Date published: 2025-9-5

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6-Aminoquinoline (CAS 580-15-4)

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Alternate Names:
6-Quinolinamine
CAS Number:
580-15-4
Molecular Weight:
144.17
Molecular Formula:
C9H8N2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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6-Aminoquinoline is extensively used in the field of chemical synthesis and material science. Researchers employ this compound for the development of complex organic molecules and as a building block in the synthesis of various heterocyclic compounds. Its presence is in studies related to fluorescence properties, where 6-Aminoquinoline acts as a fluorophore in the design of new imaging agents. The compound is also pivotal in environmental science research, particularly in the detection and analysis of metals and pollutants through complexation reactions. Furthermore, 6-Aminoquinoline′s role in catalysis is studied to refine and enhance reactions in organic synthesis, demonstrating its versatility and importance in advancing various branches of chemical research.


6-Aminoquinoline (CAS 580-15-4) References

  1. Towards aspirin-inspired self-immolating molecules which target the cyclooxygenases.  |  Drake, CR., et al. 2015. Org Biomol Chem. 13: 11078-86. PMID: 26400105
  2. 6-Polyamino-substituted quinolines: synthesis and multiple metal (CuII, HgII and ZnII) monitoring in aqueous media.  |  Abel, AS., et al. 2019. Org Biomol Chem. 17: 4243-4260. PMID: 30860543
  3. [Determination of 18 amino acids in three different kinds of milk powder by ultra performance liquid chromatography coupled with pre-column derivatization].  |  Qu, L., et al. 2021. Se Pu. 39: 472-477. PMID: 34227331
  4. Structural, Electronic and NLO Properties of 6-aminoquinoline: A DFT/TD-DFT Study.  |  Pandey, N., et al. 2021. J Fluoresc. 31: 1719-1729. PMID: 34427839
  5. Solvatochromism and estimation of ground and excited state dipole moments of 6-aminoquinoline.  |  Pandey, N., et al. 2022. Spectrochim Acta A Mol Biomol Spectrosc. 267: 120498. PMID: 34740005
  6. Enhanced carboxypeptidase efficacies and differentiation of peptide epimers.  |  Sung, YS., et al. 2022. Anal Biochem. 642: 114451. PMID: 34774536
  7. Photophysical, photostability, and ROS generation properties of new trifluoromethylated quinoline-phenol Schiff bases.  |  Rocha, IO., et al. 2021. Beilstein J Org Chem. 17: 2799-2811. PMID: 34925619
  8. Fast and Sensitive Quantification of AccQ-Tag Derivatized Amino Acids and Biogenic Amines by UHPLC-UV Analysis from Complex Biological Samples.  |  Guba, A., et al. 2022. Metabolites. 12: PMID: 35323715
  9. Need and Viability of Newborn Screening Programme in India: Report from a Pilot Study.  |  Raveendran, A., et al. 2022. Int J Neonatal Screen. 8: PMID: 35466197
  10. Development of antiparallel-type triplex-forming oligonucleotides containing quinoline derivatives capable of recognizing a T-A base pair in a DNA duplex.  |  Nishizawa, S., et al. 2022. Bioorg Med Chem. 71: 116934. PMID: 35921784
  11. Teicoplanin aglycone media and carboxypeptidase Y: Tools for finding low-abundance D-amino acids and epimeric peptides.  |  Sung, YS., et al. 2023. Chirality.. PMID: 36929217
  12. A novel fluorogenic reporter substrate for 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-2 (PLCγ2): Application to high-throughput screening for activators to treat Alzheimer's disease.  |  Visvanathan, R., et al. 2023. SLAS Discov. 28: 170-179. PMID: 36933698
  13. Photocurrent Generation and Polarity Switching in Electrochemical Cells through Light-induced Excited State Proton Transfer of Photoacids and Photobases.  |  Yucknovsky, A., et al. 2023. Angew Chem Int Ed Engl. 62: e202301541. PMID: 37190933

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

6-Aminoquinoline, 1 g

sc-239088
1 g
$49.00