M29606
9-Methylanthracene
98%
Synonym(s):
9-Methylanthracene
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About This Item
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Quality Level
Assay
98%
bp
196-197 °C/12 mmHg (lit.)
mp
77-79 °C (lit.)
density
1.066 g/mL at 25 °C (lit.)
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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Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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
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
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
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.
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