[go: up one dir, main page]

GB985484A - New triazine compounds - Google Patents

New triazine compounds

Info

Publication number
GB985484A
GB985484A GB43243/61A GB4324361A GB985484A GB 985484 A GB985484 A GB 985484A GB 43243/61 A GB43243/61 A GB 43243/61A GB 4324361 A GB4324361 A GB 4324361A GB 985484 A GB985484 A GB 985484A
Authority
GB
United Kingdom
Prior art keywords
substituted
alkoxy
alkylthio
aryloxy
groups
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
GB43243/61A
Inventor
John Reginald Atkinson
Sidney Hartley
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 GB43243/61A priority Critical patent/GB985484A/en
Priority to CH1417862A priority patent/CH437324A/en
Priority to CH1731166A priority patent/CH443324A/en
Priority to FR917547A priority patent/FR1345260A/en
Publication of GB985484A publication Critical patent/GB985484A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D251/00Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/14Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
    • C07D251/16Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D251/00Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D251/14Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
    • C07D251/16Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
    • C07D251/20Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom with no nitrogen atoms directly attached to a ring carbon atom
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B6/00Anthracene dyes not provided for above
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00Systems containing at least three condensed rings
    • C07C2603/02Ortho- or ortho- and peri-condensed systems
    • C07C2603/04Ortho- or ortho- and peri-condensed systems containing three rings
    • C07C2603/22Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
    • C07C2603/24Anthracenes; Hydrogenated anthracenes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

The invention comprises triazine brightening agents of the formula <FORM:0985484/C2/1> wherein A represents a polycyclic aromatic group containing at least three condensed rings, R1 represents a chloro, substituted amino, alkoxy, substituted alkoxy, aryloxy, alkylthio or substituted alkylthio group, and R2 represents a substituted amino, alkoxy, substituted alkoxy, aryloxy, alkythio, or substituted alkythio group. The above compounds may be prepared by reacting a triazine of the formula <FORM:0985484/C2/2> with one or more molecular proportions of an amine or substituted amine in the presence of an acid binding agent (which may be excess of amine reactant), or of the sodium derivative of an alcohol, substituted alcohol, phenol, mercaptan or substituted mercaptan. Specified polycyclic aromatic groups are those derived from pyrene, anthracene, acenaphthene and chrysene. Substituted amino groups include hydroxyalkylamino, sulphoarylamino, morpholino, alkylamino, arylamino, sulphatoalkylamino and acetoxyalkylamino groups. Substituted alkoxy groups include hydroxyalkoxy groups. Substituted alkylthio groups include carboxyalkylthio groups. The dichlorotriazine starting materials are prepared by reacting an appropriate hydrocarbon A-H with cyanuric chloride in the presence of anhydrous aluminium chloride.ALSO:Polymeric materials such as polyamides (e.g. nylon), polyesters (e.g. polyethylene terephthalate) and polyurethanes, are brightened by addition to the molton or plasticized form thereof of triazines of the formula:- <FORM:0985484/C3/1> wherein A represents a polycyclic aromatic group containing at least three condensed rings, R1 represents a chloro, substituted amino, alkoxy, substituted alkoxy, aryloxy, alkylthio or substituted alkylthio group, and R2 represents a substituted amino, alkoxy, substituted alkoxy, aryloxy, alkylthio or substituted alkylthio group.ALSO:Soaps or detergents such as fatty alcohol ethylene oxide condensates or sulphonated alkylnaphthalenes may contain triazine brightening agents of the formula <FORM:0985484/C4-C5/1> wherein A represents a polycyclic aromatic group containing at least three condensed rings, R1 represents a chloro, substituted amino, alkoxy, substituted alkoxy, aryloxy, alkylthio or substituted alkylthio group, and R2 represents a substituted amino, alkoxy, substituted alkoxy, aryloxy, alkylthio or substituted alkylthio group.ALSO:Paper and fibres formed from cotton, silk, wool, secondary cellulose acetate, cellulose triacetate, regenerated cellulose, nylon, polyethylene terephthalate, polyurethanes, polyacrylonitrile, hydrolysed polyacrylonitrile, poly (methyl methacrylate), polystyrene, polyethylene and polypropylene are brightened by treatment at temperatures of between 60 DEG C. and 100 DEG C. with an aqueous suspension of a triazine compound of the formula:- <FORM:0985484/D1-D2/1> wherein A represents a polycyclic aromatic group containing at least three condensed rings, R1 represents a chloro, substituted amino, alkoxy, substituted alkoxy, aryloxy, alkylthio or substituted alkylthio group, and R2 represents a substituted amino, alkoxy, substituted alkoxy, aryloxy, alkylthio or substituted alkylthio group, or a water-soluble salt thereof. The materials to be brightened may alternatively be padded at room temperature with the aqueous suspension of brightening agent and subsequently dried by heating to between 150 DEG and 200 DEG C. in air for a short period such as 20 to 30 seconds. Specified polycyclic aromatic groups are those derived from pyrene, anthracene, acenaphthene and chrysene. Substituted amino groups include hydroxyalkyl-amino, sulphoarylamino, morpholino, alkylamino, arylamino, sulphatoalkylamino and acetoxyalkylamino. Substituted alkoxy groups include hydroxyalkoxy groups. Substituted alkylthio groups include carboxyalkylthio groups. The above brightening agents may be used in conjunction with other brightening agents, for example substituted 4,41-ditriazinylamino-stilbene-2, 21-disulphonic acids, and also in conjunction with soaps and detergents such as fatty alcohol ethylene oxide condensates and sulphonated alkylnaphthalenes.
GB43243/61A 1961-12-04 1961-12-04 New triazine compounds Expired GB985484A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
GB43243/61A GB985484A (en) 1961-12-04 1961-12-04 New triazine compounds
CH1417862A CH437324A (en) 1961-12-04 1962-12-03 Process for the preparation of new triazine compounds
CH1731166A CH443324A (en) 1961-12-04 1962-12-03 Process for the preparation of new triazine compounds
FR917547A FR1345260A (en) 1961-12-04 1962-12-04 New substituted polycyclo-triazines, production and applications

