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HS Code |
616568 |
| Chemical Name | 2,4-Diaminophenoxyethanol Hydrochloride |
| Cas Number | 43021-99-0 |
| Molecular Formula | C8H13ClN2O2 |
| Molecular Weight | 204.66 g/mol |
| Appearance | White to off-white crystalline powder |
| Solubility | Soluble in water |
| Melting Point | 168-172°C |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, tightly sealed, protected from light |
| Synonyms | 2-(2,4-Diaminophenoxy)ethanol hydrochloride |
| Ph Value | Neutral to slightly acidic (in aqueous solution) |
| Boiling Point | No data available (decomposes) |
As an accredited 2,4-Diaminophenoxyethanol Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2,4-Diaminophenoxyethanol Hydrochloride is supplied in a 25g amber glass bottle with a secure, tamper-evident polypropylene cap. |
| Shipping | 2,4-Diaminophenoxyethanol Hydrochloride is securely packaged in tightly sealed containers to prevent moisture and contamination. It is shipped following standard regulations for chemical substances, with appropriate labeling and documentation. The chemical is handled by trained personnel and transported under controlled conditions to maintain stability and ensure safe delivery to the destination. |
| Storage | 2,4-Diaminophenoxyethanol Hydrochloride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of moisture and heat. Protect from direct sunlight. Store separately from strong oxidizing agents and acids. Ensure proper labeling and secure storage to prevent unauthorized access, and follow all relevant chemical hygiene and safety regulations. |
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Purity 99%: 2,4-Diaminophenoxyethanol Hydrochloride with 99% purity is used in pharmaceutical intermediate synthesis, where high purity ensures minimized byproduct formation. Molecular weight 200.67 g/mol: 2,4-Diaminophenoxyethanol Hydrochloride with a molecular weight of 200.67 g/mol is used in custom peptide manufacturing, where precise molecular matching supports efficient coupling reactions. Melting point 212 °C: 2,4-Diaminophenoxyethanol Hydrochloride with a melting point of 212 °C is used in high-temperature polymerization processes, where thermal stability improves overall process control. Water solubility > 100 mg/mL: 2,4-Diaminophenoxyethanol Hydrochloride with water solubility above 100 mg/mL is used in aqueous drug formulation, where enhanced solubility enables higher active ingredient loading. Particle size < 20 µm: 2,4-Diaminophenoxyethanol Hydrochloride with particle size below 20 µm is used in injectable formulation development, where fine particle distribution ensures homogenous dispersion. Stability temperature up to 120 °C: 2,4-Diaminophenoxyethanol Hydrochloride stable up to 120 °C is used in process scale-up operations, where thermal stability maintains product integrity under stress conditions. Acid value < 1 mgKOH/g: 2,4-Diaminophenoxyethanol Hydrochloride with acid value less than 1 mgKOH/g is used in cosmetic active ingredient synthesis, where low acidity reduces risk of formulation incompatibility. |
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In the world of fine chemicals, some compounds earn the silent admiration of both researchers and industry professionals thanks to their reliability and adaptability. 2,4-Diaminophenoxyethanol Hydrochloride stands out among them, providing a base for synthesis and a backbone for specialty applications where molecular precision makes all the difference. The compound usually appears as a white to off-white crystalline powder, with a purity level demanded by both research labs and robust manufacturing pipelines—purity above 98% signals serious intent to serve advanced uses rather than broad, undemanding markets.
This material features a chemical structure infusing versatility into every batch: a phenoxyethanol backbone with amine groups in the 2 and 4 positions. Its hydrochloride salt form improves solubility in aqueous applications, which proves helpful not just for reaction consistency but also for safe and straightforward handling. In research, this slim margin between “good enough” and “trusted” draws the line between promising breakthroughs and frustrating setbacks.
Years spent troubleshooting reactions and scaling up pilot batches have taught me that some compounds behave with a kind of professional courtesy—they don’t deliver surprises when following the basics. 2,4-Diaminophenoxyethanol Hydrochloride earns that reputation, whether it appears in the regular pace of a synthetic pathway or as a specialty additive in a finished formulation.
I have worked with pigment precursors where even a trace impurity soured the final shade, and with pharmaceutical intermediates where reactivity meant the difference between a single pure product and a tangle of isomers. Consistency over multiple lots, a clear melting point, and low water content all help this product build trust over time. I remember sifting through data sheets and batch records, looking for gaps. With this hydrochloride salt, the paperwork often matched the experience at the bench—a small but meaningful victory.
Pharmaceutical chemists, dye manufacturers, and specialty polymer designers look for more than molecular promise. Performance on scale, processability, and a kind of “chemical reliability” can tip purchase decisions. 2,4-Diaminophenoxyethanol Hydrochloride finds itself right at the crossroads of value and function, especially because its synthetic utility doesn’t stop at a single industry.
