Date published: 2025-12-1

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(S)-2-Aminohexane (CAS 70492-67-0)

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Alternate Names:
(S)-2-Hexylamine
CAS Number:
70492-67-0
Molecular Weight:
101.19
Molecular Formula:
C6H15N
Supplemental Information:
This is 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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(S)-2-Aminohexane is an amino acid derivative that is used in many scientific research applications. It is an important intermediate in the synthesis of many other compounds, as well as a precursor for the synthesis of other amino acids. Specifically, it can be used to develop peptides, peptidomimetics, leucine, and isoleucine. (S)-2-Aminohexane is also used in various biochemical and physiological studies, and is a key component of many laboratory experiments. The compound plays a role in modulating metabolic pathways and participating in neurotransmitter synthesis, such as serotonin and dopamine. Additionally, it is involved in gene expression regulation, exerts an influence on the immune system, helps control inflammation, and regulates cell growth.


(S)-2-Aminohexane (CAS 70492-67-0) References

  1. Improved racemate resolution of pentan-2-ol and trans-(Z)-cyclooct-5-ene-1,2-diol by lipase catalysis.  |  Graber, M., et al. 2016. J Biotechnol. 238: 60-68. PMID: 27671695
  2. Macroscopic helical chirality and self-motion of hierarchical self-assemblies induced by enantiomeric small molecules.  |  Yang, Y., et al. 2018. Nat Commun. 9: 3808. PMID: 30228273
  3. Bioprospecting Reveals Class III ω-Transaminases Converting Bulky Ketones and Environmentally Relevant Polyamines.  |  Coscolín, C., et al. 2019. Appl Environ Microbiol. 85: PMID: 30413473
  4. Protein-based scaffolds for enzyme immobilization.  |  Zhang, G., et al. 2019. Methods Enzymol. 617: 323-362. PMID: 30784408
  5. Water-soluble chiral tetrazine derivatives: towards the application of circularly polarized luminescence from upper-excited states to photodynamic therapy.  |  He, T., et al. 2019. Chem Sci. 10: 4163-4168. PMID: 31057744
  6. Light on Chirality: Absolute Asymmetric Formation of Chiral Molecules Relevant in Prebiotic Evolution.  |  Myrgorodska, I., et al. 2017. Chempluschem. 82: 74-87. PMID: 31961503
  7. Anisotropy spectroscopy of chiral alcohols, amines, and monocarboxylic acids: Implications for the analyses of extraterrestrial samples  |  Cornelia Meinert a b, Nykola C. Jones c, Søren V. Hoffmann c, Uwe J. Meierhenrich b. 2016. Journal of Photochemistry and Photobiology A: Chemistry. 331: 130-137.
  8. Chiral Zn–salen complexes: a new class of fluorescent receptors for enantiodiscrimination of chiral amines  |  Roberta Puglisi,a Francesco P. Ballistreri,a Chiara M. A. Gangemi,a Rosa Maria Toscano,a Gaetano A. Tomaselli, a Andrea Pappalardo*ab and Giuseppe Trusso Sfrazzetto *a . 2017. New J. Chem. 41: 911-915.
  9. In situ removal of inhibitory products with ion exchange resins for enhanced synthesis of chiral amines using ω-transaminase  |  Sang-Woo Han, Jong-Shik Shin. 2020. Biochemical Engineering Journal. 162.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

(S)-2-Aminohexane, 250 mg

sc-236805
250 mg
$102.00