DE2701681C2 - - Google Patents
Info
- Publication number
- DE2701681C2 DE2701681C2 DE2701681A DE2701681A DE2701681C2 DE 2701681 C2 DE2701681 C2 DE 2701681C2 DE 2701681 A DE2701681 A DE 2701681A DE 2701681 A DE2701681 A DE 2701681A DE 2701681 C2 DE2701681 C2 DE 2701681C2
- Authority
- DE
- Germany
- Prior art keywords
- herbicidal
- odorant
- bipyridylium
- acid
- alkyl
- 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
- 239000000203 mixture Substances 0.000 claims description 25
- 230000002363 herbicidal effect Effects 0.000 claims description 21
- -1 alkyl carboxylic acid Chemical class 0.000 claims description 18
- 150000001768 cations Chemical class 0.000 claims description 17
- 239000003205 fragrance Substances 0.000 claims description 16
- 150000003839 salts Chemical class 0.000 claims description 16
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 claims description 14
- 239000004094 surface-active agent Substances 0.000 claims description 13
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 claims description 10
- 150000001450 anions Chemical class 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 8
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims description 7
- 239000007864 aqueous solution Substances 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical group 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 description 11
- 239000012141 concentrate Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- INFDPOAKFNIJBF-UHFFFAOYSA-N paraquat Chemical compound C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 INFDPOAKFNIJBF-UHFFFAOYSA-N 0.000 description 5
- 239000000575 pesticide Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000002518 antifoaming agent Substances 0.000 description 4
- IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 239000004009 herbicide Substances 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 3
- 235000010234 sodium benzoate Nutrition 0.000 description 3
- 239000004299 sodium benzoate Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- XTEGARKTQYYJKE-UHFFFAOYSA-M Chlorate Chemical compound [O-]Cl(=O)=O XTEGARKTQYYJKE-UHFFFAOYSA-M 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003093 cationic surfactant Substances 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- WITARNULLOXUGF-UHFFFAOYSA-L 1-[4-[1-(2-oxopropyl)pyridin-1-ium-4-yl]pyridin-1-ium-1-yl]propan-2-one;dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](CC(=O)C)=CC=C1C1=CC=[N+](CC(C)=O)C=C1 WITARNULLOXUGF-UHFFFAOYSA-L 0.000 description 1
- WXJYKXOIFICRPR-UHFFFAOYSA-L 1-methyl-4-(1-methylpyridin-1-ium-4-yl)pyridin-1-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.COS([O-])(=O)=O.C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 WXJYKXOIFICRPR-UHFFFAOYSA-L 0.000 description 1
- OVSKIKFHRZPJSS-DOMIDYPGSA-N 2-(2,4-dichlorophenoxy)acetic acid Chemical compound OC(=O)[14CH2]OC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-DOMIDYPGSA-N 0.000 description 1
- RGZIBEBILGCELM-UHFFFAOYSA-N 2-[4-[1-(2-amino-2-oxoethyl)pyridin-1-ium-4-yl]pyridin-1-ium-1-yl]acetamide;dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](CC(=O)N)=CC=C1C1=CC=[N+](CC(N)=O)C=C1 RGZIBEBILGCELM-UHFFFAOYSA-N 0.000 description 1
- CBQDTCDOVVBGMN-UHFFFAOYSA-N 2-methyl-3-octylphenol Chemical compound CCCCCCCCC1=CC=CC(O)=C1C CBQDTCDOVVBGMN-UHFFFAOYSA-N 0.000 description 1
