|
HS Code |
588890 |
| Iupac Name | (1S,2S)-N,N'-Dimethylcyclohexane-1,2-diamine |
| Cas Number | 215761-45-0 |
| Molecular Formula | C8H18N2 |
| Molecular Weight | 142.25 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 243-245°C |
| Density | 0.93 g/cm³ (approximate) |
| Optical Rotation | +57° (c=1, CHCl3) |
| Solubility | Soluble in water and common organic solvents |
| Purity | Typically ≥98% |
| Synonyms | (+)-N,N'-Dimethyl-trans-1,2-cyclohexanediamine |
| Smiles | CN[C@@H]1CCCC[C@@H]1NC |
| Chirality | (1S,2S)-enantiomer |
| Refractive Index | 1.495 (at 20°C) |
As an accredited (1S,2S)-(+)-N,N'-Dimethylcyclohexane-1,2-diamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | (1S,2S)-(+)-N,N'-Dimethylcyclohexane-1,2-diamine (25g) is supplied in a sealed amber glass bottle with a Sigma-Aldrich label. |
| Shipping | Shipping for **(1S,2S)-(+)-N,N'-Dimethylcyclohexane-1,2-diamine** (Sigma Aldrich/Merck/TCI, Chemical Grade) typically involves secure, leak-proof packaging according to chemical safety regulations. The product is shipped in compliance with local and international hazardous materials guidelines, often requiring labeling, accompanying safety data sheets, and temperature control depending on specific storage recommendations. |
| Storage | (1S,2S)-(+)-N,N'-Dimethylcyclohexane-1,2-diamine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Store at room temperature, unless otherwise specified on the product label. Always follow your institution’s chemical storage guidelines and consult the safety data sheet (SDS). |
Competitive (1S,2S)-(+)-N,N'-Dimethylcyclohexane-1,2-diamine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to sales7@bouling-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@bouling-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Producing (1S,2S)-(+)-N,N'-Dimethylcyclohexane-1,2-diamine for over a decade has given our team a grounded appreciation of its hands-on role in countless innovation cycles. This compound, often valued for its pronounced stereochemical purity, supports precise processes where selectivity determines the integrity of the end product. Many have come to rely on its ability to introduce both the diamine function and tailored steric environment in synthesis. In our experience, the consistency of enantiomeric excess and batch reliability remains crucial, as these characteristics can make the difference between a research breakthrough and a dead end.
As manufacturers, our daily effort centers on tuning reaction parameters — careful temperature regulation, strict moisture control, and relentless testing — to offer a dependable supply of (1S,2S)-(+)-N,N'-dimethylcyclohexane-1,2-diamine. Over time, we learned to adapt workflows and raw material sourcing to meet shifts in standards and customer feedback from labs, pilot plants, and full-scale production lines. Improvements in purification methods and the drive for greener chemistry have shaped how we approach batch processing and waste reduction for this material.
Where some amine reagents offer only basic functionality, the cyclohexane scaffold of (1S,2S)-(+)-N,N'-dimethylcyclohexane-1,2-diamine lends useful rigidity and selectivity. In asymmetric synthesis or chiral ligand design, the (1S,2S) orientation delivers reliable stereocontrol; this point comes up often in feedback from process chemists in pharmaceutical and fine chemical manufacturing. The methylated nitrogen arrangement reduces side reactions commonly observed with less substituted analogs, especially under harsher conditions or in multistep routes.
We often work with researchers tackling high-value targets — specialty pharmaceuticals, agrochemicals, or even next-stage catalysts — who demand precise input on isomer ratios and trace impurity profiles. Those requests reflect a reality: small differences in molecular structure lead to major changes in biological performance or separation characteristics. Our production floor sees these challenges firsthand, motivating ever-finer analytical controls and record-keeping.
Reproducibility stands at the core of everything we do. Early in our manufacturing journey, inconsistent results from raw material vendors led to costly delays and frustrated customers. Today, sourcing raw cyclohexane and methylamine intermediates with robust paper trails is standard protocol. Rigorous chromatography and chiral HPLC analysis ensure every lot delivers on purity and enantiomeric excess. Analytical chemists on our team test for residual solvents, trace metal content, and organic contaminants — going beyond industry minimums.
