CS220778B2 - Herbicide means - Google Patents

Herbicide means Download PDF

Info

Publication number: CS220778B2
Authority: CS; Czechoslovakia
Prior art keywords: formula; compounds; weeds; active; phenyl
Prior art date: 1979-06-22

Application number

CS435580A

Other languages

Czech (cs)

English (en)

Inventor

Harald Leitner

Franz Raninger

Alfred Diskus

Engelbert Auer

Original Assignee

Chemie Linz 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.)

1979-06-22

Filing date

1980-06-16

Publication date

1983-04-29

1980-06-16 Application filed by Chemie Linz Ag filed Critical Chemie Linz Ag

1983-04-29 Publication of CS220778B2 publication Critical patent/CS220778B2/cs

Links

230000002363 herbicidal effect Effects 0.000 title claims abstract description 12
239000004009 herbicide Substances 0.000 title description 5
150000001875 compounds Chemical class 0.000 claims abstract description 31
239000000203 mixture Substances 0.000 claims abstract description 23
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 8
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 8
229910052760 oxygen Inorganic materials 0.000 claims abstract description 8
239000001301 oxygen Substances 0.000 claims abstract description 8
229910052794 bromium Inorganic materials 0.000 claims abstract description 7
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 6
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 6
229910052740 iodine Inorganic materials 0.000 claims abstract description 6
125000000217 alkyl group Chemical group 0.000 claims abstract description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 4
239000000460 chlorine Substances 0.000 claims abstract description 4
229910052801 chlorine Inorganic materials 0.000 claims abstract description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 4
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims abstract description 3
239000011630 iodine Substances 0.000 claims abstract 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 10
229910052717 sulfur Chemical group 0.000 claims description 9
125000004434 sulfur atom Chemical group 0.000 claims description 6
239000004480 active ingredient Substances 0.000 claims description 5
125000006702 (C1-C18) alkyl group Chemical group 0.000 claims description 3
239000011593 sulfur Chemical group 0.000 claims description 3
WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 claims description 2
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 claims 1
241000196324 Embryophyta Species 0.000 abstract description 29
230000002195 synergetic effect Effects 0.000 abstract description 7
235000013339 cereals Nutrition 0.000 abstract description 5
240000008042 Zea mays Species 0.000 abstract description 3
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 abstract description 3
235000002017 Zea mays subsp mays Nutrition 0.000 abstract description 3
235000009973 maize Nutrition 0.000 abstract description 3
238000000034 method Methods 0.000 abstract description 2
239000005864 Sulphur Chemical group 0.000 abstract 3
125000004432 carbon atom Chemical group C* 0.000 abstract 2
239000013543 active substance Substances 0.000 description 7
230000000694 effects Effects 0.000 description 7
240000005702 Galium aparine Species 0.000 description 6
235000014820 Galium aparine Nutrition 0.000 description 6
238000011156 evaluation Methods 0.000 description 6
-1 n-octyl Chemical group 0.000 description 6
239000005606 Pyridate Substances 0.000 description 5
JTZCTMAVMHRNTR-UHFFFAOYSA-N Pyridate Chemical compound CCCCCCCCSC(=O)OC1=CC(Cl)=NN=C1C1=CC=CC=C1 JTZCTMAVMHRNTR-UHFFFAOYSA-N 0.000 description 5
239000003995 emulsifying agent Substances 0.000 description 5
UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 description 4
241001508646 Galeopsis tetrahit Species 0.000 description 4
240000006694 Stellaria media Species 0.000 description 4
239000005489 Bromoxynil Substances 0.000 description 3
QBEXFUOWUYCXNI-UHFFFAOYSA-N Ioxynil octanoate Chemical compound CCCCCCCC(=O)OC1=C(I)C=C(C#N)C=C1I QBEXFUOWUYCXNI-UHFFFAOYSA-N 0.000 description 3
244000042664 Matricaria chamomilla Species 0.000 description 3
235000007232 Matricaria chamomilla Nutrition 0.000 description 3
239000000126 substance Substances 0.000 description 3
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 description 3
238000012360 testing method Methods 0.000 description 3
240000006122 Chenopodium album Species 0.000 description 2
229920000742 Cotton Polymers 0.000 description 2
240000006503 Lamium purpureum Species 0.000 description 2
235000009193 Lamium purpureum Nutrition 0.000 description 2
240000002702 Lapsana communis Species 0.000 description 2
