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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 | 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. |
Applications of 2,3-Dimethoxybenzylamine in Industrial Manufacturing2,3-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
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2. Specialty Dye and Pigment ManufacturingFine 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
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3. Agrochemical Active Ingredient SynthesisAgricultural 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
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4. Polymer Modifier and Curing Agent ProductionAdvanced 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
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