Date published: 2025-10-15

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5-Amino-1-pentanol (CAS 2508-29-4)

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CAS Number:
2508-29-4
Purity:
≥95%
Molecular Weight:
103.16
Molecular Formula:
C5H13NO
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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5-Amino-1-pentanol is a chemical compound that functions as a nucleophilic reagent in organic synthesis. It acts as a building block for the preparation of various fine chemicals. The primary amine group in 5-Amino-1-pentanol allows it to participate in nucleophilic substitution reactions, making it a useful reagent for the synthesis of a wide range of compounds. Its mechanism of action involves the formation of covalent bonds with electrophilic substrates, enabling the introduction of the amino group into organic molecules. 5-Amino-1-Pentanol′s functional role lies in its ability to serve as a versatile intermediate for the preparation of diverse chemical compounds, contributing to the development of new materials and compounds in research and development applications.


5-Amino-1-pentanol (CAS 2508-29-4) References

  1. Microwave-assisted functionalization of the Aurivillius phase Bi2SrTa2O9: diol grafting and amine insertion vs. alcohol grafting.  |  Wang, Y., et al. 2018. Chem Sci. 9: 7104-7114. PMID: 30310631
  2. Phosphonic acid-functionalized poly(amido amine) macromers for biomedical applications.  |  Altuncu, S., et al. 2020. J Biomed Mater Res A. 108: 2100-2110. PMID: 32319210
  3. Suprachoroidal gene transfer with nonviral nanoparticles.  |  Shen, J., et al. 2020. Sci Adv. 6: PMID: 32937452
  4. Ureido Functionalization through Amine-Urea Transamidation under Mild Reaction Conditions.  |  Guerrero-Alburquerque, N., et al. 2021. Polymers (Basel). 13: PMID: 34069157
  5. Non-Covalent Interactions in Molecular Systems: Thermodynamic Evaluation of the Hydrogen-Bond Strength in Amino-Ethers and Amino-Alcohols.  |  Siewert, R., et al. 2022. Chemistry. 28: e202200080. PMID: 35293642
  6. Study of Renal Accumulation of Targeted Polycations in Acute Kidney Injury.  |  Tang, W., et al. 2022. Biomacromolecules. 23: 2064-2074. PMID: 35394757
  7. Poly(Beta-Amino Ester)s as High-Yield Transfection Reagents for Recombinant Protein Production.  |  Luly, KM., et al. 2022. Int J Nanomedicine. 17: 4469-4479. PMID: 36176585
  8. Hyperbranched Poly(β-amino ester)s (HPAEs) Structure Optimisation for Enhanced Gene Delivery: Non-Ideal Termination Elimination.  |  Li, Y., et al. 2022. Nanomaterials (Basel). 12: PMID: 36364669
  9. A New Optimization Strategy of Highly Branched Poly(β-Amino Ester) for Enhanced Gene Delivery: Removal of Small Molecular Weight Components.  |  Li, Y., et al. 2023. Polymers (Basel). 15: PMID: 36987297
  10. Poly(β-amino ester)s-Based Delivery Systems for Targeted Transdermal Vaccination.  |  Puigmal, N., et al. 2023. Pharmaceutics. 15: PMID: 37111746
  11. Non-Viral Gene Delivery to Hepatocellular Carcinoma via Intra-Arterial Injection.  |  Vaughan, HJ., et al. 2023. Int J Nanomedicine. 18: 2525-2537. PMID: 37197026
  12. Branch Unit Distribution Matters for Gene Delivery.  |  Li, Y., et al. 2023. ACS Macro Lett. 12: 780-786. PMID: 37220212

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

5-Amino-1-pentanol, 10 g

sc-239022
10 g
$52.00