I2399
イミダゾール
ACS reagent grade, ≥99% (titration)
別名:
1,3-ジアザ-2,4-シクロペンタジエン, グリオキサリン
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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
PubChem Substance ID:
eCl@ss:
39161001
UNSPSC Code:
12352005
EC Number:
206-019-2
MDL number:
Beilstein/REAXYS Number:
103853
製品名
イミダゾール, ACS reagent, ≥99% (titration)
InChI key
RAXXELZNTBOGNW-UHFFFAOYSA-N
InChI
1S/C3H4N2/c1-2-5-3-4-1/h1-3H,(H,4,5)
SMILES string
c1c[nH]cn1
grade
ACS reagent
vapor pressure
<1 mmHg ( 20 °C)
assay
≥99% (titration)
impurities
≤0.2% water
ign. residue
≤0.1%
pH
9.5-11.0 (25 °C, 5% in H2O)
pKa (25 °C)
6.95
bp
256 °C (lit.)
mp
88-91 °C (lit.)
cation traces
Fe: ≤0.001%
Quality Level
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Other Notes
Legal Information
Redi-Dri is a trademark of Sigma-Aldrich Co. LLC
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。
General description
イミダゾールは、天然に存在する多くの化合物に認められる五員複素環化合物です。これは、酸性と塩基性の両方の特性を示します。また、トロンボキサン形成の阻害剤であると報告されています。その垂直スペクトルと無放射崩壊が記録され分析されています。
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
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
S Moncada et al.
Prostaglandins, 13(4), 611-618 (1977-04-01)
Imidazole inhibits the enzymic conversion of the endoperoxides (PGG2 and PGH2) to thromboxane A2 by platelet microsomes (IC50: 22 MICRONG/ML; DETERMINED BY BIOASSAY). The inhibitor is selective, for prostaglandin cyclo-oxygenase is only affected at high doses. Radiochemical data confirms that
Zhong Jin
Natural product reports, 28(6), 1143-1191 (2011-04-08)
A great number of structurally diverse natural products containing five-membered heterocyclic subunits, such as imidazole, oxazole, thiazole, and their saturated congeners, are abundant in nature. These naturally occurring metabolites often exhibit extensive and pharmacologically important biological activities. The latest progress
UV excitation and radiationless deactivation of imidazole.
Barbatti M, et al.
J. Chem. Phys. , 130(3), 034305-034305 (2009)
Peter Canning et al.
Journal of molecular biology, 426(13), 2457-2470 (2014-04-29)
The discoidin domain receptors (DDRs), DDR1 and DDR2, form a unique subfamily of receptor tyrosine kinases that are activated by the binding of triple-helical collagen. Excessive signaling by DDR1 and DDR2 has been linked to the progression of various human
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
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