Basic information Safety Supplier Related

3-Hydroxy-1-methylpiperidine

Basic information Safety Supplier Related

3-Hydroxy-1-methylpiperidine Basic information

Product Name:
3-Hydroxy-1-methylpiperidine
Synonyms:
  • 1-Methyl-3-hydroxypiperidine
  • 1-methyl-3-piperidino
  • 3-HYDROXY-N-METHYLPIPERIDINE
  • NM3PPOL
  • N-METHYL-3-HYDROXY PIPERIDINE
  • N-METHYL-3-PIPERIDINOL
  • 3-HYDROXY-1-METHYLPIPERIDINE
  • 1-METHYL-3-PIPERIDINOL
CAS:
3554-74-3
MF:
C6H13NO
MW:
115.17
EINECS:
222-609-2
Product Categories:
  • Piperidine
  • API intermediates
  • Building Blocks
  • C5 to C7
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Piperidines
Mol File:
3554-74-3.mol
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3-Hydroxy-1-methylpiperidine Chemical Properties

Boiling point:
76-78 °C11 mm Hg(lit.)
Density 
0.999 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.475
Flash point:
158 °F
pka
14.95±0.20(Predicted)
form 
liquid
color 
Clear, orange
Water Solubility 
Fully misicible in water.
BRN 
103017
CAS DataBase Reference
3554-74-3(CAS DataBase Reference)
NIST Chemistry Reference
3-Piperidinol, 1-methyl-(3554-74-3)
EPA Substance Registry System
3-Piperidinol, 1-methyl- (3554-74-3)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-6/37/38
Safety Statements 
26-36
WGK Germany 
3
Hazard Note 
Irritant
TSCA 
Yes
HS Code 
29333990

MSDS

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3-Hydroxy-1-methylpiperidine Usage And Synthesis

Uses

Reactant for:• ;Optimization of Novobiocin scaffold to produce antitumor agents1• ;Formation of carbamates and N-alkylimidazoles2Reactant for synthesis of:• ;Pyridine derivatives as CDK5 inhibitors3• ;Phenylcarbamate derivatives as ligands for nicotinic acetylcholine receptors4• ;Amino phosphite ligands5• ;Mexiletine enantiomers by nucleophilic aromatic substitution6

Uses

Reactant for Optimization of Novobiocin scaffold to produce antitumor agents, Formation of carbamates and N-alkylimidazoles. Reactant for synthesis of Pyridine derivatives as CDK5 inhibitors Phenylcarbamate derivatives as ligands for nicotinic acetylcholine receptors, Amino phosphite ligands, Mexiletine enantiomers by nucleophilic aromatic substitution.

Uses

Reactant for:

  • Optimization of Novobiocin scaffold to produce antitumor agents
  • Formation of carbamates and N-alkylimidazoles

Reactant for synthesis of:
  • Pyridine derivatives as CDK5 inhibitors
  • Phenylcarbamate derivatives as ligands for nicotinic acetylcholine receptors
  • Amino phosphite ligands
  • Mexiletine enantiomers by nucleophilic aromatic substitution

3-Hydroxy-1-methylpiperidine Preparation Products And Raw materials

Raw materials

3-Hydroxy-1-methylpiperidineSupplier

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