Our quality assurance doesn’t stop after production. Storage conditions for chiral diamines require vigilance; exposure to moisture or excessive heat triggers degradation, affecting subsequent applications. We take these lessons into packaging, with airtight containers and controlled warehousing that minimizes the risk of cross-contamination. These everyday precautions guard the reputation of our material and, by extension, the results of those who work with it.
While patents and literature often highlight the merits of (1S,2S)-(+)-N,N'-dimethylcyclohexane-1,2-diamine as a chiral auxiliary or ligand, our time spent at the reactor gives a different angle. The compound’s reliably solid form — not sticky, not hygroscopic — translates into ease of handling at scale, an overlooked but valuable trait for technicians and engineers who juggle dozens of steps on tight schedules. It dissolves smoothly in standard organic solvents, which makes integration into automated dispensing and mixing easier than with some higher molecular-weight diamines.
From the feedback we gather and our own troubleshooting, many users push the product’s limits in transition metal catalysis and enantioselective stage construction. Physical robustness, combined with the predictable behavior under diverse thermal and pH ranges in catalytic applications, streamlines downstream purification and reduces material losses. These practical factors boost throughput for labs trying to transition from bench to pilot plant.
Throughout our years in the lab and on the production line, dozens of diamine variants have crossed our benches. The symmetrical substitution pattern of (1S,2S)-(+)-N,N'-dimethylcyclohexane-1,2-diamine separates it from more basic options like ethylenediamine or the less sterically defined m-xylylenediamines. Chirality, in combination with methyl substitution, enhances selectivity and thermal stability.
Our chemists observed that competitors using racemic or less sterically hindered diamines often report inconsistent results in stereoselective transformations. With our product, the sharply defined (1S,2S) configuration grants end users more predictable outcomes, which matter most in regulated sectors like fine chemistry or pharmaceuticals.
Standard analytical certificates for this compound from our site include rotation data, detailed impurity breakdown, and rigorous moisture analysis, not just gross purity. For users, the assurance of full traceability and analytical support means fewer surprises between R&D and full-scale production. Our technical staff, many of whom have worked on both R&D and industrial teams, regularly run collaborative troubleshooting with key users — catching batch anomalies, assessing new synthetic challenges, or planning larger campaigns.
Some manufacturers blend advanced process control with surface-level testing, but our chemists recall cases where only deep impurity profiling flagged precursors to larger process problems. This compound’s clean synthesis route and relatively narrow impurity spectrum make troubleshooting more transparent, encouraging joint improvement efforts with industry partners.
As environmental and workplace safety standards evolve, we’re under growing pressure to adapt chemical processes. This is not abstract. Our daily pursuit means exploring steps that minimize hazardous byproducts and solvent peaks in downstream distillation. (1S,2S)-(+)-N,N'-dimethylcyclohexane-1,2-diamine, by virtue of its structure, enables fewer side products than non-methylated cyclohexane diamines, especially in coupling reactions that traditionally generate problematic impurities.
Our journey adopting reduced-footprint processes included real-time emissions monitoring and implementing waste reduction targets batch-by-batch. For users who track total process hazard scores or run comparative lifecycle assessments, the purity and manageable physical properties of this compound reduce both clean-up needs and post-reaction remediation. Handling fewer hazardous contaminants benefits those managing batch records or workplace safety compliance.
One of the most important lessons from manufacturing specialty amines like (1S,2S)-(+)-N,N'-dimethylcyclohexane-1,2-diamine is the value of transparent dialogue with users. Problems encountered on the bench don’t always fit neatly in published specs. A recent project with a European pharma research firm highlighted this — spectral data flagged a micro-level anomaly for only a single batch, but follow-up revealed a process tweak at the plant had shifted a precursor’s impurity profile.
