GB886381A - Monoazo dyestuffs containing haloacylamino groups - Google Patents

Monoazo dyestuffs containing haloacylamino groups

Info

Publication number
GB886381A
GB886381A GB3284060A GB3284060A GB886381A GB 886381 A GB886381 A GB 886381A GB 3284060 A GB3284060 A GB 3284060A GB 3284060 A GB3284060 A GB 3284060A GB 886381 A GB886381 A GB 886381A
Authority
GB
United Kingdom
Prior art keywords
benzene
amino
dyes
chloropropionylamino
specified
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
GB3284060A
Inventor
Richard Fleischhauer
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.)
Cassella Farbwerke Mainkur AG
Original Assignee
Cassella Farbwerke Mainkur 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 Cassella Farbwerke Mainkur AG filed Critical Cassella Farbwerke Mainkur AG
Priority to GB3284060A priority Critical patent/GB886381A/en
Publication of GB886381A publication Critical patent/GB886381A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M159/00—Lubricating compositions characterised by the additive being of unknown or incompletely defined constitution
    • C10M159/005—Macromolecular compounds, e.g. macromolecular compounds composed of alternatively specified monomers not covered by the same main group
    • 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
    • C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
    • C09B62/44—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
    • C09B62/465—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring the reactive group being an acryloyl group, a quaternised or non-quaternised aminoalkyl carbonyl group or a (—N)n—CO—A—O—X or (—N)n—CO—A—Hal group, wherein A is an alkylene or alkylidene group, X is hydrogen or an acyl radical of an organic or inorganic acid, Hal is a halogen atom, and n is 0 or 1
    • C09B62/47—Azo dyes
    • C09B62/473—Monoazo dyes

Abstract

The invention comprises dyes of formula <FORM:0886381/IV (c)/1> where R is H or an alkyl, cycloalkyl, aralkyl or substituted or unsubstituted benzene residue, Z is SO3H or COOH and the aryl residue is of the benzene series. The dyes are made in conventional fashion from appropriate aniline diazo, and naphthol coupling, components, coupling being effected in acid media. Cl, Br and I are specified halogens. Representative of specified diazo components are 1-amino-3- and - 4 - (b - chloropropionylamino) - benzene - 6 - sulphonic and -carboxylic acids, 1-amino-3-(b -bromo- and -iodo-propionylamino)-benzene-6-sulphonic acids, 1-amino-4-(b -chloropropionylamino)-3-chlorobenzene-6-carboxylic acid and 1 - amino - 3 - (b - chloropropionylamino) - 4 - methyl-, -methoxy- and -chloro-benzene-6-sulphonic acids. Representative of specified values for R are methyl, isopropyl, n-butyl, cyclohexyl, benzyl and phenyl. The dyes colour cotton bluish-red shades, steaming in the presence of an acid-binding agent being required. An example is provided of the preparation of the dyes and their use in colouring processes. Specifications 545,806 and 868,492 also are referred to.
GB3284060A 1958-02-27 1958-02-27 Monoazo dyestuffs containing haloacylamino groups Expired GB886381A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3284060A GB886381A (en) 1958-02-27 1958-02-27 Monoazo dyestuffs containing haloacylamino groups

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3284060A GB886381A (en) 1958-02-27 1958-02-27 Monoazo dyestuffs containing haloacylamino groups

Publications (1)

Publication Number Publication Date
GB886381A true GB886381A (en) 1962-01-03

Family

ID=10344766

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3284060A Expired GB886381A (en) 1958-02-27 1958-02-27 Monoazo dyestuffs containing haloacylamino groups

Country Status (1)

Country Link
GB (1) GB886381A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2393834A1 (en) * 1977-06-08 1979-01-05 Ici Ltd NEW REAGENT COLORS CONTAINING THE RESIDUE OF 1-HYDROXY-7-AMINO-8- (5'-AMINO-2 ', 4'-DISULFOPHENYLAZO) NAPHTHALENE-3,6-DISULFONIC, THEIR PRODUCTION PROCESS AND THEIR TINCTORIAL APPLICATIONS

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2393834A1 (en) * 1977-06-08 1979-01-05 Ici Ltd NEW REAGENT COLORS CONTAINING THE RESIDUE OF 1-HYDROXY-7-AMINO-8- (5'-AMINO-2 ', 4'-DISULFOPHENYLAZO) NAPHTHALENE-3,6-DISULFONIC, THEIR PRODUCTION PROCESS AND THEIR TINCTORIAL APPLICATIONS

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