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6,6'-Dithiodinicotinic Acid

    • Product Name 6,6'-Dithiodinicotinic Acid
    • Alias DTNA
    • Einecs 236-948-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    941835

    Cas Number 3416-14-2
    Molecular Formula C12H6N2O4S2
    Molecular Weight 322.32
    Appearance Off-white to yellow powder
    Purity Typically ≥98%
    Melting Point Approximately 260-263°C (decomposition)
    Solubility Slightly soluble in water, soluble in DMSO and DMF
    Synonyms 6,6'-Dithiodinicotinic acid; DTNA
    Storage Temperature Store at 2-8°C, protected from light
    Chemical Structure Disulfide-linked nicotinic acid dimer
    Inchikey VFWBINTDSIWFOT-UHFFFAOYSA-N
    Smiles C1=CC(=NC=C1C(=O)O)SSc2cccc(n2)C(=O)O

    As an accredited 6,6'-Dithiodinicotinic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g of 6,6'-Dithiodinicotinic Acid comes sealed in an amber glass bottle with a secure, chemical-resistant screw cap for safety.
    Shipping 6,6'-Dithiodinicotinic Acid is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. It is transported according to relevant regulations for hazardous materials, ensuring proper labeling and documentation. The chemical is stored in a cool, dry place, shielded from light and incompatible substances during transit to maintain stability and safety.
    Storage 6,6'-Dithiodinicotinic Acid should be stored in a cool, dry, and well-ventilated area, away from incompatible materials such as strong oxidizing agents. Keep the container tightly closed and protected from light and moisture. Store at room temperature, preferably in a chemical storage cabinet, and ensure proper labeling to avoid accidental misuse. Handle with appropriate personal protective equipment.
    Application of 6,6'-Dithiodinicotinic Acid

    Applications of 6,6'-Dithiodinicotinic Acid in Industrial Manufacturing

    6,6'-Dithiodinicotinic Acid serves key roles in several specialty chemical sectors that demand advanced molecular structures with sulfur linkages and nitrogen heterocycles. Our production expertise ensures consistent quality for high-performance applications in organic synthesis, electronic materials, and polymer modification. Below are core industrial scenarios where customers regularly integrate our material into their workflows.

    1. Pharmaceutical Intermediate for Thiolated Drug API Synthesis

    Multinational and regional pharmaceutical firms use 6,6'-Dithiodinicotinic Acid as a building block in advanced active pharmaceutical ingredient (API) synthesis, particularly for thiolated heterocyclic drugs. Its disulfide bond supports the construction of molecular scaffolds found in enzyme inhibitors, antitumor agents, and redox-active drug candidates. Integrators introduce this material during protected intermediate steps ahead of final deprotection and salt formation. Strict analytical controls validate sulfur content and ensure reaction completion before moving to purification and crystallization.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP-NF and Ph. Eur. monographs where applicable
    • FDA cGMP 21 CFR Part 210/211
    • Chinese Pharmacopoeia (ChP) standards for intermediates

    Typical usage ratio

    • 0.2–1.5 molar equivalents in coupling steps, adjusted per reaction scale and target moiety
    • Excess levels (up to 2 eq) for reactions requiring complete disulfide linkage transfer

    Downstream process integration

    • Entry at the condensation or cyclization stage of multi-step organic syntheses
    • Separate charging under inert atmosphere; temperature controlled addition
    • Subsequent extraction, filtration, and solvent exchange after reaction

    Final product types

    • Thio-nicotinate-based APIs
    • Enzyme modulator pharmaceuticals with disulfide bridges
    • Intermediates for heterocyclic drug families
    • Contract-manufactured custom drug scaffolds

    2. Advanced Ligand Synthesis for Metal Chelation in Catalysis

    Process chemistry teams in catalyst manufacturing and fine chemical engineering specify 6,6'-Dithiodinicotinic Acid as a precursor for designing specialty ligands. Its molecular structure allows precise chelation with transition metals such as palladium, platinum, and ruthenium. Plant operators perform ligand synthesis parallel to transition metal incorporation, where the acid group coordinates with the metal center — forming stable catalysts used in C–C and C–N bond formation. This enables batch and continuous flow processes demanding dependable ligand supply.

    Industry compliance standards

    • EU REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals)
    • ISO 9001:2015 certified production for catalyst intermediates
    • OSHA Hazard Communication Standard for chemical handling

    Typical usage ratio

    • 0.8–1.2 eq. to metal content, tunable per chelation efficiency targets
    • Adjusted based on metal type and process batch size

    Downstream process integration

    • Initial dissolution in organic or aqueous solvent; pH control for ligand activation
    • Combining with metal salt precursor under controlled agitation
    • Purification via crystallization or solvent stripping to yield the chelated ligand complex

    Final product types

    • Homogeneous and heterogeneous transition metal catalysts
    • Organometallic complexes for cross-coupling reactions
    • Special-purpose chelating agents for hydrometallurgy
    • Custom ligand systems for R&D pilot reactors

    3. Functional Polymer Modifier in High-Performance Materials

    Producers of engineering plastics and electronic resins deploy 6,6'-Dithiodinicotinic Acid as a functional cross-linking agent or chain modifier. Its disulfide group imparts tunable reactivity, enabling end-group modification and polymer backbone integration. The material enters melt compounding and solution polymerization steps, where quality teams monitor dispersion and covalent bond formation. The product advances mechanical resilience, thermal stability, and electrical conductivity in specialty resins.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances Directive) for electronics materials
    • UL 94 (flammability rating for plastics)
    • ISO 9001-certified polymer production lines
    • EN 60216 (Polymer thermal endurance testing)

    Typical usage ratio

    • 0.1–2 wt% as a cross-linker, depending on polymer and required modification depth
    • Optimized through pilot studies for blend compatibility

    Downstream process integration

    • Direct addition to polymerization vessel during the reactive blending stage
    • Pre-mixing with plasticizers or fillers to ensure uniform distribution
    • Monitoring via GPC or FTIR to confirm incorporation and cross-link density

    Final product types

    • Electronic encapsulation resins
    • High-temperature engineering plastics
    • ESD (electrostatic discharge) polymer compounds
    • Polymer composites for automotive and aerospace parts

    4. Disulfide Exchange Agent in Biochemical Research Reagents

    Specialty life science reagent manufacturers incorporate 6,6'-Dithiodinicotinic Acid as a disulfide exchange agent in protein modification and labeling systems. Its unique dithiol-disulfide balance supports stable yet reversible cross-links with biomacromolecules. Analytical laboratories value this reactivity for protein folding studies, thiol quantification, or redox-driven conjugation. Strict raw material traceability and batch quality records support regulatory submission and research publication integrity.

    Industry compliance standards

    • ISO 13485 for medical device reagents
    • ISO 17025 for laboratory testing materials
    • GLP (Good Laboratory Practice) guidelines

    Typical usage ratio

    • 10–100 μM in buffer solutions, depending on substrate and protein concentration
    • User-controlled for specific reaction kinetics

    Downstream process integration

    • Added to buffered aqueous solutions during protein incubation
    • Parallel use with reducing or oxidizing agents for redox cycling
    • Final removal by dialysis, ultrafiltration, or chromatography

    Final product types

    • Protein labeling reagent kits
    • Thiolation and cross-linking agents for biochemical research
    • Reagent grade standards for analytical laboratories
    • Protein folding and redox control tools
    Free Quote

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