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HS Code |
261642 |
| Product Name | DL-3-(3,4-Dimethoxyphenyl)-2-Methyl-2-Hydrazine Propionic Acid |
| Molecular Formula | C12H18N2O4 |
| Molecular Weight | 254.28 g/mol |
| Cas Number | 1193-21-1 |
| Appearance | White to off-white solid |
| Melting Point | 160-163°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in water and methanol |
| Storage Temperature | 2-8°C (Refrigerated) |
| Synonyms | α-Methyl-α-hydrazino-3,4-dimethoxyphenylpropionic acid |
| Hazard Class | Irritant |
| Canonical Smiles | CC(C1=CC(=C(C=C1)OC)OC)(N)C(=O)O |
| Usage | Research chemical |
As an accredited DL-3-(3,4-Dimethoxyphenyl)-2-Methyl-2-Hydrazine Propionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, sealed HDPE bottle containing 25 grams of DL-3-(3,4-Dimethoxyphenyl)-2-Methyl-2-Hydrazine Propionic Acid with safety labeling. |
| Shipping | This chemical, DL-3-(3,4-Dimethoxyphenyl)-2-Methyl-2-Hydrazine Propionic Acid, is shipped in sealed, chemical-resistant containers under ambient conditions unless otherwise specified. Packaging complies with applicable safety and regulatory guidelines. Transportation includes hazard labeling and documentation to ensure secure and compliant delivery. Handle with care to avoid exposure and contamination during transit. |
| Storage | DL-3-(3,4-Dimethoxyphenyl)-2-Methyl-2-Hydrazine Propionic Acid should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances. Store at 2–8°C (refrigerator). Ensure the storage area is well-ventilated and access is restricted to trained personnel. Follow all relevant safety guidelines, including labeling and spill containment, to prevent decomposition or hazardous exposure. |
Applications of DL-3-(3,4-Dimethoxyphenyl)-2-Methyl-2-Hydrazine Propionic Acid in Industrial ManufacturingAs a manufacturer specializing in DL-3-(3,4-Dimethoxyphenyl)-2-Methyl-2-Hydrazine Propionic Acid, we support specialized downstream production where the unique structure of this raw material enables targeted synthesis steps. Here we present core industrial application scenarios where our product plays a significant role, based on actual manufacturing integration practices and industry requirements. 1. Active Pharmaceutical Ingredient (API) Synthesis for Cardiovascular DrugsThis compound functions as a crucial intermediate in the synthesis pathway of specific anti-arrhythmic and antihypertensive APIs. Its hydrazine group structure supports regioselective substitution reactions, allowing manufacturers to efficiently construct complex molecular scaffolds required for these finished APIs. Regulatory conformity is a fundamental requirement in all process stages, including batching, reaction controls, and purification. Industry compliance standards
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2. Fine Chemical Intermediates for CNS Drug ResearchResearchers and fine chemical producers apply this hydrazine compound as a key building block for synthesizing molecules in central nervous system (CNS) drug discovery. Its dimethoxyphenyl motif is essential for constructing frameworks found in certain mood disorder candidates. Stringent lab and pilot-scale compliance practices prevail at this development stage. Industry compliance standards
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3. Specialty Agrochemical Intermediate ManufacturingThis compound serves as a designated precursor in the production of select herbicidal and fungicidal agents. The electron-donating methoxy groups contribute to the compound’s compatibility with modern heterocycle-based agrochemical synthesis routes, critical for producing plant protection solutions. Industrial-scale production must ensure adherence to agrochemical precursor regulations and batch traceability. Industry compliance standards
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4. Advanced Organic Electronic Material Precursor SynthesisManufacturers in the field of organic electronics use this compound as a starting material to create electron donor-acceptor molecules for OLED emissive layers or thin-film transistors. The dual methoxy substitutions and hydrazine backbone facilitate precise control over electronic properties during conjugated polymer fabrication and are selected for their performance in solution-processing environments. Industry compliance standards
Typical usage ratio
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Standing on the production floor, we see every stage from raw feedstock to finished DL-3-(3,4-Dimethoxyphenyl)-2-Methyl-2-Hydrazine Propionic Acid. Our team works through each batch, monitoring color and crystallinity, ensuring each kilogram meets the standards we set for ourselves. In our world, quality comes from hands-on experience and an eye for the subtle signs: the shine of purified powder, the way it handles moisture, the faint etherous scent we recognize after years spent beside reaction vessels.
This compound, sometimes abbreviated as DMHPMPA among technical staff, stands out in our product line for its unique combination of structural features. We have watched increasing demand from pharmaceutical developers and chemical researchers, and it’s easy to see why. The 3,4-dimethoxyphenyl ring structure lends distinctive electronic properties, while the hydrazine and methyl groups on the propionic acid side chain give it a reactivity profile few analogues can mimic.
