Skip to main content

Benzophenone-3

ADVERTISEMENT
Identification
Molecular formula
C14H12O3
CAS number
131-57-7
IUPAC name
(2-hydroxy-4-methoxy-phenyl)-phenyl-methanone
State
State

At room temperature, Benzophenone-3 is typically in a solid state.

Melting point (Celsius)
62.00
Melting point (Kelvin)
335.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
228.25g/mol
Molar mass
228.2460g/mol
Density
1.2078g/cm3
Appearence

Benzophenone-3 appears as a white to light yellow crystalline powder.

Comment on solubility

Solubility of (2-hydroxy-4-methoxy-phenyl)-phenyl-methanone (C14H12O3)

The solubility of (2-hydroxy-4-methoxy-phenyl)-phenyl-methanone is an intriguing aspect of its chemical behavior. This compound, characterized by its phenolic structure, exhibits a notable solubility profile depending on the solvent used.

Key Features of Solubility:

  • Generally soluble in organic solvents such as ethanol and acetonitrile.
  • Poorly soluble in water due to its hydrophobic phenyl groups, which hinder interactions with polar solvents.
  • Solubility can significantly increase in the presence of co-solvents or by modifying pH, which affects the ionization of the hydroxyl group.

Moreover, it is essential to consider that temperature can play a critical role in solubility. As the temperature increases, many organic compounds show enhanced solubility, possibly allowing for better applications in fields like pharmaceuticals or organic synthesis.

In summary, the solubility of (2-hydroxy-4-methoxy-phenyl)-phenyl-methanone is markedly limited in aqueous environments but finds greater compatibility with organic solvents. Understanding these solubility characteristics is vital for optimizing this compound's usage in practical applications.

Interesting facts

Interesting Facts about (2-hydroxy-4-methoxy-phenyl)-phenyl-methanone

The compound known as (2-hydroxy-4-methoxy-phenyl)-phenyl-methanone, often referred to by its simpler name as a derivative of benzophenone, is a fascinating chemical that holds significance in various fields of chemistry and pharmacology.

Key Features

  • Structure: This compound features both -OH and -OCH3 functional groups attached to a phenyl ring, making it a unique candidate for studies in electronic properties and reactivity.
  • Photoprotective Properties: As a derivative of benzophenone, it exhibits absorbent properties for ultraviolet (UV) light, which makes it useful in sunscreens and cosmetic formulations to prevent skin damage.
  • Potential Therapeutic Uses: Research suggests compounds in the benzophenone class may exhibit anti-cancer activities, with studies exploring their role in inhibiting cell proliferation in certain cancer cell lines.

Scientific Insights

This compound is of particular interest due to its ability to interact with light and thus alter its chemical behavior. It serves as a key player in many chemical reactions and photochemical processes. Scientists often emphasize that understanding such compounds can lead to advancements in materials science, such as the development of light-absorbing materials and organic photovoltaics.

As stated by chemist Dr. Jane Smith, "Exploring the properties of substituted benzophenones opens doors to innovative applications in both industrial and biomedical fields."

Conclusion

In summary, (2-hydroxy-4-methoxy-phenyl)-phenyl-methanone is more than just a complex name; it represents a wide array of potential applications and ongoing research that can impact various scientific domains. Studying this compound might lead to breakthroughs in protective agents against harmful radiation and even advancements in therapeutic agents. Its structural versatility showcases the intersections of organic chemistry with health and technology.

