Date published: 2025-10-15

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12-Aminododecanoic acid (CAS 693-57-2)

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Alternate Names:
12-Aminolauric acid
CAS Number:
693-57-2
Molecular Weight:
215.33
Molecular Formula:
C12H25NO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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12-Aminododecanoic acid is a compound that functions as a building block in the synthesis of polymers and materials. It acts as a monomer in the formation of polyamides, contributing to the structural integrity and properties of the resulting polymer. At the molecular level, 12-Aminododecanoic acid undergoes condensation reactions with other monomers, forming amide linkages that create long chains of repeating units. 12-Aminododecanoic acid′s mechanism of action involves participating in polymerization reactions, where it becomes integrated into the polymer structure, influencing its mechanical and chemical properties.


12-Aminododecanoic acid (CAS 693-57-2) References

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  2. A unidirectional crosslinking strategy for HIV-1 protease dimerization inhibitors.  |  Hwang, YS. and Chmielewski, J. 2004. Bioorg Med Chem Lett. 14: 4297-300. PMID: 15261290
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  4. Adsorption of fluorescently labeled protein residues on poly(ethylene-co-acrylic acid) films modified with affinity functionalities.  |  Luo, N., et al. 2006. Colloids Surf B Biointerfaces. 50: 89-96. PMID: 16750613
  5. Poly(ethylene terephthalate)/clay nanocomposites based on aminododecanoic acid-modified clay: effect of compatibilizer reactivity on clay dispersion.  |  Hao, J., et al. 2006. J Nanosci Nanotechnol. 6: 3981-4. PMID: 17256367
  6. Self-assembled monolayers of alkanoic acids on the native oxide surface of SS316L by solution deposition.  |  Raman, A. and Gawalt, ES. 2007. Langmuir. 23: 2284-8. PMID: 17266343
  7. The role of surface charge on the uptake and biocompatibility of hydroxyapatite nanoparticles with osteoblast cells.  |  Chen, L., et al. 2011. Nanotechnology. 22: 105708. PMID: 21289408
  8. Novel Bradykinin Analogues Modified in the N-Terminal Part of the Molecule with a Variety of Acyl Substituents.  |  Sleszyńska, M., et al. 2012. Int J Pept Res Ther. 18: 117-124. PMID: 22593719
  9. Emtricitabine prodrugs with improved anti-HIV activity and cellular uptake.  |  Agarwal, HK., et al. 2013. Mol Pharm. 10: 467-76. PMID: 22917277
  10. Identification of novel transaminases from a 12-aminododecanoic acid-metabolizing Pseudomonas strain.  |  Wilding, M., et al. 2015. Microb Biotechnol. 8: 665-72. PMID: 25912724
  11. Efficient production of the Nylon 12 monomer ω-aminododecanoic acid methyl ester from renewable dodecanoic acid methyl ester with engineered Escherichia coli.  |  Ladkau, N., et al. 2016. Metab Eng. 36: 1-9. PMID: 26969251
  12. A β-Alanine Catabolism Pathway Containing a Highly Promiscuous ω-Transaminase in the 12-Aminododecanate-Degrading Pseudomonas sp. Strain AAC.  |  Wilding, M., et al. 2016. Appl Environ Microbiol. 82: 3846-3856. PMID: 27107110
  13. Crystal structure of a putrescine aminotransferase from Pseudomonas sp. strain AAC.  |  Wilding, M., et al. 2017. Acta Crystallogr F Struct Biol Commun. 73: 29-35. PMID: 28045391
  14. Adsorption of cadmium on clay-organic associations in different pH solutions: The effect of amphoteric organic matter.  |  Xu, W., et al. 2022. Ecotoxicol Environ Saf. 236: 113509. PMID: 35421828
  15. Synthesis of fluorescent and radiolabeled analogues of phosphatidic acid.  |  Longmuir, KJ., et al. 1985. Chem Phys Lipids. 36: 197-207. PMID: 4006033

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

12-Aminododecanoic acid, 1 g

sc-265116
1 g
$46.00