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Key Documents

H20059

Sigma-Aldrich

Acido 4-idrossibenzoico

ReagentPlus®, 99%

Sinonimo/i:

p-HBA, p-Hydroxybenzoic acid

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About This Item

Formula condensata:
HOC6H4CO2H
Numero CAS:
Peso molecolare:
138.12
Beilstein:
970950
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

Livello qualitativo

Nome Commerciale

ReagentPlus®

Saggio

99%

Punto di fusione

213-217 °C (lit.)

Solubilità

alcohol: freely soluble

Stringa SMILE

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)
FJKROLUGYXJWQN-UHFFFAOYSA-N

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Descrizione generale

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

Applicazioni

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.

Note legali

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

Pittogrammi

CorrosionExclamation mark

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

Eye Dam. 1 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves


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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)
2?Hydroxy?3, 5?diiodobenzoic Acid.
Woollett G H and Johnson W W
Organic Syntheses, 14, 52-52 (1943)
Behrooz Darbani
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L C Goudas et al.
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