Date published: 2025-10-31

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2,6-Diaminoanthraquinone (CAS 131-14-6)

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CAS Number:
131-14-6
Molecular Weight:
238.24
Molecular Formula:
C14H10N2O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2,6-Diaminoanthraquinone (2,6-DAAQ) is a highly versatile organic compound widely utilized in scientific research. Its broad range of applications encompasses both organic and inorganic chemistry, making it an essential tool in various scientific endeavors. It plays a role in the investigation of biochemical and physiological processes. Its applications extend to the study of DNA and protein structure and function, as well as the examination of enzyme-catalyzed reactions. One of the key characteristics of 2,6-Diaminoanthraquinone is its role as an electron acceptor in various biochemical and physiological processes. It exhibits the ability to accept electrons from molecules such as proteins and enzymes, subsequently facilitating their transfer to other molecules. Moreover, 2,6-Diaminoanthraquinone can also function as an electron donor, enabling the transfer of electrons to other molecules.


2,6-Diaminoanthraquinone (CAS 131-14-6) References

  1. [Intensified Electrosorption of Pb2+ by 2,6-diaminoanthraquinone/Graphene Composite Electrode].  |  Jin, SY., et al. 2019. Huan Jing Ke Xue. 40: 4091-4097. PMID: 31854872
  2. A Reduced-Symmetry Heterobimetallic [PdPtL4 ]4+ Cage: Assembly, Guest Binding, and Stimulus-Induced Switching.  |  Lisboa, LS., et al. 2020. Angew Chem Int Ed Engl. 59: 11101-11107. PMID: 32220036
  3. A 2D donor-acceptor covalent organic framework with charge transfer for supercapacitors.  |  Li, T., et al. 2020. Chem Commun (Camb). 56: 14187-14190. PMID: 33107874
  4. Electro-enhanced solid-phase microextraction with covalent organic framework modified stainless steel fiber for efficient adsorption of bisphenol A.  |  Pang, YH., et al. 2021. Anal Chim Acta. 1142: 99-107. PMID: 33280708
  5. Porous Organic Polymer Synthesized by Green Diazo-Coupling Reaction for Adsorptive Removal of Methylene Blue.  |  Shen, Y., et al. 2021. ACS Omega. 6: 3202-3208. PMID: 33553936
  6. Covalent Triazine Framework as an Efficient Photocatalyst for Regeneration of NAD(P)H and Selective Oxidation of Organic Sulfide.  |  Chaubey, S., et al. 2022. Photochem Photobiol. 98: 150-159. PMID: 34390001
  7. Self-Assembled Carbon Superstructures Achieving Ultra-Stable and Fast Proton-Coupled Charge Storage Kinetics.  |  Song, Z., et al. 2021. Adv Mater. 33: e2104148. PMID: 34622501
  8. Heterotrimetallic Double Cavity Cages: Syntheses and Selective Guest Binding.  |  Lisboa, LS., et al. 2022. Angew Chem Int Ed Engl. 61: e202201700. PMID: 35194905
  9. Anthraquinone-2,6-disulfamidic acid: an anolyte with low decomposition rates at elevated temperatures.  |  Rohland, P., et al. 2021. RSC Adv. 11: 38759-38764. PMID: 35493233
  10. Metal-Free Photocatalysts for Conversion of H2 O into Hydrogen Peroxide.  |  Wang, Q., et al. 2022. ChemSusChem. 15: e202201514. PMID: 36177848
  11. Organic Small-Molecule Electrodes: Emerging Organic Composite Materials in Supercapacitors for Efficient Energy Storage.  |  He, Y., et al. 2022. Molecules. 27: PMID: 36431793
  12. COF-Based Electrodes with Vertically Supported Tentacle Array for Ultrahigh Stability Flexible Energy Storage.  |  He, Y., et al. 2022. ACS Appl Mater Interfaces. 14: 57328-57339. PMID: 36525593
  13. Selective oxidation of amines powered with green light and oxygen over an anthraquinone covalent organic framework.  |  Xiong, K., et al. 2023. J Colloid Interface Sci. 643: 340-349. PMID: 37080041
  14. Iodine doping induced activation of covalent organic framework cathodes for Li-ion batteries.  |  Ren, G., et al. 2023. RSC Adv. 13: 18983-18990. PMID: 37362603

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2,6-Diaminoanthraquinone, 5 g

sc-225760
5 g
$49.00