Thermo Scientific Chemicals

1-(2-Aminoethyl)piperidine, 98%, Thermo Scientific Chemicals

Catalog number: A18373.06
5 g, Each
Thermo Scientific Chemicals

1-(2-Aminoethyl)piperidine, 98%, Thermo Scientific Chemicals

Catalog number: A18373.06
5 g, Each
Quantity
Catalog number: A18373.06
also known as A18373-06
Price (USD)
Price: 48.70
Online price: 41.65
Your price:
Quantity
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Chemical Identifiers

CAS
27578-60-5
IUPAC Name
2-(piperidin-1-yl)ethan-1-amine
Molecular Formula
C7H16N2
InChI Key
CJNRGSHEMCMUOE-UHFFFAOYSA-N
SMILES
NCCN1CCCCC1
Appearance (Color)
Clear colorless to pale yellow
Assay (GC)
≥97.5%
Refractive Index
1.4725-1.4765 @ 20?C
Form
Liquid

Description

1-(2-Aminoethyl)piperidine is used in modification of vinylbenzyl chloride/divinylbenzene gel copolymer bead and in the synthesis of linkage isomers trans-bis[1-(2-aminoethyl)piperidine]dinitronickel and trans-bis[1-(2-aminoethyl)-piperidine]dinitritonickel. It is also used as a reactant for synthesis of: analogs of anticancer agents, inhibitor of botulinum neurotoxin serotype A light chain, P. falciparum malaria, and Ebola filovirus, cannabinoid CB1 receptor antagonists, small molecules that restore E-cadherin expression and reduce invasion in colorectal carcinoma cells, potent and selective 5-HT6 antagonists and N-mustards as anticancer agents. 1-(2-Aminoethyl)piperidine on [1+1] condensation reaction with 3-methoxy salicylaldehyde yields tridentate Schiff base ligand.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
1-(2-Aminoethyl)piperidine is used in modification of vinylbenzyl chloride/divinylbenzene gel copolymer bead and in the synthesis of linkage isomers trans-bis[1-(2-aminoethyl)piperidine]dinitronickel and trans-bis[1-(2-aminoethyl)-piperidine]dinitritonickel. It is also used as a reactant for synthesis of: analogs of anticancer agents, inhibitor of botulinum neurotoxin serotype A light chain, P. falciparum malaria, and Ebola filovirus, cannabinoid CB1 receptor antagonists, small molecules that restore E-cadherin expression and reduce invasion in colorectal carcinoma cells, potent and selective 5-HT6 antagonists and N-mustards as anticancer agents. 1-(2-Aminoethyl)piperidine on [1+1] condensation reaction with 3-methoxy salicylaldehyde yields tridentate Schiff base ligand.

Solubility
Partly miscible in water.

Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents, acid chlorides and acid anhydrides. It is sensitive to air.
RUO – Research Use Only

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