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HS Code |
221788 |
| Chemical Name | 3,5-Dimethoxybenzylamine |
| Molecular Formula | C9H13NO2 |
| Molecular Weight | 167.21 g/mol |
| Cas Number | 10250-27-8 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 294 °C |
| Density | 1.10 g/cm³ |
| Purity | Typically ≥98% |
| Solubility | Soluble in water and organic solvents |
| Smiles | COC1=CC(=CC(=C1)OC)CN |
| Inchi | InChI=1S/C9H13NO2/c1-11-8-3-7(6-10)4-9(5-8)12-2 |
| Refractive Index | n20/D 1.545 |
| Storage Conditions | Store at 2-8°C, tightly closed |
As an accredited 3,5-Dimethoxybenzylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g amber glass bottle with a secure screw cap, labeled "3,5-Dimethoxybenzylamine" and safety precaution details, safely sealed. |
| Shipping | 3,5-Dimethoxybenzylamine is shipped in tightly sealed containers, protected from light and moisture. It is typically packed in amber glass bottles or certified chemical-resistant packaging. Transport follows all relevant regulations for chemicals, including labeling for hazards. Shipping documentation includes safety data, and carriers must comply with regional handling and storage guidelines. |
| Storage | 3,5-Dimethoxybenzylamine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect it from light and moisture. Store at room temperature or as specified on the safety data sheet, and ensure proper labeling for easy identification and safe handling. |
Applications of 3,5-Dimethoxybenzylamine in Industrial Manufacturing3,5-Dimethoxybenzylamine serves as a key chemical intermediate for multiple specialized industrial sectors. As an original manufacturer, we support established customers in pharmaceuticals, agrochemicals, advanced materials, and specialty dyes, with product quality and processability validated at industrial scale. The following application scenarios reflect actual production use and compliance requirements within their respective downstream markets. 1. Pharmaceutical API Synthesis (CNS Drugs)Our material acts as an essential amine building block for manufacturing CNS-active pharmaceutical ingredients, particularly those involving substituted phenethylamine derivatives. Active use occurs during multi-stage API synthesis for several central nervous system therapies. Customers typically introduce this raw material in protected or unprotected form depending on route selection and regulatory impurity control. Demand centers around consistent impurity profiles and support for validated GMP processes, especially where targeted methylation patterns are required to comply with pharmacopeial specifications. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingLeading agrochemical formulators employ our raw material to construct advanced herbicide and fungicide intermediates. The amine functionality and di-methoxy substitution are especially favored in the synthesis of triazole-based agro actives and complex phenethyl structures. Use is common in closed, automated reactor systems to ensure exposure control and reproducible impurity removal, with strict adherence to global agricultural chemical standards covering both product traceability and residual amine assessments in final actives. Industry compliance standards
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3. Advanced Dye and Pigment SynthesisProducers of functional dyes and pigments rely on the unique substitution pattern of this benzylamine for synthesizing high-performance azo and anthraquinone dyes, especially in electronics and specialty textile applications. Batch formulations require tight control of amine concentration during coupling and diazotization stages, as N-methylated impurities directly affect chroma and fastness properties. Final colorant grades undergo comprehensive QC for EU and US textile chemical safety compliance, and all batches maintain documented trace aminated impurity limits. Industry compliance standards
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4. Peptide and Amino Acid Derivative SynthesisSpecialty peptide and amino acid manufacturers use this benzylamine in the synthesis of novel N-functionalized building blocks, where its electron-rich ring facilitates selective coupling during solid-phase or solution-phase peptide assembly. Regulatory focus in this niche aligns with biopharma-grade trace impurity thresholds and full backward traceability, while batch-specific QC confirms the absence of genotoxic and reactive side-products in downstream protected amino acid derivatives. Industry compliance standards
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5. Organic Electronic Material Building BlocksProducers of organic electronic and advanced optoelectronic materials use this compound to generate select functionalized benzylamine cores, which form the backbone of organic semiconductors and charge-transport layers. Consistency of the methoxy substitution is crucial for tuning electronic band gaps and controllable stacking in device-grade films. Manufacturing and quality standards emphasize low alkali and halide contamination, with tailored dosage based on targeted synthesis of electronic performance polymers or small molecules. Industry compliance standards
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Each day, people working in benches and reactors see raw materials transformed into the substances that shape today’s laboratories and manufacturing lines. 3,5-Dimethoxybenzylamine has earned its place here because of the steady demand from pharmaceutical developers, agrochemical producers, and fine chemical synthesis teams. Experience matters a great deal for this molecule. Over countless batches, with process controls honed and scaled, we’ve seen its properties and uses develop alongside trends at the research core. The steady feedback loop from customers and our own QA team drives improvements in how this compound reaches the next user.
Let’s talk about the material itself. 3,5-Dimethoxybenzylamine carries the CAS number 4167-47-5. It crystallizes as a white to off-white solid, notable for its mild aromatic amine odor and its practical solubility in organic solvents such as methanol, ethanol, and ethyl acetate. When we prepare each lot, consistent control means the melting point stays within the narrow range customers require – usually between 46°C and 50°C. Here, batch HPLC tracks let us confirm a typical purity of 98% and above. Handling starts with dedicated vessels, then each run is dried and packed to minimize trace moisture, so the amine stays as specified from drum to package.
