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HS Code |
317141 |
| Productname | 2-Cyanoethyl N,N,N',N'-Tetraisopropylphosphorodiamidite |
| Casnumber | 102054-39-1 |
| Molecularformula | C14H32N3OP |
| Molecularweight | 289.40 |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically ≥98% |
| Boilingpoint | 132-134°C at 0.2 mmHg |
| Density | 0.94 g/cm³ (approximate) |
| Solubility | Soluble in organic solvents such as acetonitrile and dichloromethane |
| Storagetemperature | 2-8°C, under an inert atmosphere |
| Synonyms | Tetraisopropyl (2-cyanoethyl)phosphorodiamidite |
| Refractiveindex | 1.438-1.443 |
As an accredited 2-Cyanoethyl N,N,N',N'-Tetraisopropylphosphorodiamidite factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 10g 2-Cyanoethyl N,N,N',N'-Tetraisopropylphosphorodiamidite is packaged in a sealed amber glass bottle with tamper-evident cap. |
| Shipping | 2-Cyanoethyl N,N,N',N'-Tetraisopropylphosphorodiamidite is shipped in tightly sealed, inert containers under a dry nitrogen or argon atmosphere. The packaging prevents moisture and air exposure, as the chemical is highly sensitive to hydrolysis. It is handled as a hazardous material and shipped in compliance with relevant chemical transport regulations. |
| Storage | 2-Cyanoethyl N,N,N',N'-Tetraisopropylphosphorodiamidite should be stored under an inert atmosphere, such as argon or nitrogen, in a tightly sealed container. Keep it in a cool, dry place, protected from moisture and direct sunlight. Ideally, store at 2–8 °C (refrigerator). Avoid contact with oxidizing agents and acids, as the compound is moisture- and air-sensitive, and may degrade upon exposure. |
Applications of 2-Cyanoethyl N,N,N',N'-Tetraisopropylphosphorodiamidite in Industrial ManufacturingAs an experienced manufacturer of specialty chemical intermediates, we have established reliable supply solutions for 2-cyanoethyl N,N,N',N'-tetraisopropylphosphorodiamidite in several high-value industrial segments. This phosphorodiamidite is well-recognized for its unique reactivity and purity critical in oligonucleotide synthesis and related downstream chemistries. The following sections describe real downstream applications, compliance standards, usage ratios, process points, and final product types. 1. Automated Oligonucleotide Synthesis for TherapeuticsAutomated solid-phase oligonucleotide synthesizers across pharmaceutical and CDMO facilities require high-purity phosphorodiamidites as key monomer activators during nucleic acid elongation. The 2-cyanoethyl tetraisopropylamide structure supports precise phosphodiester formation and improved shelf stability, becoming indispensable in large-scale antisense, siRNA, and aptamer drug development. Regulatory authorities mandate traceability for reagents engaged in GMP active pharmaceutical ingredient processes, while end-users demand quantifiable consistency and contaminant control at every batch release. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Custom DNA/RNA Synthesis for Genomics and ResearchContract synthesis and in-house laboratories involved in genomics research utilize this reagent for controlled phosphoramidite chemistry in the scalable production of DNA and RNA strands. The tight control over side reactions, hydrolysis, and isomer formation directly correlates to assay quality, PCR fidelity, and sequence purity. Sequence customization, labeling, and incorporation of modified bases rely on monomers synthesized using this phosphorodiamidite, with clear requirements for research-use-only grade chemicals. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Manufacture of Diagnostic Probes and Microarray ChipsProducers of molecular diagnostics and microarray substrates employ 2-cyanoethyl N,N,N',N'-tetraisopropylphosphorodiamidite for the surface-coupled synthesis of capture probes and tagging oligonucleotides. On-chip synthesis workflows depend on reagent stability and rapid, even deposition. Manufacturing must accommodate batch identification, impurity profiling, and support ISO-regulated tracebacks for sensitive healthcare applications. Any change in reagent purity or formulation impacts hybridization efficiency in diagnostic testing. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Synthesis of Modified Nucleic Acid Building BlocksSpecialty chemical firms and biotechnology R&D centers use this reagent as a core phosphitylation agent when making custom-modified nucleotides, such as fluorescent, biotinylated, or reactive group-carrying monomers. The electron-withdrawing cyanoethyl group improves reactivity during the modification phase, while the isopropyl substituents assist with solubility and purification. Quality assessment for custom monomer production always considers residual base impurities, reaction byproducts, and batch documentation for regulated environments. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Chemical synthesis asks for precision. In our daily production runs, 2-Cyanoethyl N,N,N',N'-Tetraisopropylphosphorodiamidite—sometimes called “Tetraisopropylphosphorodiamidite” in short—stands out as a reliable phosphitylating reagent for DNA and RNA oligo manufacturing. Our teams on the factory floor and in the quality labs have watched the growth of demand for nucleic acid-based therapeutics and diagnostics with keen eyes. More than just a reagent, this compound forms the backbone of solid-phase oligonucleotide chemistry, and there’s no shortcut: the process calls for consistency, low impurity levels, and chemical stability that only fine-tuned manufacturing controls can deliver.
