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この商品について
実験式(ヒル表記法):
C3H4N2
CAS番号:
分子量:
68.08
NACRES:
NA.21
UNSPSC Code:
12352005
Beilstein/REAXYS Number:
103853
MDL number:
製品名
イミダゾール, ReagentPlus®, 99%, Redi-Dri™, free-flowing
SMILES string
c1c[nH]cn1
InChI
1S/C3H4N2/c1-2-5-3-4-1/h1-3H,(H,4,5)
InChI key
RAXXELZNTBOGNW-UHFFFAOYSA-N
vapor pressure
<1 mmHg ( 20 °C)
product line
ReagentPlus®
Redi-Dri™
assay
99%
form
powder
quality
free-flowing
pH
9-11 at 100 g/L (23 °C)
pKa (25 °C)
6.95
bp
256 °C (lit.)
mp
85-92 °C
88-91 °C (lit.)
Quality Level
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Application
pH 6.2~7.8の範囲におけるバッファーとして優れています。
Imidazole is commonly used as a buffer component for purification of the histidine-tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC).
Features and Benefits
- Redi-Dri packaging controls moisture for hygroscopic chemicals that commonly clump
- Anhydrous powder remains free-flowing and easy to use
- Safer to handle and weigh out for routine use in lab
- Eliminates clumps to maintain product moisture and quality
General description
Imidazole is a buffering agent employed in various research applications, with a pH 9 -11, it is often used to maintain a stable pH for protein samples. Imidazole is a heterocyclic compound with a five-membered planar ring that is amphoteric, highly polar, and commonly used for affinity chromatography. Its ability to bind to metal ions makes it particularly useful for purification and separation of proteins.
Other Notes
For additional information on our range of Biochemicals, please complete this form.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
Redi-Dri is a trademark of Sigma-Aldrich Co. LLC
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 1B - Skin Corr. 1C
保管分類
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 2
flash_point_f
293.0 °F - closed cup
flash_point_c
145 °C - closed cup
Three-Dimensional Covalent Co-Assembly between Inorganic Supertetrahedral Clusters and Imidazolates.
Wu T, et al.
Angewandte Chemie (International Edition in English), 50(11), 2536-2539 (2011)
Cobalt imidazolate framework as precursor for oxygen reduction reaction electrocatalysts.
Ma S, et al.
Chemistry?A European Journal , 17(7), 2063-2067 (2011)
Ali Tebbi et al.
The Journal of biological chemistry, 290(22), 14077-14090 (2015-04-17)
Ribonucleotide reductase (RnR) is a key enzyme synthesizing deoxyribonucleotides for DNA replication and repair. In mammals, the R1 catalytic subunit forms an active complex with either one of the two small subunits R2 and p53R2. Expression of R2 is S
Pam M Van Ry et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 23(8), 1285-1297 (2015-06-09)
Duchenne muscular dystrophy (DMD) is a fatal neuromuscular disease caused by mutations in the dystrophin gene, leading to the loss of a critical component of the sarcolemmal dystrophin glycoprotein complex. Galectin-1 is a small 14 kDa protein normally found in skeletal
Michael D Clark et al.
Proceedings of the National Academy of Sciences of the United States of America, 112(28), E3669-E3678 (2015-07-01)
Acetylation is correlated with chromatin decondensation and transcriptional activation, but its regulation by histone deacetylase (HDAC)-bearing corepressor complexes is poorly understood. Here, we describe the mechanism of assembly of the mammalian Sin3L/Rpd3L complex facilitated by Sds3, a conserved subunit deemed
資料
Redi-Dri™ prevents hygroscopic powders, such as inorganic salts, from absorbing moisture and forming clumps, leaving the salts free-flowing every time.
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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