Our team’s decades of combined bench and plant work allow us to bridge these gaps. Technicians appreciate support on scaling, work-up advice, or even just an honest answer when an application is outside the product’s proven range. Our role extends to collaborating directly on trouble-shooting, especially during scale-up, where unexpected byproducts or process modifications come to light only at pilot scale. More than a few synthesis teams have relied on our technical support to refine filtration, optimize solvent swaps, or adjust mixing protocols, saving both time and resources downstream.
Direct access to production and analytical staff matters for those with time-sensitive development timelines — we maintain a flexible batch scheduling system to accommodate rush pilot runs or urgent investigations. Unexpected plant shutdowns or shipping delays can derail critical syntheses; our contingency planning balances reliability for regular customers with production capacity for special needs.
We have witnessed the changing demands of various sectors over the years. Pharmaceutical and specialty chemical syntheses drive calls for chiral building blocks that offer more than theoretical appeal. Real-application chemists want predictable results, safe handling, and cost-effective processability. Our approach combines data-driven analysis, bench-scale feedback, and honest discussions about the material’s behavior.
Regulatory agencies continue pushing for more documentation, lower impurity thresholds, and cleaner records at every stage of the procurement and production cycle. Our experience navigating shifting documentation requirements, auditing trails, and global logistics streamlines the route from plant to laboratory. We update compliance procedures in step with market evolution, liaising with regulatory consultants and customer safety officers as new standards emerge.
Our supply chain resilience has been tested repeatedly, not just by regulatory changes but by raw material shortages and transportation snags. We collaborate with trusted logistics groups, monitor geopolitical factors affecting raw chemical supply, and reserve emergency material stocks for critical production runs. Downstream users, especially those in highly regulated fields, need assurance that the material supplied this month matches the certificates, purity, and performance of the last shipment. Day-to-day, meeting that expectation guides every aspect of our operation.
Continuous improvement, for us, emerged not from corporate philosophy but from real-world process breakdowns. A minor yield drop once cascaded into weeks of troubleshooting, delaying customer runs and prompting an overhaul of our catalyst recycling protocol. A recurring solvent contamination prompted detailed sourcing investigations, leading to long-term supplier changes. Our lessons taught the value of staff training refreshers, tighter environmental controls, and record reviews before each major campaign.
Technicians on our floors run hands-on experiments alongside the chemists responsible for synthesis optimization. Batch notebook reviews, inline spectroscopic checks, and feedback from users shape the incremental updates we deploy. Whether adjusting distillation parameters or investing in better GC-MS instruments, every change traces back to real process gaps or customer input. The product you receive builds on hundreds of adjustments, each rooted in concrete operational need.
Our technical team actively surveys the literature, attends synthesis and catalysis symposia, and communicates with leading-edge users developing new applications. Open channels to academia and industry spark collaborative process improvements — a recent project introduced a new, greener work-up based on insights from an academic partner, skipping steps considered mandatory for years.
Manufacturing (1S,2S)-(+)-N,N'-dimethylcyclohexane-1,2-diamine has reinforced the notion that experience at the reactor tells a different story than catalogs or spec sheets. With every batch, our plant staff apply hard-earned lessons from process failures, customer pilot campaigns, and new regulatory hurdles. The depth of understanding across our plant means advice on this product isn’t guesswork, but informed by hundreds of kilograms run and dozens of scale-up support cases resolved.
In a climate where new supply partners appear rapidly yet often lack field-tested backing, our utility depends on relationships built over years of repeat supply, lab visits, and technical troubleshooting. We invest in ongoing staff training, knowledge-sharing sessions, and fostering connections with material users across pharma, agroscience, and specialty chemical markets. By remaining responsive and grounded, we aim to deliver both quality product and expertise tailored to the realities of modern synthesis.
(1S,2S)-(+)-N,N'-dimethylcyclohexane-1,2-diamine represents more than a reagent — it ties together chiral control, ease of process, and reliability rooted in ongoing manufacturing practice. We continue to adapt, guided by both operational insight and user feedback, confident that dedication to service, technical support, and careful production will keep it a preferred choice for those striving for excellence in complex chemical synthesis.