DE2436789A1 - Verwendung von harnstoffderivaten als selektive getreideherbizide - Google Patents
Verwendung von harnstoffderivaten als selektive getreideherbizideInfo
- Publication number
- DE2436789A1 DE2436789A1 DE2436789A DE2436789A DE2436789A1 DE 2436789 A1 DE2436789 A1 DE 2436789A1 DE 2436789 A DE2436789 A DE 2436789A DE 2436789 A DE2436789 A DE 2436789A DE 2436789 A1 DE2436789 A1 DE 2436789A1
- Authority
- DE
- Germany
- Prior art keywords
- spp
- substituted
- dichloro
- phenyl
- salts
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
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- 241000405217 Viola <butterfly> Species 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 125000001931 aliphatic 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
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 1
- 239000001166 ammonium sulphate Substances 0.000 description 1
- 235000011130 ammonium sulphate Nutrition 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 229940075522 antidotes Drugs 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- BUSBFZWLPXDYIC-UHFFFAOYSA-N arsonic acid Chemical class O[AsH](O)=O BUSBFZWLPXDYIC-UHFFFAOYSA-N 0.000 description 1
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- 235000009052 artemisia Nutrition 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
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 125000000480 butynyl group Chemical group [*]C#CC([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Inorganic materials [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 239000001175 calcium sulphate Substances 0.000 description 1
- 235000011132 calcium sulphate Nutrition 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 150000002019 disulfides Chemical class 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
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 238000005516 engineering process Methods 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 group 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
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- XXOYNJXVWVNOOJ-UHFFFAOYSA-N fenuron Chemical compound CN(C)C(=O)NC1=CC=CC=C1 XXOYNJXVWVNOOJ-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation 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
- 230000012010 growth Effects 0.000 description 1
- 150000001469 hydantoins Chemical group 0.000 description 1
- 229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 229960001330 hydroxycarbamide Drugs 0.000 description 1
- 150000002460 imidazoles Chemical group 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical group 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 235000012245 magnesium oxide Nutrition 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 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
- 238000003801 milling Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- 150000002791 naphthoquinones Chemical group 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 239000012044 organic layer Substances 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 group O=C1CON=NC1=O SDRLFDJOSQLRPB-UHFFFAOYSA-N 0.000 description 1
- 150000004866 oxadiazoles Chemical group 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- REJGOFYVRVIODZ-UHFFFAOYSA-N phosphanium;chloride Chemical group P.Cl REJGOFYVRVIODZ-UHFFFAOYSA-N 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical group [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
- 125000003386 piperidinyl group Chemical group 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- BFZYLUGEHGYJKJ-UHFFFAOYSA-N pyrazolidine-3-thione Chemical group S=C1CCNN1 BFZYLUGEHGYJKJ-UHFFFAOYSA-N 0.000 description 1
- 150000004892 pyridazines Chemical group 0.000 description 1
- 150000005299 pyridinones Chemical group 0.000 description 1
- 150000003230 pyrimidines Chemical group 0.000 description 1
- 150000008318 pyrimidones Chemical class 0.000 description 1
- 150000003235 pyrrolidines Chemical group 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
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring 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
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- OLPRIZQBWZMBAS-UHFFFAOYSA-N thiadiazolidine 1,1-dioxide Chemical group O=S1(=O)CCNN1 OLPRIZQBWZMBAS-UHFFFAOYSA-N 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical group 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 group 0.000 description 1
- 150000003852 triazoles Chemical group 0.000 description 1
- 229940047183 tribulus Drugs 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C275/32—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms
- C07C275/34—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by singly-bound oxygen atoms having nitrogen atoms of urea groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/64—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups singly-bound to oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (18)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2436789A DE2436789A1 (de) | 1974-07-31 | 1974-07-31 | Verwendung von harnstoffderivaten als selektive getreideherbizide |
