GB189922886A - Improvements in the Manufacture of Colouring Matters. - Google Patents

Improvements in the Manufacture of Colouring Matters.

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Publication number
GB189922886A
GB189922886A GB189922886DA GB189922886A GB 189922886 A GB189922886 A GB 189922886A GB 189922886D A GB189922886D A GB 189922886DA GB 189922886 A GB189922886 A GB 189922886A
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GB
United Kingdom
Prior art keywords
acids
homologues
disulphonic
alphylsulphamidonaphthol
acid
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
Inventor
Harris Lake Henry
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.)
Sandoz AG
Original Assignee
Sandoz 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 Sandoz AG filed Critical Sandoz AG
Application granted granted Critical
Publication of GB189922886A publication Critical patent/GB189922886A/en
Expired legal-status Critical Current

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Abstract

22,886. Lake, H. H., [Chemical Works formerly Sandoz]. Nov. 16. Dyes, artificial; alphylsulphamidonaphthol sulphonic acids.-Relates to new azo dyes which dye wool and silk in an acid bath bright bluish-red to violet . shades, and consist in combining 1 : 8 - alphylsulphamidonaphthol disulphonic acids with the diazo derivatives of an aromatic compound, such as aniline, o- or p-toluidine, m- or p-xylidine, mono- or di-chloraniline or their homologues, pamidoacetanilide, m - or p - nitraniline, or their homologues, o-anisidine, p-phenetidine, m-amido-pcresol ether, aniline sulphonic acids or their homologues, amidobenzoic acids, amidoazobenzene, amidoazotoluene or their sulphonic acids, alpha- or ,3- naphthylamine or mono- or di-sulphonic acids thereof. The bluest products are those derived from p-phenylenediamine and its homologues and obtained from diazotized p-amidoacetanilide or p-nitraniline. The diazo compounds combine only in alkaline solution, except in the case of diazotized nitro- or dichloro-benzenes which combine in acid or alkaline solution. The alphylsulphamidonaphthol disulphonic acids employed are produced by heating 1 : 8-amidonaphthol-3 : 6-, -2 : 4-, or -4: 6-disulphonic acid with an alphylsulphochloride, such as benzene-, o- or p-toluene-, or xylene - sulphochloride, in presence of powdered chalk at about 80‹ C. until a sample ceases to yield a diazo compound. The dialkylsulphamidonaphthol disulphonic acid thus produced is boiled with caustic soda in order to split off the alphylsulpho radicle combined with the hydroxylic oxygen. The alkaline mixture is then neutralized, the lime is precipitated by soda, and the solution is filtered off and used for the production of the azo dyes as above described. The amido group is neutralized by the presence of the alphyl-sulpho radicle, and the products have consequently the properties of naphtholsulphonic acids.
GB189922886D 1899-11-16 1899-11-16 Improvements in the Manufacture of Colouring Matters. Expired GB189922886A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB189922886T 1899-11-16

Publications (1)

Publication Number Publication Date
GB189922886A true GB189922886A (en) 1900-09-08

Family

ID=32618148

Family Applications (1)

Application Number Title Priority Date Filing Date
GB189922886D Expired GB189922886A (en) 1899-11-16 1899-11-16 Improvements in the Manufacture of Colouring Matters.

Country Status (1)

Country Link
GB (1) GB189922886A (en)

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