BE631384A - - Google Patents
Info
- Publication number
- BE631384A BE631384A BE631384A BE631384A BE631384A BE 631384 A BE631384 A BE 631384A BE 631384 A BE631384 A BE 631384A BE 631384 A BE631384 A BE 631384A BE 631384 A BE631384 A BE 631384A
- Authority
- BE
- Belgium
- Prior art keywords
- methyl
- solution
- salt
- water
- potassium
- Prior art date
Links
- 150000002148 esters Chemical class 0.000 claims description 17
- 239000000203 mixture Substances 0.000 claims description 16
- -1 ester salts Chemical class 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 5
- 230000002363 herbicidal effect Effects 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 30
- 239000000243 solution Substances 0.000 description 23
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 16
- 239000000047 product Substances 0.000 description 15
- 239000007787 solid Substances 0.000 description 15
- 150000003839 salts Chemical class 0.000 description 12
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical group [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 239000001103 potassium chloride Substances 0.000 description 8
- 235000011164 potassium chloride Nutrition 0.000 description 8
- 241000196324 Embryophyta Species 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 235000007320 Avena fatua Nutrition 0.000 description 5
- 244000075850 Avena orientalis Species 0.000 description 5
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 5
- 235000005373 Uvularia sessilifolia Nutrition 0.000 description 5
- 239000002671 adjuvant Substances 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 159000000000 sodium salts Chemical class 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 241000209504 Poaceae Species 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- QTRRBBBZOZXIMT-UHFFFAOYSA-N carbamoyl benzenesulfonate Chemical compound NC(=O)OS(=O)(=O)C1=CC=CC=C1 QTRRBBBZOZXIMT-UHFFFAOYSA-N 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- 244000042664 Matricaria chamomilla Species 0.000 description 3
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- GTCAXTIRRLKXRU-UHFFFAOYSA-N carbamic acid methyl ester Natural products COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 description 3
- 241001233957 eudicotyledons Species 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 239000000395 magnesium oxide Substances 0.000 description 3
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 3
- 159000000003 magnesium salts Chemical class 0.000 description 3
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000011591 potassium Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 240000001592 Amaranthus caudatus Species 0.000 description 2
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 235000016068 Berberis vulgaris Nutrition 0.000 description 2
- 241000335053 Beta vulgaris Species 0.000 description 2
- 235000001602 Digitaria X umfolozi Nutrition 0.000 description 2
- 235000017898 Digitaria ciliaris Nutrition 0.000 description 2
- 235000005476 Digitaria cruciata Nutrition 0.000 description 2
- 235000006830 Digitaria didactyla Nutrition 0.000 description 2
- 235000005804 Digitaria eriantha ssp. eriantha Nutrition 0.000 description 2
- 235000010823 Digitaria sanguinalis Nutrition 0.000 description 2
- 241000192043 Echinochloa Species 0.000 description 2
- 244000025670 Eleusine indica Species 0.000 description 2
- 235000014716 Eleusine indica Nutrition 0.000 description 2
- 240000006240 Linum usitatissimum Species 0.000 description 2
- 235000004431 Linum usitatissimum Nutrition 0.000 description 2
- 235000017945 Matricaria Nutrition 0.000 description 2
- 241000219053 Rumex Species 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 230000002085 persistent effect Effects 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 235000011181 potassium carbonates Nutrition 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- CNPURSDMOWDNOQ-UHFFFAOYSA-N 4-methoxy-7h-pyrrolo[2,3-d]pyrimidin-2-amine Chemical class COC1=NC(N)=NC2=C1C=CN2 CNPURSDMOWDNOQ-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241000132536 Cirsium Species 0.000 description 1
- 241000508725 Elymus repens Species 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 240000002024 Gossypium herbaceum Species 0.000 description 1
