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1-Phenylethanol

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Identification
Molecular formula
C8H10O
CAS number
98-85-1
IUPAC name
1-phenylethanol
State
State

1-Phenylethanol is a liquid at room temperature.

Melting point (Celsius)
-20.00
Melting point (Kelvin)
253.15
Boiling point (Celsius)
203.00
Boiling point (Kelvin)
476.15
General information
Molecular weight
122.17g/mol
Molar mass
122.1660g/mol
Density
1.0203g/cm3
Appearence

1-Phenylethanol is a colorless liquid that has a rose-like odor. It is a chiral compound and can exist as either racemic mixture or as one of its enantiomers. It is commonly used in the fragrance industry due to its pleasant smell.

Comment on solubility

Solubility of 1-Phenylethanol

1-Phenylethanol, known for its aromatic characteristics, exhibits interesting solubility properties that reflect its molecular structure. This organic compound, with the formula C8H10O, is primarily soluble in organic solvents.


Solubility Characteristics:

  • Solvent Compatibility: 1-Phenylethanol is soluble in various organic solvents such as ethanol, methanol, and ether.
  • Water Solubility: Although it has some degree of solubility in water, it is only slightly soluble, making it less favorable for aqueous applications.
  • Temperature Effects: Its solubility tends to increase with temperature, showcasing typical behavior of organic compounds.

In summary, the unique solubility profile of 1-phenylethanol renders it a versatile compound in various chemical applications. As noted, particular care should be taken when considering its integration with polar solvents due to its limited water solubility. This makes 1-phenylethanol particularly suited for reactions and formulations in non-polar environments.

Interesting facts

Interesting Facts about 1-Phenylethanol

1-Phenylethanol, also known as α-phenylethanol, is a fascinating compound in the world of organic chemistry. Here are some intriguing insights about this compound:

  • Natural Occurrence: 1-Phenylethanol can be found in nature, particularly in essential oils of various plants and flowers. It contributes to the aroma of certain fragrances, making it a valuable substance in the perfume industry.
  • Uses in Industry: This compound is widely used as a solvent and as an intermediate in the synthesis of other organic compounds. Its ability to act as a chiral building block makes it an essential component in pharmaceuticals and agrochemicals.
  • Flavoring Agent: Due to its pleasant aroma and taste, 1-phenylethanol is also used as a flavoring agent in food products, enhancing the overall sensory experience.
  • Chirality: The compound is chiral, which means it has two enantiomers, each differing in their spatial arrangement. This property is crucial for its biological activity; one enantiomer might be more effective than the other in certain applications.
  • Biological Applications: Research has shown that 1-phenylethanol possesses antimicrobial properties, making it a subject of interest in the field of biochemistry and drug development.

In summary, 1-phenylethanol is more than just a simple organic compound; its roles in nature, industry, and research can lead to significant advancements and applications in various fields. As chemists continue to explore its properties, who knows what new discoveries await!

