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Merck
CN

V900153

Sigma-Aldrich

咪唑

Vetec, reagent grade, 98%

别名:

1,3-二氮杂-2,4-环戊二烯, 甘恶啉

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About This Item

经验公式(希尔记法):
C3H4N2
CAS号:
分子量:
68.08
Beilstein:
103853
EC 号:
MDL编号:
UNSPSC代码:
12161700
PubChem化学物质编号:

等级

reagent grade

蒸汽压

<1 mmHg ( 20 °C)

产品线

Vetec

检测方案

98%

形式

crystalline

pH值(酸碱度)

9.5-11 (25 °C, 6.8 g/L)

pKa (25 °C)

6.95

bp

256 °C (lit.)

mp

88-91 °C (lit.)

SMILES字符串

c1c[nH]cn1

InChI

1S/C3H4N2/c1-2-5-3-4-1/h1-3H,(H,4,5)

InChI key

RAXXELZNTBOGNW-UHFFFAOYSA-N

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应用

特别适用于 pH 6.2-7.8 范围内的缓冲液

法律信息

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

警示用语:

Danger

危险声明

危险分类

Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 1B - Skin Corr. 1C

WGK

WGK 2

闪点(°F)

closed cup

闪点(°C)

closed cup


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Eleonora Petryayeva et al.
Langmuir : the ACS journal of surfaces and colloids, 29(3), 977-987 (2013-01-10)
Methods have been developed for the solid-phase detection of nucleic acids using mixed films of quantum dots (QDs) and oligonucleotide probes in microtiter plates. Polystyrene microwells were functionalized with multidentate imidazole ligands to immobilize QDs. Oligonucleotide hybridization was transduced using
Aviva Levina et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(11), 3609-3619 (2013-01-31)
An anti-metastatic drug, NAMI-A ((ImH)[Ru(III) Cl4 (Im)(dmso)]; Im=imidazole, dmso=S-bound dimethylsulfoxide), and a cytotoxic drug, KP1019 ((IndH)[Ru(III) Cl4 (Ind)2 ]; Ind=indazole), are two Ru-based anticancer drugs in human clinical trials. Their reactivities under biologically relevant conditions, including aqueous buffers, protein solutions
Joy Rathjen et al.
Reproduction, fertility, and development, 26(5), 703-716 (2013-06-14)
Human embryonic stem (ES) cells have been proposed as a renewable source of pluripotent cells that can be differentiated into various cell types for use in research, drug discovery and in the emerging area of regenerative medicine. Exploitation of this
Thangavel Vaijayanthi et al.
Bioorganic & medicinal chemistry, 21(4), 852-855 (2013-01-15)
Fluorophores that are conjugated with N-methylpyrrole-N-methylimidazole (Py-Im) polyamides postulates versatile applications in biological and physicochemical studies. Here, we show the design and synthesis of new types of pyrene-conjugated hairpin Py-Im polyamides (1-5). We evaluated the steady state fluorescence of the
Alexandar L Hansen et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(17), E1705-E1712 (2014-04-16)
The histidine imidazole side chain plays a critical role in protein function and stability. Its importance for catalysis is underscored by the fact that histidines are localized to active sites in ∼ 50% of all enzymes. NMR spectroscopy has become

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