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2,2,6,6-Tetramethyl-4-Piperidinol

    • Product Name 2,2,6,6-Tetramethyl-4-Piperidinol
    • Alias TMP
    • Einecs 219-207-7
    • 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

    650345

    Name 2,2,6,6-Tetramethyl-4-Piperidinol
    Chemical Formula C9H19NO
    Molecular Weight 157.26 g/mol
    Cas Number 2403-88-5
    Appearance White to off-white crystalline solid
    Melting Point 62-66 °C
    Boiling Point 113 °C at 15 mmHg
    Solubility In Water Slightly soluble
    Density 0.98 g/cm³
    Flash Point 110 °C
    Pka 9.93 (at 25 °C)
    Synonyms TMPOL, 4-Hydroxy-2,2,6,6-tetramethylpiperidine

    As an accredited 2,2,6,6-Tetramethyl-4-Piperidinol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100-gram amber glass bottle, tightly sealed with a screw cap, labeled "2,2,6,6-Tetramethyl-4-Piperidinol, 99% purity."
    Shipping 2,2,6,6-Tetramethyl-4-piperidinol should be shipped in tightly sealed containers, protected from light and moisture. It is generally classified as non-hazardous but should be handled with appropriate care. Comply with local, national, and international regulations. Standard packaging includes amber bottles or drums, cushioned and labelled as a chemical substance.
    Storage 2,2,6,6-Tetramethyl-4-piperidinol should be stored in a cool, dry, well-ventilated area, away from sources of heat and ignition. Keep the container tightly closed and protected from moisture. Store it separately from oxidizing agents, acids, and strong bases. Always use appropriate chemical storage cabinets, and label the container clearly. Avoid direct sunlight and incompatible materials.
    Application of 2,2,6,6-Tetramethyl-4-Piperidinol

    Applications of 2,2,6,6-Tetramethyl-4-Piperidinol in Industrial Manufacturing

    2,2,6,6-Tetramethyl-4-Piperidinol serves as a critical intermediate and additive in several specialized manufacturing sectors. Its use enables advanced polymer modification, light stabilizer synthesis, fine chemicals production, and coatings technology. Please find detailed application scenarios below, including compliance, dosing guidance, integration points, and final goods for each sector.

    1. Hindered Amine Light Stabilizers (HALS) Production

    Downstream polymer industries utilize this raw material as a core precursor in synthesizing HALS compounds. These stabilizers prevent polymer degradation from UV exposure, especially in outdoor applications. Manufacturers select it for consistent reaction yield and high purity, crucial for producing stable and high-performance stabilizer molecules requiring tight process control.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • ISO 9001:2015 for quality management throughout production
    • FDA CFR Title 21—Part 177.1520 for food-contact polymer applications (end-use verification required)
    • RoHS Directive 2011/65/EU for plastics in electronics

    Typical usage ratio

    • 10–40 wt% based on target HALS molecule synthesis route
    • Precise amounts adjusted according to the required HALS output and side reaction minimization

    Downstream process integration

    • Direct addition during condensation or cyclization step in HALS synthesis
    • Batch or continuous flow reaction vessels for precise temperature and pressure control
    • In-line monitoring for conversion efficiency and impurity control

    Final product types

    • Polyolefin and PVC stabilizers
    • HALS masterbatches for plastics processors
    • Light-stabilized agricultural films and automotive polymers
    • Coating additives for exterior paints and sealants

    2. Specialty Polyurethane Catalyst Systems

    Polyurethane formulators employ this molecule as a chain-structure modifier and catalyst precursor in select rigid and flexible foam production. Its tertiary amine group provides controlled nucleophilicity for reaction pathway tuning, especially where conventional catalysts create unwanted side products. This allows downstream blenders to optimize foam density and cell structure through accurate dosing and reactor monitoring.

