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Merck
CN

40079

Supelco

Phenanthrene solution

new

certified reference material, 5000 μg/mL in methanol

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About This Item

CAS Number:
85-01-8
Beilstein:
1905428
MDL number:
MFCD00001168
UNSPSC Code:
41116105
PubChem Substance ID:
24864953

Key Documents

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grade

certified reference material
TraceCERT®

product line

TraceCERT®

CofA

current certificate can be downloaded

packaging

ampule of 1 mL

concentration

5000 μg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

environmental

format

single component solution

storage temp.

2-8°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), CYP2A6(1548)
mouse ... Cyp2a5(13087)

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General description

Phenanthrene can be synthesized, via a multi-step synthesis process, using Haworth method involving, naphthalene and succinic anhydride as the starting materials. It can undergo chlorination in acetic acid to obtain a mixture of cis- and trans-9,10-dichloro-9,10-dihydrophenanthrenes as the major products.
This compound is listed in the SVHC (Substances of very high concern) candidate list of ECHA (European Chemicals Agency)

Other Notes

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Legal Information

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Flam. Liq. 2 - STOT SE 1

Target Organs

Eyes

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

51.8 °F - closed cup

Flash Point(C)

11 °C - closed cup

Regulatory Information

危险化学品
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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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Hepworth.DJ, et al. et al.
Aromatic Chemistry, 13 (2002)
Fei Dong et al.
Wei sheng wu xue bao = Acta microbiologica Sinica, 52(8), 985-993 (2012-11-24)
To identify the relationship between salicylate 5-hydroxylase activity and the degradation rate of phenanthrene by moderately halophilic Martelella sp. AD-3, and to investigate their enzymatic characteristics. The products resulted from degradation of salicylic acid using the crude enzyme produced by
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
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)
Stephen S Hecht et al.
Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals, 18(2), 144-150 (2013-01-23)
The extent of metabolism of [D10]phenanthrene to [D(10)]r-1,t-2,3,c-4-tetrahydroxy-1,2,3,4-tetradeuterophenanthrene ([D10]PheT) could be a biomarker of human metabolic activation of carcinogenic polycyclic aromatic hydrocarbons, leading to identification of smokers particularly susceptible to lung cancer. The longitudinal stability of [D10]PheT was evaluated in
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