1-Octylbenzimidazole, >98%
Price range: $230.65 through $3,558.56
Product Code: KI-0045-HPCAS NO: 42032-46-2
- Chemical Formula: C15H22N2
- Synonyms: N-Octylbenzimidazole
*This product will incur a $97.00 HazMat fee when the order is placed.*
SUM Formula: C15H22N2
Molecular Weight: 230.35
Purity: >98%
- SUM Formula: C15H22N2
- Molecular Weight: 230.35
1-Octylbenzimidazole, CAS: 42032-46-2
Key Applications:
Electrochemical and Energy Systems
- Serves as a precursor or coโligand in the synthesis of ionic liquids and moltenโsalt electrolytes designed for highโtemperature or nonโaqueous electrochemical environments.
- Functions as an additive in battery and capacitor electrolytes where benzimidazole motifs improve film formation, ionic mobility, and oxidative stability.
- Supports corrosionโinhibitor formulations for metals by adsorbing onto surfaces through the benzimidazole ring while the octyl chain enhances hydrophobic barrier formation.
Coordination Chemistry and Catalysis
- Acts as a neutral or weakly basic ligand for transitionโmetal complexes used in homogeneous catalysis, photochemical systems, and organometallic synthesis.
- Enables the design of amphiphilic catalytic assemblies due to its hydrophobic tail, improving solubility in organic media and facilitating phaseโtransfer processes.
Materials Science and Surface Engineering
- Used in the preparation of functional coatings, selfโassembled monolayers, and surfaceโmodification agents where the benzimidazole headgroup anchors to metal or oxide surfaces.
- Contributes to the fabrication of hydrophobic or amphiphilic polymer systems, including specialty resins and compatibilizers.
- Incorporated into advanced lubricants and antiโwear additives where nitrogenโrich heterocycles enhance metal affinity and boundaryโfilm formation.
Organic Synthesis and Specialty Chemical Development
- Serves as a building block for synthesizing benzimidazoleโbased surfactants, corrosion inhibitors, and specialty intermediates.
- Useful in structureโproperty tuning studies where alkylโchain length influences solubility, reactivity, and interfacial behavior.
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