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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
LRAD2498
LRAC8436
LRAC3583
LRAC0550
LC27042V

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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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US EPA Method 610 describes the analysis of polynuclear aromatic hydrocarbons (commonly referred to as PAHs or PNAs) by both HPLC and GC.

HPLC Analysis of PAHs on SUPELCOSIL™ LC-PAH

HPLC Analysis of PAHs on SUPELCOSIL™ LC-PAH

GC Analysis of Polynuclear Aromatic Hydrocarbons (PAHs) in Salmon on SPB®-608 (20 m x 0.18 mm I.D., 0.18 µm) after QuEChERS Cleanup using Supel™ QuE Z-Sep, Fast GC Analysis

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