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Piperidine hydrochloride_Molecular_structure_CAS_6091-44-7)
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Piperidine hydrochloride

Catalog No. 80680 Name Sigma Aldrich
CAS Number 6091-44-7 Website http://www.sigmaaldrich.com
M. F. C5H12ClN Telephone 1-800-521-8956
M. W. 121.60848 Fax
Purity ≥99.0% (AT) Email
Storage Chembase ID: 76876

SYNONYMS

Title
哌啶 盐酸盐
IUPAC name
piperidine hydrochloride
IUPAC Traditional name
piperidine hydrochloride

DATABASE IDS

CAS Number 6091-44-7
MDL Number MFCD00012770
Beilstein Number 3611699
PubChem SID 24887579
EC Number 228-033-8

PROPERTIES

Empirical Formula (Hill Notation) C5H11N · HCl
Grade purum
Purity ≥99.0% (AT)
Quality crystallized
Flash Point 113 °C
Flash Point 235.4 °F
Melting Point 245-248 °C(lit.)
Melting Point 245-250 °C
Vapor Density 2.94 (vs air)
GHS Pictograms GHS06
GHS Signal Word Danger
GHS Hazard statements H301
European Hazard Symbols Toxic Toxic (T)
MSDS Link Download
Personal Protective Equipment Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
GHS Precautionary statements P301 + P310
RID/ADR UN 2811 6.1/PG 3
Risk Statements 25-37
RTECS TN0400000
Safety Statements 36/37/39-45
Hazard Class 6.1
UN Number 2811
Packing Group 3
German water hazard class 3

DETAILS

Description (English)
Application
Reagent for synthesis of:
• Quinoline selenium compounds1
• Peripheral seratonin 5-HT3 receptor ligands2Reactant for synthesis of phthalazinone derivatives as topically active phosphodiesterase 4 inhibitors3Reactant for:
• Mannich reactions4
• Asymmetric hydrogenation of quinolines5
• Chemoselective reductive amination of carbonyl compounds6
Description (简体中文)
Application
Reagent for synthesis of:
• Quinoline selenium compounds1
• Peripheral seratonin 5-HT3 receptor ligands2Reactant for synthesis of phthalazinone derivatives as topically active phosphodiesterase 4 inhibitors3Reactant for:
• Mannich reactions4
• Asymmetric hydrogenation of quinolines5
• Chemoselective reductive amination of carbonyl compounds6

REFERENCES