Date published: 2025-12-18

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9,10-Diphenylanthracene (CAS 1499-10-1)

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CAS Number:
1499-10-1
Molecular Weight:
330.42
Molecular Formula:
C26H18
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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9,10-Diphenylanthracene is a polycyclic aromatic hydrocarbon that is used as a fluorophore in various biochemical and biophysical studies. It is a solid, crystalline compound that exhibits strong fluorescence properties when excited by ultraviolet light. This makes it valuable for studying the dynamics and interactions of biomolecules, such as proteins and nucleic acids, in a variety of experimental applications. Due to its rigid and planar structure, 9,10-diphenylanthracene is high photostable, which allows for prolonged observation of biological processes without significant photobleaching.Its relatively long fluorescence lifetime makes it suitable for time-resolved fluorescence measurements, providing a better understanding of the kinetics of biomolecular events. The hydrophobic nature of 9,10-diphenylanthracene allows for its incorporation into lipid membranes, where it can serve as a sensitive probe for studying membrane dynamics and organization. The unique optical properties of 9,10-diphenylanthracene make it indispensable for investigating various aspects of biochemistry and biophysics.


9,10-Diphenylanthracene (CAS 1499-10-1) References

  1. A peroxyoxalate chemiluminescence-based assay for the evaluation of hydrogen peroxide scavenging activity employing 9,10-diphenylanthracene as the fluorophore.  |  Arnous, A., et al. 2002. J Pharmacol Toxicol Methods. 48: 171-7. PMID: 14986866
  2. Functional macromolecules from single-walled carbon nanotubes: synthesis and photophysical properties of short single-walled carbon nanotubes functionalised with 9,10-diphenylanthracene.  |  Aprile, C., et al. 2008. Chemistry. 14: 5030-8. PMID: 18418827
  3. Electrogenerated chemiluminescence of 9,10-diphenylanthracene, rubrene, and anthracene in fluorinated aromatic solvents.  |  Vinyard, DJ., et al. 2008. J Phys Chem A. 112: 8529-33. PMID: 18729443
  4. Upconversion-powered photoelectrochemistry.  |  Khnayzer, RS., et al. 2012. Chem Commun (Camb). 48: 209-11. PMID: 22080384
  5. 9,10-Diphenylanthracene as a matrix for MALDI-MS electron transfer secondary reactions.  |  Boutaghou, MN. and Cole, RB. 2012. J Mass Spectrom. 47: 995-1003. PMID: 22899508
  6. Electrogenerated chemiluminescence of BODIPY, Ru(bpy)3(2+), and 9,10-diphenylanthracene using interdigitated array electrodes.  |  Nepomnyashchii, AB., et al. 2013. ACS Appl Mater Interfaces. 5: 5931-6. PMID: 23740271
  7. Highly Efficient Blue Organic-Light Emitting Diodes Based on 9,10-Diphenylanthracene End-Capped 5H-Pyrido[3,2-b]lndole Groups.  |  Lee, SB., et al. 2015. J Nanosci Nanotechnol. 15: 7804-7. PMID: 26726417
  8. Morphology-Controlled 9,10-Diphenylanthracene Nanoblocks as Electrochemiluminescence Emitters for MicroRNA Detection with One-Step DNA Walker Amplification.  |  Liu, JL., et al. 2018. Anal Chem. 90: 5298-5305. PMID: 29564887
  9. Interplay of exciton-excimer dynamics in 9,10-diphenylanthracene nanoaggregates and thin films revealed by time-resolved spectroscopic studies.  |  Nandi, A., et al. 2019. Phys Chem Chem Phys. 21: 11193-11202. PMID: 31099362
  10. Triplet fusion upconversion using sterically protected 9,10-diphenylanthracene as the emitter.  |  Gao, C., et al. 2020. Phys Chem Chem Phys. 22: 6300-6307. PMID: 32133470
  11. A chromatography-free total synthesis of a ferrocene-containing dendrimer exhibiting the property of recognizing 9,10-diphenylanthracene.  |  Kasprzak, A., et al. 2021. Dalton Trans. 50: 2483-2492. PMID: 33514975
  12. Organic Semiconductor Single Crystals for X-ray Imaging.  |  Chen, M., et al. 2021. Adv Mater. 33: e2104749. PMID: 34545653
  13. Triplet-Triplet Annihilation via the Triplet Channel in Crystalline 9,10-Diphenylanthracene.  |  Yago, T., et al. 2022. J Phys Chem Lett. 13: 8768-8774. PMID: 36102694
  14. Photochemically deoxygenating gels for triplet-triplet annihilation photon-upconversion performed under air.  |  Zhou, H., et al. 2022. Phys Chem Chem Phys. 24: 29151-29158. PMID: 36444712
  15. Ratiometric Singlet Oxygen Sensor Based on BODIPY-DPA Dyad.  |  Pakhomov, AA., et al. 2022. Molecules. 27: PMID: 36558192

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

9,10-Diphenylanthracene, 250 mg

sc-239146
250 mg
$56.00

9,10-Diphenylanthracene, 1 g

sc-239146A
1 g
$55.00

9,10-Diphenylanthracene, 5 g

sc-239146B
5 g
$73.00

9,10-Diphenylanthracene, 25 g

sc-239146C
25 g
$196.00