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HS Code |
394317 |
| Chemical Name | 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine |
| Cas Number | 2662-50-4 |
| Molecular Formula | C10H12N6O |
| Molecular Weight | 232.24 g/mol |
| Appearance | White to off-white powder |
| Melting Point | 228-231°C |
| Solubility | Slightly soluble in water |
| Structure | Contains a triazine core with a 3-methoxyphenyl substituent |
| Iupac Name | 6-(3-methoxyphenyl)-1,3,5-triazine-2,4-diamine |
| Smiles | COC1=CC=CC(=C1)N2C=NC(N)=NC2=N |
As an accredited 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, opaque HDPE bottle with screw cap, labeled “1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine, 100g,” hazard and handling icons. |
| Shipping | **Shipping Description:** 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine should be shipped in tightly sealed containers, protected from moisture and sunlight. Transport in accordance with local and international chemical regulations. Use appropriate labeling and documentation. Handle with care, ensuring containers remain upright. Personal protective equipment (PPE) is recommended during handling and shipping. |
| Storage | Store **1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine** in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep away from direct sunlight, heat sources, incompatible materials (such as strong acids or oxidizers), and moisture. Label the container clearly and follow standard laboratory safety protocols. Use appropriate personal protective equipment when handling the chemical. |
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Purity 99.5%: 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine with purity 99.5% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yields and minimal by-product formation. Melting Point 210°C: 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine with melting point 210°C is used in high-temperature polymer formulations, where it provides enhanced thermal stability. Particle Size <10 μm: 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine with particle size less than 10 μm is used in advanced coatings, where it ensures uniform dispersion and optimal surface finish. Molecular Weight 220.23 g/mol: 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine with molecular weight 220.23 g/mol is used in agrochemical formulations, where it allows controlled release and precise dosing. Stability Temperature 150°C: 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine with stability temperature up to 150°C is used in electronic materials, where it maintains long-term performance under thermal stress. Water Solubility 15 mg/L: 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine with water solubility of 15 mg/L is used in aqueous dye formulations, where it offers balanced solubility and sustained color intensity. |
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1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine doesn’t show up on shelves in flashy packaging or everyday products, but its impact can be found woven through a wide range of manufacturing fields. This compound, with its precise arrangement of methoxyphenyl and triazine groups, steps into roles that often stay unnoticed by the end user. In my experience speaking with technical chemists and R&D teams, clarity often trumps fancy language: this compound brings a combination of stability, reactivity, and design flexibility that opens up options for those shaping formulary work in specialty chemicals, agriculture, and even electronics.
The name alone—1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine—points straight to its core structure. Its triazine ring carries three amine groups and a 3-methoxyphenyl side chain. This specific linkage allows for strong branching points in chemical synthesis, as well as a stable, planar core structure, which is often sought after for predictable performance under elevated temperatures or variable pH environments. Not every triazine-based compound offers the same balance. For example, if we look at standard melamine or cyanuric acid, both related triazines, the switch to a methoxyphenyl group brings different reactivity, more compatibility in certain dyes, and a sharper safety profile in many engineered conditions.
Some compounds stick to their main turf and don’t offer much flexibility. Here, 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine contrasts that reputation. While many in the chemical world recognize triazines from decades-old uses in herbicides or cross-linkers, this molecule carves its own path. It frequently appears as a building block for high-performance pigments, where color fastness and resistance to light degradation push the boundaries of what end products can take. Its methoxy functional group tunes electron density across the ring, which offers a whole new palette for those involved in color science, especially when stability under sunlight or in harsh processing conditions matters.
It doesn’t stop with pigments. Textile processing and the creation of specialty coatings often require intermediates with versatile hydrogen bonding and straightforward reactivity under controlled conditions. Personal experience tells me that researchers favor reagents that don’t force too many trade-offs between sheer reactivity and long-term physical stability. The compound’s structure helps it resist hydrolysis—a property chart in a chemistry lab often highlights how standard triazines succumb faster to moisture, while this one stands firm thanks in part to the electron-donating methoxy group. As new generation coatings and waterborne dispersions seek more reliable backbone chemistries, the reputation of 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine continues to grow.
