Skip to Content
Merck
All Photos(1)

Key Documents

417122

Sigma-Aldrich

N,N-Diethylnipecotamide

98%

Synonym(s):

N,N-Diethyl-3-piperidinecarboxamide, Piperidine-3-carboxylic acid diethylamide

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C10H20N2O
CAS Number:
Molecular Weight:
184.28
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

Assay

98%

form

liquid

refractive index

n20/D 1.489 (lit.)

bp

111 °C/6.1 mmHg (lit.)

density

0.989 g/mL at 25 °C (lit.)

SMILES string

CCN(CC)C(=O)C1CCCNC1

InChI

1S/C10H20N2O/c1-3-12(4-2)10(13)9-6-5-7-11-8-9/h9,11H,3-8H2,1-2H3

InChI key

ZXQKYQVJDRTTLZ-UHFFFAOYSA-N

General description

N,N-Diethylnipecotamide is a six-membered bidentate chelating ligand. It participates as ligand in the synthesis of dimeric halocopper(I) complexes.[1]

Application

N,N-Diethylnipecotamide may be used for the preparation of 1-substituted N,N-diethylnipecotamides.[2]
Reactant for synthesis of:
Antituberculosis drugs
Spiroimidazolidinone NPC1L1 inhibitors
Acyl-CoA:cholesterol acyltransferase inhibitors
Alpha 7 nicotinic acetylcholine receptor agonist
Antimycobacterials
Isocyanoamides useful as starting materials in IMCR

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

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

Visit the Document Library

B Kovacic et al.
European journal of pharmacology, 47(1), 37-44 (1978-01-01)
Adult male Holtzman rats were trained to barpress on a schedule whereby every fourth press earned a reward of 0.01 ml of sugar-sweetened milk (FR4). After an i.p. injection of LSD (0.1 mg/kg) or DMT (3.2 or 10 mg/kg) such
Stoichiometry, properties and kinetics of aprotic reduction of dioxygen by [LCuX]2 (L= N, N-diethylnipecotamide; X= Cl, Br).
El-Sayed MA.
Inorgorganica Chimica Acta, 197(2), 197-201 (1992)

Questions

Reviews

No rating value

Active Filters

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