GB1160674A - Method of Applying Aqueous Chemicals Compositions - Google Patents
Method of Applying Aqueous Chemicals CompositionsInfo
- Publication number
- GB1160674A GB1160674A GB3626566A GB3626566A GB1160674A GB 1160674 A GB1160674 A GB 1160674A GB 3626566 A GB3626566 A GB 3626566A GB 3626566 A GB3626566 A GB 3626566A GB 1160674 A GB1160674 A GB 1160674A
- Authority
- GB
- United Kingdom
- Prior art keywords
- specified
- xanthomonas
- phosphorodithioate
- chlorophenyl
- dimethyl
- 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 2
- 239000000126 substance Substances 0.000 title 1
- 241000589634 Xanthomonas Species 0.000 abstract 2
- 239000000084 colloidal system Substances 0.000 abstract 2
- 239000000575 pesticide Substances 0.000 abstract 2
- 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
- 239000003559 2,4,5-trichlorophenoxyacetic acid Substances 0.000 abstract 1
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 abstract 1
- HXKWSTRRCHTUEC-UHFFFAOYSA-N 2,4-Dichlorophenoxyaceticacid Chemical compound OC(=O)C(Cl)OC1=CC=C(Cl)C=C1 HXKWSTRRCHTUEC-UHFFFAOYSA-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
- -1 2-(p-tert-butylphenoxy)-isopropyl 2- chloroethyl sulphite Chemical compound 0.000 abstract 1
- GFOIDJBFWHYEIU-UHFFFAOYSA-N 2-carbamothioylsulfanylethyl carbamodithioate;sodium Chemical compound [Na].[Na].NC(=S)SCCSC(N)=S GFOIDJBFWHYEIU-UHFFFAOYSA-N 0.000 abstract 1
- RZXLPPRPEOUENN-UHFFFAOYSA-N Chlorfenson Chemical compound C1=CC(Cl)=CC=C1OS(=O)(=O)C1=CC=C(Cl)C=C1 RZXLPPRPEOUENN-UHFFFAOYSA-N 0.000 abstract 1
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 abstract 1
- YVGGHNCTFXOJCH-UHFFFAOYSA-N DDT Chemical compound C1=CC(Cl)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(Cl)C=C1 YVGGHNCTFXOJCH-UHFFFAOYSA-N 0.000 abstract 1
- NPOJQCVWMSKXDN-UHFFFAOYSA-N Dacthal Chemical compound COC(=O)C1=C(Cl)C(Cl)=C(C(=O)OC)C(Cl)=C1Cl NPOJQCVWMSKXDN-UHFFFAOYSA-N 0.000 abstract 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 abstract 1
- IDCBOTIENDVCBQ-UHFFFAOYSA-N TEPP Chemical compound CCOP(=O)(OCC)OP(=O)(OCC)OCC IDCBOTIENDVCBQ-UHFFFAOYSA-N 0.000 abstract 1
- 241001517672 Xanthomonas axonopodis pv. begoniae Species 0.000 abstract 1
- 241000589636 Xanthomonas campestris Species 0.000 abstract 1
- 241000321047 Xanthomonas campestris pv. carotae Species 0.000 abstract 1
- 241000321050 Xanthomonas campestris pv. incanae Species 0.000 abstract 1
- 241001668516 Xanthomonas citri subsp. malvacearum Species 0.000 abstract 1
- 239000000642 acaricide Substances 0.000 abstract 1
- 230000001464 adherent effect Effects 0.000 abstract 1
- 239000008365 aqueous carrier Substances 0.000 abstract 1
- 239000012736 aqueous medium Substances 0.000 abstract 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 abstract 1
- 125000002147 dimethylamino group Chemical class [H]C([H])([H])N(*)C([H])([H])[H] 0.000 abstract 1
- NAGJZTKCGNOGPW-UHFFFAOYSA-K dioxido-sulfanylidene-sulfido-$l^{5}-phosphane Chemical compound [O-]P([O-])([S-])=S NAGJZTKCGNOGPW-UHFFFAOYSA-K 0.000 abstract 1
- 239000000417 fungicide Substances 0.000 abstract 1
- 239000008103 glucose Substances 0.000 abstract 1
- 239000004009 herbicide Substances 0.000 abstract 1
- 239000002917 insecticide Substances 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- UVGZJJKEELPWRH-JSCKKFHOSA-M potassium (2S,3S,4S,5R)-2,3,4,5-tetrahydroxy-6-oxohexanoate Chemical compound [K+].O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C([O-])=O UVGZJJKEELPWRH-JSCKKFHOSA-M 0.000 abstract 1
- PDEFQWNXOUGDJR-UHFFFAOYSA-M sodium;2,2-dichloropropanoate Chemical compound [Na+].CC(Cl)(Cl)C([O-])=O PDEFQWNXOUGDJR-UHFFFAOYSA-M 0.000 abstract 1
- 239000002562 thickening agent Substances 0.000 abstract 1
- 229960002447 thiram Drugs 0.000 abstract 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 abstract 1
