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Supelco

Phenanthrene

analytical standard, for environmental analysis

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About This Item

Empirical Formula (Hill Notation):
C14H10
CAS Number:
85-01-8
Molecular Weight:
178.23
Beilstein:
1905428
EC Number:
201-581-5
MDL number:
MFCD00001168
UNSPSC Code:
12000000
PubChem Substance ID:
24872118

grade

analytical standard

CofA

current certificate can be downloaded

packaging

ampule of 5000 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

340 °C (lit.)

mp

98-100 °C (lit.)

density

1.063 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

storage temp.

2-30°C

SMILES string

c1ccc2c(c1)ccc3ccccc23

InChI

1S/C14H10/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)13/h1-10H

InChI key

YNPNZTXNASCQKK-UHFFFAOYSA-N

Gene Information

human ... CYP1A2(1544)

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General description

Phenanthrene is a polycyclic aromatic hydrocarbon often formed by incomplete combustion of organic materials.

Application

Phenanthrene may be used as an analytical reference standard for the determination of the analyte in various biological matrices at trace levels using gas chromatography-mass spectrometry.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
LRAD9854
LRAD6002
LRAD2498
LRAC8436
LRAC3583

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Catherine A Matulis et al.
Current biology : CB, 30(2), 222-236 (2020-01-14)
In visual systems, neurons adapt both to the mean light level and to the range of light levels, or the contrast. Contrast adaptation has been studied extensively, but it remains unclear how it is distributed among neurons in connected circuits
Determination of phenanthrene and hydroxyphenanthrenes in various biological matrices at trace levels using gas chromatography-mass spectrometry.
Grova N, et al.
Journal of Analytical Toxicology, 29(3), 175-181 (2005)
Yulong Zhang et al.
Chemosphere, 90(6), 1973-1979 (2012-12-04)
Two sediments were demineralized and sequentially fractionated into extracted fractions [free lipid (FL), bound lipid (BL) and lignin (LG)] and residual fractions [free lipid free (FLF), bound lipid free (BLF) and lignin free (LGF)]. The sorption isotherms of phenanthrene (Phen)
Marino Marinković et al.
Environmental science & technology, 46(22), 12679-12686 (2012-11-07)
Cellular stress responses are frequently presumed to be more sensitive than traditional ecotoxicological life cycle end points such as survival and growth. Yet, the focus to reduce test duration and to generate more sensitive end points has caused transcriptomics studies
Sebastian T Hoffmann et al.
Journal of the American Chemical Society, 135(5), 1772-1782 (2013-01-10)
In order to unravel the intricate interplay between disorder effects, molecular reorganization, and charge carrier localization, a comprehensive study was conducted on hole transport in a series of conjugated alternating phenanthrene indenofluorene copolymers. Each polymer in the series contained one
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