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2,6-Dimethoxyphenol

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Identification
Molecular formula
C8H10O3
CAS number
91-10-1
IUPAC name
2,6-dimethoxyphenol
State
State
At room temperature, 2,6-dimethoxyphenol is a solid compound that can sublimate. It is often handled as a solid at standard conditions.
Melting point (Celsius)
55.00
Melting point (Kelvin)
328.15
Boiling point (Celsius)
262.00
Boiling point (Kelvin)
535.15
General information
Molecular weight
154.17g/mol
Molar mass
154.1680g/mol
Density
1.1800g/cm3
Appearence

2,6-Dimethoxyphenol is typically seen as a pale yellow crystalline solid. It is also known for its characteristic aromatic odor, which is common to phenolic compounds.

Comment on solubility

Solubility of 2,6-Dimethoxyphenol

2,6-Dimethoxyphenol, a compound belonging to the family of phenols, exhibits interesting solubility characteristics influenced by its molecular structure. This compound can be contemplated in terms of two primary factors affecting solubility:

  • Polarity: The presence of the methoxy groups (-OCH3) attached to the aromatic ring contributes to the polarity of the molecule, which enhances its ability to dissolve in polar solvents.
  • Hydrogen Bonding: The hydroxyl group (-OH) allows 2,6-dimethoxyphenol to engage in hydrogen bonding, further increasing solubility in aqueous solutions.

In general, 2,6-dimethoxyphenol is more soluble in organic solvents such as ethanol and ether due to its hydrophobic aromatic region. However, while it shows moderate solubility in water, this represents a balance between its polar and non-polar characteristics. As a rule of thumb in chemistry, "like dissolves like," and understanding how this compound interacts with various solvents can elucidate why:

  • In water: solubility is limited due to its mostly non-polar characteristics.
  • In ethanol: solubility increases substantially, making it a good solvent for applications requiring this compound.
  • In non-polar solvents: such as hexane, solubility is generally low due to the lack of interaction with the polar functional groups.

Ultimately, the solubility of 2,6-dimethoxyphenol is a fascinating interplay of its phenolic structure and functional groups, marking it as a valuable compound in various chemical applications.

Interesting facts

Discovering 2,6-Dimethoxyphenol

2,6-Dimethoxyphenol is an intriguing compound that falls under the category of phenolic compounds, known for their distinctive properties and functionalities. Here are some fascinating aspects of this compound:

Chemical Structure

As the name suggests, 2,6-dimethoxyphenol features two methoxy groups (–OCH3) attached to the aromatic ring. This substitution enhances both the compound's reactivity and its solubility in organic solvents.

Applications

The significance of 2,6-dimethoxyphenol extends to various fields, including:

  • Pharmaceutical Industry: It serves as an important building block in the synthesis of pharmaceuticals and biologically active compounds.
  • Aromatic Chemicals: It is utilized in the production of fragrances and flavors, contributing to the sensory aspects of consumer products.
  • Antioxidant Properties: This compound exhibits antioxidative effects, making it a subject of interest in food chemistry and cosmetics.

Research Insights

Studies have revealed compelling information about the behavior of 2,6-dimethoxyphenol:

  • It shows high reactivity towards electrophiles due to the electron-donating property of the methoxy groups.
  • This compound can function as a reducing agent, which is particularly useful in organic synthesis.
  • Innovative research is exploring its potential as a natural antioxidant, which could lead to healthier alternatives in product formulations.

Quote to Ponder

Reflecting on its chemical profile, a researcher once stated, "The beauty of compounds like 2,6-dimethoxyphenol lies in their dual nature: simple in structure, yet complex in their reactivity and applications."

In conclusion, 2,6-dimethoxyphenol is more than just a chemical entity; it embodies the intersection of chemistry, industry, and nature's ingenuity. Its multifaceted applications make it a compelling subject for ongoing research and development!

Synonyms
2,6-DIMETHOXYPHENOL
91-10-1
Syringol
Pyrogallol 1,3-dimethyl ether
Phenol, 2,6-dimethoxy-
2-Hydroxy-1,3-dimethoxybenzene
1,3-Dimethyl pyrogallate
Aldrich
1,3-Dimethoxy-2-hydroxybenzene
2,6-dimethoxy phenol
2,6-dimethoxy-phenol
1,3-Di-o-methylpyrogallol
Pyrogallol dimethylether
2,6-Dwumetoksyfenol
FEMA No. 3137
2,6-Dimethoxyphenyl
MFCD00064434
2,6-Dwumetoksyfenol [Polish]
EINECS 202-041-1
UNII-4UQT464H8K
CHEBI:955
DTXSID2052607
2,6-Dimethoxyphenol(Chunk or Granule or Flakes)
4UQT464H8K
DTXCID0031180
2,6-DIMETHOXYPHENOL [FHFI]
2,6-DIMETHOXY PHENOL [FCC]
2,6-Dimethoxyphenol 99+%
33-51-2
1,3-Dimethoxy-2-hydroxybenzene; 2,6-Dimethoxyphenic acid; 2-Hydroxy-1,3-dimethoxybenzene; Pyrogallol 1,3-Dimethyl Ether; Syringol
2,6Dwumetoksyfenol
3DM
2,6-dimetoxyphenol
2,6-di-methoxyphenol
1,3DiOmethylpyrogallol
Phenol, 2,6dimethoxy
1,3Dimethyl pyrogallate
bmse010203
1,3Dimethoxy2hydroxybenzene
2Hydroxy1,3dimethoxybenzene
Pyrogallol 1,3dimethyl ether
2,6-Dimethoxyphenol, 99%
SCHEMBL156388
CHEMBL109652
2,6-Dimethoxyphenol (syringol)
2,6-Dimethoxyphenol (Standard)
FEMA 3137
HY-W003972R
Tox21_303953
BDBM50409535
2,6-Dimethoxyphenol, >=98%, FG
AKOS000120263
CS-W003972
FD34673
FS-1188
HY-W003972
2,6-Dimethoxyphenol, natural, >=96%
CAS-91-10-1
2,6-Dimethoxyphenol, analytical standard
NCGC00357187-01
BP-10363
SY018913
DB-003242
D0639
NS00010674
EN300-20299
F13351
Q421420
2,6-Dimethoxyphenol Pyrogallol 1,3-dimethyl ether
Z104477654
202-041-1
25511-61-9