DD235553A5 - Synergetische wirkstoffkombinationen enthaltende herbizide mittel - Google Patents

Synergetische wirkstoffkombinationen enthaltende herbizide mittel Download PDF

Info

Publication number: DD235553A5
Authority: DD; German Democratic Republic
Prior art keywords: methyl; nitro; ethoxy; ethyl; trifluoromethylbenzene
Prior art date: 1984-07-17

Application number

DD85278547A

Other languages

German (de)

English (en)

Inventor

Ferenc Bihari

Peter Bohus

Gyula Eifert

Edit Halasz

Andras Horvath

Peter Inczedy

Tibor Kovacs

Mihaly Pletyak

Janos Lestyan

Istvan Magyari

Mihaly Nagy

Sandor Szalai

Elemer Toemoerdi

Laszlo Wohl

Original Assignee

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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.)

1984-07-17

Filing date

1985-07-12

Publication date

1986-05-14

1985-07-12 Application filed by ��@��k�� filed Critical ��@��k��

1986-05-14 Publication of DD235553A5 publication Critical patent/DD235553A5/de

Links

230000002195 synergetic effect Effects 0.000 title abstract description 7
150000001875 compounds Chemical class 0.000 title description 7
239000004009 herbicide Substances 0.000 title description 2
241000196324 Embryophyta Species 0.000 claims abstract description 14
HHMCAJWVGYGUEF-UHFFFAOYSA-N Fluorodifen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(C(F)(F)F)C=C1[N+]([O-])=O HHMCAJWVGYGUEF-UHFFFAOYSA-N 0.000 claims abstract description 12
239000000203 mixture Substances 0.000 claims abstract description 12
239000004480 active ingredient Substances 0.000 claims abstract description 11
239000003795 chemical substances by application Substances 0.000 claims abstract description 7
230000002363 herbicidal effect Effects 0.000 claims abstract description 7
KXRLLCABBOEPSY-UHFFFAOYSA-N 2-chloro-n-ethoxy-n-(2-ethyl-6-methylphenyl)propanamide Chemical compound CCON(C(=O)C(C)Cl)C1=C(C)C=CC=C1CC KXRLLCABBOEPSY-UHFFFAOYSA-N 0.000 claims abstract description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims description 6
239000000969 carrier Substances 0.000 claims description 4
238000000034 method Methods 0.000 claims description 4
239000005909 Kieselgur Substances 0.000 claims description 3
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 3
239000007788 liquid Substances 0.000 claims description 3
239000007787 solid Substances 0.000 claims description 3
239000008096 xylene Substances 0.000 claims description 3
239000005995 Aluminium silicate Substances 0.000 claims description 2
235000019738 Limestone Nutrition 0.000 claims description 2
239000000853 adhesive Substances 0.000 claims description 2
230000001070 adhesive effect Effects 0.000 claims description 2
150000001298 alcohols Chemical class 0.000 claims description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
235000012211 aluminium silicate Nutrition 0.000 claims description 2
125000000129 anionic group Chemical group 0.000 claims description 2
239000003945 anionic surfactant Substances 0.000 claims description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
239000003431 cross linking reagent Substances 0.000 claims description 2
239000002270 dispersing agent Substances 0.000 claims description 2
150000002148 esters Chemical class 0.000 claims description 2
235000013312 flour Nutrition 0.000 claims description 2
229910052500 inorganic mineral Inorganic materials 0.000 claims 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 claims description 2
150000002576 ketones Chemical class 0.000 claims description 2
239000006028 limestone Substances 0.000 claims description 2
239000011707 mineral Substances 0.000 claims description 2
239000002736 nonionic surfactant Substances 0.000 claims description 2
239000000546 pharmaceutical excipient Substances 0.000 claims description 2
150000004760 silicates Chemical class 0.000 claims description 2
240000008042 Zea mays Species 0.000 abstract description 16
235000002017 Zea mays subsp mays Nutrition 0.000 abstract description 16
240000008114 Panicum miliaceum Species 0.000 abstract description 9
235000007199 Panicum miliaceum Nutrition 0.000 abstract description 9
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 abstract description 8
235000009973 maize Nutrition 0.000 abstract description 8
239000000700 radioactive tracer Substances 0.000 abstract 1
239000000126 substance Substances 0.000 abstract 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 8
235000005822 corn Nutrition 0.000 description 8
238000002360 preparation method Methods 0.000 description 8
VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 description 7
230000000694 effects Effects 0.000 description 7
239000002689 soil Substances 0.000 description 6
239000013543 active substance Substances 0.000 description 5
239000003814 drug Substances 0.000 description 5
229940079593 drug Drugs 0.000 description 5
241000209117 Panicum Species 0.000 description 4
235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 4
235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 4
239000004495 emulsifiable concentrate Substances 0.000 description 4
238000011282 treatment Methods 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
239000012895 dilution Substances 0.000 description 3
238000010790 dilution Methods 0.000 description 3
239000008187 granular material Substances 0.000 description 3
239000000843 powder Substances 0.000 description 3
MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 2
230000002708 enhancing effect Effects 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
238000009472 formulation Methods 0.000 description 2
230000002265 prevention Effects 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
238000012360 testing method Methods 0.000 description 2
FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical class 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
241000225517 Bario Species 0.000 description 1
KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
239000005843 Thiram Substances 0.000 description 1
150000008061 acetanilides Chemical class 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
230000003042 antagnostic effect Effects 0.000 description 1
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
239000012867 bioactive agent Substances 0.000 description 1
238000004166 bioassay Methods 0.000 description 1
230000004071 biological effect Effects 0.000 description 1
238000010170 biological method Methods 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
244000038559 crop plants Species 0.000 description 1
MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
230000007812 deficiency Effects 0.000 description 1
238000001784 detoxification Methods 0.000 description 1
-1 dichloroacetyl Chemical group 0.000 description 1
238000002845 discoloration Methods 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
244000144992 flock Species 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
230000035784 germination Effects 0.000 description 1
238000005286 illumination Methods 0.000 description 1
238000011835 investigation Methods 0.000 description 1
238000009533 lab test Methods 0.000 description 1
YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 1
229920000940 maneb Polymers 0.000 description 1
239000005416 organic matter Substances 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
238000009877 rendering Methods 0.000 description 1
238000011160 research Methods 0.000 description 1
239000004576 sand Substances 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
238000009331 sowing Methods 0.000 description 1
150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
229960002447 thiram Drugs 0.000 description 1
150000003672 ureas Chemical class 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the group; Thio analogues thereof

