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190195

Sigma-Aldrich

1-Ethylpropylamine

97%

Sinónimos:

3-Aminopentane

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About This Item

Fórmula lineal:
(C2H5)2CHNH2
Número de CAS:
616-24-0
Peso molecular:
87.16
EC Number:
210-471-6
MDL number:
MFCD00008096
UNSPSC Code:
12352100
PubChem Substance ID:
24851418
NACRES:
NA.22

Quality Level

100

assay

97%

refractive index

n20/D 1.4055 (lit.)

bp

89-91 °C (lit.)

density

0.748 g/mL at 25 °C (lit.)

SMILES string

CCC(N)CC

InChI

1S/C5H13N/c1-3-5(6)4-2/h5H,3-4,6H2,1-2H3

InChI key

PQPFFKCJENSZKL-UHFFFAOYSA-N

Categorías relacionadas

Application

1-Ethylpropylamine has been used:
  • in the synthesis of (1-ethyl-propyl)-[3-(4-methoxy-2-methylphenyl)-2-methyl-6,7-dihydro-5H-1,4,8a-triaza-s-indacen-8-yl]-amine
  • in the synthesis of monoclinic VPO4·H2O
  • as internal standard in the screening of aziridine and 2-chloroethylamine in active pharmaceutical ingredients by gas chromatography-mass spectrometry.

pictograms

FlameCorrosion
GHS02,GHS05

signalword

Danger

Hazard Classifications

Flam. Liq. 2 - Skin Corr. 1B

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

35.6 °F - closed cup

flash_point_c

2 °C - closed cup

ppe

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

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Tetsuji Saito et al.
Bioorganic & medicinal chemistry, 19(18), 5432-5445 (2011-08-26)
To identify an orally active corticotropin-releasing factor 1 receptor antagonist, a series of 6,7-dihydro-5H-cyclopenta[d]pyrazolo[1,5-a]pyrimidines and their derivatives were designed, synthesized and evaluated. An in vitro study followed by in vivo and pharmacokinetic studies of these heterotricyclic compounds led us to
Julián Zapata et al.
Journal of pharmaceutical and biomedical analysis, 55(3), 458-465 (2011-03-23)
A simple, fast and fully automated method for the screening of aziridine (AZD) and 2-chloroethylamine (CEA) in active pharmaceutical ingredients (API) has been developed. The method is based on the in-fiber derivatization of the amines extracted from the sample headspace
Reaction of vanadium phosphates with alcohols at elevated temperature and pressure.
Dong W-S, et al.
Journal of Materials Chemistry, 15(31), 3214-3220 (2005)
Roman Borisov et al.
Journal of separation science, 42(22), 3470-3478 (2019-09-14)
On-spot derivatization has been suggested for the modification of primary amine containing compounds for their analysis by thin-layer chromatography hyphenated with matrix-assisted laser desorption ionization mass spectrometry. The proposed approach was based on post-chromatographic treatment of separated analytes inside the
Jan Leipert et al.
Lab on a chip, 19(20), 3490-3498 (2019-09-19)
While LC-MS-based proteomics with high nanograms to micrograms of total protein has become routine, the analysis of samples derived from low cell numbers is challenged by factors such as sample losses, or difficulties encountered with the manual manipulation of small
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