1,3-Di-tert-butylimidazolium Hydrogencarbonate is a chemical compound widely used in catalytic reactions and organic synthesis. It serves as an effective catalyst or ligand in various chemical processes due to its unique ionic structure. This compound is particularly useful in reactions involving electron or hydrogen transfer, especially in redox processes. Its role in the laboratory is to accelerate chemical reactions and reduce the activation energy required for these reactions to proceed efficiently.
The compound's stability under specific conditions and its ability to act as an ionic conductor in solution make it a preferred choice for many applications. Its complex molecular structure allows it to bind with various metal ions, making it highly suitable for heterogeneous catalysis and reactions requiring ion interactions. This versatility enhances its utility in both research and industrial settings, where precise control over reaction conditions is essential.
In Indonesian laboratories, this compound is commonly used in organic chemistry, catalysis, and the synthesis of complex compounds. It is a key component in experimental setups that require efficient catalytic activity and stability. Many research institutions and universities in Indonesia rely on this compound for experiments involving redox reactions and ion-based chemical transformations. Its reliability and effectiveness make it a valuable tool for scientific inquiry.
Advantages (TCI brochure)
- NHC ligands and catalysts are preparable by heating.
- No salt generated during preparation.
- Applicable under neutral conditions.
- NHC hydrogencarbonate salts release H2O and CO2.
TCI brochures (PDF)
- Easily-preparable N-Heterocyclic Carbene (NHC) Precursors 2021-09-14 · p. 1
- N-Heterocyclic Carbene (NHC) Ligands and Metal Complexes 2026-02-10 · p. 1
- Ligands 2025-12-01 · p. 8
- Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 26
Related TCI products
- TCI D5498 1372124-90-7 1,3-Diisopropylimidazolium Hydrogencarbonate (contains varying amounts of 1,3-Diisopropylimidazolium-2-carboxylate)
- TCI D3711 263163-17-3 1,3-Di-tert-butylimidazolium Tetrafluoroborate
- TCI D5401 675877-56-2 1,3-Dimesitylimidazolium-2-carboxylate
- TCI D5396 536755-29-0 1,3-Dimethylimidazolium-2-carboxylate
- TCI B5603 917604-39-8 1,3-Bis(2,6-diisopropylphenyl)imidazolium-2-carboxylate
- TCI D3472 157197-53-0 1,3-Di-tert-butylimidazol-2-ylidene
- Organic synthesis reactions benefit from this compound's ability to facilitate electron and hydrogen transfer, enhancing reaction efficiency in complex molecule formation.
- Redox reactions often utilize this material due to its capacity to act as a catalyst or ligand, promoting electron transfer processes in oxidation and reduction pathways.
- Heterogeneous catalysis applications take advantage of its metal ion binding properties, enabling effective interaction with various catalysts in industrial and academic settings.
- Ion conduction in solution is supported by its ionic structure, making it suitable for electrochemical experiments requiring stable ionic transport.
- Metal complex formation is enhanced by its ability to coordinate with different metal ions, supporting the development of new catalytic systems and coordination compounds.
From the TCI brochure
- Transition metal/NHC complex catalyst preparation
| Brand | TCI |
|---|---|
| CAS number | 2893755-25-2 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Catalysis and Inorganic Chemistry > Carbon-Donor Ligands [Catalysis] |
| Pack sizes | 25 g |
| Physical form | Powder |
| Storage | Store in a cool, dry place away from moisture and direct sunlight |
This compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and humidity, which can affect its chemical properties. Due to its ionic nature, it is important to handle it with care to avoid contamination. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when working with this material. It should be kept away from incompatible substances to ensure safe storage and handling. Proper labeling of storage containers is essential for safe access and use in the laboratory setting.
References cited in the TCI brochure
- Maréva Fèvre. Imidazol(in)ium Hydrogen Carbonates as a Genuine Source of N-Heterocyclic Carbenes (NHCs): Applications to the Facile Preparation of NHC Metal Complexes and to NHC-Organocatalyzed Molecular and Macromolecular Syntheses Journal of the American Chemical Society, 2012. doi:10.1021/ja3005804
Product Categories
- Catalysis and Inorganic ChemistryCarbon-Donor Ligands [Catalysis]N-Heterocyclic Carbene (NHC)-CO2 Adducts and NHC-HCO3 Salts [Carbon-Donor Ligands]
- Catalysis and Inorganic ChemistryCross-coupling Reaction using Transition Metal Catalysts [C-C Bond Formation]N-Heterocyclic Carbene (NHC) Ligands [Cross-coupling Reaction using Transition Metal Catalysts]
- Synthetic ReagentsC-C Bond Formation [Synthetic Reagents]Cross-coupling Reaction using Transition Metal Catalysts [C-C Bond Formation]








