Date published: 2026-5-19

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4-Aminobenzylamine (CAS 4403-71-8)

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CAS Number:
4403-71-8
Molecular Weight:
122.17
Molecular Formula:
C7H10N2
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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4-Aminobenzylamine (4-AB) is a versatile organic compound extensively utilized in scientific research to explore the characteristics of amines. It serves as an essential precursor in the synthesis of numerous pharmaceuticals and diverse compounds. Its applications span a wide range, including drug synthesis, dye production, and the creation of intermediates for manufacturing various compounds. Additionally, it finds utility in the synthesis of polymers and other materials. By studying 4-Aminobenzylamine, researchers gain valuable insights into the biochemical and physiological effects of amines.


4-Aminobenzylamine (CAS 4403-71-8) References

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  2. Biocatalytic behaviour of immobilized Rhizopus oryzae lipase in the 1,3-selective ethanolysis of sunflower oil to obtain a biofuel similar to biodiesel.  |  Luna, C., et al. 2014. Molecules. 19: 11419-39. PMID: 25093983
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  4. Recyclable Self-Healing Polyurethane Cross-Linked by Alkyl Diselenide with Enhanced Mechanical Properties.  |  Qian, Y., et al. 2019. Polymers (Basel). 11: PMID: 31052422
  5. A Straightforward Approach to Multifunctional Graphene.  |  Lucherelli, MA., et al. 2019. Chemistry. 25: 13218-13223. PMID: 31298440
  6. Binding Kinetics of Methylene Blue on Monolayer Graphene Investigated by Multiparameter Surface Plasmon Resonance.  |  Kaya, NS., et al. 2018. ACS Omega. 3: 7133-7140. PMID: 31458875
  7. Dataset for synthesis of conducting polymers nanocomposites based on aniline and 4-amino-benzylamine catalyzed by chromium (III) exchanged maghnite (Algerian MMT) via in situ polymerization.  |  Zeggai, FZ., et al. 2020. Data Brief. 29: 105161. PMID: 32071960
  8. Synthesis and characterisation of thiobarbituric acid enamine derivatives, and evaluation of their α-glucosidase inhibitory and anti-glycation activity.  |  Ali, M., et al. 2020. J Enzyme Inhib Med Chem. 35: 692-701. PMID: 32156165
  9. 'Photo-Rimonabant': Synthesis and Biological Evaluation of Novel Photoswitchable Molecules Derived from Rimonabant Lead to a Highly Selective and Nanomolar 'Cis-On' CB1R Antagonist.  |  Rodríguez-Soacha, DA., et al. 2021. ACS Chem Neurosci. 12: 1632-1647. PMID: 33856764
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  12. Modulating the Fibrillization of Parathyroid-Hormone (PTH) Peptides: Azo-Switches as Reversible and Catalytic Entities.  |  Paschold, A., et al. 2022. Biomedicines. 10: PMID: 35884817
  13. Selective syntheses of thick and thin nanosheets based on correlation between thickness and lateral-size distribution.  |  Haraguchi, Y., et al. 2022. iScience. 25: 104933. PMID: 36097614
  14. Phenyloxycarbonyl (Phoc) Carbamate: Chemioselective Reactivity and Tetra-n-butylammonium Fluoride Deprotection Study.  |  Huguenot, F. and Vidal, M. 2022. ACS Omega. 7: 44861-44868. PMID: 36530256
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Aminobenzylamine, 10 g

sc-232398
10 g
$92.00