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4-Aminopiperidine Dihydrochloride

    • Product Name 4-Aminopiperidine Dihydrochloride
    • Alias 4-Aminopiperidine 2HCl
    • Einecs 629-753-3
    • 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
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    Specifications

    HS Code

    683635

    Product Name 4-Aminopiperidine Dihydrochloride
    Cas Number 40064-34-4
    Molecular Formula C5H14Cl2N2
    Molecular Weight 173.09 g/mol
    Appearance White to off-white solid
    Melting Point 235-239°C (dec.)
    Solubility In Water Soluble
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, tightly closed, dry place
    Synonyms 1,4-Piperidinediamine dihydrochloride; Piperidin-4-ylamine dihydrochloride
    Inchi Key YZVZGGQYVTXUQC-UHFFFAOYSA-N
    Ec Number 254-657-9

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

    Packing & Storage
    Packing The packaging is a sealed, amber glass bottle containing 25 grams of 4-Aminopiperidine Dihydrochloride, labeled with safety and chemical information.
    Shipping **4-Aminopiperidine Dihydrochloride** is typically shipped in sealed, airtight containers to prevent moisture absorption and contamination. The packaging complies with hazardous material regulations, ensuring safe transport. All containers are clearly labeled, and shipping includes appropriate documentation. Avoid temperature extremes and strong oxidizers during transit. Handle with gloves and protective equipment upon receipt.
    Storage 4-Aminopiperidine Dihydrochloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, heat, and incompatible substances. Keep it away from strong oxidizers. Store at room temperature and protect from light to maintain stability. Ensure storage area is marked for hazardous chemicals, and access is limited to trained personnel.
    Application of 4-Aminopiperidine Dihydrochloride

    Applications of 4-Aminopiperidine Dihydrochloride in Industrial Manufacturing

    We supply 4-Aminopiperidine Dihydrochloride with industrial scale consistency for advanced chemical synthesis. This intermediate supports precision processing in pharmaceuticals, agrochemicals, and materials sectors where batch reproducibility and strict regulatory protocols define downstream operations.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Major pharmaceutical customers use our material to build essential piperidine-based cores in CNS-active APIs and antihypertensive agents. Reactors integrate the compound during stepwise N-alkylation or acylation routes to achieve specific amine architectures. Processing demands high purity and strict documentation to support regulatory dossiers for clinical and commercial drug products.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 US FDA cGMP for Finished Pharmaceuticals
    • European Pharmacopoeia (Ph. Eur.) relevant monographs
    • USP/NF identity and impurity control standards

    Typical usage ratio

    • 0.3–1.2 molar equivalent relative to the target API intermediate; final ratio depends on target scaffold complexity and route selection

    Downstream process integration

    • Charged during selective amination or reductive alkylation; introduced after initial heterocycle formation or as the amine-building block in convergent API steps

    Final product types

    • API intermediates for CNS drugs (e.g., cevimeline analogues)
    • Hypertension therapies
    • Analytical reference standards for quality control
    • Clinical development batch materials

    2. Advanced Agrochemical Intermediates

    Crop protection manufacturers deploy this compound to synthesize selective insecticides and fungicides, combining it into multi-step heterocyclic ring-forming reactions. Downstream operations emphasize precise stoichiometry and impurity management, especially for export-grade active ingredients under country-specific registration.

    Industry compliance standards

    • FAO/WHO Technical Specifications for Pesticides
    • ISO 9001:2015 Certified Quality Systems
    • Chinese ICAMA registration requirements
    • REACH Annex IX for new agrochemical actives

    Typical usage ratio

    • 1.0–1.5 molar equivalent per final heterocyclic scaffold; optimized per cycle count in multistep process

    Downstream process integration

    • Dispersed after the initial chlorination or cyclization; used as a nucleophile for N-heterocycle introduction in the core structure

    Final product types

    • Insecticide actives with piperidine motifs
    • Fungicidal intermediates for further sulfonation or methylation
    • Technical-grade agrochemical concentrates
    • R&D synthesis reference samples

    3. Specialty Polymer Additive Synthesis

    Manufacturers of high-performance polymers apply this intermediate to prepare chain extenders and reactive modifiers, especially for block copolymers targeting electronics or membrane industries. Production lines require batch tracking and contamination controls, as these additives must meet stringent purity benchmarks for sensitive downstream engineering applications.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • RoHS Directive (2011/65/EU) for electronic materials
    • REACH (EC 1907/2006) registration for additives above 1 tonne/year
    • Applicable ASTM standards for polymer formulation

    Typical usage ratio

    • 0.1–0.5 wt% to base polymer mass, directly determined by mechanical/chemical performance targets of copolymer blends

    Downstream process integration

    • Incorporated during in situ polymerization or as part of custom chain-extending reactions before melt-blending

    Final product types

    • High-durability polyurethane foams
    • Membrane-grade copolymers for filtration systems
    • Conductive polymer composites for electronic applications
    • Specialty elastomers with enhanced flexibility

    4. Pharmaceutical Impurity and Reference Standard Preparation

    Laboratory and analytical chemical producers source this intermediate to develop certified impurity markers and reference substances, supporting pharmaceutical quality control processes. Synthesis of these standards requires isolated high-purity lots with full traceability, aiding HPLC, GC, and NMR method development for regulated markets including FDA and EMA.

    Industry compliance standards

    • USP Reference Standards Program
    • ISO/IEC 17025 for chemical testing and calibration laboratories
    • ICH Q6A – Specifications: Test Procedures and Acceptance Criteria
    • European EDQM reference substance protocols

    Typical usage ratio

    • Typically produced in milligram to low gram scale per batch; used as direct analytical standard or as precursor for impurity synthesis

    Downstream process integration

    • Processed through column purification or crystallization following targeted synthesis, then formulated for analytical laboratories

    Final product types

    • Pharmaceutical impurity standards for regulatory submissions
    • Analytical calibration kits (HPLC/GC)
    • Primary reference substances for API quality control
    • Impurity isolations for toxicological assessments

    5. Fine Chemical Building Block for Custom Synthesis

    Contract development and manufacturing organizations (CDMOs) use this amine derivative as a building block for custom, project-specific fine chemical libraries. Custom syntheses require adaptable supply and technical documentation, especially where downstream partners demand traceable origin and impurity profiles for new molecule generation.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Custom Synthesis
    • Controlled Substances Act (where applicable to derivatives)
    • Company-specific raw material traceability protocols
    • GMP-compliant documentation upon request

    Typical usage ratio

    • Variable, typically 0.2–2.0 molar equivalents based on discovery routes and design-of-experiment setups in medicinal and process chemistry

    Downstream process integration

    • Supplied as a protected or free amine; enters early discovery pipelines or late-stage elaboration of proprietary scaffolds

    Final product types

    • Custom screening compound libraries
    • Research intermediates for hit-to-lead programs
    • Protected amine derivatives for process route evaluation
    • Specialty performance chemicals for material innovation
    Free Quote

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