Synonyms
1-Phenylethanol
98-85-1
ALPHA-METHYLBENZYL ALCOHOL
1-Phenylethan-1-ol
Methylphenyl carbinol
Styralyl alcohol
Styrallyl alcohol
1-Phenethyl alcohol
1-Phenylethyl alcohol
Methylphenylcarbinol
13323-81-4
DL-1-Phenylethanol
Phenylmethylcarbinol
(+/-)-1-Phenylethanol
(1-Hydroxyethyl)benzene
sec-Phenethyl alcohol
alpha-Phenylethanol
1-Phenyl-1-hydroxyethane
alpha-Methylbenzenemethanol
Ethanol, 1-phenyl-
Methyl phenyl carbinol
DL-1-Phenethylalcohol
alpha-Phenethyl alcohol
Methanol, methylphenyl-
alpha-Phenylethyl alcohol
Styrene alcohol
Phenyl Ethanol
1-Fenylethanol
NCI-C55685
alpha-Methyl-benzmethanol
Fenyl-methylkarbinol
Benzenemethanol, .alpha.-methyl-
1-Fenylethanol [Czech]
FEMA No. 2685
FEMA Number 2685
1-PHENYL-ETHANOL
.alpha.-Methylbenzyl alcohol
Fenyl-methylkarbinol [Czech]
Benzyl alcohol, alpha-methyl-
NSC 25502
Benzenemethanol, alpha-methyl-
CCRIS 2367
(1)-alpha-Methylbenzyl alcohol
alpha-Hydroxyethylbenzene
HSDB 4164
1-phenyl ethanol
alpha-Methyl-benzyl alcohol
EINECS 202-707-1
EINECS 236-361-8
methylbenzyl alcohol
.alpha.-Methylbenzenemethanol
CHEBI:669
.alpha.-Phenylethanol
DTXSID1020859
AI3-02936
Benzyl alcohol, .alpha.-methyl-
E6O895DQ52
(+/-)-alpha-Methylbenzyl alcohol
NSC-25502
.alpha.-Phenethyl alcohol
.alpha.-Phenylethyl alcohol
DTXCID50859
EC 202-707-1
1-PHENYLETHANOL, (+/-)-
ALPHA-METHYLBENZYL ALCOHOL [FCC]
1-Phenyl ethyl alcohol
ALPHA-METHYLBENZYL ALCOHOL [HSDB]
Benzene-d5-methan-d-ol, a-(methyl-d3)-
1-PHENYLETHAN-2,2,2-D3-OL
DL-sec-Phenethyl alcohol
.ALPHA.-METHYLBENZYL ALCOHOL [FHFI]
(+/-)-.ALPHA.-METHYLBENZYL ALCOHOL
a-methylbenzyl alcohol
(R)-(+)-sec-Phenethyl Alcohol
1-phenethan-1-ol
methylphenyl methanol
methyl phenyl methanol
alpha-methyl-benzene methanol
UN2937
alpha-methyl-benzenemethanol
1phenylethanol
1Fenylethanol
UNII-E6O895DQ52
1Phenylethan1ol
(R)-(+)-alpha-Methylbenzyl alcohol
(+/-)-1-Phenylethyl Alcohol
alphaPhenylethanol
(+-)-alpha-methylbenzyl alcohol
Fenylmethylkarbinol
Ethanol, 1phenyl
1Phenethyl alcohol
methylbenzyl alcohols
phenylmethyl carbinol
1Phenylethyl alcohol
a-Hydroxyethylbenzene
Methylphenyl-Methanol
MFCD00004508
1-hydroxyethylbenzene
SYNTHACOLIN
1-phenyl-1-ethanol
1Phenyl1hydroxyethane
alphaPhenethyl alcohol
1-phenylethane-1-ol
alphaMethylbenzmethanol
rac.-1-phenylethanol
Methanol, methylphenyl
(rs)-1-phenylethanol
a-phenyl ethyl alcohol
(1Hydroxyethyl)benzene
Alcohol methyl benzylic
alphaPhenylethyl alcohol
racemic 1-phenylethanol
alpha-methylbenzylalcohol
alphaMethylbenzenemethanol
(+) alpha-phenylethanol
1-Phenylethanol, 98%
1-(Phenylethyl) alcohol
1-Phenyl-1-ethylalcohol
DL-1-Phenylethyl Alcohol
.alpha.-Hydroxyethylbenzene
Alpha-methyl benzyl alcohol
Benzenemethanol, alphamethyl
Benzyl alcohol, alphamethyl
SCHEMBL2164
(s)-(+)-1-phenylethanol
a-Methylbenzenemethanol, 9CI
a-Methylbenzyl alcohol, 8CI
racemic 1-phenylethyl alcohol
(+/-)-sec-Phenethyl Alcohol
(+/-)-a-Methylbenzyl alcohol
CHEMBL508917
WLN: QY1 & R
dl-.alpha.-Methylbenzyl alcohol
(+-)-1-PHENYLETHANOL
(+-)-SEC-PHENYLETHANOL
(RS)-ALPHA-PHENYLETHANOL
CHEBI:25281
DL-METHYL PHENYL CARBINOL
FEMA 2685
(+-)-ALPHA-PHENYLETHANOL
(RS)-SEC-PHENETHYL ALCOHOL
(.+-.)-1-PHENYLETHANOL
(.+-.)-SEC-PHENYLETHANOL
BCP24404
DL-ALPHA-PHENYLETHYL ALCOHOL
NSC25502
(+-)-SEC-PHENETHYL ALCOHOL
ALPHA-METHYL BENZENE METHANOL
METHYLBENZYL ALCOHOL (ALPHA)
Tox21_200505
(+-)-1-PHENYLETHYL ALCOHOL
(.+-.)-ALPHA-PHENYLETHANOL
(+-)-ALPHA-PHENETHYL ALCOHOL
AKOS000121326
AKOS016038258
FM71254
SB40856
UN 2937
(.+-.)-1-PHENYLETHYL ALCOHOL
(.+-.)-SEC-PHENETHYL ALCOHOL
CAS-98-85-1
(+-)-ALPHA-METHYLBENZENEMETHANOL
(.+-.)-ALPHA-PHENETHYL ALCOHOL
NCGC00248663-01
NCGC00258059-01
SY007833
SY007893
(.+-.)-ALPHA-METHYLBENZENEMETHANOL
(.+-.)-ALPHA-METHYLBENZYL ALCOHOL
DB-043114
M0163
NS00005192
EN300-21267
alpha-Methylbenzyl alcohol, >=99%, FCC, FG
C07112
alpha-Methylbenzyl alcohol [UN2937] [Poison]
(R)-(+)-1-Phenylethanol, 99%, ChiraSelect(TM)
Q3740715
Z104494956
DL-Phenylmethylcarbinol;alpha-Methylphenylcarbinol;1-Phenylethanol
(?)-Methyl phenyl carbinol;(S)-(?)-alpha-Methylbenzyl alcohol;(S)-(-)-Sec-Phenylethyl alcohol
202-707-1
236-361-8