Day after day, laboratories depend on phosphoramidite reagents to build precise DNA and RNA sequences. 2-Cyanoethyl N,N,N',N'-Tetraisopropylphosphorodiamidite allows for efficient coupling in both automated and manual phosphoramidite chemistry. We’re familiar with the problems that arise from low-purity or unstable intermediates—problems we have worked to eliminate over years of process refinement. Material shipped from our facility maintains tight control over isomeric purity, moisture content, and residual solvents, which directly improves efficiency in every coupling cycle.
The reagent supports installation of the phosphite triester linkage with high yield, something every oligo synthesis lab values. For each lot, our team carries out strict HPLC and NMR checks. Experience has shown that insufficient removal of water or amines compromises synthesis. So every drum that leaves our site comes after a thorough moisture and impurity purge in our vacuum drying and distillation lines. Phosphoramidite reagents degrade quickly in air or if improperly sealed. We’ve invested in the right argon blanketing practices and supply chain protection to tackle these real-world challenges.
It’s tempting to look only at paper specifications when sourcing chemicals. Still, there’s a gap in real performance whenever shortcuts creep in. We’ve faced customer reports of line clogs and low coupling efficiencies when they tried lower-quality alternatives. Small differences in color, viscosity, or odor point toward hydrolysis or oxidation. That’s why we target colorless to pale yellow, clear liquid material—any deviation triggers an internal investigation. Real-time feedback from our end-users helps us tighten product uniformity.
Water content consistently ranks at the top of discussion here. Our technicians have seen that even small increases in water—sometimes less than 0.05%—can slow down phosphitylation or lead to truncated oligos. Achieving Karl Fischer results below 0.02% has become standard. We monitor amine impurities using GC-MS because their presence can form byproducts that show up as ghost peaks during oligo synthesis. It’s not just statistics—each impurity peak takes hours of troubleshooting for our customers. We’ve narrowed batch variations by adjusting our distillation protocols, fine-tuning the temperature profile in our reactor trains, and improving raw material checks.
As a primary manufacturer, our teams own every step—from sourcing phosphorus trichloride and isopropylamine to the final packaging under inert gas. It’s a long way from simply buying and selling. We control the batch records, the cleaning regimes, the solvent recycling, and the worker training. Years of hands-on practice have taught us which stainless-steel reactors to use and how fast to add the 2-cyanoethanol to reduce side reactions.
There’s genuine difference between re-bottled or resold chemicals and those supported by a robust in-house process. We take customer complaints back to the plant manager’s desk and collaborate across synthesis, QA, and logistics to get to the root cause. Shipping under nitrogen, selecting proper fluoropolymer-lined containers, and holding stock in temperature-monitored storage matter to users who measure product shelf-life in weeks, not months.
Not all phosphoramidites act the same, even though they share similar core structures. Tetraisopropylphosphorodiamidite brings special properties compared to the more common diethyl or diisopropyl analogues. Our regular interactions with oligonucleotide synthesis groups reveal that steric hindrance from isopropyl groups slows hydrolysis just enough to improve shelf stability, without negative impact on coupling speeds.
Compounds with less hindered amine substituents, such as diethyl, sometimes show faster hydrolysis rates—leading to more strict storage and handling needs. Tetraisopropyl versions hold up better over longer storage, especially crucial for labs that don’t turn over inventory quickly. Based on user data, customers using our tetraisopropyl variant report higher average yields on longer DNA/RNA sequences by a few percentage points, reducing purification demand.
Some alternative reagents might cost less to produce using recycled amines or different phosphorus sources, but we’ve found the batch-to-batch irreproducibility leads to much higher costs for the end user. Cleaning clogged synthesis columns, running extra mass spec and HPLC tests, and re-purchasing failed coupling agents all hit the bottom line harder than a higher up-front chemical price. Through hundreds of syntheses, ligation, and dealkylation steps, customers provide data on side reactions that we feed back into manufacturing improvements.
Few things frustrate an oligonucleotide chemist more than receiving a shipment with degraded or contaminated reagent. From our plant, packages leave with traceable lot numbers and full environmental logging. Our logistics team learned early on that even a few days stuck in direct sun or held at an uncontrolled dock can raise impurity levels.
By investing in insulated shipping and temperature monitors, we help avoid the hot summer or freezing winter excursions that have ruined shipments for customers in less-prepared supply chains. Metal containers with PTFE linings keep moisture and oxygen out. We’ve responded to feedback from users who want easier re-sealing and better desiccant inclusion for repeated use. Our staff checks seals and overpacks so each container arrives in ready-to-use condition.
