NO750812L - - Google Patents

Info

Publication number: NO750812L
Authority: NO; Norway
Prior art keywords: substituted; active substance; salts; spp; phenyl
Prior art date: 1974-03-14

Application number

NO750812A

Other languages

English (en)

Norwegian (no)

Inventor

A Fischer

G Synnatschke

Original Assignee

Basf 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.)

1974-03-14

Filing date

1975-03-11

Publication date

1975-09-16

1975-03-11 Application filed by Basf Ag filed Critical Basf Ag

1975-09-16 Publication of NO750812L publication Critical patent/NO750812L/no

Links

239000004009 herbicide Substances 0.000 claims description 19
230000002363 herbicidal effect Effects 0.000 claims description 18
239000007900 aqueous suspension Substances 0.000 claims description 11
239000004480 active ingredient Substances 0.000 claims description 4
239000013543 active substance Substances 0.000 description 39
150000003839 salts Chemical class 0.000 description 21
239000007921 spray Substances 0.000 description 21
-1 wetting->gluing Substances 0.000 description 19
241000196324 Embryophyta Species 0.000 description 18
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
150000002148 esters Chemical class 0.000 description 16
150000001408 amides Chemical class 0.000 description 15
239000007788 liquid Substances 0.000 description 11
239000000843 powder Substances 0.000 description 11
239000002253 acid Substances 0.000 description 8
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
150000007513 acids Chemical class 0.000 description 7
OFQCQIGMURIECL-UHFFFAOYSA-N 2-[2-(diethylamino)ethyl]-2',6'-dimethylspiro[isoquinoline-4,4'-oxane]-1,3-dione;phosphoric acid Chemical compound OP(O)(O)=O.O=C1N(CCN(CC)CC)C(=O)C2=CC=CC=C2C21CC(C)OC(C)C2 OFQCQIGMURIECL-UHFFFAOYSA-N 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
239000000725 suspension Substances 0.000 description 6
238000002474 experimental method Methods 0.000 description 5
239000002245 particle Substances 0.000 description 5
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
GRTOGORTSDXSFK-XJTZBENFSA-N ajmalicine Chemical compound C1=CC=C2C(CCN3C[C@@H]4[C@H](C)OC=C([C@H]4C[C@H]33)C(=O)OC)=C3NC2=C1 GRTOGORTSDXSFK-XJTZBENFSA-N 0.000 description 4
235000013877 carbamide Nutrition 0.000 description 4
235000013339 cereals Nutrition 0.000 description 4
238000009826 distribution Methods 0.000 description 4
238000000227 grinding Methods 0.000 description 4
230000012010 growth Effects 0.000 description 4
NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical class CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
239000003513 alkali Substances 0.000 description 3
239000004202 carbamide Substances 0.000 description 3
239000000084 colloidal system Substances 0.000 description 3
239000007859 condensation product Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
229940117927 ethylene oxide Drugs 0.000 description 3
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 3
150000002790 naphthalenes Chemical class 0.000 description 3
239000003921 oil Substances 0.000 description 3
230000008635 plant growth Effects 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
230000001681 protective effect Effects 0.000 description 3
239000002689 soil Substances 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
230000000844 anti-bacterial effect Effects 0.000 description 2
230000002528 anti-freeze Effects 0.000 description 2
239000000729 antidote Substances 0.000 description 2
229940075522 antidotes Drugs 0.000 description 2
239000007798 antifreeze agent Substances 0.000 description 2
239000003899 bactericide agent Substances 0.000 description 2
239000011324 bead Substances 0.000 description 2
230000004071 biological effect Effects 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
239000003630 growth substance Substances 0.000 description 2
239000002917 insecticide Substances 0.000 description 2
239000000203 mixture Substances 0.000 description 2
239000005645 nematicide Substances 0.000 description 2
YDCVQGAUCOROHB-UHFFFAOYSA-N oxadiazolidine-4,5-dione Chemical class O=C1NNOC1=O YDCVQGAUCOROHB-UHFFFAOYSA-N 0.000 description 2
SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical class OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 description 2
239000000126 substance Substances 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
FNQJDLTXOVEEFB-UHFFFAOYSA-N 1,2,3-benzothiadiazole Chemical class C1=CC=C2SN=NC2=C1 FNQJDLTXOVEEFB-UHFFFAOYSA-N 0.000 description 1
