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3,5-Di-Tert-Butyl-4-Hydroxybenzaldehyde

    • Product Name 3,5-Di-Tert-Butyl-4-Hydroxybenzaldehyde
    • Alias DTBHB
    • Einecs 221-344-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    665484

    Name 3,5-Di-Tert-Butyl-4-Hydroxybenzaldehyde
    Cas Number 13891-11-3
    Molecular Formula C15H22O2
    Molecular Weight 234.33
    Appearance White to off-white solid
    Melting Point 104-107°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles CC(C)(C)c1cc(C=O)c(O)cc1C(C)(C)C
    Synonyms 2,6-Di-tert-butyl-4-hydroxybenzaldehyde
    Storage Conditions Store in a cool, dry place, keep container tightly closed
    Inchi InChI=1S/C15H22O2/c1-14(2,3)11-8-12(10-16)13(17)9-1115(4,5)6-7/h8-10,17H,1-7H3

    As an accredited 3,5-Di-Tert-Butyl-4-Hydroxybenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25-gram amber glass bottle with a tightly sealed cap, labeled “3,5-Di-Tert-Butyl-4-Hydroxybenzaldehyde, 25g, For laboratory use.”
    Shipping 3,5-Di-Tert-Butyl-4-Hydroxybenzaldehyde is shipped in tightly sealed, chemical-resistant containers to prevent contamination and degradation. It should be transported as a non-hazardous solid, protected from moisture, direct sunlight, and extreme temperatures. Appropriate labeling and documentation are provided, and handling should follow standard guidelines for laboratory chemicals.
    Storage 3,5-Di-Tert-Butyl-4-Hydroxybenzaldehyde should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances like strong oxidizers. Avoid exposure to direct sunlight and moisture. Label containers clearly, and ensure storage in a designated chemical storage cabinet, preferably under an inert atmosphere or nitrogen if prolonged storage is required.
    Application of 3,5-Di-Tert-Butyl-4-Hydroxybenzaldehyde

    Applications of 3,5-Di-Tert-Butyl-4-Hydroxybenzaldehyde in Industrial Manufacturing

    3,5-Di-Tert-Butyl-4-Hydroxybenzaldehyde plays a significant role as a specialty intermediate in regulated downstream industrial sectors. Below we provide a detailed breakdown of established application scenarios, compliance frameworks, formula guidance, manufacturing process entry points, and real downstream finished goods, based on customer formulation data and direct manufacturing experience.

    1. Antioxidant Synthesis for Lubricant Additives

    This compound is a key intermediate for producing high-performance hindered phenolic antioxidants in lubricant additive manufacturing. Downstream blenders value its precise substitution pattern, which ensures oxidative stability in engine, hydraulic, and gear oils subject to extreme operating temperatures and shear stress.

    Industry compliance standards

    • ASTM D4951 for engine oil antioxidants
    • API Base Oil Interchange Guidelines
    • REACH Regulation (EC) No 1907/2006 within the EU market
    • OEM-specified additive compatibility requirements (General Motors, Daimler, etc.)

    Typical usage ratio

    • Intermediate conversion: 0.8–1.1 molar equivalents in synthesis of target antioxidant
    • Final antioxidants are dosed at 0.05–1.5 wt% in oil formulations, depending on base oil quality, ash content, and thermal load

    Downstream process integration

    • Incorporated in condensation with hindered amines or phosphites under inert atmosphere
    • Post-synthesis, products undergo controlled crystallization and solvent wash to achieve targeted purity before blending into lubricant bases

    Final product types

    • Passenger vehicle motor oils
    • Industrial gear oils
    • Hydraulic fluids
    • OEM-approved multipurpose lubricants

    2. Polymer Stabilizer Intermediates in Polyolefin Production

    This material supports the synthesis of sterically hindered phenolic stabilizers, preserving polymer integrity during high-temperature extrusion and preventing degradation in polyolefins such as polyethylene and polypropylene, critical for packaging and automotive components.