Applications drive our production choices directly. Nearly every batch we make finds its way into pharmaceutical intermediates and research for new entity exploration. Researchers use 3,5-Dimethoxybenzylamine as a key building block for synthesizing complex heterocycles, customized side chains, and protected amines. Medicinal chemistry projects frequently request smaller lots, while custom manufacturing clients order on the kilogram scale for scale-up screening or early GMP campaigns. We regularly hear from peptide chemistry labs using this amine to anchor protecting groups or add methoxy-substituted aromatic rings to candidate molecules. On the chemical synthesis side, its versatile reactivity smooths downstream modifications. Amine protection, reductive aminations, and nucleophilic substitutions all run efficiently with well-prepared material.
Our role as the actual maker means quality starts at the drum of raw starting materials and finishes at the filled product vessel. Scale brings new learning. In smaller quantities, 3,5-Dimethoxybenzylamine’s purification feels straightforward, but large-scale isolation takes patience and judgment. It’s tempting to think every production run is the same, yet subtle changes in process conditions—temperature ramps, stirring rates, solvent composition—make the difference. Every kilo we send out represents multiple verification points, from in-process checks using GC-MS for trace byproducts, to careful FTIR tracking through each phase. Color, odor, and even how the solid crusts as it cools tell experienced technicians whether they are on track.
There is no shortcut to building know-how. Handling of mother liquors, correct storage to avoid secondary formation, and shipping in lined containers all stem from direct experience. Batch-to-batch consistency becomes easier through records kept on every run. If a customer calls about a difference in the spectral profile or slight variation in yield downstream, we reference archived analytical results and shipping histories to trace the root. This is not generic logistical work—every cycle of production teaches something new, and corrections are logged for the next operator in the chain. Over time, customer feedback has led us to adjust drying times and optimize particle size for easier dissolution and filtration on their end.
Chemists who work with 3,5-Dimethoxybenzylamine have shared that its performance in forming key C-N bonds can save significant steps in retrosynthetic planning. Methoxy substitutions at 3 and 5 positions block unwanted side reactions, steering the reactivity where the chemist desires—this is especially valued in multi-step synthesis. One pharmaceutical client reported that material consistent in both purity and crystal form led to reproducible assay outcomes for scale-up trials, which cut several weeks from project timelines. Peptide chemistry teams consistently request smaller particle sizes because they dissolve faster, avoiding “clumping” that slows automated synthesis cycles. Our batch history supports both pharmaceutical and agrochemical customers, as the molecule forms the base for custom herbicides and potential fungicide discovery efforts.
In our own hands, the amine’s robust nature streamlines isolation from mother liquor, compared to less substituted benzylamines. Less polar relatives have posed crystallization issues or unpredictability during purification, especially under highly humid or rapid cooling conditions. Customers note that 3,5-Dimethoxybenzylamine stores well over months, given the right container and environmental control, with minimal color change or loss to sublimation.
Production lines regularly see multiple benzylamine derivatives, but 3,5-Dimethoxybenzylamine stands out due to its electron-donating methoxy groups. These groups add both steric and electronic effects, guiding regioselectivity during further functionalization. Compared to parent benzylamine or even single-methoxy analogs, it has enhanced solubility in polar organic solvents but remains manageable on filtration and washing lines.
When scaling other methoxy isomers—notably 2,4- or 3,4-dimethoxybenzylamine—we have observed increased byproduct formation, most often N-alkylated or over-oxidized derivatives. The 3,5-dimethoxy configuration strikes a good balance between reactivity and stability. Operators have an easier time removing residual solvents and identifying finished material by clearer melting transitions. For certain syntheses, our clients specify 3,5-substitution specifically to suppress possible ortho- or para-directing issues that trouble alternate patterns.
On the performance side, users maneuver it in cross-coupling or protection reactions with far less background reactivity compared to unsubstituted benzylamine. Isolation after reaction also tends to be easier. Slight differences in scent and tactile feel—a mild aromatic amine with faint ether notes—is one of the practical markers our QC personnel use for hands-on verification, before even running the chromatograph.
Feedback from industrial buyers and regulatory teams continues to push for more sustainable handling of aromatic amines. In our plant, we rework most spent solvents and recover a significant fraction for reuse. Safety systems include real-time monitoring for airborne amines, protecting both operators and downstream effluent. Methoxybenzylamine derivatives like the 3,5-isomer present lower acute toxicity than certain other substituted amines, which informs our handling, containment, and exposure protocols. We’ve invested in on-site scrubbing capability that captures amine emissions before venting or further processing.
Proper waste management remains critical. Spent mother liquors are collected in segregated drums for incineration or chemical neutralization, avoiding cross-contamination risks. Each run’s waste footprint is logged and measured, tied directly to optimizing process economy and minimizing environmental impact. We share analytical data with any customer needing to complete their safety or regulatory dossiers, so full traceability continues at every level of the supply chain.
