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Linalyl acetate

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Identification
Molecular formula
C12H20O2
CAS number
115-95-7
IUPAC name
1,1-dimethoxy-3,7-dimethyl-octa-2,6-diene
State
State

Linalyl acetate is a liquid at room temperature, commonly used in the fragrance and perfume industry.

Melting point (Celsius)
-4.00
Melting point (Kelvin)
269.15
Boiling point (Celsius)
220.00
Boiling point (Kelvin)
493.15
General information
Molecular weight
196.30g/mol
Molar mass
196.2900g/mol
Density
0.9015g/cm3
Appearence

Linalyl acetate is a colorless liquid with a pleasant, floral odor that is reminiscent of bergamot and lavender.

Comment on solubility

Solubility of 1,1-Dimethoxy-3,7-dimethyl-octa-2,6-diene

The solubility of 1,1-dimethoxy-3,7-dimethyl-octa-2,6-diene can be quite intriguing due to its unique structure and functional groups. Here are some important considerations regarding its solubility:

  • Polar vs Nonpolar Solubility: This compound contains both methoxy groups (–OCH3) and a hydrocarbon backbone. This duality can lead to interesting solubility characteristics.
  • In Organic Solvents: It is likely to be soluble in organic solvents such as ether or acetone due to its nonpolar hydrocarbon segments.
  • Water Solubility: The methoxy groups can introduce some polarity; however, the overall hydrophobic nature of the diene might limit its solubility in water.
  • Temperature Effects: Solubility often increases with temperature, making it useful in applications where temperature variations are expected.

In summary, while 1,1-dimethoxy-3,7-dimethyl-octa-2,6-diene exhibits favorable solubility in nonpolar organic solvents, its water solubility remains limited, illustrating the classic "like dissolves like" principle in chemistry. Understanding these solubility dynamics is crucial for various applications, including synthesis and formulation processes.

Interesting facts

Exploring 1,1-Dimethoxy-3,7-dimethyl-octa-2,6-diene

1,1-Dimethoxy-3,7-dimethyl-octa-2,6-diene is a fascinating compound found in organic chemistry, particularly noteworthy for its unique structure and applications. Here are some captivating aspects:

  • Structural Diversity: The compound is classified as a diene, which means it contains two double bonds. This structural feature contributes to its reactivity and makes it an interesting subject of study for chemists interested in synthetic organic reactions.
  • Application in Synthesis: It's often utilized as a building block in the synthesis of more complex organic molecules, especially within the realm of pharmaceuticals. Due to its multifunctional groups, it opens the door to various transformations that could lead to valuable derivatives.
  • Natural Occurrence: Interestingly, compounds with similar structures can be found in nature, often contributing to flavors and aromas in plants. This raises questions about the biosynthetic pathways that lead to the formation of such compounds in living organisms.
  • Potential Benefits: Research into this compound may uncover beneficial properties, such as antioxidant or antimicrobial effects, which could be significant in developing new drugs or functional foods.

As with many organic compounds, future studies could focus on environmental impacts and sustainability, considering how we can utilize compounds like 1,1-dimethoxy-3,7-dimethyl-octa-2,6-diene in a way that is beneficial to both humans and the planet.

In summary, the exploration of 1,1-dimethoxy-3,7-dimethyl-octa-2,6-diene not only enriches the field of organic chemistry but also sparks curiosity about its potential applications and natural significance.

Synonyms
2,6-Octadiene, 1,1-dimethoxy-3,7-dimethyl-
CHEMBL3181878
DB-230123
NS00012104
NS00082439