JP50069758A JPS5814403B2 (ja) | 1974-07-31 | 1975-06-11 | コクモツサイバイニオケル センタクテキジヨソウザイ |
IL47565A IL47565A (en) | 1974-07-31 | 1975-06-25 | Method for the selective control of weeds in cereals,using3,5-dichloro-4-alkoxy phenylureas |
AU82443/75A AU8244375A (en) | 1974-07-31 | 1975-06-25 | Herbicidal urea derivatives |
CA230,778A CA1059780A (en) | 1974-07-31 | 1975-07-04 | Urea derivatives as selective herbicides in cereals |
IT50548/75A IT1040958B (it) | 1974-07-31 | 1975-07-16 | Impiego di derivati ureici comediserbanti selettivi in colture di cereali |
NL7508581A NL7508581A (nl) | 1974-07-31 | 1975-07-17 | Selectieve herbiciden. |
CS7500005261A CS185579B2 (en) | 1974-07-31 | 1975-07-25 | Selective herbicidal agent |
SE7508485A SE420040B (sv) | 1974-07-31 | 1975-07-25 | Anvendning av 1-(3,5-diklor-4-metoxifenyl-)-3-3-dimetylurinemne eller 1-(3,5-diklor-4-etoxifenyl)-3,3-dimetylurinemne som elektiva herbicider i sedesodlingar |
CH981775A CH596764A5 (enrdf_load_stackoverflow) | 1974-07-31 | 1975-07-28 | |
DD187547A DD118981A5 (enrdf_load_stackoverflow) | 1974-07-31 | 1975-07-29 | |
PL182370A PL93904B2 (enrdf_load_stackoverflow) | 1975-07-29 | ||
DK345675A DK138721C (da) | 1974-07-31 | 1975-07-30 | Anvendelse af urinstofderivater som selektive kornherbicider |
AT590175A AT342917B (de) | 1974-07-31 | 1975-07-30 | Herbizid |
GB31865/75A GB1512666A (en) | 1974-07-31 | 1975-07-30 | Use of urea derivatives as selective herbicides in cereal |
ZA00754900A ZA754900B (en) | 1974-07-31 | 1975-07-30 | Use of urea derivatives as selective herbicides in cereals |
FR7523990A FR2280320A1 (fr) | 1974-07-31 | 1975-07-31 | Utilisation de derives d'uree comme agent herbicide selectif des cereales |
BE158835A BE831992A (fr) | 1974-07-31 | 1975-07-31 | Utilisation de derives d'uree en tant qu'agents herbicide selectif dans les cereales |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2436789A DE2436789A1 (de) | 1974-07-31 | 1974-07-31 | Verwendung von harnstoffderivaten als selektive getreideherbizide |
Publications (1)
Publication Number | Publication Date |
---|---|
DE2436789A1 true DE2436789A1 (de) | 1976-02-19 |
Family
ID=5921986
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE2436789A Withdrawn DE2436789A1 (de) | 1974-07-31 | 1974-07-31 | Verwendung von harnstoffderivaten als selektive getreideherbizide |
Country Status (17)
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB177208A (en) * | 1920-11-26 | 1922-03-27 | Reginald Hind Stockdale | Improvements in or relating to railway signals |
FR1279146A (fr) * | 1960-02-10 | 1961-12-15 | Basf Ag | Produits pour détruire des végétaux indésirables |
DE1291733B (de) * | 1965-11-16 | 1969-04-03 | Lauterbach | Verfahren zur Herstellung von N-Aryl-harnstoffen |
FR2245284A1 (en) * | 1973-07-30 | 1975-04-25 | Fahlberg List Veb | N-Aryl-N-methyl ureas as selective herbicides - for pre- and post-emergent use |
-
1974
- 1974-07-31 DE DE2436789A patent/DE2436789A1/de not_active Withdrawn
-
1975
- 1975-06-11 JP JP50069758A patent/JPS5814403B2/ja not_active Expired
- 1975-06-25 AU AU82443/75A patent/AU8244375A/en not_active Expired
- 1975-06-25 IL IL47565A patent/IL47565A/xx unknown
- 1975-07-04 CA CA230,778A patent/CA1059780A/en not_active Expired
- 1975-07-16 IT IT50548/75A patent/IT1040958B/it active
- 1975-07-17 NL NL7508581A patent/NL7508581A/xx not_active Application Discontinuation
- 1975-07-25 CS CS7500005261A patent/CS185579B2/cs unknown
- 1975-07-25 SE SE7508485A patent/SE420040B/xx unknown
- 1975-07-28 CH CH981775A patent/CH596764A5/xx not_active IP Right Cessation
- 1975-07-29 DD DD187547A patent/DD118981A5/xx unknown
- 1975-07-30 ZA ZA00754900A patent/ZA754900B/xx unknown
- 1975-07-30 DK DK345675A patent/DK138721C/da not_active IP Right Cessation
- 1975-07-30 AT AT590175A patent/AT342917B/de not_active IP Right Cessation
- 1975-07-30 GB GB31865/75A patent/GB1512666A/en not_active Expired
- 1975-07-31 FR FR7523990A patent/FR2280320A1/fr active Granted
- 1975-07-31 BE BE158835A patent/BE831992A/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
FR2280320A1 (fr) | 1976-02-27 |
AU8244375A (en) | 1977-01-06 |
SE420040B (sv) | 1981-09-14 |
DD118981A5 (enrdf_load_stackoverflow) | 1976-04-05 |
AT342917B (de) | 1978-04-25 |
BE831992A (fr) | 1976-02-02 |
CS185579B2 (en) | 1978-10-31 |
CA1059780A (en) | 1979-08-07 |
IL47565A (en) | 1978-03-10 |
JPS5814403B2 (ja) | 1983-03-18 |
JPS5115624A (enrdf_load_stackoverflow) | 1976-02-07 |
ZA754900B (en) | 1976-07-28 |
PL93904B1 (enrdf_load_stackoverflow) | 1977-07-30 |
IL47565A0 (en) | 1975-08-31 |
SE7508485L (sv) | 1976-02-02 |
DK138721B (da) | 1978-10-23 |
DK345675A (da) | 1976-02-01 |
CH596764A5 (enrdf_load_stackoverflow) | 1978-03-15 |
FR2280320B1 (enrdf_load_stackoverflow) | 1979-05-11 |
DK138721C (da) | 1979-04-02 |
IT1040958B (it) | 1979-12-20 |
NL7508581A (nl) | 1976-02-03 |
GB1512666A (en) | 1978-06-01 |
ATA590175A (de) | 1977-08-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
8110 | Request for examination paragraph 44 | ||
8130 | Withdrawal |