Date published: 2026-5-21

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N-Benzylaniline (CAS 103-32-2)

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Alternate Names:
N-Phenylbenzylamine
CAS Number:
103-32-2
Molecular Weight:
183.25
Molecular Formula:
C13H13N
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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N-Benzylaniline is extensively used in research focused on organic synthesis and material science, where it serves as an important intermediate in the production of dyes, pigments, and other aromatic compounds. N-Benzylaniline is instrumental in studies related to the properties of aniline derivatives, particularly their electronic and structural characteristics, which are for developing advanced materials with specific optical and electrical properties. N-Benzylaniline is investigated for its potential use in the synthesis of bioactive and agrochemical products, exploring its reactivity and the mechanisms by which it forms more complex molecules. Its role in polymer chemistry is examined, particularly in the creation of polymers that require specific functionalities for high-performance applications. N-Benzylaniline′s utility in catalysis, especially in facilitating reactions that involve the formation of carbon-nitrogen bonds, is another significant area of study.


N-Benzylaniline (CAS 103-32-2) References

  1. N-benzylideneaniline and N-benzylaniline are potent inhibitors of lignostilbene-alpha,beta-dioxygenase, a key enzyme in oxidative cleavage of the central double bond of lignostilbene.  |  Han, SY., et al. 2003. J Enzyme Inhib Med Chem. 18: 279-83. PMID: 14506920
  2. Dissociative benzyl cation transfer versus proton transfer: loss of benzene from protonated N-benzylaniline.  |  Sun, H., et al. 2012. J Org Chem. 77: 7098-102. PMID: 22823406
  3. Functionalized Graphitic Carbon Nitride Decorated with Palladium: an Efficient Heterogeneous Catalyst for Hydrogenation Reactions Using KHCO2 as a Mild and Noncorrosive Source of Hydrogen.  |  Bahuguna, A. and Sasson, Y. 2020. ACS Omega. 5: 12302-12312. PMID: 32548413
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  5. Mimicking transition metals in borrowing hydrogen from alcohols.  |  Banik, A., et al. 2021. Chem Sci. 12: 8353-8361. PMID: 34221316
  6. Generation of Masked TiII Intermediates from TiIV Amides via β-H Abstraction or Alkyne Deprotonation: An Example of Ti-Catalyzed Nitrene-Coupled Transfer Hydrogenation.  |  Pearce, AJ., et al. 2020. Organometallics. 39: 3771-3774. PMID: 34321708
  7. Selective Para-C-H Alkynylation of Aniline Derivatives by Pd/S,O-Ligand Catalysis.  |  Deng, KZ., et al. 2022. Chemistry. 28: e202104107. PMID: 34902180
  8. Mn(ii)-Catalysed ortho-alkenylation of aromatic amines and its application in reproductive diseases.  |  Yang, J., et al. 2020. RSC Adv. 11: 164-167. PMID: 35423065
  9. Coordinatively Unsaturated Hf-MOF-808 Prepared via Hydrothermal Synthesis as a Bifunctional Catalyst for the Tandem N-Alkylation of Amines with Benzyl Alcohol.  |  Bohigues, B., et al. 2021. ACS Sustain Chem Eng. 9: 15793-15806. PMID: 35663357
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  11. Preparation of core-shell catalyst for the tandem reaction of amino compounds with aldehydes.  |  Liang, J., et al. 2023. RSC Adv. 13: 5186-5196. PMID: 36777936
  12. Designing New Magnesium Pincer Complexes for Catalytic Hydrogenation of Imines and N-Heteroarenes: H2 and N-H Activation by Metal-Ligand Cooperation as Key Steps.  |  Liang, Y., et al. 2023. J Am Chem Soc. 145: 9164-9175. PMID: 37068165
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

N-Benzylaniline, 25 g

sc-235999
25 g
$34.00