Date published: 2026-2-11

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5-(Diethylamino)pentylamine (CAS 34987-15-0)

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CAS Number:
34987-15-0
Molecular Weight:
158.28
Molecular Formula:
C9H22N2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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5-(Diethylamino)pentylamine (DEAP) is a versatile organic compound extensively employed in various scientific and industrial applications. Derived from pentylamine, 5-(Diethylamino)pentylamine consists of a five-member ring housing two nitrogen atoms and an ethyl group. This colorless liquid possesses a pungent odor and exhibits solubility in water. It is alternatively referred to as Diethylaminopentane, 5-(Diethylamino)pentylamine, and N,N-diethylpentan-2-amine. 5-(Diethylamino)pentylamine finds utility across diverse scientific research realms. It serves as a reagent in organic synthesis, a stabilizer in polymer manufacturing, and a catalyst in polyurethane production. Moreover, it plays a role in polycarbonate preparation, polyamide synthesis, and adhesive formulation. In organic synthesis, 5-(Diethylamino)pentylamine acts as a nucleophile, enabling reactions with electrophiles like alkyl halides and acyl halides. The nitrogen atom within the 5-(Diethylamino)pentylamine molecule initiates the reaction as the nucleophilic center. This reaction generates an amine compound, which subsequently undergoes further reactions with other compounds.


5-(Diethylamino)pentylamine (CAS 34987-15-0) References

  1. Synthesis and structure-activity relationships of 7-substituted 3-(2, 6-dichlorophenyl)-1,6-naphthyridin-2(1H)-ones as selective inhibitors of pp60(c-src).  |  Thompson, AM., et al. 2000. J Med Chem. 43: 3134-47. PMID: 10956222
  2. Discovery of a selective, substrate-competitive inhibitor of the lysine methyltransferase SETD8.  |  Ma, A., et al. 2014. J Med Chem. 57: 6822-33. PMID: 25032507

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

5-(Diethylamino)pentylamine, 5 g

sc-317764
5 g
$189.00