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Sigma-Aldrich

Anthraquinone-2-carboxylic acid

98%

Synonym(s):

9,10-Dihydro-9,10-dioxo-2-anthracenecarboxylic acid

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About This Item

Empirical Formula (Hill Notation):
C15H8O4
CAS Number:
117-78-2
Molecular Weight:
252.22
EC Number:
204-207-9
MDL number:
MFCD00001231
UNSPSC Code:
12352100
PubChem Substance ID:
24855233
NACRES:
NA.22

assay

98%

form

solid

mp

287-289 °C (lit.)

SMILES string

OC(=O)c1ccc2C(=O)c3ccccc3C(=O)c2c1

InChI

1S/C15H8O4/c16-13-9-3-1-2-4-10(9)14(17)12-7-8(15(18)19)5-6-11(12)13/h1-7H,(H,18,19)

InChI key

ASDLSKCKYGVMAI-UHFFFAOYSA-N

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

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Yiwen Zhu et al.
Materials (Basel, Switzerland), 13(16) (2020-08-17)
Antimicrobial and antiviral materials have attracted significant interest in recent years due to increasing occurrences of nosocomial infections and pathogenic microbial contamination. One method to address this is the combination of photoactive compounds that can produce reactive oxygen species (ROS)
Coupled Proton and Electron Transfer: Adsorbed Anthraquinone-2-carboxylic Acid Monolayers.
Forster RJ.
Journal of the Electrochemical Society, 144(4), 1165-1173 (1997)
A Bielawska et al.
Polish journal of pharmacology, 53(3), 283-287 (2002-01-12)
A series of proline analogues of anthraquinone-2-carboxylic acid (1-3) were synthesized and evaluated for cytotoxic activity in the cultured breast cancer MCF-7 cells. The concentrations of 1, 2 and 3 needed to inhibit [3H]thymidine incorporation into DNA by 50% (IC50)
Morihide Higo et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 24(3), 313-320 (2008-03-12)
The adsorption state and morphology of anthraquinone-2-carboxylic acid (AQ-2-COOH) deposited from acetone solutions (0.02 - 1.00 mg ml(-1)) onto atomically-smooth native oxide surfaces of Al(111) films were investigated by infrared reflection absorption spectroscopy, X-ray photoelectron spectroscopy, and atomic force microscopy.
Jie Sun et al.
Analytical chemistry, 90(11), 6660-6665 (2018-05-15)
To detect the redox state evolution during wound healing process, a redox-sensitive surface-enhanced Raman scattering (SERS) probe was constructed by attaching anthraquinone as a redox-sensitive molecule onto gold nanoshells, and the redox-sensitive SERS probes were loaded on one surface of
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