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Merck
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文件

V900153

Sigma-Aldrich

咪唑

Vetec, reagent grade, 98%

同義詞:

1,3-二氮杂-2,4-环戊二烯, 甘恶啉

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About This Item

經驗公式(希爾表示法):
C3H4N2
CAS號碼:
分子量::
68.08
Beilstein:
103853
EC號碼:
MDL號碼:
分類程式碼代碼:
12161700
PubChem物質ID:

等級

reagent grade

蒸汽壓力

<1 mmHg ( 20 °C)

產品線

Vetec

化驗

98%

形狀

crystalline

pH值

9.5-11 (25 °C, 6.8 g/L)

pKa (25 °C)

6.95

bp

256 °C (lit.)

mp

88-91 °C (lit.)

SMILES 字串

c1c[nH]cn1

InChI

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

InChI 密鑰

RAXXELZNTBOGNW-UHFFFAOYSA-N

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應用

特别适用于 pH 6.2-7.8 范围内的缓冲液

法律資訊

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

訊號詞

Danger

危險聲明

危險分類

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

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類(WGK)

WGK 2

閃點(°F)

293.0 °F - closed cup

閃點(°C)

145 °C - closed cup


分析證明 (COA)

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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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