DD235553A5 - Synergetische wirkstoffkombinationen enthaltende herbizide mittel - Google Patents
Synergetische wirkstoffkombinationen enthaltende herbizide mittel Download PDFInfo
- Publication number
- DD235553A5 DD235553A5 DD85278547A DD27854785A DD235553A5 DD 235553 A5 DD235553 A5 DD 235553A5 DD 85278547 A DD85278547 A DD 85278547A DD 27854785 A DD27854785 A DD 27854785A DD 235553 A5 DD235553 A5 DD 235553A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- methyl
- nitro
- ethoxy
- ethyl
- trifluoromethylbenzene
- Prior art date
Links
- 230000002195 synergetic effect Effects 0.000 title abstract description 7
- 150000001875 compounds Chemical class 0.000 title description 7
- 239000004009 herbicide Substances 0.000 title description 2
- 241000196324 Embryophyta Species 0.000 claims abstract description 14
- HHMCAJWVGYGUEF-UHFFFAOYSA-N Fluorodifen Chemical compound C1=CC([N+](=O)[O-])=CC=C1OC1=CC=C(C(F)(F)F)C=C1[N+]([O-])=O HHMCAJWVGYGUEF-UHFFFAOYSA-N 0.000 claims abstract description 12
- 239000000203 mixture Substances 0.000 claims abstract description 12
- 239000004480 active ingredient Substances 0.000 claims abstract description 11
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 7
- 230000002363 herbicidal effect Effects 0.000 claims abstract description 7
- KXRLLCABBOEPSY-UHFFFAOYSA-N 2-chloro-n-ethoxy-n-(2-ethyl-6-methylphenyl)propanamide Chemical compound CCON(C(=O)C(C)Cl)C1=C(C)C=CC=C1CC KXRLLCABBOEPSY-UHFFFAOYSA-N 0.000 claims abstract description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims description 6
- 239000000969 carrier Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 239000005909 Kieselgur Substances 0.000 claims description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- 239000008096 xylene Substances 0.000 claims description 3
- 239000005995 Aluminium silicate Substances 0.000 claims description 2
- 235000019738 Limestone Nutrition 0.000 claims description 2
- 239000000853 adhesive Substances 0.000 claims description 2
- 230000001070 adhesive effect Effects 0.000 claims description 2
- 150000001298 alcohols Chemical class 0.000 claims description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
- 235000012211 aluminium silicate Nutrition 0.000 claims description 2
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 239000003945 anionic surfactant Substances 0.000 claims description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 2
- 239000003431 cross linking reagent Substances 0.000 claims description 2
- 239000002270 dispersing agent Substances 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 235000013312 flour Nutrition 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 2
- 150000002576 ketones Chemical class 0.000 claims description 2
- 239000006028 limestone Substances 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 239000002736 nonionic surfactant Substances 0.000 claims description 2
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 2
- 150000004760 silicates Chemical class 0.000 claims description 2
- 240000008042 Zea mays Species 0.000 abstract description 16
- 235000002017 Zea mays subsp mays Nutrition 0.000 abstract description 16
- 240000008114 Panicum miliaceum Species 0.000 abstract description 9
- 235000007199 Panicum miliaceum Nutrition 0.000 abstract description 9
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 abstract description 8
- 235000009973 maize Nutrition 0.000 abstract description 8
- 239000000700 radioactive tracer Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 8
- 235000005822 corn Nutrition 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- VTNQPKFIQCLBDU-UHFFFAOYSA-N Acetochlor Chemical compound CCOCN(C(=O)CCl)C1=C(C)C=CC=C1CC VTNQPKFIQCLBDU-UHFFFAOYSA-N 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000002689 soil Substances 0.000 description 6
- 239000013543 active substance Substances 0.000 description 5
- 239000003814 drug Substances 0.000 description 5
- 229940079593 drug Drugs 0.000 description 5
- 241000209117 Panicum Species 0.000 description 4
- 235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 4
- 235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 4
- 239000004495 emulsifiable concentrate Substances 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000012895 dilution Substances 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 2