- 235000004341 Gossypium herbaceum Nutrition 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 240000004658 Medicago sativa Species 0.000 description 1
- 235000017587 Medicago sativa ssp. sativa Nutrition 0.000 description 1
- 241000205407 Polygonum Species 0.000 description 1
- 244000292697 Polygonum aviculare Species 0.000 description 1
- 235000006386 Polygonum aviculare Nutrition 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 244000111146 Sonchus arvensis Species 0.000 description 1
- 235000008132 Sonchus arvensis ssp. uliginosus Nutrition 0.000 description 1
- 244000152045 Themeda triandra Species 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 235000012735 amaranth Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 1
- XMJHPCRAQCTCFT-UHFFFAOYSA-N methyl chloroformate Chemical compound COC(Cl)=O XMJHPCRAQCTCFT-UHFFFAOYSA-N 0.000 description 1
- KBOYYSBFXHJLGU-UHFFFAOYSA-N methyl n-sulfonylcarbamate Chemical compound COC(=O)N=S(=O)=O KBOYYSBFXHJLGU-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical class [H]C([H])=* 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- 230000001473 noxious effect Effects 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
- C07C303/40—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
-
- 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
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Agronomy & Crop Science (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB32407/61A GB1040541A (en) | 1961-09-08 | 1961-09-08 | Herbicidal compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
BE631384A true BE631384A (d) | 1963-11-18 |
Family
ID=10338134
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE622214A BE622214A (d) | 1961-09-08 | 1962-09-06 | |
BE631384A BE631384A (d) | 1961-09-08 | 1963-04-22 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE622214A BE622214A (d) | 1961-09-08 | 1962-09-06 |
Country Status (12)
Country | Link |
---|---|
AT (1) | AT242434B (d) |
BE (2) | BE622214A (d) |
BR (1) | BR6242762D0 (d) |
CH (1) | CH416214A (d) |
DE (1) | DE1468220A1 (d) |
DK (2) | DK109484C (d) |
ES (1) | ES280583A1 (d) |
FR (1) | FR1340297A (d) |
GB (1) | GB1040541A (d) |
MY (1) | MY6900199A (d) |
NL (2) | NL123687C (d) |
SE (1) | SE305979B (d) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3512955A (en) * | 1967-11-06 | 1970-05-19 | Monsanto Co | Method of protecting plant growth |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3326970A (en) * | 1965-11-26 | 1967-06-20 | Olin Mathieson | N-trihalomethylthio n-(aminosulfonyl) carbamates |
JPS6055062B2 (ja) * | 1979-09-21 | 1985-12-03 | 塩野義製薬株式会社 | N↑4−フエノキシアセチルスルフアニルアミド類および除草剤 |
OA06869A (fr) * | 1980-08-13 | 1983-02-28 | May & Baker Ltd | Procédé de contrôle des mauvaises herbes utilisant un mélange de matières actives notamment de carbamate. |
DE4023040A1 (de) * | 1990-07-20 | 1992-01-23 | Bayer Ag | Herbizide auf basis von sulfonylierten (thio)carbamidsaeureestern, neue sulfonylierte carbamidsaeureester und verfahren zu deren herstellung |
FR2690918B1 (fr) * | 1992-05-06 | 2001-12-28 | Poudres & Explosifs Ste Nale | Utilisation d'un arylsulfonyluréthanne comme résine garnissante dans les vernis à ongles nitrocellulosiques. Nouveaux arylsulfonyluréthannes et nouveaux vernis à ongles nitrocellulosiques. |
EP2052606A1 (de) | 2007-10-24 | 2009-04-29 | Bayer CropScience AG | Herbizid-Kombination |
DE102008037620A1 (de) | 2008-08-14 | 2010-02-18 | Bayer Crop Science Ag | Herbizid-Kombination mit Dimethoxytriazinyl-substituierten Difluormethansulfonylaniliden |
JP6027009B2 (ja) | 2010-10-15 | 2016-11-16 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | Alsインヒビター除草剤耐性ベータ・ブルカリス植物における望ましくない植生の防除のためのalsインヒビター除草剤の使用 |
UA117447C2 (uk) | 2011-05-04 | 2018-08-10 | Байєр Інтеллектуал Проперті Гмбх | Застосування гербіцидів інгібіторів als для боротьби з небажаною рослинністю на площі вирощування brassica |
DK2931034T4 (da) | 2012-12-13 | 2022-07-18 | Bayer Cropscience Ag | Anvendelse af als-inhibitorherbicider til bekæmpelse af uønsket vegetation i als-inhibitorherbicidtolerante beta vulgaris-planter |
CN118201483A (zh) | 2021-10-15 | 2024-06-14 | 科沃施种子欧洲股份两合公司 | ALS抑制剂除草剂耐受的甜菜(Beta Vulgaris)突变体 |
-
0
- NL NL283003D patent/NL283003A/xx unknown
- NL NL123687D patent/NL123687C/xx active
-
1961
- 1961-09-08 GB GB32407/61A patent/GB1040541A/en not_active Expired
-
1962
