- Product Details
Keywords
- 2,6-Diaminopyridine
- 2,6-diamino-pyridin
- pyridine-2,6-diyldiamine
Quick Details
- ProName: 2,6-Diaminopyridine
- CasNo: 141-86-6
- Molecular Formula: C5H7N3
- Appearance: Off white crystalline powder
- Application: Pharmaceutical and Cosmetic
- DeliveryTime: in 5 days
- PackAge: 1kg/Box, 25kg/Drum
- Port: Any port of China
- ProductionCapacity: 100 Kilogram/Month
- Purity: 98%
- Storage: Requires a sealed container and keep d...
- Transportation: By Sea/Air/Courier
- LimitNum: 5 Kilogram
- Loss on Drying: 0.16%
- Water Content: 0.18%
- Sulphated Ash: 0.01%
- Melting Range: 120℃ ~ 121℃
Superiority
Wuhan Fortuna Chemical Co.,Ltd is a professional integrative chemical enterprise with 18 years exporting experience,which is being engaged in Pharmaceutical and its intermediates, Food and Feed additives, Fine chemicals.
Details
2,6-Diaminopyridine is an organic compound with the molecular formula C?H?N?. Here's a detailed overview:
Chemical Structure
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It consists of a pyridine ring (a six-membered aromatic ring with one nitrogen atom) substituted with two amine groups (-NH?) at the 2 and 6 positions relative to the nitrogen (position 1). This arrangement gives the molecule symmetry, with the amines positioned opposite each other across the ring.
Physical Properties
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Appearance: Typically a white to off-white crystalline solid.
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Solubility: Moderately soluble in water due to hydrogen bonding from the amine groups. More soluble in polar organic solvents (e.g., ethanol, DMSO).
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Melting Point: Exact values vary, but it is solid at room temperature.
Synthesis
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Prepared via nitration of pyridine derivatives followed by reduction, or through direct amination using reagents like ammonia under controlled conditions. Specific methods depend on the desired substitution pattern.
Applications
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Pharmaceuticals:
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Acts as a precursor in synthesizing drugs, particularly those targeting neurological conditions (e.g., analogues of 4-aminopyridine used in multiple sclerosis).
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Coordination Chemistry:
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Serves as a chelating ligand for metal ions (e.g., Cu²?, Fe³?), leveraging its pyridine nitrogen and amine groups to form stable complexes.
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Materials Science:
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Used in polymers, dendrimers, or supramolecular assemblies due to its ability to participate in hydrogen bonding and crosslinking.
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Agrochemicals and Dyes:
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Intermediate in the synthesis of herbicides, insecticides, or colorants.
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Safety and Handling
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Toxicity: May be harmful if inhaled, ingested, or absorbed through the skin. Causes irritation to eyes, skin, and respiratory system.
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Precautions: Use protective equipment (gloves, goggles) and work in a well-ventilated area. Proper disposal is essential to avoid environmental contamination.
Key Features
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Combines aromaticity with nucleophilic amine groups, making it reactive in electrophilic substitution and metal coordination.
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Symmetrical structure enhances its utility in creating ordered molecular architectures.
This compound bridges organic synthesis, medicinal chemistry, and materials science, highlighting its versatility in research and industrial applications.