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E12001

4-Ethylaniline

Name: 4-Ethylaniline
Brand: ALDRICH

98%

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About This Item

Linear Formula:

C₂H₅C₆H₄NH₂

CAS Number:

589-16-2

Molecular Weight:

121.18

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24894393

EC Number:

209-637-0

Beilstein/REAXYS Number:

774319

MDL number:

MFCD00007921

Assay:

98%

Form:

liquid

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Properties

Quality Level

100

assay

98%

form

liquid

refractive index

n20/D 1.554 (lit.)

bp

216 °C (lit.)

mp

−5 °C (lit.)

density

0.975 g/mL at 25 °C (lit.)

SMILES string

CCc1ccc(N)cc1

InChI

1S/C8H11N/c1-2-7-3-5-8(9)6-4-7/h3-6H,2,9H2,1H3

InChI key

HRXZRAXKKNUKRF-UHFFFAOYSA-N

Description

pictograms

GHS06,GHS08

signalword

Danger

hcodes

H301 + H311 + H331,H373

pcodes

P260 - P280 - P301 + P310 - P302 + P352 + P312 - P304 + P340 + P311 - P314

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - STOT RE 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

185.0 °F - closed cup

flash_point_c

85 °C - closed cup

ppe

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

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On the active site of liver acetyl-CoA. Arylamine N-acetyltransferase from rapid acetylator rabbits (III/J).

H H Andres et al.

The Journal of biological chemistry, 263(16), 7521-7527 (1988-06-05)

A covalent, catalytic intermediate of cytosolic liver acetyl coenzyme A: arylamine N-acetyltransferase (EC 2.3.1.5) from rapid acetylator rabbits (III/J) was isolated and chemically characterized. The active site was further studied using two covalent inhibitors, [2-3H]iodoacetic acid and bromoacetanilide. Inhibition experiments

Overtone spectra of aniline derivatives.

Vineet Kumar Rai et al.

Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 60(1-2), 53-56 (2003-12-13)

Overtone spectra of 2-ethylaniline, N-methylaniline, N-ethylaniline, N,N-dimethylaniline and N,N-diethylaniline have been studied in 2500-15000 cm(-1) region. Vibrational frequency and anharmonicity constants for aryl/alkyl C-H stretch and N-H stretch vibrations have been determined. The effect of substitution of C(2)H(5) group on

CE with multi-walled carbon nanotubes (MWCNTs). Part I. Functionalized and SDS coated MWCNTs as pseudo-stationary phases in nanoparticle EKC - Studies on retention energetics.

Sarah Alharthi et al.

Talanta, 192, 534-544 (2018-10-24)

In this study, multi-walled carbon nanotubes (MWCNTs) in either unmodified, hydroxylated (MWCNT-OH), carboxylated (MWCNT-COOH) or sulfonated (MWCNT-SO3H) forms were incorporated into the running electrolytes in capillary electrophoresis (CE) to play the role of pseudo-stationary phases (PSPs) and perform nanoparticle electrokinetic

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Global Trade Item Number

SKU	GTIN
E12001-500ML	04061836830878
E12001-100ML	04061833601433