GB1339315A - Herbicidal compositions - Google Patents
Herbicidal compositionsInfo
- Publication number
- GB1339315A GB1339315A GB3620871A GB3620871A GB1339315A GB 1339315 A GB1339315 A GB 1339315A GB 3620871 A GB3620871 A GB 3620871A GB 3620871 A GB3620871 A GB 3620871A GB 1339315 A GB1339315 A GB 1339315A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- amino
- salts
- composition
- formula
- 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 title abstract 9
- 230000002363 herbicidal effect Effects 0.000 title abstract 4
- 150000003839 salts Chemical class 0.000 abstract 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 abstract 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 abstract 3
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 abstract 3
- RHPUJHQBPORFGV-UHFFFAOYSA-N 4-chloro-2-methylphenol Chemical compound CC1=CC(Cl)=CC=C1O RHPUJHQBPORFGV-UHFFFAOYSA-N 0.000 abstract 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 abstract 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 abstract 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 abstract 2
- -1 alkali metal salts Chemical class 0.000 abstract 2
- HYJSGOXICXYZGS-UHFFFAOYSA-N benazolin Chemical compound C1=CC=C2SC(=O)N(CC(=O)O)C2=C1Cl HYJSGOXICXYZGS-UHFFFAOYSA-N 0.000 abstract 2
- VHRGRCVQAFMJIZ-UHFFFAOYSA-N cadaverine Chemical compound NCCCCCN VHRGRCVQAFMJIZ-UHFFFAOYSA-N 0.000 abstract 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 abstract 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 abstract 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 abstract 2
- ATHGHQPFGPMSJY-UHFFFAOYSA-N spermidine Chemical compound NCCCCNCCCN ATHGHQPFGPMSJY-UHFFFAOYSA-N 0.000 abstract 2
- PFNFFQXMRSDOHW-UHFFFAOYSA-N spermine Chemical compound NCCCNCCCCNCCCN PFNFFQXMRSDOHW-UHFFFAOYSA-N 0.000 abstract 2
- UODZHRGDSPLRMD-UHFFFAOYSA-N sym-homospermidine Chemical compound NCCCCNCCCCN UODZHRGDSPLRMD-UHFFFAOYSA-N 0.000 abstract 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 abstract 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- GXEKYRXVRROBEV-FBXFSONDSA-N (1r,2s,3r,4s)-7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid Chemical compound C1C[C@@H]2[C@@H](C(O)=O)[C@@H](C(=O)O)[C@H]1O2 GXEKYRXVRROBEV-FBXFSONDSA-N 0.000 abstract 1
- SMYMJHWAQXWPDB-UHFFFAOYSA-N (2,4,5-trichlorophenoxy)acetic acid Chemical compound OC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl SMYMJHWAQXWPDB-UHFFFAOYSA-N 0.000 abstract 1
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 abstract 1
- XDBHOPSEFXTSOW-UHFFFAOYSA-N 1-methyl-4-(1-methyl-2h-pyridin-4-yl)-2h-pyridine Chemical compound C1=CN(C)CC=C1C1=CCN(C)C=C1 XDBHOPSEFXTSOW-UHFFFAOYSA-N 0.000 abstract 1
- NDUPDOJHUQKPAG-UHFFFAOYSA-M 2,2-Dichloropropanoate Chemical compound CC(Cl)(Cl)C([O-])=O NDUPDOJHUQKPAG-UHFFFAOYSA-M 0.000 abstract 1
- VVJIVFKAROPUOS-UHFFFAOYSA-N 2,2-bis(aminomethyl)propane-1,3-diamine Chemical compound NCC(CN)(CN)CN VVJIVFKAROPUOS-UHFFFAOYSA-N 0.000 abstract 1
- XZIDTOHMJBOSOX-UHFFFAOYSA-N 2,3,6-TBA Chemical compound OC(=O)C1=C(Cl)C=CC(Cl)=C1Cl XZIDTOHMJBOSOX-UHFFFAOYSA-N 0.000 abstract 1
- 239000003559 2,4,5-trichlorophenoxyacetic acid Substances 0.000 abstract 1
- YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 abstract 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 abstract 1
- MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 abstract 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 abstract 1
- LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 abstract 1
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 abstract 1
- VMQAGVBDNJCBSQ-UHFFFAOYSA-N 3-amino-2,2-bis(aminomethyl)propan-1-ol Chemical compound NCC(CN)(CN)CO VMQAGVBDNJCBSQ-UHFFFAOYSA-N 0.000 abstract 1
- UIKUBYKUYUSRSM-UHFFFAOYSA-N 3-morpholinopropylamine Chemical compound NCCCN1CCOCC1 UIKUBYKUYUSRSM-UHFFFAOYSA-N 0.000 abstract 1
- FDPCVOXXUBYMTQ-UHFFFAOYSA-N 4-(4-aminobutoxy)butan-1-amine Chemical compound NCCCCOCCCCN FDPCVOXXUBYMTQ-UHFFFAOYSA-N 0.000 abstract 1
- FFEKEPNLQVJRKO-UHFFFAOYSA-N 5-(5-aminopentoxy)pentan-1-amine Chemical compound NCCCCCOCCCCCN FFEKEPNLQVJRKO-UHFFFAOYSA-N 0.000 abstract 1
- KLSJWNVTNUYHDU-UHFFFAOYSA-N Amitrole Chemical compound NC1=NC=NN1 KLSJWNVTNUYHDU-UHFFFAOYSA-N 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- HSSBORCLYSCBJR-UHFFFAOYSA-N Chloramben Chemical compound NC1=CC(Cl)=CC(C(O)=O)=C1Cl HSSBORCLYSCBJR-UHFFFAOYSA-N 0.000 abstract 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 1
- 239000005574 MCPA Substances 0.000 abstract 1
- 239000005700 Putrescine Substances 0.000 abstract 1
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 abstract 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 abstract 1
- SLINHMUFWFWBMU-UHFFFAOYSA-N Triisopropanolamine Chemical compound CC(O)CN(CC(C)O)CC(C)O SLINHMUFWFWBMU-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- QZXCCPZJCKEPSA-UHFFFAOYSA-N chlorfenac Chemical compound OC(=O)CC1=C(Cl)C=CC(Cl)=C1Cl QZXCCPZJCKEPSA-UHFFFAOYSA-N 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- DBSUDIOKJSDLAL-UHFFFAOYSA-N cyclopropane-1,2,3-triamine Chemical compound NC1C(N)C1N DBSUDIOKJSDLAL-UHFFFAOYSA-N 0.000 abstract 1
- YQLZOAVZWJBZSY-UHFFFAOYSA-N decane-1,10-diamine Chemical compound NCCCCCCCCCCN YQLZOAVZWJBZSY-UHFFFAOYSA-N 0.000 abstract 1
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical compound COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 abstract 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 abstract 1
- 229940043237 diethanolamine Drugs 0.000 abstract 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 abstract 1
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 abstract 1
- 229940043276 diisopropanolamine Drugs 0.000 abstract 1
- 229940043279 diisopropylamine Drugs 0.000 abstract 1
- 239000012153 distilled water Substances 0.000 abstract 1
- 239000004009 herbicide Substances 0.000 abstract 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 abstract 1
- 239000004312 hexamethylene tetramine Substances 0.000 abstract 1
- 229910017053 inorganic salt Inorganic materials 0.000 abstract 1
- NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 abstract 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 abstract 1
- QYPPRTNMGCREIM-UHFFFAOYSA-N methylarsonic acid Chemical compound C[As](O)(O)=O QYPPRTNMGCREIM-UHFFFAOYSA-N 0.000 abstract 1
- RWIVICVCHVMHMU-UHFFFAOYSA-N n-aminoethylmorpholine Chemical compound NCCN1CCOCC1 RWIVICVCHVMHMU-UHFFFAOYSA-N 0.000 abstract 1
- DPBLXKKOBLCELK-UHFFFAOYSA-N pentan-1-amine Chemical compound CCCCCN DPBLXKKOBLCELK-UHFFFAOYSA-N 0.000 abstract 1
- IGEIPFLJVCPEKU-UHFFFAOYSA-N pentan-2-amine Chemical compound CCCC(C)N IGEIPFLJVCPEKU-UHFFFAOYSA-N 0.000 abstract 1
- 150000003141 primary amines Chemical class 0.000 abstract 1
- ZNZJJSYHZBXQSM-UHFFFAOYSA-N propane-2,2-diamine Chemical compound CC(C)(N)N ZNZJJSYHZBXQSM-UHFFFAOYSA-N 0.000 abstract 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 abstract 1
