497312
4-Piperidinemethanol
97%
Synonym(s):
4-(Hydroxymethyl)piperidine
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About This Item
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Quality Level
Assay
97%
bp
118-120 °C/10 mmHg (lit.)
mp
55-59 °C (lit.)
functional group
hydroxyl
SMILES string
OCC1CCNCC1
InChI
1S/C6H13NO/c8-5-6-1-3-7-4-2-6/h6-8H,1-5H2
InChI key
XBXHCBLBYQEYTI-UHFFFAOYSA-N
Related Categories
General description
4-Piperidinemethanol is a cyclic secondary amine. Its standard molar enthalpies of combustion, sublimation and formation have been determined.
Application
4-Piperidinemethanol may be used in the preparation of:
- N-tert-butoxycarbonyl-4-hydroxymethyl piperidine
- desferrioxamine B (DFO) containing third generation triazine dendrimer
- ethyl 3-(4-(hydroxymethyl)piperidin-1-yl)propanoate (EHMPP)
- 4-(hydroxymethyl)piperidine-1-carbodithioic acid (HL)
- 1-[[(1E)-2-(4-chlorophenyl)ethenyl]sulfonyl]-4-piperidinemethanol
Substrate used in solid-phase organic synthesis of a secondary amine.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
230.0 °F - closed cup
Flash Point(C)
110 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Organic letters, 6(12), 1935-1938 (2004-06-05)
[reaction: see text] An expedient solid-phase synthetic approach to secondary and tertiary amines was developed. The protocol employs conversion of resin-bound amino alcohols to the corresponding iodides, followed by iodide displacement with primary or secondary amines or with unprotected amino
Synthesis, spectroscopy, and biological activity of heterobimetallic complexes containing Sn (IV) and Pd (II) with 4-(hydroxymethyl) piperidine-1-carbodithioic acid.
Russ. J. Gen. Chem., 83(12), 2380-2385 (2013)
Enzymatic synthesis, thermal and crystalline properties of a poly (β-amino ester) and poly (lactone-co-β-amino ester) copolymers.
Polymer, 53(9), 1839-1848 (2012)
Synthesis and evaluation of 1-arylsulfonyl-3-piperazinone derivatives as factor Xa inhibitor.
Chemical & Pharmaceutical Bulletin, 49(10), 1237-1244 (2001)
Bioorganic & medicinal chemistry, 18(15), 5749-5753 (2010-07-10)
The synthesis of a third generation triazine dendrimer, 1, containing multiple, iron-sequestering desferrioxamine B (DFO) groups is described. Benzoylation of the hydroxamic acid groups of DFO and formation of a reactive dichlorotriazine provide the intermediate for reaction with the second
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