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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 | 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. |
Applications of 3-(1-Piperidinylmethyl)Phenol in Industrial ManufacturingAs 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) SynthesisDrug 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
Typical usage ratio
Downstream process integration
Final product types
2. Intermediate for Agrochemical Active SubstancesMajor 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
Typical usage ratio
Downstream process integration
Final product types
3. Intermediate for Specialty Polymer ModificationPolymer 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
Typical usage ratio
Downstream process integration
Final product types
4. Intermediate for Functional Dye and Pigment SynthesisProducers 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
Typical usage ratio
Downstream process integration
Final product types
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