DD232187A5 - Synergistische herbizide zusammensetzungen - Google Patents

Synergistische herbizide zusammensetzungen Download PDF

Info

Publication number: DD232187A5
Authority: DD; German Democratic Republic
Prior art keywords: hydrogen; chlorine; chloro; item; alkyl
Prior art date: 1983-12-05

Application number

DD84270327A

Other languages

German (de)

English (en)

Inventor

Ellen Y 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.)

1983-12-05

Filing date

1984-12-05

Publication date

1986-01-22

1984-12-05 Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co

1986-01-22 Publication of DD232187A5 publication Critical patent/DD232187A5/de

Links

239000000203 mixture Substances 0.000 title claims abstract description 38
230000002195 synergetic effect Effects 0.000 title claims abstract description 16
239000004009 herbicide Substances 0.000 title description 13
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 30
239000001257 hydrogen Substances 0.000 claims abstract description 30
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 26
229910052801 chlorine Inorganic materials 0.000 claims abstract description 26
239000000460 chlorine Chemical group 0.000 claims abstract description 26
-1 pentafluoropropionamido Chemical group 0.000 claims abstract description 24
125000000217 alkyl group Chemical group 0.000 claims abstract description 22
230000002363 herbicidal effect Effects 0.000 claims abstract description 21
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 18
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 18
229910052794 bromium Chemical group 0.000 claims abstract description 18
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 7
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 6
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 6
125000003545 alkoxy group Chemical group 0.000 claims abstract description 5
125000004644 alkyl sulfinyl group Chemical group 0.000 claims abstract description 5
125000004390 alkyl sulfonyl group Chemical group 0.000 claims abstract description 5
125000004414 alkyl thio group Chemical group 0.000 claims abstract description 5
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 5
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 5
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims abstract description 4
229910052731 fluorine Inorganic materials 0.000 claims abstract description 4
239000011737 fluorine Chemical group 0.000 claims abstract description 4
125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims abstract description 4
150000002431 hydrogen Chemical group 0.000 claims description 20
238000000034 method Methods 0.000 claims description 11
230000008635 plant growth Effects 0.000 claims description 8
RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Natural products C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 7
125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 claims description 5
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 4
LLLFASISUZUJEQ-UHFFFAOYSA-N orbencarb Chemical compound CCN(CC)C(=O)SCC1=CC=CC=C1Cl LLLFASISUZUJEQ-UHFFFAOYSA-N 0.000 claims description 4
NQLVQOSNDJXLKG-UHFFFAOYSA-N prosulfocarb Chemical compound CCCN(CCC)C(=O)SCC1=CC=CC=C1 NQLVQOSNDJXLKG-UHFFFAOYSA-N 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 claims description 2
125000001183 hydrocarbyl group Chemical group 0.000 claims 1
HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 abstract description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 6
125000001309 chloro group Chemical group Cl* 0.000 abstract 3
125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 abstract 1
125000001246 bromo group Chemical group Br* 0.000 abstract 1
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
150000001875 compounds Chemical class 0.000 description 19
230000000694 effects Effects 0.000 description 12
230000012010 growth Effects 0.000 description 11
241000196324 Embryophyta Species 0.000 description 9
244000044980 Fumaria officinalis Species 0.000 description 7
235000006961 Fumaria officinalis Nutrition 0.000 description 7
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 6
238000006243 chemical reaction Methods 0.000 description 6
239000000126 substance Substances 0.000 description 6
230000006735 deficit Effects 0.000 description 5
238000009472 formulation Methods 0.000 description 5
210000004072 lung Anatomy 0.000 description 5
239000000654 additive Substances 0.000 description 4
230000003042 antagnostic effect Effects 0.000 description 4
229940125904 compound 1 Drugs 0.000 description 4
239000003921 oil Substances 0.000 description 4
239000002689 soil Substances 0.000 description 4
239000004094 surface-active agent Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
230000000996 additive effect Effects 0.000 description 3
MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 description 3
239000004495 emulsifiable concentrate Substances 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
239000000843 powder Substances 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
