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4-Benzyloxyphenol

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Identification
Molecular formula
C13H12O2
CAS number
103-16-2
IUPAC name
4-benzyloxyphenol
State
State
4-Benzyloxyphenol is typically found as a solid at room temperature. It can be handled as a crystalline powder.
Melting point (Celsius)
93.00
Melting point (Kelvin)
366.15
Boiling point (Celsius)
395.00
Boiling point (Kelvin)
668.15
General information
Molecular weight
200.23g/mol
Molar mass
200.2320g/mol
Density
1.1740g/cm3
Appearence

4-Benzyloxyphenol appears as a white to off-white crystalline solid. It has a characteristic phenolic odor.

Comment on solubility

Solubility of 4-Benzyloxyphenol

4-Benzyloxyphenol, also known by its IUPAC name, possesses interesting solubility characteristics that can be influenced by various factors. This compound is known to be:

  • Soluble in organic solvents: 4-Benzyloxyphenol generally dissolves well in non-polar solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO). Its aromatic structure contributes to its solubility in these mediums.
  • Moderately soluble in water: Its solubility in water is limited due to the hydrophobic nature of the phenol ring; however, studies show that with increasing temperature, its solubility can improve.
  • Influenced by pH: The solubility of 4-benzyloxyphenol may also be affected by the pH of the solution. For instance, higher pH levels can enhance the solubility due to the potential deprotonation of the phenolic hydroxyl group.

In summary, while 4-benzyloxyphenol may not be highly soluble in water, its affinity for organic solvents and responsiveness to pH changes make it a versatile compound in chemical applications.

Interesting facts

Interesting Facts About 4-Benzyloxyphenol

4-Benzyloxyphenol is a versatile organic compound that has garnered attention in various fields, including medicinal chemistry, materials science, and industrial applications. This compound is an aromatic ether, characterized by the presence of a benzene ring substituted with both a phenol and a benzyl group. Here are some captivating insights:

  • Chemical Versatility: 4-Benzyloxyphenol can participate in a variety of chemical reactions due to the presence of functional groups, making it a useful intermediate in organic synthesis.
  • Antioxidant Properties: Studies have shown that 4-benzyloxyphenol exhibits significant antioxidant activity, which may contribute to its use in formulations aimed at preventing oxidative stress.
  • Biological Contributions: Research has suggested potential biological activities of this compound, including antimicrobial and anti-inflammatory properties, which could lead to novel therapeutic applications.
  • Material Science Applications: 4-Benzyloxyphenol is also explored for its roles in polymer science, acting as a stabilizer in the synthesis of various materials.
  • Safety Precaution: As with many chemical compounds, proper handling and safety measures are essential to mitigate potential hazards during research and application.

With its unique structure and promising attributes, 4-benzyloxyphenol continues to be an interesting subject of study, inviting further exploration and innovation in both academic and industrial settings. As researchers delve deeper into its properties and applications, it stands to become an even more significant compound in the realm of chemistry.

Synonyms
Monobenzone
4-Benzyloxyphenol
103-16-2
4-(Benzyloxy)phenol
Hydroquinone monobenzyl ether
Benoquin
P-(BENZYLOXY)PHENOL
Benzoquin
Monobenzyl hydroquinone
Hydroquinone benzyl ether
Leucodinine
Monobenzon
Superlite
Agerite alba
4-(Phenylmethoxy)phenol
p-Hydroxyphenyl benzyl ether
Dermochinona
Carmifal
Depigman
Pigmex
Benzyl p-hydroxyphenyl ether
Monobenzyl ether hydroquinone
Alba-Dome
Monobenzona
4-(Benzyloxyl)phenol
Agerite
Benzyl hydroquinone
Phenol, 4-(phenylmethoxy)-
Monobenzonum
Monobenzone [INN]
4-phenylmethoxyphenol
Monobenzonum [INN-Latin]
Monobenzona [INN-Spanish]
Superlite (antioxidant)
P-BENZYLOXYPHENOL
Monobenzyl Ether of Hydroquinone
Alba
Hydrochinon monobenzylether [Czech]
Phenol, p-(benzyloxy)-
Hydrochinon monobenzylether
4-Benzyloxy-phenol
4-phenylmethoxy-phenol
MFCD00002333
NSC 2132
NSC-2132
9L2KA76MG5
CHEBI:34380
Monobenzone (Benoquin)
4-benzyloxy phenol
PBP
DTXSID2020717
NSC33918
NCGC00016360-01
CAS-103-16-2
WLN: QR DO1R
MONOBENZONE (MART.)
MONOBENZONE [MART.]
MONOBENZONE (USP-RS)
MONOBENZONE [USP-RS]
DTXCID00717
MONOBENZONE (USP MONOGRAPH)
MONOBENZONE [USP MONOGRAPH]
Benoquin (TN)
HSDB 4019
SR-05000001819
Monobenzone (USP/INN)
Monobenzone [USP:INN]
EINECS 203-083-3
BRN 1958305
UNII-9L2KA76MG5
4-benzoxyphenol
AI3-14325
Hydroquinone Monobenzylether; 4-Benzyloxyphenol; 4-(Benzyloxy)phenol
4-benzyloxylphenol
p-benzyloxy phenol
p-benzyloxy-phenol
Monobenzone, USP
4(benzyloxy)phenol
(p)-Benzyloxyphenol
MBEH
4-(benzyloxy)-phenol
para-(Benzyloxy)phenol
Monobenzone (Standard)
MONOBENZONE [MI]
Prestwick0_000912
Prestwick1_000912
Prestwick2_000912
Prestwick3_000912
MONOBENZONE [HSDB]
MONOBENZONE [VANDF]
CHEMBL1388
Oprea1_698781
SCHEMBL35631
BSPBio_000784
MONOBENZONE [WHO-DD]
Monobenzone;4-Benzyloxyphenol
4-(Benzyloxy)phenol, 98%
4-06-00-05728 (Beilstein Handbook Reference)
BIDD:ER0003
SPBio_002973
BPBio1_000864
GTPL6830
4-(Benzyloxy)phenol, >=99%
D11AX13
MONOBENZONE [ORANGE BOOK]
NSC2132
HMS1570H06
HMS1580P12
HMS2097H06
HMS3655K15
HMS3714H06
Pharmakon1600-01503031
4-(Benzyloxy)phenol (Monobenzone)
BCP09974
CS-B0870
Tox21_110396
Tox21_201147
4-(Benzyloxy)phenol; Hydroquinone monobenzyl ether; PBP; Monobenzone
BDBM50410520
HY-30272R
NSC-33918
NSC758211
s1652
STL283939
AKOS000119555
Tox21_110396_1
AC-2492
CCG-213094
DB00600
FH02681
NSC-758211
PS-8213
NCGC00016360-02
NCGC00016360-03
NCGC00016360-05
NCGC00016360-06
NCGC00258699-01
FH178558
HY-30272
SY001650
AB00513959
B1104
NS00001735
SW197310-3
EN300-20495
D05072
F11201
AB00513959-03
AB00513959_04
AB00513959_05
A800687
Q2768526
SR-05000001819-1
SR-05000001819-2
SR-05000001819-3
BRD-K54262262-001-01-7
BRD-K54262262-001-06-6
BRD-K54262262-001-09-0
BRD-K54262262-001-10-8
BRD-K54262262-001-11-6
BRD-K54262262-001-12-4
F0777-0782
Z104478412
Monobenzone, United States Pharmacopeia (USP) Reference Standard
4-(Benzyloxy)phenol ; Hydroquinone monobenzyl ether ; PBP ; Monobenzone
203-083-3