GB969962A - Fungicidal compositions - Google Patents
Fungicidal compositionsInfo
- Publication number
- GB969962A GB969962A GB4031560A GB4031560A GB969962A GB 969962 A GB969962 A GB 969962A GB 4031560 A GB4031560 A GB 4031560A GB 4031560 A GB4031560 A GB 4031560A GB 969962 A GB969962 A GB 969962A
- Authority
- GB
- United Kingdom
- Prior art keywords
- polymers
- poly
- groups
- hydrogen
- acrylamide
- 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
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)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
A fungicidal composition comprises a mixture of a major proportion of zinc ethylenebisdithiocarbamate and a minor proportion, preferably from 0.5 to 10% based on the weight of the zinc compound and in particular from 1-5%, of a cationic, water-dispersible polymer containing a multiplicity of nitrogenous groups and having a molecular weight between about 500 and about 100,000 and preferably not exceeding about 10,000. The polymers may be:- (a) Polyalkylenepolyamines, NH2(CnH2nNH)xH, where n has a value of 2 to 3 and x is an integer over about 12 and may be at least as large as 40; (b) Ureidopolyalkylenepolyamines, <FORM:0969962/A5-A6/1> where x1 and y are integers, the sum of which is at least about 12 (usually 12 to 40), and n has a value of 2 to 3; (c) Methylol derivatives of the above compounds; (d) Polyhydroxypolyalkylenepolyamines <FORM:0969962/A5-A6/2> where x and y are integers yielding a molecular weight of at least 500, usually 500 to 10,000, and n has a value of 2 to 3; (e) Ureidopolyhydroxypolyalkylenepolyamines <FORM:0969962/A5-A6/3> where M represents hydrogen or the -CONH2 group and x, y and z are integers, the sum of which is at least about 12 and may be as high as 40 or more, and n has a value of 2 to 3; (f) Methylol derivatives of the above compounds (d) and (e); (g) Polymers from aminoalkylacrylamides, R1R2NCnH2nNHCOC(R0)=CH2 where R1 and R2 are members of the class consisting of hydrogen and lower alkyl groups, n is an integer from 1 to 3, and R0 is a member of the class consisting of hydrogen and the methyl group. Specified polymers of this type are N - (2 - dimethylaminoethyl)acrylamide, N - (dimethylaminoethylamino - ethyl)acrylamide, N - (3 - dimethylaminopropyl)acrylamide, N - (2 - (3 - dimethylaminopropyl) aminoethyl) acrylamide, or N-3-diethylamino-propyl)acrylamide, N - (2 - dimethylaminoethyl) - methacrylamide, N - tert. - butylaminoethylacrylamide, and N - tert. - butylaminoethoxyethylacrylamide. Similar members of this class include polyaminoalkyl-substituted poly(methyl acrylate), formed by reacting poly(methyl acrylate) or poly(methyl methacrylate) with an alkylenepolyamine in excess, such as the ethylenediamine, diethylenetriamine, aminopropylaminoethylamine, aminoethylamino - propylaminoethylamine, <FORM:0969962/A5-A6/4> triethylenetetramine, tetraethylenepentamine. (h) Polymers from polyaminoalkylacrylamides, <FORM:0969962/A5-A6/5> where x is an integer from 1 to 4, n is an integer from 2 to 3, and R1, R2 and R0 are as above; (i) Polymers of aminoalkyl acrylic esters, R1R2NAOOCC(R0)=CH2 where R1 is a member of the class consisting of hydrogen and lower alkyl groups and R2 is a lower alkyl group, A is an alkylene group of 2 to 3 carbon atoms, and R0 is a member of the class consisting of hydrogen and the methyl group; specified polymers of this type are dimethylaminoethyl, dimethylaminopropyl, diethylaminoethyl, or diethylaminopropyl acrylates or methacrylates; (j) Polyvinyl amino resins, <FORM:0969962/A5-A6/6> where m is an integer of at least about 12, R1 and R2 are hydrogen or lower alkyl groups or equivalent groups in which R1 and R2 form a heterocycle as in morpholine or piperidine. Tertiary amine groups may be quaternized. (k) Polyvinyl amino resins, in which the vinyl polymer chain is joined to the amino group through a benzene nucleus or a methylene group (here represented by A), <FORM:0969962/A5-A6/7> (l) Polymers