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Merck

H52406

Sigma-Aldrich

3-(4-Hydroxyphenyl)propionic acid

98%

Sinónimos:

3-(p-Hydroxyphenyl)propionic acid, Phloretic acid

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About This Item

Fórmula lineal:
HOC6H4CH2CH2CO2H
Número de CAS:
Peso molecular:
166.17
Beilstein/REAXYS Number:
2209841
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

mp

129-131 °C (lit.)

fluorescence

λex 320 nm; λem 404 nm (buffer, pH 8.6)

SMILES string

OC(=O)CCc1ccc(O)cc1

InChI

1S/C9H10O3/c10-8-4-1-7(2-5-8)3-6-9(11)12/h1-2,4-5,10H,3,6H2,(H,11,12)

InChI key

NMHMNPHRMNGLLB-UHFFFAOYSA-N

Application

3-(4-Hydroxyphenyl)propionic acid can be used:
  • To derive hydrogel based on chitosan, gelatin or poly(ethylene glycol).
  • To synthesize novel symmetric and asymmetric bolaamphiphiles.
  • As an acyl donor for the enzymatic synthesis of sugar alcohol esters.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Biocatalytic acylation of sugar alcohols by 3-(4-hydroxyphenyl) propionic acid.
Croitoru R, et al.
Process Biochemistry (Oxford, United Kingdom), 47(12), 1894-1902 (2012)
Efficient syntheses of bolaform surfactants from L-rhamnose and/or 3-(4-hydroxyphenyl) propionic acid.
Akong F O and Bouquillon S
Green Chemistry, 17(6), 3290-3300 (2015)
Seon-Min Jeon et al.
Translational research : the journal of laboratory and clinical medicine, 149(1), 15-21 (2007-01-02)
This study was conducted to compare the hypocholesterolemic and antioxidant effects of naringenin (0.02%), and its metabolites, rho-hyproxyphenylpropionic acid (PHPP, 0.012%) and rho-hydroxybenzoic acid (PHB, 0.012%), in 1% cholesterol diet-fed rats. All supplements significantly lowered the plasma total-cholesterol (total-C), triglyceride
Tailorable cell culture platforms from enzymatically cross-linked multifunctional poly (ethylene glycol)-based hydrogels.
Menzies D J, et al.
Biomacromolecules, 14(2), 413-423 (2013)
Eliana Capecchi et al.
Nanomaterials (Basel, Switzerland), 8(6) (2018-06-20)
Sustainable catalysts for the oxidation of phenol derivatives under environmentally friendly conditions were prepared by the functionalization of lignin nanoparticles with tyrosinase. Lignin, the most abundant polyphenol in nature, is the main byproduct in the pulp and paper manufacturing industry

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