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3-Hydroxyphenyl acetate

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Identification
Molecular formula
C8H8O3
CAS number
621-26-1
IUPAC name
(3-hydroxyphenyl) acetate
State
State

At room temperature, 3-Hydroxyphenyl acetate is in a solid state. It is typically handled as a solid powder or crystalline substance for most of its applications.

Melting point (Celsius)
67.00
Melting point (Kelvin)
340.15
Boiling point (Celsius)
265.00
Boiling point (Kelvin)
538.15
General information
Molecular weight
166.17g/mol
Molar mass
166.1660g/mol
Density
1.2374g/cm3
Appearence

3-Hydroxyphenyl acetate appears as a white to off-white crystalline solid. It is often used in chemical research and industrial applications. The compound is relatively stable under normal conditions, but should be stored in a cool, dry place, away from light and moisture to maintain its purity.

Comment on solubility

Solubility of (3-Hydroxyphenyl) Acetate

(3-Hydroxyphenyl) acetate, represented by the chemical formula C8H8O3, exhibits notable solubility characteristics. Its solubility is influenced by both its structure and the functional groups present in the molecule.

Factors Affecting Solubility

  • Polarity: The hydroxyl (-OH) group contributes to the polarity of the molecule, enhancing its ability to form hydrogen bonds with water, making it more soluble in polar solvents.
  • Hydrogen Bonding: The presence of the hydroxyl group allows for effective intermolecular hydrogen bonding, particularly with water, which facilitates its solubility.
  • Aromatic Nature: The aromatic ring structure may limit solubility in non-polar solvents, as aromatic compounds tend to have lower solubility in water compared to aliphatic compounds.

In practical terms, (3-hydroxyphenyl) acetate is generally soluble in organic solvents like ethanol and acetone but may be only sparingly soluble in water. This illustrates a common trend where compounds with a balance of hydrophilic and hydrophobic features can exhibit variable solubility profiles.

Summary

As a compound of interest, (3-hydroxyphenyl) acetate showcases the complexity of solubility that arises from molecular interactions. Its ability to dissolve in various solvents highlights the importance of structural characteristics in predicting solubility behavior, emphasizing that "like dissolves like" is an essential consideration in chemical solubility.

Interesting facts

Interesting Facts about (3-Hydroxyphenyl) Acetate

(3-Hydroxyphenyl) acetate, often referred to in scientific communities as 3-hydroxyphenyl acetate, is a compound that presents intriguing characteristics and applications within various fields. Here are some captivating insights:

  • Structural Significance: This compound features a phenolic hydroxyl group and an acetate moiety, contributing to its unique reactivity and interaction with other substances.
  • Biological Activity: Research has indicated that compounds like (3-hydroxyphenyl) acetate exhibit potential antioxidant properties. Antioxidants are crucial in combating oxidative stress in biological systems.
  • Fragrance and Flavor: The aroma profile of (3-hydroxyphenyl) acetate is noteworthy, as it can impart sweet, floral fragrances. This makes it a candidate for utilization in perfumes and flavorings.
  • Natural Occurrence: This compound is sometimes found in various plants and can be extracted from natural sources. Its derivation from plant materials adds a layer of sustainability to its use in consumer products.
  • Potential in Medicine: The chemical structure of (3-hydroxyphenyl) acetate opens avenues for its exploration in medicinal chemistry, particularly in developing therapeutic agents that target specific pathways.

In conclusion, (3-hydroxyphenyl) acetate stands out not only for its structural properties but also for its potential applications in biochemistry, food science, and pharmaceutical research. As we continue to delve into the world of chemical compounds, the significance of such seemingly simple structures becomes ever more apparent.

Synonyms
RESORCINOL MONOACETATE
102-29-4
3-Hydroxyphenyl acetate
Euresol
Acetylresorcinol
3-Acetoxyphenol
Remonol
Resorcitate
1,3-Benzenediol, 1-acetate
(3-hydroxyphenyl) acetate
1,3-Benzenediol, monoacetate
resorcinol acetate
m-Hydroxyphenyl acetate
Resorcin acetate
Resorcin monoacetate
m-Acetoxyphenol
Resorcinol, monoacetate
Resorcinol (monoacetate)
UNII-YL6O37RD1S
Acetylresorcinol;Resorcin monoacetate
EINECS 203-022-0
YL6O37RD1S
NSC 40511
Resorcinol, acetate
Resorcinol monoacetate [USP]
BRN 1865490
DTXSID6045901
CHEBI:29672
AI3-02359
MFCD00002266
NSC-40511
1,3-benzenediol monoacetate
Resorcinol monoacetate (USP)
DTXCID4025901
Acetic Acid 3-Hydroxyphenyl Ester
Acetic acid, 3-hydroxyphenyl ester
RESORCINOL MONOACETATE [MI]
4-06-00-05672 (Beilstein Handbook Reference)
RESORCINOL MONOACETATE [MART.]
RESORCINOL MONOACETATE [WHO-DD]
NCGC00095054-01
RESORCINOL MONOACETATE [USP MONOGRAPH]
RESORCINOL MONOACETATE (MART.)
CAS-102-29-4
RESORCINOL MONOACETATE (USP MONOGRAPH)
Resorcinmonoacetat
Euresol (TN)
resorcinol-monoacetate
(resorcin monoacetate)
Spectrum_001737
Spectrum3_000967
Spectrum4_001086
Spectrum5_001091
3-Hydroxyphenyl acetate #
SCHEMBL27801
BSPBio_002573
KBioGR_001472
KBioSS_002217
DivK1c_000300
SPECTRUM1503500
CHEMBL1593874
HMS500O22
KBio1_000300
KBio2_002217
KBio2_004785
KBio2_007353
KBio3_001793
NINDS_000300
HMS1922C22
HMS2093G09
Pharmakon1600-01503500
Acetic acid 3-hydroxy-phenyl ester
HY-B0894
NSC40511
Tox21_111406
CCG-40330
NSC758475
AKOS015916482
Tox21_111406_1
DB15480
FA71057
NSC-758475
Resorcinol monoacetate, technical grade
IDI1_000300
NCGC00095054-02
NCGC00095054-03
NCGC00095054-05
DA-67167
SY051508
SBI-0051828.P002
NS00014035
R0009
Resorcinol monoacetate;3-Hydroxyphenylacetate
D02393
E77870
EN300-120015
AB00052359_02
SR-05000002069
SR-05000002069-1
BRD-K85603128-001-01-9
BRD-K85603128-001-02-7
BRD-K85603128-001-03-5
BRD-K85603128-001-04-3
Q27110220