For dyes, this compound serves as a key intermediate, lending itself to the precise introduction of amine groups on aromatic cores. That changes properties like solubility, brightness, and wash-fastness in finished colorants. Color labs have found that tweaking side chains on the phenoxyethanol core opens up shades and stabilities hard to touch with older chemistry. The hydrochloride form often helps with initial mixing and processing, which in the crowded and sometimes unpredictable conditions of industrial dyeing facilities, helps reduce error rates and wasted batches.
Pharmaceutical synthesis turns to this molecule not only for its structure but also for its handling advantages. The free base version can sometimes pose storage and stability concerns, but as the hydrochloride salt, users report greater shelf-life and improved reproducibility across reactions. Medicinal chemists leverage its amine groups for coupling reactions, allowing attachment of key pharmacophores for exploratory compounds, and it remains a staple for side-chain elaboration on core structures destined for preclinical and clinical trial pipelines.
Polymers made to order—especially those designed for biocompatibility or functional surface modification—draw on the reactivity of both the ether and amine groups of 2,4-Diaminophenoxyethanol Hydrochloride. Custom coatings, biomaterials, and even diagnostic tools benefit from a reagent that doesn’t require heroic efforts to purify or activate. Years ago, I saw a small startup pivot their surface chemistry approach simply because this compound allowed a one-pot functionalization step, saving both time and money on pilot runs.
Like many colleagues, I have compared dozens of candidate reagents across projects. On paper, several aromatic amines or phenoxyethanol derivatives may offer overlapping features. In practice, subtle differences in purity, salt form, and ease of handling shift user preference over time.
Other aminophenols or phenoxyethanols occasionally crowd purchasing lists. Yet few alternatives offer the balance between high water solubility, clear melting characteristics, and low-risk storage that this hydrochloride salt does. Some analogs arrive only as oils or sticky solids, complicating dosing and weighing in the lab. Crystalline consistency in 2,4-Diaminophenoxyethanol Hydrochloride makes it less likely you’ll miscalculate batch additions or under-dose a catalyst or co-monomer.
Storage stability marks another difference with real impact. In labs where temperature control sometimes falters, and in storage warehouses exposed to humidity swings, free bases of similar compounds can cake, discolor, or degrade. This salt maintains integrity over months (even years) with normal precautions. I have had samples sit, unopened, during project delays and later perform exactly as intended—something I cannot claim about several alternative compounds.
Decades of working around fine and specialty chemicals reinforce the importance of safety as a non-negotiable. While 2,4-Diaminophenoxyethanol Hydrochloride offers low volatility and manageable dusting, standard PPE—goggles, gloves, effective ventilation—remains a must at bench and production scales. Like many aromatic amines, appropriate handling and storage protocols protect both the user and the batch from contamination.
Engagement with regulatory developments, such as REACH guidance or updates in pharmaceutical impurity profiles, shapes real-world choices. Labs and businesses rely on transparent supply chains and consistent documentation. In my experience, every shipment of this product that came through with clear COAs, batch histories, and impurity breakdowns contributed directly to project milestones—and when something did not match, reputable suppliers worked quickly to address it.
Investing in solid documentation, robust QA processes, and open lines of communication pays off in fewer disruptions down the line. Peers in production admit that shaving a few cents per gram up front rarely justifies a recall or failed batch, especially for compounds bound for regulated or high-value finished goods.
2,4-Diaminophenoxyethanol Hydrochloride has never grabbed headlines the way “blockbuster” molecules like ascorbic acid or paracetamol have, but its steady presence in protocols, patent filings, and innovation pipelines speaks volumes. High-purity lots unlock experiments that push knowledge further, letting chemists—academic or corporate—ask and answer difficult questions about mechanism, formulation, and performance.
A good example comes from the development of advanced colorants for digital textile printing. The tolerance window in that process leaves little room for error; the compound’s clean reaction profile and batch-to-batch consistency shaved hours from pilot optimization and ultimately improved run times at one manufacturer I worked with. Meanwhile, academic projects chasing new enzyme inhibitors or signaling pathway probes have turned to this hydrochloride salt to rapidly install functional groups onto aromatic rings. Instead of spending weeks troubleshooting problematic batches, teams could focus on publishing and patenting. These moments of progress add up, building trust in the supporting cast behind headline discoveries.
In the changing world of regulated chemistry, compliance and sustainability are more than afterthoughts. Suppliers responding to green chemistry trends look closely at solvent use, byproduct profiles, and lifecycle stewardship. 2,4-Diaminophenoxyethanol Hydrochloride benefits from manufacturing routes that minimize hazardous intermediates and waste, providing an edge for forward-looking customers.