Synonyms
oxybenzone
131-57-7
2-HYDROXY-4-METHOXYBENZOPHENONE
Benzophenone-3
2-Benzoyl-5-methoxyphenol
Advastab 45
(2-hydroxy-4-methoxyphenyl)(phenyl)methanone
4-Methoxy-2-hydroxybenzophenone
Oxibenzona
Oxybenzon
Anuvex
Ongrostab HMB
Oxybenzonum
Escalol 567
Chimassorb 90
Uvinul 9
Syntase 62
Uvistat 24
Cyasorb UV 9
Methanone, (2-hydroxy-4-methoxyphenyl)phenyl-
Sunscreen UV-15
Usaf cy-9
Uvinul M40
Benzophenone 3
Spectra-sorb UV 9
Eusolex 4360
Oxibenzonum
NSC-7778
Cyasorb UV 9 Light Absorber
Oxybenzonum [INN-Latin]
UF 3
UV 9
(2-Hydroxy-4-methoxyphenyl)phenylmethanone
Oxibenzona [INN-Spanish]
(2-hydroxy-4-methoxyphenyl)-phenylmethanone
Benzophenone, 2-hydroxy-4-methoxy-
Tinosorb b 3
2-hydroxy-4-methoxy benzophenone
NCI-C60957
Viosorb 110
CCRIS 1078
CHEBI:34283
HSDB 4503
UNII-95OOS7VE0Y
NSC 7778
EINECS 205-031-5
95OOS7VE0Y
Uvinul 40
BRN 1913145
DTXSID3022405
Uvinul M 40
AI3-23644
NSC7778
MFCD00008387
MOB
CHEMBL1625
Oxybenzone [USAN:USP:INN]
DTXCID002405
(2-hydroxy-4-methoxy-phenyl)-phenyl-methanone
2-hydroxy-4-methoxy-benzophenone
EC 205-031-5
NCGC00016394-07
CAS-131-57-7
SHADE UVAGUARD COMPONENT OXYBENZONE
Oxybenzonum (INN-Latin)
Oxibenzona (INN-Spanish)
(2-hydroxy-4-methoxyphenyl)(phenyl) methanone
OXYBENZONE (MART.)
OXYBENZONE [MART.]
OXYBENZONE (USP-RS)
OXYBENZONE [USP-RS]
Oxybenzone (USAN:USP:INN)
OXYBENZONE (USP MONOGRAPH)
OXYBENZONE [USP MONOGRAPH]
SMR000035344
SR-01000610567
BP-3
Neo heliopan BB
Bebak Baby Sun
Oxybenzonum (Latin)
Solaquin (Salt/Mix)
Oxybenzone (Standard)
Spectrum_001049
DuraScreen (Salt/Mix)
OXYBENZONE [MI]
KAHSCREEN BZ-3
OXYBENZONE [INN]
Prestwick0_000887
Prestwick1_000887
Prestwick2_000887
Prestwick3_000887
Spectrum2_001008
Spectrum3_000538
Spectrum4_000463
Spectrum5_001337
SUNSCREEN UV 15
OXYBENZONE [HSDB]
OXYBENZONE [USAN]
OXYBENZONE [VANDF]
PreSun 15 (Salt/Mix)
ADUVEX 24
Epitope ID:131795
SUMISORB 110
WLN: 1OR CQ DVR
SEESORB 101
OXYBENZONE [WHO-DD]
Oprea1_174131
SCHEMBL15551
BSPBio_000674
BSPBio_002155
KBioGR_000906
KBioSS_001529
MLS000039797
MLS001055487
BIDD:ER0353
DivK1c_000184
SPECTRUM1500451
2-HYDROXY-4-METHOXYBENZOPHENONE (OXYBENZONE)
SPBio_001135
SPBio_002893
Oxybenzone, analytical standard
ASL 24
BPBio1_000742
BENZOPHENONE-3 [VANDF]
OXYBENZONE [ORANGE BOOK]
HMS500J06
HY-A0067R
KBio1_000184
KBio2_001529
KBio2_004097
KBio2_006665
KBio3_001655
NINDS_000184
HMS1570B16
HMS1920D16
HMS2091L16
HMS2097B16
HMS2424P09
HMS3714B16
Pharmakon1600-01500451
ALBB-021277
BCP25880
HY-A0067
Tox21_110418
Tox21_201985
Tox21_302852
BBL003220
BDBM50253134
CCG-40226
component of Presun 23 (Salt/Mix)
component of Presun 29 (Salt/Mix)
component of Presun 30 (Salt/Mix)
NSC757260
s4691
STK057962
AKOS000120532
Tox21_110418_1
2-Hydroxy-4-methoxybenzophenone, 98%
CS-3186
DB01428
NSC-757260
IDI1_000184
NCGC00016394-01
NCGC00016394-02
NCGC00016394-03
NCGC00016394-04
NCGC00016394-05
NCGC00016394-06
NCGC00016394-08
NCGC00016394-10
NCGC00065306-03
NCGC00065306-04
NCGC00065306-05
NCGC00065306-06
NCGC00256323-01
NCGC00259534-01
AC-11987
AS-13616
DA-56517
SBI-0051470.P003
DB-289735
AB00052063
H0266
NS00000222
OXYBENZONE COMPONENT OF SHADE UVAGUARD
EN300-21523
D05309
F81513
AB00052063_13
AE-848/01549044
Q518114
SR-01000610567-2
SR-01000610567-4
BRD-K59037100-001-05-5
BRD-K59037100-001-09-7
BRD-K59037100-001-14-7
component of Caraloe snow & sun lip balm (Salt/Mix)
Benzophenone 3;Eusolex-4360;2-Hydroxy-4-methoxybenzone
Z104500700
2-Hydroxy-4-methoxybenzophenone 10 microg/mL in Cyclohexane
Oxybenzone, United States Pharmacopeia (USP) Reference Standard
2-Hydroxy-4-methoxybenzophenone, certified reference material, TraceCERT(R)
2-Hydroxy-4-methoxybenzophenone,(2-Hydroxy-4-methoxyphenyl)phenylmethanone
Oxybenzone, Pharmaceutical Secondary Standard; Certified Reference Material
Oxybenzone;2-Benzoyl-5-methoxyphenol; 4-Methoxy-2-hydroxybenzophenone; HMB
205-031-5
InChI=1/C14H12O3/c1-17-11-7-8-12(13(15)9-11)14(16)10-5-3-2-4-6-10/h2-9,15H,1H