152986
1-Benzyl-4-hydroxypiperidine
96%
Synonym(s):
1-Benzyl-4-piperidinol
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About This Item
Empirical Formula (Hill Notation):
C12H17NO
CAS Number:
Molecular Weight:
191.27
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
96%
form
solid
bp
127-128 °C/2 mmHg (lit.)
mp
61-63 °C (lit.)
functional group
hydroxyl
phenyl
SMILES string
OC1CCN(CC1)Cc2ccccc2
InChI
1S/C12H17NO/c14-12-6-8-13(9-7-12)10-11-4-2-1-3-5-11/h1-5,12,14H,6-10H2
InChI key
BPPZXJZYCOETDA-UHFFFAOYSA-N
Application
1-Benzyl-4-hydroxypiperidine was used as an alternative molecule to study the ligand concentration attached to the epoxy-activated Sepharose 6B.
Reactant for synthesis of:
Muscarinic acetylcholine receptor antagonist and beta 2 adrenoceptor agonist
Fatty acid amide hydrolase inhibitors
PI3 kinase-alpha inhibitors
Flavonoid derivatives used as dual binding acetylcholinesterase inhibitors
Urotensin-II receptor antagonists
Rho kinase inhibitors
Muscarinic acetylcholine receptor antagonist and beta 2 adrenoceptor agonist
Fatty acid amide hydrolase inhibitors
PI3 kinase-alpha inhibitors
Flavonoid derivatives used as dual binding acetylcholinesterase inhibitors
Urotensin-II receptor antagonists
Rho kinase inhibitors
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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X Santarelli et al.
Journal of chromatography. B, Biomedical sciences and applications, 739(1), 63-72 (2000-04-01)
New pseudo-affinity chromatographic supports for penicillin acylase were prepared and evaluated with three different samples: pure penicillin acylase, industrial clarified feedstock and crude extract. The different gels were studied for their purification fold (three to six) and their recovery power
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