GB976528A - Treatment of synthetic products for rendering them antibacterial and antimycotic - Google Patents
Treatment of synthetic products for rendering them antibacterial and antimycoticInfo
- Publication number
- GB976528A GB976528A GB2134062A GB2134062A GB976528A GB 976528 A GB976528 A GB 976528A GB 2134062 A GB2134062 A GB 2134062A GB 2134062 A GB2134062 A GB 2134062A GB 976528 A GB976528 A GB 976528A
- Authority
- GB
- United Kingdom
- Prior art keywords
- agents
- carbon atoms
- group containing
- emulsions
- synthetic resins
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/30—Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- Environmental Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Biochemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Textile Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Synthetic resins and cellulose esters are rendered antibacterial and antimycotic by applying to or incorporating therein a compound of the general formula: <FORM:0976528/C3/1> in which X represents oxygen or sulphur, and R represents a phenyl group that may be substituted by at least one halogen atom or an alkyl or alkoxy group containing 1 to 4 carbon atoms or at least one -CF3, -OH, -NO2, -CN, -SCN, -SO3H, -SR1, -SO2R1, <FORM:0976528/C3/2> , -COOA, <FORM:0976528/C3/3> or <FORM:0976528/C3/4> group, in which R1 represents an alkyl group containing 1 to 4 carbon atoms, and A and A1 each represent a hydrogen atom or an alkyl group containing 1 to 4 carbon atoms. Numerous resins are specified typical examples of which are polyvinylchloride and nylon. In an example a vinyl resin lacquer comprising PVC, dioctyl phthalate, methyl ethyl ketone ketone is rendered antimicrobial by mixing it with 3,31,4-tri-(trifluoromethyl)-41-chloro-N,N1 -diphenyl thio-urea in acetone solution. The synthetic resins and cellulose esters may be in the form of textile or non textile fibres, castings, stratified structures, coatings foils, emulsions and solutions. The active materials may be mixed with the monomers or precondensates and are advantageously dissolved in plasticizers e.g. the dialkyl adipates and phthalates, aliphatic sulphonic acid esters and triglycol acetate. Fibrous materials may be treated by spraying, immersion or absorption from an aqueous bath preferably containing surface active agents. The active compounds may be used in the form of pastes, powders, emulsions, suspensions solutions emulsion concentrates or wettable powders which may contain (i) anionic, non-ionic or cationic surface active agents (2) dyestuffs, pigments, matting agents, optical brightening agents, softening agents, antioxidants and (3) insecticides, acaricides or bactericides such as 3:4-dichlorobenzyl alcohol, cetyl pyridinium chloride, cetyltrimethyl-ammonium bromide, tetra-methyl thiuram-disulphide, salicylanilides dichloro-, dibromo-, tribromo- and tetrachlorosalicylanilides and 2:21-dihydroxy-3:5:6:31:51:61 -hexachloro-diphenyl methane.ALSO:Synthetic resins and cellulose esters are rendered antibacterial and antimycotic by applying to or incorporating therein a compound of the general formula <FORM:0976528/A5-A6/1> in which X represents oxygen or sulphur, and R represents a phenyl group that may be substituted by at least one halogen atom or an alkyl or alkoxy group containing 1 to 4 carbon atoms or at least one -CF3, -OH, -NO2, -CN, -SCN, -SO3H, -SR1, -SO2R1, <FORM:0976528/A5-A6/2> group, in which R1 represents an alkyl group containing 1 to 4 carbon atoms, and A and A1 each represent a hydrogen atom or an alkyl group containing 1 to 4 carbon atoms. Numerous resins are specified typical examples of which are polyvinyl chloride and nylon. In an example a vinyl resin lacquer comprising PVC, dioctyl phthalate, methyl ethyl ketone ketone is rendered antimicrobial by mixing it with 3,31,4 - tri - (trifluoromethyl) - 41 - chloro N,N1-diphenyl thiourea in acetone solution. The synthetic resins and cellulose esters may be in the form of textile or non-textile fibres, castings, stratified structures, coatings, foils, emulsions and solutions. The active materials may be mixed with the monomers or precondensates and are advantageously dissolved in plasticizers, e.g. the dialkyl adipates and phthalates, aliphatic sulphonic acid esters and triglycol acetate. Fibrous materials may be treated by spraying, immersion or absorption from an aqueous bath preferably containing surface active agents. The active compounds may be used in the form of pastes, powders, emulsions, suspensions solutions emulsion concentrates or wettable powders which may contain (i) anionic, non-ionic or cationic surface active agents; (2) dyestuffs, pigments, matting agents, optical brightening agents, softening agents, antioxidants; and (3) insecticides, acaricides or bactericides such as 3 : 4-dichlorobenzyl alcohol, cetyl pyridinium chloride, cetyl-trimethyl-ammonium bromide, tetra-methyl thiuram-disulphide, salicylanilides, dichloro-, dibromo-, tribromo- and tetrachloro-salicylanilides and 2 : 21-dihydroxy - 3 : 5 : 6 : 31 : 51 : 61 - hexachloro-diphenyl methane.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2134062A GB976528A (en) | 1962-06-01 | 1962-06-01 | Treatment of synthetic products for rendering them antibacterial and antimycotic |
US199660A US3200035A (en) | 1962-06-01 | 1962-06-04 | Treatment of synthetic products, especially synthetic fibers |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2134062A GB976528A (en) | 1962-06-01 | 1962-06-01 | Treatment of synthetic products for rendering them antibacterial and antimycotic |
Publications (1)
Publication Number | Publication Date |
---|---|
GB976528A true GB976528A (en) | 1964-11-25 |
Family
ID=10161232
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2134062A Expired GB976528A (en) | 1962-06-01 | 1962-06-01 | Treatment of synthetic products for rendering them antibacterial and antimycotic |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB976528A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CZ297581B6 (en) * | 2005-05-26 | 2007-01-10 | Universita Karlova v Praze, Farmaceutická fakulta v Hradci Králové | Antimycotic and antimycobacterial thiosalicylanilides and process of their preparation |
WO2008039999A1 (en) * | 2006-09-28 | 2008-04-03 | Arete Therapeutics, Inc. | Soluble epoxide hydrolase inhibitors |
WO2012021963A1 (en) * | 2010-07-09 | 2012-02-23 | Metasignal Therapeutics Inc. | Novel sulfonamide compounds for inhibition of metastatic tumor growth |
-
1962
- 1962-06-01 GB GB2134062A patent/GB976528A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CZ297581B6 (en) * | 2005-05-26 | 2007-01-10 | Universita Karlova v Praze, Farmaceutická fakulta v Hradci Králové | Antimycotic and antimycobacterial thiosalicylanilides and process of their preparation |
WO2008039999A1 (en) * | 2006-09-28 | 2008-04-03 | Arete Therapeutics, Inc. | Soluble epoxide hydrolase inhibitors |
WO2012021963A1 (en) * | 2010-07-09 | 2012-02-23 | Metasignal Therapeutics Inc. | Novel sulfonamide compounds for inhibition of metastatic tumor growth |
CN103221388A (en) * | 2010-07-09 | 2013-07-24 | 玛特辛格纳治疗股份有限公司 | Novel sulfonamide compounds for inhibition of metastatic tumor growth |
CN103221388B (en) * | 2010-07-09 | 2016-09-28 | 维理生物技术公司 | For the novel sulfonamide compounds suppressing metastatic tumo(u)r to grow |
US9463171B2 (en) | 2010-07-09 | 2016-10-11 | Welichem Biotech Inc. | Sulfonamide compounds for inhibition of metastatic tumor growth |
US9962398B2 (en) | 2010-07-09 | 2018-05-08 | Welichem Biotech Inc. | Sulfonamide compounds for inhibition of metastatic tumor growth |
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