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156507

Sigma-Aldrich

9,10-Phenanthrenequinone

≥99%

Synonym(s):

9,10-Phenanthrenedione

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About This Item

Empirical Formula (Hill Notation):
C14H8O2
CAS Number:
84-11-7
Molecular Weight:
208.21
Beilstein/REAXYS Number:
608838
EC Number:
201-515-5
MDL number:
MFCD00001163
UNSPSC Code:
12352103
PubChem Substance ID:
24849615
NACRES:
NA.23
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Quality Level

100

assay

≥99%

impurities

<0.1% anthraquinone

mp

209-212 °C (lit.)

λmax

420 nm

SMILES string

O=C1C(=O)c2ccccc2-c3ccccc13

InChI

1S/C14H8O2/c15-13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)14(13)16/h1-8H

InChI key

YYVYAPXYZVYDHN-UHFFFAOYSA-N

Gene Information

human ... PTPN1(5770) , PTPRC(5788)

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1 of 4

This Item
275034D22908778885
9,10-Phenanthrenequinone &#8805;99%

156507

9,10-Phenanthrenequinone

9,10-Phenanthrenequinone 95%

275034

9,10-Phenanthrenequinone

9,10-Diaminophenanthrene 97%

D22908

9,10-Diaminophenanthrene

(11R,12R)-9,10-Dihydro-9,10-ethanoanthracene-11,12-diamine &#8805;95.0% (HPLC)

778885

(11R,12R)-9,10-Dihydro-9,10-ethanoanthracene-11,12-diamine

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

-

mp

209-212 °C (lit.)

mp

209-212 °C (lit.)

mp

164-166 °C (lit.)

mp

-

impurities

<0.1% anthraquinone

impurities

-

impurities

-

impurities

≤5% water

λmax

420 nm

λmax

-

λmax

-

λmax

-

Gene Information

human ... PTPN1(5770), PTPRC(5788)

Gene Information

human ... PTPN1(5770), PTPRC(5788)

Gene Information

-

Gene Information

-

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H319,H400

Hazard Classifications

Aquatic Acute 1 - Eye Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

473.0 °F

flash_point_c

245 °C

ppe

dust mask type N95 (US), Eyeshields, Gloves

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    Certificates of Analysis (COA)

    Lot/Batch Number
    MKBG9712V
    MKBG1112V
    STBB8076V
    STBB8076
    S79639

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    9, 10-Phenanthrenequinone binary complexes of iron, cobalt, and nickel
    Floriani, C., R. Henzi, and F. Calderazzo
    J. Chem. Soc., Dalton Trans., 23, 2640-2642 (1972)
    Molecular Properties of 9, 10-Phenanthrenequinone and Benzil
    Muddasir, H., Lu, P., Gu, C., Wang, Z. M., Yang, S. M., Yang, B., &amp; Ma, Y. G.
    Chemical Research in Chinese Universities, 25(6), 950-956 (2009)
    Electronic structure and band alignment of 9, 10-phenanthrenequinone passivated silicon surfaces
    Avasthi, Sushobhan, et al.
    Surface Science, 605(13), 1308-1312 (2011)
    Petr Milko et al.
    Inorganic chemistry, 48(24), 11734-11742 (2009-11-26)
    With the use of the model complexes [(PQ)FeCl(CH(3)O)](+), [(phen)FeCl(CH(3)O)](+), and [(PQ)(phen)FeCl(CH(3)O)](+), where PQ is 9,10-phenanthraquinone and phen is 1,10-phenanthroline, the reactivity of phenanthraquinone in complexes with iron(III) is investigated. It is shown that 9,10-phenanthraquinone takes part in redox processes occurring
    Michael C Byrns et al.
    Biochemical pharmacology, 75(2), 484-493 (2007-10-24)
    Aldo-keto reductase (AKR) 1C3 (type 2 3alpha-HSD, type 5 17beta-HSD, and prostaglandin F synthase) regulates ligand access to steroid hormone and prostaglandin receptors and may stimulate proliferation of prostate and breast cancer cells. NSAIDs are known inhibitors of AKR1C enzymes.
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