8.14223
Imidazole
for synthesis
Synonym(s):
Imidazole, Glyoxaline, Iminazole
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About This Item
grade
synthesis grade
Quality Level
vapor pressure
0.003 hPa ( 20 °C)
assay
≥99% (GC)
form
solid
autoignition temp.
480 °C
potency
970 mg/kg LD50, oral (Rat)
dilution
(for synthesis)
pH
10.5 (20 °C, 67 g/L in H2O)
bp
256 °C/1013 hPa
mp
90 °C
transition temp
flash point 145 °C
solubility
633 g/L
density
1.233 g/cm3 at 20 °C
bulk density
500‑600 kg/m3
storage temp.
2-30°C
SMILES string
[nH]1cncc1
InChI
1S/C3H4N2/c1-2-5-3-4-1/h1-3H,(H,4,5)
InChI key
RAXXELZNTBOGNW-UHFFFAOYSA-N
Application
- Integrated metabolomic and transcriptomic analysis reveals the regulatory mechanisms of flavonoid and alkaloid biosynthesis in the new and old leaves of Murraya tetramera Huang.: This study examines the biochemical pathways in Murraya tetramera, with a focus on the interaction between flavonoids and alkaloids, which may include imidazole-based compounds (Zhou et al., 2024).
- Unraveling the complex nexus: Interplay of volatile compounds, free amino acids, and metabolites in oat solid state fermentation.: Discusses the roles of various biochemicals, including potentially imidazole, in oat fermentation, providing insights into food science and biochemistry (Sun et al., 2024).
- Application of copper (I) selective ligands for PET imaging of reactive oxygen species through metabolic trapping.: This article explores the use of imidazole ligands in PET imaging, contributing to advanced techniques in medical imaging and diagnostics (Tada et al., 2024).
Analysis Note
Melting range (lower value): ≥ 88 °C
Melting range (upper value): ≤ 91 °C
Identity (IR): passes test
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 1B - Skin Corr. 1C
wgk
WGK 2
flash_point_f
293.0 °F - closed cup
flash_point_c
145 °C - closed cup
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
Certificates of Analysis (COA)
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