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HS Code |
194856 |
| Cas Number | 96-20-8 |
| Iupac Name | 2-Aminobutan-1-ol |
| Molecular Formula | C4H11NO |
| Molar Mass | 89.14 g/mol |
| Appearance | Colorless liquid |
| Boiling Point | 175-178 °C |
| Melting Point | -1 °C |
| Density | 0.913 g/cm³ |
| Solubility In Water | Miscible |
| Flash Point | 83 °C |
| Pka | 9.76 (amino group) |
| Refractive Index | 1.445 |
| Smiles | CC(CO)N |
As an accredited 2-Aminobutanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Aminobutanol is supplied in a 500g amber glass bottle with a secure screw cap, labeled with handling, hazard, and storage information. |
| Shipping | 2-Aminobutanol should be shipped in tightly sealed containers, protected from moisture and incompatible substances. Handle with care to prevent leaks or spills. Label the package according to local and international regulations for hazardous chemicals. Store and transport at room temperature, away from strong oxidizers and acids, ensuring proper ventilation during transit. |
| Storage | 2-Aminobutanol should be stored in a tightly closed container in a cool, dry, and well-ventilated area away from heat, sparks, and open flames. It should be kept separate from strong oxidizing agents and acids. Proper labeling is essential, and containers should be inspected regularly for signs of leakage. Personal protective equipment should be used when handling the chemical. |
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Purity 99%: 2-Aminobutanol with purity of 99% is used in API synthesis, where high product yield and minimized impurities are achieved. Viscosity grade 20 cP: 2-Aminobutanol with a viscosity grade of 20 cP is used in intermediate formulations, where uniform mixing and consistent reactivity are ensured. Molecular weight 89.14 g/mol: 2-Aminobutanol of molecular weight 89.14 g/mol is used in chiral building block production, where precise molecular incorporation is essential for enantioselectivity. Melting point 14°C: 2-Aminobutanol with a melting point of 14°C is used in controlled crystallization processes, where stable phase behavior improves processing efficiency. Stability temperature 120°C: 2-Aminobutanol with a stability temperature of 120°C is used in high-temperature reactions, where chemical integrity is maintained during synthesis. Water content <0.5%: 2-Aminobutanol with water content below 0.5% is used in moisture-sensitive catalysis, where unwanted side reactions are minimized. Assay 98%: 2-Aminobutanol with an assay of 98% is used in fine chemical manufacturing, where consistent product quality and batch reproducibility are required. Particle size <50 μm: 2-Aminobutanol with particle size below 50 μm is used in solid-state formulations, where rapid dissolution and enhanced homogeneity are provided. |
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2-Aminobutanol walks a path that may seem narrow, but it supports a broad part of today's chemical progress. With the formula C4H11NO, this molecule finds space in labs and factories, most often in the form of a clear or light yellow liquid. The compound features an amino group and a hydroxyl group, giving it a flexible edge. Its physical and chemical features make it more than just a line on a chemist's checklist—it stands as a bridge between simple precursors and more complex molecules. Teachers and students brush against it in lessons, while professionals count on its qualities for consistency and reactivity.
With a boiling point close to 174°C and a melting point near 0°C, 2-aminobutanol holds its own in typical production settings. Purity counts for more than just bragging rights; it dictates whether a batch will serve its intended purpose. I've seen projects stumble when contaminants sneak in, especially during synthesis or pharmaceutical work, so a high-purity grade—98% and above—stays in demand. The density, usually around 0.92 g/cm³, finds its place in calculations when preparing reaction mixtures.
For many, the draw of 2-aminobutanol stretches well beyond its structural makeup. In pharmaceuticals, it's more than a stepping stone—it often takes part in the synthesis of important drug intermediates. Its presence helps create some antiviral and antihypertensive agents. Outside the world of medicine, I've met researchers who rely on this compound to build specialty surfactants. Industrial chemists find value in its dual reactivity; both the amine and alcohol groups set the scene for modifications.
I remember a project focusing on stabilizing sensitive materials in the lab. 2-Aminobutanol played a quiet but steady hand by preventing unwanted side reactions due to its mild basicity and low volatility. Its use as a chiral building block in the preparation of specific enantiomers stands out to anyone who's ever worked on asymmetric synthesis. That quality has helped unlock new methods for producing optically active compounds—no minor feat for fields like agrochemicals and fine chemicals.
