All Photos(1)

Documents

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

Sign Into View Organizational & Contract Pricing

All Photos(1)

About This Item

Linear Formula:

HOC₆H₄CH₂CO₂H

CAS Number:

156-38-7

Molecular Weight:

152.15

Beilstein:

1448766

EC Number:

205-851-3

MDL number:

MFCD00004347

UNSPSC Code:

12352100

PubChem Substance ID:

24895664

NACRES:

NA.22

Quality Level

200

Assay

98%

mp

148-151 °C (lit.)

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

Looking for similar products? Visit Product Comparison Guide

Related Categories

Organic Building Blocks

General description

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

Application

Reagent used in the acylation of phenols and amines.

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Precautionary Statements

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

Hazard Classifications

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

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

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)

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

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

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