Imidazole CAS#288-32-4

Versatile Heterocyclic Building Block: Imidazole is an important five-membered aromatic heterocyclic compound widely used as a key intermediate in pharmaceutical, agrochemical, and fine chemical synthesis.

Unique Amphoteric Properties: With both acidic and basic characteristics, imidazole readily forms salts with strong bases and exhibits versatile chemical reactivity in a variety of synthesis processes.

Excellent Catalytic Performance: The imidazole ring combines the chemical features of pyridine and pyrrole, making it an effective catalytic and acyl-transfer structural unit in numerous chemical and biochemical reactions.

Biologically Significant Structure: Imidazole derivatives are widely found in biological systems, including important biomolecules such as histidine, DNA-related compounds, and hemoglobin, highlighting their broad scientific and industrial value.

Products Description of Imidazole CAS#288-32-4

Imidazole (molecular formula: C₃H₄N₂) is an organic compound belonging to the diazole family. It is a five-membered aromatic heterocyclic compound containing two non-adjacent nitrogen atoms within its ring structure. The lone pair of electrons on the nitrogen atom at the 1-position participates in cyclic conjugation, reducing the electron density of the nitrogen atom and allowing the hydrogen attached to it to be readily released as a proton.

Imidazole exhibits both acidic and basic properties and is capable of forming salts with strong bases. Its chemical behavior combines characteristics of both pyridine and pyrrole. In biological systems, the imidazole ring is an essential structural component of histidine, where it functions as an acyl-transfer group involved in lipid hydrolysis and plays an important catalytic role in enzymatic reactions. Imidazole derivatives are widely distributed in living organisms and are of greater significance than imidazole itself in scientific research and industrial applications, with important examples including DNA- and hemoglobin-related compounds.

1783994297715248.jpg.webp

Imidazole Chemical Properties

Melting point 

88-91 °C(lit.)

Boiling point 

256 °C(lit.)

density 

1.01 g/mL at 20 °C

vapor pressure 

<1 mm Hg ( 20 °C)

refractive index 

1.4801

Fp 

293 °F

storage temp. 

Store below +30°C.

solubility 

H2O: 0.1 M at 20 °C, clear, colorless

pka

6.953(at 25℃)

form 

crystalline

color 

white

Specific Gravity

1.03

Odor

Amine like

PH Range

9.5 - 11

PH

9.5-11.0 (25℃, 50mg/mL in H2O)

Water Solubility 

633 g/L (20 ºC)

Sensitive 

Hygroscopic

λmax

λ: 260 nm Amax: 0.10

λ: 280 nm Amax: 0.10

Merck 

144912

BRN 

103853

Dielectric constant

23.0(Ambient)

Stability:

Stable. Incompatible with acids, strong oxidizing agents. Protect from moisture.

InChIKey

RAXXELZNTBOGNW-UHFFFAOYSA-N

LogP

-0.02 at 25℃

CAS DataBase Reference

288-32-4(CAS DataBase Reference)

NIST Chemistry Reference

1H-Imidazole(288-32-4)

EPA Substance Registry System

Imidazole (288-32-4)

Hazard Codes 

C,Xi,T

Risk Statements 

36/38-63-34-22-20/21/22-61

Safety Statements 

26-36/37/39-45-22-36-27-53

RIDADR 

UN 2923 8/PG 3

WGK Germany 

1

RTECS 

NI3325000

Autoignition Temperature

480 °C

TSCA 

Yes

HazardClass 

8

PackingGroup 

III

HS Code 

29332990

Hazardous Substances Data

288-32-4(Hazardous Substances Data)

Toxicity

LD50 in mice (mg/kg): 610 i.p.; 1880 orally (Nishie)

1783994305533113.jpg.webp

Product Application of Imidazole CAS#288-32-4

Imidazole is slightly more basic than pyrazole and readily forms stable salts, including picrates and nitrates. One of its important applications is in the purification of His-tagged proteins using immobilized metal affinity chromatography (IMAC).

During the purification process, His-tagged proteins selectively bind to nickel ions immobilized on the chromatography resin. An imidazole-containing elution buffer is then used to compete with the His tag for nickel binding, allowing the target protein to be released from the column and collected with high purity.

1783994317103105.jpg.webp

Online Consultation

Please fill out the form below and we will contact you as soon as possible