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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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Properties

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

Description

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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Introducing chemiluminescence resonance energy transfer into immunoassay in a microfluidic format for an improved assay sensitivity.

Shulin Zhao et al.

Chemical communications (Cambridge, England), 48(5), 699-701 (2011-12-03)

We report on a novel strategy to improve microfluidic immunoassay sensitivity by introducing chemiluminescence resonance energy transfer (CRET) into the immunoreactions. The proposed CRET-based immunoassay for estradiol (E2, as a model analyte) is one of the most sensitive immunoassay with

Configuration and optimization of a common two-site immunoassay for human prolactin using a chemiluminescent tracer and an enzymatic tracer.

L Farina et al.

Journal of bioluminescence and chemiluminescence, 4(1), 587-593 (1989-07-01)

We have developed a two-site immunoassay for human prolactin using two monoclonal antibodies: one of them immobilized on the solid phase and the other labelled with biotin. The serum is incubated simultaneously with the antibody-coated bead, the biotinylated antibody and

Liquid chromatographic analysis of carboxylic acids using N-(4-aminobutyl)-N-ethylisoluminol as chemiluminescent label: determination of ibuprofen in saliva.

O M Steijger et al.

Journal of chromatography, 615(1), 97-110 (1993-05-19)

N-(4-Aminobutyl)-N-ethylisoluminol was used for labelling of carboxylic acids. The derivatization reaction was carried out with 1-hydroxybenzotriazole as pre-activator of the carboxylic acid function and N-ethyl-N'-(3-dimethylaminopropyl)carbodiimide as the coupling reagent. Optimum conditions for the derivatization were determined by using factorial design

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Global Trade Item Number

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