Date published: 2026-4-25

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(+)-Dehydroabietylamine (CAS 1446-61-3)

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Alternate Names:
1,4a-Dimethyl-7-isopropyl-1,2,3,4,4a,9,10,10a-octahydro-1-phenanthrenemethylamine
CAS Number:
1446-61-3
Molecular Weight:
285.48
Molecular Formula:
C20H31N
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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(+)-Dehydroabietylamine, a derivative of abietic acid found in rosin, is a compound of significant interest in various research domains due to its unique bioactivity. Its mechanism of action, while not entirely elucidated, is thought to involve interaction with biological membranes and proteins, leading to modulation of cellular processes. This characteristic makes it useful in the study of cellular biochemistry and the development of novel materials. In research applications, (+)-Dehydroabietylamine serves as a scaffold for the synthesis of more complex molecules, owing to its rigid tricyclic structure, which provides a versatile framework for chemical modifications. This has facilitated its use in creating functional materials with potential applications in biotechnology and material science, such as the development of antimicrobial coatings and environmentally friendly polymers. Its role in research continues to expand as scientists explore its properties and potential applications in various fields.


(+)-Dehydroabietylamine (CAS 1446-61-3) References

  1. (+)-Dehydroabietylamine derivatives target triple-negative breast cancer.  |  Ling, T., et al. 2015. Eur J Med Chem. 102: 9-13. PMID: 26241873
  2. Synthesis and applications of secondary amine derivatives of (+)-dehydroabietylamine in chiral molecular recognition.  |  Laaksonen, T., et al. 2015. Org Biomol Chem. 13: 10548-55. PMID: 26337032
  3. Anti-herpetic and anti-dengue activity of abietane ferruginol analogues synthesized from (+)-dehydroabietylamine.  |  Roa-Linares, VC., et al. 2016. Eur J Med Chem. 108: 79-88. PMID: 26638041
  4. Synthesis of (-)-Chamobtusin A from (+)-Dehydroabietylamine.  |  Mori, N., et al. 2016. J Org Chem. 81: 11866-11870. PMID: 27768308
  5. Synthesis and bio-molecular study of (+)-N-Acetyl-α-amino acid dehydroabietylamine derivative for the selective therapy of hepatocellular carcinoma.  |  Mustufa, MA., et al. 2016. BMC Cancer. 16: 883. PMID: 27842576

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

(+)-Dehydroabietylamine, 100 g

sc-486628
100 g
$102.00