H52406
3-(4-Hydroxyphenyl)propionic acid
98%
Sinônimo(s):
3-(p-Hydroxyphenyl)propionic acid, Phloretic acid
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About This Item
Fórmula linear:
HOC6H4CH2CH2CO2H
Número CAS:
Peso molecular:
166.17
Beilstein:
2209841
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Nível de qualidade
Ensaio
98%
pf
129-131 °C (lit.)
fluorescência
λex 320 nm; λem 404 nm (buffer, pH 8.6)
cadeia de caracteres SMILES
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)
chave InChI
NMHMNPHRMNGLLB-UHFFFAOYSA-N
Aplicação
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.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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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)
Enhanced tissue adhesiveness of injectable gelatin hydrogels through dual catalytic activity of horseradish peroxidase.
Hoang T T T, et al.
Biopolymers, 109(1), e23077-e23077 (2018)
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
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)
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)
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