Date published: 2026-4-24

1-800-457-3801

SCBT Portrait Logo
Seach Input

Piperidinium acetate (CAS 4540-33-4)

0.0(0)
Write a reviewAsk a question

CAS Number:
4540-33-4
Molecular Weight:
145.20
Molecular Formula:
C7H15NO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Piperidinium acetate, an organic compound falling within the piperidines family, showcases a distinctive nitrogen atom bound to four carbon atoms. This white, crystalline solid possesses a melting point of 120-122° C and a boiling point of 222° C. Due to its versatility, Piperidinium acetate finds widespread application in the chemical industry, as well as research laboratories. Its various uses range from synthesizing complex molecules to acting as a reliable source of hydrogen for hydrogenation reactions. In scientific research, Piperidinium acetate is highly favored for its multifaceted applications. It serves as a reagent in organic synthesis and catalyzes hydrogenation reactions, proving invaluable as a hydrogen source. The compound is instrumental in peptide and protein synthesis and plays a role in the creation of other organic compounds. Although the exact mechanism of action of Piperidinium acetate remains partially veiled, it is believed that the piperidine nitrogen atom assumes the role of a Lewis acid, reacting with acetic anhydride to form an intermediate product. Subsequently, this intermediate undergoes a series of reactions leading to the desired end product. Furthermore, the piperidine nitrogen atom is thought to participate in the formation of hydrogen bonds with acetic anhydride, contributing to the stabilization of the intermediate product. Piperidinium acetate stands as a versatile and valuable compound with broad applications in various industries and research fields, supporting the advancement of scientific understanding and the synthesis of compounds.


Piperidinium acetate (CAS 4540-33-4) References

  1. Concise preparation of the (3E,5Z)-alkadienyl system. New approach to the synthesis of principal insect sex pheromone constituents.  |  Ragoussis, V., et al. 2004. J Agric Food Chem. 52: 5047-51. PMID: 15291473
  2. Synthesis of novel 6-enaminopurines.  |  Carvalho, MA., et al. 2004. Org Biomol Chem. 2: 2340-5. PMID: 15305216
  3. A regioselective [4 + 2] annulation approach to 5-acylindolizine-7-carbonitriles: generation of poly-substituted pyridines.  |  Kim, S., et al. 2021. Org Biomol Chem. 19: 5806-5817. PMID: 34113946
  4. Diastereoselective Synthesis of Densely Functionalized 3a,8a-Dihydro-8H-furo[3,2-a]pyrrolizines through One-Pot Three-Component Assembly.  |  Lee, S., et al. 2021. J Org Chem. 86: 12367-12377. PMID: 34479403
  5. Impact of an aryl bulky group on a one-pot reaction of aldehyde with malononitrile and N-substituted 2-cyanoacetamide.  |  Vala, RM., et al. 2019. RSC Adv. 9: 28886-28893. PMID: 35529659
  6. Tandem cyclocondensation of 1,3-bis-sulfonylpropan-2-ones with arylaldehydes. One-pot synthesis of tris-sulfonyl 3-arylphenols.  |  Hsueh, NC. and Chang, MY. 2022. Org Biomol Chem. 20: 8471-8483. PMID: 36260065

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Piperidinium acetate, 5 g

sc-483655
5 g
$206.00

Piperidinium acetate, 25 g

sc-483655A
25 g
$707.00

Piperidinium acetate, 100 g

sc-483655B
100 g
$2448.00