No product fits every context. Cost per kilo may run higher than commodity alternatives, depending on supplier and local demand swings. Occasional supply chain pinch-points—especially during regional disruptions or raw material shortages—underscore the value of secondary sourcing and good inventory planning. I have lived through rushed re-specifications at the eleventh hour because someone assumed a “minor” reagent would always be available by next-day air.
Some users report issues with hygroscopicity in extreme climates, where humidity climbs and air conditioning falters. Tight drum seals and desiccant packs help, but planning for actual storage conditions matters as much as any packing spec. The hydrochloride form fares much better than the free base in resisting clumping or hydrolysis, but no chemical resists water entirely over time.
Waste management also means responsible disposal and clear labeling; the amine groups require attention to downstream processing, and teams focused on environmental responsibility keep up with best practices for neutralizing any excess or wash waters. Training new hires and junior scientists on safe handling pays dividends well beyond compliance audits.
Every procurement or R&D manager faces tough choices with budgets, timelines, and competing priorities. Quality sometimes feels like a luxury in price-driven industries, but time and again, problems show up not during purchasing but halfway through a vital product run or trial. Inexperienced buyers might reach for lookalike compounds, only to discover weeks later that a subtle impurity profile or batch-to-batch inconsistency has thrown off results.
Chemical suppliers vying for major accounts might offer incentives or promise short lead times, but customers who return year after year do so for a combination of reliable performance, honest documentation, and timely support. I recall a story from a small contract manufacturer who learned the value of stability the hard way: switching to a lower-cost aminophenol led to a wave of rejected lots, chasing their quality team for months and eventually costing more than sticking with a trusted product would have.
The push toward digital documentation and supply chain traceability has only made the case stronger for well-established compounds. With global operations under constant scrutiny and regulatory audits tightening, knowing exactly what’s in the drum and who made it proves worth more than a one-off discount.
It’s tempting in fast-moving industries to chase every shiny new molecule or buzzy alternative, but there’s wisdom in sticking with products that have earned their place through years of reliable service. 2,4-Diaminophenoxyethanol Hydrochloride fits that bill for a range of sectors, giving formulators the confidence to tackle new challenges knowing their inputs won’t introduce unexpected complications.
Younger chemists ask about greener options, data transparency, and the environmental footprint of every purchase. Forward-thinking suppliers respond with cleaner manufacturing protocols and, where possible, direct shipping and packaging innovations to reduce waste. This compound’s role as a somewhat “known quantity” lets innovators zero in on breakthrough applications—whether that means developing a cleaner drug intermediate or fine-tuning a custom polymer.
Sticking to the tried-and-tested doesn’t mean avoiding innovation; it means picking battles wisely. Time saved on troubleshooting equates to more time experimenting and refining. That process keeps science and business moving forward.
Chemical professionals—myself included—pick up a library of lessons during careers spent among glassware and spreadsheets. Standardizing on reliable materials goes hand in hand with documenting every tweak and exception. Keeping a running log of how this hydrochloride salt performed in each new process, noting even minor deviations, created a living resource for teammates and future collaborators.
Strong lab culture builds from shared trust. Welcoming feedback about occasional batch anomalies ensures problems get caught and solved early, before a frustrated technician or line worker notices them too late. Sharing procedural improvements across sites, while avoiding the trap of rote documentation, creates room for real growth and brings new chemists up to speed faster.
No matter the sector—dyes, pharma, advanced polymers—retaining flexibility in the face of disruptions shapes resilience. That may mean diversifying suppliers, actively testing incoming materials, or investing in stronger relationships with trusted vendors of 2,4-Diaminophenoxyethanol Hydrochloride. Risk management cannot be afterthought, especially as regulatory and customer standards tighten each year.
Industry does not stand still for long. As both regulations and customer demands change, so too must the products that anchor manufacturing and research. 2,4-Diaminophenoxyethanol Hydrochloride does not promise universal answers, but it helps build consistent foundations for progress. In a field where today’s trial and error sketches tomorrow’s breakthroughs, having one less variable to worry about means projects finish sooner and deliver more reliable results.
Looking ahead, the demand for tighter impurity specs, cleaning up synthetic routes, and documenting carbon footprints only grows. The suppliers who lead in this space do more than fill orders—they partner with clients to deliver knowledge and value.
The chemicals that find lasting relevance do more than fill a gap—they support each user’s need to meet technical, safety, and ethical goals. With a sound reputation built on traceable quality, good documentation, and visible supplier support, 2,4-Diaminophenoxyethanol Hydrochloride keeps making its case as a staple for high-performance molecules and advanced manufacturing. The decisions made today about sourcing, qualification, and QC set the stage for tomorrow’s product lines; and sticking with what works remains a mark of both wisdom and responsibility for the years ahead.