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252727

Anthraquinone-2-carboxylic acid

Name: Anthraquinone-2-carboxylic acid
Brand: ALDRICH

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

NACRES:

NA.22

PubChem Substance ID:

24855233

UNSPSC Code:

12352100

EC Number:

204-207-9

MDL number:

MFCD00001231

Assay:

98%

Form:

solid

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Properties

Quality Level

100

assay

98%

form

solid

mp

287-289 °C (lit.)

functional group

carboxylic acid, ketone

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

Description

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Possible cause of G-C-->C-G transversion mutation by guanine oxidation product, imidazolone.

K Kino et al.

Chemistry & biology, 8(4), 369-378 (2001-04-28)

The genome is constantly assaulted by oxidation reactions which are likely to be associated with oxygen metabolism, and oxidative lesions are generated by many types of oxidants. Such genotoxin-induced alterations in the genomic message have been implicated in aging and

Adsorption state and morphology of anthraquinone-2-carboxylic acid deposited from solution onto the atomically-smooth native oxide surface of Al(111) films studied by infrared reflection absorption spectroscopy, X-ray photoelectron spectroscopy, and atomic force microscopy.

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.

Detection of Redox State Evolution during Wound Healing Process Based on a Redox-Sensitive Wound Dressing.

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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Global Trade Item Number

SKU	GTIN
252727-5G	04061831810257
252727-1G	04061825973593