3807-81-6

Basic information

• Product Name: 5-Nitro-1,2,3-benzenetricarboxylic acid
• Synonyms: 1-NITROBENZENE-3,4,5-TRICARBOXYLIC ACID;5-NITRO-1,2,3-BENZENETRICARBOXYLIC ACID;5-NITRO-BENZENE-1,2,3-TRICARBOXYLIC ACID;5-Nitro-1,2,3-nitroacetophenone
• CAS NO: 3807-81-6
• Molecular Formula: C₉H₅NO₈
• Molecular Weight: 255.14
• EINECS: 1312995-182-4
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
• Mol File: 3807-81-6.mol
• Article Data: 4

Chemical Properties

• Melting Point: 208 °C
• Boiling Point: 546.4 °C at 760 mmHg
• Flash Point: 240.4 °C
• Appearance: /
• Density: 1.837 g/cm₃
• Vapor Pressure: 8.97E-13mmHg at 25°C
• Refractive Index: 1.698
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 2.09±0.30(Predicted)
• CAS DataBase Reference: 5-Nitro-1,2,3-benzenetricarboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 5-Nitro-1,2,3-benzenetricarboxylic acid(3807-81-6)
• EPA Substance Registry System: 5-Nitro-1,2,3-benzenetricarboxylic acid(3807-81-6)

Safety Data

• Hazardous Substances Data: 3807-81-6(Hazardous Substances Data)

Usage

General Description

5-Nitro-1,2,3-benzenetricarboxylic acid, also known as nitrilotribenzoic acid, is a nitro-substituted aromatic compound derived from trimesic acid. Its chemical formula is C9H5NO8 and it is a yellow crystalline solid at room temperature. The presence of both carboxylic and nitro functional groups makes it a versatile chemical, with applications in the synthesis of dyes, pharmaceuticals, and coordination complexes. It is commonly used as a building block in organic synthesis and as a ligand in coordination chemistry, due to its ability to chelate metal ions. Additionally, its nitro group can be reduced to produce 1,2,3-benzenetricarboxylic acid, which has applications in the production of high-strength polymers. Overall, 5-Nitro-1,2,3-benzenetricarboxylic acid is a valuable chemical with a wide range of industrial and scientific uses.

InChI:InChI=1/C9H5NO8/c11-7(12)4-1-3(10(17)18)2-5(8(13)14)6(4)9(15)16/h1-2H,(H,11,12)(H,13,14)(H,15,16)

Upstream product

• 569-51-7 benzene-1,2,3-tricarboxlic acid 
• 526-73-8 1,2,3-trimethylbenzene 
• 16134-13-7 1-Hydroxy-3.5-diacetoxymethyl-7-nitro-1H-benzopyran-⁽²⁾ 
• 15999-91-4 Tri-K-Salz von Hemimellitsaeure 

Downstream Products

• 65537-83-9 5-Iodo-1,2,3-tris-trifluoromethyl-benzene 
• 65537-86-2 2-{(2-Hydroxy-ethyl)-[3-methyl-4-(3,4,5-tris-trifluoromethyl-phenylazo)-phenyl]-amino}-ethanol 
• 65537-85-1 Dimethyl-[4-(3,4,5-tris-trifluoromethyl-phenylazo)-phenyl]-amine 
• 65537-79-3 3,4,5-Tris-(trifluormethyl)-nitrobenzol 
• 1236108-27-2 3,4,5-tricarboxyl-(3′,4′,5′-tricarboxylazophenyl)benzene 

Relevant articles and documents

Preparing method for 5-iodine-1, 2, 3-benzenetricarboxylic acid

The invention relates to a preparing method for an organic iodine substituted compound, in particular to a preparing method for 5-iodine-1, 2, 3-benzenetricarboxylic acid. The preparing method includes the steps that firstly a reaction is performed when p

4-(Monoalkylamino) benzene polycarboxylic acids

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