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HS Code |
485235 |
| Iupac Name | (R)-3,3-Dimethyl-2-aminobutane |
| Molecular Formula | C6H15N |
| Cas Number | 19447-91-5 |
| Smiles | CC(C)(C)[C@H](C)N |
| Inchi | InChI=1S/C6H15N/c1-5(7)4-6(2,3)8/h5H,4,7-8H2,1-3H3/t5-/m1/s1 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 99-101°C |
| Density | 0.75 g/mL at 25°C |
| Optical Rotation | [α]20/D +16° (c=1, EtOH) |
As an accredited (R)-3,3-Dimethyl-2-Aminobutane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of (R)-3,3-Dimethyl-2-Aminobutane, securely sealed with a tamper-evident cap and labeled. |
| Shipping | (R)-3,3-Dimethyl-2-Aminobutane should be shipped in tightly sealed, clearly labeled containers, protected from heat and direct sunlight. It must comply with regulations for transporting flammable and hazardous chemicals, including appropriate documentation and safety data sheets. Handle and store in a cool, well-ventilated area away from incompatible substances during transit. |
| Storage | (R)-3,3-Dimethyl-2-aminobutane should be stored in a tightly sealed container, kept in a cool, dry, well-ventilated area, and away from direct sunlight, incompatible substances (such as strong oxidizers, acids), and ignition sources. Store at ambient temperature and avoid moisture exposure. Ensure proper labeling and keep away from food and drink. Use secondary containment to prevent accidental spillage or leaks. |
Applications of (R)-3,3-Dimethyl-2-Aminobutane in Industrial ManufacturingAs a direct manufacturer of (R)-3,3-Dimethyl-2-Aminobutane, we supply this specialty intermediate to multiple industries using proprietary synthesis routes. Our product serves downstream customers in enantioselective synthesis, fine chemical production, chiral pharmaceutical development, agrochemical manufacturing, and specialized polymer sectors where consistent chiral purity and traceability are critical to manufacturing performance. 1. Chiral Intermediate for Active Pharmaceutical Ingredient (API) SynthesisThis material acts as a key chiral building block in the production of certain enantiomerically enriched pharmaceutical APIs. Medicinal chemistry projects utilize it for asymmetric synthesis pathways, typically in multi-step routes for small molecule APIs, where the tert-butyl-like skeleton and steric profile are required. Quality control batches use validated analytical methods to monitor enantiomeric excess and process impurities throughout production. Industry compliance standards
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2. Selective Catalytic Ligand ProductionAdvanced catalyst manufacturing operations employ (R)-3,3-Dimethyl-2-Aminobutane as an integral component in the construction of chiral ligands for transition-metal systems. These ligands facilitate highly selective hydrogenations and asymmetric catalytic reactions, particularly in fine chemical synthesis where enantioselectivity and reproducibility must pass rigorous batch QC analysis. Industry compliance standards
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3. Agrochemical Intermediate SynthesisWe supply this compound to agrochemical synthesis plants as a precursor for specialty amines and chiral building blocks used in high-value pesticide and herbicide actives. Its specific framework supports sterically demanding reaction conditions, yielding finished agrochemical molecules with required technical-grade purity, toxicological profiling, and field stability. Industry compliance standards
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4. Functional Monomer Precursor in Specialty Polymer ManufacturingIn advanced materials sectors, manufacturers utilize (R)-3,3-Dimethyl-2-Aminobutane to introduce functionalized chiral moieties into custom polyamides and polyimides. These specialty polymers deliver enhanced toughness, optical activity, or chemical resistance for niche engineering, electronics, and membrane applications. End-users require batch-specific documentation on chirality incorporation and purity indices for final goods certification. Industry compliance standards
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Few molecules in our catalog get the amount of discussion in the lab as (R)-3,3-Dimethyl-2-Aminobutane. From our production floors to the development benches, chemists reach for this particular amine when they want reliable chiral building blocks that stand up to the complexities of modern synthesis. Having seen this compound shape projects across pharmaceutical, agrochemical, and material science applications, we’ve come to appreciate what sets it apart from the bulk of amine intermediates in use today.
Every year, thousands of kilograms of generic amines roll off manufacturing lines. Still, the (R)-enantiomer of 3,3-dimethyl-2-aminobutane always gets extra scrutiny—for good reason. Chirality controls the biological properties in asymmetric synthesis. Pharmacological activity, selectivity, and downstream success often depend on optical purity. Racemates cloud results and undercut performance in active pharmaceutical ingredients. Putting in the time to produce the single (R)-stereoisomer matters for formulation and regulation alike.
