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M29606

Sigma-Aldrich

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
Beilstein:
1907463
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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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Pictograms

Environment

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

M29606-1G:
M29606-10G:
M29606-5G:
M29606-BULK:
M29606-VAR:


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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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
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