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05F—ORGANIC FERTILISERS NOT COVERED BY SUBCLASSES C05B, C05C, e.g. FERTILISERS FROM WASTE OR REFUSE
- C05F11/00—Other organic fertilisers
- C05F11/08—Organic fertilisers containing added bacterial cultures, mycelia or the like
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
1,160,674. Pesticides in adherent aqueous media. KELCO CO. 12 Aug., 1966, No. 36265/66. Heading A5E. [Also in Division C1] A pesticide is employed in an aqueous carrier comprising 0.02-2% of a Xanthomonas hydrophilic colloid (as thickening agent). The composition may have a viscosity of 400-1,200 centipoises. The colloid is a polymer containing mannose, glucose, potassium glucuronate and acetyl radicals and is produced by known Xanthomonas bacteria, e.g. Xanthomonas campestris, carotae, incanae, begoniae, or malvacearum. Herbicides specified are dimethyl 2,3,5,6-tetrachloro terephthalate, sodium 2,2- dichloropropionate, 2,4,5-trichlorophenoxyacetic acid, 2-(2,4-dichloro phenoxy) propionic acid, and 2,4-dichlorophenoxyacetic acid and dimethylamine salt. Fungicides specified are N-trichloromethylmercapto-4-yclohexene-1, 2- dicarboximide, tetramethyl thiuram disulphide, 1,2,3,4,5,6-hexachlorobenzeine, and disodium ethylene bisdithiocarbamate. Insecticides specified are 1,2,4,5,6,7,8,8-octachloro-3a,4,7,7atetrahydro-4,7-methanoindane; 1,1,1-trichloro- 2,2-bis(p-chlorophenyl)-ethane, 1,2,3,4,5,6-hexachlorocyclohexane, 0,0-dimethyl S-(1,2-dicarbethoxyethyl) phosphorodithioate, and 3-(1- methyl-2-(pyrrolidyl) pyridine. Miticides specified are 2-(p-tert-butylphenoxy)-isopropyl 2- chloroethyl sulphite, p-chlorophenyl p-chlorobenzenesulphonate, tetraethyl pyrophosphate, and 0,0-diethyl s-(chlorophenylthiomethyl), phosphorodithioate.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3626566A GB1160674A (en) | 1966-08-12 | 1966-08-12 | Method of Applying Aqueous Chemicals Compositions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3626566A GB1160674A (en) | 1966-08-12 | 1966-08-12 | Method of Applying Aqueous Chemicals Compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1160674A true GB1160674A (en) | 1969-08-06 |
Family
ID=10386525
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3626566A Expired GB1160674A (en) | 1966-08-12 | 1966-08-12 | Method of Applying Aqueous Chemicals Compositions |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1160674A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4144046A (en) * | 1970-11-02 | 1979-03-13 | Amchem Products, Inc. | Method of stimulating the flow of latex and compositions used therein |
| EP0045280A1 (en) * | 1980-07-24 | 1982-02-03 | Sipuro Ag | Composition for the control of slugs and snails, container for this composition and use of substances in pesticides for slugs and snails |
| FR2590118A1 (en) * | 1985-11-19 | 1987-05-22 | Vignolles Jean | Highly persistent liquid anti-cryptogamic composition based on parachlorometacresol |
-
1966
- 1966-08-12 GB GB3626566A patent/GB1160674A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4144046A (en) * | 1970-11-02 | 1979-03-13 | Amchem Products, Inc. | Method of stimulating the flow of latex and compositions used therein |
| EP0045280A1 (en) * | 1980-07-24 | 1982-02-03 | Sipuro Ag | Composition for the control of slugs and snails, container for this composition and use of substances in pesticides for slugs and snails |
| WO1982000237A1 (en) * | 1980-07-24 | 1982-02-04 | Rohrer H | Preparation to control slugs,container for such preparation and utilization of substances |
| FR2590118A1 (en) * | 1985-11-19 | 1987-05-22 | Vignolles Jean | Highly persistent liquid anti-cryptogamic composition based on parachlorometacresol |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PLE | Entries relating assignments, transmissions, licences in the register of patents | ||
| PE | Patent expired |