I2399
咪唑
ACS reagent grade, ≥99% (titration)
别名:
1,3-二氮杂-2,4-环戊二烯, 甘恶啉
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关于此项目
经验公式（希尔记法）:
C3H4N2
化学文摘社编号:
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
产品名称
咪唑, 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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Application
特别适用于 pH 6.2-7.8 范围内的缓冲液
General description
咪唑是一种五元杂环化合物，存在于许多天然化合物中。它兼有酸性和碱性特性。据报道，它是血栓形成的抑制剂。其垂直谱和无辐射衰减已得到记录和分析。
Other Notes
Legal Information
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
存储类别
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
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)
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
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
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
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