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190195

Sigma-Aldrich

1-Ethylpropylamin

97%

Synonym(e):

3-Amino-pentan

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About This Item

Lineare Formel:
(C2H5)2CHNH2
CAS-Nummer:
616-24-0
Molekulargewicht:
87.16
EG-Nummer:
210-471-6
MDL-Nummer:
MFCD00008096
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24851418
NACRES:
NA.22

Qualitätsniveau

100

Assay

97%

Brechungsindex

n20/D 1.4055 (lit.)

bp

89-91 °C (lit.)

Dichte

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

InChIKey

PQPFFKCJENSZKL-UHFFFAOYSA-N

Verwandte Kategorien

Anwendung

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.

Piktogramme

FlameCorrosion
GHS02,GHS05

Signalwort

Danger

H-Sätze

H225 - H314

Gefahreneinstufungen

Flam. Liq. 2 - Skin Corr. 1B

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

35.6 °F - closed cup

Flammpunkt (°C)

2 °C - closed cup

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

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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
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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.
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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
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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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