241000209764 Avena fatua Species 0.000 description 2
235000007320 Avena fatua Nutrition 0.000 description 2
244000025254 Cannabis sativa Species 0.000 description 2
240000005702 Galium aparine Species 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
239000004480 active ingredient Substances 0.000 description 2
VJYIFXVZLXQVHO-UHFFFAOYSA-N chlorsulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)Cl)=N1 VJYIFXVZLXQVHO-UHFFFAOYSA-N 0.000 description 2
229940125782 compound 2 Drugs 0.000 description 2
229940126214 compound 3 Drugs 0.000 description 2
229940125898 compound 5 Drugs 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
230000003993 interaction Effects 0.000 description 2
239000003208 petroleum Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000007921 spray Substances 0.000 description 2
238000011282 treatment Methods 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
KKYIAOSXVVCZKM-UHFFFAOYSA-N 2,2-diphenoxypentanoic acid Chemical class C=1C=CC=CC=1OC(C(O)=O)(CCC)OC1=CC=CC=C1 KKYIAOSXVVCZKM-UHFFFAOYSA-N 0.000 description 1
HKROQOWBHZLRCU-UHFFFAOYSA-N 2,2-diphenoxypropanoic acid Chemical class C=1C=CC=CC=1OC(C(O)=O)(C)OC1=CC=CC=C1 HKROQOWBHZLRCU-UHFFFAOYSA-N 0.000 description 1
GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 1
125000006282 2-chlorobenzyl group Chemical group [H]C1=C([H])C(Cl)=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
240000001592 Amaranthus caudatus Species 0.000 description 1
235000009328 Amaranthus caudatus Nutrition 0.000 description 1
235000004535 Avena sterilis Nutrition 0.000 description 1
235000021533 Beta vulgaris Nutrition 0.000 description 1
241000335053 Beta vulgaris Species 0.000 description 1
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
235000008427 Brassica arvensis Nutrition 0.000 description 1
244000056139 Brassica cretica Species 0.000 description 1
235000003351 Brassica cretica Nutrition 0.000 description 1
244000024671 Brassica kaber Species 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
VNQLUYRZOKNUFM-UHFFFAOYSA-N CC(C)C(C)C1=C(NC([O-])=O)[S+](CCCC2=CC=CC=C2)C=C1 Chemical compound CC(C)C(C)C1=C(NC([O-])=O)[S+](CCCC2=CC=CC=C2)C=C1 VNQLUYRZOKNUFM-UHFFFAOYSA-N 0.000 description 1
GWYUISFLFLFSLO-UHFFFAOYSA-N CCC1=C(S(C=C1)(CC2=CC=CC=C2)C(C)(C)CC)NC(=O)O Chemical compound CCC1=C(S(C=C1)(CC2=CC=CC=C2)C(C)(C)CC)NC(=O)O GWYUISFLFLFSLO-UHFFFAOYSA-N 0.000 description 1
101150065749 Churc1 gene Proteins 0.000 description 1
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 1
235000014820 Galium aparine Nutrition 0.000 description 1
241000209219 Hordeum Species 0.000 description 1
241000209510 Liliopsida Species 0.000 description 1
240000004296 Lolium perenne Species 0.000 description 1
244000292693 Poa annua Species 0.000 description 1
102100038239 Protein Churchill Human genes 0.000 description 1
235000021536 Sugar beet Nutrition 0.000 description 1
QHTQREMOGMZHJV-UHFFFAOYSA-N Thiobencarb Chemical compound CCN(CC)C(=O)SCC1=CC=C(Cl)C=C1 QHTQREMOGMZHJV-UHFFFAOYSA-N 0.000 description 1
241000209140 Triticum Species 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
241001166549 Veronica hederifolia Species 0.000 description 1
241000607479 Yersinia pestis Species 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
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
239000012736 aqueous medium Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 1
QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
238000009835 boiling Methods 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000007865 diluting Methods 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
VOMHMJILNADLNM-UHFFFAOYSA-N ethyl 4-[4-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxyphenoxy]-3-hydroxypentanoate Chemical compound C1=CC(OC(C)C(O)CC(=O)OCC)=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl VOMHMJILNADLNM-UHFFFAOYSA-N 0.000 description 1
241001233957 eudicotyledons Species 0.000 description 1
230000003631 expected effect Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000000295 fuel oil Substances 0.000 description 1
208000037824 growth disorder Diseases 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
238000007689 inspection Methods 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
150000004668 long chain fatty acids Chemical class 0.000 description 1
VRZKGXNOIKPXBW-UHFFFAOYSA-N methyl 4-[4-[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxyphenoxy]-3-hydroxypentanoate Chemical compound C1=CC(OC(C)C(O)CC(=O)OC)=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl VRZKGXNOIKPXBW-UHFFFAOYSA-N 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
150000003235 pyrrolidines Chemical class 0.000 description 1
150000004040 pyrrolidinones Chemical class 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
241000894007 species Species 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
239000000725 suspension Substances 0.000 description 1
150000003918 triazines 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
- 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