Stacking up 2-aminobutanol against close relatives such as ethanolamine or isopropanolamine brings several differences into focus. Ethanolamine, with one carbon fewer, often ends up in detergents and emulsifiers. It brings a higher degree of water solubility but lacks the same steric bulk. Isopropanolamine, on the other hand, serves as a corrosion inhibitor but features a branched structure, changing its reactivity profile.
The straight-chain nature of 2-aminobutanol, along with its additional carbon atom, shifts how it interacts in chemical reactions. In cases demanding a balance between hydrophobic and hydrophilic behavior, this molecule lays out a sound middle path. End users in pharmaceuticals or fine chemicals keep coming back to it because its chemistry supports more precise control over molecule design. One example lies in the preparation of certain beta-blockers, where the chain length affects both efficacy and side-effect profiles. Subtle changes at the molecular level ripple through to production costs and final product reliability.
Having spent years in chemical environments, I don't overlook the importance of safe handling and practical logistics. 2-Aminobutanol brings a moderate odor and a slight viscosity. Handling reminds me of straightforward alcohols, but with an eye on its amine component. Gloves, goggles, and well-ventilated spaces are not negotiable in practice. While its flammability stays low compared to pure alcohols, a careful approach guards against long-term health concerns.
I’ve watched production lines where slight spills happen. Thanks to its relatively low volatility, 2-aminobutanol doesn't race into the air at room temperature, which adds a measure of workplace safety. Still, liquid phase exposure asks for good absorption protocols, and cleaning should never get lazy. Disposal rules follow the playbook for amines and alcohols: containment, neutralization if needed, and secure waste management. While all this may seem routine, failing to take these basics seriously will erode trust among skilled workers and management alike.
The world doesn’t run on paperwork and data sheets alone. Sourcing quality 2-aminobutanol remains a test of trust between supplier and end-user. Those who’ve weathered supply chain delays—especially in the wake of global disruptions—know that reliability matters as much as technical features. Pricing swings track with shifts in production costs for basic raw materials and energy inputs.
Conversations with colleagues remind me that the real value of this compound finds roots in how it streamlines project goals. Whether purifying a new drug molecule or building up a research lab’s chemical toolkit, having a dependable supply lets everyone stay focused on innovation rather than troubleshooting bad batches. This reliability shines brightest during experiments that demand strict control over inputs. A good supply partner stands just as tall as lab grit and creativity.
I see plenty of new directions every year involving 2-aminobutanol. Lab teams explore its potential as a precursor for novel ligands and specialty chelating agents. Since both the amine and hydroxyl groups can latch onto metals or react with substituents, inventive minds keep discovering ways to tweak downstream reactions. I’ve met synthetic chemists turning to this compound when hoping to sidestep tedious protection and deprotection steps during multi-stage synthesis.
Researchers keep coming up with greener and more efficient ways to produce and use this compound. Demand for energy-saving and waste-reducing processes has pushed many to experiment with enzymatic or catalytic transformations involving 2-aminobutanol. Some breakthroughs have included using biocatalysts for asymmetric ketone reduction, improving selectivity and minimizing byproducts.
The chemical world doesn’t run in a vacuum—regulations, environmental plans, and green chemistry principles shape how compounds like 2-aminobutanol fit into the bigger picture. Waste management, recycling, and sourcing from renewable resources make up more of the day-to-day conversation. Direct experience teaches that proper design—with waste reduction in mind—translates into fewer headaches and stronger community trust.
Compared to bulk chemicals like methanol or ethylene glycol, specialty amines receive scrutiny for their fate in the environment. 2-Aminobutanol degrades primarily through microbial action, yet this doesn't excuse careless disposal. Emphasizing closed systems, process refinement, and safe recovery lifts both the plant’s reputation and its bottom line. Regulatory guidelines on emission and discharge make up a crucial guardrail, shaping decisions from R&D to full-scale manufacture.
Trouble often starts when labs and factories cut corners on verifying chemical identity and quality. I’ve heard stories of batches failing analytic tests due to impurities or mislabeled packaging. Smart purchasing teams invest time in vetting suppliers and confirming batch-to-batch consistency. This might look like routine testing for pH, color, or residual solvent, but behind every good result stands diligence and shared knowledge.
