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A0156

Sigma-Aldrich

N-(4-Aminobutyl)-N-ethylisoluminol

≥90%

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Synonym(s):
4-(N1-Ethyl-4-aminobutylamino)phthalic hydrazide, 6-[N-(4-Aminobutyl)-N-ethylamino]-2,3-dihydro-1,4-phthalazinedione, ABEI
Empirical Formula (Hill Notation):
C14H20N4O2
CAS Number:
Molecular Weight:
276.33
Beilstein/REAXYS Number:
920895
MDL number:
PubChem Substance ID:
NACRES:
NA.83

Quality Level

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

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Show Differences

1 of 4

This Item
A8264SML3029SML1560
N-(4-Aminobutyl)-N-ethylisoluminol ≥90%

A0156

N-(4-Aminobutyl)-N-ethylisoluminol

4-Aminophthalhydrazide

A8264

4-Aminophthalhydrazide

HG-9-91-01 >95% (HPLC)

SML3029

HG-9-91-01

Azoramide ≥98% (HPLC)

SML1560

Azoramide

solubility

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

solubility

2 M NH4OH: 50 mg/mL, clear to slightly hazy

solubility

DMSO: 2 mg/mL, clear

solubility

DMSO: 30 mg/mL, clear

form

powder

form

powder

form

powder

form

powder

storage temp.

2-8°C

storage temp.

-

storage temp.

2-8°C

storage temp.

2-8°C

mp

259-260 °C (lit.)

mp

300 °C (lit.)

mp

-

mp

-

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Customers Also Viewed

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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
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
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
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
K E Achyuthan
Journal of bioluminescence and chemiluminescence, 13(1), 1-11 (1998-06-03)
A novel and sensitive chemiluminescent assay is described to quantitate the acyl transfer activities of blood coagulation factor XIIIa or liver transglutaminase using aminobutyl-N-ethylisoluminol as acyl acceptor and N,N-dimethylcasein, human plasma fibrinogen or fibronectin as acyl donors. The method involved

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