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A0156

N-(4-Aminobutyl)-N-ethylisoluminol

Name: <I>N</I>-(4-Aminobutyl)-<I>N</I>-ethylisoluminol
Brand: SIGMA

≥90%, powder

Synonym(s):

4-(N¹-Ethyl-4-aminobutylamino)phthalic hydrazide, 6-[N-(4-Aminobutyl)-N-ethylamino]-2,3-dihydro-1,4-phthalazinedione, ABEI

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About This Item

Empirical Formula (Hill Notation):

C₁₄H₂₀N₄O₂

CAS Number:

66612-29-1

Molecular Weight:

276.33

NACRES:

NA.83

PubChem Substance ID:

24890404

UNSPSC Code:

12352204

MDL number:

MFCD00010559

Beilstein/REAXYS Number:

920895

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Product Name

N-(4-Aminobutyl)-N-ethylisoluminol, ≥90%

Quality Level

200

assay

≥90%

form

powder

mp

259-260 °C (lit.)

solubility

glacial acetic acid: 50 mg/mL, clear, colorless to yellow

storage temp.

2-8°C

SMILES string

CCN(CCCCN)c1ccc2C(=O)NNC(=O)c2c1

InChI

1S/C14H20N4O2/c1-2-18(8-4-3-7-15)10-5-6-11-12(9-10)14(20)17-16-13(11)19/h5-6,9H,2-4,7-8,15H2,1H3,(H,16,19)(H,17,20)

InChI key

LEOJISUPFSWNMA-UHFFFAOYSA-N

Related Categories

Proteins & Enzymes

Detection Substrates & Enzymes

Features and Benefits

Efficient chemiluminescent NH₂-coupling reagent for detection of a wide variety of proteins down to the picomole range.

Other Notes

Reportedly, the use of this material in chemiluminescent assays has distinct advantages over conventional radioimmunoassay.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Electrochemiluminescent aptamer biosensor for the determination of ochratoxin A at a gold-nanoparticles-modified gold electrode using N-(aminobutyl)-N-ethylisoluminol as a luminescent label.

Zhouping Wang et al.

Analytical and bioanalytical chemistry, 398(5), 2125-2132 (2010-09-14)

A highly selective electrochemiluminescent biosensor for the detection of target nephrotoxic toxin, ochratoxin A (OTA), was developed using a DNA aptamer as the recognition element and N-(4-aminobutyl)-N-ethylisoluminol (ABEI) as the signal-producing compound. The electrochemiluminescent aptamer biosensor was fabricated by immobilizing

Chemiluminescence energy transfer: a new technique applicable to the study of ligand--ligand interactions in living systems.

A Patel et al.

Analytical biochemistry, 129(1), 162-169 (1983-02-15)

Chemiluminescent molecules can be readily detected in the range 10(-15) to 10(-18) mol, and potentially at least down to 10(-20) mol reacting/s. The chemiluminescent compound aminobutylethylisoluminol (ABEI) and its isothiocyanate derivative have been synthesized. The ABEI was coupled to rabbit

High-performance liquid chromatography-chemiluminescence determination of methamphetamine in human serum using N-(4-aminobutyl)-N-ethylisoluminol as a chemiluminogen.

K Nakashima et al.

Journal of chromatography, 530(1), 154-159 (1990-08-24)

Electrochemiluminescence biosensor for the assay of small molecule and protein based on bifunctional aptamer and chemiluminescent functionalized gold nanoparticles.

Ying Chai et al.

Analytica chimica acta, 715, 86-92 (2012-01-17)

An electrochemiluminescence (ECL) biosensor for simultaneous detection of adenosine and thrombin in one sample based on bifunctional aptamer and N-(aminobutyl)-N-(ethylisoluminol) functionalized gold nanoparticles (ABEI-AuNPs) was developed. A streptavidin coated gold nanoparticles modified electrode was utilized to immobilize biotinylated bifunctional aptamer

Detection of DNA hybridization by ABEI electrochemiluminescence in DNA-chip compatible assembly.

M-L Calvo-Muñoz et al.

Bioelectrochemistry (Amsterdam, Netherlands), 66(1-2), 139-143 (2005-04-19)

The electrochemiluminescence (ECL) of a luminol derivate (ABEI) generated both by a carbon electrode and a polypyrrole-coated carbon electrode was examined. It was found that the polypyrrole film (ppy) did not inhibit the ECL. After that, ABEI anchored on a

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Global Trade Item Number

SKU	GTIN
A0156-25MG	04061833326978
A0156-250MG	04061833326961

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