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2-N-Methyl-2-Pyridylaminoethanol

    • Product Name 2-N-Methyl-2-Pyridylaminoethanol
    • Alias N-(2-Hydroxyethyl)-N-methyl-2-pyridinamine
    • Einecs 401-780-0
    • 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

    860245

    Chemical Name 2-N-Methyl-2-Pyridylaminoethanol
    Cas Number 16232-40-1
    Molecular Formula C8H12N2O
    Molecular Weight 152.19
    Appearance Colorless to pale yellow liquid
    Solubility Soluble in water and common organic solvents
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry, and well-ventilated place
    Synonyms 2-[(N-Methyl-2-pyridyl)amino]ethanol
    Smiles CN(Cc1ncccc1)CCO
    Inchi Key DQGQGCUUOZDIFB-UHFFFAOYSA-N

    As an accredited 2-N-Methyl-2-Pyridylaminoethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g bottle of 2-N-Methyl-2-Pyridylaminoethanol comes in a tightly sealed amber glass container with detailed hazard labeling.
    Shipping 2-N-Methyl-2-Pyridylaminoethanol is shipped in tightly sealed containers, protected from light and moisture. It should be packed according to regulations for chemical substances, with appropriate hazard labeling. Enclosures must prevent leaks and spills, and transport must comply with applicable safety and environmental guidelines for potentially harmful organic chemicals.
    Storage 2-N-Methyl-2-Pyridylaminoethanol should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a well-ventilated, cool, dry area, and segregate it from oxidizers, acids, and incompatible substances. Properly label the storage area, and ensure access is limited to trained personnel. Use secondary containment to prevent spills or leaks.
    Application of 2-N-Methyl-2-Pyridylaminoethanol

    Applications of 2-N-Methyl-2-Pyridylaminoethanol in Industrial Manufacturing

    As a direct manufacturer with specialized synthesis capabilities, we support our clients with high-purity 2-N-Methyl-2-Pyridylaminoethanol for critical intermediate needs across diverse chemical sectors. Below we present focused, true-to-market applications reflecting current industry requirements, regulatory frameworks, and operational best practices for this material.

    1. Pharmaceutical Intermediates: API Synthesis

    2-N-Methyl-2-Pyridylaminoethanol serves as a selective building block in the multi-stage synthesis of anti-infective APIs and certain antihypertensives. In process chemistry, it enables pyridyl-based moiety construction for key intermediates. GMP-based manufacturing lines integrate the material during late-stage amide coupling or as a nucleophilic partner in N-alkylation reactions, often preceding critical hydrogenation or protection/deprotection steps. Its purity and trace metal content are controlled to meet stringent regulatory filings for regulated markets.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) requirements for intermediates
    • USP <467> Residual Solvents guidelines

    Typical usage ratio

    • 0.5–5 molar equivalents per coupling step, adjusted by stoichiometry and side reaction profile

    Downstream process integration

    • Introduced post-grignard reaction or methylation step; direct feed to batch or flow reactors
    • Followed by phase separation, aqueous work-up, or distillation

    Final product types

    • Pharmaceutical APIs including quinolone derivatives, anti-infective agents, and beta-blockers where pyridyl groups are structural

    2. Agrochemical Formulation: Herbicide Intermediate

    The compound acts as a core intermediate in the synthesis of modern pyridine-based herbicides. Formulation facilities apply controlled batch reactions, using this raw material to build nitrogen-containing heterocycles essential for selectivity in crop protection products. Compliance requires accurate documentation and traceability of each batch to ensure the absence of banned impurities and environmental toxins in the supply chain.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Agrochemical Synthesis
    • FAO/WHO specifications for pesticide ingredients
    • REACH Registration, Evaluation, and Authorization of Chemicals—EU requirements
    • China ICAMA product registration standards for active formulations

    Typical usage ratio

    • 10–25% by weight in pre-final coupling or cyclization stages; varies with crop protection active design

    Downstream process integration

    • Dosed into jacketed reactors for nucleophilic substitution or amidation
    • Intermediate purified by liquid-liquid extraction before crystallization of actives

    Final product types

    • Nitrogen-heterocycle herbicide actives (e.g. pyridyl-based selective weed control agents)
    • Commercial pesticide technical concentrates (TCs)

