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MilliporeSigma

48569

Supelco

Phenanthrene

analytical standard, for environmental analysis

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About This Item

Empirical Formula (Hill Notation):
C14H10
CAS Number:
Molecular Weight:
178.23
Beilstein/REAXYS Number:
1905428
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
Technical Service
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grade

analytical standard

Quality Level

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.
This compound is listed in the SVHC (Substances of very high concern) candidate list of ECHA (European Chemicals Agency)

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

signalword

Warning

hcodes

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


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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)
Raïssa Kom Regonne et al.
Environmental pollution (Barking, Essex : 1987), 180, 145-151 (2013-06-19)
Efficient bioremediation of PAH-contaminated sites is limited by the hydrophobic character and poor bioavailability of pollutants. In this study, stable isotope probing (SIP) was implemented to track bacteria that can degrade PAHs adsorbed on hydrophobic sorbents. Temperate and tropical soils
Geoffrey Marchal et al.
Environmental pollution (Barking, Essex : 1987), 181, 200-210 (2013-07-23)
Sorption of PAHs to carbonaceous soil amendments reduces their dissolved concentrations, limiting toxicity but also potentially biodegradation. Therefore, the maximum abiotic desorption of freshly sorbed phenanthrene (≤5 mg kg(-1)) was measured in three soils amended with activated carbon (AC), biochar
Wenyan Li et al.
Environmental pollution (Barking, Essex : 1987), 176, 228-233 (2013-02-26)
Nanoparticles (NPs) in soils may participate in essential ecological services, since they have special characteristics arising from their nanoscale sizes and large surface areas. We did aqueous solubility enhancement experiments to derive the partition coefficients of phenanthrene between water and

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