Tyrosol | Solubility of Things

Identification

Molecular formula

C₈H₁₀O₂

CAS number

501-94-0

IUPAC name

4-(2-hydroxyethyl)phenol

State

At room temperature, Tyrosol is in a solid state. It forms stable crystals and is commonly found in both natural and laboratory settings in this physical form.

Melting point (Celsius)

91.00

Melting point (Kelvin)

364.15

Boiling point (Celsius)

154.00

Boiling point (Kelvin)

427.15

General information

Molecular weight

138.16g/mol

Molar mass

138.1640g/mol

Density

1.1214g/cm³

Appearence

Tyrosol is a colorless crystalline solid. It often appears as white crystals or powder and can have a faint phenolic odor. The compound is known for its solubility in water, alcohol, and ether.

Comment on solubility

Solubility of 4-(2-hydroxyethyl)phenol

4-(2-hydroxyethyl)phenol, a compound with the formula C₁₀H₁₄O₂, exhibits notable solubility characteristics that are worth discussing.

Solubility Properties

This compound is primarily soluble in:

Water: Due to the presence of the hydroxyl (-OH) group, 4-(2-hydroxyethyl)phenol can interact favorably with water molecules, leading to increased solubility.
Alcohols: Its hydrophilic nature also allows it to dissolve effectively in various alcohols, enhancing its applicability in organic synthesis.
Organic solvents: The presence of the aromatic ring further supports solubility in common organic solvents like acetone and ether.

Key Considerations

However, it is essential to note that while 4-(2-hydroxyethyl)phenol is soluble in these media, solubility can vary based on:

Temperature: Higher temperatures may increase its solubility rates.
Concentration: At specific concentrations, solubility might reach saturation, limiting potential applications.
pH Levels: The solubility can also be influenced by the pH of the solution, as acidic or basic conditions might alter the ionization of the compound.

In summary, the solubility of 4-(2-hydroxyethyl)phenol is significantly affected by its structural attributes, making it a versatile chemical in various applications, especially in environments rich in polar solvents.

Interesting facts

Interesting Facts about 4-(2-hydroxyethyl)phenol

4-(2-hydroxyethyl)phenol, often recognized for its vital role in various applications, is a fascinating compound that showcases the intersection of chemistry and practical utility. Here are some intriguing aspects of this compound:

Antioxidant Properties: This compound is known for its potent antioxidant activity. It is often utilized in formulations to protect against oxidative stress, making it essential in various cosmetic products.
Industrial Applications: 4-(2-hydroxyethyl)phenol plays a critical role in the production of phenolic resins, which are widely employed in the construction and automotive industries due to their strength and durability.
Biological Relevance: As a phenolic compound, it’s important in research related to microbial activity and potential health benefits. Studies have indicated that compounds like 4-(2-hydroxyethyl)phenol may exhibit antibacterial properties.
Versatility: This compound can be synthesized in various ways, allowing chemists to explore different reaction conditions and pathways, illustrating the flexibility within organic synthesis.
Regulatory Insight: While 4-(2-hydroxyethyl)phenol is generally recognized as safe in specific applications, it’s crucial to consider regulatory guidelines when introducing new products to the market.

The compound is truly a testament to the diverse capabilities of phenolic derivatives. As you delve deeper into its chemistry, you’ll appreciate the complexities and potential innovations it offers across different fields of science.

Synonyms

Tyrosol

2-(4-Hydroxyphenyl)ethanol

501-94-0

4-(2-Hydroxyethyl)phenol

4-Hydroxyphenylethanol

4-Hydroxybenzeneethanol

p-Hydroxyphenethyl alcohol

p-Tyrosol

Tyrosol C

NSC 59876

UNII-1AK4MU3SNX

1AK4MU3SNX

EINECS 207-930-8

beta-(4-Hydroxyphenyl)ethanol

CHEBI:1879

NSC-59876

DTXSID8060111

HYDROXYPHENETHYL ALCOHOL, P-

n-tyrosol

para-hydroxyphenylethanol

METOPROLOL TARTRATE IMPURITY G (EP IMPURITY)

METOPROLOL TARTRATE IMPURITY G [EP IMPURITY]

METOPROLOL SUCCINATE IMPURITY G (EP IMPURITY)

METOPROLOL SUCCINATE IMPURITY G [EP IMPURITY]

DTXCID7040780

TYROSOL (CONSTITUENT OF RHODIOLA ROSEA)

207-930-8

4-Hydroxyphenethyl alcohol

Benzeneethanol, 4-hydroxy-

4-Hydroxyphenylethyl alcohol

MFCD00002902

2-(4-Hydroxyphenyl)ethyl Alcohol

p-Thyrosol

p-HPEA

2-(P-HYDROXYPHENYL)ETHANOL

Metoprolol IMpurity 07

4-hydroxy-Benzeneethanol

p-Hydroxyphenylethyl alcohol

4-(2-Hydroxy-ethyl)-phenol

CHEMBL53566

p-hydroxyphenylethanol

SMR000857159

4-hydroxyphenethylalcohol

4-tyrosol

YRL

Tyrosol (Standard)

2-(4-Hydroxyphenyl)ethanol (Tyrosol)

4-hydroxybenzenethanol

4-(Hydroxyethyl)phenol

p-Hydroxy-benzeneethanol

TYROSOL [MI]

b-(p-Hydroxyphenyl)ethanol

bmse000173

b-(4-Hydroxyphenyl)ethanol

4-Hydroxyphenylmethylcarbinol

2-(p-hydroxyphenyl) ethanol

SCHEMBL43838

(4-Hydroxyphenethyl) alcohol

2-(4-hydroxyphenyl) ethanol

2-(4-hydroxyphenyl)-ethanol

beta-(p-Hydroxyphenyl)ethanol

MLS001332423

MLS001332424

Phenethyl alcohol, p-hydroxy-

Ethanol, 2-(4-hydroxyphenyl)

SCHEMBL10620528

.beta.-(p-Hydroxyphenyl)ethanol

2-(4-Hydroxyphenyl)-1-ethanol

Ethanol, 2-(4-hydroxyphenyl)-

HY-N0474R

.beta.-(4-Hydroxyphenyl)ethanol

4-Hydroxyphenethyl alcohol [ISO]

HMS2230E12

2-(4-Hydroxyphenyl)ethanol, 98%

BCP34277

HY-N0474

NSC59876

STR02735

BDBM50339585

s3773

AKOS000280287

AC-2493

CCG-266147

CS-W019782

FH15593

KS-5274

NCGC00246994-01

NCGC00246994-03

SY001653

DB-019455

Tyrosol;2-(4-Hydroxyphenyl)ethanol;p-HPEA

H0720

NS00014657

C06044

EN300-116733

2-(4-Hydroxyphenyl)ethanol, analytical standard

NSC 59876; p-HPEA;4-Hydroxyphenethyl alcohol

Q402607

TYROSOL (CONSTITUENT OF RHODIOLA ROSEA) [DSC]

F0001-1309

Z1250886919

947D0361-23C6-4863-8346-22AB05108AC5

4-hydroxy-Benzeneethanol;4-Hydroxyphenylethanol;beta-(4-Hydroxyphenyl)ethanol

InChI=1/C8H10O2/c9-6-5-7-1-3-8(10)4-2-7/h1-4,9-10H,5-6H