Our production runs begin with carefully sourced 3,4-dimethoxybenzene derivatives. At the reactor, we employ controlled conditions—forging a bond between the aromatic nucleus and first methyl, then working in the hydrazine and carboxylic acid units with the precision required to avoid byproducts that can crop up in less disciplined batches. Each synthesis cycle is monitored using HPLC and NMR to track purity and side product formation. Years back, yields would swing unpredictably, but dedicated process improvement stabilized rates near 89–92%, balancing efficiency and purity.
Chemists in our plant know the quirks: stir speeds matter, pH mustn’t drift, even the temperature ramp between alkylation and hydrazine addition shapes the purity outcome. We purify the crude material through a crystallization protocol that wastes little solvent and recovers most of the active, all while keeping the overall footprint small. Our technicians run LC-MS spot checks at multiple stages—trust comes not from assumption, but from what the instruments tell us during each run.
DMHPMPA appears as a crystalline powder, off-white to pale beige depending on trace amounts of natural impurities. From lots calcined at higher temperatures, we sometimes see larger crystals; most users prefer the standard medium particle size, which flows more easily and dissolves consistently in common laboratory solvents. Several of our customers have remarked that consistency of color and texture means fewer downstream hiccups, like variable dissolution times or clogging of filters, issues that can plague batches sourced from less careful facilities.
Its melting point tends to fall in a narrow range, batch after batch. This helps end-users predict reaction onset or processing conditions downstream. Stability profiles show long shelf life under standard storage, although we recommend a cool, dry environment to reduce the risk of oxidation or hydrolysis. Some competitors offer material with inconsistent performance—chalky, clumpy, or faintly discolored—but we pride ourselves on uniform appearance, borne from rigorous process control.
People wonder why research organizations fixate on this molecule. Most turn to DMHPMPA as a building block or active intermediate in custom syntheses, especially in pharmaceutical development. Its hydrazine group, rarely available in a propionic acid framework paired with a dimethoxyphenyl ring, serves as a springboard for further functionalization. We’ve seen it used in creating novel CNS-active compounds, specialty ligand frameworks, and as a masked amine in combinatory synthesis projects.
Each buyer comes with a new application. Some require tight specifications for their process—ultra-low metal ion content, high optical purity, or a particle size range compatible with high-throughput screening. We accommodate these through batch selection and, when needed, customized purification or grinding steps, leveraging our small-batch flexibility. Our hands-on technical team coordinates directly with client chemists: we share our spectral data, field practical questions about reactivity, and keep open channels for troubleshooting.
On one level, a molecule is a molecule. But in reality, synthetic chemistry is shaped by the details: the ratio of regioisomers, the handling requirements, the contaminant profile, even subtle differences in crystalline habit. Some in the industry package white powders in a drum and call it a day. We’ve dealt with rushed orders from small resellers—what showed up was flaky, full of sticky clumps, and reeked of residual solvent. Our approach solves that. Each batch earns a comprehensive certificate, backed by direct analysis results—not just a line on a spreadsheet, but the actual chromatograms and spectra.
Workflow is transparent here, never mysterious. Teams can track batch history, and if a customer voices a concern, we pull up the actual run records—a practice we’ve followed for decades. Some clients send a trainee to check our line, and we open the doors. Our operators talk them through the steps, from raw material storage to packaging under nitrogen, so they see every variable is managed. The people composing those technical emails have actually stood at the distillation column or cleaned the rotary evaporator. This isn’t a brokerage; this is chemical manufacturing with months of real effort behind each kilogram.
Many researchers compare DMHPMPA to other hydrazine-based intermediates, or to simpler 3,4-dimethoxyphenyl acids and amines. The difference isn’t just one of subtle structure, but of practical outcome. The additional methyl group and side-chain configuration mean this compound behaves differently in a range of synthetic routes. We talked with a group developing central nervous system agents; they tried the parent acid and mono-methyl analogues, but those lacked the solubility in methanol and acetonitrile needed for their pilot steps. Our material dissolved swiftly, leaving none of the undissolved grit that complicated their reactions with other alternatives.
It also stands apart from 3-(3,4-dimethoxyphenyl)-2-propionic acid due to the hydrazine’s increased nucleophilicity. When forming hydrazones or related linkers, direct substitution becomes faster and yields rise compared to single-amino or carboxyl-only analogues. Some labs report fewer byproducts and a cleaner product profile, saving countless hours in downstream purification. This isn’t something seen on paper; it’s learned by running the reactions, recovering product, and tallying the cost of rework.
We’ve invested heavily in on-site analytics. Each batch is scanned by HPLC and GC, scrutinized for residual solvents and related impurities. FTIR confirms ring substitution, and our NMR results show clean spectra with minimal side product interference—something less regulated vendors sometimes gloss over. Every order includes a spectrum set, so those running their own QC see exactly what we saw.