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)

DD85278547A 1984-07-17 1985-07-12 Synergetische wirkstoffkombinationen enthaltende herbizide mittel DD235553A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
HU842773A HU193214B (en)	1984-07-17	1984-07-17	Synergic herbicide compositions for extirpating panicum miliaceum containing chloro-acetamide derivatives and substituted benzene derivatives as active agents

Publications (1)

Publication Number	Publication Date
DD235553A5 true DD235553A5 (de)	1986-05-14

Family

ID=10961036

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD85278547A DD235553A5 (de)	1984-07-17	1985-07-12	Synergetische wirkstoffkombinationen enthaltende herbizide mittel

Country Status (13)

Country	Link
JP (1)	JPS6193103A (ro)
BR (1)	BR8503390A (ro)
CH (1)	CH664258A5 (ro)
CS (1)	CS261226B2 (ro)
DD (1)	DD235553A5 (ro)
DE (1)	DE3525371A1 (ro)
ES (1)	ES8608282A1 (ro)
FR (1)	FR2567718B1 (ro)
GB (1)	GB2163349B (ro)
HU (1)	HU193214B (ro)
IT (1)	IT1207061B (ro)
PL (1)	PL143071B1 (ro)
RO (1)	RO93277A (ro)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19958381A1 (de)	1999-12-03	2001-06-07	Bayer Ag	Herbizide auf Basis von N-Aryl-uracilen

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL136904C (ro) *	1962-02-08
GB1407205A (en) *	1971-09-17	1975-09-24	Girling Ltd	Vehicle braking systems
JPS5350328A (en) *	1976-10-16	1978-05-08	Kumiai Chem Ind Co Ltd	Composition for herbicides
JPS5555107A (en) *	1978-10-19	1980-04-22	Nissan Chem Ind Ltd	Herbicidal composition
TW286443B (ro) *	1994-10-25	1996-09-21	Fridolin Alois Frech

