Description

N(1),N(6)-Bis(2,3-Dihydroxybenzoyl)-1,6-Diaminohexane is a specialized synthetic compound featuring a hexamethylene diamine core symmetrically functionalized with catechol-derived benzoyl groups. This molecular architecture makes it a highly effective metal-chelating agent, particularly for iron(III), offering superior binding affinity and selectivity. It is primarily utilized in advanced research and industrial applications where precise control of metal ion concentration and speciation is critical. The compound's unique structure provides a versatile platform for developing novel materials and biochemical tools.

Application

• Research Chemical for Siderophore Studies: Serves as a model compound or synthetic analog of natural siderophores for investigating microbial iron acquisition and transport mechanisms.
• Metal Chelation & Sequestration: Used in laboratory and industrial processes to selectively bind and remove transition metal ions, especially iron, from solutions to prevent catalysis of unwanted oxidation reactions.
• Pharmaceutical Intermediate: Potential building block for the synthesis of novel therapeutic agents targeting iron metabolism, such as chelation therapy drugs or antimicrobials.
• Analytical Chemistry Reagent: Employed as a chromogenic or fluorogenic agent in the development of sensitive and selective sensors or assays for the detection of specific metal ions.
• Material Science Precursor: Utilized in the synthesis of functional polymers, coatings, or nanocomposites where integrated catechol groups can provide adhesive, antioxidant, or metal-binding properties.
• Agricultural & Nutritional Research: Investigated for its potential role in plant iron nutrition or as a component in specialized nutrient delivery systems.

Basic Information

Product Name	N(1),N(6)-Bis(2,3-Dihydroxybenzoyl)-1,6-Diaminohexane
CAS No.	73630-99-6
Molecular Formula	C20H24N2O6
Molecular Weight	388.42 g/mol
Synonyms	1,6-Hexanediamine, N,N'-bis(2,3-dihydroxybenzoyl)-; N,N'-Bis(2,3-dihydroxybenzoyl)-1,6-hexanediamine; 2,3-Dihydroxy-N-[6-[(2,3-dihydroxybenzoyl)amino]hexyl]benzamide; 1,6-Bis(2,3-dihydroxybenzamido)hexane; Catecholamide-based hexadentate chelator; Synthetic Catecholamide Siderophore Analog; Iron(III) Chelator 73630-99-6
EINECS	Contact for details

Quality Control

Our N(1),N(6)-Bis(2,3-Dihydroxybenzoyl)-1,6-Diaminohexane is manufactured under controlled conditions to ensure batch-to-batch consistency and high purity. Each lot undergoes rigorous analytical testing, including HPLC for purity assessment and spectroscopic methods for structural confirmation. We provide comprehensive Certificates of Analysis (COA) detailing all relevant specifications, ensuring the material meets the stringent requirements of research and development applications. Custom synthesis and purification to meet specific project criteria are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its light-sensitive and easily oxidized nature, prolonged exposure to light, air, or elevated temperatures should be avoided. For long-term storage, consider maintaining the product under an inert atmosphere such as argon or nitrogen.

Specification

Item	Specification
Appearance	Off-white to light tan powder
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 95.0%
Loss on Drying	≤ 2.0%
Residue on Ignition	≤ 0.5%
Heavy Metals (as Pb)	≤ 20 ppm
Iron (Fe) Content	≤ 50 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.