In manufacturing, a chemical’s recorded purities and specification details speak volumes for reliability in scale-up. Through years spent in process scale-up labs, I’ve learned that triazine intermediates come with a variety of purity grades, often tailored to their planned use. When suppliers talk about 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine, the focus usually lands on achieving chemical purities upwards of 98%, along with tight control on moisture and trace metals. These numbers might not catch the imagination, but without them, large-scale reactions quickly spin out of control or stall when faced with regulatory hurdles.
This level of control becomes critical when integrating the compound into custom dye synthesis, where trace contaminants can alter shade intensity or reproducibility. On the flip side, in electronics—think specialty insulating films or advanced optical discs—cleanliness and structure predictability mark the difference between marketing a breakthrough product or sending piles of scrap to the waste stream. Noticeable here is the role specification plays not just in chemical safety, but in plant efficiency, downstream waste, and regulatory compliance. Purity underpins every risk assessment, and in many regions, that also paves the way for easier registration or market entry.
Comparing this compound with more commonly referenced triazines highlights where it fits well and where it might not. Traditional melamine, the poster child of triazine chemistry, takes a central role in forming resins for laminates or adhesives. It brings high nitrogen content, but lacks the aromatic punch and edge-case stability that a methoxyphenyl group introduces. Standard triazines often serve broad markets but don’t tap into the depth of specialty dye work, where slight shifts in electron density can make or break a formulation. Switching in a methoxyphenyl not only brings different UV-absorbing qualities but allows easier fine-tuning of end-use properties like solvent compatibility or heat resistance.
Another close neighbor, cyanuric chloride, wears the badge of a reactive anchor in pharmaceuticals and agrochemical synthesis. Its high reactivity sometimes becomes a problem when controlled, nuanced chemistry is needed. By comparison, 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine offers a step-down in raw reactivity but a step-up in precision. Instead of brute force, formulators can shape and direct the reactivity window with more confidence, which becomes essential as product liability and traceability clamp down across the chemical sector.
Evolving regulations in Europe, North America, and much of Asia continue to impose stricter scrutiny on intermediary chemicals. I remember facing a drawn-out registration process for a substance with only vague data on toxicity and bioaccumulation—a frustrating barrier for companies of every size. Here, 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine benefits from a well-documented structure and relatively clear legacy in pigment and coating industries. That transparency lends itself both to compliance and to safety assessment, as detailed studies often accompany decades of practical use.
In risk assessment meetings and calls with environmental health professionals, one expectation stands clear: manufacturers don't accept “good enough” safety profiles anymore. The transparent structure, moderate volatility, and manageable byproducts during synthesis help position this molecule a notch above less-documented triazines. Workers dealing with synthesis or downstream processing demand both reliable safety data and guidance for handling; in industries moving closer to human and environmental health standards, these factors now decide product selection far more than cost or tradition alone.
During collaborative projects between specialty chemical suppliers and research teams, I’ve watched the drive for new high-performance materials center around intermediates like 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine. This isn’t happenstance. Research labs count on such compounds for iterative testing, thanks to both manageable reactivity and consistent output from batch to batch. In dye chemistry, where small tweaks to substituent groups create profound color impacts, this molecule’s methoxyphenyl group acts as a crucial dial for innovators seeking the next leap in color reproduction or weather-fast durability.
Chemists in textiles continue chasing new routes toward washfastness and resistance to repeated exposure to detergents or sunlight. More than once, I’ve seen project managers wrestle with legacy chemicals producing only incremental improvements. By turning to intermediates with a richer set of modifiable groups (such as the tri-amine and methoxy functions present here), they stand a better chance of meeting or exceeding targets. This kind of direct link between chemical structure and real-world product outcomes remains the holy grail for any R&D department seeking better performance and longer life from their creations.
Industries moving at different speeds also change what they seek from specialty intermediates. Pigment manufacturers keep a wary eye on long-term light stability, often after seeing colors fade or transform under sunlight. Coating formulators tend to prioritize shelf-life and predictable reactivity with curing agents. Electronics producers zero in on dielectric properties and insulation resistance.
1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine walks a careful line among these requirements. Its structure brings in the right aromaticity for color work, but pairs it with the chemical backbone needed for demanding electronic film applications. Speaking with engineers over coffee or during training sessions, the verdict is pretty consistent: compounds that bridge these application gaps open new business and allow faster entry into adjacent markets.