Chemists can tell the difference. The shape, electronic profile, and behavior in reaction mechanisms all differ between enantiomers. In daily production, our technical teams tailor enantioselective routes, hand-pick selective catalysts, and control distillation procedures tightly. We keep optical purity levels well above 99% ee on commercial lots—no shortcuts here. Extra effort means one less worry for the process chemist, one less variable sabotaging yield or impurity profiles.
Sourcing chiral amines never felt like shopping for a generic solvent. In our experience supporting drug discovery, only the pure (R)-3,3-dimethyl-2-aminobutane fits when synthesis walks that fine line between reactivity and selectivity. Route scouts in pharma, especially those building advanced intermediates for API development, keep returning to this precise chiral amine for direct N-alkylation sequences, subtle protecting group chemistry, or constructing quaternary centers.
Materials teams using rigid aliphatic structures know that the steric influence of two methyls around the chiral center grants more than just geometric fun—these groups drive selectivity, create new scaffold spaces, and block unwanted migration. Epimerization stays minimal, and the molecule’s handshake with a chiral catalyst stays clear during late-stage synthesis. That repeatable, predicable performance gives formulators the confidence to move quickly from route scouting to pilot-scale production.
Our technicians, who measure and move barrels every day, know (R)-3,3-dimethyl-2-aminobutane as a clear, colorless liquid. With a boiling point near 99°C at standard pressure, the compound never demands unusual equipment. Storage does not suffer from the air- or moisture sensitivity of some more exotic diamines or hindered bases. Spills, cleanups, and equipment rinses run along familiar lines in our plant, with staff acclimated to its strong, typical amine odor.
Solubility favors most of the usual suspects in organic solvents: ether, alcohols, and light hydrocarbons. Evaporation rates match the use in rotary evaporation and batch distillation, leaving no persistent residue to foul downstream vessels. Hazard profiles line up with other small aliphatic amines—reasonable precautions, prompt ventilation, routine PPE, and standard detection methods keep daily routines efficient and safe.
We built our processes from the ground up for chiral selectivity, not cost-minimization or fast-resale. Our reactors hold multi-ton lots where each crystallization, extraction, and filtration step draws on years of scale-up trials. Batch logs tell their own stories, as tweaks in temperature or solvent blend can swing enantiomeric ratios unexpectedly for less-experienced shops. Working as direct manufacturers means we carry full responsibility for every drop of product, from purification to certification.
Any chemical supplier can hand you a bottle, but only someone with skin in the game runs full QC on chiral HPLC, NMR, and IR spectra for every production lot. Optical rotation gets checked with every shift, and we never ship until it matches reference values. Unwanted color or odor means automatic reprocessing. Our internal standards set targets beyond most compendial minimums—because no downstream customer wants to troubleshoot their process with a wobbly intermediate or a barely-good-enough specification.
Years of working with our pharmaceutical partners showed us that a single bad lot of chiral amine can stall research timelines, cause failed validations, or even set clinical programs back by months. Reliable supply chains start at the roots, and running a vertically integrated factory means we call the shots on every critical parameter. If process research teams need kilograms for library synthesis or a pilot plant demands multi-ton runs for scale-up, we can flex production rapidly based on real-world experience, not market guesswork.
Our close relationships with drug discovery teams breed a steady exchange of observation and improvement. Lab-scale insights inform bulk-scale adjustments. Seasonal shifts in solvent purity or a subtle tweak in hydrogenation temperature sometimes flip the script on enantioselectivity—we learned early that feedback from real users beats relying solely on academic literature or catalog claims.
Global logistics upended expectations for chemical manufacturing over the past decade. Having raw starting material stocks on hand, responsive process chemistry, and in-house purification enable us to smooth out market bumps. While traders and resellers chase inventory, we prioritize forward contracts and maintain consistent output thanks to redundant plant sites and solvent recovery systems.
Our operations team double-checks every metric during order fulfillment, shipment preparation, and customs handling. We support both small customers—project teams and research chemists—and bulk buyers with equal attention. We resolve supply hiccups before they disrupt your formulation schedules or clinical pipeline milestones.
We field questions every quarter: Why not settle for the racemate? Or the (S)-enantiomer? The difference lies in the details. (R)-3,3-dimethyl-2-aminobutane consistently yields different biological activity profiles compared to its (S)-counterpart or the non-enantiopure materials. For chiral pharmaceutical leads, regulatory agencies demand exacting stereochemical documentation—and failing to nail your starting material means doubling analysis downstream.
