|
HS Code |
742227 |
| Product Name | 2,4-Dichlorobenzylamine |
| Cas Number | 89-98-5 |
| Molecular Formula | C7H7Cl2N |
| Molecular Weight | 176.05 |
| Appearance | White to off-white crystalline solid |
| Melting Point | 47-51°C |
| Boiling Point | 267-268°C |
| Solubility In Water | Slightly soluble |
| Density | 1.34 g/cm³ |
| Purity | Typically ≥98% |
| Flash Point | 121°C |
| Storage Temperature | Store at room temperature |
| Iupac Name | 2,4-dichlorobenzylamine |
| Synonyms | 2,4-DCBA; Benzylamine, 2,4-dichloro- |
As an accredited 2,4-Dichlorobenzylamine (109#) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,4-Dichlorobenzylamine (109#), 100g, is packaged in a sealed amber glass bottle with a secure screw cap and chemical label. |
| Shipping | 2,4-Dichlorobenzylamine (109#) is shipped in tightly sealed containers, protected from moisture and direct sunlight. It should be handled with appropriate safety measures, including gloves and eye protection. Transport follows standard hazardous chemical regulations to prevent spillage, exposure, or environmental release. Keep away from incompatible substances during transit. |
| Storage | **2,4-Dichlorobenzylamine (109#)** should be stored in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed when not in use. Use appropriate chemical-resistant containers and ensure proper labeling. Implement secondary containment to prevent accidental release or spills. |
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Purity 99%: 2,4-Dichlorobenzylamine (109#) with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and consistent product quality. Melting Point 73°C: 2,4-Dichlorobenzylamine (109#) with a melting point of 73°C is used in agrochemical formulation, where it provides thermal stability during processing. Molecular Weight 176.04 g/mol: 2,4-Dichlorobenzylamine (109#) at molecular weight 176.04 g/mol is used in specialty chemical manufacturing, where it supports precise stoichiometric reactions. Low Volatility: 2,4-Dichlorobenzylamine (109#) with low volatility is used in polymer additive production, where it minimizes loss during high-temperature compounding. Stability Temperature 120°C: 2,4-Dichlorobenzylamine (109#) stable up to 120°C is used in resin synthesis, where it maintains chemical integrity under elevated conditions. Particle Size <50 µm: 2,4-Dichlorobenzylamine (109#) with particle size less than 50 µm is used in fine chemical blending, where it enhances dispersion and uniformity. Moisture Content <0.5%: 2,4-Dichlorobenzylamine (109#) with moisture content below 0.5% is used in electronics chemical processing, where it prevents unwanted hydrolysis reactions. |
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In today’s world, finding a chemical intermediate that delivers real consistency can make all the difference across industrial, laboratory, and research settings. 2,4-Dichlorobenzylamine, often labeled as 109#, draws attention for this very reason. Anyone who’s spent much time in chemical synthesis or formulation knows that success often depends on starting materials that predictably perform. 2,4-Dichlorobenzylamine fits that bill, offering not only dependable quality but a combination of purity and versatility that keeps it relevant, year after year.
Manufacturers and scientists both appreciate materials that balance stability with reactivity. 2,4-Dichlorobenzylamine typically comes as a crystalline solid, white to pale yellow, with a characteristic amine odor. The 109# model indicates a specific synthesis route that prioritizes low levels of byproducts and stable shelf characteristics. Many chemists recall the headaches of erratic starting points; here, 2,4-Dichlorobenzylamine shines by cutting down on surprises during production or scale-up.
Common packaging goes from kilogram-level bottles for research to fiber drums sized for bulk manufacturing. Chemical supply chains thrive on predictability, and with 2,4-Dichlorobenzylamine, you rarely hear complaints about delayed delivery or stock-outs thanks to a steady worldwide source base. Knowing what you get, and getting it when you need it—simple, but far from guaranteed elsewhere.
Direct application often depends on the setting. In pharmaceutical manufacturing, it’s used as a key intermediate in the synthesis of antiviral drugs, antimicrobials, and sometimes as a step toward more complex compounds. Agricultural labs recognize its usefulness in designing new crop protection agents and growth regulators where specific substitution on the benzylamine backbone leads to precise biological activity.
It’s not just drug or agrochemical labs tapping into its potential. Anyone dealing with specialty synthesis—fine chemicals for polymers, resins, or even some aromatic compounds—has likely come across 2,4-Dichlorobenzylamine in their process development files. Over the years, stories have emerged of researchers hitting roadblocks with generic benzylamines, only to flip the script by switching to this substituted variant.
