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2-Amino-7-nitrofluorene (CAS 1214-32-0)

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Alternate Names:
7-Nitro-9H-fluoren-2-amine
Application:
2-Amino-7-nitrofluorene is an aromatic nitro compound
CAS Number:
1214-32-0
Molecular Weight:
226.23
Molecular Formula:
C13H10N2O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2-Amino-7-nitrofluorene is a fluorescent aromatic nitro compound that finds utility in diverse biochemical and physiological investigations. Primarily, it serves as a fluorescent dye for the detection and quantification of proteins, nucleic acids, and other biomolecules. Widely employed for biomolecule analysis, it also facilitates the detection of environmental pollutants and contributes to the development of biosensors. Furthermore, 2-Amino-7-nitrofluorene plays a role in pharmaceutical synthesis and aids in the study of cell metabolism and signaling pathways.


2-Amino-7-nitrofluorene (CAS 1214-32-0) References

  1. Heterogeneity in a room-temperature ionic liquid: persistent local environments and the red-edge effect.  |  Hu, Z. and Margulis, CJ. 2006. Proc Natl Acad Sci U S A. 103: 831-6. PMID: 16418271
  2. A study of the time-resolved fluorescence spectrum and red edge effect of ANF in a room-temperature ionic liquid.  |  Hu, Z. and Margulis, CJ. 2006. J Phys Chem B. 110: 11025-8. PMID: 16771357
  3. Charge-transfer-induced twisting of the nitro group.  |  Mondal, JA., et al. 2007. J Phys Chem A. 111: 6122-6. PMID: 17591761
  4. Solvation oscillations and excited-state dynamics of 2-amino- and 2-hydroxy-7-nitrofluorene and its 2'-deoxyriboside.  |  Karunakaran, V., et al. 2008. J Phys Chem A. 112: 4294-307. PMID: 18386856
  5. Diffusion-viscosity decoupling in solute rotation and solvent relaxation of coumarin153 in ionic liquids containing fluoroalkylphosphate (FAP) anion: a thermophysical and photophysical study.  |  Das, SK., et al. 2013. J Phys Chem B. 117: 636-47. PMID: 23256462
  6. Difluoroboron β-diketonate polylactic acid oxygen nanosensors for intracellular neuronal imaging.  |  Zhuang, M., et al. 2021. Sci Rep. 11: 1076. PMID: 33441771
  7. Some arsonic acids of fluorene and its derivatives  |  Cislak, F. E., & Hamilton, C. S. 1931. Journal of the American Chemical Society. 53(2): 746-749.
  8. Calculated values for the solubility product constants of the metallic sulfides  |  Goates, J. R., Gordon, M. B., & Faux, N. D. 1952. Journal of the American Chemical Society. 74(3): 835-836.
  9. Organic dye laser properties and orientational relaxation processes  |  Gronau, B., Lippert, E., & Rapp, W. 1972. Berichte der Bunsengesellschaft für physikalische Chemie. 76(5): 432-437.
  10. Time-resolved fluorescence spectroscopy of 2-amino-7-nitrofluorene in two-solvent solutions  |  Hallidy, L. A., & Topp, M. R. 1978. The Journal of Physical Chemistry. 82(22): 2415-2419.
  11. Picosecond optical pulse sampling by frequency conversion. Studies of solvent-induced molecular relaxation  |  Hallidy, L., & Topp, M. 1978. The Journal of Physical Chemistry. 82(21): 2273-2277.
  12. Progress towards a generalized solvent polarity scale: The solvatochromism of 2‐(dimethylamino)‐7‐nitrofluorene and its homomorph 2‐fluoro‐7‐nitrofluorene  |  Catalán, J., López, V., Pérez, P., Martin‐Villamil, R., & Rodríguez, J. G. 1995. Liebigs Annalen. 1995(2): 241-252.
  13. Femtosecond relaxation of 2-amino-7-nitrofluorene in acetonitrile: Observation of the oscillatory contribution to the solvent response  |  Ruthmann, J., Kovalenko, S. A., Ernsting, N. P., & Ouw, D. 1998. The Journal of chemical physics. 109(13): 5466-5468.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Amino-7-nitrofluorene, 250 mg

sc-209062
250 mg
$331.00