63768-01-4 Usage
Description
1-(butylamino)-4-hydroxyanthraquinone is a synthetic organic compound that belongs to the anthraquinone class of chemicals. It is characterized by its vivid, reddish-brown color and is known for its high stability and resistance to fading.
Uses
Used in Textile Industry:
1-(butylamino)-4-hydroxyanthraquinone is used as a dye and colorant for imparting a reddish-brown color to textiles. Its high stability and resistance to fading make it a preferred choice in this industry.
Used in Plastics Industry:
In the plastics industry, 1-(butylamino)-4-hydroxyanthraquinone is used as a colorant to provide a reddish-brown hue to various plastic products. Its stability ensures that the color remains vibrant over time.
Used in Printing Inks Industry:
1-(butylamino)-4-hydroxyanthraquinone is utilized as a pigment in the production of printing inks, offering a distinctive reddish-brown color that is resistant to fading and maintains its vibrancy.
Used in Pharmaceutical Industry:
Due to its potential antioxidant and anti-inflammatory properties, 1-(butylamino)-4-hydroxyanthraquinone is being explored for its possible medicinal uses in the pharmaceutical industry. Its ability to combat oxidative stress and inflammation may lead to the development of new therapeutic agents.
Please note that the provided materials do not mention any specific applications of glycerol. The uses listed are based on the general knowledge of 1-(butylamino)-4-hydroxyanthraquinone and its potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 63768-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,6 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 63768-01:
(7*6)+(6*3)+(5*7)+(4*6)+(3*8)+(2*0)+(1*1)=144
144 % 10 = 4
So 63768-01-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H17NO3/c1-2-3-10-19-13-8-9-14(20)16-15(13)17(21)11-6-4-5-7-12(11)18(16)22/h4-9,19-20H,2-3,10H2,1H3
63768-01-4Relevant articles and documents
Synthesis of new cytotoxic aminoanthraquinone derivatives via nucleophilic substitution reactions
Nor, Siti Mariam Mohd,Sukari, Mohd Aspollah Hj Md,Azziz, Saripah Salbiah Syed Abdul,Fah, Wong Chee,Alimon, Hasimah,Juhan, Siti Fadilah
, p. 8046 - 8062 (2013/08/23)
Aminoanthraquinones were successfully synthesized via two reaction steps. 1,4-Dihydroxyanthraquinone (1) was first subjected to methylation, reduction and acylation to give an excellent yield of anthracene-1,4-dione (3), 1,4-dimethoxyanthracene- 9,10-dione (5) and 9,10-dioxo-9,10-dihydroanthracene-1, 4-diyl diacetate (7). Treatment of 1, 3, 5 and 7 with BuNH2 in the presence of PhI(OAc)2 as catalyst produced seven aminoanthraquinone derivatives 1a, b, 3a, and 5a-d. Amination of 3 and 5 afforded three new aminoanthraquinones, namely 2-(butylamino)anthracene-1,4-dione (3a), 2-(butylamino)anthracene-9,10-dione (5a) and 2,3-(dibutylamino)anthracene-9,10-dione (5b). All newly synthesised aminoanthraquinones were examined for their cytotoxic activity against MCF-7 (estrogen receptor positive human breast) and Hep-G2 (human hepatocellular liver carcinoma) cancer cells using MTT assay. Aminoanthraquinones 3a, 5a and 5b exhibited strong cytotoxicity towards both cancer cell lines (IC50 1.1-13.0 μg/mL).
The Direct Alkylamination of α-Substituted Antraquinones Promoted bu Metal Ions
Matsuoka, Masaru,Takei, Toshio,Nakamura, Isao
, p. 2225 - 2226 (2007/10/02)
The reaction of 1-amino-4-acylaminoantraquinones with piperidine in the presence of CoCl2 and atmospheric oxygen gave the 2-aminated products in 75-80percent and similar reaction of 1-hydroxyantraquinone or 1-aminoantraquinone-2-sulfonic acid with butylamine gave the corresponding 4-aminated products, respectively.The effects of the α-substituents and the role of metal salts were discussed.
