BE612550A - - Google Patents
Info
- Publication number
- BE612550A BE612550A BE612550DA BE612550A BE 612550 A BE612550 A BE 612550A BE 612550D A BE612550D A BE 612550DA BE 612550 A BE612550 A BE 612550A
- Authority
- BE
- Belgium
- Prior art keywords
- carbamate
- methyl
- dichlorophenyl
- herbicidal
- sep
- Prior art date
Links
- 230000002363 herbicidal Effects 0.000 claims description 33
- 239000000203 mixture Substances 0.000 claims description 25
- WOZQBERUBLYCEG-UHFFFAOYSA-N SWEP Chemical compound COC(=O)NC1=CC=C(Cl)C(Cl)=C1 WOZQBERUBLYCEG-UHFFFAOYSA-N 0.000 claims description 17
- 239000007787 solid Substances 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 5
- 239000002671 adjuvant Substances 0.000 claims description 3
- 230000000240 adjuvant Effects 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 2
- 239000002689 soil Substances 0.000 claims description 2
- 238000000034 method Methods 0.000 claims 4
- 238000004519 manufacturing process Methods 0.000 claims 2
- 229920001098 polystyrene-block-poly(ethylene/propylene) Polymers 0.000 description 26
- 239000000843 powder Substances 0.000 description 11
- 241000196324 Embryophyta Species 0.000 description 10
- 239000004009 herbicide Substances 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000004480 active ingredient Substances 0.000 description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 7
- 239000002270 dispersing agent Substances 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Substances CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 230000000875 corresponding Effects 0.000 description 5
- 231100000331 toxic Toxicity 0.000 description 5
- 230000002588 toxic Effects 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- KXDHJXZQYSOELW-UHFFFAOYSA-M carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 244000075850 Avena orientalis Species 0.000 description 3
- 235000007319 Avena orientalis Nutrition 0.000 description 3
- 240000000772 Brassica cretica Species 0.000 description 3
- 235000003351 Brassica cretica Nutrition 0.000 description 3
- 235000003343 Brassica rupestris Nutrition 0.000 description 3
- 229920000742 Cotton Polymers 0.000 description 3
- 240000002860 Daucus carota Species 0.000 description 3
- 235000002767 Daucus carota Nutrition 0.000 description 3
- 240000006962 Gossypium hirsutum Species 0.000 description 3
- 240000008415 Lactuca sativa Species 0.000 description 3
- 235000003228 Lactuca sativa Nutrition 0.000 description 3
- 241000209082 Lolium Species 0.000 description 3
- PWXJULSLLONQHY-UHFFFAOYSA-M N-phenylcarbamate Chemical class [O-]C(=O)NC1=CC=CC=C1 PWXJULSLLONQHY-UHFFFAOYSA-M 0.000 description 3
- -1 alkyl N-phenylcarbamates Chemical class 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 235000010460 mustard Nutrition 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N oxane Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 231100000167 toxic agent Toxicity 0.000 description 3
- 239000003440 toxic substance Substances 0.000 description 3
- 239000004563 wettable powder Substances 0.000 description 3
- 239000000080 wetting agent Substances 0.000 description 3
- MFUVCHZWGSJKEQ-UHFFFAOYSA-N 3,4-Dichlorphenylisocyanate Chemical compound ClC1=CC=C(N=C=O)C=C1Cl MFUVCHZWGSJKEQ-UHFFFAOYSA-N 0.000 description 2
- SDYWXFYBZPNOFX-UHFFFAOYSA-N 3,4-dichloroaniline Chemical compound NC1=CC=C(Cl)C(Cl)=C1 SDYWXFYBZPNOFX-UHFFFAOYSA-N 0.000 description 2
- 240000001452 Canavalia ensiformis Species 0.000 description 2
- 210000003763 Chloroplasts Anatomy 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N Isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 235000010617 Phaseolus lunatus Nutrition 0.000 description 2
- 240000005158 Phaseolus vulgaris Species 0.000 description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
- HWKQNAWCHQMZHK-UHFFFAOYSA-N Trolnitrate Chemical compound [O-][N+](=O)OCCN(CCO[N+]([O-])=O)CCO[N+]([O-])=O HWKQNAWCHQMZHK-UHFFFAOYSA-N 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 230000002745 absorbent Effects 0.000 description 2
- 239000002250 absorbent Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000008055 alkyl aryl sulfonates Chemical group 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- 235000005824 corn Nutrition 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000004495 emulsifiable concentrate Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
- UAVOCTDYPKOULU-UHFFFAOYSA-N methylchloranuidyl formate Chemical compound C[Cl-]OC=O UAVOCTDYPKOULU-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 1
- PZZYQPZGQPZBDN-UHFFFAOYSA-N Aluminium silicate Chemical compound O=[Al]O[Si](=O)O[Al]=O PZZYQPZGQPZBDN-UHFFFAOYSA-N 0.000 description 1
- 229940054025 Carbamate anxiolytics Drugs 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N Dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- UVMTZTPUIFOAGM-UHFFFAOYSA-M N-(3-chlorophenyl)carbamate Chemical compound [O-]C(=O)NC1=CC=CC(Cl)=C1 UVMTZTPUIFOAGM-UHFFFAOYSA-M 0.000 description 1
- AAPAVYWERMFERN-UHFFFAOYSA-M N-ethyl-N-phenylcarbamate Chemical compound CCN(C([O-])=O)C1=CC=CC=C1 AAPAVYWERMFERN-UHFFFAOYSA-M 0.000 description 1
- 206010034972 Photosensitivity reaction Diseases 0.000 description 1
- VXPLXMJHHKHSOA-UHFFFAOYSA-N Propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 description 1
