A0156
N-(4-Aminobutyl)-N-ethylisoluminol
≥90%, powder
동의어(들):
4-(N1-Ethyl-4-aminobutylamino)phthalic hydrazide, 6-[N-(4-Aminobutyl)-N-ethylamino]-2,3-dihydro-1,4-phthalazinedione, ABEI
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모든 사진(1)
About This Item
실험식(Hill 표기법):
C14H20N4O2
CAS Number:
Molecular Weight:
276.33
Beilstein:
920895
MDL number:
UNSPSC 코드:
12352204
PubChem Substance ID:
NACRES:
NA.83
추천 제품
product name
N-(4-Aminobutyl)-N-ethylisoluminol, ≥90%
Quality Level
분석
≥90%
형태
powder
mp
259-260 °C (lit.)
solubility
glacial acetic acid: 50 mg/mL, clear, colorless to yellow
저장 온도
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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특징 및 장점
Efficient chemiluminescent NH2-coupling reagent for detection of a wide variety of proteins down to the picomole range.
기타 정보
Reportedly, the use of this material in chemiluminescent assays has distinct advantages over conventional radioimmunoassay.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
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)
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
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
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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