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2,6-Dimethylphenol

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Identification
Molecular formula
C8H10O
CAS number
576-26-1
IUPAC name
2,6-dimethylphenol
State
State

At room temperature, 2,6-dimethylphenol is a solid. Its physical state contributes to its utility in a variety of chemical applications, including as a precursor in the synthesis of antioxidants, polymers, and other chemical intermediates.

Melting point (Celsius)
45.00
Melting point (Kelvin)
318.15
Boiling point (Celsius)
204.00
Boiling point (Kelvin)
477.15
General information
Molecular weight
122.16g/mol
Molar mass
122.1640g/mol
Density
0.9698g/cm3
Appearence

2,6-Dimethylphenol typically appears as a white crystalline solid. It can become yellowish upon exposure to air and light due to oxidation. It may also have a phenolic odor, which is characteristic of aromatic compounds containing a hydroxyl group.

Comment on solubility

Solubility of 2,6-Dimethylphenol

2,6-Dimethylphenol, a member of the phenolic compounds, exhibits a relatively low solubility in water due to its hydrophobic methyl groups. However, its solubility profile can be understood through a few key points:

  • Water Solubility: 2,6-Dimethylphenol is only slightly soluble in water, typically around 1.5 g/L at room temperature. This limited solubility can be attributed to the nonpolar characteristics of the methyl groups attached to the aromatic ring.
  • Solubility in Organic Solvents: In contrast, this compound displays good solubility in organic solvents such as ethanol, diethyl ether, and chloroform. This is significant for applications where organic solvents are used.
  • Impact of Temperature: The solubility of 2,6-dimethylphenol increases with temperature, as commonly observed in most substances. Heating the solution may enhance its ability to dissolve.
  • pH Dependence: The solubility can also be affected by the pH of the solution, though this compound does not ionize significantly under typical conditions.

In summary, while 2,6-dimethylphenol shows a preference for organic environments over aqueous solutions, understanding its solubility can help tailor its usage in various applications and experiments.

Interesting facts

Interesting Facts about 2,6-Dimethylphenol

2,6-Dimethylphenol is a fascinating aromatic compound that has captured the interest of chemists and industrialists alike due to its unique properties and applications. Here are some intriguing aspects of this compound:

  • Structural Characteristics: As a derivative of phenol, 2,6-dimethylphenol contains two methyl groups attached to the benzene ring in the 2 and 6 positions. This substitution pattern not only influences its chemical behavior but also its physical properties.
  • Uses in Industry: This compound is primarily used as an intermediate in the production of various chemical products. For example, it plays a crucial role in synthesizing antioxidants and surfactants, making it valuable in the manufacturing of plastics, resins, and coatings.
  • Biological Significance: Research indicates that 2,6-dimethylphenol exhibits antimicrobial properties, which could lead to its use in biocides and preservatives. This adds an additional layer of interest from a biochemical perspective.
  • Environmental Considerations: Like many organic compounds, the environmental impact of 2,6-dimethylphenol is an important consideration. It is essential to study its degradation products and potential effects on ecosystems, ensuring safe handling and usage.
  • Research Potential: Ongoing studies aim to explore the compound's behavior in various chemical reactions. Its reactivity can yield a wide range of derivatives useful in pharmaceuticals and agriculture.

In summary, 2,6-dimethylphenol is more than just a simple aromatic compound; it is a compound with significant industrial, biological, and environmental implications. The interplay of its chemical structure and reactivity not only highlights the beauty of chemistry but also opens doors to innovative applications.

Synonyms
2,6-DIMETHYLPHENOL
2,6-Xylenol
Phenol, 2,6-dimethyl-
2-Hydroxy-m-xylene
Vic-m-xylenol
2,6-Dmp
2,6-Dimethyl-phenol
Xylenol 235
Dimethylphenol, 2,6-
2-Hydroxy-1,3-dimethylbenzene
NSC 2123
HSDB 5697
UNII-I8N0RO87OV
EINECS 209-400-1
m-2-Xylenol
1,3-Dimethyl-2-hydroxybenzene
DTXSID9024063
AI3-08524
FEMA 3249
1,2,6-Xylenol
1,3,2-Xylenol
NSC-2123
2,6-Xylenol, 8CI
2,6-XYLENOL [FHFI]
DTXCID404063
1-Hydroxy-2, 6-dimethylbenzene
EC 209-400-1
XYLENOL 2,6-DIMETHYLPHENOL
2,6-DIMETHYLPHENOL [HSDB]
XYLENOL 2,6-DIMETHYLPHENOL [MI]
METACRESOL IMPURITY D [EP IMPURITY]
MEXILETINE HYDROCHLORIDE IMPURITY A [EP IMPURITY]
METACRESOL IMPURITY D (EP IMPURITY)
MEXILETINE HYDROCHLORIDE IMPURITY A (EP IMPURITY)
Vicmxylenol
2,6xylenol
Phenol, 2,6dimethyl
1Hydroxy2,6dimethylbenzene
2Hydroxy1,3dimethylbenzene
BENZENE,1,3-DIMETHYL,2-HYDROXY MFC8 H10 O1
209-400-1
2,6dmp
inchi=1/c8h10o/c1-6-4-3-5-7(2)8(6)9/h3-5,9h,1-2h
nxxykounuywiha-uhfffaoysa-n
un2261
576-26-1
2,6-Dimethyl phenol
1-Hydroxy-2,6-dimethylbenzene
FEMA No. 3249
MFCD00002240
I8N0RO87OV
CHEMBL30106
CAS-576-26-1
vic.-m-Xylenol
2MY
Mexiletine Hydrochloride Imp. A (EP); Mexiletine Imp. A (EP); 2,6-Dimethylphenol; Mexiletine Hydrochloride Impurity A; Mexiletine Impurity A
2.6-xylenol
2,6 Dimethylphenol
2,6-di-methylphenol
Phenol,2,6-dimethyl-
MEXILETINE_met014
SCHEMBL64141
2,6-Dimethylphenol, 99%
WLN: QR B1 F1
2,6-Xylenol, >=99%
26XY
NSC2123
3f37
3f38
CHEBI:180557
2,6-Dimethylphenol, >=99.5%
Tox21_201274
Tox21_300157
BBL011609
BDBM50240430
STL163336
AKOS000118743
2,6-Dimethylphenol, analytical standard
NCGC00091680-01
NCGC00091680-02
NCGC00091680-03
NCGC00254005-01
NCGC00258826-01
AC-10727
VS-02985
D0776
NS00004310
EN300-19433
2,6-Dimethylphenol 100 microg/mL in Methanol
A806014
A831530
AB-131/40171179
Q1055852
2,6-Dimethylphenol, PESTANAL(R), analytical standard
BENZENE,1,3-DIMETHYL,2-HYDROXY MFC8 H10 O1
F0001-1500
Z104473832