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等級
ACS reagent
品質等級
蒸汽壓力
<1 mmHg ( 20 °C)
化驗
≥99% (titration)
雜質
≤0.2% water
燃燒殘留物
≤0.1%
pH值
9.5-11.0 (25 °C, 5% in H2O)
pKa (25 °C)
6.95
bp
256 °C (lit.)
mp
88-91 °C (lit.)
正離子痕跡
Fe: ≤0.001%
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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一般說明
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。
應用
特别适用于 pH 6.2-7.8 范围内的缓冲液
法律資訊
Redi-Dri is a trademark of Sigma-Aldrich Co. LLC
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
個人防護裝備
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
其他客户在看
UV excitation and radiationless deactivation of imidazole.
J. Chem. Phys., 130(3), 034305-034305 (2009)
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
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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
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
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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