Content uniformity is not a buzzword here; it shows in the control charts compiled each quarter. Where deviations arise—a shift in melting point, a spectral impurity—we stop and find the source, usually long before a drum leaves our doors. This culture of hands-on quality cuts out so many headaches: no batches quarantined at importation, no delays waiting for retesting, and no obscure supply chain drama.
Customers often call after receiving a shipment, concerned about storage and safe handling. In practice, this compound resists air and light fairly well, but best results come from keeping containers tightly sealed and in a low humidity environment. Scooping or pouring is straightforward, with little tendency for dust formation—a relief for those with limited personal protection setups.
Standard lab glassware handles the acid well. In acid solution, the molecule displays reliable stability through routine heating cycles. One customer tried using an automatic powder dispenser and reported smooth dosing, with no clumping or bridging. Our team keeps an open line for practical handling questions, and we share methods built on years of internal use and direct customer feedback.
From day one, we took pride in supporting researchers learning their craft. Graduate students and rising process chemists ask questions that push us to explore new purification methods, or tweak particle size profiles for better solubility. Sometimes, these collaborations reveal improvements that flow right back into our plant: a shift in recrystallization solvent, a tweak to the drying protocol, or a new insight into polymorphic forms.
Open communication builds trust on both sides. Users know the people making their starting materials, and we keep learning what matters in the lab and at the bench. These shared experiences—mistakes and successes—shape every improvement in our process.
Recent years brought evolving regulatory standards and environmental mandates, so we take steps to ensure each synthesis batch respects both worker safety and environmental protection. Solvent recovery loops, closed-system transfer, and careful waste segregation are standard on our plant floor, not afterthoughts. Our HSE team trains operators and chemists on hazard recognition and best practices. Each lot leaves not just as a certificate number, but as a record of diligent stewardship.
We have also introduced energy-efficient reaction vessels and phased out certain longstanding solvents to reduce our emissions profile. These aren’t decisions made under duress, but improvements that help long-term sustainability of chemical manufacturing. Our customers benefit from knowing the products in their labs come from a source committed to safe, responsible production, monitored continuously.
New entrants to the field often focus on price or short-term supply, but we have seen that real value comes from reliability and support. Batches with unknown impurity profiles may pass unnoticed in simple applications, but these almost always lead to headaches as tolerance windows tighten and projects move to pilot scale. Our team solves this the old-fashioned way: by investing in up-to-date instrumentation, ongoing operator training, and a culture that favors root-cause analysis over symptom patching.
If an upstream issue affects purity, we identify it early and issue full disclosure to any affected user, sometimes providing interim solutions or technical guidance. Many long-term clients have switched over after encountering supply chain problems or unexplained delays elsewhere. A transparent approach differentiates us: the lab and the manufacturing plant are closely linked, avoiding miscommunication and delays.
We once assisted a customer who had ordered 3-(3,4-dimethoxyphenyl) derivatives from several suppliers for side-by-side trials. Other samples arrived with variable particle size, crystalline habit, or reactivity. Our batch, by contrast, required no additional processing and fit seamlessly into their protocol, saving days of bench work. That sort of reliability is not accidental—it stems from robust process documentation, skilled workers, and the decision to make quality assurance everyone’s responsibility.
It is not uncommon for researchers to face late-stage problems due to seemingly minor specification differences. What reads like a tiny shift in melting point or trace impurity shows up later as a stubborn byproduct or unexpected signal in chromatography. Our habit is to flag even the minor anomalies, double-check protocols, and communicate findings upfront. This approach means process chemists scale up with fewer surprises, and that makes a difference in competitive fields.
Every year, our technical support team compiles feedback not just from power users, but from occasional buyers and smaller research groups. They voice concerns about order turnaround, technical support, or documentation detail. Taking this feedback seriously, we have added additional online resources, offered live troubleshooting sessions, and revised our labeling and documentation systems to suit actual user practice.
On the plant floor, feedback from the end-user side has shaped the way DMHPMPA is packaged and shipped. Protective liners, moisture barriers, and traceable seals arise not from abstract best practices, but from real stories—once, a shipment to a damp coastal city arrived clumped. By redesigning packaging, that problem disappeared. These iterative improvements yield a better experience for all users.
Our philosophy rests on producing more than chemical commodities. Each batch represents an agreement: we will deliver not only the stated molecule, but a product shaped by the hard lessons of daily hands-on practice and honest communication. Researchers seeking DL-3-(3,4-Dimethoxyphenyl)-2-Methyl-2-Hydrazine Propionic Acid can trust that our version reflects this long-term commitment—produced with care, evaluated with professional rigor, and backed by a team whose experience is always available to support your next breakthrough.