Looking back, even top-performing labs run into unexpected roadblocks from small differences in raw materials. A reagent’s minor impurity can put weeks of work at risk. Teams that keep robust quality checks and open lines of communication with suppliers dodge many avoidable headaches. Peer review among chemists helps surface recurring problems, leading to community-driven solutions. Leadership in science often means admitting what didn't work and building better habits from those lessons.
Raising standards for both quality and environmental footprint takes patience and teamwork. Several improvements have delivered real progress over the years. Digital inventory and tracking help labs flag inconsistencies early. Automated dispensing minimizes human error and spillage, especially in busy production spaces. Real-time analytics give feedback during complex reactions, showing whether the aminobutanol is playing its expected part. These practical changes save more research hours than flashy innovations.
Knowledge exchange—through regular workshops and open-access data—raises the bar for everyone. I’ve seen good ideas grow from casual conversations at conferences. Sharing tips on purification or handling tricks can smooth out some bumps. Those who develop new applications or find better ways to recycle waste don’t just build their company’s bottom line; they help the wider community climb higher.
Genuine improvements in the 2-aminobutanol supply chain tend to follow clear needs. If a process improves yield by a few percent or trims hazardous byproducts, adoption spreads quickly. Labs working on tight budgets still value reliability and quality, even if it means paying a bit more upfront. Cheap, unreliable chemicals rarely pay off in the long run due to higher waste and failed projects.
Market demand isn’t just about volume; it’s about solving specific problems and opening new doors in synthesis. A specialty pharmaceutical manufacturer may look for a supplier with strong track records and documentation, while a research group might place flexibility and custom batch sizes near the top of the wish list. The most successful suppliers often work closely with users to fine-tune specifications.
Talking to others who actually use 2-aminobutanol, stories revolve around its reliability and versatility. Medicinal chemists describe its essential place in synthesizing key intermediates, often noting that a reliable, pure source felt like a safety net in challenging projects. From chemical engineering shops to big pharma labs, users praise it for balancing reactivity with manageable hazards.
Failures often come from small lapses—missing a storage guideline, underestimating environmental risks, or losing track of a new impurity. Open discussion among industry groups brings those risks to the surface. Seasoned professionals lean on experience and shared war stories more than flashy brochures. Building smarter routines for monitoring chemical health and tracking performance has paid off in both productivity and safety.
The science surrounding 2-aminobutanol isn’t finished evolving. Analysts see signs that demand could shift as green chemistry and biopharma trends expand. Synthetic approaches that shrink environmental impact and costs have gradually moved from pilot scale to larger production, promising a stronger place for this compound in future applications. Emerging uses in new drug delivery systems and advanced materials might push existing boundaries on both process efficiency and purity needs.
The challenge remains finding the sweet spot between innovation, safety, and environmental responsibility. Regulatory watchdogs increase their scrutiny year after year. New opportunities for recycling, process refinement, and creative reuse hold promise for reducing long-term costs. Labs willing to invest in new methods and transparency rarely regret the effort; trust among partners and colleagues grows in quiet but lasting ways.
Mentoring new chemists and operators means teaching more than just reaction protocols or safety drills. Sharing real stories about the shifting demands of industry—along with the lessons learned from both success and failure—gives newcomers a better foundation. Guided group discussions that dissect recent production hiccups, or walk through the details of process optimization, build a culture where everyone grows.
Experience shows that incremental change, driven by honest feedback loops, transforms daily work. Those who stay flexible—adapting storage practices, tightening safety checks, or responding to customer needs—find that quality problems shrink, and long-term results improve. Familiarity with the specifics of 2-aminobutanol only goes so far; willingness to keep learning sets apart effective teams from the rest.
The journey of 2-aminobutanol, from production plant to end-user, reflects ongoing progress in science and industry. It succeeds in both simple and specialized roles because of its unique traits, but also through the shared commitment of those who produce, handle, and apply it wisely. Quality, safety, and environmental focus all play a part.
Those who depend on 2-aminobutanol—whether in research, teaching, or manufacturing—benefit most when the whole community maintains high standards. By valuing honest partnership, rigorous verification, and ongoing innovation, users and providers build more than just better chemicals. They set the groundwork for real progress and genuine trust in the growing, interconnected field of modern chemistry.