Search
項目搜尋
結構搜尋
Thermo Scientific Chemicals
3-(3-Hydroxyphenyl)propionic acid, 98+%
CAS: 621-54-5 | C9H10O3 | 166.176 g/mol
Have Questions?
變更視圖
化學識別
CAS621-54-5
IUPAC Name3-(3-hydroxyphenyl)propanoic acid
Molecular FormulaC9H10O3
InChI KeyQVWAEZJXDYOKEH-UHFFFAOYSA-N
SMILESOC(=O)CCC1=CC=CC(O)=C1
檢視更多
規格
規格表
規格表FormCrystals or powder or crystalline powder
Assay (Silylated GC)≥98.0%
Melting Point (clear melt)110.0-116.0?C
Appearance (Color)Cream to brown
Identification (FTIR)Conforms
檢視更多
3-Hydroxyphenylpropionic acid acts as a urinary metabolite of procyanidins in pigs. It also serves as an intermediate in the preparation of various synthetic organic products. Further, it is used in the preparation of 3-(3-hydroxy-phenyl)-propionic acid methyl ester.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
3-Hydroxyphenylpropionic acid acts as a urinary metabolite of procyanidins in pigs. It also serves as an intermediate in the preparation of various synthetic organic products. Further, it is used in the preparation of 3-(3-hydroxy-phenyl)-propionic acid methyl ester.
Solubility
Soluble in chloroform and methanol.
Notes
Incompatible with bases, oxidizing agents and reducing agents.
3-Hydroxyphenylpropionic acid acts as a urinary metabolite of procyanidins in pigs. It also serves as an intermediate in the preparation of various synthetic organic products. Further, it is used in the preparation of 3-(3-hydroxy-phenyl)-propionic acid methyl ester.
Solubility
Soluble in chloroform and methanol.
Notes
Incompatible with bases, oxidizing agents and reducing agents.
RUO – Research Use Only
General References:
- Wiese, S.; Esatbeyoglu, T.; Winterhalter, P.; Kruse, H. P.; Winkler, S.; Bub, A.; Kulling, S. E. Comparative biokinetics and metabolism of pure monomeric, dimeric, and polymeric flavan-3-ols: A randomized cross-over study in humans. Mol. Nutr. Food Res. 2015, 59 (4), 610-621.
- Margalef, M.; Pons, Z.; Bravo, F. I.; Muguerza, B.; Arola-Arnal, A. Plasma kinetics and microbial biotransformation of grape seed flavanols in rats. J. Funct. Foods 2015, 12, 478-488.