1099-02-1

Basic information

• Product Name: N,N,N',N'-1,4-PHENYLENEDIAMINETETRAACETIC ACID
• Synonyms: LABOTEST-BB LT00455236;N,N,N',N'-1,4-PHENYLENEDIAMINETETRAACETIC ACID
• CAS NO: 1099-02-1
• Molecular Formula: C14H16N2O8
• Molecular Weight: 340.29
• Mol File: 1099-02-1.mol
• Article Data: 3

Chemical Properties

• Melting Point: 205°C (dec.)
• Boiling Point: 744.2°Cat760mmHg
• Flash Point: 403.9°C
• Appearance: /
• Density: 1.62g/cm³
• PKA: 1.68±0.10(Predicted)
• BRN: 2823470
• CAS DataBase Reference: N,N,N',N'-1,4-PHENYLENEDIAMINETETRAACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: N,N,N',N'-1,4-PHENYLENEDIAMINETETRAACETIC ACID(1099-02-1)
• EPA Substance Registry System: N,N,N',N'-1,4-PHENYLENEDIAMINETETRAACETIC ACID(1099-02-1)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36
• Hazardous Substances Data: 1099-02-1(Hazardous Substances Data)

Usage

General Description

N,N,N',N'-1,4-Phenylenediaminetetraacetic Acid (PDTA) is a complexing agent that forms highly stable complexes with most metal ions. This organic chemical compound is structurally similar to Ethylenediaminetetraacetic acid (EDTA) with two benzene rings. It's not naturally occurring, thus, it's synthetically produced for use in various industrial applications, which include agriculture, water treatment, and cleaning products. Its high chelation ability is utilized for removing heavy metals and minerals from solutions. However, exposure to this chemical at high rates can be harmful to health and the environment, primarily due to its non-biodegradable characteristic.

Upstream product

• 3926-62-3 sodium monochloroacetic acid 
• 106-50-3 1,4-phenylenediamine 
• 64-69-7 Iodoacetic acid 

Downstream Products

• 780738-83-2 Mn⁽²⁺⁾*C₁₄H₁₂N₂O₈^(4-)=Mn(C₁₄H₁₂N₂O₈)^(2-) 

Relevant articles and documents

Formation of a one-dimensional water chain containing two linking patterns of planar water tetra-mers

The self-assembly of the title dinuclear complex, namely (-p-phenyl-enediamine-N,N,N′,N′-tetra-acetato)bis-[aqua-(1, 10-phenanthroline)nickel(II)] dodecahydrate, [Ni2(C14H12N2O8)(C12H8N2)2(H2O)2] ·12H2O, through intricate noncovalent inter-actions results in a two-dimensional sheet-like structure. The dimer lies about an inversion centre at the centre of the p-phenylenediamine ring. Uncoordinated water mol-ecules form one-dimensional chains in which cyclic water tetra-mers act as two types of building blocks. The water mol-ecules play a significant role in the stabilization of the three-dimensional supra-molecular framework. Intra-molecular aryl-metal chelate ring π-π inter-actions are also observed. International Union of Crystallography 2007.

Electrochemical assay method and novel p-phenylenediamine compound

An enzyme electrode, specific binding or the like electrochemical assay method capable of performing always stably high detection sensitivity (responsibility) and reappearance even in the case of blood, urine and the like samples that contain interfering