CS255870B2 - Synergic herbicide - Google Patents

Synergic herbicide Download PDF

Info

Publication number: CS255870B2
Authority: CS; Czechoslovakia
Prior art keywords: dinitro; compound; trifluoro; butyl; effective amount
Prior art date: 1985-04-08

Application number

CS862538A

Other languages

Czech (cs)

English (en)

Other versions

CS253886A2 (en

Inventor

David J Bracey

Ellen Mojica

Original Assignee

Stauffer Chemical Co

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.)

1985-04-08

Filing date

1986-04-08

Publication date

1988-03-15

1986-04-08 Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co

1987-07-16 Publication of CS253886A2 publication Critical patent/CS253886A2/cs

1988-03-15 Publication of CS255870B2 publication Critical patent/CS255870B2/cs

Links

230000002363 herbicidal effect Effects 0.000 title claims abstract description 16
230000002195 synergetic effect Effects 0.000 title claims abstract description 8
239000004009 herbicide Substances 0.000 title description 11
239000000203 mixture Substances 0.000 claims abstract description 19
CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 claims abstract description 7
-1 benzene derivative compound Chemical class 0.000 abstract description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 2
125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
SPNQRCTZKIBOAX-UHFFFAOYSA-N Butralin Chemical compound CCC(C)NC1=C([N+]([O-])=O)C=C(C(C)(C)C)C=C1[N+]([O-])=O SPNQRCTZKIBOAX-UHFFFAOYSA-N 0.000 abstract 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
PTFJIKYUEPWBMS-UHFFFAOYSA-N Ethalfluralin Chemical compound CC(=C)CN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O PTFJIKYUEPWBMS-UHFFFAOYSA-N 0.000 abstract 1
NEKOXWSIMFDGMA-UHFFFAOYSA-N Isopropalin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(C)C)C=C1[N+]([O-])=O NEKOXWSIMFDGMA-UHFFFAOYSA-N 0.000 abstract 1
UMKANAFDOQQUKE-UHFFFAOYSA-N Nitralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(S(C)(=O)=O)C=C1[N+]([O-])=O UMKANAFDOQQUKE-UHFFFAOYSA-N 0.000 abstract 1
SMDHCQAYESWHAE-UHFFFAOYSA-N benfluralin Chemical compound CCCCN(CC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O SMDHCQAYESWHAE-UHFFFAOYSA-N 0.000 abstract 1
229910052794 bromium Chemical group 0.000 abstract 1
239000000460 chlorine Chemical group 0.000 abstract 1
229910052801 chlorine Inorganic materials 0.000 abstract 1
125000000753 cycloalkyl group Chemical group 0.000 abstract 1
239000001257 hydrogen Substances 0.000 abstract 1
229910052739 hydrogen Inorganic materials 0.000 abstract 1
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
UNAHYJYOSSSJHH-UHFFFAOYSA-N oryzalin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(S(N)(=O)=O)C=C1[N+]([O-])=O UNAHYJYOSSSJHH-UHFFFAOYSA-N 0.000 abstract 1
230000004044 response Effects 0.000 description 15
239000000654 additive Substances 0.000 description 12
241000196324 Embryophyta Species 0.000 description 11
230000000996 additive effect Effects 0.000 description 11
229940125904 compound 1 Drugs 0.000 description 8
229940125782 compound 2 Drugs 0.000 description 8
150000001875 compounds Chemical class 0.000 description 8
239000004495 emulsifiable concentrate Substances 0.000 description 5
230000009036 growth inhibition Effects 0.000 description 5
239000000243 solution Substances 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
230000012010 growth Effects 0.000 description 4
239000004094 surface-active agent Substances 0.000 description 4
240000002791 Brassica napus Species 0.000 description 3
239000005591 Pendimethalin Substances 0.000 description 3
244000098338 Triticum aestivum Species 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
239000000843 powder Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 2
241000335053 Beta vulgaris Species 0.000 description 2
235000011293 Brassica napus Nutrition 0.000 description 2
NPOJQCVWMSKXDN-UHFFFAOYSA-N Dacthal Chemical compound COC(=O)C1=C(Cl)C(Cl)=C(C(=O)OC)C(Cl)=C1Cl NPOJQCVWMSKXDN-UHFFFAOYSA-N 0.000 description 2
240000005979 Hordeum vulgare Species 0.000 description 2
235000007340 Hordeum vulgare Nutrition 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
240000001090 Papaver somniferum Species 0.000 description 2
235000021307 Triticum Nutrition 0.000 description 2
240000005592 Veronica officinalis Species 0.000 description 2
239000004480 active ingredient Substances 0.000 description 2
150000001555 benzenes Chemical class 0.000 description 2
239000000969 carrier Substances 0.000 description 2
235000013339 cereals Nutrition 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
230000003993 interaction Effects 0.000 description 2
230000000051 modifying effect Effects 0.000 description 2
239000003208 petroleum Substances 0.000 description 2
