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Key Documents

Altri documenti

45793

Supelco

9-Methylanthracene

analytical standard

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About This Item

Formula empirica (notazione di Hill):
C15H12
Numero CAS:
779-02-2
Peso molecolare:
192.26
Beilstein:
1907463
Numero CE:
212-299-7
Numero MDL:
MFCD00001261
Codice UNSPSC:
41116107
ID PubChem:
329756955
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

P. eboll.

196-197 °C/12 mmHg (lit.)

Punto di fusione

77-79 °C (lit.)

Densità

1.066 g/mL at 25 °C (lit.)

applicazioni

environmental

Formato

neat

Stringa SMILE

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
CPGPAVAKSZHMBP-UHFFFAOYSA-N

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Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pittogrammi

Environment
GHS09

Avvertenze

Warning

Indicazioni di pericolo

H410

Consigli di prudenza

P273 - P391 - P501

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCCG6105
BCBT8597
SZBC243XV
SZB9243XV
SZE9243X

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Phenanthrene 98%

Sigma-Aldrich

P11409

Phenanthrene

Naphthalene analytical standard

Supelco

84679

Naphthalene

Acetonitrile suitable for HPLC, gradient grade, ≥99.9%

Sigma-Aldrich

34851

Acetonitrile

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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