1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride

Catalog Number	ACM250285326
CAS	250285-32-6
Structure
Description	1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride, also known as BIPI, is an organic compound that has found a variety of applications in the scientific research field. BIPI is a quaternary ammonium salt, which is composed of two isopropylphenyl groups and an imidazolium ring. As a result of its unique structure, BIPI has a variety of properties that make it an attractive choice for a wide range of scientific research applications. This paper will discuss the synthesis method, scientific research applications, mechanism of action, biochemical and physiological effects, advantages and limitations for lab experiments, and potential future directions for BIPI research.
Synonyms	1,3-BIS(2,6-DI-I-PROPYLPHENYL)IMIDAZOLIUM CHLORIDE; 1,3-BIS(2,6-DIISOPROPYLPHENYL)IMIDAZOLIUM CHLORIDE; 1,3-BIS(2,6-DIISOPROPYLPHENYL)IMIDAZOLI&; 1,3-Bis(2,6-di-i-propylphenyl)imidazoliumchloride,min.95%; 1,3-BIS(2,6-DI-I-PROPYLPHENYL) IMIDAZOLIUM CHLORI
IUPAC Name	1,3-bis[2,6-di(propan-2-yl)phenyl]imidazol-1-ium;chloride
Molecular Weight	425 g/mol
Molecular Formula	C27H37ClN2
Canonical SMILES	CC(C)C1=C(C(=CC=C1)C(C)C)N2C=C[N+](=C2)C3=C(C=CC=C3C(C)C)C(C)C.[Cl-]
InChI	InChI=1S/C27H37N2.ClH/c1-18(2)22-11-9-12-23(19(3)4)26(22)28-15-16-29(17-28)27-24(20(5)6)13-10-14-25(27)21(7)8;/h9-21H,1-8H3;1H/q+1;/p-1
InChI Key	AVJBQMXODCVJCJ-UHFFFAOYSA-M
Melting Point	278 °C(dec.)(lit.)
Purity	98%+
Appearance	Solid
Application	1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride has found a variety of applications in the scientific research field. It has been used as a catalyst in a variety of organic reactions, including the synthesis of heterocyclic compounds and the preparation of polymers. 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride has also been used as a stabilizer in the synthesis of polymers and as a surfactant in the preparation of emulsions. Additionally, 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride has been used as an ionic liquid in the extraction of organic compounds from aqueous solutions.
Complexity	421
Covalently-Bonded Unit Count	2
Exact Mass	424.265g/mol
GHS Pictogram	Corrosive; Acute Toxic; Irritant; Environmental Hazard
Heavy Atom Count	30
Isomeric SMILES	CC(C)C1=C(C(=CC=C1)C(C)C)N2C=C[N+](=C2)C3=C(C=CC=C3C(C)C)C(C)C.[Cl-]
Monoisotopic Mass	424.265g/mol
Properties	1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride has been studied for its potential biochemical and physiological effects. Studies have shown that 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride can act as an antioxidant and can reduce the toxicity of certain compounds. Additionally, 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride has been shown to have anti-inflammatory, anti-microbial, and anti-cancer properties. Furthermore, 1,3-Bis(2,6-diisopropylphenyl)imidazolium chloride has been studied for its potential ability to reduce cholesterol levels and to improve cardiovascular health.
Rotatable Bond Count	6
Topological Polar Surface Area	8.8A^2