Purity plays a role that goes beyond what’s written on a certificate of analysis. Every chemist remembers struggling with difficult purifications, which drain time and budget, especially when planning for multi-step syntheses. The biggest advantage here is that the usual specification for 2,4-Dichlorobenzylamine 109# lists high purity levels—often 98 percent or above. Lower content of related impurities means less risk for downstream failures and cleaner reaction profiles. That translates into fewer reruns, leaner solvent use, and a lower environmental footprint. It’s not only about comfort in the lab; it’s about responsible practice at scale.
Specifications aren’t just up to buyer’s choice—regulations for pharmaceutical and crop protection chemicals keep tightening globally. For manufacturers, the assurance that each lot matches rigorous criteria saves headaches when submitting to regulatory agencies. It also helps companies maintain trust with their end users, whether those are researchers, patients, or farmers expecting pesticides to work without risky contaminants.
Choice matters in chemical supply. Compared to generic benzylamines or non-chlorinated analogs, 2,4-Dichlorobenzylamine 109# brings reliable selectivity and enhanced activity for many targets. This arises from the chlorine substitutions at the 2 and 4 positions on the benzene ring, which tweak reactivity while offering better compatibility with a range of synthesis steps.
Think about the alternatives: regular benzylamine lacks the same steric and electronic effects, leading to broader, sometimes less predictable behavior in catalytic or coupling reactions. I’ve witnessed colleagues push through countless failed attempts using unmodified starting materials, only to see results snap into place when switching to this more specialized amine. Chlorinated variants other than the 2,4- form might not offer the same downstream versatility, and in some cases, their physical properties make them less convenient to handle or transport—liquids are messier, while solids with inconsistent grain can gum up automated feeders.
Years at the bench teach one to value consistent crystallinity and melting points as much as theoretical yields. More than once, we’ve faced the fallout of poorly defined raw materials: clumpy powders, batches that degrade too quickly in humid weather, and endless, costly troubleshooting. Looking through quality reports for 2,4-Dichlorobenzylamine 109#, the lot-to-lot repeatability stands out. This reliability shields product developers and production chemists from abrupt troubleshooting marathons and lost batches.
Stability also matters for shipping and storage. 2,4-Dichlorobenzylamine stores well under standard conditions—low humidity, sealed packaging, out of direct sunlight—so buyers can stock up without racing against cracking drums or runaway degradation. That’s peace of mind rarely found with less robust precursors.
The push for greener, safer processes grows stronger each year. Many chemical players now aim to shrink waste, reduce toxic emissions, and cut hazardous byproducts. 2,4-Dichlorobenzylamine, produced to high standards, can support those ambitions. High-purity batches tend to run cleaner, which means lower burdens on purification plants and less environmental impact from waste disposal. Modern suppliers now trace routes back to responsible feedstocks and cleaner reaction technologies, adding further reassurance for those committed to environmental and social governance.
Even as regulations shift—including REACH and other frameworks governing toxic subtances—2,4-Dichlorobenzylamine’s long track record offers confidence. This isn’t some market newcomer with hidden surprises; labs and plants both small and large have integrated it into robust, documented workstreams. Alongside quality, this heritage plays its own part—there’s less risk of hidden impurities or outlier batches knocking critical projects off track.
R&D teams often juggle the risk of spending months on a promising synthesis route, only to find commercial supply won’t support scale-up. That doesn’t happen as often with 2,4-Dichlorobenzylamine 109#. Supply chains in Asia, Europe, and North America mean that producers respond quickly to demand shifts, both for kilo-scale research orders and tonnage-level production runs.
Quality aside, scalable handling matters for chemists moving from flask to drum. Packing formats work for glassware, continuous processes, or semi-automated pilot lines. This flexibility goes a long way in environments that need to flip quickly between project prototypes and full-scale output. Chemical R&D can be a gamble, but losing to practical logistics shouldn’t be the reason a promising compound gets axed.
Establishing real trust in a chemical ingredient rests on good documentation. As someone who’s both ordered and audited supply chains, I’ve seen firsthand how problems often stem from missing data or sketchy compliance records. With 2,4-Dichlorobenzylamine, established protocols cover everything from production traceability to safety profiles, and batch-level certificates clear most regulatory hurdles without much fuss. This helps downstream users avoid the grind of ‘extra paperwork’ or stalled trials, which many remember all too well with less-documented chemicals.
