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Merck
CN

N10970

Anthraquinone

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C14H8O2
CAS Number:
84-65-1
Molecular Weight:
208.21
Beilstein:
390030
EC Number:
201-549-0
MDL number:
MFCD00001188
UNSPSC Code:
41116107
PubChem Substance ID:
329818484

Key Documents

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grade

analytical standard

vapor density

7.16 (vs air)

vapor pressure

1 mmHg ( 190 °C)

packaging

ampule of 1 g

manufacturer/tradename

Chem Service, Inc. PS-926

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

379-381 °C (lit.)

mp

284-286 °C (lit.)

format

neat

SMILES string

O=C1c2ccccc2C(=O)c3ccccc13

InChI

1S/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H

InChI key

RZVHIXYEVGDQDX-UHFFFAOYSA-N

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Danger

Hazard Statements

H317,H350

Hazard Classifications

Carc. 1B - Skin Sens. 1

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

Flash Point(F)

482.0 °F - closed cup

Flash Point(C)

250 °C - closed cup

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Certificates of Analysis (COA)

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Sana Zafar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 114, 164-169 (2013-06-19)
Nonlinear optical properties of 1,4-Diamino-9,10-Anthraquinone dye in solution at different concentrations are investigated by utilizing single beam Z-scan technique using a low power continuous wave laser (λ=532 nm). The anthraquinone dye is found to exhibit self-defocusing and reverse saturable absorption
Erin E Podlesny et al.
The Journal of organic chemistry, 78(2), 466-476 (2012-12-20)
The development of the first asymmetric synthesis of a chiral anthraquinone dimer is outlined, resulting in the first total synthesis of (S)-bisoranjidiol. Rather than a biomimetic dimerization retrosynthetic disconnection, the anthracenyl ring systems are generated after formation of the axially
Yasuhiro Kobori et al.
Journal of the American Chemical Society, 133(42), 16770-16773 (2011-10-07)
To elucidate how the protein-ligand docking structure affects electronic interactions in the electron-transfer process, we have analyzed time-resolved electron paramagnetic resonance spectra of photoinduced charge-separated (CS) states generated by light excitation of 9,10-anthraquinone-1-sulfonate (AQ1S(-)) bound to human serum albumin at
Myriam Bonose-Crosnier de Bellaistre et al.
Journal of chromatography. A, 1218(6), 778-786 (2011-01-14)
Chromatographic study of natural products helps to determine their molecular composition and to identify their sources (biological, geographical, etc.). However, identifying anthraquinoids is still a challenge because this chemical family is composed of more than half a thousand molecules. In
Marino Convertino et al.
Protein science : a publication of the Protein Society, 18(4), 792-800 (2009-03-25)
Amyloid aggregation is linked to a number of neurodegenerative syndromes, the most prevalent one being Alzheimer's disease. In this pathology, the beta-amyloid peptides (Abeta) aggregate into oligomers, protofibrils, and fibrils and eventually into plaques, which constitute the characteristic hallmark of
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