- 150000003335 secondary amines Chemical class 0.000 abstract 1
- 229940063673 spermidine Drugs 0.000 abstract 1
- 229940063675 spermine Drugs 0.000 abstract 1
- 150000003512 tertiary amines Chemical class 0.000 abstract 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 abstract 1
- WCLDITPGPXSPGV-UHFFFAOYSA-N tricamba Chemical compound COC1=C(Cl)C=C(Cl)C(Cl)=C1C(O)=O WCLDITPGPXSPGV-UHFFFAOYSA-N 0.000 abstract 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 abstract 1
- RKBCYCFRFCNLTO-UHFFFAOYSA-N triisopropylamine Chemical compound CC(C)N(C(C)C)C(C)C RKBCYCFRFCNLTO-UHFFFAOYSA-N 0.000 abstract 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
- A01N25/02—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 containing liquids as carriers, diluents or solvents
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)
Abstract
1339315 Herbicidal compositions CIBAGEIGY CANADA Ltd 2 Aug 1971 [25 Nov 1970] 36208/71 Heading A5E A herbicidal composition comprises a mixture of at least two different salts of at least one herbicidally active compound, said mixture of salts being miscible with a liquid polar carrier such as water and having the property of being liquid at 20‹C for at least 24 hours, said composition having an absolute surface tension of not more than 35 dynes/cm, when measured at 25‹C in distilled water at a 1% active herbicide concentration. Suitable salts are those of primary amines of formula R-NH 2 , secondary amines of formula RR'NH, tertiary amines of formula RR'R 2 N, quaternary ammonium salts of formula RR'R 2 R 3 N<SP>+</SP>, wherein the radicals R, R', R 2 and R 3 are selected from alkyl, hydroxy-substituted alkyl and alkoxy groups having 1 to 6 carbon atoms, ammonium and alkali metal salts. Suitable herbicidally active acids include 2, 4-dichlorophenoxyacetic acid, 2, 4-dichlorophenoxypropionic acid, 2, 4-dichlorophenoxybutyric acid, 2-methyl-4-chlorophenoxyacetic acid, 2-methyl- 4-chlorophenoxybutyric acid, 2, 4, 5-trichlorophenoxyacetic acid, 2, 3, 6-trichlorobenzoic acid, 2-methoxy-3, 5, 6-trichlorobenzoic acid, 2-methoxy-3, 6-dichlorobenzoic acid, 4-chloro- 2-oxobenzothiazolin-3-ylacetic acid, 3, 5-dibromo-4-hydroxybenzonitrile, 3, 5-diiodo-4-hydroxybenzonitrile, 4-amino-3, 5, 6-trichloropicolinic acid, trichloroacetic acid, 2, 2-dichloropropionic acid, 3-amino-2, 5-dichlorobenzoic acid, methane arsonic acid, 2, 3, 6-trichlorophenylacetic acid and 3, 6-endoxo-hexahydrophthalic acid, 4-amino-3, 5, 6-trichloropicolinic acid, 4-chloro-2-oxobenzothiazolin -3- ylacetic acid. The composition may include a carboxylic or inorganic salt of 3-amino-1, 2, 4- triazole or 1, 1'-dimethyl-4, 4'-bipyridine. Suitable salts include methylamine, ethylamine, isopropylamine, propylamine, n-butylamine, 1- amino-pentane, 2-amino-pentane, cyclohexylamine, monoethanolamine, monoisopropanolamine, dimethylamine, diethylamine, diisopropylamine, diethanolamine, diisopropanolamine, trimethylamine, triethylamine, triisopropylamine, tri-n-butylamine, triethanolamine, triisopropanolamine, diethylaminoacetal, 1, 2-diaminoethane, 1, 2- and 1, 3-diaminopropane, putrescine, cadaverine, 1, 6-diamino-n-hexane, 1, 10-diaminodecane, 1, 2, 3-triaminocyclopropane, spermidine, sym-homo-spermidine, 1- hydroxy-2, 2, 2-triaminomethylethane, tetra (aminomethyl) methane, hexamethylenetetramine, spermine, bis (4-aminobutyl) ether, bis-(5- aminopentyl)-ether, 4(2-aminoethyl) morpholine, 4(3-aminopropyl) morpholine. A method of preparing the above composition and a method of controlling undesired vegetation by use of the composition are also claimed.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CA879602A CA879602A (en) | 1970-11-25 | 1970-11-25 | Herbicidal compositions |
