H50004

4-Hydroxyphenylacetic acid

Name: 4-Hydroxyphenylacetic acid
Brand: ALDRICH

98%

Synonym(s):

(4-Hydroxyphenyl)acetic acid, (p-Hydroxyphenyl)acetic acid, 2-(4′-Hydroxyphenyl)acetic acid, 2-[4-(Hydroxy)phenyl]acetic acid, 4-(Carboxymethyl)phenol, 4-Hydroxybenzeneacetic acid, 4′-Hydroxyphenylacetic acid, p-Hydroxybenzeneacetic acid

Select a Size

All Photos(1)

About This Item

Linear Formula:

HOC₆H₄CH₂CO₂H

CAS Number:

156-38-7

Molecular Weight:

152.15

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24895664

EC Number:

205-851-3

Beilstein/REAXYS Number:

1448766

MDL number:

MFCD00004347

Product Name

4-Hydroxyphenylacetic acid, 98%

SMILES string

OC(=O)Cc1ccc(O)cc1

InChI

1S/C8H8O3/c9-7-3-1-6(2-4-7)5-8(10)11/h1-4,9H,5H2,(H,10,11)

InChI key

XQXPVVBIMDBYFF-UHFFFAOYSA-N

assay

98%

mp

148-151 °C (lit.)

Quality Level

200

Looking for similar products? Visit Product Comparison Guide

Related Categories

Chemical Building Blocks

Chemistry & Biochemicals

Organic Building Blocks

Application

Reagent used in the acylation of phenols and amines.

General description

4-Hydroxyphenylacetic acid is a phenolic acid that is esterified with various alcohols to synthesize esters.

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Journal of the Chemical Society. Perkin Transactions 1, 3005-3005 (1991)

Characterization of negative tone photoresist based on acid catalyzed dehydration crosslinking of novolac resins having pendant carboxyl groups

Liu HH, et al.

Journal of Polymer Research, 9, 251-256 (2002)

Korean J. Med. Chem., 1, 2-2 (1991)

Processed foods drive intestinal barrier permeability and microvascular diseases.

Matthew Snelson et al.

Science advances, 7(14) (2021-04-02)

Intake of processed foods has increased markedly over the past decades, coinciding with increased microvascular diseases such as chronic kidney disease (CKD) and diabetes. Here, we show in rodent models that long-term consumption of a processed diet drives intestinal barrier

Competing pathways in the photo-Favorskii rearrangement and release of esters: studies on fluorinated p-hydroxyphenacyl-caged GABA and glutamate phototriggers.

Kenneth Stensrud et al.

The Journal of organic chemistry, 74(15), 5219-5227 (2009-07-04)

Three new trifluoromethylated p-hydroxyphenacyl (pHP)-caged gamma-aminobutyric acid (GABA) and glutamate (Glu) derivatives have been examined for their efficacy as photoremovable protecting groups in aqueous solution. Through the replacement of hydrogen with fluorine, e.g., a m-trifluoromethyl or a m-trifluoromethoxy versus m-methoxy

View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service