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)
Degasification And Air Bubble Elimination (AREA)
Medicines Containing Plant Substances (AREA)

DD84270327A 1983-12-05 1984-12-05 Synergistische herbizide zusammensetzungen DD232187A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US55799483A	1983-12-05	1983-12-05

Publications (1)

Publication Number	Publication Date
DD232187A5 true DD232187A5 (de)	1986-01-22

Family

ID=24227718

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD84270327A DD232187A5 (de)	1983-12-05	1984-12-05	Synergistische herbizide zusammensetzungen

Country Status (19)

Country	Link
EP (1)	EP0146835A3 (cs)
JP (1)	JPS60139604A (cs)
KR (1)	KR850004379A (cs)
AU (1)	AU559251B2 (cs)
CA (1)	CA1235919A (cs)
CS (1)	CS939084A2 (cs)
DD (1)	DD232187A5 (cs)
DK (1)	DK573784A (cs)
ES (1)	ES8604407A1 (cs)
FI (1)	FI74385C (cs)
HU (1)	HUT36801A (cs)
IL (1)	IL73720A (cs)
NO (1)	NO844828L (cs)
NZ (1)	NZ210424A (cs)
PL (1)	PL141435B1 (cs)
PT (1)	PT79607A (cs)
RO (1)	RO89784A (cs)
TR (1)	TR22091A (cs)
ZA (1)	ZA849421B (cs)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FI76671C (fi) *	1983-12-05	1988-12-12	Stauffer Chemical Co	Synergistisk herbicidblandning och foerfarande foer bekaempning av icke oenskvaerd vaextlighet.
PT2198712T (pt) *	2004-12-17	2018-10-18	Syngenta Participations Ag	Composições herbicidas compreendendo prossulfocarbe

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS49134839A (cs) *	1973-05-10	1974-12-25
JPS5036637A (cs) *	1973-08-08	1975-04-05
JPS5127734B2 (cs) *	1973-11-16	1976-08-14
FR2305434A1 (fr) *	1975-03-28	1976-10-22	Stauffer Chemical Co	Procede de preparation pour l'emploi en tant qu'herbicides d'halo-2-pyrrolidinones n-substituees, de types acycliques, alicycliques, monocycliques, aromatiques ou phenyliques

1984
- 1984-11-20 FI FI844548A patent/FI74385C/fi not_active IP Right Cessation
- 1984-12-03 PT PT79607A patent/PT79607A/pt unknown
- 1984-12-03 DK DK573784A patent/DK573784A/da not_active Application Discontinuation
- 1984-12-04 HU HU844478A patent/HUT36801A/hu unknown
- 1984-12-04 NO NO844828A patent/NO844828L/no unknown
- 1984-12-04 RO RO84116513A patent/RO89784A/ro unknown
- 1984-12-04 KR KR1019840007639A patent/KR850004379A/ko not_active Abandoned
- 1984-12-04 IL IL73720A patent/IL73720A/xx unknown
- 1984-12-04 NZ NZ210424A patent/NZ210424A/en unknown
- 1984-12-04 EP EP84114739A patent/EP0146835A3/en not_active Ceased
- 1984-12-04 ZA ZA849421A patent/ZA849421B/xx unknown
- 1984-12-04 AU AU36262/84A patent/AU559251B2/en not_active Ceased
- 1984-12-04 CA CA000469254A patent/CA1235919A/en not_active Expired
- 1984-12-04 PL PL1984250712A patent/PL141435B1/pl unknown
- 1984-12-05 DD DD84270327A patent/DD232187A5/de unknown
- 1984-12-05 TR TR22091A patent/TR22091A/xx unknown
- 1984-12-05 CS CS849390A patent/CS939084A2/cs unknown
- 1984-12-05 JP JP59257318A patent/JPS60139604A/ja active Pending
- 1984-12-05 ES ES538300A patent/ES8604407A1/es not_active Expired

Also Published As

Publication number	Publication date
AU559251B2 (en)	1987-03-05
JPS60139604A (ja)	1985-07-24
NO844828L (no)	1985-06-06
FI844548A0 (fi)	1984-11-20
FI74385B (fi)	1987-10-30
DK573784A (da)	1985-06-06
FI74385C (fi)	1988-02-08
KR850004379A (ko)	1985-07-15
AU3626284A (en)	1985-06-13
PL250712A1 (en)	1985-07-30
EP0146835A3 (en)	1986-01-15
ES538300A0 (es)	1986-02-01
RO89784A (ro)	1986-07-30
FI844548L (fi)	1985-06-06
DK573784D0 (da)	1984-12-03
IL73720A (en)	1988-06-30
CS939084A2 (en)	1988-08-16
HUT36801A (en)	1985-10-28
NZ210424A (en)	1987-06-30
PL141435B1 (en)	1987-07-31
ZA849421B (en)	1985-10-30
CA1235919A (en)	1988-05-03
ES8604407A1 (es)	1986-02-01
IL73720A0 (en)	1985-03-31
EP0146835A2 (en)	1985-07-03
PT79607A (en)	1985-01-01
TR22091A (tr)	1986-03-30

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DE19605786A1 (de)	1997-08-21	Ölsuspensionskonzentrate
DE10141618A1 (de)	2003-03-06	Fungizide Wirkstoffkombinationen
DE3688844T2 (de)	1994-01-05	Synergistische, herbizide Kombinationen und Verfahren zur Anwendung.
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DE69820499T2 (de)	2004-05-27	Fungizide Mischung, enthaltend ein N-Acetonylbenzamid und Phosphorigsäure
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CH663514A5 (de)	1987-12-31	Schneckenbekaempfungsmittel.
DD218268A5 (de)	1985-02-06	Herbizide zusammensetzung
DD231979A5 (de)	1986-01-15	Synergistische herbizide zusammensetzungen
DE69216905T2 (de)	1997-05-15	Herbizide Zusammensetzungen mit verbesserter Getreide-Sicherheit
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