Date published: 2025-12-6

1-800-457-3801

SCBT Portrait Logo
Seach Input

L-(−)-α-Amino-ε-caprolactam hydrochloride (CAS 26081-07-2)

0.0(0)
Write a reviewAsk a question

Alternate Names:
(S)-3-Amino-hexahydro-2-azepinone hydrochloride; L-Lysine lactam hydrochloride
CAS Number:
26081-07-2
Molecular Weight:
164.63
Molecular Formula:
C6H12N2O•HCl
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

L-(−)-α-Amino- -caprolactam hydrochloride functions as a precursor in the synthesis of polymers and other organic compounds. It acts as a monomer in the production of nylon-6, which is used in various industrial applications. The chemical participates in ring-opening polymerization reactions, leading to the formation of long-chain polymers with high tensile strength and thermal stability. At the molecular level, L-(−)-α-Amino- -caprolactam hydrochloride undergoes nucleophilic attack by an amine group, initiating the polymerization process. L-(−)-Å-Amino- -Caprolactam Hydrochloride′s mechanism of action involves its incorporation into the growing polymer chain, contributing to the material′s mechanical properties and overall performance. In the context of research and development, L-(−)-α-Amino- -caprolactam hydrochloride serves as a building block for the synthesis of advanced materials with tailored properties.


L-(−)-α-Amino-ε-caprolactam hydrochloride (CAS 26081-07-2) References

  1. Total synthesis of Bengamide E and analogues by modification at C-2 and at terminal olefinic positions.  |  Sarabia, F. and Sánchez-Ruiz, A. 2005. J Org Chem. 70: 9514-20. PMID: 16268627
  2. Tricyclic pharmacophore-based molecules as novel integrin alpha(v)beta3 antagonists. Part III: synthesis of potent antagonists with alpha(v)beta3/alpha(IIb)beta3 dual activity and improved water solubility.  |  Ishikawa, M., et al. 2006. Bioorg Med Chem. 14: 2131-50. PMID: 16307881
  3. In Silico Identification for α-Amino-ε-Caprolactam Racemases by Using Information on the Structure and Function Relationship.  |  Payoungkiattikun, W., et al. 2015. Appl Biochem Biotechnol. 176: 1303-14. PMID: 26206345
  4. Total Synthesis of Mycobacterium tuberculosis Dideoxymycobactin-838 and Stereoisomers: Diverse CD1a-Restricted T Cells Display a Common Hierarchy of Lipopeptide Recognition.  |  Cheng, JM., et al. 2017. Chemistry. 23: 1694-1701. PMID: 27925318
  5. Resolution of the Confusion in the Assignments of Configuration for the Ciliatamides, Acylated Dipeptides from Marine Sponges.  |  Takada, K., et al. 2017. J Nat Prod. 80: 2845-2849. PMID: 29016113
  6. Vinyl Monomers, Polymers and Supramolecular Assemblies from Aminocaprolactam  |   and Eylem Tarkin-Tas, Huseyin Tas, Lon J. Mathias. March 2012. Macromolecular Symposia. Volume313-314, Issue1 Special Issue: Functional Polymeric Materials and Composites: Pages 79-89.
  7. Hydrogen-bonded supramolecular polymers from derivatives of α-amino-ε-caprolactam: A bio-based material  |   and Eylem Tarkin-Tas, Christopher A. Lange, Lon J. Mathias. 1 June 2011. Journal of Polymer Science Part A: Polymer Chemistry. Volume49, Issue11: Pages 2451-2460.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

L-(−)-α-Amino-ε-caprolactam hydrochloride, 1 g

sc-255229
1 g
$143.00