| ZA730955A ZA73955B (en) | 1970-11-25 | 1973-02-09 | Herbicidal compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1339315A true GB1339315A (en) | 1973-12-05 |
Family
ID=25666644
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3620871A Expired GB1339315A (en) | 1970-11-25 | 1971-08-02 | Herbicidal compositions |
Country Status (10)
| Country | Link |
|---|---|
| AT (1) | AT312986B (en) |
| AU (1) | AU456852B2 (en) |
| BE (1) | BE770822A (en) |
| CA (1) | CA879602A (en) |
| DD (1) | DD101273A5 (en) |
| DE (1) | DE2138556A1 (en) |
| FR (1) | FR2115138B1 (en) |
| GB (1) | GB1339315A (en) |
| NL (1) | NL7110636A (en) |
| ZA (1) | ZA73955B (en) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0432092A1 (en) * | 1989-11-23 | 1991-06-12 | Ciba-Geigy Ag | Pesticide composition |
| US5104873A (en) * | 1989-11-23 | 1992-04-14 | Ciba-Geigy Corporation | Pesticide composition |
| AU2007100527B4 (en) * | 2006-06-23 | 2007-08-23 | Nufarm Australia Limited | Phenoxy alkanoate herbicidal composition and method of preparation and use |
| WO2008069826A1 (en) * | 2006-12-06 | 2008-06-12 | Akzo Nobel N.V. | Compatibility agents for herbicidal formulations comprising 2,4-(dichlorophenoxy) acetic acid salts |
| WO2010071936A1 (en) * | 2008-12-23 | 2010-07-01 | Nufarm Australia Limited | Auxin herbicide composition |
| US8293683B2 (en) | 2006-12-06 | 2012-10-23 | Akzo Nobel N.V. | Alkylamidopropyl dialkylamine surfactants as adjuvants |
| AU2010202620B2 (en) * | 2008-12-23 | 2013-10-31 | Nufarm Australia Limited | Dicamba herbicide composition |
| EP2582240A4 (en) * | 2010-06-21 | 2013-12-18 | Nufarm Australia Ltd | HERBICIDE PICOLINE ACID SALT COMPOSITION |
| AU2014200518B2 (en) * | 2008-12-23 | 2015-08-13 | Nufarm Australia Limited | Auxin herbicide composition |
| WO2018197418A1 (en) * | 2017-04-24 | 2018-11-01 | Taminco Bvba | Highly concentrated solutions of alkanolamine salts of dicamba |
| WO2019173859A1 (en) * | 2018-03-13 | 2019-09-19 | Adama Australia Pty Ltd | Herbicide formulation |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4971630A (en) * | 1983-07-15 | 1990-11-20 | Pbi/Gordon Corporation | Liquid herbicidal composition having extended penetrating and systemic activity |
-
1970
- 1970-11-25 CA CA879602A patent/CA879602A/en not_active Expired
-
1971
- 1971-08-02 FR FR7128225A patent/FR2115138B1/fr not_active Expired
- 1971-08-02 DD DD156898A patent/DD101273A5/xx unknown
- 1971-08-02 NL NL7110636A patent/NL7110636A/xx unknown
- 1971-08-02 AT AT674371A patent/AT312986B/en active
- 1971-08-02 GB GB3620871A patent/GB1339315A/en not_active Expired
- 1971-08-02 DE DE19712138556 patent/DE2138556A1/en active Pending
- 1971-08-02 BE BE770822A patent/BE770822A/en not_active IP Right Cessation
- 1971-08-03 AU AU31947/71A patent/AU456852B2/en not_active Expired
-
1973
- 1973-02-09 ZA ZA730955A patent/ZA73955B/en unknown
Cited By (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0432092A1 (en) * | 1989-11-23 | 1991-06-12 | Ciba-Geigy Ag | Pesticide composition |
