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Raspberry Ketone

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Identification
Molecular formula
C10H12O4
CAS number
5471-51-2
IUPAC name
1-(2,4,5-trihydroxyphenyl)butan-1-one
State
State

At room temperature, raspberry ketone is typically found as a solid. It is stable under standard conditions and used in a variety of chemical formulations for its aromatic properties.

Melting point (Celsius)
82.00
Melting point (Kelvin)
355.15
Boiling point (Celsius)
285.00
Boiling point (Kelvin)
558.15
General information
Molecular weight
164.17g/mol
Molar mass
164.1730g/mol
Density
1.0340g/cm3
Appearence

Raspberry ketone is a natural phenolic compound that is responsible for the aroma of red raspberries. It appears as a white to pale yellow crystalline powder. It can be synthesized or extracted for use in various applications especially in the flavor and aroma industries.

Comment on solubility

Solubility of 1-(2,4,5-trihydroxyphenyl)butan-1-one

1-(2,4,5-trihydroxyphenyl)butan-1-one exhibits **interesting solubility characteristics** due to its molecular structure. This compound features multiple hydroxy groups, which can significantly influence its solubility in various solvents.

Polar Solvents

In polar solvents such as water and alcohols, 1-(2,4,5-trihydroxyphenyl)butan-1-one typically shows:

  • **High solubility** due to hydrogen bonding between hydroxy groups and solvent molecules.
  • Enhanced dissolution in **ethanol and methanol**, where the polar nature aids in solvation.

Non-Polar Solvents

Conversely, the solubility in non-polar solvents is expected to be:

  • **Limited**, as the hydrophilic hydroxy groups are incompatible with non-polar environments.
  • The compound may precipitate or remain undissolved in **hexane or benzene**, significantly reducing its solubility.

In summary, the solubility of 1-(2,4,5-trihydroxyphenyl)butan-1-one is largely determined by its **functional groups** and **molecular interactions**, making it soluble in polar environments while substantially insoluble in non-polar solvents.

Interesting facts

Exploring 1-(2,4,5-trihydroxyphenyl)butan-1-one

1-(2,4,5-trihydroxyphenyl)butan-1-one, often referred to as a compound of notable interest in the field of organic chemistry, presents a multitude of intriguing characteristics that make it a subject of study and discussion among scientists and students alike.

Chemical Structure and Functionality

This compound features a unique structure that consists of:

  • Three hydroxyl (-OH) groups attached to a phenyl ring, enhancing its reactivity.
  • A butan-1-one structure that contributes to its functional properties.

The presence of the hydroxyl groups indicates potential for hydrogen bonding, leading to increased solubility in various solvents and an ability to participate in numerous chemical reactions.

Natural Occurrence

Interestingly, compounds similar to 1-(2,4,5-trihydroxyphenyl)butan-1-one can be found in nature. Some of these natural products are known for their biological activities, sparking a keen interest in their medicinal properties. Research indicates that:

  • Hydroxylated phenolic compounds can exhibit antioxidant properties.
  • These compounds may play a role in the protection against cellular damage caused by free radicals.

Applications and Importance

The applications of 1-(2,4,5-trihydroxyphenyl)butan-1-one are diverse and show great promise, particularly in:

  • Pharmaceutical industry: Due to its potential therapeutic effects.
  • Research: As a foundational compound for developing new drugs and treatments.

As a result, the study of such compounds can lead to groundbreaking discoveries in fields ranging from biochemistry to pharmacology.

Conclusion

In summary, 1-(2,4,5-trihydroxyphenyl)butan-1-one stands out as a fascinating compound due to its chemical structure, biological significance, and practical applications. Its ability to participate in important biochemical processes makes it a key subject for ongoing research and exploration within the scientific community.

Synonyms
1421-63-2
2,4,5-TRIHYDROXYBUTYROPHENONE
1-(2,4,5-trihydroxyphenyl)butan-1-one
2',4',5'-Trihydroxybutyrophenone
1-Butanone, 1-(2,4,5-trihydroxyphenyl)-
USAF EK
1-(2,4,5-Trihydroxyphenyl)-1-butanone
Butyrophenone, 2',4',5'-trihydroxy-
NSC 73478
CCRIS 6281
HSDB 4288
EINECS 215-824-8
UNII-KN729W3LR0
BRN 2577028
KN729W3LR0
DTXSID2026232
AI3-26870
NSC-73478
DTXCID706232
4-08-00-02753 (Beilstein Handbook Reference)
1-butanone, 1-(2,4,5-trihydroxyphenyl)
2,4,5-TRIHYDROXYBUTYROPHENONE [MI]
2,4,5-TRIHYDROXYBUTYROPHENONE [HSDB]
BUTYROPHENONE, TRIHYDROXY-
1(2,4,5Trihydroxyphenyl)1butanone
Butyrophenone, 2',4',5'trihydroxy
1Butanone, 1(2,4,5trihydroxyphenyl)
PROPYL 2,4,5-TRIHYDROXYPHENYL KETONE
1421-63-252262-23-4
trihydroxybutyrophenone
un2811
Thbp
NCGC00091839-03
2,5-Trihydroxybutyrophenone
SCHEMBL43001
WLN: QR BQ DQ EV3
BIDD:ER0369
2',5'-Trihydroxybutyrophenone
CHEMBL1531716
5-Butanoyl-1,2,4-benzeneetriol
Butyrophenone,4',5'-trihydroxy-
CHEBI:173969
2 ,4 ,5 -Trihydroxybutyrophenone
2,'4',5'-Trihydroxybutyrophenone
NSC73478
1-Butanone,4,5-trihydroxyphenyl)-
Tox21_400052
2',4',5'-Trihydroxy-Butyrophenone
MFCD00020019
AKOS003297818
PS-5892
2'4'5'-TRIHYDROXYBUTYROPHENONE
NCGC00091839-01
NCGC00091839-02
NCGC00091839-04
NCGC00091839-05
2',4',5'-Trihydroxybutyrophenone, 8CI
FT131181
CAS-1421-63-2
1 - (2,4,5-trihydroxyphenyl) 1-butanone
CS-0446336
NS00021649
F11160
Q27282340