87-66-1

  • Product Name:Pyrogallic Acid
  • Molecular Formula:C6H6O3
  • Purity:99%
  • Molecular Weight:126.112
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Product Details

pd_meltingpoint:43-47 °C(lit.)

Appearance:white crystalline solid

Factory Supply industrial standard Pyrogallic Acid 87-66-1 In Stock

  • Molecular Formula:C6H6O3
  • Molecular Weight:126.112
  • Appearance/Colour:white crystalline solid 
  • Vapor Pressure:10 mm Hg ( 167.7 °C) 
  • Melting Point:43-47 °C(lit.) 
  • Refractive Index:n20/D 1.387  
  • Boiling Point:309 °C at 760 mmHg 
  • PKA:pK1:9.03(0);pK2:11.63(+1) (25°C) 
  • Flash Point:164.4 °C 
  • PSA:60.69000 
  • Density:1.488 g/cm3 
  • LogP:0.80340 

Pyrogallol(Cas 87-66-1) Usage

Production Methods

Pyrogallol is prepared by heating dried gallic acid at about 200°C with the loss of carbon dioxide or by the chlorination of cyclohexanol to tetrachlorocyclohexanone, followed by hydrolysis.

Definition

ChEBI: A benzenetriol carrying hydroxy groups at positions 1, 2 and 3.

General Description

Odorless white to gray solid. Sinks and mixes with water.

Air & Water Reactions

Turns gray on exposure to light or air. Water soluble.

Reactivity Profile

Pyrogallol is a strong reducing agent. Reacts with alkalis, NH3, antipyrine, camphor, phenol, iron and lead salts, iodine, lime water, menthol and KMnO4.

Hazard

Toxic by ingestion and skin absorption.

Health Hazard

The toxic symptoms are similar to those of phenol. It can enter the body by absorption through skin and ingestion. The poisoning effects are nausea, vomiting, gastritis, hemolysis, methemoglobinemia, kidney and liver damage, convulsions, and congestion of lungs. High doses can cause death. Ingestion of 2–3 g of solid can be fatal to humans. The LD50 values varied widely in species. The oral LD50 value in mice is about 300 mg/kg.

Fire Hazard

Pyrogallol is probably combustible.

Contact allergens

Pyrogallol belongs to the phenols group. It is an old photograph developer and a low sensitizer in hair dyes.

Biochem/physiol Actions

Pyrogallol also referred to as 1,2,3-trihydroxybenzene inhibits the response to nitric oxide (NO) in the rat anococcygeus muscle.

Safety Profile

Human poison by ingestion and subcutaneous routes. An experimental poison by ingestion, subcutaneous, intravenous, and intraperitoneal routes. Experimental teratogenic and reproductive effects. Questionable carcinogen with experimental tumorigenic data. Mutation data reported. 1 198 PPRSOO PYROSULFURYL CHLORIDE Readdy absorbed through the skin. Human systemic effects by ingestion: convulsions, dyspnea, gastrointestinal effects. A severe skin and eye irritant. Incompatible with alkalies, NH3, antipyrine, phenol, iron and lead salts, iodine, KMn04. When heated to decomposition it emits acrid smoke and irritating fumes. Used as a topical antibacterial agent, as an intermediate, hair dye component, and analytical reagent.

Carcinogenicity

Pyrogallol was not carcinogenic in mouse and rabbit chronic dermal studies. Mice were treated twice weekly with pyrogallol in acetone (50%) on the shaved flank for life. There was no increase in dermal or systemic tumors. A similar study in rabbits also revealed no skin tumors, although positive controls showed an increase in tumors in both mice and rabbits. Pyrogallol was considered to be cocarcinogenic when administered dermally three times a week together with the skin carcinogen benzo[a]pyrene for 440 days; pyrogallol administered alone caused no increase in skin tumors.

InChI:InChI=1/C6H6O3/c7-4-2-1-3-5(8)6(4)9/h1-3,7-9H

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87-66-1 Process route

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1,2,4-Trihydroxybenzene

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Conditions
Conditions Yield
With sodium chloride; at 340 ℃; for 1h; Yield given;
With sodium chloride; at 340 ℃; for 1h; Yield given. Further byproducts given. Yields of byproduct given;
With sodium chloride; at 315 ℃; for 2h; Yield given. Further byproducts given. Yields of byproduct given;
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1,2,4-Trihydroxybenzene

hydroxy-2-propanone
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hydroxy-2-propanone

levoglucosan
498-07-7

levoglucosan

2-hydroxyresorcinol
87-66-1

2-hydroxyresorcinol

Conditions
Conditions Yield
With sodium chloride; at 340 ℃; for 1h; Yield given. Further byproducts given. Yields of byproduct given;

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