M29606
9-Methylanthracene
98%
Synonym(s):
9-Methylanthracene
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About This Item
Empirical Formula (Hill Notation):
C15H12
CAS Number:
Molecular Weight:
192.26
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
212-299-7
Beilstein/REAXYS Number:
1907463
MDL number:
Product Name
9-Methylanthracene, 98%
InChI key
CPGPAVAKSZHMBP-UHFFFAOYSA-N
InChI
1S/C15H12/c1-11-14-8-4-2-6-12(14)10-13-7-3-5-9-15(11)13/h2-10H,1H3
SMILES string
Cc1c2ccccc2cc3ccccc13
assay
98%
bp
196-197 °C/12 mmHg (lit.)
mp
77-79 °C (lit.)
density
1.066 g/mL at 25 °C (lit.)
Quality Level
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Related Categories
signalword
Warning
hcodes
pcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
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
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Wenyan Shi et al.
Polymers, 11(3) (2019-04-10)
Membrane inlet mass spectrometry (MIMS) is commonly used for detecting the components in liquid samples. When a liquid sample flows through a membrane, certain analytes will permeate into the vacuum chamber of a mass spectrometer from the solution. The properties
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
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
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
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