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H20059

Sigma-Aldrich

4-Hydroxybenzoic acid

ReagentPlus®, 99%

Synonym(s):

p-HBA, p-Hydroxybenzoic acid

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About This Item

Linear Formula:
HOC6H4CO2H
CAS Number:
99-96-7
Molecular Weight:
138.12
Beilstein:
970950
EC Number:
202-804-9
MDL number:
MFCD00002547
UNSPSC Code:
12352100
PubChem Substance ID:
24895495
NACRES:
NA.22

product line

ReagentPlus®

Assay

99%

mp

213-217 °C (lit.)

solubility

alcohol: freely soluble

SMILES string

OC(=O)c1ccc(O)cc1

InChI

1S/C7H6O3/c8-6-3-1-5(2-4-6)7(9)10/h1-4,8H,(H,9,10)

InChI key

FJKROLUGYXJWQN-UHFFFAOYSA-N

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General description

4-Hydroxybenzoic acid (PHBA) is a phenolic derivative of benzoic acid, used as a building block in polymer synthesis.

Application

4-Hydroxybenzoic acid can be used as a starting material to synthesize organic intermediates such as 4-acetoxybenzoic acid and 4-hydroxy-3,5-diiodobenzoic acid.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H318,H335

Hazard Classifications

Eye Dam. 1 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

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’.

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2?Hydroxy?3, 5?diiodobenzoic Acid.
Woollett G H and Johnson W W
Organic Syntheses, 14, 52-52 (1943)
Formation of novel polymeric films derived from 4-hydroxybenzoic acid
Ferreira L, et al.
Materials Chemistry and Physics, 129, 46-52 (2011)
Esterification of Carboxylic Acids with Trialkyloxonium Salts: Ethyl and Methyl 4?Acetoxybenzoates: Benzoic acid, 4?(acetyloxy)?, ethyl and methyl esters.
Douglas J, et al.
Organic Syntheses, 56, 59-59 (1977)
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