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07-2760

Sigma-Aldrich

Diethylamine

SAJ special grade, ≥99.0%

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About This Item

Linear Formula:
(C2H5)2NH
CAS Number:
Molecular Weight:
73.14
Beilstein/REAXYS Number:
605268
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
Pricing and availability is not currently available.

grade

SAJ special grade

vapor density

2.5 (vs air)

vapor pressure

14.14 psi ( 55 °C)
180 mmHg ( 20 °C)
3.51 psi ( 20 °C)

assay

≥99.0%

form

liquid

autoignition temp.

594 °F

expl. lim.

10.1 %

availability

available only in Japan

refractive index

n20/D 1.385 (lit.)

pH

13 (20 °C, 100 g/L)

bp

55 °C (lit.)

mp

−50 °C (lit.)

density

0.707 g/mL at 25 °C (lit.)

SMILES string

CCNCC

InChI

1S/C4H11N/c1-3-5-4-2/h5H,3-4H2,1-2H3

InChI key

HPNMFZURTQLUMO-UHFFFAOYSA-N

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Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

-14.8 °F

flash_point_c

-26 °C


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Jennifer C Irvine et al.
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Journal of chromatography. A, 1217(3), 250-255 (2009-12-05)
A salting-out assisted liquid extraction coupled with back-extraction by a water/acetonitrile/dichloromethane ternary component system combined with high-performance liquid chromatography with diode-array detection (HPLC-DAD) was developed for the extraction and determination of sulfonamides in solid tissue samples. After the homogenization of
Manuel Ventura et al.
Journal of chromatography. A, 1220, 147-155 (2011-12-22)
Supercritical fluid chromatography is routinely utilized by analytical separations groups in the pharmaceutical industry to efficiently handle separations for discovery medicinal chemistry purposes. Purifications are performed on samples ranging from a few milligrams up to hundreds of grams. Basic additives
Katina S S Dossou et al.
Journal of chromatography. A, 1216(44), 7450-7455 (2009-06-26)
A polysaccharide-based chiral stationary phase (Sepapak-4), with cellulose tris(4-chloro-3-methylphenylcarbamate) as chiral selector, has been investigated in liquid chromatography (LC). Its enantioresolution power was evaluated towards 13 basic amino-drugs with widely different structures and polarities, using polar organic mobile phases. After
Roberto Cirilli et al.
Analytical chemistry, 81(9), 3560-3570 (2009-03-28)
Second-order rate constants of the diethylamine-promoted enantiomerization of 2-[2-(1-methyl-1H-pyrrol-2-yl)-2-oxo-1-phenylethyl]-isoindole-1,3-dione, a chiral alpha-substituted ketone endowed with high anti-MAO activity type-A, were measured by dynamic high-performance liquid chromatography (DHPLC), stopped-flow high-performance liquid chromatography (sf-HPLC), and a classical method based on enantioselective HPLC

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