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D98807

N,N-Diethylnicotinamide

Name: <I>N,N</I>-Diethylnicotinamide
Brand: ALDRICH

99%

Synonym(s):

DENC, Nicotinic acid diethylamide, Nikethamide

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About This Item

Empirical Formula (Hill Notation):

C₁₀H₁₄N₂O

CAS Number:

59-26-7

Molecular Weight:

178.23

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24894117

EC Number:

200-418-5

Beilstein/REAXYS Number:

5743

MDL number:

MFCD00006386

Assay:

99%

Form:

liquid

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Properties

Quality Level

200

assay

99%

form

liquid

refractive index

n20/D 1.524 (lit.)

bp

296-300 °C (lit.)

mp

23 °C (lit.)

density

1.06 g/mL at 25 °C (lit.)

SMILES string

CCN(CC)C(=O)c1cccnc1

InChI

1S/C10H14N2O/c1-3-12(4-2)10(13)9-6-5-7-11-8-9/h5-8H,3-4H2,1-2H3

InChI key

NCYVXEGFNDZQCU-UHFFFAOYSA-N

Description

Application

N,N-Diethylnicotinamide (DENC) is commonly used as a ligand to prepare tetranuclear copper complexes.

pictograms

GHS06

signalword

Danger

hcodes

H301,H319

pcodes

P264 - P280 - P301 + P310 - P305 + P351 + P338 - P337 + P313 - P405

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 1

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Synthesis and properties of mixed-valence copper molecules (. mu.-Y) N4CuII2CUI2X4 (N= N, N-diethylnicotinamide; Y= 3, 4, 5, 6-tetrachlorocatecholate; X= Cl, Br, I) and the products and kinetics of their reactions with dioxygen and nitrobenzene.

El-Sayed M A and Davies G

Inorganic Chemistry, 29(24), 4891-4897 (1990)

Transmetalation reactions of tetranuclear copper (II) complexes. 2. Stoichiometry and products of reaction of [(DENC) CuCl] 4O2,[(DENC) CuCl] 4 (CO3) 2,[(DENC) CuCl] 4Cl4, and (DENC) 4Cu4Cl6O (DENC= N, N-diethylnicotinamide) with Ni (NS) 2, the kinetics of product isomerization in aprotic solvents, and inhibition of copper-catalyzed phenolic. oxidativecoupling by dioxygen through transmetalation.

El-Toukhy A, et al.

Journal of the American Chemical Society, 106(16), 4596-4605 (1984)

Effects of ethylene glycol-based graft, star-shaped, and dendritic polymers on solubilization and controlled release of paclitaxel.

Tooru Ooya et al.

Journal of controlled release : official journal of the Controlled Release Society, 93(2), 121-127 (2003-11-26)

New methods and pharmaceutical compositions were developed to increase the aqueous solubility of paclitaxel (PTX), a poorly water-soluble drug. Graft and star-shaped graft polymers consisting of poly(ethylene glycol) (PEG400) graft chains increased the PTX solubility in water by three orders

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Global Trade Item Number

SKU	GTIN
D98807-25G	04061837669514
D98807-500G	04061833591260
D98807-100G	04061833591253