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| Synonyms | Dicobalt hexacarbonyl t-butylacetylene, 99%;(3,3-Dimethyl-1-butyne)dicobalthexacarbonyl,98%;(3,3-DIMETHYL-1-BUTYNE)DICOBALT HEXACARBONYL;(3,3-Dimethyl-1-butyne)dicobalt hexacarbonyl, 98% CCTBA |
| Appearance | Dark red liquid |
| Molecular Weight | 368.07 |
| Boiling Point | 52°C / 0.8 |
| Sensitivity | Air sensitive |
| Purity | ≧ 98% |
| Package Information | 100g, 500g, 1kg, or customized |
(3,3-dimethyl-1-butyne) dicobalt hexacarbonyl has high purity (≥98%), maintains excellent chemical stability under sealed conditions, and exhibits strong reaction selectivity.
As a transition metal catalyst or catalytic precursor, CCTBA exhibits excellent catalytic activity in olefin hydroformylation, carbonylation, and hydrogenation reactions.
This compound allows for easy adjustment of reaction temperature and solvent system, making it suitable for both research and industrial-scale processes requiring high yield and selectivity.
CCTBA is compatible with a wide variety of ligands and substrates, making it suitable for organometallic chemistry studies in diverse systems.
CCTBA is commonly used as a key catalyst in carbonylation and hydroformylation reactions, significantly increasing reaction rates and product yields.
(3,3-dimethyl-1-butyne) dicobalt hexacarbonyl can be used as a structural template or intermediate in organometallic synthesis and the preparation of transition metal complexes.
In materials chemistry and novel coordination polymer research, CCTBA, due to its unique coordination properties, has been used to design novel metal-organic framework (MOF) precursors.
CCTBA is easily decomposed by reaction with oxygen and should be stored in a sealed dry container.
When using, wear chemical-resistant gloves and goggles to avoid direct skin contact.
Mixing with strong acids or oxidants may cause exothermic reactions or decomposition, so avoid coexistence with acids and oxidants.
1. How do you control the purity of CCTBA?
We use a multi-stage refining process under inert atmosphere to ensure product purity of ≥98%. We also provide a complete COA report.
2. What types of catalytic reactions are suitable for CCTBA?
It is primarily used in transition metal catalytic systems such as carbonylation, hydrogenation, and coupling reactions, and is particularly well-suited for organic synthesis and coordination chemistry research.
Wolfa professionally supplies CCTBA, supporting small-batch sampling and large-volume procurement needs. Packaging options include ordinary glass bottles, glass ampoules, metal ampoules, etc.
For product analysis reports (such as COA) or procurement consulting, please feel free to contact us at jomin@wolfabio.com at any time.
| Synonyms | Dicobalt hexacarbonyl t-butylacetylene, 99%;(3,3-Dimethyl-1-butyne)dicobalthexacarbonyl,98%;(3,3-DIMETHYL-1-BUTYNE)DICOBALT HEXACARBONYL;(3,3-Dimethyl-1-butyne)dicobalt hexacarbonyl, 98% CCTBA |
| Appearance | Dark red liquid |
| Molecular Weight | 368.07 |
| Boiling Point | 52°C / 0.8 |
| Sensitivity | Air sensitive |
| Purity | ≧ 98% |
| Package Information | 100g, 500g, 1kg, or customized |
(3,3-dimethyl-1-butyne) dicobalt hexacarbonyl has high purity (≥98%), maintains excellent chemical stability under sealed conditions, and exhibits strong reaction selectivity.
As a transition metal catalyst or catalytic precursor, CCTBA exhibits excellent catalytic activity in olefin hydroformylation, carbonylation, and hydrogenation reactions.
This compound allows for easy adjustment of reaction temperature and solvent system, making it suitable for both research and industrial-scale processes requiring high yield and selectivity.
CCTBA is compatible with a wide variety of ligands and substrates, making it suitable for organometallic chemistry studies in diverse systems.
CCTBA is commonly used as a key catalyst in carbonylation and hydroformylation reactions, significantly increasing reaction rates and product yields.
(3,3-dimethyl-1-butyne) dicobalt hexacarbonyl can be used as a structural template or intermediate in organometallic synthesis and the preparation of transition metal complexes.
In materials chemistry and novel coordination polymer research, CCTBA, due to its unique coordination properties, has been used to design novel metal-organic framework (MOF) precursors.
CCTBA is easily decomposed by reaction with oxygen and should be stored in a sealed dry container.
When using, wear chemical-resistant gloves and goggles to avoid direct skin contact.
Mixing with strong acids or oxidants may cause exothermic reactions or decomposition, so avoid coexistence with acids and oxidants.
1. How do you control the purity of CCTBA?
We use a multi-stage refining process under inert atmosphere to ensure product purity of ≥98%. We also provide a complete COA report.
2. What types of catalytic reactions are suitable for CCTBA?
It is primarily used in transition metal catalytic systems such as carbonylation, hydrogenation, and coupling reactions, and is particularly well-suited for organic synthesis and coordination chemistry research.
Wolfa professionally supplies CCTBA, supporting small-batch sampling and large-volume procurement needs. Packaging options include ordinary glass bottles, glass ampoules, metal ampoules, etc.
For product analysis reports (such as COA) or procurement consulting, please feel free to contact us at jomin@wolfabio.com at any time.
