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ChemicalBook > Product Catalogue >Organic Chemistry >Carboxylic acids and derivatives >2-(4-Hydroxybenzoyl)benzoic acid

2-(4-Hydroxybenzoyl)benzoic acid

2-(4-Hydroxybenzoyl)benzoic acid Structure
  • ₹0
  • Product name: 2-(4-Hydroxybenzoyl)benzoic acid
  • CAS: 85-57-4
  • MF: C14H10O4
  • MW: 242.23
  • EINECS:201-616-4
  • MDL Number:MFCD00016507
  • Synonyms:2-(4-hydroxybenzoyl)-benzoicaci ;o-(p-hydroxybenzoyl)-benzoicaci ;o-(p-hydroxybenzoyl)benzoicacid ;phthaleinacid ;2-(P-HYDROXYBENZOYL)BENZOIC AC ID;AKOS B028764;2-(4-HYDROXYBENZOYL)BENZOIC ACID;2-(4-hydroxybenzoyI)benzoic acid
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Properties

Melting point :213 °C
Boiling point :512.6±35.0 °C(Predicted)
Density :1.356±0.06 g/cm3(Predicted)
storage temp. :Inert atmosphere,Room Temperature
form :Powder
pka :3.35±0.36(Predicted)
CAS DataBase Reference :85-57-4(CAS DataBase Reference)
EPA Substance Registry System :2-(4-Hydroxybenzoyl)benzoic acid (85-57-4)

Safety Information

Symbol(GHS): GHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H315 Causes skin irritation Skin corrosion/irritation Category 2 Warning GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 Causes serious eye irritation Serious eye damage/eye irritation Category 2A Warning GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 May cause respiratory irritation Specific target organ toxicity, single exposure;Respiratory tract irritation Category 3 Warning GHS hazard pictograms
Precautionary statements:
P261 Avoid breathing dust/fume/gas/mist/vapours/spray.
P271 Use only outdoors or in a well-ventilated area.
P280 Wear protective gloves/protective clothing/eye protection/face protection.

Description

2-(4-Hydroxybenzoyl)benzoic acid is a white crystalline powder. It is sparingly soluble in water but soluble in organic solvents like ethanol and acetone. The compound has a melting point range of approximately 245-250 ℃. The synthesis of 2-(4-Hydroxybenzoyl)benzoic acid involves the reaction of 4-hydroxybenzoic acid (also known as p-hydroxybenzoic acid) with benzoyl chloride or benzoyl anhydride. The reaction occurs through an acylation process where the benzoyl group is added to the benzene ring of the 4-hydroxybenzoic acid. This compound has potential applications in various fields, including pharmaceuticals and materials science. It can serve as a building block for synthesising other organic compounds or as a starting material for preparing pharmaceutical intermediates. Additionally, it may exhibit certain properties that make it useful in developing materials or coatings.

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