[1,1'-Biphenyl]-4-ethanol, with the CAS number 37729-18-3, is an organic compound characterized by its biphenyl structure substituted with a hydroxyl group at the para position of one of the phenyl rings. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its moderate solubility in organic solvents and limited solubility in water due to the hydrophobic nature of the biphenyl moiety. The presence of the hydroxyl group imparts some polar characteristics, allowing for potential hydrogen bonding interactions. [1,1'-Biphenyl]-4-ethanol may exhibit interesting chemical reactivity, including the ability to undergo oxidation or participate in various substitution reactions. Its applications can range from serving as an intermediate in organic synthesis to being utilized in the development of pharmaceuticals or agrochemicals. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.

[1,1'-Biphenyl]-4-ethanol

37729-18-3: 2-p-Biphenylethanol(6CI), 2-(4-Biphenylyl)ethyl alcohol, 4-Biphenylethanol

4-Phenylphenethyl alcohol

Biphenyl-4-Ethanol

Biphenyl-4-ethanol is an organic compound that belongs to the group of phenols. It is an efficient adsorbent for isosafrole, which is a contaminant in gasoline and diesel fuel. Biphenyl-4-ethanol has a high affinity with aromatic compounds, such as 4-biphenylmethanol. It also has specificities that are not shared by other adsorbents, such as acetonitrile, which are used in the petroleum industry. This product can be used to remove hydroxylase enzymes from fungal cells and it also removes hydrocarbon contaminants from water sources.

CAS 37729-18-3: [1,1'-Biphenyl]-4-ethanol

4-Phenylphenethyl alcohol

Ref: 10-F400282

Biphenyl-4-Ethanol

Ref: IN-DA00CJ3S

Biphenyl-4-Ethanol

Ref: 3D-FB179556

4-(2-Hydroxyethyl)biphenyl

Ref: 54-OR16854