DE2522471C2 - Agrochemisches Mittel - Google Patents
Agrochemisches MittelInfo
- Publication number
- DE2522471C2 DE2522471C2 DE2522471A DE2522471A DE2522471C2 DE 2522471 C2 DE2522471 C2 DE 2522471C2 DE 2522471 A DE2522471 A DE 2522471A DE 2522471 A DE2522471 A DE 2522471A DE 2522471 C2 DE2522471 C2 DE 2522471C2
- Authority
- DE
- Germany
- Prior art keywords
- pyrazolium
- ccc
- wild oats
- chloroethyl
- salt
- 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
- 239000003795 chemical substances by application Substances 0.000 title claims description 6
- 239000003905 agrochemical Substances 0.000 title claims description 4
- 235000007320 Avena fatua Nutrition 0.000 claims description 19
- 244000075850 Avena orientalis Species 0.000 claims description 17
- 235000005373 Uvularia sessilifolia Nutrition 0.000 claims description 17
- 241000209140 Triticum Species 0.000 claims description 10
- 235000021307 Triticum Nutrition 0.000 claims description 10
- 235000013339 cereals Nutrition 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- -1 pyrazolium cation Chemical class 0.000 claims description 6
- 239000007921 spray Substances 0.000 claims description 5
- 240000005979 Hordeum vulgare Species 0.000 claims description 3
- 235000007340 Hordeum vulgare Nutrition 0.000 claims description 3
- 235000007238 Secale cereale Nutrition 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 3
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 claims description 2
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- 244000082988 Secale cereale Species 0.000 claims 1
- UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical compound [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 description 25
- 241000196324 Embryophyta Species 0.000 description 11
- 239000004009 herbicide Substances 0.000 description 11
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical class C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 10
- 230000002363 herbicidal effect Effects 0.000 description 10
- 150000001768 cations Chemical class 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 229920000136 polysorbate Polymers 0.000 description 6
- 230000006378 damage Effects 0.000 description 5
- 230000005764 inhibitory process Effects 0.000 description 5
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 5
- 230000012010 growth Effects 0.000 description 4
- 241000894007 species Species 0.000 description 4
- 240000001592 Amaranthus caudatus Species 0.000 description 3
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 3
- 229920001213 Polysorbate 20 Polymers 0.000 description 3
- 230000008635 plant growth Effects 0.000 description 3
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 3
- 230000001105 regulatory effect Effects 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 230000000007 visual effect Effects 0.000 description 3
- 244000237956 Amaranthus retroflexus Species 0.000 description 2
- 235000013479 Amaranthus retroflexus Nutrition 0.000 description 2
- 241001647031 Avena sterilis Species 0.000 description 2
- 235000004535 Avena sterilis Nutrition 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- WTKZEGDFNFYCGP-UHFFFAOYSA-O Pyrazolium Chemical compound C1=CN[NH+]=C1 WTKZEGDFNFYCGP-UHFFFAOYSA-O 0.000 description 2
- 241000209056 Secale Species 0.000 description 2
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 2
- 239000005648 plant growth regulator Substances 0.000 description 2
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- OCWGRWAYARCRTQ-UHFFFAOYSA-N 2-chloro-n,n-dimethylpropan-1-amine;hydron;chloride Chemical compound Cl.CC(Cl)CN(C)C OCWGRWAYARCRTQ-UHFFFAOYSA-N 0.000 description 1
- PHHDQWZIARFHPV-UHFFFAOYSA-M 2-chloroethyl(triethyl)azanium;chloride Chemical compound [Cl-].CC[N+](CC)(CC)CCCl PHHDQWZIARFHPV-UHFFFAOYSA-M 0.000 description 1
- 235000014224 Ceanothus americanus Nutrition 0.000 description 1
- 235000001904 Ceanothus herbaceus Nutrition 0.000 description 1
- 125000000174 L-prolyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])([H])[C@@]1([H])C(*)=O 0.000 description 1