    Industry compliance standards

    • ISO 9001:2015 quality system in catalyst manufacture
    • Directive 2002/95/EC (RoHS) for use in electrical insulation foams
    • EU Regulation (EC) No 1935/2004 for food-contact polyurethane, where applicable
    • US EPA TSCA requirements for new intermediates

    Typical usage ratio

    • 0.1–2.0 wt% of total catalyst blend
    • Adjusted for polyurethane type, density target, and process (batch/slabstock or molded)

    Downstream process integration

    • Pre-dissolved into polyol blend before metering
    • Metered inline to reactor for high consistency
    • Entry point optimized for catalysis selectivity and foam rise profile

    Final product types

    • Rigid polyurethane insulation panels
    • Automotive seat foams
    • Medical diagnostic foam pads
    • High-resilience furniture cushioning

    3. Pharmaceutical Intermediate for Piperidinol Derivatives

    Our piperidinol has established use as an advanced intermediate in active pharmaceutical ingredient (API) synthesis for drugs requiring hindered tertiary amines. Regulatory-driven batch traceability and impurity profiling enable pharmaceutical clients to satisfy all cGMP and pharmacopoeial demands for the finished API. This material enters critical alkylation and deprotection steps—where unambiguous identity and purity are strictly assured by our plant-level controls.

    Industry compliance standards

    • International Council for Harmonisation (ICH Q7) for API production
    • Good Manufacturing Practice (GMP) as per WHO and EU GMP guidelines
    • USP/NF and European Pharmacopoeia grade material on request
    • TSE/BSE risk-free for pharmaceutical processing

    Typical usage ratio

    • Stoichiometric amounts, typically 1–1.2 molar equivalents based on API pathway
    • All batch ratios specified by validated route and regulatory filing

    Downstream process integration

    • Charged to initial reaction vessel for alkylation or amidation
    • May serve as a protecting group or nucleophile in multi-step synthesis
    • Removal and downstream transformation tracked by validated in-process QC

    Final product types

    • CNS-active pharmaceutical intermediates
    • Specialty oncology drug precursors
    • Molecules for regulated clinical research pipelines
    • Generic drug intermediates for global drug markets

    4. Epoxy Resin Additives for Industrial Coatings

    Coatings producers use this ingredient as a reactive additive to improve UV resistance and color stability of advanced epoxy systems. Its incorporation in curing or modification steps reduces photodegradation in industrial paints and heavy-duty epoxy topcoats. Our consistency in amine content supports batch-to-batch performance and minimizes rework at formulation stages.

    Industry compliance standards

    • ASTM D6386 for coating durability assessment
    • ISO 12944-6 for anti-corrosion coatings
    • GB/T 9754–2007 for gloss and weatherability in paints
    • LEV III and EU VOC regulations for industrial paints

    Typical usage ratio

    • 0.5–3.0 wt% of total resin weight, depending on UV stability target
    • Adjusted upward for high-exposure outdoor applications

    Downstream process integration

    • Dispersed directly into epoxy base prior to crosslinker addition
    • Compatible with both hot-melt and ambient cure blending
    • Monitored during application for color holdout and gloss retention effects

    Final product types

    • Protective epoxy coatings for structural steel
    • Industrial flooring resins
    • Automotive underbody and chassis paints
    • Marine environment coatings

    5. Advanced Agrochemical Formulation Synthesis

    Agrochemical compounders adopt this raw material for building specific amine-based active ingredients and intermediates, especially in herbicide and pesticide scaffold production. It supports secure, closed-loop synthesis required for controlled-substance tracking and purity, and ensures predictable conversion rates during large-scale batch operations. Multi-point QC sampling during formulation guarantees no unwanted conversion or loss during high-throughput manufacturing.

    Industry compliance standards

    • FAO/WHO specifications for technical-grade agrochemicals
    • ISO 9001:2015 in agrochemical production system
    • EPA inert ingredient database for US pesticide use
    • Regulation (EC) No 1107/2009 for agricultural chemical registration

    Typical usage ratio

    • 5–25 wt% by total mass of intermediate batch
    • Ratio selected based on downstream synthetic target and regulatory file

    Downstream process integration

    • Charged into core cyclization or amidation reactors
    • Integrated at post-neutralization step for derivative finishing
    • In-line monitored for amine purity before downstream formulation

    Final product types

    • Pyridine-based herbicide actives
    • N-substituted pesticide intermediates
    • Specialty fungicide scaffolds
    • Crop-protection chemical blends
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    Competitive 2,2,6,6-Tetramethyl-4-Piperidinol prices that fit your budget—flexible terms and customized quotes for every order.

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