- ODPOAESBSUKMHD-UHFFFAOYSA-L 6,7-dihydrodipyrido[1,2-b:1',2'-e]pyrazine-5,8-diium;dibromide Chemical compound [Br-].[Br-].C1=CC=[N+]2CC[N+]3=CC=CC=C3C2=C1 ODPOAESBSUKMHD-UHFFFAOYSA-L 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 239000005630 Diquat Substances 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M Formate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- YWTQVACKTMAQRT-UHFFFAOYSA-M N,N-diethyl-2-(4-pyridin-1-ium-4-ylpyridin-1-ium-1-yl)acetamide dichloride Chemical compound [Cl-].[Cl-].CCN(CC)C(=O)C[N+]1=CC=C(C=C1)C1=CC=[NH+]C=C1 YWTQVACKTMAQRT-UHFFFAOYSA-M 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- DTKVWOOPKHTIFT-UHFFFAOYSA-M [Cl-].[Cl-].CN(C(=O)C[N+]1=CC=C(C=C1)C1=CC=[NH+]C=C1)C Chemical compound [Cl-].[Cl-].CN(C(=O)C[N+]1=CC=C(C=C1)C1=CC=[NH+]C=C1)C DTKVWOOPKHTIFT-UHFFFAOYSA-M 0.000 description 1
- MZFYPAVURASXHI-UHFFFAOYSA-L [Cl-].[Cl-].OCCC=1[C+]=NC=CC=1C1=C[CH+]N(C=C1)C Chemical compound [Cl-].[Cl-].OCCC=1[C+]=NC=CC=1C1=C[CH+]N(C=C1)C MZFYPAVURASXHI-UHFFFAOYSA-L 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 229940077388 benzenesulfonate Drugs 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 description 1
- MXZACTZQSGYANA-UHFFFAOYSA-N chembl545463 Chemical compound Cl.C1=CC(OC)=CC=C1C(N=C1)=CN2C1=NC(C)=C2O MXZACTZQSGYANA-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- ZQMFXSROVKWNMZ-UHFFFAOYSA-N dimethyl sulfate;1-methyl-4-(1-methylpyridin-1-ium-4-yl)pyridin-1-ium Chemical compound COS(=O)(=O)OC.C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 ZQMFXSROVKWNMZ-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- JVCVWQYGXOSMDW-UHFFFAOYSA-L ethyl 2-[4-[1-(2-ethoxy-2-oxoethyl)pyridin-1-ium-4-yl]pyridin-1-ium-1-yl]acetate;dibromide Chemical compound [Br-].[Br-].C1=C[N+](CC(=O)OCC)=CC=C1C1=CC=[N+](CC(=O)OCC)C=C1 JVCVWQYGXOSMDW-UHFFFAOYSA-L 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 229940104869 fluorosilicate Drugs 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 230000003054 hormonal effect Effects 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 229940049920 malate Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- IIACRCGMVDHOTQ-UHFFFAOYSA-M sulfamate Chemical compound NS([O-])(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-M 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 229940005605 valeric acid Drugs 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (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 |
|---|---|---|---|
| GB2174/76A GB1570981A (en) | 1976-01-20 | 1976-01-20 | Herbicidal compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2701681A1 DE2701681A1 (de) | 1977-07-21 |
| DE2701681C2 true DE2701681C2 (en, 2012) | 1988-03-03 |
Family
ID=9734883
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19772701681 Granted DE2701681A1 (de) | 1976-01-20 | 1977-01-17 | Herbizide massen |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US4075005A (en, 2012) |
| JP (1) | JPS5290631A (en, 2012) |
| AU (1) | AU504775B2 (en, 2012) |
| BE (1) | BE849874A (en, 2012) |
| BR (1) | BR7700314A (en, 2012) |
| CA (1) | CA1097096A (en, 2012) |
| DE (1) | DE2701681A1 (en, 2012) |
| FR (1) | FR2338649A1 (en, 2012) |
| GB (1) | GB1570981A (en, 2012) |
| GR (1) | GR59189B (en, 2012) |
| IE (1) | IE44322B1 (en, 2012) |
| IL (1) | IL51150A (en, 2012) |
| IT (1) | IT1124750B (en, 2012) |
