DE1913266C2 - Herbizid - Google Patents
HerbizidInfo
- Publication number
- DE1913266C2 DE1913266C2 DE19691913266 DE1913266A DE1913266C2 DE 1913266 C2 DE1913266 C2 DE 1913266C2 DE 19691913266 DE19691913266 DE 19691913266 DE 1913266 A DE1913266 A DE 1913266A DE 1913266 C2 DE1913266 C2 DE 1913266C2
- Authority
- DE
- Germany
- Prior art keywords
- active ingredient
- triazine
- mixtures
- ethylamino
- vii
- 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.)
- Expired
Links
- 230000002363 herbicidal effect Effects 0.000 title claims description 9
- 239000004009 herbicide Substances 0.000 title claims description 6
- 239000000203 mixture Substances 0.000 claims description 22
- 239000004480 active ingredient Substances 0.000 description 76
- 241000196324 Embryophyta Species 0.000 description 13
- 240000008042 Zea mays Species 0.000 description 13
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
- 230000006378 damage Effects 0.000 description 9
- 235000007244 Zea mays Nutrition 0.000 description 8
- 244000038559 crop plants Species 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 244000237956 Amaranthus retroflexus Species 0.000 description 6
- 235000013479 Amaranthus retroflexus Nutrition 0.000 description 6
- 241001506766 Xanthium Species 0.000 description 6
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 6
- 229960000278 theophylline Drugs 0.000 description 6
- 150000003918 triazines Chemical class 0.000 description 6
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 244000285774 Cyperus esculentus Species 0.000 description 4
- 235000005853 Cyperus esculentus Nutrition 0.000 description 4
- 244000075634 Cyperus rotundus Species 0.000 description 4
- 235000016854 Cyperus rotundus Nutrition 0.000 description 4
- 244000152970 Digitaria sanguinalis Species 0.000 description 4
- 235000010823 Digitaria sanguinalis Nutrition 0.000 description 4
- 240000006597 Poa trivialis Species 0.000 description 4
- 241001355178 Setaria faberi Species 0.000 description 4
- 239000013543 active substance Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 241000234653 Cyperus Species 0.000 description 3
- 240000005702 Galium aparine Species 0.000 description 3
- 235000014820 Galium aparine Nutrition 0.000 description 3
- 244000042664 Matricaria chamomilla Species 0.000 description 3
- 235000007232 Matricaria chamomilla Nutrition 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 244000067505 Xanthium strumarium Species 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 125000001309 chloro group Chemical group Cl* 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- -1 α-methyl-β-methoxy-ethyl Chemical group 0.000 description 3
- ACAHVXOSWOUZAB-UHFFFAOYSA-N 4,6-dichloro-n-ethyl-1,3,5-triazin-2-amine Chemical compound CCNC1=NC(Cl)=NC(Cl)=N1 ACAHVXOSWOUZAB-UHFFFAOYSA-N 0.000 description 2
- HNUALPPJLMYHDK-UHFFFAOYSA-N C[CH]C Chemical group C[CH]C HNUALPPJLMYHDK-UHFFFAOYSA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- 241000209082 Lolium Species 0.000 description 2
- 244000292693 Poa annua Species 0.000 description 2
- 244000062793 Sorghum vulgare Species 0.000 description 2
- 244000098338 Triticum aestivum Species 0.000 description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 2
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 235000005822 corn Nutrition 0.000 description 2
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 2
- 235000019713 millet Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 241001621841 Alopecurus myosuroides 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
- 101100511458 Epichloe uncinata lolT1 gene Proteins 0.000 description 1
- 101100511459 Epichloe uncinata lolT2 gene Proteins 0.000 description 1
- 241000209219 Hordeum Species 0.000 description 1
- 244000100545 Lolium multiflorum Species 0.000 description 1
- 240000004296 Lolium perenne Species 0.000 description 1
- 125000000066 S-methyl group Chemical group [H]C([H])([H])S* 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 241000209140 Triticum Species 0.000 description 1
- 241000700605 Viruses Species 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- PXWUKZGIHQRDHL-UHFFFAOYSA-N atraton Chemical compound CCNC1=NC(NC(C)C)=NC(OC)=N1 PXWUKZGIHQRDHL-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- LCPDWSOZIOUXRV-UHFFFAOYSA-N phenoxyacetic acid Chemical class OC(=O)COC1=CC=CC=C1 LCPDWSOZIOUXRV-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- WJNRPILHGGKWCK-UHFFFAOYSA-N propazine Chemical compound CC(C)NC1=NC(Cl)=NC(NC(C)C)=N1 WJNRPILHGGKWCK-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
- C07D251/16—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
- C07D251/18—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom with nitrogen atoms directly attached to the two other ring carbon atoms, e.g. guanamines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/48—Two nitrogen atoms
- C07D251/50—Two nitrogen atoms with a halogen atom attached to the third ring carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/15—Six-membered rings
