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MilliporeSigma
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Documentos

37879

Supelco

Azulene

analytical standard

Sinónimos:

Bicyclo[5.3.0]decapentaene

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About This Item

Fórmula empírica (notación de Hill):
C10H8
Número de CAS:
275-51-4
Peso molecular:
128.17
Beilstein/REAXYS Number:
969517
EC Number:
205-993-6
MDL number:
MFCD00003810
UNSPSC Code:
41116107
PubChem Substance ID:
329755704
NACRES:
NA.24

grade

analytical standard

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

242 °C (lit.)

mp

98-100 °C (lit.)

application(s)

environmental

format

neat

SMILES string

c1ccc2cccc2cc1

InChI

1S/C10H8/c1-2-5-9-7-4-8-10(9)6-3-1/h1-8H

InChI key

CUFNKYGDVFVPHO-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.

Recommended products

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

pictograms

Environment
GHS09

hcodes

H411

Hazard Classifications

Aquatic Chronic 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificados de análisis (COA)

Lot/Batch Number
BCCD7841
BCCB7702
BCBW5128
SZBD011XV
SZB9345XV

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Mine Ince et al.
Chemical communications (Cambridge, England), 48(34), 4058-4060 (2012-03-22)
A novel supramolecular electron donor-acceptor hybrid (2·1) and an electron donor-acceptor conjugate (3), both exhibiting a remarkably shifted Q band in the NIR region of the solar spectrum, were prepared. Irradiation of the supramolecular ensemble 2·1 within the visible range
Dawei Zhao et al.
The Journal of chemical physics, 131(18), 184307-184307 (2009-11-18)
The infrared (IR) spectrum of protonated azulene (AzuH(+), C(10)H(9)(+)) has been measured in the fingerprint range (600-1800 cm(-1)) by means of IR multiple photon dissociation (IRMPD) spectroscopy in a Fourier transform ion cyclotron resonance mass spectrometer equipped with an electrospray
Hiromi Mitsuhashi et al.
European journal of pharmacology, 551(1-3), 152-155 (2006-10-19)
Oral ulcerative mucositis is a common and painful toxicity associated with chemotherapy for cancer. Current treatment for chemotherapy-induced oral mucositis is largely palliative, and no adequate treatment with conclusive evidence exists. The purpose of this study was to evaluate the
Stefan Löber et al.
ChemMedChem, 4(3), 325-328 (2009-02-03)
Blue makes it happen: The non-uniform charge distribution of the blue colored azulene framework is highly suitable for the bioisosteric replacement of bicyclic heteroarene moieties. Showing an analogous binding mode as heterocyclic dopamine D4 receptor-selective lead compounds, the induction of
A F M Mustafizur Rahman et al.
Chemical communications (Cambridge, England), (10)(10), 1196-1198 (2008-03-01)
In spite of having small pi-conjugation systems, azulenes show large binding constants (10(4)-10(5)) to C(60) and C(70), which are larger than those of monoporphyrins and alternant aromatic hydrocarbons.
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