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45793

Supelco

9-Methylanthracene

analytical standard

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About This Item

Fórmula empírica (notación de Hill):
C15H12
Número de CAS:
779-02-2
Peso molecular:
192.26
Beilstein/REAXYS Number:
1907463
EC Number:
212-299-7
MDL number:
MFCD00001261
UNSPSC Code:
41116107
PubChem Substance ID:
329756955
NACRES:
NA.24

grade

analytical standard

Quality Level

100

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

196-197 °C/12 mmHg (lit.)

mp

77-79 °C (lit.)

density

1.066 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

SMILES string

Cc1c2ccccc2cc3ccccc13

InChI

1S/C15H12/c1-11-14-8-4-2-6-12(14)10-13-7-3-5-9-15(11)13/h2-10H,1H3

InChI key

CPGPAVAKSZHMBP-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

Environment
GHS09

signalword

Warning

hcodes

H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCG6105
BCBT8597

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Sigma-Aldrich

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Acetonitrilo

K Takegoshi et al.
Solid state nuclear magnetic resonance, 11(3-4), 189-196 (1998-08-07)
The locus of the photodimerization reaction of 9-methylanthracene in the crystal was examined by high-resolution solid-state 13C NMR techniques. Examination of the 13C spectra of the products showed that only the trans dimer is formed by the solid state photodimerization
H S Lamparczyk et al.
Xenobiotica; the fate of foreign compounds in biological systems, 16(4), 325-333 (1986-04-01)
The metabolism of 9-methylanthracene by liver microsomal preparations from 3-methylcholanthrene-treated rats was examined. The principal metabolites identified were 9-hydroxymethylanthracene, the 1,2- and 3,4-dihydrodiols of the parent hydrocarbon and the 3,4-dihydrodiol of the 9-hydroxymethyl derivative. A small amount of a product
Samantha L Jenkins et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 62(4-5), 1131-1139 (2005-06-15)
Reaction of single crystals of benzoic and trans-cinnamic acids with 200 Torr pressure of ammonia gas in a sealed glass bulb at 20 degrees C generates the corresponding ammonium salts; there is no sign of any 1:2 adduct as has
Klaus Pittertschatscher et al.
Analytical biochemistry, 308(2), 300-306 (2002-11-07)
A novel one-step ethylchloroformate (ECF) derivatization of histamine in biological liquid matrices that allows the sensitive quantification by gas chromatography and mass spectroscopic detection (GC-MS) from small volumes of blood plasma or cell culture supernatants within 15 min is described.
Kamlesh Awasthi et al.
The journal of physical chemistry. A, 113(40), 10603-10609 (2009-10-02)
Photoluminescence of electron donor-acceptor pairs that show photoinduced electron transfer (PIET) has been measured in a polymer film under simultaneous application of electric field and magnetic field. Fluorescence emitted from the locally excited state (LE fluorescence) of 9-methylanthracene (MAnt) and
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