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About This Item
Empirical Formula (Hill Notation):
C10H14N2O
CAS Number:
Molecular Weight:
178.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-418-5
Beilstein/REAXYS Number:
5743
MDL number:
Assay:
99%
Form:
liquid
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
SMILES string
CCN(CC)C(=O)c1cccnc1
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.)
Quality Level
Application
N,N-Diethylnicotinamide (DENC) is commonly used as a ligand to prepare tetranuclear copper complexes.
signalword
Danger
hcodes
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
Regulatory Information
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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)
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)
Synthesis, structure and properties of the tetranuclear complexes [(DENC) CuX] 4 (DENC= N, N-diethylnicotinamide; X= Cl, Br, I) and the kinetics of oxidation of the chloride and bromide by dioxygen in aprotic solvents.
Churchill M R, et al.
Inorganic Chemistry, 21(3), 995-1001 (1982)
K Elkharraz et al.
International journal of pharmaceutics, 314(2), 127-136 (2006-02-24)
The aim of this study was to prepare different types of paclitaxel-loaded, PLGA-based microparticles and lipidic implants, which can directly be injected into the brain tissue. Releasing the drug in a time-controlled manner over several weeks, these systems are intended
[Disturbed functioning of enzyme systems of the microsomal oxidation, glucuro- and glutathione conjugation of xenobiotics in the liver of rats intoxicated by deoxycholate and their correction].
M I Bushma et al.
Biulleten' eksperimental'noi biologii i meditsiny, 129(1), 56-60 (2000-03-11)
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