Date published: 2025-12-14

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2-Amino-5-methylhexane (CAS 28292-43-5)

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Alternate Names:
1,4-Dimethylpentylamine; 5-Methyl-2-hexylamine
Application:
2-Amino-5-methylhexane is an aliphatic amine used in the preparation of pyridines
CAS Number:
28292-43-5
Purity:
≥98%
Molecular Weight:
115.22
Molecular Formula:
C7H17N
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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2-Amino-5-methylhexane is a compound that functions as a substrate in the synthesis of various organic compounds. It acts as a building block in the formation of complex molecules, contributing to the creation of new chemical entities. At the molecular level, 2-Amino-5-methylhexane participates in reactions that lead to the formation of diverse chemical structures, allowing for the exploration of different chemical pathways and the development of novel compounds. Its mechanism of action involves participating in chemical reactions as a reactant, leading to the production of derivatives with potential applications in various research and development applications. 2-Amino-5-methylhexane plays a role in the modification and synthesis of organic molecules, contributing to the expansion of chemical libraries and the exploration of new chemical space. Its involvement in synthetic processes allows for the generation of diverse chemical entities, enabling the investigation of their properties and potential applications in experimental applications.


2-Amino-5-methylhexane (CAS 28292-43-5) References

  1. Molecular mechanism of uncompetitive inhibition of human placental and germ-cell alkaline phosphatase.  |  Hoylaerts, MF., et al. 1992. Biochem J. 286 (Pt 1): 23-30. PMID: 1520273
  2. A synthetic stimulant never tested in humans, 1,3-dimethylbutylamine (DMBA), is identified in multiple dietary supplements.  |  Cohen, PA., et al. 2015. Drug Test Anal. 7: 83-7. PMID: 25293509
  3. Functional characterization of PLP fold type IV transaminase with a mixed type of activity from Haliangium ochraceum.  |  Zeifman, YS., et al. 2019. Biochim Biophys Acta Proteins Proteom. 1867: 575-585. PMID: 30902765
  4. Naphthalene diimides with improved solubility for visible light photoredox catalysis.  |  Reiß, B. and Wagenknecht, HA. 2019. Beilstein J Org Chem. 15: 2043-2051. PMID: 31501672
  5. Improving Catalytic Efficiency and Changing Substrate Spectrum for Asymmetric Biocatalytic Reductive Amination.  |  Jiang, W. and Wang, Y. 2020. J Microbiol Biotechnol. 30: 146-154. PMID: 31546300
  6. Beyond Substituted p-Phenylenediamine Antioxidants: Prevalence of Their Quinone Derivatives in PM2.5.  |  Wang, W., et al. 2022. Environ Sci Technol. 56: 10629-10637. PMID: 35834306

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-Amino-5-methylhexane, 1 g

sc-225146
1 g
$617.00