CSNIZNHTOVFARY-UHFFFAOYSA-N 1,2-benzothiazole Chemical class C1=CC=C2C=NSC2=C1 CSNIZNHTOVFARY-UHFFFAOYSA-N 0.000 description 1
MFVFDTCSVFBOTL-UHFFFAOYSA-N 1,3-diazetidine Chemical class C1NCN1 MFVFDTCSVFBOTL-UHFFFAOYSA-N 0.000 description 1
FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical class OS(O)(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC FKKAGFLIPSSCHT-UHFFFAOYSA-N 0.000 description 1
XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
QZEDXQFZACVDJE-UHFFFAOYSA-N 2,3-dibutylnaphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(O)(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 QZEDXQFZACVDJE-UHFFFAOYSA-N 0.000 description 1
HXDXZZNFARDZLT-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid;2-(2-hydroxyethylamino)ethanol Chemical compound OCCNCCO.CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O HXDXZZNFARDZLT-UHFFFAOYSA-N 0.000 description 1
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
UOCUSOBVEHOMMB-UHFFFAOYSA-N 2h-1$l^{6},2,3-benzothiadiazine 1,1-dioxide Chemical class C1=CC=C2S(=O)(=O)NN=CC2=C1 UOCUSOBVEHOMMB-UHFFFAOYSA-N 0.000 description 1
HQQTZCPKNZVLFF-UHFFFAOYSA-N 4h-1,2-benzoxazin-3-one Chemical class C1=CC=C2ONC(=O)CC2=C1 HQQTZCPKNZVLFF-UHFFFAOYSA-N 0.000 description 1
241000743985 Alopecurus Species 0.000 description 1
241000219318 Amaranthus Species 0.000 description 1
241000208477 Anagallis Species 0.000 description 1
241000404028 Anthemis Species 0.000 description 1
235000005781 Avena Nutrition 0.000 description 1
244000075850 Avena orientalis Species 0.000 description 1
235000008427 Brassica arvensis Nutrition 0.000 description 1
244000024671 Brassica kaber Species 0.000 description 1
235000004977 Brassica sinapistrum Nutrition 0.000 description 1
235000011305 Capsella bursa pastoris Nutrition 0.000 description 1
240000008867 Capsella bursa-pastoris Species 0.000 description 1
240000004385 Centaurea cyanus Species 0.000 description 1
235000005940 Centaurea cyanus Nutrition 0.000 description 1
241000219312 Chenopodium Species 0.000 description 1
244000192528 Chrysanthemum parthenium Species 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
244000152970 Digitaria sanguinalis Species 0.000 description 1
235000010823 Digitaria sanguinalis Nutrition 0.000 description 1
241000551547 Dione <red algae> Species 0.000 description 1
241000221079 Euphorbia <genus> Species 0.000 description 1
244000214240 Galinsoga parviflora Species 0.000 description 1
235000018914 Galinsoga parviflora Nutrition 0.000 description 1
240000005702 Galium aparine Species 0.000 description 1
235000014820 Galium aparine Nutrition 0.000 description 1
241000209219 Hordeum Species 0.000 description 1
241000520028 Lamium Species 0.000 description 1
241000209510 Liliopsida Species 0.000 description 1
235000017945 Matricaria Nutrition 0.000 description 1
235000007232 Matricaria chamomilla Nutrition 0.000 description 1
241000221026 Mercurialis annua Species 0.000 description 1
229930192627 Naphthoquinone Natural products 0.000 description 1
241000209094 Oryza Species 0.000 description 1
240000008114 Panicum miliaceum Species 0.000 description 1
235000007199 Panicum miliaceum Nutrition 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
241000209504 Poaceae Species 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
241000205407 Polygonum Species 0.000 description 1
239000004721 Polyphenylene oxide Substances 0.000 description 1
WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical class C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
240000000111 Saccharum officinarum Species 0.000 description 1
235000007201 Saccharum officinarum Nutrition 0.000 description 1
241000209056 Secale Species 0.000 description 1
235000005775 Setaria Nutrition 0.000 description 1
241000232088 Setaria <nematode> Species 0.000 description 1
241000488874 Sonchus Species 0.000 description 1
240000006694 Stellaria media Species 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
240000008488 Thlaspi arvense Species 0.000 description 1
235000008214 Thlaspi arvense Nutrition 0.000 description 1
240000005592 Veronica officinalis Species 0.000 description 1
241000219873 Vicia Species 0.000 description 1
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
238000004026 adhesive bonding Methods 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
150000001447 alkali salts Chemical class 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000005215 alkyl ethers Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