| US5104873A (en) * | 1989-11-23 | 1992-04-14 | Ciba-Geigy Corporation | Pesticide composition |
| AU2007100527B4 (en) * | 2006-06-23 | 2007-08-23 | Nufarm Australia Limited | Phenoxy alkanoate herbicidal composition and method of preparation and use |
| AU2007328454B2 (en) * | 2006-12-06 | 2014-02-27 | Akzo Nobel Chemicals International B.V. | Compatibility agents for herbicidal formulations comprising 2,4-(Dichlorophenoxy) acetic acid salts |
| US8293683B2 (en) | 2006-12-06 | 2012-10-23 | Akzo Nobel N.V. | Alkylamidopropyl dialkylamine surfactants as adjuvants |
| US9012365B2 (en) | 2006-12-06 | 2015-04-21 | Akzo Nobel N.V. | Compatibility agents for herbicidal formulations comprising 2,4-(Dichlorophenoxy) acetic acid salts |
| WO2008069826A1 (en) * | 2006-12-06 | 2008-06-12 | Akzo Nobel N.V. | Compatibility agents for herbicidal formulations comprising 2,4-(dichlorophenoxy) acetic acid salts |
| WO2010071936A1 (en) * | 2008-12-23 | 2010-07-01 | Nufarm Australia Limited | Auxin herbicide composition |
| AU2009329825B2 (en) * | 2008-12-23 | 2013-10-31 | Nufarm Australia Limited | Auxin herbicide composition |
| AU2010202620B2 (en) * | 2008-12-23 | 2013-10-31 | Nufarm Australia Limited | Dicamba herbicide composition |
| US9179673B2 (en) * | 2008-12-23 | 2015-11-10 | Nufarm Australia Limited | Auxin herbicide composition |
| AU2014200518B2 (en) * | 2008-12-23 | 2015-08-13 | Nufarm Australia Limited | Auxin herbicide composition |
| US8871683B2 (en) | 2008-12-23 | 2014-10-28 | Nufarm Australia Limited | Dicamba herbicide composition |
| US8877685B2 (en) | 2008-12-23 | 2014-11-04 | Nufarm Australia Limited | Auxin herbicide composition |
| US20150018212A1 (en) * | 2008-12-23 | 2015-01-15 | Nufarm Australia Limited | Auxin Herbicide Composition |
| AU2011269714B2 (en) * | 2010-06-21 | 2014-10-30 | Nufarm Australia Limited | Herbicidal picolinic acid salt composition |
| US20150031538A1 (en) * | 2010-06-21 | 2015-01-29 | Nufarm Australia Limited | Herbicidal picolinic acid salt composition |
| US8865625B2 (en) | 2010-06-21 | 2014-10-21 | Nufarm Australia Limited | Herbicidal picolinic acid salt composition |
| US9137993B2 (en) * | 2010-06-21 | 2015-09-22 | Nufarm Australia Limited | Herbicidal picolinic acid salt composition |
| EP2582240A4 (en) * | 2010-06-21 | 2013-12-18 | Nufarm Australia Ltd | HERBICIDE PICOLINE ACID SALT COMPOSITION |
| WO2018197418A1 (en) * | 2017-04-24 | 2018-11-01 | Taminco Bvba | Highly concentrated solutions of alkanolamine salts of dicamba |
| CN110545667A (en) * | 2017-04-24 | 2019-12-06 | 塔明克公司 | Highly concentrated solutions of alkanolamine salts of dicamba |
| US11109591B2 (en) | 2017-04-24 | 2021-09-07 | Taminco Bvba | Single phase liquids of alkanolamine salts of dicamba |
| WO2019173859A1 (en) * | 2018-03-13 | 2019-09-19 | Adama Australia Pty Ltd | Herbicide formulation |
Also Published As
| Publication number | Publication date |
|---|---|
| ZA73955B (en) | 1974-02-27 |
| AU3194771A (en) | 1973-02-08 |
| DD101273A5 (en) | 1973-11-05 |
| FR2115138B1 (en) | 1974-12-20 |
| DE2138556A1 (en) | 1972-06-08 |
| AU456852B2 (en) | 1975-01-16 |
| BE770822A (en) | 1972-02-02 |
| CA879602A (en) | 1971-08-31 |
| AT312986B (en) | 1974-01-25 |
| NL7110636A (en) | 1972-05-29 |
| FR2115138A1 (en) | 1972-07-07 |
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| Date | Code | Title | Description |
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| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |