Date published: 2025-12-14

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1-Pyrenecarboxaldehyde (CAS 3029-19-4)

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Alternate Names:
1-Pyrenealdehyde; 1-Formylpyrene
Application:
1-Pyrenecarboxaldehyde is a novel base-discriminating fluorescent (BDF) compound
CAS Number:
3029-19-4
Purity:
≥99%
Molecular Weight:
230.26
Molecular Formula:
C17H10O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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1-Pyrenecarboxaldehyde is a fluorescent organic compound used as a probe in biochemistry. It has ability to react with amino acids and proteins, making it useful in studying protein structure and function. 1-Pyrenecarboxaldehyde is particularly useful in the study of protein folding and aggregation, as its fluorescence properties allow for the monitoring of conformational changes and interactions between proteins. It is sensitive to changes in the local environment, such as pH and temperature, making it versatile for studying the behavior of proteins under different conditions. Its unique fluorescent properties and reactivity with proteins make it important in biochemistry.


1-Pyrenecarboxaldehyde (CAS 3029-19-4) References

  1. Solvent effects on the kinetics of the interaction of 1-pyrenecarboxaldehyde with calf thymus DNA.  |  Secco, F., et al. 2010. J Phys Chem B. 114: 4686-91. PMID: 20297772
  2. Convenient and efficient approach to the permanent or reversible conjugation of RNA and DNA sequences with functional groups.  |  Cieślak, J., et al. 2012. Curr Protoc Nucleic Acid Chem. Chapter 4: Unit4.52. PMID: 22956458
  3. Synthesis of carboxylate-functionalized graphene nanosheets for high dispersion of platinum nanoparticles based on the reduction of graphene oxide via 1-pyrenecarboxaldehyde.  |  Kuang, Y., et al. 2013. Nanotechnology. 24: 395604. PMID: 24013585
  4. Oxidized polyethylene films for orienting polar molecules for linear dichroism spectroscopy.  |  Razmkhah, K., et al. 2014. Analyst. 139: 1372-82. PMID: 24482800
  5. Decomposition and transformation of pyrene-derivative micelles at intracellular milieu and their influence on cytoviability.  |  Wang, H., et al. 2014. Macromol Biosci. 14: 1748-54. PMID: 25205202
  6. Synergetic spin crossover and fluorescence in one-dimensional hybrid complexes.  |  Wang, CF., et al. 2015. Angew Chem Int Ed Engl. 54: 1574-7. PMID: 25504738
  7. Fluorescent imino and secondary amino chitosans as potential sensing biomaterials.  |  Jatunov, S., et al. 2015. Carbohydr Polym. 123: 288-96. PMID: 25843861
  8. Ion Sensor Properties of Fluorescent Schiff Bases Carrying Dipicolylamine Groups. A Simple Spectrofluorimetric Method to Determine Cu (II) in Water Samples.  |  Vanlı, E., et al. 2017. J Fluoresc. 27: 1759-1766. PMID: 28536848
  9. A highly selective and reversible turn-off fluorescent chemosensor for Cu2+ based on electrospun nanofibrous membrane modified with pyrenecarboxaldehyde.  |  Cui, X., et al. 2019. Spectrochim Acta A Mol Biomol Spectrosc. 207: 173-182. PMID: 30243105
  10. Polymeric Ionic Liquid-Based Fluorescent Amphiphilic Block Copolymer Micelle for Selective and Sensitive Detection of p-Phenylenediamine.  |  Gao, LF., et al. 2018. ACS Appl Mater Interfaces. 10: 43049-43056. PMID: 30457315
  11. An efficient new dual fluorescent pyrene based chemosensor for the detection of bismuth (III) and aluminium (III) ions and its applications in bio-imaging.  |  Saravanan, A., et al. 2019. Talanta. 198: 249-256. PMID: 30876558
  12. Organic Dots Embedded in Mesostructured Silica Xerogel as High-Performance ECL Emitters: Preparation and Application for MicroRNA-126 Detection.  |  Tu, TT., et al. 2020. ACS Appl Mater Interfaces. 12: 3945-3952. PMID: 31877251
  13. A facile and total water-soluble fluorescent organic nanoparticles-based sensor for Hg2+ detection and its application in tea samples.  |  Wang, Y., et al. 2022. Spectrochim Acta A Mol Biomol Spectrosc. 265: 120358. PMID: 34509892

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-Pyrenecarboxaldehyde, 5 g

sc-208694
5 g
$106.00