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45793

Supelco

9-Methylanthracene

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C15H12
CAS Number:
779-02-2
Molecular Weight:
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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Certificates of Analysis (COA)

Lot/Batch Number
BCCG6105
BCBT8597

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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
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
L S Von Tungeln et al.
Carcinogenesis, 7(7), 1135-1141 (1986-07-01)
Stereoselective metabolism of 9-methylanthracene (9-M-A), 9-hydroxymethylanthracene (9-OHM-A) and 9,10-dimethylanthracene (9,10-DM-A) by liver microsomes from untreated rats, and from rats pretreated with either 3-methylcholanthrene or phenobarbital was studied. The metabolites were separated by h.p.l.c. and characterized by analysis of the u.v.-visible
Capillary gas chromatography/pulsed supersonic jet/fluorescence excitation spectroscopy for the identification of methylanthracenes in a complex environmental sample.
B V Pepich et al.
Analytical chemistry, 58(13), 2825-2830 (1986-11-01)
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