935557

3-O-p-Coumaroylquinic acid

≥95%

• Synonym(s): 3-O-p-Coumaroylquinic acid, (1S,3R,4R,5R)-1,3,4-Trihydroxy-5-[[3-(4-hydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]cyclohexanecarboxylic acid,, 3-O-p-Coumarylquinic acid, Cinnamic acid, p-hydroxy-, 3-ester with 1,3,4,5-tetrahydroxycyclohexanecarboxylic acid, Cyclohexanecarboxylic acid, 1,3,4-trihydroxy-5-[[3-(4-hydroxyphenyl)-1-oxo-2-propen-1-yl]oxy]-, (1S,3R,4R,5R)
• Empirical Formula (Hill Notation): C₁₆H₁₈O₈
• CAS Number: 1899-30-5
• Molecular Weight: 338.31
• MDL number: MFCD00928770
• UNSPSC Code: 12352106
• NACRES: NA.21

Properties

• Quality Level: 100
• Assay: ≥95%
• form: solid
• color: white to light yellow
• bp: 613.2 °C
• density: 1.554 g/cm³
• storage temp.: 2-8°C
• SMILES string: O=C([C@]1(O)C[C@@H](O)[C@@H](O)[C@H](OC(/C=C/C2=CC=C(O)C=C2)=O)C1)O
• InChI: InChI=1S/C16H18O8/c17-10-4-1-9(2-5-10)3-6-13(19)24-12-8-16(23,15(21)22)7-11(18)14(12)20/h1-6,11-12,14,17-18,20,23H,7-8H2,(H,21,22)/t11-,12-,14-,16+/m1/s1
• InChI key: BMRSEYFENKXDIS-OTCYKTEZSA-N

Description

Application

A naturally occurring substance discovered in plants, which possesses antibacterial characteristics and may serve as a substitute for antibiotics in combatting opportunistic fungal infections.

Features and Benefits

The hypoglycemic effects of 3-p-Coumaroylquinic acid are attributed to its capacity to hinder glucose uptake in the intestines.

Safety Information

• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 3
• Flash Point(F): Not applicable
• Flash Point(C): Not applicable