230000008635 plant growth Effects 0.000 description 2
NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 description 2
239000002689 soil Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
239000008096 xylene Substances 0.000 description 2
VGPLIJIUBXEKJJ-UHFFFAOYSA-N 3,4-dimethyl-2,6-dinitro-5-pentan-3-ylaniline Chemical compound CCC(CC)C1=C(C)C(C)=C([N+]([O-])=O)C(N)=C1[N+]([O-])=O VGPLIJIUBXEKJJ-UHFFFAOYSA-N 0.000 description 1
240000001592 Amaranthus caudatus Species 0.000 description 1
235000009328 Amaranthus caudatus Nutrition 0.000 description 1
235000007320 Avena fatua Nutrition 0.000 description 1
241000209764 Avena fatua Species 0.000 description 1
244000075850 Avena orientalis Species 0.000 description 1
235000016068 Berberis vulgaris Nutrition 0.000 description 1
235000021533 Beta vulgaris Nutrition 0.000 description 1
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
241000219198 Brassica Species 0.000 description 1
235000008427 Brassica arvensis Nutrition 0.000 description 1
235000003351 Brassica cretica Nutrition 0.000 description 1
244000024671 Brassica kaber Species 0.000 description 1
235000006008 Brassica napus var napus Nutrition 0.000 description 1
235000003343 Brassica rupestris Nutrition 0.000 description 1
235000004977 Brassica sinapistrum Nutrition 0.000 description 1
241000544808 Bromus sterilis Species 0.000 description 1
241000283707 Capra Species 0.000 description 1
241000271532 Crotalus Species 0.000 description 1
206010011878 Deafness Diseases 0.000 description 1
244000044980 Fumaria officinalis Species 0.000 description 1
235000006961 Fumaria officinalis Nutrition 0.000 description 1
240000005702 Galium aparine Species 0.000 description 1
235000014820 Galium aparine Nutrition 0.000 description 1
206010053759 Growth retardation Diseases 0.000 description 1
240000004296 Lolium perenne Species 0.000 description 1
244000042664 Matricaria chamomilla Species 0.000 description 1
235000007232 Matricaria chamomilla Nutrition 0.000 description 1
235000011096 Papaver Nutrition 0.000 description 1
235000008753 Papaver somniferum Nutrition 0.000 description 1
241000745991 Phalaris Species 0.000 description 1
244000081757 Phalaris arundinacea Species 0.000 description 1
244000100170 Phaseolus lunatus Species 0.000 description 1
235000010617 Phaseolus lunatus Nutrition 0.000 description 1
235000014676 Phragmites communis Nutrition 0.000 description 1
244000292693 Poa annua Species 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
235000021536 Sugar beet Nutrition 0.000 description 1
235000005545 Veronica americana Nutrition 0.000 description 1
LZKWCGKJBCBCAQ-UHFFFAOYSA-N [O-]C(NC1=CC=C[S+]1CC1=CC=CC=C1)=O Chemical class [O-]C(NC1=CC=C[S+]1CC1=CC=CC=C1)=O LZKWCGKJBCBCAQ-UHFFFAOYSA-N 0.000 description 1
125000003158 alcohol group Chemical group 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
230000003042 antagnostic effect Effects 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
238000003556 assay Methods 0.000 description 1
QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
239000013043 chemical agent Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
239000002283 diesel fuel 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
239000002270 dispersing agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
238000009472 formulation Methods 0.000 description 1
125000003827 glycol group Chemical group 0.000 description 1
208000037824 growth disorder Diseases 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
230000001788 irregular Effects 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
150000002646 long chain fatty acid esters Chemical class 0.000 description 1
238000000034 method Methods 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000004576 sand Substances 0.000 description 1
238000009331 sowing Methods 0.000 description 1
239000007921 spray Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
230000001629 suppression Effects 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000005737 synergistic response Effects 0.000 description 1
239000000080 wetting agent 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
- 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
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring

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)

CS862538A 1985-04-08 1986-04-08 Synergic herbicide CS255870B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US72126285A	1985-04-08	1985-04-08

Publications (2)

Publication Number	Publication Date
CS253886A2 CS253886A2 (en)	1987-07-16
CS255870B2 true CS255870B2 (en)	1988-03-15

Family

ID=24897223

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS862538A CS255870B2 (en)	1985-04-08	1986-04-08	Synergic herbicide

Country Status (12)