- GXCLVBGFBYZDAG-UHFFFAOYSA-N N-[2-(1H-indol-3-yl)ethyl]-N-methylprop-2-en-1-amine Chemical compound CN(CCC1=CNC2=C1C=CC=C2)CC=C GXCLVBGFBYZDAG-UHFFFAOYSA-N 0.000 description 1
- 240000000103 Potentilla erecta Species 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 230000008485 antagonism Effects 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 125000004966 cyanoalkyl group Chemical group 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 235000012055 fruits and vegetables Nutrition 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 208000006278 hypochromic anemia Diseases 0.000 description 1
- 125000005358 mercaptoalkyl group Chemical group 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 231100001184 nonphytotoxic Toxicity 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000005082 stem growth Effects 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000011885 synergistic combination Substances 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 239000013585 weight reducing agent Substances 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/02—Amines; Quaternary ammonium compounds
- A01N33/12—Quaternary ammonium compounds
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
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 |
|---|---|---|---|
| US47353374A | 1974-05-28 | 1974-05-28 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2522471A1 DE2522471A1 (de) | 1975-12-11 |
| DE2522471C2 true DE2522471C2 (de) | 1984-12-20 |
Family
ID=23879926
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2522471A Expired DE2522471C2 (de) | 1974-05-28 | 1975-05-21 | Agrochemisches Mittel |
Country Status (17)
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2260485C2 (de) * | 1971-12-17 | 1983-12-29 | American Cyanamid Co., Wayne, N.J. | 1,2-Dialkyl-3,5-diphenylpyrazoliumsalze und diese enthaltende herbizide Mittel |
-
1975
- 1975-04-21 CA CA225,044A patent/CA1049282A/en not_active Expired
- 1975-04-21 AR AR258440A patent/AR229922A1/es active
- 1975-04-28 GB GB1763375A patent/GB1466634A/en not_active Expired
- 1975-05-12 IT IT49532/75A patent/IT1057898B/it active
- 1975-05-13 TR TR18239A patent/TR18239A/xx unknown
- 1975-05-21 NL NL7505964A patent/NL7505964A/xx not_active Application Discontinuation
- 1975-05-21 DE DE2522471A patent/DE2522471C2/de not_active Expired
- 1975-05-22 CS CS7500003607A patent/CS181786B2/cs unknown
- 1975-05-26 IE IE1172/75A patent/IE41071B1/xx unknown
- 1975-05-27 DD DD186272A patent/DD119699A5/xx unknown
- 1975-05-27 DK DK233475AA patent/DK136751B/da unknown
- 1975-05-27 BE BE156739A patent/BE829528A/xx not_active IP Right Cessation
- 1975-05-28 FR FR7516683A patent/FR2272603B1/fr not_active Expired
- 1975-05-28 FI FI751556A patent/FI57042C/fi not_active IP Right Cessation
- 1975-05-28 ES ES437989A patent/ES437989A1/es not_active Expired
- 1975-05-28 SU SU7502137882A patent/SU580798A3/ru active
- 1975-05-28 SE SE7506105A patent/SE425940B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IE41071L (en) | 1975-11-28 |
| DK136751C (US07122603-20061017-C00187.png) | 1978-05-29 |
| NL7505964A (nl) | 1975-12-02 |
| FR2272603B1 (US07122603-20061017-C00187.png) | 1978-05-19 |
| CS181786B2 (en) | 1978-03-31 |
| SE425940B (sv) | 1982-11-29 |
| DD119699A5 (US07122603-20061017-C00187.png) | 1976-05-12 |
| SE7506105L (sv) | 1975-12-01 |
| FI57042C (fi) | 1980-06-10 |
| IE41071B1 (en) | 1979-10-10 |
| FI751556A (US07122603-20061017-C00187.png) | 1975-11-29 |
| DE2522471A1 (de) | 1975-12-11 |
| SU580798A3 (ru) | 1977-11-15 |
| CA1049282A (en) | 1979-02-27 |
| GB1466634A (en) | 1977-03-09 |
| IT1057898B (it) | 1982-03-30 |
| AR229922A1 (es) | 1984-01-31 |
| TR18239A (tr) | 1976-11-05 |
| ES437989A1 (es) | 1977-04-01 |
| AU8054475A (en) | 1976-10-28 |
| DK233475A (US07122603-20061017-C00187.png) | 1975-11-29 |
| BE829528A (fr) | 1975-11-27 |
| FI57042B (fi) | 1980-02-29 |
| FR2272603A1 (US07122603-20061017-C00187.png) | 1975-12-26 |
| DK136751B (da) | 1977-11-21 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8110 | Request for examination paragraph 44 | ||
| 8128 | New person/name/address of the agent |
Representative=s name: SPOTT, G., DIPL.-CHEM. DR.RER.NAT., PAT.-ANW., 800 |
|
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |