granted
- 1979-09-07 AU AU50680/79A patent/AU527466B2/en not_active Ceased
- 1979-09-07 CA CA000335216A patent/CA1160468A/fr not_active Expired
1980
- 1980-10-27 PH PH24771A patent/PH17459A/en unknown
- 1980-10-27 PH PH24770A patent/PH16629A/en unknown
1982
- 1982-01-22 US US06/341,803 patent/US4692181A/en not_active Expired - Lifetime
1985
- 1985-12-30 MY MY552/85A patent/MY8500552A/xx unknown
1986
- 1986-10-30 US US06/925,701 patent/US4830658A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
US4830658A (en)	1989-05-16
ZA794748B (en)	1980-08-27
PH15592A (en)	1983-02-28
PH17459A (en)	1984-08-29
JPS5538379A (en)	1980-03-17
PH16629A (en)	1983-12-05
ATE127T1 (de)	1981-08-15
EP0009620A1 (fr)	1980-04-16
BR7905732A (pt)	1980-05-20
IL58188A0 (en)	1979-12-30
AR243057A1 (es)	1993-07-30
MY8500552A (en)	1985-12-31
EP0009620B1 (fr)	1981-08-05
JPH0132801B2 (fr)	1989-07-10
ES483791A1 (es)	1980-05-16
CA1160468A (fr)	1984-01-17
IL58188A (en)	1983-02-23
US4692181A (en)	1987-09-08
AU5068079A (en)	1980-03-13
AU527466B2 (en)	1983-03-03
DE2839087A1 (de)	1980-03-20
DE2960580D1 (en)	1981-11-05

Publication	Publication Date	Title
DD145695A5 (de)	1981-01-07	Herbizide mittel
DE69607743T2 (de)	2000-09-07	Insektizide kombinationen enthaltend ein insektizid der chloronikotinyl-reihe und ein insektizid mit eine pyrazol-, pyrrol oder phenylimidazol-gruppe
DE3650670T2 (de)	1998-07-30	Flüssige phytoaktive Zusammensetzungen und Verfahren zu ihrer Verwendung
DE19911165B4 (de)	2008-03-13	Entlaubungsmittel
DE69723750T2 (de)	2004-06-03	Herbizide Kombinationen
EP0036106A2 (fr)	1981-09-23	Mélanges synergistiques de phosphinothricine
EP0557308B1 (fr)	1998-03-04	Herbicides synergiques
DE68903902T2 (de)	1993-04-22	Herbizide zusammensetzung.
DE69114746T2 (de)	1996-04-18	Herbizide Zusammenschluss enthaltender Aclonifen und mindestens einen substituierten Harnstoff.
EP1290944B1 (fr)	2004-03-17	Composition herbicide
DE1301173B (de)	1969-08-14	Mittel zur Bekaempfung von unerwuenschtem Pflanzenwuchs
EP2238835B1 (fr)	2016-04-06	Défoliant à base de thidiazuron et de flufénacet
EP0495748A1 (fr)	1992-07-22	Agents acaricides
EP0614608B1 (fr)	1999-01-07	Mélange synergique pour la contrÔle de queue-de-renard
EP0431545A2 (fr)	1991-06-12	Agent herbicide sélectif et agent fongicide
DD210196A5 (de)	1984-06-06	Herbizide mittel
WO1998047356A2 (fr)	1998-10-29	Herbicide
EP0007573B1 (fr)	1981-12-23	Compositions et procédés pour le contrôle sélectif des mauvaises herbes dans les céréales
EP0009616B1 (fr)	1982-01-27	Agent herbicide et procédé pour combattre les mauvaises herbes
DE69216905T2 (de)	1997-05-15	Herbizide Zusammensetzungen mit verbesserter Getreide-Sicherheit
DE4428982C1 (de)	1996-05-15	Neue synergistische Herbizide, insbesondere zur Bekämpfung von Ackerfuchsschwanz
WO2007098841A2 (fr)	2007-09-07	Défoliant
EP0070929B1 (fr)	1986-12-10	Agents pour combattre sélectivement les mauvaises herbes, et leur application
DD211471A5 (de)	1984-07-18	Synergetische herbizide mittel
DE2438598A1 (de)	1975-03-06	Herbizide mittel