Eugenol | Solubility of Things

Identification

Molecular formula

C₁₀H₁₂O₂

CAS number

97-53-0

IUPAC name

2-methoxy-4-vinyl-phenol

State

At room temperature, eugenol exists as a liquid. Its oily consistency and aromatic nature frequently identify it in a liquid state, rendering it useful in various industrial and medicinal applications.

Melting point (Celsius)

-9.00

Melting point (Kelvin)

264.15

Boiling point (Celsius)

254.50

Boiling point (Kelvin)

527.65

General information

Molecular weight

164.20g/mol

Molar mass

164.2010g/mol

Density

1.0829g/cm³

Appearence

Eugenol typically appears as a colorless to pale yellow aromatic oily liquid, often observed within clove oil, some nutmeg, cinnamon, and bay leaf products. Its distinct aroma is reminiscent of cloves and plays a vital role in its use in perfumery, flavorings, and essential oils.

Comment on solubility

Solubility of 2-methoxy-4-vinyl-phenol

The solubility of 2-methoxy-4-vinyl-phenol (C₁₀H₁₂O₂) is an important characteristic that influences its applications in various fields. This compound, being amphiphilic in nature due to the hydrophilic methoxy (-OCH₃) and hydroxyl (-OH) groups as well as the hydrophobic vinyl group, shows distinct solubility behaviors in different solvents.

Key Solubility Insights:

Solvent Compatibility: 2-methoxy-4-vinyl-phenol is generally soluble in organic solvents such as ethanol, methanol, and acetone due to its polar functional groups.
Water Solubility: While it can show limited solubility in water, the presence of the extensive hydrocarbon backbone somewhat hinders its complete dissolution.
Temperature Dependency: The solubility may increase with temperature, as higher temperatures typically improve the dissolution of organic compounds in solvents.
pH Influence: The solubility can also be pH-dependent; variations in pH can affect the ionization of the hydroxyl group, altering solubility in aqueous environments.

To summarize, 2-methoxy-4-vinyl-phenol exhibits a complex solubility profile influenced by its molecular structure, interaction with solvents, and environmental conditions, making it an interesting compound for further study.

Interesting facts

Exploring 2-Methoxy-4-vinyl-phenol

2-Methoxy-4-vinyl-phenol, often referred to as a versatile organic compound, belongs to the family of phenolic compounds. Its unique structure and functional groups endow it with several interesting characteristics:

Versatile Reactivity: The presence of both a methoxy group and a vinyl group makes this compound highly reactive and adaptable in various chemical reactions, including polymerization and substitution reactions.
Biological Significance: Some studies suggest that compounds resembling 2-methoxy-4-vinyl-phenol exhibit potential biological activities, including antimicrobial and antioxidant properties. This opens avenues for further research into its applications in pharmaceuticals.
Industrial Applications: Due to its chemical structure, this compound can be utilized in the formulation of coatings and adhesives, showcasing its play in improving product durability and performance.
Environmental Considerations: As with many organic compounds, understanding the environmental impact and degradation pathways of 2-methoxy-4-vinyl-phenol is crucial for sustainable chemistry practices.

Moreover, the intricate balance of its physical and chemical properties positions 2-methoxy-4-vinyl-phenol as a subject of interest for ongoing research, particularly in the fields of medicinal chemistry and materials science. Its potential for innovation in these areas is exciting for both scientists and industry professionals.

As we delve deeper into the world of organic compounds, quotes like "Every compound tells a story; it’s our job to listen" remind us of the vast knowledge waiting to be uncovered in the realm of chemistry.

Synonyms

2-Methoxy-4-vinylphenol

7786-61-0

4-vinylguaiacol

p-Vinylguaiacol

4-Hydroxy-3-methoxystyrene

4-ETHENYL-2-METHOXYPHENOL

Phenol, 4-ethenyl-2-methoxy-

o-methoxy-p-vinylphenol

para-vinylguaiacol

Guaiacol, 4-vinyl-

p-Vinyl guaiacol

4-vinyl-2-methoxyphenol

Phenol, 2-methoxy-4-vinyl-

4-Hydroxy-3-methoxyvinylbenzene

FEMA No. 2675

3-Methoxy-4-hydroxystyrene

Varamol 106

CCRIS 548

CHEBI:42438

2-METHOXY-4-VINYL-PHENOL

Vinylcatechol-O-methyl ether, P-

UNII-DA069CTH0O

EINECS 232-101-2

2M4VP

DA069CTH0O

Guaiacol, 4-vinyl

BRN 2044521

4-hydroxy-3-methoxyphenylethene

DTXSID7052529

2-(4-hydroxy-3-methoxyphenyl)ethene

2-Methoxy-4-ethenylphenol

Phenol, 2-methoxy-4-ethenyl

Phenol, 4-vinyl, 2-methoxy

CHEMBL1232595

DTXCID8031102

(4-Hydroxy-3-methoxyphenyl)ethene

3-06-00-04981 (Beilstein Handbook Reference)

4-vinyl guaiacol

EUG

Vinyl guaiacol

p-Vinyl guaicol

4-vinylguaiacole

4-Ethenylguaiacol

MFCD00015437

4-Vinyl-O-guaiacol

2-Methoxy-vinylphenol

31853-85-7

2-Metoxy-4-vinyl-phenol

bmse010071

4-ethenyl-2-methoxy-phenol

SCHEMBL54199

BCP27800

HY-W019940R

2-Methoxy-4-vinylphenol (Standard)

Tox21_304024

BDBM50548720

AKOS015890494

DB03514

FM35629

FS-3782

HY-W019940

2-methoxy-4-vinylphenol (vinylguaiacol)

2-METHOXY-4-VINYLPHENOL [FHFI]

2-Methoxy-4-vinylphenol, >=98%, FG

NCGC00357234-01

Vinylguaiacol (4-vinyl-2-methoxyphenol)

BP-11167

PD006849

CAS-7786-61-0

2-Methoxy-4-vinylphenol (4-vinylguaiacol)

4-Vinyl-2-methoxyphenol (4-vinylguaiacol)

DB-003488

2-Methoxy-4-vinylphenol, analytical standard

4-Vinyl-2-methoxyphenol ( p-vinylguaiacol)

CS-0031749

NS00005168

C17883

EN300-1832370

Q4596898

2-METHOXY-4-VINYLPHENOL (STABILIZED WITH TBC)

232-101-2

4M4