- 230000002708 enhancing effect Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 230000002265 prevention Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical class COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
- 241000225517 Bario Species 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 239000005843 Thiram Substances 0.000 description 1
- 150000008061 acetanilides Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000012867 bioactive agent Substances 0.000 description 1
- 238000004166 bioassay Methods 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 238000010170 biological method Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 244000038559 crop plants Species 0.000 description 1
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000001784 detoxification Methods 0.000 description 1
- -1 dichloroacetyl Chemical group 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 244000144992 flock Species 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 1
- 229920000940 maneb Polymers 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 150000003672 ureas Chemical class 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/26—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the group; Thio analogues thereof
Landscapes
- 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)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU842773A HU193214B (en) | 1984-07-17 | 1984-07-17 | Synergic herbicide compositions for extirpating panicum miliaceum containing chloro-acetamide derivatives and substituted benzene derivatives as active agents |
Publications (1)
Publication Number | Publication Date |
---|---|
DD235553A5 true DD235553A5 (de) | 1986-05-14 |
Family
ID=10961036
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DD85278547A DD235553A5 (de) | 1984-07-17 | 1985-07-12 | Synergetische wirkstoffkombinationen enthaltende herbizide mittel |
Country Status (13)
Country | Link |
---|---|
JP (1) | JPS6193103A (fr) |
BR (1) | BR8503390A (fr) |
CH (1) | CH664258A5 (fr) |
CS (1) | CS261226B2 (fr) |
DD (1) | DD235553A5 (fr) |
DE (1) | DE3525371A1 (fr) |
ES (1) | ES8608282A1 (fr) |
FR (1) | FR2567718B1 (fr) |
GB (1) | GB2163349B (fr) |
HU (1) | HU193214B (fr) |
IT (1) | IT1207061B (fr) |
PL (1) | PL143071B1 (fr) |
RO (1) | RO93277A (fr) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19958381A1 (de) | 1999-12-03 | 2001-06-07 | Bayer Ag | Herbizide auf Basis von N-Aryl-uracilen |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE628133A (fr) * | 1962-02-08 | |||
GB1407205A (en) * | 1971-09-17 | 1975-09-24 | Girling Ltd | Vehicle braking systems |
JPS5350328A (en) * | 1976-10-16 | 1978-05-08 | Kumiai Chem Ind Co Ltd | Composition for herbicides |
JPS5555107A (en) * | 1978-10-19 | 1980-04-22 | Nissan Chem Ind Ltd | Herbicidal composition |
TW286443B (fr) * | 1994-10-25 | 1996-09-21 | Fridolin Alois Frech |
-
1984
- 1984-07-17 HU HU842773A patent/HU193214B/hu not_active IP Right Cessation
-
1985
- 1985-07-03 GB GB08516880A patent/GB2163349B/en not_active Expired
- 1985-07-09 FR FR8510467A patent/FR2567718B1/fr not_active Expired
- 1985-07-12 CH CH3031/85A patent/CH664258A5/de not_active IP Right Cessation
- 1985-07-12 DD DD85278547A patent/DD235553A5/de unknown
- 1985-07-15 RO RO85119567A patent/RO93277A/fr unknown
- 1985-07-16 PL PL1985254561A patent/PL143071B1/pl unknown
- 1985-07-16 JP JP60156848A patent/JPS6193103A/ja active Pending
- 1985-07-16 IT IT8521575A patent/IT1207061B/it active
- 1985-07-16 BR BR8503390A patent/BR8503390A/pt unknown
- 1985-07-16 DE DE19853525371 patent/DE3525371A1/de not_active Withdrawn
- 1985-07-17 CS CS855306A patent/CS261226B2/cs unknown
- 1985-07-17 ES ES545327A patent/ES8608282A1/es not_active Expired
Also Published As
Publication number | Publication date |
---|---|
PL143071B1 (en) | 1988-01-30 |
IT8521575A0 (it) | 1985-07-16 |
ES8608282A1 (es) | 1986-07-16 |
FR2567718B1 (fr) | 1988-10-14 |
HU193214B (en) | 1987-08-28 |
DE3525371A1 (de) | 1986-07-10 |
CS261226B2 (en) | 1989-01-12 |
RO93277A (fr) | 1988-03-30 |
RO93277B (ro) | 1987-12-31 |
JPS6193103A (ja) | 1986-05-12 |
GB2163349B (en) | 1988-05-05 |
FR2567718A1 (fr) | 1986-01-24 |
GB8516880D0 (en) | 1985-08-07 |
ES545327A0 (es) | 1986-07-16 |
BR8503390A (pt) | 1986-04-08 |
IT1207061B (it) | 1989-05-17 |
GB2163349A (en) | 1986-02-26 |
HUT39565A (en) | 1986-10-29 |
CS530685A2 (en) | 1988-05-16 |
PL254561A1 (en) | 1986-06-17 |
CH664258A5 (de) | 1988-02-29 |
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