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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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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

Development of a solid-phase chemiluminescence immunoassay for plasma progesterone.

F Kohen et al.

Steroids, 38(1), 73-88 (1981-07-01)

A solid-phase immunoassay procedure for the determination of progesterone in human plasma is described, which utilizes chemiluminescence as the end-point. A progesterone-isoluminol conjugate serves as the chemiluminescent marker. An IgG fraction of antiserum to progesterone-11 alpha-hemisuccinate bovine serum albumin is

End-column chemiluminescence detection for pressurized capillary electrochromatographic analysis of norepinephrine and epinephrine.

Zian Lin et al.

Journal of chromatography. A, 1170(1-2), 118-121 (2007-10-02)

A simple and convenient end-column chemiluminescence (CL) detection coupled to pressurized capillary electrochromatography (pCEC) was described. Luminol and N-(4-aminobutyl)-N-ethylisoluminol (ABEI) were adopted as mode compounds to evaluate the feasibility of end-column reactor. Detailed analysis of ABEI revealed that the high

Synthesis of N-(aminobutyl)-N-(ethylisoluminol) functionalized gold nanomaterials for chemiluminescent bio-probe.

Dayong Tian et al.

Chemical communications (Cambridge, England), 47(17), 4959-4961 (2011-03-25)

A novel strategy for the synthesis of CF-AuNMs by reducing HAuCl(4) with ABEI in aqueous solution at room temperature is reported. No additional stabilizing and reducing reagents are needed, and various morphologies of CF-AuNMs can be obtained. It could be

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Global Trade Item Number

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

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