Years of fielding technical calls have shown us the value of direct contact with bench chemists and production lines. Common challenges include plugging of synthesis columns, variable coupling efficiency, or color changes during storage. Listening to customers has led to several in-process adjustments: extra polishing on the final product, revised packaging formats for high-throughput labs, and even small-scale custom lots for process development work.
Some research groups need a reagent that tolerates a slower coupling schedule, while others look for faster deprotection or minimal residual contamination in final oligos. Our technical support is trained to translate these needs back to the plant—if a customer’s sequencer develops ghost peaks or if dry-box handling proves difficult, these issues trigger internal improvement projects.
As interest in gene therapy, antisense oligonucleotides, mRNA vaccines, and aptamer development grows, worldwide regulation has increased. Customers ask us about REACH registration, controlled class shipment, import/export documentation, and trace element profiles for GMP environments. From our perspective, documentation quality is inseparable from product quality.
We maintain long-term audit trails, stability studies, and change control logs for every material shipped. This has allowed us to work with customers under NDA for patented or confidential process development and scale-up runs. Our batch traceability extends through supplier documentation—we require our raw material vendors to certify every solvent, every lot of amine, and every drum of 2-cyanoethanol, and we check each in-house before use.
Each year, improvements in automation, sequence length, and throughput force us to adapt. Earlier, oligonucleotide applications focused on short primers and probes. Today the market looks for long RNA, high-fidelity gene editing strands, or even library-scale combinatorial synthesis. These needs drive stricter control of trace impurities and greater flexibility in packaging—requests for kilogram-scale drums now come as often as demand for single-use vials.
We collaborate with equipment manufacturers and academic groups to anticipate where oligo chemistry will head next. Feedback from users about synthesis cycle time, compatibility with new automated platforms, and integration with LNP and CRISPR delivery workflows help us calibrate product specifications. For example, the purity, density, and volatility profile of our tetraisopropyl product undergo constant benchmarking against published standards and in-house controls.
Manufacturing phosphorus compounds brings health and environmental risks. We enforce strict PPE, ventilation, and containment standards to protect our teams. Wastewater from cleaning and spent solvents goes through in-house treatment facilities to reduce organic and phosphate load before discharge. Regular third-party inspections help verify procedures meet current environmental rules.
By maintaining full R&D and production in one site, we can act quickly—a quality excursion in manufacturing triggers batch segregation and remediation before a single drum leaves. Every safety incident, employee concern, or environmental complaint becomes a driver for internal process improvements. We focus both on compliance and on creating a workplace culture where staff feel empowered to raise safety concerns as soon as they arise.
Our experience supplies valuable lessons. Small changes in feedstock purity or equipment temperature can lead to batch failures or minor degradations that only appear in final oligo yield data. By systematically recording every process parameter, and by linking customer technical support tickets directly to our manufacturing analytics, we close the loop between issue and solution much faster than could a trader or outsourced producer.
Direct production means we never lose visibility—there’s no opacity on where a reagent came from or how it handles real-world use. Fast communication between our manufacturing, QA, and technical support groups ensures that problems don’t fester. Over time, this gives our customers greater confidence that every liter of 2-Cyanoethyl N,N,N',N'-Tetraisopropylphosphorodiamidite truly matches what the project demands.
Chemistry is a hands-on business; reliability grows from understanding the real-life context in which a product gets used. We supply institutions running cutting-edge research in cancer diagnostics or infectious disease monitoring, but also help startups and multinational pharma establish robust large-scale synthesis lines. Each group approaches risk, cost, and schedule differently. Our approach: focus on delivering on-time shipments, minimal impurities, and responsive technical support to limit troubleshooting and downtime.
As new requirements emerge—like higher throughput, more extensive sequence libraries, or tighter impurity limits—we continue adapting. This means frequent equipment upgrades, staff training, and close collaboration with analytic labs and equipment makers. Direct ties with users help us refine the product and anticipate tomorrow’s challenges rather than chasing after them.
2-Cyanoethyl N,N,N',N'-Tetraisopropylphosphorodiamidite plays a central role in oligonucleotide chemistry, and meeting these demands requires more than just technical knowledge. It calls for experience, a drive for quality at every step, and a willingness to listen and improve based on direct feedback from users. Having manufactured and shipped this compound for many years, we’ve built a relationship with the scientists who rely on it. This ongoing partnership helps us keep pushing the quality, shelf life, and usability forward in line with the evolving needs of the field.
Every process tweak, packaging improvement, or specification update comes from experience and from user stories we hear. So, each bottle carries the lessons of a manufacturing floor committed to serving the real-world, practical needs of oligonucleotide chemists around the world.