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2,3-Dimethoxybenzylamine

    • Product Name 2,3-Dimethoxybenzylamine
    • Alias Veratrylamine
    • Einecs 217-740-8
    • 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

    540007

    Product Name 2,3-Dimethoxybenzylamine
    Cas Number 4134-29-4
    Molecular Formula C9H13NO2
    Molecular Weight 167.21
    Appearance Colorless to pale yellow liquid
    Boiling Point 140-142°C at 15 mmHg
    Density 1.105 g/cm³
    Refractive Index 1.553
    Purity Typically ≥97%
    Solubility Soluble in organic solvents like ethanol and ether
    Synonyms 2,3-Dimethoxyphenylmethylamine
    Smiles COC1=CC=CC(=C1N)OC
    Inchi Key FMVIGRQZZYMVKX-UHFFFAOYSA-N
    Storage Condition Store at 2-8°C

    As an accredited 2,3-Dimethoxybenzylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle, tightly sealed with a plastic screw cap and labeled with chemical name, quantity, hazards, and supplier details.
    Shipping 2,3-Dimethoxybenzylamine is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It should be packed according to standard hazardous material protocols, protected from heat, moisture, and direct sunlight. Appropriate labeling and documentation are provided, ensuring compliance with transport regulations for safe handling and delivery.
    Storage 2,3-Dimethoxybenzylamine should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. Protect the chemical from moisture and direct sunlight. Recommended storage is at room temperature or lower, ensuring proper labeling and keeping it away from acids and bases to prevent hazardous reactions.
    Application of 2,3-Dimethoxybenzylamine

    Applications of 2,3-Dimethoxybenzylamine in Industrial Manufacturing

    2,3-Dimethoxybenzylamine finds active use in multiple specialized chemical synthesis channels. As a direct manufacturer, we serve industrial partners from regulated pharmaceutical lines to fine chemical production.

    1. Pharmaceutical Intermediate Synthesis for Active Pharmaceutical Ingredients (APIs)

    Leading drug manufacturers incorporate 2,3-dimethoxybenzylamine to build essential amine-containing intermediates during the synthesis of small-molecule APIs, particularly for neuroactive compounds and antihypertensive agents. Pharmaceutical process chemists introduce this amine as a nucleophilic building block in multi-step routes starting with aromatic substitution or reductive amination. Critical stages include controlling reaction temperatures, pH, and solvent ratios to ensure integration of the dimethoxy functional group while achieving high enantiopurity and isolated yields. Batch QC follows pharmacopeia standards for identity, purity, and trace amines before further processing towards the final API form.

    Industry compliance standards

    • USP–NF Monographs for related substances
    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II for starting materials
    • Japanese Pharmacopoeia, General Notices for raw material controls

    Typical usage ratio

    • 0.05–0.3 molar equivalents, variable based on molar input of coupling substrate; specific ratios depend on the desired molecular scaffold and final step yield optimization

    Downstream process integration

    • Introduced in early to mid-stage intermediate synthesis, commonly after initial aromatic substitution or halogen exchange steps. Downstream transformation involves reductive amination or amide coupling prior to purification and conversion to bulk API form.

    Final product types

    • Neuroactive pharmaceutical intermediates
    • Antihypertensive agent building blocks
    • Psychoactive compound precursors
    • Custom-synthesized API intermediates for clinical trial supply

    2. Specialty Dye and Pigment Manufacturing

    Fine chemical producers employ 2,3-dimethoxybenzylamine in condensation or coupling reactions to assemble advanced chromophores required for high-performance organic dye manufacturing. The amine group acts as a functional handle in azo and anthraquinone dye synthesis, contributing to desired solubility profiles and color stability. Production follows established routes such as diazotization, Schiff base formation, or Ullmann condensation, with precise monitoring of pH, batch temperature, and amine loading. All process lines utilize closed transfer systems and in-line analytics for batch consistency and purity control.

    Industry compliance standards

    • EN 71-3 for migration of heavy metals (toys, textiles)
    • OEKO-TEX Standard 100, Appendix 6, for textile dye chemistry
    • REACH Annex XVII for industrial dyes
    • ISO 105-A02 for color fastness testing parameters

    Typical usage ratio

    • 5–30% by mass of primary reactants in dye coupling stages; actual ratio adapted based on color depth, desired molar absorption, and solubility attributes of the target dye product

    Downstream process integration

    • Charged to the condensation reactor following thorough premixing with core chromophore-forming reactants. Subsequent work-up includes filtration, multistage washing, and spray-drying to furnish highly pure dye granules.

    Final product types

    • Water-soluble textile dyes
    • Permanent ink pigments
    • High-speed printing dye intermediates
    • Photostable industrial colorants

    3. Agrochemical Active Ingredient Synthesis

    Agricultural chemical manufacturers utilize 2,3-dimethoxybenzylamine in the assembly of key amine-derived intermediates essential to proprietary herbicide and growth regulator molecules. The material enters via direct amination or N-alkylation under controlled batch conditions using pressure-resistant reactors and catalytic systems. Downstream integration focuses on minimizing by-product formation and maximizing amine conversion. Each agrochemical plant implements dedicated solvent recovery and purification lines to ensure compliance with active ingredient and impurity level specifications.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides (JMPS Codes)
    • EPA 40 CFR §180.1001 for inert ingredients
    • ISO 9001:2015 for quality management of synthesis process
    • GLP (Good Laboratory Practice) for batch traceability

    Typical usage ratio

    • 0.1–1.2 mole equivalents based on active molecule structure; titration adjusted to mole ratio of core aromatic or aliphatic partners in amination, targeting >98% conversion

    Downstream process integration

    • Typically fed into intermediate coupling reactions during middle phase of AI synthesis. The processed intermediate is then purified through liquid–liquid extraction, isolation, and crystallization steps ahead of formulation packaging.

    Final product types

    • Selective herbicide intermediates
    • Plant growth regulator precursors
    • Custom synthesis intermediates for contract agrochemical manufacturing
    • Off-patent generic AI building blocks

    4. Polymer Modifier and Curing Agent Production

    Advanced polymer formulators select 2,3-dimethoxybenzylamine to manufacture specialty curing agents, chain extenders, and polymer functionalization additives. The compound acts as a primary amine hardener in epoxy resin systems, or reacts as a nucleophile in custom polyamide and polyimide modification. Technicians optimize integration temperature and mixture ratios to achieve target cross-linking density, mechanical strength, and thermal behavior. End-to-end QC testing ensures absence of unreacted amines and consistently controls molecular weight distribution in finished modifiers and resins.

    Industry compliance standards

    • ASTM D1652 for epoxy resin amine value determination
    • ISO 9001:2015 for continuous production quality
    • RoHS Directive 2011/65/EU for electronic encapsulants
    • REACH registration for industrial chemical use

    Typical usage ratio

    • 7–25 parts per hundred parts resin (phr), adjusted according to amine value and cross-linking stoichiometry needed for target polymer properties

    Downstream process integration

    • Directly dosed into resin blend during prepolymer melt or solution blending stage. Integration typically precedes casting, molding, or extrusion of the finished polymer system, depending on final application specification.

    Final product types

    • Epoxy curing agents and chain extenders
    • Functionalized polyamides with custom side chains
    • Thermal-resistant polyimide additives
    • Industrial polymer composite additives
    Free Quote

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