1-Phenylethane-1,2-diol

CAT: 0804-HY-W015788-01Size: 5 gDry Ice: NoHazardous: No
CAT#:0804-HY-W015788-01Size:5 g
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Description
1-Phenylethane-1,2-diol (Styrene Glycol) is a benzyl diol compound, which is the major metabolite of Styrene. 1-Phenylethane-1,2-diol can be oxidized to hydroxyl ketone (2-hydroxy-1-phenylethan-1-one) selectively with variety of catalysts, including organocatalysts, metal complexes, non-noble metal oxides, bimetallics[1][2][3].
CAS Number
[93-56-1]
Product Name Alternative
Styrene Glycol
UNSPSC
12352005
Hazard Statement
H302, H315, H319, H335
Target
Biochemical Assay Reagents; Drug Metabolite
Type
Natural Products
Related Pathways
Metabolic Enzyme/Protease; Others
Field of Research
Neurological Disease
Assay Protocol
https://www.medchemexpress.com/1-phenylethane-1-2-diol.html
Concentration
10mM
Purity
99.92
Solubility
DMSO : 100 mg/mL (ultrasonic)
Smiles
OC(C1=CC=CC=C1)CO
Molecular Formula
C8H10O2
Molecular Weight
138.17
Precautions
H302, H315, H319, H335
References & Citations
[1]Fangwei Zhang, et al. Oxidation of 1-Phenylethane-1,2-Diol to 2-Hydroxy-1-Phenylethan-1-One Catalyzed by Gold Nanocrystals. ChemistrySelect. Volume 3, Issue 48 p. 13638-13640|[2]Bandyopadhyaya A K, et al. Synthesis of both enantiomers of 1-phenylethane-1, 2-diol via chirality transfer from bile acid derivatives[J]. Tetrahedron: Asymmetry, 2000, 11 (17) : 3463-3466.|[3]Kohn J, et al. Assessment of the neurotoxicity of styrene, styrene oxide, and styrene glycol in primary cultures of motor and sensory neurons. Toxicol Lett. 1995 Jan;75 (1-3) :29-37.
Shipping Conditions
Room Temperature
Storage Conditions
-20°C, 3 years; 4°C, 2 years (Powder)
Scientific Category
Natural Products
Clinical Information
No Development Reported

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