CAS 492-89-7
:3-Pentadecylcatechol
Description:
3-Pentadecylcatechol, with the CAS number 492-89-7, is an organic compound characterized by its long aliphatic chain and catechol structure. It features a catechol moiety, which consists of a benzene ring with two hydroxyl groups positioned at the 1 and 2 positions, and a pentadecyl group (a 15-carbon straight-chain alkyl group) attached to the 3-position of the catechol. This unique structure imparts both hydrophilic and hydrophobic properties, making it amphiphilic. As a result, 3-pentadecylcatechol can interact with various substances, potentially serving as a surfactant or emulsifier in different applications. The compound is typically solid at room temperature and may exhibit low solubility in water due to its long hydrocarbon chain, while being more soluble in organic solvents. Its properties make it of interest in fields such as materials science, biochemistry, and pharmaceuticals, where it may be utilized in the development of novel materials or as a biochemical probe. Safety and handling precautions should be observed, as with any chemical substance, due to potential health hazards.
Formula:C21H36O2
InChI:InChI=1S/C21H36O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-16-19-17-15-18-20(22)21(19)23/h15,17-18,22-23H,2-14,16H2,1H3
InChI key:InChIKey=DQTMTQZSOJMZSF-UHFFFAOYSA-N
SMILES:C(CCCCCCCCCCCCCC)C1=C(O)C(O)=CC=C1
Synonyms:- 3-Pentadecyl-1,2-benzenediol
- (15:0)-Urushiol
- Hydrourushiol
- 492-89-7
- 3-Pentadecylbenzene-1,2-diol
- 1,2-benzenediol, 3-pentadecyl-
- Pyrocatechol, 3-pentadecyl-
- 3-Pentadecyl-1,2-benzenediol
- 1,2-Benzenediol, 3-pentadecyl-
- Dihydrorhengol
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.
Hydrourushiol
CAS:<p>Hydrourushiol is a natural product that can be used as a reference standard. The CAS number of Hydrourushiol is 492-89-7.</p>Formula:C21H36O2Color and Shape:SolidMolecular weight:320.517Pentadecylcatechol
CAS:<p>Pentadecylcatechol is a naturally occurring allergenic compound, which is a primary constituent in the oily resin of poison ivy, poison oak, and poison sumac. These plants belong to the genus Toxicodendron, and the irritant properties are due to the urushiol oil, which contains this specific catechol derivative.</p>Formula:C21H36O2Purity:Min. 95%Molecular weight:320.5 g/mol