1984
- 1984-07-17 HU HU842773A patent/HU193214B/hu not_active IP Right Cessation
1985
- 1985-07-03 GB GB08516880A patent/GB2163349B/en not_active Expired
- 1985-07-09 FR FR8510467A patent/FR2567718B1/fr not_active Expired
- 1985-07-12 DD DD85278547A patent/DD235553A5/de unknown
- 1985-07-12 CH CH3031/85A patent/CH664258A5/de not_active IP Right Cessation
- 1985-07-15 RO RO85119567A patent/RO93277A/ro unknown
- 1985-07-16 JP JP60156848A patent/JPS6193103A/ja active Pending
- 1985-07-16 PL PL1985254561A patent/PL143071B1/pl unknown
- 1985-07-16 DE DE19853525371 patent/DE3525371A1/de not_active Withdrawn
- 1985-07-16 IT IT8521575A patent/IT1207061B/it active
- 1985-07-16 BR BR8503390A patent/BR8503390A/pt unknown
- 1985-07-17 ES ES545327A patent/ES8608282A1/es not_active Expired
- 1985-07-17 CS CS855306A patent/CS261226B2/cs unknown

Also Published As

Publication number	Publication date
GB2163349B (en)	1988-05-05
RO93277B (ro)	1987-12-31
FR2567718B1 (fr)	1988-10-14
ES545327A0 (es)	1986-07-16
FR2567718A1 (fr)	1986-01-24
BR8503390A (pt)	1986-04-08
IT1207061B (it)	1989-05-17
DE3525371A1 (de)	1986-07-10
HU193214B (en)	1987-08-28
PL254561A1 (en)	1986-06-17
GB8516880D0 (en)	1985-08-07
HUT39565A (en)	1986-10-29
ES8608282A1 (es)	1986-07-16
CS261226B2 (en)	1989-01-12
CS530685A2 (en)	1988-05-16
RO93277A (ro)	1988-03-30
PL143071B1 (en)	1988-01-30
CH664258A5 (de)	1988-02-29
IT8521575A0 (it)	1985-07-16
GB2163349A (en)	1986-02-26
JPS6193103A (ja)	1986-05-12

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EP1541023B1 (de)	2007-01-10	Biozid-wirksame Kombination für landwirtschaftliche Anwendungen
DE19911165B4 (de)	2008-03-13	Entlaubungsmittel
DE2135768A1 (de)	1972-01-20	Herbizidmischung
DE2250085B2 (ro)	1978-12-07
DE2440787A1 (de)	1975-03-06	Verfahren zur selektiven bekaempfung von unkraut in kentucky-blaugras
DE60222438T2 (de)	2008-06-12	Zusammensetzung zur bekämpfung von pflanzenpathogenen bakterien und verfahren zur bekämpfung von pflanzenpathogenen bakterien
DE69011975T2 (de)	1995-01-12	Herbizide Mischung auf der Basis Bromoxynil oder eines seiner Derivate.
DD235553A5 (de)	1986-05-14	Synergetische wirkstoffkombinationen enthaltende herbizide mittel
DE1177407B (de)	1964-09-03	Mittel zur Bekaempfung von Pflanzenrosterregern
CH657750A5 (de)	1986-09-30	Schaedlingsbekaempfungsmittel.
DE1792143C3 (de)	1979-05-03	Selektiv wirkendes, herbicides Mittel auf Basis von N-3,4-Dichlorphenyl-N'-methyl-N'-n-butylharnstoff
DE3045799C2 (de)	1984-07-05	Fungicide Gemische auf Basis von Alkoxycarbonsäureimid-Derivaten
DE2602591C3 (ro)	1978-09-14
AT253861B (de)	1967-04-25	Insektizide Mischung
DE1542901A1 (de)	1970-05-27	Insektizide Mittel
DE1567218C3 (de)	1973-09-27	Verwendung von 4-Chlorphenoxyessigsäureamid-Derivaten als Herbizide
DD211471A5 (de)	1984-07-18	Synergetische herbizide mittel
DE962658C (de)	1957-04-25	Pflanzenphysiologisch wirksame Mittel, insbesondere zur Bekaempfung von Unkraeutern in Kulturen
DD264568A3 (de)	1989-02-08	Mittel gegen stress und umweltnoxen bei landwirtschaftlichen und gaertnerischen nutzpflanzen
DD212887A1 (de)	1984-08-29	Fungizide mittel
DE1966665B2 (de)	1977-02-17	Verwendung einer kombination auf der basis von aryloxymonothioessigsaeureestern
DD293040A5 (de)	1991-08-22	Mittel zur beizung landwirtschaftlichen und gaertnerischen erntegutes, vorzugsweise fuer kartoffeln
DE3803313A1 (de)	1989-08-17	Herbizidgemisch und verfahren zu seiner anwendung
DE3130719A1 (de)	1983-02-17	"fungizide mittel"
DE1036564B (de)	1958-08-14	Bekaempfung von Pilzen und Nematoden