    3. Polymer Modification: Specialty Engineering Plastics

    Manufacturers of advanced polymers employ this material in specialty resin synthesis, targeting functional monomer introduction to modify electrical or thermal performance. It contributes as a chain modifier or as part of the backbone in custom polyamides and polyimides. Formulators precisely meter the material into continuous or batch reactors, maintaining process conditions to maximize reactivity and chain length control, critical for downstream extrusion or molding performance.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001 Environmental Management
    • RoHS Directive (2011/65/EU) compliance for flame retardant and additives in E&E plastics
    • UL 94 flammability standards for end-use polymer parts
    • FDA 21 CFR 177 sub-requirements when targeting food-contact polymers

    Typical usage ratio

    • 0.1–3.0 phr (parts per hundred resin); optimized per polymer matrix and end-use specification

    Downstream process integration

    • Fed as neat liquid or in solution at initial polymerization charging
    • Added before catalyst introduction in step-growth or ring-opening polymerizations

    Final product types

    • High-performance polyamides and polyimides for electronics
    • Functionalized engineering plastics for automotive lightweighting

    4. Corrosion Inhibitor Formulation: Oil & Gas Sector

    Processing facilities in the oil and gas industry incorporate 2-N-Methyl-2-Pyridylaminoethanol as a foundational component when blending imidazoline-based and amine-based corrosion inhibitors for pipeline and drilling fluids. It reacts with fatty acids or acyl chlorides to generate surface-active agents tailored for harsh downhole or subsea pipeline applications. Trace contaminant control, water miscibility, and amine content require strict monitoring throughout blending and QC release according to sector expectations.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical manufacture
    • API 682: Packing and Sealing systems—relevant for additive components
    • REACH—SVHC (Substances of Very High Concern) declaration
    • NACE MR0175/ISO 15156 for materials exposed to hydrogen sulfide in oilfield environments

    Typical usage ratio

    • 5–15% by weight in corrosion inhibitor blend; fine-tuned due to brine composition, temperature, and metal type

    Downstream process integration

    • Combined with fatty acids and alkylating agents in batch reactors at controlled temperatures
    • Final inhibitor solution adjusted for pH and viscosity before canning

    Final product types

    • Pigging and pipeline corrosion inhibitors
    • Wellbore protection fluids for exploration and production

    5. Electroplating Additives: Metal Finishing Chemicals

    Electroplating factories use this molecule as a functional additive to adjust deposit morphology and plating bath stability in copper and nickel processes. During electrolyte make-up, operators add the material for complexation and leveling properties, directly influencing smoothness, brightness, and ductility of plated coatings, especially in electronics, PCB manufacturing, and decorative hardware finishing steps.

    Industry compliance standards

    • IEC 62321: Determination of certain substances in EEE—relevant for heavy metal limits in formulations
    • ANSI/EIA-364 for connector and PCB component quality
    • RoHS & WEEE directives for waste minimization and recycling control
    • ISO 9001:2015 for specialty chemical QC

    Typical usage ratio

    • 20–200 ppm in electrolyte bath; concentration set by current density, metal ion concentration, and bath turnover rate

    Downstream process integration

    • Dosed inline during bath makeup or as a continuous additive in recirculating systems
    • Participates in chelation and surface adsorption during voltage-controlled plating cycles

    Final product types

    • High-brightness copper and nickel coatings for semiconductors
    • Decorative metal finishings for automotive and architectural parts

    6. Fine Chemical Synthesis: Laboratory & Pilot Scale Reagents

    Custom synthesis groups and fine chemical producers employ 2-N-Methyl-2-Pyridylaminoethanol as a multi-purpose intermediate in targeted heterocycle and ligand development. Its dual functional groups allow for the construction of bi- or tri-dentate ligands and advanced pyridine derivatives, feeding specialized research projects and pilot scale proof-of-concept batches. These syntheses operate under meticulous control, including low temperature handling, specific catalyst uses, and post-reaction vacuum distillation.

    Industry compliance standards

    • ISO/IEC 17025: General requirements for laboratory competence
    • GHS/OSHA hazard communication for laboratory handling
    • Responsible Care® guidelines for chemical manufacturers
    • IATA/IMDG transport restrictions for sample shipment

    Typical usage ratio

    • 0.1–1.5 molar equivalents per synthetic transformation; scaled by target molecule and literature precedents

    Downstream process integration

    • Added at low temperature or under inert conditions when required by sensitivity of co-reactants
    • Integrated into iterative batch synthesis with in-process FTIR/NMR monitoring

    Final product types

    • Pharmaceutical and agrochemical intermediates for lead optimization
    • Specialty ligands for homogeneous catalysis development
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