GB694451A - Improvements relating to polyazine dyestuffs - Google Patents

Improvements relating to polyazine dyestuffs

Info

Publication number
GB694451A
GB694451A GB2829050A GB2829050A GB694451A GB 694451 A GB694451 A GB 694451A GB 2829050 A GB2829050 A GB 2829050A GB 2829050 A GB2829050 A GB 2829050A GB 694451 A GB694451 A GB 694451A
Authority
GB
United Kingdom
Prior art keywords
hydrazine
reacted
terephthalaldehyde
dialdehyde
tetra
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
GB2829050A
Inventor
James Rex Naylor
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.)
Calico Printers Association Ltd
Original Assignee
Calico Printers Association 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 Calico Printers Association Ltd filed Critical Calico Printers Association Ltd
Priority to GB2829050A priority Critical patent/GB694451A/en
Publication of GB694451A publication Critical patent/GB694451A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C251/00Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
    • C07C251/72Hydrazones
    • 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
    • C09B26/00Hydrazone dyes; Triazene dyes
    • C09B26/02Hydrazone dyes

Landscapes

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

Abstract

Insoluble coloured polyazines are made by reacting hydrazine, its hydrate or a salt thereof with an aromatic p- or m dialdehyde or a tetra-acetate thereof in substantially an aqueous medium the hydrazine, its hydrate or its salt being used in the proportion of at least 1 mol. to 1 mol. of the dialdehyde; 80-90 DEG C. are preferred temperatures. Water-miscible organic solvents, e.g. lower aliphatic alcohols, may be present. The dialdehyde may be substituted and specified dialdehydes are terephthal-, isophthal-, 4-methoxy-, isophthal-, 2,5-dichloroterephthal-, 5-hydroxy-isophthal-, 2,5-dibromoterephthal and 2,5-dimethoxy-terephthal-aldehyde. The pigments are yellow. The tetra-acetates may be made by oxidizing the corresponding dimethyl compound with chromium trioxide and sulphuric acid in the presence of acetic acid and anhydride. In examples: (1) terephthalaldehyde tetra-acetate is reacted in aqueous ethanol with hydrazine sulphate in the presence of sulphuric acid, (5) 4-methoxy-isophthalaldehyde is reacted in aqueous ethanol with hydrazine sulphate, (6) 2,5-dichloro-terephthalaldehyde tetra-acetate is reacted in aqueous ethanol with hydrazine hydrate in the presence of sulphuric acid, (7) 5-acetoxy-isophthalaldehyde tetra-acetate is reacted in aqueous ethanol with hydrazine sulphate and (8) 2,5-dibromo-terephthaldehyde in aqueousethanol is reacted with hydrazine sulphate.ALSO:Insoluble coloured polyazines used in dyeing processes are made by reacting hydrazine, its hydrate or a salt thereof with an aromatic p-or m-dialdehyde or a tetra-acetate thereof in substantially an aqueous medium, the hydrazine, its hydrate or its salt being used in the proportion of at least 1 mol. to 1 mol. of the dialdehyde. 80-90 DEG C. are preferred temperatures. Water-miscible organic solvents, e.g. a lower aliphatic alcohol, may be present. The dialdehyde may be substituted and specified dialdehydes are terephthal-, isophthal-, 4-methoxy-isophthal-, 2,5-dichloro-terephthal-, 5-hydroxy - isophthal-, 2,5 - dibromo - terephthal and 2,5-dimethoxy-terephthal-aldehyde. The pigments are yellow. The tetra-acetates may be made by oxidizing the corresponding dimethyl compound with chromium trioxide and sulphuric acid in the presence of acetic acid and anhydride. In the dyeing of textiles the polyazine may be caused to form on the materials, e.g. by impregnating with a solution of the dialdehyde, and after removal of excess liquid the material is run, with or without drying, through an aqueous solution containing the hydrazine compound, preferably at an elevated temperature, the fabric finally being washed and dried. Alternatively treatment with the hydrazine compound may precede that with dialdehyde. Pattern effects are produced by applying one or both reagents in selected areas only. The polyazine may be caused to form subsequently, e.g. by steaming, tetraacetates being particularly useful in this respect since they require hydrolysis before they react. In examples: (1) terephthalaldehyde tetraacetate is reacted in aqueous ethanol with hydrazine sulphate in the presence of sulphuric acid; (5) 4-methoxy-isophthalaldehyde is reacted in aqueous ethanol with hydrazine sulphate; (6) 2,5-dichloro-terephthalaldehyde tetra-acetate is reacted in aqueous ethanol with hydrazine hydrate in the presence of sulphuric acid; (7) 5-acetoxy-isophthalaldehyde tetraacetate is reacted in aqueous ethanol with hydrazine sulphate and (8) 2,5-dibromo-terephthalaldehyde in aqueous-ethanol is reacted with hydrazine sulphate; in (2) a cotton fabric is impregnated with a 5 per cent aqueous ethanol solution of terephthalaldehyde and run through a 5 per cent aqueous solution of hydrazine sulphate to be dyed a bright lemon yellow; (3) a cotton fabric is impregnated with a solution containing terephthalaldehyde tetraacetate and hydrazine hydrate, dried and the colour developed by passing through steam and formic acid vapour; (4) a cotton fabric is printed with a paste containing terephthalaldehyde tetracetate, hydrazine hydrate and tragacanth thickening, dried and steamed to develop the colour and in (9) a cotton fabric is impregnated with an aqueous alcohol solution of 2,5-dimethoxy terephthalaldehyde, dried and further impregnated with an aqueous solution of hydrazine sulphate, dried and steamed to yield an orange dyeing.
GB2829050A 1950-11-20 1950-11-20 Improvements relating to polyazine dyestuffs Expired GB694451A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2829050A GB694451A (en) 1950-11-20 1950-11-20 Improvements relating to polyazine dyestuffs

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2829050A GB694451A (en) 1950-11-20 1950-11-20 Improvements relating to polyazine dyestuffs

Publications (1)

Publication Number Publication Date
GB694451A true GB694451A (en) 1953-07-22

Family

ID=10273305

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2829050A Expired GB694451A (en) 1950-11-20 1950-11-20 Improvements relating to polyazine dyestuffs

Country Status (1)

Country Link
GB (1) GB694451A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2953987A4 (en) * 2013-02-06 2016-09-28 Avertica Inc Polymers, substrates, methods for making such, and devices comprising the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2953987A4 (en) * 2013-02-06 2016-09-28 Avertica Inc Polymers, substrates, methods for making such, and devices comprising the same

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