150000008052 alkyl sulfonates Chemical class 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
125000002490 anilino group Chemical class [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
210000000436 anus Anatomy 0.000 description 1
BUSBFZWLPXDYIC-UHFFFAOYSA-N arsonic acid Chemical class O[AsH](O)=O BUSBFZWLPXDYIC-UHFFFAOYSA-N 0.000 description 1
125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 description 1
150000005130 benzoxazines Chemical class 0.000 description 1
BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
150000002019 disulfides Chemical group 0.000 description 1
239000012990 dithiocarbamate Substances 0.000 description 1
150000004659 dithiocarbamates Chemical class 0.000 description 1
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
239000000428 dust Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
QQSGDKKFXBGYON-UHFFFAOYSA-N ethoxy-methylperoxy-(6-methyl-2-propan-2-ylpyrimidin-4-yl)oxy-sulfanylidene-$l^{5}-phosphane Chemical class CCOP(=S)(OOC)OC1=CC(C)=NC(C(C)C)=N1 QQSGDKKFXBGYON-UHFFFAOYSA-N 0.000 description 1
241001233957 eudicotyledons Species 0.000 description 1
239000000194 fatty acid Chemical class 0.000 description 1
229930195729 fatty acid Chemical class 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
230000008014 freezing Effects 0.000 description 1
238000007710 freezing Methods 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
GOQYKNQRPGWPLP-UHFFFAOYSA-N heptadecan-1-ol Chemical class CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
150000001469 hydantoins Chemical class 0.000 description 1
229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
150000002460 imidazoles Chemical class 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000000034 method Methods 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
150000002791 naphthoquinones Chemical class 0.000 description 1
230000001069 nematicidal effect Effects 0.000 description 1
QNMLMAVEXUCXRG-UHFFFAOYSA-N oxadiazinane-4,5-dione Chemical group O=C1CONNC1=O QNMLMAVEXUCXRG-UHFFFAOYSA-N 0.000 description 1
SDRLFDJOSQLRPB-UHFFFAOYSA-N oxadiazine-4,5-dione Chemical class O=C1CON=NC1=O SDRLFDJOSQLRPB-UHFFFAOYSA-N 0.000 description 1
150000004866 oxadiazoles Chemical class 0.000 description 1
230000035515 penetration Effects 0.000 description 1
230000002085 persistent effect Effects 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
REJGOFYVRVIODZ-UHFFFAOYSA-N phosphanium;chloride Chemical class P.Cl REJGOFYVRVIODZ-UHFFFAOYSA-N 0.000 description 1
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
150000003009 phosphonic acids Chemical class 0.000 description 1
235000011007 phosphoric acid Nutrition 0.000 description 1
150000003016 phosphoric acids Chemical class 0.000 description 1
150000003053 piperidines Chemical class 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
235000019422 polyvinyl alcohol Nutrition 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
239000000047 product Substances 0.000 description 1
150000003217 pyrazoles Chemical class 0.000 description 1
150000003222 pyridines Chemical class 0.000 description 1
150000003230 pyrimidines Chemical class 0.000 description 1
150000008318 pyrimidones Chemical class 0.000 description 1
NYCVCXMSZNOGDH-UHFFFAOYSA-N pyrrolidine-1-carboxylic acid Chemical class OC(=O)N1CCCC1 NYCVCXMSZNOGDH-UHFFFAOYSA-N 0.000 description 1
150000003235 pyrrolidines Chemical class 0.000 description 1
150000004040 pyrrolidinones Chemical class 0.000 description 1
150000003246 quinazolines Chemical class 0.000 description 1
150000003248 quinolines Chemical class 0.000 description 1
239000004576 sand Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
125000003011 styrenyl group Chemical class [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
OLPRIZQBWZMBAS-UHFFFAOYSA-N thiadiazolidine 1,1-dioxide Chemical class O=S1(=O)CCNN1 OLPRIZQBWZMBAS-UHFFFAOYSA-N 0.000 description 1
150000003566 thiocarboxylic acids Chemical class 0.000 description 1
150000003582 thiophosphoric acids Chemical class 0.000 description 1
150000003585 thioureas Chemical class 0.000 description 1
239000011573 trace mineral Substances 0.000 description 1
235000013619 trace mineral Nutrition 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
150000003672 ureas Chemical class 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D237/14—Oxygen atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
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)

