1-Amino-4-hydroxyanthraquinone (CAS 116-85-8)
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1-Amino-4-hydroxyanthraquinone is an organic compound utilized extensively in the field of dye chemistry and materials science research. It serves as a key intermediate in the synthesis of a variety of anthraquinone dyes and pigments, which are of interest for their colorfast properties and applications in textile and paper. In addition to its use in colorant synthesis, this compound′s photophysical properties are investigated for potential use in advanced materials, such as organic semiconductors and photovoltaic cells. The presence of both amino and hydroxy functional groups makes it a versatile molecule for surface modification studies, where it is used to alter the properties of fibers and surfaces to create novel material interactions. Furthermore, 1-Amino-4-hydroxyanthraquinone is studied for its potential role in the development of optical sensors and electronic devices, leveraging its ability to undergo redox reactions and its distinctive electronic absorption characteristics.
1-Amino-4-hydroxyanthraquinone (CAS 116-85-8) References
- Optochemical sensor for an ornidazole assay using 1-amino-4-allyloxyanthraquinone as a fluorescent indicator. | Tan, SZ., et al. 2005. Anal Sci. 21: 967-71. PMID: 16122170
- Complexes of some rare earth metals with 1-amino-4-hydroxyanthraquinone. | Jain, AK., et al. 1972. Talanta. 19: 1481-2. PMID: 18961210
- Complexation equilibria and spectrophotometric determination of iron(III) with 1-amino-4-hydroxyanthraquinone. | Abu-Bakr, MS., et al. 1994. Talanta. 41: 1669-74. PMID: 18966119
- Disperse red 15 (DR15) impedes biofilm formation of uropathogenic Escherichia coli. | Miryala, S., et al. 2020. Microb Pathog. 138: 103772. PMID: 31589910
- Performance and enhancement mechanism of redox mediator for nitrate removal in immobilized bioreactor with preponderant microbes. | Zhang, S., et al. 2021. Water Res. 209: 117899. PMID: 34861436
- Friedel-Crafts reactions of amino compounds. New method for the preparation of 1-amino-4-hydroxyanthraquinone | Aggarwala, V. P., Gopal, R., & Garg, S. P. 1973. The Journal of Organic Chemistry. 38(6): 1247-1247.
- Fluorimetric determination of vanadium based on its reaction with 1-amino-4-hydroxyanthraquinone | Salinas, F., Garcia-Sanchez, F., & Genestar, C. 1982. Microchemical Journal. 27(1): 26-31.
- Spectrofluorimetric determination of beryllium based on the inclusion complex of 1-amino-4-hydroxyanthraquinone with β-cyclodextrin as ligand | Sanchez, F. G., Lopez, M. H., & Heredia, A. 1986. Analytica chimica acta. 187: 147-155.
- Spectrophotometric study of the complexation equilibria of zirconium (IV) with 1-amino-4-hydroxyanthraquinone and the determination of zirconium | Idriss, K. A., Seleim, M. M., Saleh, M. S., Abu-Bakr, M. S., & Sedaira, H. 1988. Analyst. 113(11): 1643-1647.
- Spektrophotometrische Bestimmung von Mikromengen Yttrium mit 1-Amino-4-hydroxyanthrachinon | Saleh, M. S. 1995. Monatshefte für Chemie/Chemical Monthly. 126: 621-629.
- Solubility of 1-amino-4-hydroxyanthraquinone in water-amide mixtures | Prusova, S. M., & Baranov, A. V. 2002. Russian journal of applied chemistry. 75: 375-377.
- Solubility of anthraquinone derivatives in supercritical carbon dioxide | Tamura, K., & Alwi, R. S. 2015. Dyes and Pigments. 113: 351-356.
- Design, synthesis, and stability of (1-amino-4-(3-bromopropoxy) anthracene-9, 10‑dione) pentacarbonylrhenium (I) triflate: first X-ray crystallographic structure of a Re (CO) 5 (N-donor) | Tay, J. J. J., Karve, N. R. O., & Chan, K. H. 2023. Journal of Organometallic Chemistry. 987: 122632.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
1-Amino-4-hydroxyanthraquinone, 5 g | sc-264660 | 5 g | $99.00 |