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4-Benzylpiperidine_Molecular_structure_CAS_31252-42-3)
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4-Benzylpiperidine

Catalog No. 13820 Name Sigma Aldrich
CAS Number 31252-42-3 Website http://www.sigmaaldrich.com
M. F. C12H17N Telephone 1-800-521-8956
M. W. 175.27008 Fax
Purity ≥95% (GC) Email
Storage Chembase ID: 24827

SYNONYMS

Title
4-苄基哌啶
IUPAC name
4-benzylpiperidine
IUPAC Traditional name
4-benzylpiperidine
Synonyms
苯基(4-哌啶基)甲烷
Phenyl(4-piperidyl)methane

DATABASE IDS

Beilstein Number 132339
CAS Number 31252-42-3
MDL Number MFCD00006006
EC Number 250-535-0

PROPERTIES

GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
RTECS TM4728000
Safety Statements 26-36
German water hazard class 3
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
Empirical Formula (Hill Notation) C12H17N
Grade technical
Purity ≥95% (GC)
Boiling Point 279 °C(lit.)
Density 0.997 g/mL at 25 °C(lit.)
Flash Point 112 °C
Flash Point 233.6 °F
Melting Point 6-7 °C(lit.)
Refractive Index n20/D 1.537(lit.)
Refractive Index n20/D 1.538

DETAILS

Description (English)
Application
Reactant for synthesis of:
• Antiproliferatives1
• GABA uptake inhibitors2
• Pyridines3
• Histamine H3 antagonists4
• Multipotent drugs with cholinergic and neuroprotective properties for the treatment of Alzheimers and neuronal vascular diseases5
• Antiserotoninergic, antiplatelet, hemorheologic, antiarrythmic and antioxidant molecules via nucleophilic substitution6
Description (简体中文)
Application
Reactant for synthesis of:
• Antiproliferatives1
• GABA uptake inhibitors2
• Pyridines3
• Histamine H3 antagonists4
• Multipotent drugs with cholinergic and neuroprotective properties for the treatment of Alzheimers and neuronal vascular diseases5
• Antiserotoninergic, antiplatelet, hemorheologic, antiarrythmic and antioxidant molecules via nucleophilic substitution6

REFERENCES