Skip to main content

Glycerol phenyl ether

ADVERTISEMENT
Identification
Molecular formula
C9H12O3
CAS number
7473-05-8
IUPAC name
1-phenylpropane-1,2,3-triol
State
State

At room temperature, 1-Phenylpropane-1,2,3-triol is generally found as a viscous liquid but can also form a solid depending on environmental conditions.

Melting point (Celsius)
34.00
Melting point (Kelvin)
307.15
Boiling point (Celsius)
333.00
Boiling point (Kelvin)
606.15
General information
Molecular weight
168.20g/mol
Molar mass
168.1970g/mol
Density
1.2290g/cm3
Appearence

1-Phenylpropane-1,2,3-triol is a colorless to pale yellow viscous liquid commonly used as an intermediate in chemical synthesis. It may also be found as a white crystalline solid, depending on its purity and storage conditions.

Comment on solubility

Solubility of 1-phenylpropane-1,2,3-triol

1-phenylpropane-1,2,3-triol, also known as phenyl glycerol, exhibits interesting solubility characteristics that are important for its applications in various fields. Its solubility can be described as follows:

  • Solvating Behavior: The presence of multiple hydroxyl groups (-OH) in the structure of 1-phenylpropane-1,2,3-triol enhances its polarity, allowing it to interact favorably with polar solvents.
  • Water Solubility: This compound is generally soluble in water due to its ability to form hydrogen bonds with water molecules.
  • Organic Solvents: It also exhibits good solubility in various polar organic solvents such as alcohols and ketones.

However, its solubility in non-polar solvents is limited, making it less compatible with hydrocarbons or other similar substances. This distinctive solubility profile is particularly valuable in chemical reactions and formulation processes.

In conclusion, the solubility of 1-phenylpropane-1,2,3-triol can be summarized as highly soluble in water and polar solvents, while showing restricted solubility in non-polar environments.

Interesting facts

Interesting Facts about 1-Phenylpropane-1,2,3-triol

1-Phenylpropane-1,2,3-triol, commonly referred to as a phenolic compound, possesses unique characteristics that intrigue both chemists and students alike. Here are some fascinating points about this compound:

  • Chemical Structure: The structure of 1-phenylpropane-1,2,3-triol features a propane backbone with three hydroxyl groups and a phenyl ring. This combination contributes to its reactivity and interaction with biological systems.
  • Hydroxyl Groups: The presence of multiple hydroxyl (–OH) groups allows this compound to engage in hydrogen bonding, which can influence its solubility and reactivity in various chemical reactions.
  • Biological Activity: Compounds containing phenolic structures are often of great interest in pharmacology due to their potential antioxidant and antimicrobial properties. This makes 1-phenylpropane-1,2,3-triol a candidate for exploration in medicinal chemistry.
  • Applications: Beyond its role in research, this compound can serve as an intermediate in organic synthesis and may find applications in creating more complex organic compounds.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." As you delve into the study of 1-phenylpropane-1,2,3-triol, consider the vast opportunities for innovation and discovery that lie within such compounds.

Overall, 1-phenylpropane-1,2,3-triol exemplifies the intricate relationship between structure and function in organic chemistry, making it a compound worth studying and understanding.

Synonyms
1-phenylpropane-1,2,3-triol
[S(R*,R*)]-1-phenylglycerol
63157-81-3
16354-95-3
D-Threo-1-phenylglycerol
(S(R*,R*))-1-Phenylglycerol
16354-93-1
phenylglycerin
EINECS 240-414-0
EINECS 263-975-3
SCHEMBL117950
CHEMBL1836134
DTXSID20936837
CCFAGRVEHSCROQ-UHFFFAOYSA-N
(1S,2R)-1-phenylpropane-1,2,3-triol
NS00120630