GB113141A - Manufacture of New Copper Compounds of Substantive Azodyestuffs. - Google Patents

Manufacture of New Copper Compounds of Substantive Azodyestuffs.

Info

Publication number
GB113141A
GB113141A GB1950/17A GB195017A GB113141A GB 113141 A GB113141 A GB 113141A GB 1950/17 A GB1950/17 A GB 1950/17A GB 195017 A GB195017 A GB 195017A GB 113141 A GB113141 A GB 113141A
Authority
GB
United Kingdom
Prior art keywords
acid
phenyl
dianisidine
copper compounds
acetyl
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
GB1950/17A
Inventor
Oliver Imray
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to GB1950/17A priority Critical patent/GB113141A/en
Publication of GB113141A publication Critical patent/GB113141A/en
Expired legal-status Critical Current

Links

Classifications

    • 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
    • C09B35/00Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
    • C09B35/02Disazo dyes
    • C09B35/039Disazo dyes characterised by the tetrazo component
    • C09B35/08Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl
    • C09B35/10Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl from two coupling components of the same type
    • C09B35/16Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of biphenyl from two coupling components of the same type from hydroxy-amines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

113,141. Imray, O., (Soc. of Chemical Industry in Basle). Feb. 8, 1917. Disazo dyes, copper compounds of. The substantive disazo dyes obtained by coupling a tetrazotized p-diamine of the diphenyl series, having at least one alhyloxy group in o-position to an amino group, with one molecular proportion of 2 : 5 : 7-aminonaphthol sulphonic acid or an alkyl, aryl, or acidyl derivative thereof and one molecular proportion of a 1 : 8-aminonaphthol sulphonic acid or a derivative thereof, or with two molecular proportions of 2 : 5 : 7 - acid or a derivative thereof, are converted by treatment with copper or copper compounds into soluble copper compounds which dye cotton, wool, silk, mixed goods, straw, wood, paper, leather, etc.; they may also be used in printing or for the manufacture of lakes. Examples are given of the production of copper compounds of the dyes obtained from the following sets of components :- dianisidine, 1 - acetylamino - 8 - naphthol - 2 : 4 - disulphonic acid and phenyl - 2 : 5 : 7 - acid; dianisidine, 1 : 8 : 2 : 4 - acid, and phenyl - 2 : 5 : 7 - acid; dianisidine, acetyl - 1: 8 : 3 : 6 - acid, and acetyl-2 : 5: 7 - acid; dianisidine and two molecules of phenyl - 2 : 5 : 7 - acid; diphenetidine, 1 : 8 : 2 : 4 - acid, and phenyl - 2 : 5 : 7 - acid; 3-ethoxybenzidine, 1 : 8 : 3 : 6 - acid, and phenyl - 2 : 5 : 7 - acid; 6-methyl - 3 - ethoxybenzidine, 1 : 8 : 2 : 4 - acid, and phenyl 2 : 5 : 7 - acid; 5 - bromdianisidine, acetyl - 1 : 8 : 2 : 4 - acid, and phenyl - 2 : 5 : 7 - acid; 3 - ethoxybenzidine - 6 - sulphonic acid, acetyl - 1: 8: 4 - acid, and phenyl - 2 : 5 : 7 - acid. Specifications 12250/15, 12932/15, 101,601, 102,881, and 103,251 are referred to. 5 - Bromdianisidine is prepared by treating dianisidine with sodium bromide in sulphuric acid solution.
GB1950/17A 1917-02-08 1917-02-08 Manufacture of New Copper Compounds of Substantive Azodyestuffs. Expired GB113141A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1950/17A GB113141A (en) 1917-02-08 1917-02-08 Manufacture of New Copper Compounds of Substantive Azodyestuffs.

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1950/17A GB113141A (en) 1917-02-08 1917-02-08 Manufacture of New Copper Compounds of Substantive Azodyestuffs.

Publications (1)

Publication Number Publication Date
GB113141A true GB113141A (en) 1918-02-08

Family

ID=32481343

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1950/17A Expired GB113141A (en) 1917-02-08 1917-02-08 Manufacture of New Copper Compounds of Substantive Azodyestuffs.

Country Status (1)

Country Link
GB (1) GB113141A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2536957A (en) * 1946-10-17 1951-01-02 Ciba Ltd Process of making metalliferous azo dyestuffs
US2567828A (en) * 1947-12-29 1951-09-11 Ciba Ltd Process of making disazo dyestuffs

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2536957A (en) * 1946-10-17 1951-01-02 Ciba Ltd Process of making metalliferous azo dyestuffs
US2567828A (en) * 1947-12-29 1951-09-11 Ciba Ltd Process of making disazo dyestuffs

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