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Sigma-Aldrich

Picric acid

moistened with water, ≥98%

Synonyme(s) :

2,4,6-Trinitrophenol, PA

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About This Item

Formule linéaire :
(O2N)3C6H2OH
Numéro CAS:
88-89-1
Poids moléculaire :
229.10
Numéro C.I. (Colour Index):
10305
Numéro Beilstein :
423400
Numéro MDL:
MFCD00007102
Code UNSPSC :
12352100
ID de substance PubChem :
57647805

Densité de vapeur

7.9 (vs air)

Niveau de qualité

200

Pression de vapeur

1 mmHg ( 195 °C)

Pureté

≥98%

Forme

powder or crystals (with a top layer of Liquid)

Contient

≥35% water

Limite d'explosivité

0.01 %

Pf

122-123 °C (dried material) (lit.)

Solubilité

alcohol: 1 (g/12 mL)(lit.)
benzene: 1 g/10 mL
chloroform: 1 (g/35 mL)
diethyl ether: 1 (g/65 mL)

Densité

1.763 g/cm3

Chaîne SMILES 

Oc1c(cc(cc1[N+]([O-])=O)[N+]([O-])=O)[N+]([O-])=O

InChI

1S/C6H3N3O7/c10-6-4(8(13)14)1-3(7(11)12)2-5(6)9(15)16/h1-2,10H

Clé InChI

OXNIZHLAWKMVMX-UHFFFAOYSA-N

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Description générale

Picric acid (PA, 2,4,6-trinitrophenol) is a polynitrated aromatic acid. It is strongly acidic in nature. Since it readily dissolves in water, it can easily pollute the environment on exposure. Sensitive detection of PA by tris-imidazolium salt, fluorescent [3+2] self-assembled nanoscopic organic cage and rhodamine based sensors have been reported. It is widely used for the determination of various organic compounds by spectrophotometric and extractive spectrophotometric methods.

Application

Picric acid has been used in the preparation of Bouin′s fixative and picric acid/sodium azide/multi-walled carbon nanotubes.
Picric acid was used in the quantitative determination of bisoprolol.

Pictogrammes

FlameSkull and crossbones
GHS02,GHS06

Mention d'avertissement

Danger

Mentions de danger

H206,H302,H311 + H331

Classification des risques

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Desen. Expl. 1

Code de la classe de stockage

4.1A - Other explosive hazardous materials

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

302.0 °F - closed cup

Point d'éclair (°C)

150 °C - closed cup

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Mario Sanhueza et al.
Journal of visualized experiments : JoVE, (111)(111), doi:10-doi:10 (2016-05-24)
Most studies on morphogenesis rely on qualitative descriptions of how anatomical traits are affected by the disruption of specific genes and genetic pathways. Quantitative descriptions are rarely performed, although genetic manipulations produce a range of phenotypic effects and variations are
Bijan Roy et al.
The Journal of organic chemistry, 78(3), 1306-1310 (2013-01-12)
Two new anthracene-functionalized fluorescent tris-imidazolium salts have been synthesized, characterized, and proven to be selective sensors for picric acid, which is a common constituent of many powerful explosives. Theoretical studies revealed an unusual ground-state electron transfer from picrate anion to
Koushik Acharyya et al.
Chemical communications (Cambridge, England), 50(99), 15788-15791 (2014-11-06)
Dynamic covalent imine chemistry has been utilized to synthesize a fluorescent [3+2] self-assembled nanoscopic organic cage. The fluorescent nature of the reduced analogue of the cage was further exploited for the highly selective detection of the explosive picric acid (PA).
Alina-Diana Panainte et al.
Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi, 117(2), 520-524 (2013-12-18)
Bisoprolol is a drug belonging to beta blockers drugs used primarily for the treatment of cardiovascular diseases. A spectrophotometric method for quantitative determination of bisoprolol was developed based on the formation of a complex combination between bisoprolol and picric acid.
Rhodamine based selective turn-on sensing of picric acid.
Sivaraman G, et al.
Royal Society of Chemistry Advances, 4(58), 30828-30831 (2014)
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