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4-Benzylpiperidine

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4-Benzylpiperidine Basic information

Product Name:
4-Benzylpiperidine
Synonyms:
  • 4-(phenylmethyl)-piperidin
  • 4-benzyl-piperidin
  • LABOTEST-BB LTBB000752
  • PHENYL(4-PIPERIDYL)METHANE
  • Piperidine, 4-(phenylmethyl)-
  • Piperidine, 4-benzyl-
  • 4-BENZYLPIPERIDINE
  • 4-(PHENYLMETHYL)PIPERIDINE
CAS:
31252-42-3
MF:
C12H17N
MW:
175.27
EINECS:
250-535-0
Product Categories:
  • B
  • Bioactive Small Molecules
  • Building Blocks
  • C12
  • Cell Biology
  • Chemical Synthesis
  • Piperidine
  • Piperidine Series
  • Heterocyclic Building Blocks
  • Piperidines
Mol File:
31252-42-3.mol
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4-Benzylpiperidine Chemical Properties

Melting point:
6-7 °C (lit.)
Boiling point:
279 °C (lit.)
Density 
0.997 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.537(lit.)
Flash point:
>230 °F
storage temp. 
Store below +30°C.
form 
Viscous Liquid
pka
10.58±0.10(Predicted)
color 
Clear colorless to yellow
BRN 
132339
CAS DataBase Reference
31252-42-3(CAS DataBase Reference)
EPA Substance Registry System
Piperidine, 4-(phenylmethyl)- (31252-42-3)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
RTECS 
TM4728000
TSCA 
Yes
HazardClass 
IRRITANT
HS Code 
29333990

MSDS

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4-Benzylpiperidine Usage And Synthesis

Chemical Properties

clear colourless to yellow viscous liquid.

Uses

4-Benzylpiperidine was studied as acid corrosion inhibitor for iron. It was also used to study potential utility of dopamine-welective releaser as a treatment for cocaine dependence. In an assay of cocaine discrimination, 4-Benzylpiperidine had the most rapid onset and shortest duration of action.

Preparation

4-Benzylpiperidine can be prepared by reacting 4-cyanopyridine with toluene. Catalytic hydrogenation of the pyridine ring then completes the synthesis.

Application

Reactant for synthesis of:
Antiproliferatives
GABA uptake inhibitors
Pyridines
Histamine H3 antagonists
Multipotent drugs with cholinergic and neuroprotective properties for the treatment of Alzheimer′s and neuronal vascular diseases
Antiserotoninergic, antiplatelet, hemorheologic, antiarrythmic and antioxidant molecules via nucleophilic substitution

Synthesis Reference(s)

Synthesis, p. 741, 1980 DOI: 10.1055/s-1980-29196

General Description

4-Benzylpiperidine is dopamine-selective releaser. It is a potential candidate for treatments for cocaine dependence.

Biochem/physiol Actions

4-Benzylpiperidine inhibits the activity of rat brain monoamine oxidase-A and -B, with IC50 values of 0.02 mM and 2 mM respectively. It acts as a monoamine releasing agent with 20- to 48-fold selectivity for releasing dopamine versus serotonin. It is most efficacious as a releaser of norepinephrine, with an ec50 of 109/41.4/5246nM for DA/NE/5HT, respectively . It has a fast onset of action and a short duration. It also functions as a monoamine oxidase inhibitor (MAOI) with preference for MAO-A.

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