GB1452322A - Disperse monoazo dyestuffs - Google Patents

Disperse monoazo dyestuffs

Info

Publication number
GB1452322A
GB1452322A GB3371873A GB3371873A GB1452322A GB 1452322 A GB1452322 A GB 1452322A GB 3371873 A GB3371873 A GB 3371873A GB 3371873 A GB3371873 A GB 3371873A GB 1452322 A GB1452322 A GB 1452322A
Authority
GB
United Kingdom
Prior art keywords
alkyl
aminobenzenesulphonamides
monoazo dyestuffs
disperse monoazo
disperse
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
GB3371873A
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 GB3371873A priority Critical patent/GB1452322A/en
Priority to NL7409526A priority patent/NL7409526A/en
Priority to CH972874A priority patent/CH584264A5/xx
Priority to JP8162974A priority patent/JPS5028530A/ja
Priority to DE19742434228 priority patent/DE2434228A1/en
Priority to ES428300A priority patent/ES428300A2/en
Publication of GB1452322A publication Critical patent/GB1452322A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00—Monoazo dyes prepared by diazotising and coupling
    • C09B29/34—Monoazo dyes prepared by diazotising and coupling from other coupling components
    • C09B29/36—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
    • C09B29/3604—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom
    • C09B29/3617—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom
    • C09B29/3621—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring
    • C09B29/3626—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring from a pyridine ring containing one or more hydroxyl groups (or = O)
    • C09B29/363—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring from a pyridine ring containing one or more hydroxyl groups (or = O) from diazotized amino carbocyclic rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Abstract

1452322 Aminobenzenesulphonamides IMPERIAL CHEMICAL INDUSTRIES Ltd 4 June 1974 [16 July 1973] 33718/73 Addition to 1,256,093 Heading C2C [Also in Division C4] Aminobenzenesulphonamides of formula (where R 1 is H 1 alkyl, aryl, cycloalkyl or aralkyl; R 2 is alkyl or at least 5 carbon atoms and B may be further substituted by NO 2 , CN, alkyl, alkoxy, Cl, Br, phenyl or phenoxy) are prepared by reacting the corresponding acetylaminobenzenesulphonchlorides with the appropriate amine followed by hydrolysis of the acetyl group.
GB3371873A 1973-07-16 1973-07-16 Disperse monoazo dyestuffs Expired GB1452322A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
GB3371873A GB1452322A (en) 1973-07-16 1973-07-16 Disperse monoazo dyestuffs
NL7409526A NL7409526A (en) 1973-07-16 1974-07-15 PROCEDURES FOR THE PREPARATION AND USE OF MONOAZO DYES.
CH972874A CH584264A5 (en) 1973-07-16 1974-07-15
JP8162974A JPS5028530A (en) 1973-07-16 1974-07-16
DE19742434228 DE2434228A1 (en) 1973-07-16 1974-07-16 DISPERSE Azo Dyes
ES428300A ES428300A2 (en) 1973-07-16 1974-07-16 Disperse monoazo dyestuffs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3371873A GB1452322A (en) 1973-07-16 1973-07-16 Disperse monoazo dyestuffs

Publications (1)

Publication Number Publication Date
GB1452322A true GB1452322A (en) 1976-10-13

Family

ID=10356560

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3371873A Expired GB1452322A (en) 1973-07-16 1973-07-16 Disperse monoazo dyestuffs

Country Status (6)

Country Link
JP (1) JPS5028530A (en)
CH (1) CH584264A5 (en)
DE (1) DE2434228A1 (en)
ES (1) ES428300A2 (en)
GB (1) GB1452322A (en)
NL (1) NL7409526A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4883254A (en) * 1989-03-24 1989-11-28 Sloan Valve Company Flush valve handle assembly

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH585246A5 (en) * 1973-05-17 1977-02-28 Basf Ag

Also Published As

Publication number Publication date
ES428300A2 (en) 1976-11-16
CH584264A5 (en) 1977-01-31
JPS5028530A (en) 1975-03-24
NL7409526A (en) 1975-01-20
DE2434228A1 (en) 1975-02-06

Similar Documents

Publication Publication Date Title
GB1292238A (en) Cationic anthraquinone dyestuffs, process for their manufacture and their use
GB1441056A (en) Phenyl-pyridazines their preparation and use as herbicides
GB1061530A (en) Improvements in or relating to the preparation of organylmercaptoalkyl amines
GB1180616A (en) Improvements in or relating to Hexahydroazepine Compounds and the Manufacture thereof
GB1452322A (en) Disperse monoazo dyestuffs
GB1360279A (en) Styryl compounds processes for theirmanufacture and their use
GB1398638A (en) Furan 2-or 3-carboxylic and amides compositions thereof and methods for using same
GB1474896A (en) Salts of phenylpyridazines and the preparation thereof
GB1359171A (en) Azo dye-stuffs their manufacture and use
GB1507414A (en) Hydantoin derivatives
GB1270784A (en) Processes for carrying out chemical reactions initiated by free-radicals using 1,2-diaryl-1,2-dicyano-ethane compounds as radical initiators
GB1369386A (en) Glycidyl-urethane compounds processes for their manufacture and their use
GB1471479A (en) Nitrothiazole azo compounds
GB1470461A (en) Process fot the manufacture of cyano-substituted bis-styryl compounds
GB1237658A (en) Substituted 1-oxy-1-thiono-3-halogen- or -3-alkyl phospholines
GB1239106A (en)
GB1384609A (en) Substituted n- 3-aminocarbonyloxyphenyl-n,-methylureas
GB1398741A (en) Water-insoluble monoazo dyestuffs
GB1271110A (en) Process for polymerising vinyl compounds using acyl azo compounds as polymerisation catalysts
GB1492683A (en) Chromium complex dyes their manufacture and use
GB1368470A (en) Antiviral compositions containing bisbasic ketones of dibenzofu ran and methods of treating viruses therewith
GB1132665A (en) Acrylonitrile copolymers containing sulphonic groups
GB1325944A (en) Bisoxalic acid diamides
GB1415635A (en) Monoazo dyestuffs their preparation and use for dyeing fibrous materials
GB1471902A (en) Styrylsulphonylamidines

Legal Events

Date Code Title Description
PS Patent sealed
48S Specification amended (sect. 8/1949)
SP Amendment (slips) printed
PE20 Patent expired after termination of 20 years