235000006761 Lapsana communis Nutrition 0.000 description 2
240000004674 Papaver rhoeas Species 0.000 description 2
235000007846 Papaver rhoeas Nutrition 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
125000005228 aryl sulfonate group Chemical group 0.000 description 2
239000000969 carrier Substances 0.000 description 2
230000001186 cumulative effect Effects 0.000 description 2
238000011161 development Methods 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
230000008029 eradication Effects 0.000 description 2
239000000945 filler Substances 0.000 description 2
238000009472 formulation Methods 0.000 description 2
NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
238000009736 wetting Methods 0.000 description 2
DQKWXTIYGWPGOO-UHFFFAOYSA-N (2,6-dibromo-4-cyanophenyl) octanoate Chemical compound CCCCCCCC(=O)OC1=C(Br)C=C(C#N)C=C1Br DQKWXTIYGWPGOO-UHFFFAOYSA-N 0.000 description 1
HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 1
239000005631 2,4-Dichlorophenoxyacetic 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
WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 description 1
XWSSUYOEOWLFEI-UHFFFAOYSA-N 3-phenylpyridazine Chemical class C1=CC=CC=C1C1=CC=CN=N1 XWSSUYOEOWLFEI-UHFFFAOYSA-N 0.000 description 1
240000007124 Brassica oleracea Species 0.000 description 1
235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
244000157790 Buglossoides arvense Species 0.000 description 1
235000004256 Buglossoides arvense Nutrition 0.000 description 1
235000007866 Chamaemelum nobile Nutrition 0.000 description 1
235000009344 Chenopodium album Nutrition 0.000 description 1
235000011498 Chenopodium album var missouriense Nutrition 0.000 description 1
235000013328 Chenopodium album var. album Nutrition 0.000 description 1
235000014052 Chenopodium album var. microphyllum Nutrition 0.000 description 1
235000014050 Chenopodium album var. stevensii Nutrition 0.000 description 1
235000013012 Chenopodium album var. striatum Nutrition 0.000 description 1
241001289540 Fallopia convolvulus Species 0.000 description 1
239000005574 MCPA Substances 0.000 description 1
101000986989 Naja kaouthia Acidic phospholipase A2 CM-II Proteins 0.000 description 1
235000008753 Papaver somniferum Nutrition 0.000 description 1
241000218180 Papaveraceae Species 0.000 description 1
241000205407 Polygonum Species 0.000 description 1
241000555745 Sciuridae Species 0.000 description 1
WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 1
LEHOTFFKMJEONL-UHFFFAOYSA-N Uric Acid Chemical compound N1C(=O)NC(=O)C2=C1NC(=O)N2 LEHOTFFKMJEONL-UHFFFAOYSA-N 0.000 description 1
241001166549 Veronica hederifolia Species 0.000 description 1
240000005592 Veronica officinalis Species 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
230000003115 biocidal effect Effects 0.000 description 1
230000008033 biological extinction Effects 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
244000038559 crop plants Species 0.000 description 1
230000006378 damage Effects 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
235000013312 flour Nutrition 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
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000007788 liquid Substances 0.000 description 1
240000004308 marijuana Species 0.000 description 1
MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
239000011707 mineral Substances 0.000 description 1
239000006072 paste Substances 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
239000005648 plant growth regulator Substances 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920000056 polyoxyethylene ether Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000011435 rock Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
150000004760 silicates Chemical class 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
IZWPGJFSBABFGL-GMFCBQQYSA-M sodium;2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS([O-])(=O)=O IZWPGJFSBABFGL-GMFCBQQYSA-M 0.000 description 1
239000000243 solution Substances 0.000 description 1
241000894007 species Species 0.000 description 1
239000007921 spray Substances 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000004563 wettable powder Substances 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
- A01N47/02—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 no bond to a nitrogen atom
- A01N47/06—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 no bond to a nitrogen atom containing —O—CO—O— groups; 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)

CS435580A 1979-06-22 1980-06-16 Herbicide means CS220778B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19792925335 DE2925335A1 (de)	1979-06-22	1979-06-22	Herbizides mittel

Publications (1)