Our technical teams have compared every permutation—both in reaction kinetics and performance as key intermediates. Minor impurities in the wrong hand cost weeks in purification and scrap. Crossover contamination with non-chiral batches never happens on our lines thanks to dedicated reactors, shared only among optically active amine projects. Experience has taught us there’s no shortcut when enantiopurity intertwines with activity and safety.
The synthetic organic chemistry landscape keeps changing. As drug candidates grow in complexity and regulatory frameworks tighten, routine supply of high-purity, high-selectivity intermediates shapes the success of not just single programs, but entire therapeutic platforms. Our investment in chiral amine production—especially with challenging motifs like the tert-butyl adjacent to an amine on a chiral, quaternary-structured backbone—reflects a deep commitment to real-world application, not just filling an order book.
Material scientists, agrochemical innovators, and biotech researchers push us to dial up purity, reduce batch-to-batch variation, and tailor supply to evolving process demands. Custom synthesis and scale-out support aren’t buzzwords here: they come from ongoing collaboration, repeated process runs, and analytical verification inside our walls. Our troubleshooting rarely starts with a chart; it starts with people talking about what works and what needs improvement on the factory floor and in partner labs.
Staying ahead of the development curve means never coasting on past performance. Pharmaceutical quality management, green chemistry initiatives, process intensification—they all intersect with how we produce (R)-3,3-dimethyl-2-aminobutane. From solvent recycling to waste minimization and even lifecycle assessments, direct manufacturing means we can respond fast to new customer requests or regulatory changes.
The transition from lab to pilot and then to commercial-scale production often reveals subtle bottlenecks. Maybe it’s thermal sensitivity during quenching, scale-up of hydrogenation steps, or impurity carryover at the multi-ton scale. Our teams live these details daily. Investigations in our pilot facilities sometimes uncover breakdown products that never appeared in small-scale runs; years of repetition have taught us where to look, and how to eliminate surprises before they reach end users.
Too many stories in our industry revolve around poor communication between producers and end users. Our entire process—from inbound raw material qualification to finished product dispatch—draws from ongoing conversations with research and process clients. If a customer in peptide synthesis needs custom packaging to minimize air exposure, or a formulation chemist requires specification tweaks for downstream compatibility, we handle revisions quickly. Questions don’t route through sales channels—they go directly to production supervisors, analytical chemists, or R&D scientists with hands-on experience.
In cases where researchers request support interpreting analytic data or troubleshooting failed reactions, we offer guidance based on direct lab knowledge, not reused documentation or generic responses. Our commitment remains to solve problems before they impact project timelines.
For every lot of (R)-3,3-dimethyl-2-aminobutane that leaves our plant, full traceability remains available on demand. Certificate of analysis reports detail both chiral and chemical purity, as well as any relevant physical parameters and gas chromatography profiles. Should a client need clarification, the technical staff who generated the original data always remain on hand to explain their findings and decisions.
Having walked the floors with both the operators and QC chemists, we see firsthand how transparency improves long-term relationships. Production notes stay connected to every shipment; lessons from a delayed crystallization or an anomalous analytic run go into process improvements for future batches. This cycle of ongoing review and adjustment keeps us honest and responsive.
Staying relevant as a manufacturer requires more than churning out intermediates—it demands smart process evolution, technical integrity, and real engagement with customers. We invested in scalable chiral catalysis and high-throughput purification, not because market trends told us to, but because our partners needed these capabilities for their own innovation. These deep-rooted investments make our products—especially bounded chiral amines like (R)-3,3-dimethyl-2-aminobutane—sources of confident progress for teams tackling tomorrow’s toughest chemistry problems.
Our goal centers on getting things right, every run, every kilogram. Feedback cycles, both internal and external, push us to tweak, improve, and sometimes completely overhaul our processes. Training never stops, and neither does our search for cleaner, faster, and more reliable ways to support our customers’ most urgent and difficult challenges using our chemistry.
After decades making, packaging, shipping, and supporting (R)-3,3-dimethyl-2-aminobutane, our take remains straightforward: real reliability and real purity come from real, hard-earned expertise. Traders and resellers can quote prices and availability, but long-term partnerships depend on owning the entire lifecycle of a chemical, start to finish. For customers whose work depends on absolute confidence in their chiral building blocks, our direct, informed approach keeps projects on track and innovation moving forward.