Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

H42001

Sigma-Aldrich

N-Methyl-3-piperidinol

98%

Synonym(s):

1-Methyl-3-piperidinol, 3-Hydroxy-1-methylpiperidine

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C6H13NO
CAS Number:
3554-74-3
Molecular Weight:
115.17
Beilstein/REAXYS Number:
103017
EC Number:
222-609-2
MDL number:
MFCD00006495
UNSPSC Code:
12352100
PubChem Substance ID:
24895628

assay

98%

refractive index

n20/D 1.474 (lit.)

bp

76-78 °C/11 mmHg (lit.)

density

0.999 g/mL at 25 °C (lit.)

SMILES string

CN1CCCC(O)C1

InChI

1S/C6H13NO/c1-7-4-2-3-6(8)5-7/h6,8H,2-5H2,1H3

InChI key

UKANCZCEGQDKGF-UHFFFAOYSA-N

Application

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

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

158.0 °F - closed cup

flash_point_c

70 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCBN1449V
BCBJ0852V
BCBB0049V
BCBB0049
1417285

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Hafiz Awais Nawaz et al.
Journal of materials chemistry. B, 9(9), 2295-2307 (2021-02-23)
Injectable gelatine-based hydrogels are valuable tools for drug and cell delivery due to their extracellular matrix-like properties that can be adjusted by the degree of cross-linking. We have established anhydride-containing oligomers for the cross-linking of gelatine via anhydride-amine-conjugation. So far

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service