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2,6-Di-Tert-Butylpyridine

    • Product Name 2,6-Di-Tert-Butylpyridine
    • Alias DTBP
    • Einecs 221-823-9
    • 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

    245901

    Chemical Name 2,6-Di-Tert-Butylpyridine
    Cas Number 728-36-9
    Molecular Formula C13H21N
    Molecular Weight 191.32 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 253-255 °C
    Melting Point -20 °C
    Density 0.900 g/mL at 25 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Flash Point 113 °C
    Refractive Index 1.505 at 20 °C
    Storage Conditions Store in a cool, dry place, tightly closed

    As an accredited 2,6-Di-Tert-Butylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100g amber glass bottle with a tightly sealed cap, labeled "2,6-Di-Tert-Butylpyridine" and hazard warnings.
    Shipping **2,6-Di-Tert-Butylpyridine** is shipped in sealed, chemical-resistant containers to prevent moisture and contamination. It is transported as a non-hazardous, stable liquid under normal conditions. Ensure upright positioning, avoid extreme temperatures, and use proper labeling per regulatory guidelines. Consult the safety data sheet (SDS) for detailed handling and emergency information.
    Storage 2,6-Di-Tert-Butylpyridine should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizing agents and acids. Keep it away from heat and sources of ignition. Protect from moisture and light to prevent degradation. Store under an inert atmosphere if prolonged storage or sensitive applications are required.
    Application of 2,6-Di-Tert-Butylpyridine

    Applications of 2,6-Di-Tert-Butylpyridine in Industrial Manufacturing

    2,6-Di-Tert-Butylpyridine functions as a specialized hindered base across industrial synthesis, ensuring precise control during key transformation steps. This material provides unique selectivity due to its steric and electronic properties, supporting consistent output in several demanding downstream sectors. We manufacture to tight specifications for direct use in regulated production chains.

    1. Pharmaceutical Active Ingredient Synthesis

    Producers of active pharmaceutical ingredients (APIs) use 2,6-Di-Tert-Butylpyridine to suppress unwanted side reactions, especially during alkylation, acylation, or halogenation steps. Its bulk and non-nucleophilicity help chemists achieve high yields and target purity, particularly in macrolide antibiotics and cardiovascular product lines. We supply this base for integration in batch and continuous synthesis, supporting controlled conditions meeting ICH and regional health authority guidelines.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • 21 CFR Part 211 (US FDA regulations)
    • EU GMP Directive 2003/94/EC
    • Chinese Pharmacopoeia production quality system

    Typical usage ratio

    • 0.5%–2.0% by weight of total reaction mass
    • Adjustable according to target substrate and reaction scale
    • Lower end for less reactive starting materials
    • Exceptions: Higher base levels for selective protection strategies

    Downstream process integration

    • Introduced during the base-promoted step in multi-stage synthesis
    • Added after temperature set-point stabilization but before electrophile addition
    • Removed during aqueous workup and solvent extraction
    • Presence monitored by in-process HPLC or titration methods

    Final product types

    • Antibiotics (e.g., macrolides, cephalosporin derivatives)
    • Statins for cholesterol management
    • API intermediates for antihypertensive drugs
    • Chirally pure pharmaceutical intermediates

    2. Fine Chemical Synthesis for Agrochemical Active Substances

    Agrochemical manufacturers turn to 2,6-Di-Tert-Butylpyridine as a base during key condensation and functionalization steps, especially in the preparation of herbicide and fungicide intermediates. Its bulky structure prevents side-chain alkylation and halogen exchange, crucial for controlling isomer ratios in pyridine- or pyrimidine-based agrochemicals. Compliance with regional agrochemical standards drives uniformity and traceability from base chemical to registered crop protection agent.

    Industry compliance standards

    • ISO 9001:2015 for chemical production
    • FAO/WHO pesticide specifications
    • REACH Registration (Europe)
    • China GB chemical safety standards

    Typical usage ratio

    • 1.0%–5.0% based on weight of core substrate
    • Ratio depends on acidity/basicity of reaction system
    • Lower for aromatic substitution reactions
    • Higher for strongly electrophilic steps or where byproducts are a risk

    Downstream process integration

    • Charged directly to the reactor with other base components
    • Engaged during key condensation or cyclization step
    • Careful removal during downstream separation to avoid interference in formulation
    • QA/QC tracks residuals in each batch discharge

    Final product types

    • Pyrazole and pyridine herbicides
    • Triazole fungicide intermediates
    • Growth regulator bases for regulated markets
    • Chemical building blocks for insecticides

    3. Catalyst Poisoning Prevention in Olefin Polymer Production

    Producers of specialty polyolefins and elastomers use this hindered base to deactivate trace acidic components or moisture that can poison sensitive Ziegler-Natta or metallocene catalyst systems. Careful dosing helps maintain active catalyst lifetime and polymer property control. This material supports the production of advanced material grades, especially where tight molecular weight distribution and mechanical performance are required for auto, film, and cable applications.

    Industry compliance standards

    • ISO 14001 environmental management for petrochemical plants
    • ASTM D4020 for polystyrene and polyolefin purity
    • EU REACH for polymer additives
    • US EPA TSCA Inventory List

    Typical usage ratio

    • 0.05%–0.2% by weight of total catalyst/activator load
    • Dosing adjusted based on ppm acid contaminant levels
    • Often fed by in-line dosing pump
    • Periodically verified by titration of system impurities

    Downstream process integration

    • Injected into monomer feed or directly into reactor pre-catalyst zone
    • Dosage controlled by on-line impedance monitoring
    • Removed by downstream polymer washing and filtration steps
    • Residual check by FTIR or chromatography on final resin

    Final product types

    • High-performance polyethylene grades
    • Polypropylene for medical and consumer packaging
    • Thermoplastic elastomers for industrial tubing
    • Insulating compounds for power cables

    4. Laboratory and Commercial-Scale Organic Synthesis R&D

    Academic and industrial R&D teams apply 2,6-Di-Tert-Butylpyridine during the development of novel synthesis routes, especially where sterically hindered base is essential for selectivity. This material helps screen optimal reaction conditions, scale up new synthesis pathways, and troubleshoot problematic transformations in pilot and kilo labs. Accurate dosing and high batch-to-batch purity are essential for reproducibility before commercialization.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for research
    • ISO 17025 for chemical analytics
    • In-house SOPs for safe chemical handling
    • Material traceability as per GxP guidance

    Typical usage ratio

    • 0.2–1.5 molar equivalents relative to main substrate
    • Varies by reaction type—often 1:1 with acid or electrophile present
    • Adjusted by chemist based on desired selectivity or suppression of by-products
    • Screened in parallel reactions for best outcome

    Downstream process integration

    • Added at start of reaction trial as dry or in solution
    • Interacts during kinetic studies and reaction optimization
    • Isolated by extraction and removed by silica gel or distillation in workup
    • Monitored by NMR or TLC spot assay

    Final product types

    • New small-molecule reference standards
    • Experimental bioactives for pharma screening
    • Organic intermediates for specialty polymer research
    • Custom compounds for analytical study
    Free Quote

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