N-(2-Aminoethyl)piperidine Chemical Properties

Melting point:

67-70 °C(Solv: ligroine (8032-32-4); dichloromethane (75-09-2))

Boiling point:

186 °C(lit.)

Density 

0.899 g/mL at 25 °C(lit.)

refractive index 

n20/D 1.473(lit.)

Flash point:

136 °F

storage temp. 

under inert gas (nitrogen or Argon) at 2–8 °C

form 

Liquid

pka

pK1: 6.38;pK2: 9.89 (30°C)

color 

Clear colorless to yellow

Water Solubility 

Partly miscible in water.

Sensitive 

Air Sensitive

BRN 

103469

CAS DataBase Reference

27578-60-5(CAS DataBase Reference)

NIST Chemistry Reference

1-Piperidineethanamine(27578-60-5)

Safety Information

Hazard Codes 

C,Xi

Risk Statements 

34

Safety Statements 

26-36/37/39-45

RIDADR 

UN 2734 8/PG 2

WGK Germany 

3

Hazard Note 

Irritant

HazardClass 

3

PackingGroup 

III

HS Code 

29333990

MSDS

• Language:English Provider:N-(2-Aminoethyl)piperidine
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N-(2-Aminoethyl)piperidine Usage And Synthesis

Chemical Properties

CLEAR COLOURLESS TO YELLOW LIQUID

Uses

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.

General Description

1-(2-Aminoethyl)piperidine on [1+1] condensation reaction with 3-methoxy salicylaldehyde yields tridentate Schiff base ligand.

N-(2-Aminoethyl)piperidine(27578-60-5)Related Product Information

• N-Aminoethylpiperazine
• Triacetonediamine
• 2-(2-Aminoethylamino)ethanol
• Haloperidol
• DROPERIDOL
• Piperidine
• Diphenoxylate
• 2-PIPERIDINOACETAMIDOXIME
• KETANSERIN TARTRATE
• VERRUCULOGEN
• D-PHE-PIP-ARG-PNA
• 2-PIPERIDINOETHYL ISOTHIOCYANATE
• Ketanserin
• 4-(2-Aminoethyl)piperidine, N2-BOC protected,4-(BOC-AMINOETHYL)PIPERIDINE,4-(N-BOC-2-AMINOETHYL)PIPERIDINE,4-(2-BOC-AMINOETHYL) PIPERIDINE
• 2-(boc-aminoethyl)piperidine,1-Boc-2-(aminoethyl)piperidine
• 4-(2-AMINOETHYL)PIPERIDINE 2HCL,4-(2'-AMINOETHYL)PIPERIDINE DIHYDROCHLORIDE,4-(2-AMINOETHYL)-PIPERIDINE DIHYDROCHLORIDE
• (S)-1-Boc-3-(2-Aminoethyl)-Piperidine
• N-BOC-3-AMINOETHYL-PIPERIDINE,1-Boc-3-(2-Aminoethyl)-Piperidine