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GB1530486A - Quaternised 1-(pyrazolinylphenylsulphonyl)-piperazines - Google Patents

Quaternised 1-(pyrazolinylphenylsulphonyl)-piperazines

Info

Publication number
GB1530486A
GB1530486A GB9026/76A GB902676A GB1530486A GB 1530486 A GB1530486 A GB 1530486A GB 9026/76 A GB9026/76 A GB 9026/76A GB 902676 A GB902676 A GB 902676A GB 1530486 A GB1530486 A GB 1530486A
Authority
GB
United Kingdom
Prior art keywords
radical
alkyl
represents hydrogen
unsubstituted
carbon atoms
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
GB9026/76A
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.)
Novartis AG
Original Assignee
Ciba Geigy 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 Geigy AG filed Critical Ciba Geigy AG
Publication of GB1530486A publication Critical patent/GB1530486A/en
Expired legal-status Critical Current

Links

Classifications

    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02—Charge-receiving layers
    • G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
    • G03G5/0622—Heterocyclic compounds
    • G03G5/0644—Heterocyclic compounds containing two or more hetero rings
    • G03G5/0661—Heterocyclic compounds containing two or more hetero rings in different ring systems, each system containing at least one hetero ring
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
    • D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
    • D06L4/60—Optical bleaching or brightening
    • G—PHYSICS
    • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00—Photosensitive materials
    • G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/815—Photosensitive materials characterised by the base or auxiliary layers characterised by means for filtering or absorbing ultraviolet light, e.g. optical bleaching
    • G03C1/8155—Organic compounds therefor
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01S—DEVICES USING THE PROCESS OF LIGHT AMPLIFICATION BY STIMULATED EMISSION OF RADIATION [LASER] TO AMPLIFY OR GENERATE LIGHT; DEVICES USING STIMULATED EMISSION OF ELECTROMAGNETIC RADIATION IN WAVE RANGES OTHER THAN OPTICAL
    • H01S3/00—Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range
    • H01S3/14—Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range characterised by the material used as the active medium
    • H01S3/20—Liquids
    • H—ELECTRICITY
    • H01—ELECTRIC ELEMENTS
    • H01S—DEVICES USING THE PROCESS OF LIGHT AMPLIFICATION BY STIMULATED EMISSION OF RADIATION [LASER] TO AMPLIFY OR GENERATE LIGHT; DEVICES USING STIMULATED EMISSION OF ELECTROMAGNETIC RADIATION IN WAVE RANGES OTHER THAN OPTICAL
    • H01S3/00—Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range
    • H01S3/14—Lasers, i.e. devices using stimulated emission of electromagnetic radiation in the infrared, visible or ultraviolet wave range characterised by the material used as the active medium
    • H01S3/20—Liquids
    • H01S3/213—Liquids including an organic dye

Landscapes

  • Physics & Mathematics (AREA)
  • Electromagnetism (AREA)
  • Engineering & Computer Science (AREA)
  • Optics & Photonics (AREA)
  • Plasma & Fusion (AREA)
  • General Physics & Mathematics (AREA)
  • Materials Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Textile Engineering (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Paper (AREA)
  • Detergent Compositions (AREA)

Abstract

1530486 Quaternized 1-(pyrazoliniumphenylsulphonyl)piperazines CIBA GEIGY AG 5 March 1976 [6 March 1975] 9026/76 Heading C2C [Also in Division C5] The invention comprises compounds of general formula wherein the rings A and B optionally have one or more nonchromophoric and nonionic substituents; R 1 represents an unsubstituted or substituted alkyl radical or an alkenyl radical, R 2 represents an unsubstituted or substituted alkyl or aryl radical; R 3 , R 4 , R 5 and R 6 each independently represent hydrogen or halogen, or an alkyl, cycloalkyl, aralkyl or aryl radical; R 7 represents hydrogen, an unsubstituted alkyl or phenyl radical, or a phenyl radical substituted with chlorine, alkyl or alkoxy; R 8 represents hydrogen or alkyl, or together with the o-position of the ring B an ethylene bridge, or R 7 and R 8 together represent a radical of the formula wherein U 1 represents hydrogen or cyano, U 2 represents hydrogen, cyano, carboxy, carbalkoxy having 2 to 5 carbon atoms, hydroxysubstituted carbalkoxy having 2 to 5 carbon atoms, or carbamoyl, and U 3 represents hydrogen or carbalkoxy having 2 to 5 carbon atoms, or U 2 and U 3 together represent a fusedon benzene radical; and Y represents halogen, an alkyl sulphate radical or a phenylsulphonate radical which is unsubstituted or substituted by halogen and/or an alkyl radical having 1 to 4 carbon atoms. These compounds are prepared by quaternizing a compound of formula with a compound R 1 Y. The compounds are optical brighteners and may be used for treating textiles.
GB9026/76A 1975-03-06 1976-03-05 Quaternised 1-(pyrazolinylphenylsulphonyl)-piperazines Expired GB1530486A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH284975A CH603880B5 (en) 1975-03-06 1975-03-06

Publications (1)

Publication Number Publication Date
GB1530486A true GB1530486A (en) 1978-11-01

Family

ID=4242959

Family Applications (1)

Application Number Title Priority Date Filing Date
GB9026/76A Expired GB1530486A (en) 1975-03-06 1976-03-05 Quaternised 1-(pyrazolinylphenylsulphonyl)-piperazines

Country Status (9)

Country Link
JP (1) JPS51113885A (en)
BE (1) BE839228A (en)
BR (1) BR7601362A (en)
CH (2) CH603880B5 (en)
DE (1) DE2608648A1 (en)
ES (2) ES445795A1 (en)
FR (1) FR2303012A1 (en)
GB (1) GB1530486A (en)
NL (1) NL7602215A (en)

Also Published As

Publication number Publication date
BE839228A (en) 1976-09-06
DE2608648A1 (en) 1976-09-16
FR2303012B1 (en) 1978-05-19
ES445795A1 (en) 1977-06-01
BR7601362A (en) 1976-09-14
NL7602215A (en) 1976-09-08
CH603880B5 (en) 1978-08-31
CH284975A4 (en) 1977-08-31
JPS51113885A (en) 1976-10-07
FR2303012A1 (en) 1976-10-01
ES451274A1 (en) 1978-10-16

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Legal Events

Date Code Title Description
PS Patent sealed
49R Reference inserted (sect. 9/1949)
SP Amendment (slips) printed
PCNP Patent ceased through non-payment of renewal fee