Country	Link
EP (1)	EP0200935A3 (fr)
AU (1)	AU581074B2 (fr)
CS (1)	CS255870B2 (fr)
DK (1)	DK158786A (fr)
FI (1)	FI861469A7 (fr)
GR (1)	GR860923B (fr)
HU (1)	HUT41231A (fr)
IL (1)	IL78426A0 (fr)
NO (1)	NO861339L (fr)
PT (1)	PT82293B (fr)
RO (1)	RO93894A (fr)
ZA (1)	ZA862559B (fr)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2334563A1 (de) *	1973-07-07	1975-01-30	Basf Ag	Herbizid
JPS527052B2 (fr) *	1973-08-30	1977-02-26
DE3307768A1 (de) *	1983-03-04	1984-09-06	Torfstreuverband Gmbh, 2900 Oldenburg	Verfahren und mittel zur gewinnung unkrautfreier torfprodukte

1986
- 1986-03-27 PT PT82293A patent/PT82293B/pt unknown
- 1986-04-07 IL IL78426A patent/IL78426A0/xx unknown
- 1986-04-07 RO RO86122920A patent/RO93894A/fr unknown
- 1986-04-07 EP EP86104727A patent/EP0200935A3/fr not_active Withdrawn
- 1986-04-07 AU AU55699/86A patent/AU581074B2/en not_active Ceased
- 1986-04-07 FI FI861469A patent/FI861469A7/fi not_active Application Discontinuation
- 1986-04-07 ZA ZA862559A patent/ZA862559B/xx unknown
- 1986-04-07 NO NO861339A patent/NO861339L/no unknown
- 1986-04-07 HU HU861453A patent/HUT41231A/hu unknown
- 1986-04-08 GR GR860923A patent/GR860923B/el unknown
- 1986-04-08 DK DK158786A patent/DK158786A/da not_active IP Right Cessation
- 1986-04-08 CS CS862538A patent/CS255870B2/cs unknown

Also Published As

Publication number	Publication date
FI861469L (fi)	1986-10-09
EP0200935A3 (fr)	1988-12-28
AU581074B2 (en)	1989-02-09
HUT41231A (en)	1987-04-28
AU5569986A (en)	1986-10-16
NO861339L (no)	1986-10-09
RO93894A (fr)	1988-03-30
FI861469A7 (fi)	1986-10-09
FI861469A0 (fi)	1986-04-07
PT82293B (en)	1988-01-11
DK158786A (da)	1986-10-09
ZA862559B (en)	1987-06-24
CS253886A2 (en)	1987-07-16
DK158786D0 (da)	1986-04-08
GR860923B (en)	1986-08-11
IL78426A0 (en)	1986-08-31
PT82293A (en)	1986-04-01
EP0200935A2 (fr)	1986-11-12

Publication	Publication Date	Title
CS254984B2 (en)	1988-02-15	Agent for selective weed killing
EP0795269B1 (fr)	2003-07-30	Associations herbicides
BG110457A (bg)	2010-03-31	Синергични хербицидни смеси
PL173338B1 (pl)	1998-02-27	Kompozycja chwastobójcza
EP0347950B1 (fr)	1993-08-04	Combinaisons herbicides synergiques et méthode d'application
HU208237B (en)	1993-09-28	Herbicidal compositions comprising aklonifen and a substituted urea and process for weed control
DE69204415T2 (de)	1996-02-01	Herbizide Zusammensetzung.
JPH0416441B2 (fr)	1992-03-24
EA036339B1 (ru)	2020-10-28	Синергетическая гербицидная композиция
CZ286811B6 (cs)	2000-07-12	Herbicidní prostředek
CS255870B2 (en)	1988-03-15	Synergic herbicide
CZ153598A3 (cs)	1998-09-16	Nové herbicidní prostředky obsahující 4-benzoylisoxazoly a aclonifen
JP2016521267A (ja)	2016-07-21	殺虫性を有する活性化合物の組合せ
US4123253A (en)	1978-10-31	Herbicidal compositions
CN116439256B (zh)	2025-09-16	除草组合物、除草剂及其应用
KR950002851B1 (ko)	1995-03-27	제초 조성물
CS235339B2 (en)	1985-05-15	Synergic herbicide agent
CS246093B2 (en)	1986-10-16	Synergically affecting herbicide
WO2024163845A1 (fr)	2024-08-08	Compositions herbicides et procédés associés
JPS62185003A (ja)	1987-08-13	除草組成物
US20050124493A1 (en)	2005-06-09	Herbicidal composition
EP0039535B1 (fr)	1984-10-24	Compositions herbicides synergiques et leur application
WO2025223988A1 (fr)	2025-10-30	Formulation de concentré émulsifiable (ce)
AU595010B2 (en)	1990-03-22	Synergistic herbicidal compositions and method of use
HU191900B (en)	1987-04-28	Sinergetic herbicides containing as active substance 2-/alfa-naftoxi/-n,n-diethyl propionamid and n-benzil-n-izoprophil-piralamid