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137529

Sigma-Aldrich

N,N-Diethylacetamide

97%

Sinónimos:

Acetic acid diethylamide

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About This Item

Fórmula lineal:
CH3CON(C2H5)2
Número de CAS:
685-91-6
Peso molecular:
115.17
Beilstein/REAXYS Number:
1209428
EC Number:
211-685-2
MDL number:
MFCD00009047
UNSPSC Code:
12352100
PubChem Substance ID:
24848334
NACRES:
NA.22

assay

97%

form

liquid

refractive index

n20/D 1.440 (lit.)

bp

182-186 °C (lit.)

density

0.925 g/mL at 25 °C (lit.)

SMILES string

CCN(CC)C(C)=O

InChI

1S/C6H13NO/c1-4-7(5-2)6(3)8/h4-5H2,1-3H3

Inchi Key

AJFDBNQQDYLMJN-UHFFFAOYSA-N

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General description

N,N-Diethylacetamide is commonly used as drug solvent.

Application

N,N-Diethylacetamide was used to investigate the spectroscopic properties of N,N-diethyl-2-[(4-substituted)phenylsulfinyl] acetamides.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - 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

168.8 °F - closed cup

flash_point_c

76 °C - closed cup

ppe

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

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R Budden et al.
Arzneimittel-Forschung, 28(9), 1571-1579 (1978-01-01)
The drug solvents diethyleneglycol monoethylether (Transcutol), N,N-diethylacetamide, and dimethylsulfoxide were examined for their pharmacodynamic properties in the following tests: i.p. toxicity, "sign pattern", inclined screen test, balance rod test, and potentiation of hexobarbitone sleeping time in mice, spasmolytic activity in
Spectroscopic and theoretical studies of some N,N-diethyl-2-[(4-substituted) phenylsulfinyl] acetamides.
Olivato PR, et al.
Journal of Molecular Structure, 827(1), 25-34 (2007)
M Silvia et al.
Biochemical pharmacology, 48(4), 717-726 (1994-08-17)
This study was undertaken to investigate: (1) the effect of N,N-diethylacetamide (DEAC) and N,N-dimethylacetamide (DMAC) administration to rats on drug-metabolizing enzymes in the liver; (2) the in vitro dealkylation of DEAC and DMAC by hepatic microsomes from rats treated with
Action of N,N-diethylacetamide on hepatic microsomal drug-metabolizing enzymes.
F E Beyhl et al.
Food and cosmetics toxicology, 19(5), 627-629 (1981-10-01)
Vijay Gupta et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(12), 2658-2665 (2019-12-04)
A new triazole-functionalized tetracarboxylic acid ligand (H4 L) has been synthesized and utilized for the fabrication of a 3D ZnII organic framework with a Zn4 (-COO)6 cluster as the secondary building unit. The framework exhibits very good thermal stability and

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