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Diethylstilbestrol

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Identification
Molecular formula
C18H20O2
CAS number
56-53-1
IUPAC name
4-[1-ethyl-2-(4-hydroxyphenyl)butyl]phenol
State
State

At room temperature, Diethylstilbestrol is in a solid state.

Melting point (Celsius)
169.00
Melting point (Kelvin)
442.15
Boiling point (Celsius)
528.00
Boiling point (Kelvin)
801.15
General information
Molecular weight
268.35g/mol
Molar mass
268.3510g/mol
Density
1.2830g/cm3
Appearence

Diethylstilbestrol appears as a white crystalline powder.

Comment on solubility

Solubility of 4-[1-ethyl-2-(4-hydroxyphenyl)butyl]phenol (C18H20O2)

The solubility of 4-[1-ethyl-2-(4-hydroxyphenyl)butyl]phenol is an intriguing aspect due to its complex organic structure. This compound, with its notable functional groups, exhibits certain characteristics that determine its solubility behavior:

  • Polar and Nonpolar Characteristics: Due to the presence of a hydroxyl group (-OH) in its structure, 4-[1-ethyl-2-(4-hydroxyphenyl)butyl]phenol is expected to have some degree of solubility in polar solvents. However, the large hydrocarbon chains contribute to its overall nonpolar characteristics, making it less soluble in water.
  • Solubility in Organic Solvents: This compound is likely to dissolve more readily in organic solvents such as ethanol, acetone, or dichloromethane, where the interactions with the solvent molecules can effectively accommodate its structural nature.
  • Hydrogen Bonding: The hydroxyl functional group may participate in hydrogen bonding with polar solvents, enhancing solubility to some extent, especially in alcohols or ethers, further illustrating the duality of its solubility profile.

In conclusion, while 4-[1-ethyl-2-(4-hydroxyphenyl)butyl]phenol demonstrates limited solubility in water due to its hydrophobic qualities, it reveals a more favorable interaction with organic solvents, highlighting the importance of molecular structure in solubility behavior.

Interesting facts

Interesting Facts about 4-[1-ethyl-2-(4-hydroxyphenyl)butyl]phenol

4-[1-ethyl-2-(4-hydroxyphenyl)butyl]phenol, also known as a branched chain phenolic compound, exhibits a unique structure that combines both ethyl and hydroxyphenyl groups. This intriguing arrangement contributes to its diverse applications and properties. Here are some interesting points:

  • Versatile Ingredient: This compound often functions as a key ingredient in various chemical formulations, including cosmetic products, pharmaceuticals, and industrial applications.
  • Antioxidant Properties: The presence of hydroxyl groups in its structure allows this compound to exhibit significant antioxidant activity, which helps combat oxidative stress in biological systems.
  • Potential Health Benefits: Some studies suggest that derivatives of phenolic compounds can have protective effects against diseases such as cancer and heart disease, making them a focus of ongoing research.
  • Functionalization: The ability to modify the phenolic structure enables chemists to tailor specific properties for targeted applications, enhancing its functionality and efficiency in usage.
  • Environmental Impact: As with many organic compounds, understanding the environmental fate of this compound is essential, especially regarding its degradation and potential accumulation in ecosystems.

In conclusion, 4-[1-ethyl-2-(4-hydroxyphenyl)butyl]phenol serves as a prime example of how organic compounds can play vital roles across various fields. Its rich chemistry and promising utility make it a subject of interest for further exploration and understanding.

Synonyms
hexestrol
5635-50-7
Dihydrodiethylstilbestrol
Vitestrol
Hexoestrolum
4,4'-(1,2-Diethylethylene)diphenol
Exestrol
Stilbestrol, dihydro-
4,4'-(hexane-3,4-diyl)diphenol
Phenol, 4,4'-(1,2-diethyl-1,2-ethanediyl)bis-
4-[4-(4-hydroxyphenyl)hexan-3-yl]phenol
Hexane, 3,4-bis(4-hydroxyphenyl)-
Synoestrolum
Phenol, 4,4'-(1,2-diethylethylene)di-
CHEBI:31669
3,4-Bis(p-hydroxyphenyl)hexane
Hexanestrol
NSC 9894
Hormoestrol; Mesohexestrol; NSC 9894; Sinestrol
Esestrolo [DCIT]
Hexestrolum
Esestrolo
Hexestrolum [INN-Latin]
MFCD00068996
Hexestrol [INN:NF]
4,2-Diethylethylene)diphenol
SR-05000001870
EINECS 227-082-2
NSC-9894
Phenol,4'-(1,2-diethylethylene)di-
Prestwick_80
1,4-Dicyano-2,3,5,6-tetrachlorobenzene; 2,3,5,6-Tetrachloro-1,4-benzenedicarbonitrile; 2,3,5,6-Tetrachloro-1,4-dicyanobenzene; 2,3,5,6-Tetrachloroterephthalonitrile; Tetrachloroterephthalodinitrile
Spectrum_000487
Hexestrol (JAN/INN)
Prestwick0_000699
Prestwick1_000699
Prestwick2_000699
Prestwick3_000699
Spectrum2_000891
Spectrum3_000560
Spectrum4_000392
Spectrum5_001475
4-[1-ethyl-2-(4-hydroxyphenyl)butyl]phenol
CHEMBL6615
Oprea1_380638
BSPBio_000857
BSPBio_002239
KBioGR_000943
KBioSS_000967
MLS002153963
DivK1c_000443
SCHEMBL154886
SPECTRUM1500632
SPBio_000702
SPBio_002778
BPBio1_000943
GTPL2823
4,4'-hexane-3,4-diyldiphenol
Hexane,4-bis(4-hydroxyphenyl)-
HMS501G05
KBio1_000443
KBio2_000967
KBio2_003535
KBio2_006103
KBio3_001739
DTXSID30859129
NINDS_000443
3,4-bis(4-hydroxyphenyl) hexane
4,4'-(3,4-Hexanediyl)diphenol
HMS1570K19
HMS1921M07
HMS2097K19
HMS2235O21
HMS3369N07
HMS3656I04
HMS3714K19
Pharmakon1600-01500632
BCP03061
QYB47612
CCG-39630
NSC229419
NSC757393
STK366320
AKOS005442984
NSC-229419
NSC-757393
4,4\'-(1,2-Diethylethylene)Diphenol
IDI1_000443
NCGC00094818-01
NCGC00094818-02
NCGC00094818-03
NCGC00094818-04
NCGC00094818-05
NCGC00094818-06
NCGC00094818-08
AC-12485
AS-56141
SMR001233302
SBI-0051565.P002
AB00052132
D0494
NS00003872
D01641
Phenol,4'-(1,2-diethyl-1,2-ethanediyl)bis-
AB00052132_08
Q5896882
SR-05000001870-1
SR-05000001870-3
SR-05000001870-4
BRD-A01078468-001-05-6
BRD-A01078468-001-08-0
BRD-A01078468-001-14-8