Procurement experts and project managers tell us that traceability and genuine technical support affect everything downstream. Each time labs use 3,5-Dimethoxybenzylamine for a new route—and encounter an unexpected impurity or sporadic yield drop—direct lines to the original producer become crucial. We have answered dozens of detailed technical requests stemming from subtle batch-to-batch variation caused by differences in storage, transfer conditions, or seasonal humidity. Process engineers crawl through historical manufacturing records to trace root causes and offer practical corrections.
Forward transparency saves money and time because it eliminates guesswork. Examples range from a customer who needed a certificate for endotoxin testing due to stringent pharma standards, to a pilot plant requesting additional sieving just before running their campaign, all coordinated through integrated production and QA teams. This openness stands in contrast to secondary distributors who may pass on product without the deeper knowledge or access to original records.
Recent years have shown that security of supply hinges on direct engagement. Geopolitical developments and transport disruptions have forced the market to look closely at their supply networks. Our response draws on finished stock monitoring, redundant raw supplier qualification, and rapid lot-trace feedback from the manufacturing suite. This means the pipeline from synthesis to the client's door remains resilient during unpredictable periods—delay scenarios covered by emergency reserves and air-freight contingency allotments.
Every operator here recognizes the subtle cues that only come from hands-on contact. They keep records not only on batch yields and analytical results, but also on seasonal issues that affect production—summer humidity lengthens drying times, while winter ramps slow exothermic steps. Project managers rely on this knowledge to tweak schedules and preempt bottlenecks. When a run turns up unexpected coloration or a shifting melting point range, the floor tech communicates it upstream and downstream immediately.
Regular workshop sessions allow process upgrades to filter through every team. The drying suite team recorded a solution for caking during a wet season by layering over anhydrous sodium sulfate and adjusting the final vacuum pull. Operators log this for future batches, and the insight then heads to process development when evaluating new derivatives or larger-scale projects.
Almost every improvement in our 3,5-Dimethoxybenzylamine consistently comes from customer data or lab bench experience, not from abstract analysis. Major requests have included better flow in dust-free dispensing, so we invested in a new granulator. Multiple buyers prefer a specific mesh size—QC responded with sieving screens to reach a more uniform cut. Pharmaceutical buyers demanded HPLC verification for specific low-level byproducts, so our analytical staff updated the routine certificate of analysis to match.
This kind of two-way communication never ends. Teams from peptide research to specialty polymer labs describe outcomes where purity and ease of handling lifted overall yields or reduced time-to-result. Someone might notice a flask sticking in winter conditions, which translates to tweaks in the warehouse’s moisture controls the next season. Sharing best practices between users—whether they dissolve the amine in alcohol or chloroform—refines the next lot we deliver.
Even with decades spent producing 3,5-Dimethoxybenzylamine, issues occasionally surface. Our most experienced operators remember specific years where an unseasonable run of high-humidity weeks complicated isolation and drying. Hands-on troubleshooting—adjusting solvent picks and batch times—helped recover expected yields and maintain release specifications.
We see similar complexities with long-term storage. If the container’s seal weakens or exposure to light increases, a faint yellowing appears sooner than expected. Regular checks and lot-specific recommendations from the plant floor help buyers prevent such degradation. Should a downstream process display increased side product or new impurity peaks in the HPLC trace, our technical team reviews archived manufacturing and analytical data to find the intersection of equipment maintenance, process change, or new operator error.
Improvements take many forms. For a customer facing inhalation exposure control issues at their site, our response included repacking under inert gas and tighter secondary seals. If a research client faces difficulty dissolving the material in their chosen solvent, our feedback based on solubility data—and a few tested approaches from our own QA routine—can save attempts and wasted time.
Chemical manufacturers sit in a unique position to view the evolution of how a compound is used. Early in its commercial life, 3,5-Dimethoxybenzylamine attracted interest from peptide and pharmaceutical researchers as an amine building block that added both functionality and solubility. Over subsequent years, we tracked new uses in specialty polymers, and more recently, in materials chemistry where aryl amine units offer electron-donating effects for advanced monomers.
With attention shifting to more sustainable reaction conditions, calls for larger batches of this molecule reflect new process intensification strategies or green solvent shifts. Certain synthetic teams now favor this amine because it can deliver faster conversions under milder conditions—reducing waste, saving energy, and minimizing the need for excess reagents. Our own chemists help troubleshoot unexpected bottlenecks or suggest alternate purification options, based on hundreds of production and quality runs behind the scenes.
Real understanding grows through continuous production, feedback, and adaptation. Making 3,5-Dimethoxybenzylamine is never just a matter of following a formula, but a dynamic, cooperative process between experienced operators, technical support, and chemists in the field. Each lot embodies countless adjustments made over time, and every new request further evolves our routines and knowledge base.
Direct contact between user and manufacturer forms the basis for credible, high-quality supply chains. Process data, analytical support, and meaningful operator insight translate to fewer delays and better project results. From the manufacturing floor to the next synthesis breakthrough, our experience with 3,5-Dimethoxybenzylamine draws on fact, feedback, and the daily reality of making chemistry work as intended.