6471-02-9

Usage

Uses

Used in Textile Industry:
N-(4-amino-9,10-dioxo-anthracen-1-yl)acetamide is used as a colorant in the textile industry for its vibrant red light purple hue. It provides excellent light fastness, ironing fastness, perspiration fastness, and washing fastness, making it a suitable choice for various textile applications.
Used in ISO Standards:
N-(4-amino-9,10-dioxo-anthracen-1-yl)acetamide meets the ISO standards for various fastness properties, including light fastness (rated 6-7), ironing fastness (rated 5), perspiration fastness (rated 3-4), and washing fastness (rated 4). These ratings indicate its high performance and reliability in different applications.

Preparation

in the control condition will be N-(4-acetamido-9,10-dioxo-9,10-dihydroanthracene-1-yl)acetamide?take off a acetyl groups.

Standard(Vinegar fiber)

Ironing Fastness

Fading

Stain

InChI:InChI=1/C16H12N2O3/c1-8(19)18-12-7-6-11(17)13-14(12)16(21)10-5-3-2-4-9(10)15(13)20/h2-7H,17H2,1H3,(H,18,19)

Upstream product

• 128-95-0 1,4-diamino-9,10-anthraquinone 
• 108-24-7 acetic anhydride 
• 6534-28-7 N-(4-acetylamino-9,10-dioxo-9,10-dihydro-anthracene-1-yl)-acetamide 
• 5327-72-0 1,4-diamino-anthracene-9,10-diol 
• 75-36-5 acetyl chloride 
• 64-19-7 acetic acid 

Downstream Products

• 52062-63-2 1,4-diamino-2-piperidinoantraquinone 
• 79207-93-5 1-amino-2-piperidino-4-acetylantraquinone 

Relevant academic research and scientific papers

EFFECT OF SRUCTURAL FACTORS ON THE FORMATION AND PROPERTIES OF ACYLAMINOANTHRAQUINONES

The N-methyl group prevents the acylation of α-aminoanthraquinones by acetic anhydride in the absence of acid catalysis.This is explained by hindrances for the abstraction of hydrogen atom from the 1-methylamino group, which is connected by an intramolecular hydrogen bond.Acid catalysis levels out the differences in the reactivity of the α-amino and α-methyl amino groups.The α-acetylamino groups have lower hydrolytic stability than the α-N-acetylmethylamino groups.These characteristics make it possible to realize a directed synthesis of acyl derivatives at theprimary or secondary α-amino groups of polyaminoanthraquinones.The introduction of acyl residues into the secondary α-amino groups completely excludes them conjugation with the anthraquinone ring, and an unexpectedly small hypsochromic shift of the absorption is observed in the 4-amino, 4-alkylamino, and particularly the 4-arylamino derivatives of 1-acylaminoanthraquinones.

Triazinyl dyes

Vat dyestuffs of the formula EQU1 wherein R represents alkyl with 1 to 4 carbon atoms, R1 and R2 represent hydrogen or alkyl with 1 to 4 carbon atoms and each of A1 and A2 represents a vattable radical with 3 to 7 condensed rings are characterized by improved resistance to alkali and are suitable for dyeing and printing the most diverse materials, in particular fibers made from natural or regenerated cellulose.