Those aiming for new international markets can lean on the well-established identity of 2,4-Dichlorobenzylamine. Labs building up at the cutting edge rarely have the patience for long-winded negotiations over chemical provenance. With this product, its history stands behind it.
Medicinal chemistry enjoys the substituent’s effect that directs selectivity and allows fine-tuning for specific targets, especially in early lead discovery. Manufacturers share plenty of anecdotes about how using a robust chlorinated amine intermediate keeps side reactions to a minimum. In agrochemical projects, precise placement of those chlorine atoms brings out needed bioactivity without adding unforeseen toxicity. Experienced chemists see such reliable performance as the backbone of many patent filings and successful registrations.
Sometimes the benefit lies in reducing downstream headaches. Solid, consistent melting and handling profiles mean formulation teams don’t scramble to adjust every time a new batch comes in. Tech transfer from lab to production floor can be tough, but using a trusted raw material lets project teams spend more time innovating, less time tracking down the source of small, compounding errors.
There’s no such thing as zero risk in chemical handling, but responsible suppliers and users work together to reduce hazards. 2,4-Dichlorobenzylamine calls for competent handling—nobody wants to take chances with skin or respiratory contact and most labs have the protocols to match. The upside: clear, accessible safety data means fewer ambiguous situations for workers, and modern packaging improves containment, reducing incident rates compared to loose, dusty powders or volatile liquids. In firms with a strong safety culture, reliable SDS documentation and label clarity make life easier for both new hires and seasoned hands.
Beyond lab walls, safer materials bring confidence on the supply-chain and regulatory sides. Any project developing substances for further human or environmental contact takes this seriously, and established chemical inputs help keep surprises to a minimum. Battles with unclear toxicology data or regulatory status—common with lesser-known, specialty amines—mostly disappear with this product.
Real-world budgets rarely stretch as far as teams might hope, so sourcing decisions often come down to total cost. 2,4-Dichlorobenzylamine sits at a sweet spot—affordable for high-volume runs, but not so commoditized that quality slips. This balance lets manufacturers keep project budgets steady and avoid the price spikes that sometimes sneak in when betting on rare or niche alternatives. Consistent demand means suppliers keep pace with output, and buyers don’t have to chase after substitutes that may not perform the same way in sensitive syntheses.
Discussing alternatives, many have debated switching to less expensive, structurally-simpler amine sources. Each time, they wind up back with 2,4-Dichlorobenzylamine after tallying up costs from added purification runs, lower yields, and regulatory uncertainty. Over time, the small difference in unit price gets dwarfed by the savings in labor, waste, and project delays.
Chemistry moves quickly, and every year someone announces a new synthetic platform or reactivity method. 2,4-Dichlorobenzylamine benefits from this relentless innovation while staying relevant—its established reactivity and physical properties bring out the best in new catalytic systems, combinatorial approaches, and greener synthesis. My time in both academic and industrial labs has shown that ingredients with flexibility and reliability win out, even when projects take sharp left turns. Whether building old drugs in fresh ways or developing something entirely novel, the right benzylamine intermediate forms the backbone of smart strategy.
Upcoming trends focus on even tighter impurity control and sourcing transparency. Here, 2,4-Dichlorobenzylamine 109# stays competitive by meeting international testing standards and adapting to client needs fast. If global routes shift—whether through regulatory update, economic turbulence, or supply chain realignment—producers of this compound typically bounce back with alternate sources, consistent packaging, and documented lot reliability.
Over years of sourcing, testing, and applying organic intermediates, many chemicals have come and gone in my own work and across the wider industry. Very few combine the dependability, versatility, and well-documented background that 2,4-Dichlorobenzylamine 109# brings to scientific and industrial teams. It’s gained a trustworthy reputation because—put simply—it delivers what practitioners expect, without excess drama or unnecessary compromise. Older colleagues who’ve worked through decades of changing regulations and shifting technologies often mention this intermediate as a staple of their labs and factories.
Choosing the right chemical building block matters, whether you’re after new patents, tightening up efficiency, or aiming for tighter environmental standards. In real-world practice, the simple fact is that fewer unknowns at the foundation of a synthesis ripple into fewer problems later in development. 2,4-Dichlorobenzylamine offers that solid bedrock: robust purity, steady supply, and a proven ability to adapt to the ever-evolving demands of research and industry. It’s one less thing to worry about, and in the business of getting chemical projects right, that sometimes makes all the difference.