- 1962-09-03 CH CH1047162A patent/CH416214A/fr unknown
- 1962-09-05 FR FR908679A patent/FR1340297A/fr not_active Expired
- 1962-09-06 ES ES0280583A patent/ES280583A1/es not_active Expired
- 1962-09-06 BR BR142762/62A patent/BR6242762D0/pt unknown
- 1962-09-06 BE BE622214A patent/BE622214A/xx unknown
- 1962-09-07 DK DK391862AA patent/DK109484C/da active
- 1962-09-07 DK DK391962AA patent/DK107326C/da active
- 1962-09-07 DE DE19621468220 patent/DE1468220A1/de active Pending
- 1962-09-07 AT AT716262A patent/AT242434B/de active
- 1962-09-07 SE SE9714/62A patent/SE305979B/xx unknown
-
1963
- 1963-04-22 BE BE631384A patent/BE631384A/fr unknown
-
1969
- 1969-12-31 MY MY1969199A patent/MY6900199A/xx unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3512955A (en) * | 1967-11-06 | 1970-05-19 | Monsanto Co | Method of protecting plant growth |
Also Published As
Publication number | Publication date |
---|---|
BE622214A (d) | 1963-03-06 |
MY6900199A (en) | 1969-12-31 |
CH416214A (fr) | 1966-06-30 |
AT242434B (de) | 1965-09-10 |
GB1040541A (en) | 1966-09-01 |
ES280583A1 (es) | 1962-12-01 |
FR1340297A (fr) | 1963-10-18 |
DK107326C (da) | 1967-05-16 |
NL123687C (d) | |
BR6242762D0 (pt) | 1973-05-10 |
DE1468220A1 (de) | 1970-01-15 |
DK109484C (da) | 1968-04-29 |
SE305979B (d) | 1968-11-11 |
NL283003A (d) |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BE631384A (d) | ||
DE69118070T2 (de) | Benzofuranyl- und Benzothiophenyl-substituierte Uracilderivate, ihre Herstellung und ihre Verwendung als Herbizide | |
HU188525B (en) | Herbicidal preparations containing tetrahydrophthalimide derivatives and process for the production of the active substance | |
FR3119622A1 (fr) | Nouvelle forme cristalline de pyroxasulfone, procédés de préparation et utilisation de celle-ci | |
EP0097547B1 (fr) | Acides halogénobenzhydrylsulfinylacétohydroxamiques, procédé de préparation et utilisation en thérapeutique | |
EP0142769A2 (en) | Tetrahydrobenzotriazoles, their production and use | |
CH368151A (fr) | Procédé de fabrication d'agents antidiabétiques | |
FR2594437A1 (fr) | Nouveaux derives du cyano-2 benzimidazole, leur preparation, les compositions les contenant et leur utilisation comme fongicide | |
FR2560007A1 (fr) | Compositions fongicides comprenant des derives de phenoxy benzaldehyde | |
FR2571589A1 (fr) | Compositions herbicides selectives ayant une action prolongee et contenant, a titre d'ingredient actif, des derives d'a-chloracetamide | |
FR2467191A1 (fr) | Nouveaux 5-(2'-chloro-4'-trifluoromethylphenoxy)-2-nitrostyrenes, leur procede de production, composition herbicide les contenant et leur application a la destruction de vegetaux | |
BE818849A (fr) | Derives de cyclohexane | |
FR2549831A1 (fr) | Nouveaux derives d'acides aryloxybenzoiques, et leur utilisation comme herbicides | |
EP0060955A1 (fr) | Nouveaux uraciles substitués comportant un groupement 2-tétra-hydropyranyle, leur procédé de préparation et les compositions pesticides les renfermant | |
EP0131522B1 (fr) | Nouveaux uraciles substitués comportant en position 1 un groupement phényloxy carbonyl substitué, leur préparation et les compositions herbicides les renfermant | |
BE799932A (fr) | Nouvelles 6-amino-s-triazinediones utiles comme herbicdes | |
FR2460110A1 (fr) | Nouveaux agents fongicides et bactericides a base d'halogenoacetamides | |
FR2465719A1 (fr) | Procede de preparation de n4-phenoxyalcanoylsulfanilamides, nouveaux produits ainsi obtenus et compositions herbicides les renfermant | |
BE608352A (d) | ||
FR2480278A1 (fr) | Nouveaux derives du terpene, procede pour leur preparation et compositions insecticides contenant ces derives | |
BE550303A (d) | ||
CH634067A5 (en) | Thiophenecarboxamidoxime derivatives, their preparation and phytohormonal and herbicidal compositions containing them | |
FR2787788A1 (fr) | Compose de l'uracile optiquement actif, son utilisation comme herbicide, composition herbicide et procede de lutte contre les mauvaises herbes l'utilisant | |
FR2521130A1 (fr) | Procede pour augmenter le sucre recuperable provenant de betteraves a sucre, en traitant ces plantes avec des benzamides d'acide 2-methoxy-3,6-dichlorobenzoique | |
BE787656A (fr) | Nouveaux sels de thenylammonium quaternaire, leur procede de preparation et leur application comme regulateurs de croissance des vegetaux. |