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3-(1-Piperidinylmethyl)Phenol

    • Product Name 3-(1-Piperidinylmethyl)Phenol
    • Alias 3-(Piperidin-1-ylmethyl)phenol
    • Einecs 626-144-4
    • 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

    748825

    Chemical Name 3-(1-Piperidinylmethyl)phenol
    Molecular Formula C12H17NO
    Molecular Weight 191.27 g/mol
    Cas Number 17142-28-2
    Appearance White to off-white solid
    Boiling Point Unknown
    Melting Point Unknown
    Solubility Soluble in organic solvents, low solubility in water
    Density Unknown
    Synonyms 3-(Piperidin-1-ylmethyl)phenol
    Structure Type Aromatic phenol with piperidine substitution
    Smiles C1CCN(CC1)CC2=CC(=CC=C2)O
    Inchi InChI=1S/C12H17NO/c14-12-6-2-5-11(9-12)10-13-7-3-1-4-8-13/h2,5-6,9,14H,1,3-4,7-8,10H2

    As an accredited 3-(1-Piperidinylmethyl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100g, screw cap, with hazard labels and chemical name `3-(1-Piperidinylmethyl)Phenol` clearly printed on label.
    Shipping Shipping of **3-(1-Piperidinylmethyl)phenol** requires secure, sealed packaging with appropriate labeling according to chemical transport regulations. The chemical should be shipped in a cool, dry environment, away from incompatible substances. Material Safety Data Sheet (MSDS) and hazard information must accompany the package, and handling should comply with local and international chemical shipment guidelines.
    Storage Store **3-(1-Piperidinylmethyl)phenol** in a tightly closed, labeled container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizing agents and acids. Protect from moisture and direct sunlight. Keep away from heat sources and ignition. Use secondary containment if possible, and restrict access to authorized and trained personnel only. Follow standard chemical hygiene procedures.
    Application of 3-(1-Piperidinylmethyl)Phenol

    Applications of 3-(1-Piperidinylmethyl)Phenol in Industrial Manufacturing

    As a direct manufacturer of 3-(1-Piperidinylmethyl)Phenol, we supply this raw material to specialized downstream sectors that require precise functional additives for advanced synthesis and formulation tasks. Below, we detail major industrial application scenarios where this intermediate is reliably utilized, specifying technical standards, formulation guidance, downstream processing points, and examples of finished product types.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Drug manufacturers use 3-(1-Piperidinylmethyl)Phenol primarily as a building block in multi-step synthesis routes for APIs, particularly in central nervous system (CNS) compound development. It serves as a coupling partner for stepwise N-alkylation and aromatic substitution reactions that enable the creation of key structural frameworks in finished medicines. Its purity profiles and batch consistency are tightly controlled to minimize impurities that can interfere with downstream reactions or regulatory drug master file submissions.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/EP/JP relevant general chapters for starting material quality
    • 21 CFR Part 210/211 (US FDA cGMPs)
    • EU Directive 2001/83/EC requirements for pharmaceutical ingredients

    Typical usage ratio

    • 0.8%–2.5% w/w in API synthesis batch, optimized by yield and downstream reactivity; exact ratio determined by stoichiometric calculations based on specific API structure

    Downstream process integration

    • Charged during the intermediate formation stage, typically prior to condensation or cyclization; introduced after pH adjustment where nucleophilicity is maximized; quality checked by HPLC before downstream transfer

    Final product types

    • Central nervous system therapeutic APIs such as novel antipsychotics and analgesics
    • Custom synthesized heterocyclic drugs
    • Pain management pharmaceutical intermediates
    • Small molecule R&D candidates

    2. Intermediate for Agrochemical Active Substances

    Major agrochemical producers incorporate 3-(1-Piperidinylmethyl)Phenol in the development of pesticide actives, particularly as a nucleophile for forming piperidinyl-phenolic backbones in herbicidal and fungicidal agents. Its chemical stability supports scale-up during large-batch syntheses. This precursor contributes to the synthesis of molecules with selective mode-of-action in crop protection chemicals, and must meet specific analytical standards for agrochemical registration.

    Industry compliance standards

    • FAO/WHO specifications for technical active ingredients
    • OECD guidelines for chemical testing and residue analysis
    • ISO 9001:2015 certified QC management in agrochemical ingredient production
    • Globally Harmonized System (GHS) for labeling, transport, and MSDS requirements

    Typical usage ratio

    • 1.0%–3.0% w/w in technical concentrate synthesis, adjusted for target molecule; final dose refined based on desired target content and process yield during pilot scaling

    Downstream process integration

    • Dosed alongside halogenated reactants in staged couplings, followed by neutralization and solvent recovery; introduced post-chlorination but prior to crystallization and purification trains

    Final product types

    • Herbicide actives for cereals and broad-leaf crops
    • Systemic fungicide bases for crop protection formulations
    • Agrochemical technical concentrates and pre-mixes
    • Seed treatment additives based on piperidinyl moieties

    3. Intermediate for Specialty Polymer Modification

    Polymer manufacturers exploit the phenolic and piperidinyl functionalities of this molecule to produce modified resins and specialty plastics with tailored thermal and mechanical profiles. Introduced as a chain stopper or crosslinker, this intermediate supports the formation of resins for electronics encapsulation and thermoset adhesives. Its dosing impacts polymer chain length distribution, so material addition must be carefully controlled for target end-use properties.

    Industry compliance standards

    • ISO 9001 for quality management in chemical processing
    • REACH (EC 1907/2006) compliance on polymer raw materials
    • RoHS Directive 2011/65/EU for electronic grade polymers
    • ASTM D638 for mechanical properties of finished resins

    Typical usage ratio

    • 0.2%–1.5% w/w relative to total monomer mass; precise concentration depends on required molecular weight control and degree of crosslinking

    Downstream process integration

    • Added at the pre-polymer stage in melt or solution polymerization; introduced with initiators and catalysts before cure; monitored via GPC for chain structure validation

    Final product types

    • Thermosetting epoxy and phenolic resins for electronic encapsulation
    • Modified polymer casting compounds for automotive connectors
    • Specialty thermoset adhesives for circuit board lamination
    • Heat-resistant polymeric coatings

    4. Intermediate for Functional Dye and Pigment Synthesis

    Producers of specialty dyestuffs employ 3-(1-Piperidinylmethyl)Phenol as a precursor for high-affinity, high-fastness dyes, specifically via Mannich condensation and aromatic substitution. Its unique ring structure enables tuning of color depth and solubility for reactive and metal-complex dyes targeting textile and ink applications. Stringent analytical controls on raw material input directly influence purity and color strength of the final pigment or dye formulation.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile safety
    • ISO 105 for color fastness testing in dyed textiles
    • EN 71-3 for migration of chemical elements (when used in inks and coatings for toys)
    • Registration under REACH Annex IV for dye intermediates

    Typical usage ratio

    • 0.5%–2.0% w/w in total dye intermediate mass; amount set by stoichiometry of target chromophore synthesis

    Downstream process integration

    • Introduced during coupling or condensation steps after pre-drying and solvent activation; batch QC by thin layer chromatography or HPLC pre- and post-synthesis

    Final product types

    • Reactive and vat dyes for cotton and synthetic fibers
    • Disperse dyes and pigment intermediates
    • Colorant concentrates for inkjet and textile printing
    • Special effect pigments for high-performance coatings
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