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GB969962A - Fungicidal compositions - Google Patents

Fungicidal compositions

Info

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
Application number
GB4031560A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Rohm and Haas Co
Original Assignee
Rohm and Haas Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Rohm and Haas Co filed Critical Rohm and Haas Co
Publication of GB969962A publication Critical patent/GB969962A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N25/00Biocides, 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
    • A01N25/30Biocides, 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.
GB4031560A 1959-12-01 1960-11-23 Fungicidal compositions Expired GB969962A (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Cited By (4)

* Cited by examiner, † Cited by third party
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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