    Industry compliance standards

    • FDA 21 CFR 178.2010 for indirect food additives (polymer stabilization)
    • EU Plastics Regulation (EU) No 10/2011 for food contact materials
    • ISO 9001 for quality management in compounding operations
    • UL Yellow Card compliance for electrical and flame-retardant grades

    Typical usage ratio

    • Used as an intermediate at 0.95–1.2 molar equivalents when preparing final stabilizer agents
    • Polymer masterbatch addition: 500–2500 ppm (0.05–0.25 wt%), adjusted for thermal exposure and end-use certification needs

    Downstream process integration

    • Condensation with acid anhydrides or secondary amines, catalyst-assisted
    • Post-synthesis blending into polymer melts during extrusion or compounding at temperatures of 180–240°C

    Final product types

    • Food-grade packaging films (PE/PP)
    • Automotive trim parts
    • Cable insulation granules
    • Consumer blow-molded containers

    3. Synthesis of Pharmaceuticals Intermediates (API, Bulk Drug Synthesis)

    In the pharmaceutical sector, the aldehyde group of this raw material enables its use in advanced chemical transformations, such as forming building blocks for certain cardiovascular and neuroprotective APIs through condensation and cyclization reactions, under strict GMP standards for traceability and impurity control.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) and European Pharmacopoeia (Ph. Eur.) monographs
    • FDA DMF (Drug Master File) submission protocols
    • GMP cleanroom synthesis (ISO 14644/Class 100000 or better)

    Typical usage ratio

    • Intermediate scale: 1.0–1.3 molar equivalents, based on downstream core structure and yield optimization
    • API production loads: Micro-molar to tens of kilo-scale, dictated by batch size and purity targets

    Downstream process integration

    • Enters multi-step synthesis starting with condensation (e.g., Knoevenagel, Mannich), followed by isolation under reduced pressure and crystallization protocols
    • Downstream transformation includes reduction, acylation, or ring-closure before final API purification and validation

    Final product types

    • Cardiotonic agents
    • Neuroprotective precursor molecules
    • Specialty intermediates for custom synthesis APIs
    • Custom reference standards for pharmaceutical QC

    4. Light Stabilizer Precursor for Coatings and Pigments

    End-users rely on this benzaldehyde derivative for creating hindered phenol-based light stabilizers, which enhance the durable optical and fade-resistance properties of outdoor architectural coatings and highly pigmented industrial paints subjected to UV exposure and atmospheric pollutants.

    Industry compliance standards

    • EN 71-3:2019 Safety of toys—Migration of certain elements (for toy coatings)
    • ISO 16000-9 (VOC emissions in indoor coatings)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in electrical coatings)
    • German Blue Angel Ecolabel for low-emission paints

    Typical usage ratio

    • Precursor input: 1.0–1.2 molar equivalents per stabilizer batch, optimized for maximum UV block performance
    • Light stabilizer dosage: 0.2–0.8 wt% in formulation, variable according to PVC resin or epoxy content and intended weatherability

    Downstream process integration

    • Undergoes condensation with acrylic or alkyd monomers in controlled reactors
    • Product is dispersed into paint or coating emulsion as a late-stage additive during letdown to avoid thermal decomposition

    Final product types

    • Exterior architectural paints
    • Industrial equipment coatings
    • Plastic and metal primer formulations
    • UV-resistant toy enamels

    5. Performance Resin Modifier in Adhesive Formulations

    Formulators in the adhesives sector utilize this molecule to impart antioxidant character and hydrolysis resistance in specialty phenolic and urethane-based adhesives, which need stable performance in heat or chemical exposure such as those encountered in automotive assembly lines or electronics encapsulation.

    Industry compliance standards

    • ISO 4587 for adhesives—Determination of tensile lap-shear strength of rigid-to-rigid bonded assemblies
    • REACH Annex XVII compliance regarding restricted substances in adhesives
    • RoHS Directive for electronics-related adhesives
    • ASTM D1002 for shear strength measurement in metals

    Typical usage ratio

    • Phenolic resin synthesis: 0.5–2.0 mol% relative to total aldehyde content
    • Urethane adhesive: 0.03–0.2 wt% as a stabilizing agent, adjusted to required shelf life and curing profile

    Downstream process integration

    • Added to resin kettle prior to final chain extension, under strict temperature and inert gas controls
    • Stabilizer homogeneously blended during mixing, prior to catalyst initiation and packaging

    Final product types

    • Heat-resistant automotive adhesives
    • Electronic potting compounds
    • Structural bonding resins for metal, glass, and composites
    • Assembly adhesives for white goods and appliances
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    Tel: +8615371019725

    Email: sales7@sinochem-nanjing.com

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