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Merck

A0156

Sigma-Aldrich

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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About This Item

经验公式(希尔记法):
C14H20N4O2
CAS号:
分子量:
276.33
Beilstein:
920895
MDL號碼:
分類程式碼代碼:
12352204
PubChem物質ID:
NACRES:
NA.83

product name

N-(4-氨基丁基)-N-乙基异鲁米诺, ≥90%

化驗

≥90%

形狀

powder

mp

259-260 °C (lit.)

溶解度

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

儲存溫度

2-8°C

SMILES 字串

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 密鑰

LEOJISUPFSWNMA-UHFFFAOYSA-N

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特點和優勢

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。

其他說明

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。

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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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)
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
Shulin Zhao et al.
Analytical biochemistry, 393(1), 105-110 (2009-06-23)
A microchip electrophoresis (MCE) method with chemiluminescence (CL) detection was developed for the determination of carnosine-related peptides, including carnosine, homocarnosine, and anserine, in biological samples. A simple integrated MCE-CL system was built to perform the assays. The highly sensitive CL
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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