Scaling from laboratory synthesis to industrial batch runs comes with headaches familiar to anyone who’s walked an operations floor. With 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine, producers often comment that its relatively compact molecular weight and crystalline nature simplify handling and dosing compared to some larger, oily intermediates. Its ease of crystallization out of standard organic solvents helps remove much of the variability that plagues batch-to-batch consistency.
At larger scale, the focus shifts to throughput, cleaning protocols, and containment. This compound’s moderate dustiness does prompt rigorous filter maintenance and worker training—nodes often missed in spec sheets but crucial for long-term plant reliability. On more than one occasion, process managers have highlighted the improved yield-on-purification compared against triazines bearing bulkier or multi-ring substituents, which tend to clog equipment or require harsher solvents for processing. These details shape not just cost models, but long-term investment in a facility’s capability to serve evolving customer segments.
The chemical world has weathered its share of supply disruptions over the past decade. Natural disasters, geopolitical disputes, and regulatory changes push buyers to reassess single-source dependencies. In roundtable discussions with purchasing specialists, mention of 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine comes with a nod to its place in relatively simple synthetic routes, allowing buyers to pivot between qualified suppliers when needed. This resilience in the supply chain not only supports stable pricing but also reduces lead time risks.
It’s worth noting that as more regional producers sign on to manufacture triazine derivatives, access to this specialty intermediate widens. Companies seeking alternatives to traditional imports can now check competitive pricing models and reduce the risk associated with bottlenecked supply nodes. For R&D and manufacturing alike, secure sourcing drives both innovation and on-time project delivery—two targets that stay high on the wishlists of any agile business.
As industries push for lowered emissions, less waste, and safer end products, the spotlight turns to intermediates that help achieve those targets without fundamental trade-offs. When contacting sustainability leads and reading through producer sustainability reports, clear patterns emerge: molecules that offer measurable efficiency improvements carry more weight. The methoxy substituent on this compound often means fewer halogenated byproducts during downstream synthetic steps, which translates to safer waste and more straightforward effluent treatment—a point not lost on operators tasked with daily compliance.
In real-world terms, the push for greener chemistry drives formulators and researchers to scrutinize not just a molecule’s performance, but also the fate of its leftovers. Here, 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine often wins out over more reactive or less stable triazines by offering a safer-by-design profile. Less chance of side reactions means less need for expensive post-reaction cleanup and fewer surprises in field performance—a major advantage in cost calculations over a product’s life.
Common production headaches—batch-to-batch variability, post-reaction purification, or occasional stability doubts—show up across nearly every specialty chemical. With 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine, success leans on simple but powerful measures. Reducing moisture uptake during storage, controlling particle size, and keeping a close eye on impurities upstream in the supply chain all lead to smoother production cycles.
Many industry colleagues recommend doubling down on staff training around handling and dosing. Ensuring that reagents see minimal air exposure curbs unexpected hydrolysis or degradation, especially in humid climates. Forward-thinking manufacturers invest in humidity-controlled bulk storage and real-time monitoring, swapping out traditional open-drum approaches for sealed systems. These shifts don’t just bring peace of mind—they lower the cost and stress of troubleshooting, month after month.
Where the technical edge meets market reality, choices carry weight. During launches of new pigment or forays into electronic insulation films, product managers look for molecules like 1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine to give them just enough differentiation to edge past existing solutions. Its chemical design allows precision adjustment of performance attributes, helping formulators stretch product lines momentarily stuck in older, less flexible models.
End users rarely care about the name or spelling of what’s inside their colored shirt or high-speed data cable. But for those inside technical teams, the ability to fine-tune how a product ages, processes, or appears under tough conditions builds both brand reputation and customer trust. With regulatory, economic, and performance pressures turning more intense, the value of adaptable, well-documented intermediates continues to grow.
1-(3-Methoxyphenyl)-1,3,5-triazin-2,4,6-triamine looks unremarkable as lines on a chemical structure diagram, but its reach spans from creative color chemistry to the guts of advanced coatings and electronics. Across continents and sectors, eager chemists and operations leaders share the same goals: predictable materials, safe and easy handling, and the chance to shift gears fast when the market changes. In my years talking with those on the production floor, in the lab, or at the end of the supply chain, I hear the value in compounds that bridge the gap between high performance and daily practicality. Products built on solid, well-studied intermediates like this one keep possibilities open and raise the bar for what new inventions can do.