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Geranyl tiglate

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Identification
Molecular formula
C15H24O2
CAS number
1125-17-9
IUPAC name
3,7-dimethylocta-2,6-dienyl 2-methylbut-2-enoate
State
State

Geranyl tiglate is a liquid at room temperature.

Melting point (Celsius)
-12.00
Melting point (Kelvin)
261.15
Boiling point (Celsius)
124.00
Boiling point (Kelvin)
397.15
General information
Molecular weight
236.36g/mol
Molar mass
236.3580g/mol
Density
0.8860g/cm3
Appearence

Geranyl tiglate is typically a clear or pale yellow liquid with a pleasant floral odor. It is slightly oily in texture and may exhibit a slight viscous nature depending on temperature conditions.

Comment on solubility

Solubility of 3,7-Dimethylocta-2,6-dienyl 2-methylbut-2-enoate

The solubility of 3,7-dimethylocta-2,6-dienyl 2-methylbut-2-enoate is influenced by several factors, including its molecular structure and the presence of functional groups. This compound, often characterized by its hydrophobic nature, demonstrates interesting solubility properties:

  • Solvent Interactions: It tends to be more soluble in organic solvents such as hexane or ethyl acetate due to its non-polar characteristics.
  • Aqueous Solubility: The compound has limited solubility in water, which is common for many organic compounds with long hydrocarbon chains.
  • Temperature Effects: Increasing temperature can enhance solubility in organic solvents, as kinetic energy allows for better interaction with solvent molecules.

It's essential to note that the solubility can also be affected by:

  • Presence of impurities or other solutes in the solution.
  • The pH of the solution, which can alter the ionization of functional groups.

In summary, while 3,7-dimethylocta-2,6-dienyl 2-methylbut-2-enoate shows excellent solubility in non-polar solvents, its solubility in polar solvents like water is significantly hindered, emphasizing the compound's hydrophobic behavior.

Interesting facts

Interesting Facts about 3,7-dimethylocta-2,6-dienyl 2-methylbut-2-enoate

The compound known as 3,7-dimethylocta-2,6-dienyl 2-methylbut-2-enoate is a fascinating organic molecule that belongs to the family of esters. Esters are characterized by their unique properties and are essential in various applications, from flavorings to plastics. Below are some notable aspects of this compound:

  • Natural Sources: This compound is often found in essential oils and plant extracts, contributing to the aroma and flavor profiles of many natural products.
  • Synthetic Pathways: The synthesis of this compound can involve the reaction of an alcohol and a carboxylic acid, demonstrating key principles of organic chemistry such as nucleophilic attack and esterification.
  • Use in Scent and Flavor: Due to its pleasant scent, this compound may be used in perfumes and as a flavoring agent in food products.
  • Biological Activity: Some studies suggest that compounds similar to 3,7-dimethylocta-2,6-dienyl 2-methylbut-2-enoate may exhibit anti-inflammatory or antioxidant properties, making them of interest in pharmacology.
  • Structural Insights: The presence of multiple double bonds and a long carbon chain gives this molecule interesting geometric isomers that can impact how it interacts with biological systems.

Furthermore, the naming of this compound highlights the importance of IUPAC nomenclature in chemistry, which provides a systematic way to convey the structure of more complex molecules. As chemists explore and manipulate compounds like this one, understanding their structure and reactivity can lead to innovations in fields ranging from drug development to material science.

If you’re interested in organic chemistry, keep an eye on compounds like 3,7-dimethylocta-2,6-dienyl 2-methylbut-2-enoate, as they often serve as building blocks for even more complex synthetic molecules in research and industry!

Synonyms
DTXSID8069511
2-Butenoic acid, 2(or 3)-methyl-, (2E)-3,7-dimethyl-2,6-octadienyl ester
DTXCID8043151
Geranium extract
Geranyltiglate
61827-81-4
Geranium oil, Chinese
PD056736
Q67879903