- C07D285/16—Thiadiazines; Hydrogenated thiadiazines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (19)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19691913266 DE1913266C2 (de) | 1969-03-15 | 1969-03-15 | Herbizid |
| AT126770A AT299605B (de) | 1969-03-15 | 1970-02-12 | Herbizid |
| AT424671A AT299610B (de) | 1969-03-15 | 1970-02-12 | Herbizid |
| BG017879A BG19075A3 (bg) | 1969-03-15 | 1970-02-17 | Хербецид |
| BG013999A BG20268A3 (bg) | 1969-03-15 | 1970-02-17 | Хербицид |
| CH233270A CH532887A (de) | 1969-03-15 | 1970-02-18 | Herbizid |
| BE746889D BE746889A (fr) | 1969-03-15 | 1970-03-05 | Herbicide |
| CA076,617,A CA950224A (en) | 1969-03-15 | 1970-03-05 | Herbicide |
| CS161770A CS172324B2 (ref) | 1969-03-15 | 1970-03-11 | |
| SU1416266A SU404188A1 (ru) | 1970-03-11 | Гербицидный состав | |
| GB1213270A GB1294021A (en) | 1969-03-15 | 1970-03-13 | Herbicide |
| NL7003629A NL7003629A (ref) | 1969-03-15 | 1970-03-13 | |
| TR1676470A TR16764A (tr) | 1969-03-15 | 1970-03-13 | Zararli bitkileri oeldueruecue maddeler |
| FR7009058A FR2034967B1 (ref) | 1969-03-15 | 1970-03-13 | |
| DK127470A DK125723B (da) | 1969-03-15 | 1970-03-13 | Herbicid. |
| PL13939870A PL87255B1 (ref) | 1969-03-15 | 1970-03-14 | |
| ES377508A ES377508A1 (es) | 1969-03-15 | 1970-03-14 | Procedimiento para la obtencion de composiciones herbici- das. |
| DK492471A DK126226B (da) | 1969-03-15 | 1971-10-11 | Herbicid. |
| US334195A US3920441A (en) | 1969-03-15 | 1973-02-21 | Selective herbicide compositions containing a substituted triazine derivative and a benzo-2-thia-1,3-diazinone-(4)-2,2-dioxide |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19691913266 DE1913266C2 (de) | 1969-03-15 | 1969-03-15 | Herbizid |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE1913266A1 DE1913266A1 (de) | 1970-11-05 |
| DE1913266C2 true DE1913266C2 (de) | 1985-07-18 |
Family
ID=5728260
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19691913266 Expired DE1913266C2 (de) | 1969-03-15 | 1969-03-15 | Herbizid |
Country Status (14)
| Country | Link |
|---|---|
| AT (2) | AT299610B (ref) |
| BE (1) | BE746889A (ref) |
| BG (2) | BG20268A3 (ref) |
| CA (1) | CA950224A (ref) |
| CH (1) | CH532887A (ref) |
| CS (1) | CS172324B2 (ref) |
| DE (1) | DE1913266C2 (ref) |
| DK (2) | DK125723B (ref) |
| ES (1) | ES377508A1 (ref) |
| FR (1) | FR2034967B1 (ref) |
| GB (1) | GB1294021A (ref) |
| NL (1) | NL7003629A (ref) |
| PL (1) | PL87255B1 (ref) |
| TR (1) | TR16764A (ref) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2217722C2 (de) * | 1972-04-13 | 1982-11-04 | Basf Ag, 6700 Ludwigshafen | Herbizid |
| DE29506462U1 (de) * | 1995-04-11 | 1995-08-31 | Eduard Wandzel KG, 93413 Cham | Archiv-Schachtel bzw. Beleg-Depot |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA685638A (en) * | 1964-05-05 | Hooker Chemical Corporation | Synergistic herbicidal composition | |
| NL244878A (ref) * | 1958-11-05 | |||
| DE1670100A1 (de) * | 1966-07-02 | 1970-08-13 | Basf Ag | Herbizide |
| BE702877A (ref) * | 1966-08-30 | 1968-02-21 |
-
1969
- 1969-03-15 DE DE19691913266 patent/DE1913266C2/de not_active Expired
-
1970
- 1970-02-12 AT AT424671A patent/AT299610B/de not_active IP Right Cessation
- 1970-02-12 AT AT126770A patent/AT299605B/de not_active IP Right Cessation
- 1970-02-17 BG BG013999A patent/BG20268A3/xx unknown
- 1970-02-17 BG BG017879A patent/BG19075A3/xx unknown
- 1970-02-18 CH CH233270A patent/CH532887A/de not_active IP Right Cessation
- 1970-03-05 CA CA076,617,A patent/CA950224A/en not_active Expired
- 1970-03-05 BE BE746889D patent/BE746889A/xx not_active IP Right Cessation
- 1970-03-11 CS CS161770A patent/CS172324B2/cs unknown
- 1970-03-13 NL NL7003629A patent/NL7003629A/xx unknown
- 1970-03-13 TR TR1676470A patent/TR16764A/xx unknown
- 1970-03-13 FR FR7009058A patent/FR2034967B1/fr not_active Expired
- 1970-03-13 DK DK127470A patent/DK125723B/da not_active IP Right Cessation
- 1970-03-13 GB GB1213270A patent/GB1294021A/en not_active Expired
- 1970-03-14 PL PL13939870A patent/PL87255B1/pl unknown
- 1970-03-14 ES ES377508A patent/ES377508A1/es not_active Expired
-
1971
- 1971-10-11 DK DK492471A patent/DK126226B/da not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| TR16764A (tr) | 1973-05-01 |
| SU404188A3 (ref) | 1973-10-26 |
| FR2034967B1 (ref) | 1974-05-24 |
| AT299610B (de) | 1972-06-26 |
| CA950224A (en) | 1974-07-02 |
| ES377508A1 (es) | 1973-02-01 |
| DK125723B (da) | 1973-04-30 |
| PL87255B1 (ref) | 1976-06-30 |
| GB1294021A (en) | 1972-10-25 |
| DE1913266A1 (de) | 1970-11-05 |
| CH532887A (de) | 1973-01-31 |
| BE746889A (fr) | 1970-09-07 |
| FR2034967A1 (ref) | 1970-12-18 |
| AT299605B (de) | 1972-06-26 |
| BG19075A3 (bg) | 1975-04-30 |
| NL7003629A (ref) | 1970-09-17 |
| CS172324B2 (ref) | 1976-12-29 |
| DK126226B (da) | 1973-06-25 |
| BG20268A3 (bg) | 1975-11-05 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8330 | Complete disclaimer |