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Merck
CN

40079

菲 溶液

certified reference material, 5000 μg/mL in methanol

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化学文摘社编号:
PubChem Substance ID:
UNSPSC Code:
41116105
Beilstein/REAXYS Number:
1905428
MDL number:
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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

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

Gene Information

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

signalword

Danger

存储类别

3 - Flammable liquids

wgk

WGK 2

flash_point_f

51.8 °F - closed cup

flash_point_c

11 °C - closed cup

Hazard Classifications

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

target_organs

Eyes,Central nervous system

法规信息

危险化学品
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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
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
Xinghui Xia et al.
Environmental toxicology and chemistry, 32(4), 894-901 (2013-01-22)
Carbon nanotubes have attracted attention around the world because of their high sorption capacity for hydrophobic organic compounds (HOCs); however, the bioavailability of HOCs sorbed on carbon nanotubes to bacteria is not well known. In the present study, (14) C-labeled
Lei Wang et al.
Journal of hazardous materials, 244-245, 268-275 (2012-12-29)
To study the impact of organic matter (OM) properties on different sorption domain of hydrophobic organic contaminants, phenanthrene sorption on chemically modified geosorbents and synthesized charcoals (SCs) was investigated and explored using Dual-Mode model (DMM). Sorption of phenanthrene on two

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