GB976528A - Treatment of synthetic products for rendering them antibacterial and antimycotic - Google Patents

Treatment of synthetic products for rendering them antibacterial and antimycotic

Info

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
Application number
GB2134062A
Inventor
Henry Martin
Andreas Ruperti
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.)
BASF Schweiz AG
Original Assignee
Ciba AG
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 Ciba AG filed Critical Ciba AG
Priority to GB2134062A priority Critical patent/GB976528A/en
Priority to US199660A priority patent/US3200035A/en
Publication of GB976528A publication Critical patent/GB976528A/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
    • A01N47/00Biocides, 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
    • A01N47/08Biocides, 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
    • A01N47/28Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/30Derivatives containing the group >N—CO—N aryl or >N—CS—N—aryl
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M16/00Biochemical 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.
GB2134062A 1962-06-01 1962-06-01 Treatment of synthetic products for rendering them antibacterial and antimycotic Expired GB976528A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (7)

* Cited by examiner, † Cited by third party
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

Similar Documents

Publication Publication Date Title
US3133916A (en) -ch chj
DE1543701A1 (en) Alkanolamine derivatives and processes for their preparation
GB947981A (en) New thiophene derivatives
DE2704825C3 (en) Fluorescent dyes, processes for their production and their use for tinting organic materials white
GB976528A (en) Treatment of synthetic products for rendering them antibacterial and antimycotic
GB925320A (en) Fungicidal compositions containing benzimidazole derivatives
GB1013454A (en) Sulphone-substituted derivatives of pyrazoline
GB1274786A (en) New azole compounds, processes for their manufacture and their use
GB1283095A (en) Acidic zinc electrolytes
GB1588447A (en) Brightener mixtures
EP0359039A3 (en) Process for the wash-and-wear finishing of textiles
GB974111A (en) Organic compositions incorporating ultra-violet light absorbers
AT225663B (en) Optical brighteners
GB1201719A (en) Triazinylaminocoumarin compounds
GB1178778A (en) Finishing Cellulosic Fibrous Material
GB1121905A (en) Chelate-forming polyfluorinated ketones, alcohols and esters
GB906960A (en) Process for brightening fibrous materials
DE2133655B2 (en) Color photographic recording material
US4462925A (en) Stable solutions of optical brighteners
AT230838B (en) Optical brighteners
DE1670852B2 (en) 5-ARYLOTRIAZOLYL-2-STYRYLBENZOTRIAZOLES
GB1350939A (en) Styryltriazoles their use for the optical brightening or organic materials and processes for their manufacture
AT233526B (en) Protective agent against ultraviolet radiation
EP0173932A3 (en) Hair dyeing composition
GB1218168A (en) Finishing agent for textile material