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Ethyl vanillate

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Identification
Molecular formula
C10H12O5
CAS number
121-32-4
IUPAC name
ethyl 4-hydroxy-3,5-dimethoxy-benzoate
State
State
Ethyl vanillate is typically found in a solid crystalline form at room temperature, bearing its characteristic sweet vanilla scent.
Melting point (Celsius)
40.00
Melting point (Kelvin)
313.15
Boiling point (Celsius)
306.00
Boiling point (Kelvin)
579.15
General information
Molecular weight
196.19g/mol
Molar mass
196.1920g/mol
Density
1.2043g/cm3
Appearence

Ethyl vanillate appears as a solid, often in the form of colorless to off-white crystals. The compound is known for its vanilla-like aroma which makes it not only an object of chemical studies but also interesting in flavor and fragrance applications.

Comment on solubility

Solubility of Ethyl 4-Hydroxy-3,5-Dimethoxy-Benzoate

Ethyl 4-hydroxy-3,5-dimethoxy-benzoate, with its intriguing structure, exhibits unique solubility characteristics that are worth noting. Its solubility can be influenced by several factors:

  • Polarity: This compound contains both hydrophobic (the ethyl and methoxy groups) and hydrophilic (the hydroxy group) components, which can lead to interesting solubility behaviors.
  • Solvent Interactions: Ethyl 4-hydroxy-3,5-dimethoxy-benzoate is generally soluble in organic solvents such as ethanol, acetone, and chloroform, but may show limited solubility in water due to the predominance of hydrophobic groups.
  • Temperature Effects: Like many organic compounds, solubility may increase with temperature, making it more favorable to dissolve in warmer solutions.

In summary, the solubility of ethyl 4-hydroxy-3,5-dimethoxy-benzoate is largely influenced by its structural characteristics and the nature of the solvent. Understanding these factors can aid in the effective use of this compound in various chemical applications.

Interesting facts

Interesting Facts about Ethyl 4-Hydroxy-3,5-Dimethoxy-Benzoate

Ethyl 4-hydroxy-3,5-dimethoxy-benzoate, often referred to in chemical terms as ethyl vanillate, is a fascinating compound that belongs to the class of benzoate esters. This compound is largely appreciated in the fields of chemistry and food science due to its diverse applications and delightful properties.

Key Applications:

  • Flavoring Agent: Ethyl vanillate is frequently utilized in the food industry as a natural flavoring agent, imparting a sweet and creamy vanilla taste to various products.
  • Fragrance Component: In perfumery, this compound plays a crucial role as it provides a warm and rich scent profile, often used in products like lotions, soaps, and perfumes.
  • Medicinal Uses: Research has indicated potential health benefits, as compounds similar to ethyl vanillate exhibit antioxidant and anti-inflammatory properties.

Chemical Significance:

As a derivative of vanillin, ethyl 4-hydroxy-3,5-dimethoxy-benzoate shares similarities in its chemical structure, which contributes to its unique sensory characteristics. Its structure includes:

  • A hydroxy group, which is crucial for its solubility and interaction with other compounds.
  • Two methoxy groups that enhance its overall stability and flavor profile.

Quote to Reflect: "The beauty of chemistry lies not only in the compounds themselves but also in their transformations and various applications." Through the exploration of such compounds, we understand the interconnectedness of nature, chemistry, and our daily lives.

Conclusion:

Overall, ethyl 4-hydroxy-3,5-dimethoxy-benzoate exemplifies the synergy between chemistry and sensory experiences. Whether in culinary arts or perfumery, it showcases how thoughtful chemical composition can lead to extraordinary outcomes, enhancing our tastes and experiences.

Synonyms
ethyl 4-hydroxy-3,5-dimethoxybenzoate
3943-80-4
ethyl 4-hydroxy-3,5-dimethoxy-benzoate
BENZOIC ACID, 3,5-DIMETHOXY-4-HYDROXY-, ETHYL ESTER
Ethyl syringate
3,5-Dimethoxy-4-hydroxybenzoic acid ethyl ester
Ethyl4-hydroxy-3,5-dimethoxybenzoate
BRN 2113673
Ester etylowy kwasu syringowego [Polish]
Ester etylowy kwasu syringowego
Ethyl syringoate
Benzoic acid, 4-hydroxy-3,5-dimethoxy-, ethyl ester
ethyl 3,5-dimethoxy-4-hydroxybenzoate
syringic acid ethyl ester
SCHEMBL582920
DTXSID40192599
DAA94380
AKOS016003287
DB-069813
E79234