Picric acid: Difference between revisions

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== Description ==
== Description ==


A yellow acid dye.  Picric acid was prepared in 1771 by Woulfe by treating [[indigo|indigo]] with [[nitric%20acid|nitric acid]].  It was first used as a textile dye for [[wool|wool]] and [[silk|silk]].  Picric acid has poor washfastness and is explosive.  As a textile colorant, it was replaced by naphthol dyes by the late 1800s. However, it was still used as an explosive until it was replaced by the less powerful, but safer, trinitrotoluene (TNT) in 1902.
A yellow acid dye that was prepared in 1771 by Woulfe by treating [[indigo|indigo]] with [[nitric%20acid|nitric acid]].  Picric acid had early use as a textile dye for [[wool|wool]] and [[silk|silk]].  It was quickly learned that picric acid had poor washfastness and was explosive.  As a textile colorant, it was replaced by naphthol dyes by the late 1800s. However, it was still used as an explosive until it was replaced by the less powerful, but safer, trinitrotoluene (TNT) in 1902.


== Synonyms and Related Terms ==
== Synonyms and Related Terms ==


2,4,6-trinitrophenol; CI 10305; carbazitic acid; picronitric acid; melinite; acide picrique (Fr.); ácido pícrico (Esp., Port.)
2,4,6-trinitrophenol; CI 10305; acide picrique (Fr.); ácido pícrico (Esp., Port.); 1,3,5-trinitrophenol; TNP; carbozitic acid; carbozotic acid; picronitric acid; phenol trinitrate; Melinite


== Risks ==
== Risks ==


* Flammable solid.  Flash point = 150 C.  Explosive at 300C.   
* Flammable solid.  Flash point = 150 C.  Explosive at 300C.   
* Harmful by ingestion, inhalation, and skin absorption.
* Harmful by ingestion, inhalation, and skin absorption.  
* Keep away from metals as metal salts are more sensitive to explosion.
* Fisher Scientific: [https://www.fishersci.com/store/msds?partNumber=SP9200100&productDescription=PICRIC+ACID%2C+SAT%2C+100ML&vendorId=VN00006705&countryCode=US&language=en SDS]
* Fisher Scientific: [https://www.fishersci.com/store/msds?partNumber=SP9200100&productDescription=PICRIC+ACID%2C+SAT%2C+100ML&vendorId=VN00006705&countryCode=US&language=en SDS]


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* Composition = C6H3(NO2)3O (mol. wt. = 229.11 g/ml)
* Composition = C6H3(NO2)3O (mol. wt. = 229.11 g/ml)
* CAS = 88-89-1
* CAS = 88-89-1
* Melting Point = 122 C
* Melting Point = 122 C (burns after melting with a sooty flame and characteristic whistling noise)
* Density 1.77 g/ml
* Density 1.77 g/ml



Latest revision as of 11:00, 25 April 2026

Description

A yellow acid dye that was prepared in 1771 by Woulfe by treating indigo with nitric acid. Picric acid had early use as a textile dye for wool and silk. It was quickly learned that picric acid had poor washfastness and was explosive. As a textile colorant, it was replaced by naphthol dyes by the late 1800s. However, it was still used as an explosive until it was replaced by the less powerful, but safer, trinitrotoluene (TNT) in 1902.

Synonyms and Related Terms

2,4,6-trinitrophenol; CI 10305; acide picrique (Fr.); ácido pícrico (Esp., Port.); 1,3,5-trinitrophenol; TNP; carbozitic acid; carbozotic acid; picronitric acid; phenol trinitrate; Melinite

Risks

  • Flammable solid. Flash point = 150 C. Explosive at 300C.
  • Harmful by ingestion, inhalation, and skin absorption.
  • Keep away from metals as metal salts are more sensitive to explosion.
  • Fisher Scientific: SDS

Physical and Chemical Properties

  • Soluble in water, ethanol, ether
  • Composition = C6H3(NO2)3O (mol. wt. = 229.11 g/ml)
  • CAS = 88-89-1
  • Melting Point = 122 C (burns after melting with a sooty flame and characteristic whistling noise)
  • Density 1.77 g/ml

Resources and Citations

  • A.Scharff, "Synthetic dyestuffs for textiles and their fastness to washing" in ICOM Preprints, Lyon, 1999. p.654-660.
  • Wikipedia: Picric acid Accessed April 2026