4-Hydroxybenzoic acid, 99%
4-Hydroxybenzoic acid, 99%
4-Hydroxybenzoic acid, 99%
4-Hydroxybenzoic acid, 99%
Thermo Scientific Chemicals

4-Hydroxybenzoic acid, 99%

CAS: 99-96-7 | C7H6O3 | 138.12 g/mol
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Catalog number A13700.0I
also known as A13700-0I
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Quantity:
5000 g
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Price (USD)
339.00
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Chemical Identifiers
CAS99-96-7
IUPAC Name4-hydroxybenzoic acid
Molecular FormulaC7H6O3
InChI KeyFJKROLUGYXJWQN-UHFFFAOYSA-N
SMILESOC(=O)C1=CC=C(O)C=C1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)White
FormPowder
Assay (Aqueous acid-base Titration)≥98.5 to ≤101.5% (non-U.S. sourced material)
Assay (Silylated GC)≥98.5% (non-U.S. sourced material)
Assay from Supplier's CofA≥98.5 (U.S. sourced material)
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This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Suitable for battery materials development.

Applications
4-Hydroxybenzoic acid is used as an intermediate for dyes, antiseptics and active pharmaceutical ingredients. It is also used as a food preservative, corrosion inhibitor, anti-oxidant and an emulsifier. It reacts with 6-hydroxynaphthalene-2-carboxylic acid to prepare aromatic polyester called Vectran fiber. It acts as a precursor to prepare p-hydroxyphenylbenzoate, p-acetoxybenzoyl chloride and 4,4′-dihydroxybenzophenone. Further, it is used in paint additives, coating additives, processing aids, electrical and electronic products. In addition to this, it acts as a preservative in cosmetics and some ophthalmic solutions.

Solubility
Soluble in water, alcohol, ethanol, ether, n-butanol and acetone. Slightly soluble in chloroform. Insoluble in carbon disulfide.

Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Froissard, D.; Rapior, S.; Bessiere, J. M.; Buatois, B.; Fruchier, A.; Sol, V.; Fons, F. Asplenioideae Species as a Reservoir of Volatile Organic Compounds with Potential Therapeutic Properties. Nat. Prod. Commun. 2015, 10 (6), 1079-1083.
  2. Albarran, G.; Esparza, M.; Mendoza, E. Oxidation of hydroxybenzoic acids by ∙OH radical produced radiolytically. Radiat. Phys. Chem. 2015, 107, 109-114.