NO750812A 1974-03-14 1975-03-11 NO750812L (ja)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2412270A DE2412270A1 (de)	1974-03-14	1974-03-14	Herbizid

Publications (1)

Publication Number	Publication Date
NO750812L true NO750812L (ja)	1975-09-16

Family

ID=5910073

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO750812A NO750812L (ja)	1974-03-14	1975-03-11

Country Status (16)

Country	Link
JP (1)	JPS50125032A (ja)
AU (1)	AU7836075A (ja)
BE (1)	BE826538A (ja)
DD (1)	DD117587A5 (ja)
DE (1)	DE2412270A1 (ja)
DK (1)	DK102375A (ja)
FI (1)	FI750665A (ja)
FR (1)	FR2263691A1 (ja)
IL (1)	IL46667A0 (ja)
LU (1)	LU72037A1 (ja)
NL (1)	NL7503016A (ja)
NO (1)	NO750812L (ja)
RO (1)	RO72089A (ja)
SE (1)	SE7502912L (ja)
TR (1)	TR18579A (ja)
ZA (1)	ZA751558B (ja)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2547968A1 (de) *	1975-10-27	1977-05-05	Basf Ag	Herbizid
DE2909158A1 (de) *	1979-03-08	1980-09-11	Basf Ag	Herbizide mischungen

1974
- 1974-03-14 DE DE2412270A patent/DE2412270A1/de active Pending
1975
- 1975-02-19 IL IL46667A patent/IL46667A0/xx unknown
- 1975-02-19 AU AU78360/75A patent/AU7836075A/en not_active Expired
- 1975-03-07 FR FR7507236A patent/FR2263691A1/fr active Granted
- 1975-03-07 FI FI750665A patent/FI750665A/fi not_active Application Discontinuation
- 1975-03-11 TR TR18579A patent/TR18579A/xx unknown
- 1975-03-11 BE BE154216A patent/BE826538A/xx unknown
- 1975-03-11 JP JP50028717A patent/JPS50125032A/ja active Pending
- 1975-03-11 NO NO750812A patent/NO750812L/no unknown
- 1975-03-12 LU LU72037A patent/LU72037A1/xx unknown
- 1975-03-12 DD DD184723A patent/DD117587A5/xx unknown
- 1975-03-12 RO RO7581611A patent/RO72089A/ro unknown
- 1975-03-13 ZA ZA00751558A patent/ZA751558B/xx unknown
- 1975-03-13 DK DK102375A patent/DK102375A/da unknown
- 1975-03-13 NL NL7503016A patent/NL7503016A/xx unknown
- 1975-03-14 SE SE7502912A patent/SE7502912L/xx not_active Application Discontinuation

Also Published As

Publication number	Publication date
JPS50125032A (ja)	1975-10-01
DD117587A5 (ja)	1976-01-20
AU7836075A (en)	1976-08-19
FI750665A (ja)	1975-09-15
FR2263691B1 (ja)	1978-04-21
DK102375A (ja)	1975-09-15
FR2263691A1 (en)	1975-10-10
RO72089A (ro)	1982-05-10
LU72037A1 (ja)	1975-08-20
TR18579A (tr)	1977-04-13
DE2412270A1 (de)	1975-09-25
NL7503016A (nl)	1975-09-16
SE7502912L (ja)	1975-09-15
IL46667A0 (en)	1975-04-25
ZA751558B (en)	1976-03-31
BE826538A (fr)	1975-09-11

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CA2082572A1 (en)	1993-05-27	Hydroxypyridonecarboxamides, their manufacture and use
NO750812L (ja)	1975-09-16
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NO142983B (no)	1980-08-18	Vandig herbicid suspensjon paa basis av 1-fenyl-4-amino-5-klor (eller -5-brom)-pyridazon-(6)
EP0427695A2 (en)	1991-05-15	Herbicidal compositions
AU594853B2 (en)	1990-03-15	Herbicidal composition
AU595974B2 (en)	1990-04-12	Herbicidal composition
NO750265L (ja)	1975-08-25
PL126706B1 (en)	1983-08-31	Herbicide
EP0067712B1 (en)	1985-01-23	A herbicidal composition and method for controlling the growth of plants
EP0264736B1 (en)	1992-05-13	Herbicidal composition
NO139332B (no)	1978-11-13	Herbicid preparat som inneholder blandinger av 2,1,3-benzotiadiazinon-(4)-2,2-dioksyd- og teroksysmoersyre-derivater
US4025544A (en)	1977-05-24	O-alkylsulfonylglycolic anilides
NO743390L (ja)	1975-05-12
CS202523B2 (en)	1981-01-30	Herbicide means
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NO741858L (ja)	1975-01-06
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GB2068233A (en)	1981-08-12	Herbicidal compositions comprising 1-(3,4-dichlorobenzyl)imidazole- N,N%-dimethyl-4,5-dicarboxamide