- 235000015450 Tilia cordata Nutrition 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- CNFUKOAVELXSRS-UHFFFAOYSA-M [O-]C(=O)N(Cl)C1=CC=CC=C1 Chemical class [O-]C(=O)N(Cl)C1=CC=CC=C1 CNFUKOAVELXSRS-UHFFFAOYSA-M 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 230000000855 fungicidal Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000008079 hexane Substances 0.000 description 1
- 229910003480 inorganic solid Inorganic materials 0.000 description 1
- 230000000749 insecticidal Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- IAGUPODHENSJEZ-UHFFFAOYSA-N methyl N-phenylcarbamate Chemical compound COC(=O)NC1=CC=CC=C1 IAGUPODHENSJEZ-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000017066 negative regulation of growth Effects 0.000 description 1
- 230000001069 nematicidal Effects 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N o-xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 231100000018 phototoxicity Toxicity 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- DAJSVUQLFFJUSX-UHFFFAOYSA-M sodium;dodecane-1-sulfonate Chemical compound [Na+].CCCCCCCCCCCCS([O-])(=O)=O DAJSVUQLFFJUSX-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- SMDQFHZIWNYSMR-UHFFFAOYSA-N sulfanylidenemagnesium Chemical compound S=[Mg] SMDQFHZIWNYSMR-UHFFFAOYSA-N 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE612550A true BE612550A (de) |
Family
ID=193216
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE612550D BE612550A (de) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE612550A (de) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5981532A (en) * | 1992-01-29 | 1999-11-09 | Basf Aktiengesellschaft | Carbamates and crop protection agents containing them |
-
0
- BE BE612550D patent/BE612550A/fr unknown
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5981532A (en) * | 1992-01-29 | 1999-11-09 | Basf Aktiengesellschaft | Carbamates and crop protection agents containing them |
| US6075148A (en) * | 1992-01-29 | 2000-06-13 | Basf Aktiengesellschaft | Carbamates and crop protection agents containing them |
| US6252083B1 (en) | 1992-01-29 | 2001-06-26 | Basf Aktiengesellschaft | Carbamates and crop protection agents containing them |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP2102148B1 (de) | Neue bis(dialkylamid)verbindungen, verfahren zu ihrer herstellung und anwendungen davon | |
| BE529063A (de) | ||
| FR2568749A1 (fr) | Composition a base d'un derive de thiolcarbamate, procede pour prolonger l'action des herbicides et compositions herbicides ayant une action prolongee | |
| FR2779032A1 (fr) | Composition pesticide synergique contenant du 3,5-dichloro-1 (3,3-dichloro-2-propenyloxy)-4-(3-(5trifluoromethyl-2-yloxy) propoxybenzene et un pyrethrinoide et procede de lutte contre les nuisibles | |
| BE612550A (de) | ||
| FR2618053A1 (fr) | Procede de lutte contre la vegetation indesirable dans une culture de graminees et composition pour sa mise en oeuvre | |
| EP0034556B1 (de) | Das Pflanzenwachstum regulierende Zusammensetzungen, die als aktive Substanz Derivate von 2-Methylen-succinamidsäure enthalten, und Derivate dieser Säure, die in diesen Zusammensetzungen verwendbar sind | |
| EP0239508A2 (de) | 2-Cyano-benzimidazol-Derivate, Verfahren zu deren Herstellung und Anwendung als Fungizide, deren Assoziation mit anderen Fungiziden | |
| FR2591593A1 (fr) | Composes heterocycliques oxygenes ou soufres de 5 a 7 chainons et substitues en position 2, compositions nematicides et insecticides les contenant et procede pour leur preparation | |
| FR2465417A1 (fr) | Produit et composition acaricides et procede de destruction des tiques et des acariens | |
| CH660365A5 (fr) | Benzoate de tricyclohexyletain comme derive organique de l'etain. | |
| LU86116A1 (fr) | Compositions herbicides selectives ayant une action prolongee et contenant,a titre d'ingredient actif,des derives d'alpha-chloracetamide | |
| FR2560007A1 (fr) | Compositions fongicides comprenant des derives de phenoxy benzaldehyde | |
| FR2645404A1 (fr) | Compositions herbicides contenant un antidote et compositions antidotes ainsi obtenues | |
| EP0249567A2 (de) | Propargyloxybenzolderivate, ihre Herstellung und sie enthaltende fungizide Zusammensetzungen | |
| BE1022655B1 (fr) | Composition herbicide améliorée, procédé et utilisation | |
| FR2509580A1 (fr) | 1-phenyl-1,2,3-triazoles utilisables comme anti-appetants et leur preparation | |
| IL31823A (en) | Alkylcarbamoylamoxylphenyl N-Aloxy urea compounds and their use in weed control | |
| LU83229A1 (fr) | Procede de preparation de 2-haloacetamides a radicaux heterocyclylmethyles,nouveaux produits ainsi obtenus et leur utilisation comme herbicides | |
| FR2519338A1 (fr) | Nouveaux derives de 3-nitrobenzenesulfonanilide, compositions fongicides les contenant comme ingredients actifs et procede pour lutter contre la hernie du chou les utilisant | |
| LU83237A1 (fr) | Composes de n-hydrocarbyloxymethyl-2-haloacetanilide et compositions herbicides les renfermant | |
| BE852417Q (fr) | Application de composes cycliques a la lutte contre des depredateurs | |
| EP0197250A2 (de) | Herbizide Zusammensetzungen, basierend auf Carbamyloxyphenylcarbamate und mineralisches Petroleumöl | |
| CH668070A5 (fr) | Derives de trihalogeno-imidazole et compositions insecticides les contenant. | |
| BE876077A (fr) | Derives de diphenylamine |