Skip to Content
MilliporeSigma
All Photos(2)

Documents

126993

Sigma-Aldrich

N-Ethylbenzylamine

97%

Synonym(s):

N-Benzylethylamine

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
C6H5CH2NHCH2CH3
CAS Number:
14321-27-8
Molecular Weight:
135.21
Beilstein/REAXYS Number:
386023
EC Number:
238-265-1
MDL number:
MFCD00009031
UNSPSC Code:
12352100
PubChem Substance ID:
24847753
NACRES:
NA.22

assay

97%

form

liquid

refractive index

n20/D 1.511 (lit.)

bp

191-194 °C (lit.)

density

0.909 g/mL at 25 °C (lit.)

SMILES string

CCNCc1ccccc1

InChI

1S/C9H13N/c1-2-10-8-9-6-4-3-5-7-9/h3-7,10H,2,8H2,1H3

InChI key

HVAAHUDGWQAAOJ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

N-Ethylbenzylamine has been used to demonstrate the reactivity of NDTE (2,5-dihydroxyphenylacetic acid, 2,5-bis-tetrahydropyranyl ether p-nitrophenyl ester) and HLTE (homogentisic gamma-lactone tetrahydropyranyl ether). It has also been used to prepare 2-[(N-Benzyl, N-ethyl)amino]derivative using 2-chloro-4H-pyrido[1,2-a]pyrimidin-4-one.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

156.2 °F - closed cup

flash_point_c

69 °C - closed cup

ppe

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

N-Benzylethylenediamine 97%

Sigma-Aldrich

462292

N-Benzylethylenediamine

M Di Braccio et al.
Il Farmaco; edizione scientifica, 43(9), 705-723 (1988-09-01)
The N,N-disubstituted 4-amino-2H-pyrido[1,2-a]pyrimidin-2-ones (III) and isomer 2-amino-4H-pyrido[1,2-a]pyrimidin-4-ones (IV) were obtained from the reaction of 2-aminopyridine with the N,N-disubstituted ethyl malonamate/phosphorus oxychloride reagent (II), in refluxing 1,2-dichloroethane. 2-[(N-Benzyl, N-ethyl)amino]derivative (IV b) was also prepared in excellent yield by treating 2-chloro-4H-pyrido[1,2-a]pyrimidin-4-one (V)
M J Rose et al.
Analytical chemistry, 71(11), 2221-2230 (1999-06-15)
Two new reagents, NDTE (2,5-dihydroxyphenylacetic acid, 2,5-bis-tetrahydropyranyl ether p-nitrophenyl ester) and HLTE (homogentisic gamma-lactone tetrahydropyranyl ether), are described for the chemical derivatization of primary and/or secondary amines to form an electrochemically active product. These reagents undergo reaction with the aforementioned
Md Salman Shakil et al.
Biomedicines, 9(2) (2021-01-31)
Hydroxypyr(id)ones are a pharmaceutically important class of compounds that have shown potential in diverse areas of drug discovery. We investigated the 3-hydroxy-4-pyridones 1a-1c and 3-hydroxy-4-thiopyridones 1d-1f as well as their Ru(η6-p-cymene)Cl complexes 2a-2f, and report here the molecular structures of
Oh Kyung Choi et al.
Journal of hazardous materials, 403, 123636-123636 (2020-08-28)
Solvent extraction desalination (SED) is one of the liquid-liquid separation techniques that selectively uptake freshwater from high saline water, and then separate the absorbed freshwater from the solvent through temperature swing. This study evaluated the desalination performance of seven different

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service