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Benzophenone

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Identification
Molecular formula
C13H10O
CAS number
119-61-9
IUPAC name
1,2-diphenylethanone
State
State
Benzophenone is typically a solid at room temperature. It is stable under standard conditions but should be stored away from strong oxidizing agents.
Melting point (Celsius)
48.50
Melting point (Kelvin)
321.65
Boiling point (Celsius)
305.40
Boiling point (Kelvin)
578.50
General information
Molecular weight
182.22g/mol
Molar mass
182.2180g/mol
Density
1.1100g/cm3
Appearence

Benzophenone appears as white crystals or a white crystalline powder. It is often used in various industrial applications because of its UV light filtering properties and is known for its pleasant, distinctive odor.

Comment on solubility

Solubility of 1,2-Diphenylethanone

1,2-Diphenylethanone, often abbreviated as DPE, presents some intriguing characteristics when it comes to its solubility. Here are some key points to consider:

  • Solvent Compatibility: 1,2-diphenylethanone is generally soluble in organic solvents such as ethanol, acetone, and ether.
  • Water Solubility: This compound is practically insoluble in water, a trend common among many organic compounds with significant hydrophobic character.
  • Influence of Temperature: As with many organic compounds, an increase in temperature can enhance its solubility in organic solvents, making it a point of consideration in various experimental settings.
  • Structural Factors: The presence of multiple aromatic rings contributes to the compound's overall hydrophobic nature, thus impacting its interaction with polar solvents like water.

In summary, while 1,2-diphenylethanone demonstrates good solubility in several organic solvents, its limited solubility in water underscores the essence of molecular structure in determining solubility behavior.

Interesting facts

Exploring 1,2-Diphenylethanone

1,2-Diphenylethanone, often referred to in academic and industrial settings as a significant organic compound, boasts various intriguing properties and applications. This compound can be viewed as an important derivative of ketones, featuring two phenyl groups attached to a central carbonyl carbon.

Key Highlights

  • Historical Note: This compound has been studied extensively in the field of organic chemistry since the 20th century, leading to advancements in synthetic methodologies.
  • Industrial Use: It plays a crucial role in the production of various types of fragrances and flavoring agents due to its aromatic characteristics.
  • Role in Research: 1,2-Diphenylethanone is often utilized as a precursor in the synthesis of pharmaceuticals and agrochemicals.
  • Interesting Reactions: Its reactivity allows it to undergo various chemical reactions such as nucleophilic addition, making it a valuable compound in synthetic organic chemistry.
  • Photochemical Properties: This compound can absorb ultraviolet light, leading to interesting photochemical reactions that are utilized in various analytical techniques.

Furthermore, textbooks often highlight its applicability in the field of photochemistry, where it can act as a sensitizer in certain reactions. In this context, the compound serves as a fascinating example of how organic compounds can be harnessed for both practical applications and fundamental scientific inquiry. As one scholar aptly stated, "Understanding the behavior of compounds like 1,2-diphenylethanone opens doors to innovative chemical processes."

With ongoing research, 1,2-diphenylethanone continues to inspire chemists, and its versatility makes it an essential compound worthy of attention in both academic and industrial chemistry.

Synonyms
Deoxybenzoin
2-Phenylacetophenone
1,2-Diphenylethanone
451-40-1
Benzyl phenyl ketone
Ethanone, 1,2-diphenyl-
DESOXYBENZOIN
1,2-Diphenylethan-1-one
Phenyl benzyl ketone
Acetophenone, 2-phenyl-
Benzoin, deoxy-
MFCD00003081
1,2-diphenyl-ethanone
benzylphenylketone
UNII-F17V6C9PZX
EINECS 207-193-2
F17V6C9PZX
NSC 131456
BRN 1072876
DTXSID6044430
AI3-10583
NSC-131456
DTXCID4024430
1,2-DI(PHENYL)ETHANONE
4-07-00-01393 (Beilstein Handbook Reference)
WLN: RV1R
desoxybenzoine
deoxy benzoin
Benzoin, deoxy
BzBn
2Phenylacetophenone
a-phenylacetophenone
1,2diphenylethanone
Acetophenone, 2phenyl
1,2Diphenylethan1one
1, 2-diphenylethanone
1,2 diphenyl ethanone
1,2 diphenyl-ethanone
Ethanone, 1,2diphenyl
Enamine_004883
1,2-Diphenyl-1-ethanone
2-Phenylacetophenone, 97%
SCHEMBL24800
F3297-0011
CHEMBL3182695
NSC6097
HMS1407N21
HY-Y1777
NSC-6097
Tox21_302159
NSC131456
NSC249236
STL264189
AKOS001050203
CCG-103088
FP26930
NSC-249236
NCGC00255911-01
AC-11645
AS-11947
CAS-451-40-1
PD200354
SY010613
DB-051270
B0435
CS-0019389
EU-0066752
NS00021160
EN300-17086
AH-034/32462010
SR-01000388911
SR-01000388911-1
Q27277503
Z56876371
1,2-Diphenylethanone;1,2-Diphenylethan-1-one;Deoxybenzoin
207-193-2