Skip to Content
Merck
All Photos(1)

Key Documents

411027

Sigma-Aldrich

Piperidine

≥99.5%, purified by redistillation

Synonym(s):

Hexahydropyridine

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C5H11N
CAS Number:
Molecular Weight:
85.15
Beilstein:
102438
EC Number:
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

vapor density

3 (vs air)

Quality Level

vapor pressure

23 mmHg ( 20 °C)

Assay

≥99.5%

form

liquid

purified by

redistillation

refractive index

n20/D 1.452 (lit.)

bp

106 °C (lit.)

mp

−13 °C (lit.)

density

0.862 g/mL at 20 °C (lit.)

SMILES string

C1CCNCC1

InChI

1S/C5H11N/c1-2-4-6-5-3-1/h6H,1-5H2

InChI key

NQRYJNQNLNOLGT-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Piperidine may be used as a base for the oxidative homocoupling of terminal alkynes to form symmetrical 1,4-disubstituted 1,3-diynes in the presence of copper nanoparticle on polyaniline support catalyst. It may also be used for cleaving the Fmoc-group in Nα-9-fluorenylmethyloxycarbonyl (Fmoc) amino acids.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

60.8 °F - closed cup

Flash Point(C)

16 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Polymer-Supported Cu?Nanoparticle as an Efficient and Recyclable Catalyst for Oxidative Homocoupling of Terminal Alkynes.
Aziz ST
Catalysis Letters, 148(1), 205-213 (2018)
Solid?phase peptide synthesis using mild base cleavage of N?-fluorenylmethyloxycarbonylamino acids, exemplified by a synthesis of dihydrosomatostatin.
Chang CD
Chemical Biology & Drug Design, 11(3), 246-249 (1978)
Shunlei Duan et al.
Nucleic acids research, 48(12), 6530-6546 (2020-05-21)
OGG1 initiated base excision repair (BER) is the major pathway for repair of oxidative DNA base damage 8-oxoguanine (8-oxoG). Here, we report that RECQL4 DNA helicase, deficient in the cancer-prone and premature aging Rothmund-Thomson syndrome, physically and functionally interacts with
Total synthesis of (-)-kopsinine by an asymmetric one-pot [n+2+3] cyclization.
Shingo Harada et al.
Chemistry, an Asian journal, 7(10), 2196-2198 (2012-08-22)
J Phillip Turner et al.
ACS chemical neuroscience, 5(7), 552-558 (2014-04-03)
Alzheimer's disease (AD) is the most common form of dementia and the sixth leading cause of death in the United States. Plaques composed of aggregated amyloid-beta protein (Aβ) accumulate between the neural cells in the brain and are associated with

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