Publication Number	Publication Date
CS220778B2 true CS220778B2 (en)	1983-04-29

Family

ID=6073947

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS435580A CS220778B2 (en)	1979-06-22	1980-06-16	Herbicide means

Country Status (19)

Country	Link
AR (1)	AR225044A1 (tr)
AU (1)	AU526903B2 (tr)
BR (1)	BR8003872A (tr)
CA (1)	CA1139121A (tr)
CS (1)	CS220778B2 (tr)
DD (1)	DD151405A1 (tr)
DE (1)	DE2925335A1 (tr)
DK (1)	DK156982C (tr)
FR (1)	FR2459617A1 (tr)
GB (1)	GB2051578B (tr)
HU (1)	HU185893B (tr)
IT (1)	IT1129226B (tr)
KE (1)	KE3301A (tr)
PL (1)	PL122688B1 (tr)
SE (1)	SE446928B (tr)
SU (1)	SU934897A3 (tr)
TR (1)	TR20588A (tr)
UA (1)	UA6316A1 (tr)
ZA (1)	ZA803236B (tr)

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE636416A (tr) *	1962-08-30
DE2331398C3 (de) *	1973-06-20	1979-10-11	Lentia Gmbh	Ester von S-PhenyM-hydroxy-e-halogenpyridazinverbindungen, ihre Herstellung und sie enthaltende herbizide Mittel
DE2351553A1 (de) *	1973-10-13	1975-04-24	Basf Ag	Herbizid

1979
- 1979-06-22 DE DE19792925335 patent/DE2925335A1/de not_active Ceased
1980
- 1980-05-29 CA CA000353054A patent/CA1139121A/en not_active Expired
- 1980-05-30 ZA ZA00803236A patent/ZA803236B/xx unknown
- 1980-06-06 DK DK244280A patent/DK156982C/da not_active IP Right Cessation
- 1980-06-11 GB GB8019037A patent/GB2051578B/en not_active Expired
- 1980-06-12 SE SE8004382A patent/SE446928B/sv not_active IP Right Cessation
- 1980-06-16 CS CS435580A patent/CS220778B2/cs unknown
- 1980-06-17 DD DD80221891A patent/DD151405A1/de active Protection Beyond IP Right Term
- 1980-06-17 UA UA2936199A patent/UA6316A1/uk unknown
- 1980-06-17 SU SU802936199A patent/SU934897A3/ru active
- 1980-06-18 AU AU59394/80A patent/AU526903B2/en not_active Ceased
- 1980-06-18 AR AR281438A patent/AR225044A1/es active
- 1980-06-19 FR FR8013600A patent/FR2459617A1/fr active Granted
- 1980-06-20 PL PL1980225113A patent/PL122688B1/pl unknown
- 1980-06-20 HU HU801537A patent/HU185893B/hu not_active IP Right Cessation
- 1980-06-20 BR BR8003872A patent/BR8003872A/pt not_active IP Right Cessation
- 1980-06-20 IT IT67972/80A patent/IT1129226B/it active Protection Beyond IP Right Term
- 1980-06-23 TR TR20588A patent/TR20588A/tr unknown
1983
- 1983-06-27 KE KE3301A patent/KE3301A/xx unknown

Also Published As

Publication number	Publication date
CA1139121A (en)	1983-01-11
GB2051578B (en)	1983-06-02
UA6316A1 (uk)	1994-12-29
HU185893B (en)	1985-04-28
AR225044A1 (es)	1982-02-15
IT1129226B (it)	1986-06-04
DK244280A (da)	1980-12-23
PL122688B1 (en)	1982-08-31
GB2051578A (en)	1981-01-21
IT8067972A0 (it)	1980-06-20
DK156982C (da)	1990-03-26
TR20588A (tr)	1982-02-01
DD151405A1 (de)	1981-10-21
PL225113A1 (tr)	1981-05-22
SE446928B (sv)	1986-10-20
DE2925335A1 (de)	1981-01-08
KE3301A (en)	1983-08-05
AU526903B2 (en)	1983-02-03
ZA803236B (en)	1981-05-27
FR2459617A1 (fr)	1981-01-16
DK156982B (da)	1989-10-30
FR2459617B1 (tr)	1982-04-16
BR8003872A (pt)	1981-01-21
AU5939480A (en)	1981-01-08
SE8004382L (sv)	1980-12-23
SU934897A3 (ru)	1982-06-07

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