| NL (1) | NL184305C (en, 2012) |
| NZ (1) | NZ182935A (en, 2012) |
| PH (1) | PH13648A (en, 2012) |
| ZA (1) | ZA767545B (en, 2012) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2712032A1 (de) * | 1976-03-19 | 1977-09-29 | Ici Ltd | Herbizide zusammensetzungen |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4046552A (en) * | 1976-04-15 | 1977-09-06 | Imperial Chemical Industries Limited | Herbicidal compositions of bipyridylium quaternary salts and emetic amounts of s-triazolo pyrimidine derivatives |
| WO1979000838A1 (en) * | 1978-03-28 | 1979-10-18 | Michael James Sampson | New plant technique |
| IT1122094B (it) * | 1979-07-10 | 1986-04-23 | Montedison Spa | Composizione erbicida a base di sali di bipiridilio contenente una sostanza che impartisce cattivo odore |
| EP0027344B1 (en) * | 1979-10-13 | 1984-02-22 | Neville Hutchings | Process for obtaining improved yields from plants |
| US4432787A (en) * | 1982-03-22 | 1984-02-21 | American Cyanamid Company | Concentrated emetic herbicidal composition and method for the preparation thereof |
| GB8700658D0 (en) * | 1987-01-13 | 1987-02-18 | Ici Plc | Formulation process |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1406881A (en) * | 1972-04-13 | 1975-09-17 | Ici Ltd | Herbicidal compositions |
-
1976
- 1976-01-20 GB GB2174/76A patent/GB1570981A/en not_active Expired
- 1976-12-16 IE IE2754/76A patent/IE44322B1/en not_active IP Right Cessation
- 1976-12-20 ZA ZA767545A patent/ZA767545B/xx unknown
- 1976-12-21 NZ NZ182935A patent/NZ182935A/xx unknown
- 1976-12-22 AU AU20802/76A patent/AU504775B2/en not_active Expired
- 1976-12-23 IL IL51150A patent/IL51150A/xx unknown
- 1976-12-23 GR GR52472A patent/GR59189B/el unknown
- 1976-12-24 BE BE173650A patent/BE849874A/xx not_active IP Right Cessation
- 1976-12-27 US US05/757,912 patent/US4075005A/en not_active Expired - Lifetime
- 1976-12-31 NL NLAANVRAGE7614616,A patent/NL184305C/xx not_active IP Right Cessation
- 1976-12-31 IT IT31056/76A patent/IT1124750B/it active
-
1977
- 1977-01-10 FR FR7700511A patent/FR2338649A1/fr active Granted
- 1977-01-17 DE DE19772701681 patent/DE2701681A1/de active Granted
- 1977-01-18 BR BR7700314A patent/BR7700314A/pt unknown
- 1977-01-19 CA CA270,075A patent/CA1097096A/en not_active Expired
- 1977-01-19 PH PH19366A patent/PH13648A/en unknown
- 1977-01-20 JP JP449377A patent/JPS5290631A/ja active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2712032A1 (de) * | 1976-03-19 | 1977-09-29 | Ici Ltd | Herbizide zusammensetzungen |
Also Published As
| Publication number | Publication date |
|---|---|
| US4075005A (en) | 1978-02-21 |
| NL7614616A (nl) | 1977-07-22 |
| AU2080276A (en) | 1978-06-29 |
| IL51150A (en) | 1979-11-30 |
| PH13648A (en) | 1980-08-21 |
| GR59189B (en) | 1977-11-25 |
| IT1124750B (it) | 1986-05-14 |
| FR2338649B1 (en, 2012) | 1981-10-16 |
| BE849874A (fr) | 1977-06-24 |
| AU504775B2 (en) | 1979-10-25 |
| CA1097096A (en) | 1981-03-10 |
| JPS6135963B2 (en, 2012) | 1986-08-15 |
| NL184305C (nl) | 1989-06-16 |
| JPS5290631A (en) | 1977-07-30 |
| DE2701681A1 (de) | 1977-07-21 |
| GB1570981A (en) | 1980-07-09 |
| NZ182935A (en) | 1979-10-25 |
| ZA767545B (en) | 1977-11-30 |
| IE44322L (en) | 1977-07-20 |
| BR7700314A (pt) | 1977-09-20 |
| FR2338649A1 (fr) | 1977-08-19 |
| IE44322B1 (en) | 1981-10-21 |
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