Date published: 2025-12-14

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Amylamine (CAS 110-58-7)

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Alternate Names:
n-Amylamine; Pentylamine; 1-Aminopentane
Application:
Amylamine is A compound used in the production of dyes and emulsifiers
CAS Number:
110-58-7
Purity:
≥98%
Molecular Weight:
87.16
Molecular Formula:
C5H13N
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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Amylamine is a chemical compound that functions as a reactive intermediate in various processes. It acts as a nucleophile in organic reactions, participating in the formation of amides, esters, and other organic compounds. Amylamine′s mode of action involves its ability to undergo nucleophilic substitution reactions, where it donates its lone pair of electrons to form new chemical bonds with electrophilic substrates. This allows for the synthesis of complex organic molecules and the modification of functional groups within a molecular structure. Amylamine′s reactivity and nucleophilic nature make it a useful function for the creation of diverse chemical compounds and the study of organic synthesis pathways. Its mode of action at the molecular level involves its interaction with specific functional groups and its role in facilitating the formation of new chemical bonds.


Amylamine (CAS 110-58-7) References

  1. Polyamines as olfactory stimuli in the goldfish Carassius auratus.  |  Rolen, SH., et al. 2003. J Exp Biol. 206: 1683-96. PMID: 12682100
  2. Probing mechanisms of catalysis and electron transfer by methylamine dehydrogenase by site-directed mutagenesis of alpha Phe55.  |  Davidson, VL. 2003. Biochim Biophys Acta. 1647: 230-3. PMID: 12686138
  3. Retention behavior of C1-C6 aliphatic monoamines on anion-exchange and polymethacrylate resins with heptylamine as eluent.  |  Ohta, K., et al. 2004. J Chromatogr A. 1039: 179-86. PMID: 15250421
  4. Automated on-fiber derivatization with headspace SPME-GC-MS-MS for the determination of primary amines in sewage sludge using pressurized hot water extraction.  |  Llop, A., et al. 2011. J Sep Sci. 34: 1531-7. PMID: 21618429
  5. Vibrational spectra, HOMO, LUMO, MESP surfaces and reactivity descriptors of amylamine and its isomers: A DFT study.  |  Dwivedi, A., et al. 2015. Spectrochim Acta A Mol Biomol Spectrosc. 149: 343-51. PMID: 25965519
  6. Effects of reduced levels of sulfite in wine production using mixtures with lysozyme and dimethyl dicarbonate on levels of volatile and biogenic amines.  |  Ancín-Azpilicueta, C., et al. 2016. Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 33: 1518-1526. PMID: 27597233
  7. Hyperbranched Aliphatic Polyester via Cross-Metathesis Polymerization: Synthesis and Postpolymerization Modification.  |  Zeng, FR., et al. 2018. Macromol Rapid Commun. 39: PMID: 29250866
  8. Gas chromatography/mass spectrometry of bacterial amines.  |  Tavakkol, A., et al. 1985. Biomed Mass Spectrom. 12: 359-63. PMID: 2931124
  9. Hydrophobicity-Adjustable MOF Constructs Superhydrophobic MOF-rGO Aerogel for Efficient Oil-Water Separation.  |  Sun, T., et al. 2020. ACS Appl Mater Interfaces. 12: 56435-56444. PMID: 33270430
  10. Specific characters of serum MAO in dogs.  |  Ikeno, M., et al. 1978. Biochem Exp Biol. 14: 3-10. PMID: 743481
  11. Ion chromatography of amylamine and tert.-butylamine in pharmaceuticals.  |  Jagota, NK., et al. 1996. J Chromatogr A. 739: 343-9. PMID: 8765853
  12. Pseudomonas monteilii sp. nov., isolated from clinical specimens.  |  Elomari, M., et al. 1997. Int J Syst Bacteriol. 47: 846-52. PMID: 9226917
  13. Factors influencing uptake and retention of amino-containing drugs in large unilamellar vesicles exhibiting transmembrane pH gradients.  |  Maurer-Spurej, E., et al. 1999. Biochim Biophys Acta. 1416: 1-10. PMID: 9889298

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Amylamine, 25 ml

sc-239249
25 ml
$51.00

Amylamine, 50 ml

sc-239249A
50 ml
$78.00