A0156
N-(4-氨基丁基)-N-乙基异鲁米诺
≥90%, powder
别名:
4-(N1-乙基-4-氨基丁基氨基)邻苯二甲酰肼, 6-[N-(4-氨基丁基)-N-乙氨基]-2,3-二氢-1,4-邻苯二甲酰肼, ABEI
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关于此项目
经验公式（希尔记法）:
C14H20N4O2
化学文摘社编号:
分子量:
276.33
NACRES:
NA.83
PubChem Substance ID:
UNSPSC Code:
12352204
MDL number:
Beilstein/REAXYS Number:
920895
产品名称
N-(4-氨基丁基)-N-乙基异鲁米诺, ≥90%
InChI key
LEOJISUPFSWNMA-UHFFFAOYSA-N
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)
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
Quality Level
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Features and Benefits
高效的化学发光 NH2 偶联试剂，用于检测低至皮摩尔范围的各种蛋白质。
Other Notes
据报道，在化学发光测定中使用这种材料具有明显优于传统放射免疫测定的优点。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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
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
R M Lequin et al.
Journal of immunoassay, 7(3), 169-179 (1986-01-01)
Chemiluminescent labels have been shown to be interesting alternatives to radioisotope labels. Disadvantages of the latter are preparation of e.g. labelled protein/peptides every four to six weeks, and problems with storage and disposal. Amino-Butyl-Ethyl-Isoluminol(ABEI) was attached to the alpha-amino function
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