of aminoalkyl vinyl ethers, R1R2NAOCH=CH2 where R1 and R2 are members of the class consisting of hydrogen and lower alkyl groups and A is an alkylene group of 2 to 3 carbon atoms. Specified polymers of this type are poly(dimethylaminoethyl vinyl ether) or poly(N-methylaminoethyl vinyl ether), poly(aminoethyl vinyl ether), or poly(aminopropyl vinyl ether), and the corresponding thioethers. (m) Polyethylene-imine; (n) Ureides from polyethyleneimine; and (o) Methylol derivatives of (m) and (n); (p) Aminolyzed styrene polymers, e.g. by replacing chlorine in chloromethylated polystyrene with polyamine groups as from an alkylenepolyamine. Any of these may also be used in quaternary ammonium salt from or in the form of a slat formed with an acid. Other co-monomers may be used in conjunction with any of the above nitrogenous monomers, which polymerize by addition to form copolymers, the proportion of such other co-monomer or comonomers being adjusted to retain dispersibility in water. Thus, minor proportions of alkyl acrylates or methacrylates, vinyl esters, alkyl fumarates, or alkyl itaconates may be copolymerized. Likewise, copolymers may be formed with two or more nitrogen-containing monomers which polymerize by addition; (q) or a salt of any of the above compounds (a) to (o) may also be used, e.g. hydrochloride, sulphate, acetate or phosphate; (r) or polymers of compounds (g)-(i) may have quaternary ammonium groups in place of some or all of the -NR1R2 groups for example the quaternary salt formed by reacting benzyl chloride with poly - N - (3 - dimethylaminopropyl)acrylamide. U.S.A. Specifications 2,626,874, 2,643,958, 2,742,453, 2,845,408 and German Specification 1,055,810 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US85637359A | 1959-12-01 | 1959-12-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB969962A true GB969962A (en) | 1964-09-16 |
Family
ID=25323447
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4031560A Expired GB969962A (en) | 1959-12-01 | 1960-11-23 | Fungicidal compositions |
Country Status (3)
Country | Link |
---|---|
DE (1) | DE1180997B (en) |
ES (1) | ES262876A1 (en) |
GB (1) | GB969962A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2753602A1 (en) * | 1996-09-26 | 1998-03-27 | Rhone Poulenc Agrochimie | Agrochemical compositions for treating rice seeds |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2098942A (en) * | 1935-06-18 | 1937-11-16 | Du Pont | Protection of materials subject to parasitic attack |
CH264213A (en) * | 1943-12-30 | 1949-10-15 | Ciba Geigy | Process for the manufacture of preparations to be used as pesticides. |
DE844688C (en) * | 1945-05-15 | 1952-07-24 | Ciba Geigy | Process for the production of spray boilers used for pest control |
CH249068A (en) * | 1945-12-04 | 1947-06-15 | Ciba Geigy | Methods of combating pests. |
GB655427A (en) * | 1946-11-08 | 1951-07-18 | Gen Aniline & Film Corp | Biocidal composition |
GB723627A (en) * | 1952-11-03 | 1955-02-09 | Nat Res Dev | Synthetic resin compositions containing insect attractants or insect repellents |
-
1960
- 1960-11-23 GB GB4031560A patent/GB969962A/en not_active Expired
- 1960-11-23 DE DER29147A patent/DE1180997B/en active Pending
- 1960-11-30 ES ES0262876A patent/ES262876A1/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2753602A1 (en) * | 1996-09-26 | 1998-03-27 | Rhone Poulenc Agrochimie | Agrochemical compositions for treating rice seeds |
ES2129005A1 (en) * | 1996-09-26 | 1999-05-16 | Rhone Poulenc Agrochimie | Composition for the treatment of rice seeds |
AU724106B2 (en) * | 1996-09-26 | 2000-09-14 | Rhone-Poulenc Agro | Composition for the treatment of rice seeds |
US6121193A (en) * | 1996-09-26 | 2000-09-19 | Segaud; Christian | Composition for the treatment of rice seeds |
Also Published As
Publication number | Publication date |
---|---|
ES262876A1 (en) | 1961-06-01 |
DE1180997B (en) | 1964-11-05 |
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