Basic information Safety Supplier Related

1-Benzyl-4-hydroxypiperidine

Basic information Safety Supplier Related

1-Benzyl-4-hydroxypiperidine Basic information

Product Name:
1-Benzyl-4-hydroxypiperidine
Synonyms:
  • 4-HYDROXY-1-BENZYLPIPERIDINE
  • benzyl-4-piperidinol
  • 4-Piperidinol, 1-(phenylmethyl)-
  • 1-Benzyl-4-hydroxypiperidine,97%
  • NSC 72991
  • N-BENZYL-4-PIPERIDINOL
  • N-BENZYL-4-HYDROXYPIPERIDINE
  • 1-(Phenylmethyl)-4-piperidinol
CAS:
4727-72-4
MF:
C12H17NO
MW:
191.27
EINECS:
225-226-9
Product Categories:
  • Building Blocks
  • C12
  • Alcohols and Derivatives
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Piperidines
  • Non-Chiral heterocyclic compounds
  • Agro-Products
  • Aromatics
  • Heterocycles
Mol File:
4727-72-4.mol
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1-Benzyl-4-hydroxypiperidine Chemical Properties

Melting point:
61-63 °C(lit.)
Boiling point:
127-128 °C2 mm Hg(lit.)
Density 
1.0096 (rough estimate)
refractive index 
1.5212 (estimate)
Flash point:
121-123°C/0.7mm
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Chloroform, Methanol
pka
14.87±0.20(Predicted)
form 
Crystalline Powder
color 
White to yellow
Sensitive 
Hygroscopic
BRN 
146118
CAS DataBase Reference
4727-72-4(CAS DataBase Reference)
NIST Chemistry Reference
4-Piperidinol, 1-(phenylmethyl)-(4727-72-4)
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Safety Information

Hazard Codes 
T,C,Xi,Xn
Risk Statements 
25-36/37/38-20/21/22
Safety Statements 
26-45-37/39-36
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
2
HS Code 
29333990

MSDS

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1-Benzyl-4-hydroxypiperidine Usage And Synthesis

Chemical Properties

WHITE TO YELLOWISH CRYSTALLINE POWDER

Uses

A piperidine based pesticide

Uses

1-Benzyl-4-hydroxypiperidine was used as an alternative molecule to study the ligand concentration attached to the epoxy-activated Sepharose 6B.

Uses

1-Benzyl-4-hydroxypiperidine is the reactant for synthesis of: Muscarinic acetylcholine receptor antagonist and beta 2 adrenoceptor agonist1 Fatty acid amide hydrolase inhibitors PI3 kinase-alpha inhibitors Flavonoid derivatives used as dual binding acetylcholinesterase inhibitors Urotensin-II receptor antagonists Rho kinase inhibitors.

Synthesis Reference(s)

Journal of the American Chemical Society, 108, p. 3512, 1986 DOI: 10.1021/ja00272a059

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