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB43243/61A GB985484A (en) 1961-12-04 1961-12-04 New triazine compounds

Publications (1)

Publication Number Publication Date
GB985484A true GB985484A (en) 1965-03-10

Family

ID=10427891

Family Applications (1)

Application Number Title Priority Date Filing Date
GB43243/61A Expired GB985484A (en) 1961-12-04 1961-12-04 New triazine compounds

Country Status (2)

Country Link
CH (2) CH437324A (en)
GB (1) GB985484A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0020817A1 (en) * 1979-06-08 1981-01-07 Bayer Ag Process for the preparation of pyrene compounds
US4675402A (en) * 1984-10-13 1987-06-23 Hoechst Aktiengesellschaft Process for the preparation of dialkoxytriazinylpyrenes
US10982391B2 (en) 2016-06-01 2021-04-20 Ecolab Usa Inc. High-efficiency strength program used for making paper in higher charge demand system
CN116196898A (en) * 2023-02-23 2023-06-02 郑州师范学院 Nanometer ferroferric oxide-cyclodextrin hydrogel adsorbent and preparation method thereof

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0020817A1 (en) * 1979-06-08 1981-01-07 Bayer Ag Process for the preparation of pyrene compounds
US4675402A (en) * 1984-10-13 1987-06-23 Hoechst Aktiengesellschaft Process for the preparation of dialkoxytriazinylpyrenes
US10982391B2 (en) 2016-06-01 2021-04-20 Ecolab Usa Inc. High-efficiency strength program used for making paper in higher charge demand system
CN116196898A (en) * 2023-02-23 2023-06-02 郑州师范学院 Nanometer ferroferric oxide-cyclodextrin hydrogel adsorbent and preparation method thereof

Also Published As

Publication number Publication date
CH443324A (en) 1967-09-15
CH437324A (en) 1967-06-15

Similar Documents

Publication Publication Date Title
GB951445A (en) Process for the manufacture of surface-active agents on the basis of derivatives of polyalkylene glycols
US3310564A (en) Novel 4-alkoxy naphthalimides
GB965006A (en) Anthraquinone dyestuffs free from acid groups imparting water-solubility and a process for their manufacture
GB1059256A (en) Fluorescent, practically colourless, benzimidazole and benzoxazole derivatives
GB1120463A (en) Derivatives of 1,3-diazafluoranthene-1-oxide
GB985484A (en) New triazine compounds
GB888209A (en) 2:5-di[-benzimidazyl-(2)]-furanes
GB897757A (en) 1, 3-di-methylol-4, 5-bis(alkoxy)-2-imidazolidinones and use of the same
GB853129A (en) New pyrrolo derivatives and process for their manufacture
GB624052A (en) Stilbene derivatives for use in whitening textile materials
US2976288A (en) Triazine derivatives
US3157651A (en) Triazine compounds
GB982196A (en) Process for the optical brightening of cellulose material and material brightened thereby
GB1055183A (en) Benzoxazole drivatives and their use as optical brighteners
US3074963A (en) Derivatives of p-[coumarinyl-(3)]-phenyl-carbamic acid
GB961078A (en) New disazo-dyestuffs and their manufacture and use
KR20000027195A (en) Nitrogen-containing phosphoric acid ester based flame retarder having wide range of flame resistance effect
US3522265A (en) 1,2-benzisothiazolone antimicrobial preparations
GB1023205A (en) -triazino(5,6-6) indoles
GB855022A (en) Improvements in and relating to carbostyril derivatives
GB1033385A (en) Di-arylene azolyl styrene compounds and their use as optical brightening agents
GB1049149A (en) Coumarin compounds
GB1016365A (en) New azolyl-thiophene derivatives, process for their preparation and their use
GB1010231A (en) Substituted 3-phenyl-5-imino-4,5 dihydro-1,2,4-oxadiazoles, process for their manufacture and therapeutic compositions containing same
GB1077177A (en) New benzthiazole compounds and their application