Octane-2,3-dione
97%
- Product Code: 82292
CAS:
585-25-1
| Molecular Weight: | 142.20 g./mol | Molecular Formula: | C₈H₁₄O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06796191 | |
| Melting Point: | Boiling Point: | 173 °C at 760 mmHg | |
| Density: | 0.9311 g/cm3 | Storage Condition: | room temperature, dark, inert gas |
Product Description:
Octane-2,3-dione is primarily used in the flavor and fragrance industry due to its unique aroma characteristics. It is often employed as a flavoring agent to impart buttery or creamy notes in food products such as baked goods, dairy items, and confectionery. Additionally, it serves as a key intermediate in the synthesis of more complex organic compounds, particularly in the production of pharmaceuticals and agrochemicals. Its role in organic synthesis also extends to the development of specialty chemicals and fine chemicals, where it acts as a building block for various reactions. In research, octane-2,3-dione is utilized in studies related to organic chemistry and material science, particularly in the investigation of reaction mechanisms and the development of new synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,593.00 |
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Octane-2,3-dione
Octane-2,3-dione is primarily used in the flavor and fragrance industry due to its unique aroma characteristics. It is often employed as a flavoring agent to impart buttery or creamy notes in food products such as baked goods, dairy items, and confectionery. Additionally, it serves as a key intermediate in the synthesis of more complex organic compounds, particularly in the production of pharmaceuticals and agrochemicals. Its role in organic synthesis also extends to the development of specialty chemicals and fine chemicals, where it acts as a building block for various reactions. In research, octane-2,3-dione is utilized in studies related to organic chemistry and material science, particularly in the investigation of reaction mechanisms and the development of new synthetic pathways.
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