GB469022A - New fungicidal and bactericidal agents - Google Patents

New fungicidal and bactericidal agents

Info

Publication number
GB469022A
GB469022A GB136036A GB136036A GB469022A GB 469022 A GB469022 A GB 469022A GB 136036 A GB136036 A GB 136036A GB 136036 A GB136036 A GB 136036A GB 469022 A GB469022 A GB 469022A
Authority
GB
United Kingdom
Prior art keywords
ether
mercuric
parts
mercury
ethyleneglycol
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
GB136036A
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB136036A priority Critical patent/GB469022A/en
Publication of GB469022A publication Critical patent/GB469022A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F3/00Compounds containing elements of Groups 2 or 12 of the Periodic System
    • C07F3/10Mercury compounds

Abstract

Organo-mercury compounds of the formula R--[O--Alk]n--O--C2H2R<1>2--Hg--X in which R represents alkyl or aralkyl, R<1> signifies hydrogen, alkyl or aryl, n is 1 or 2, Alk stands for an alkylene residue and X represents hydroxyl or a salt-forming group, are prepared by reacting a mercuric salt, or mercuric oxide and a mercuric acid, with an olefinic compound C2H2R<1>2 in the presence of an ether-alcohol R--[O--Alk]n--OH containing no halogen. The mercuric salt may be formed in situ from yellow mercuric oxide and an acid, and the residue X may be exchanged by double decomposition. The products are useful as fungicidal and bactericidal agents and may be applied, either as dusts in admixture with carriers such as talc or in the form of aqueous solutions or dispersions. Examples are given of the interaction of (1) ethyleneglycol monoethyl ether, ethylene, and mercury acetate; instead of the said ether, ethyleneglycol monomethyl or monobutyl ether or diethyleneglycol monoethyl ether may be used and yellow mercuric oxide may be employed in addition to mercuric acetate; treatment of the product with sodium chloride yields the corresponding mercury chloride compound; (2) ethyleneglycol monoethyl ether, ethylene, yellow mercuric oxide and glacial acetic acid; (3) ethyleneglycol monomethyl or monoethyl ether, propylene, mercuric acetate and yellow mercuric oxide; addition of brine forms the chloride of the product; (4) ethyleneglycol monobenzyl ether, ethylene, yellow mercuric oxide and glacial acetic acid; the product is treated with brine; (5) ethyleneglycol monoethyl ether, styrene and mercuric acetate, and reaction of the product with oxalic acid. Other olefines mentioned are butylene and phenylethylene, and as ether alcohols diethyleneglycol monomethyl ether and trimethyleneglycol monoethyl ether are also specified. Reference is made to a dust composition for treating oats comprising 3 parts by weight of the organo-mercury compound, 3 parts of glycerine and 94 parts of talc. Specifications 335,527, [Class 81 (i)], 411,507, and 427,974 are referred to.ALSO:Compositions for the immunization or preservation of seeds, bulbs, tubers, corns, &c. consist of organo-mercury compounds of the formula R-[O-Alk]n-O-C2H2R12-Hg-X in which R represents alkyl or aralkyl, R1 signifies hydrogen, alkyl or aryl, n is 1 or 2, Alk stands for an alkylene residue and X represents hydroxyl or a salt-forming group, together with an inert carrier such as talc, or comprise an aqueous solution or dispersion of the organo-mercury compound containing wetting and spreading agents. Thus, a mixture of 3 parts by weight of organo-mercury compound, 3 parts of glycerine and 94 parts of talc may be used for the treatment of oat seed infected with leaf stripe.
GB136036A 1936-01-15 1936-01-15 New fungicidal and bactericidal agents Expired GB469022A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB136036A GB469022A (en) 1936-01-15 1936-01-15 New fungicidal and bactericidal agents

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB136036A GB469022A (en) 1936-01-15 1936-01-15 New fungicidal and bactericidal agents

Publications (1)

Publication Number Publication Date
GB469022A true GB469022A (en) 1937-07-15

Family

ID=9720661

Family Applications (1)

Application Number Title Priority Date Filing Date
GB136036A Expired GB469022A (en) 1936-01-15 1936-01-15 New fungicidal and bactericidal agents

Country Status (1)

Country Link
GB (1) GB469022A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3058877A (en) * 1960-09-09 1962-10-16 Chicopee Mfg Corp Germicidal, bactericidal and fungicidal compositions

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3058877A (en) * 1960-09-09 1962-10-16 Chicopee Mfg Corp Germicidal, bactericidal and fungicidal compositions

Similar Documents

Publication Publication Date Title
GB469022A (en) New fungicidal and bactericidal agents
DE1618985B2 (en) 4-ACETOXY ALKYLBENZYLIDENMALONIC ACID DINITRILE, THE METHOD OF MANUFACTURING IT AND THE FUNGICIDAL AGENTS CONTAINING IT
US3711477A (en) 5-amino-1,2,3-trithianes
US2273443A (en) Organic mercury compound
US2220981A (en) Fungicide
Bost et al. Sulfur studies. XVI. The synthesis of certain higher alkyl sulfonium salts and related compounds
US2875126A (en) New esters of 5-acyl-8-hydroxyquinolines and their use for the control of fungi
US2251778A (en) Mono-(organo mercury) acetylides
US2402016A (en) Sulphonium salts
US2121724A (en) aralkyl ethers of ethyl-phenol
US2555024A (en) Lauryl pyridinium 2-(5-chlorobenzothiazyl)-sulfide
US2145595A (en) Organic mercury compounds and a method of making the same
US2329884A (en) Method of preventing growth of fungi
US2356884A (en) Mercurated aliphatic amines
US1760781A (en) Manufacture of new pharmaceutical products
US2056945A (en) Aromatic mercury alcoholates of hydroxy fatty compounds
US1901316A (en) Process of preparing tribromoethyl alcohol
US2844508A (en) Substituted mercuric 8-hydroxy quinolinates
US2875122A (en) Fungicide
US2499417A (en) Trialkyl ammonium halides of benzhydryl-aminoethyl ether
US2471622A (en) Mercury compounds and process of preparing same
US2948727A (en) Thiobispiperazines
US1526627A (en) Iodine compound
US2553774A (en) N-thiotrichloromethyl morpholine and fungicidal compositions containing same
US2154488A (en) Preparation of aracyl persulphides