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A89502

Anthraflavic acid

Name: Anthraflavic acid
Brand: ALDRICH

technical grade, 90%

Synonym(s):

2,6-Dihydroxyanthraquinone, Anthraflavine

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About This Item

Empirical Formula (Hill Notation):

C₁₄H₈O₄

CAS Number:

84-60-6

Molecular Weight:

240.21

NACRES:

NA.22

PubChem Substance ID:

24891386

UNSPSC Code:

12352100

EC Number:

201-544-3

MDL number:

MFCD00001228

Assay:

90%

Form:

powder

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Properties

grade

technical grade

Quality Level

100

assay

90%

form

powder

mp

>320 °C (lit.)

SMILES string

Oc1ccc2C(=O)c3cc(O)ccc3C(=O)c2c1

InChI

1S/C14H8O4/c15-7-1-3-9-11(5-7)14(18)10-4-2-8(16)6-12(10)13(9)17/h1-6,15-16H

InChI key

APAJFZPFBHMFQR-UHFFFAOYSA-N

Description

Application

Anthraflavic acid can be used as a starting material to synthesize tetrahydroxy tetrathiafulvalene (TTF) derivatives, which are used as redox-active building blocks in supramolecular and materials science. It is also utilized to prepare phosphanylidene anthra[2,1-b]furans by reacting with dialkyl acetylenedicarboxylates and triphenylphosphine.

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Determination of the optical GAP in thin films of amorphous dilithium phthalocyanine using the Tauc and Cody models.

María Elena Sánchez-Vergara et al.

Molecules (Basel, Switzerland), 17(9), 10000-10013 (2012-08-28)

Semiconducting thin films were grown on quartz substrates and crystalline silicon wafers, using dilithium phthalocyanine and the organic ligands 2,6-dihydroxyanthraquinone and 2,6-diaminoanthraquinone as the starting compounds. The films, thus obtained, were characterized by Fourier Transform infrared (FTIR), fast atomic bombardment

Extrapolation of in vitro antimutagenicity to the in vivo situation: the case for anthraflavic acid.

C Ioannides et al.

Basic life sciences, 61, 103-110 (1993-01-01)

Exceptional activity of tannic acid among naturally occurring plant phenols in protecting against 7,12-dimethylbenz(a)anthracene-, benzo(a)pyrene-, 3-methylcholanthrene-, and N-methyl-N-nitrosourea-induced skin tumorigenesis in mice.

H Mukhtar et al.

Cancer research, 48(9), 2361-2365 (1988-05-01)

Our recent studies have shown that naturally occurring dietary plant phenols such as tannic acid, quercetin, myricetin, and anthraflavic acid are capable of inhibiting polycyclic aromatic hydrocarbon (PAH) metabolism and subsequent PAH-DNA adduct formation in epidermis of SENCAR mice (M.

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Global Trade Item Number

SKU	GTIN
A89502-5G	04061833401002