|
HS Code |
225985 |
| Cas Number | 2291-52-5 |
| Molecular Formula | C6H9N3 |
| Molecular Weight | 123.16 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 276-277 °C |
| Melting Point | -40 °C |
| Density | 1.032 g/cm3 at 20 °C |
| Solubility In Water | Miscible |
| Flash Point | 126 °C |
| Vapor Pressure | 0.003 mmHg at 25 °C |
As an accredited 3,3'-Iminodipropionitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3,3'-Iminodipropionitrile is supplied in a tightly sealed amber glass bottle, 100 grams, labeled with safety precautions and chemical information. |
| Shipping | **Shipping Description for 3,3'-Iminodipropionitrile:** Ship in tightly sealed containers, away from heat, sparks, and incompatible substances. Store in a cool, well-ventilated area. Label packages with appropriate hazard warnings. Handle with care to prevent leakage or spillage. Follow all regulations for the transport of toxic organic chemicals. Use protective equipment to minimize risk during handling. |
| Storage | 3,3'-Iminodipropionitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Keep it away from heat, sparks, and open flames. Store in a secure location, and label clearly. Use secondary containment to prevent leaks, and avoid storage near food or drink materials. |
|
Purity 98%: 3,3'-Iminodipropionitrile with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced impurity levels. Molecular Weight 136.18 g/mol: 3,3'-Iminodipropionitrile with a molecular weight of 136.18 g/mol is used in organic reagent formulations, where precise stoichiometric calculations are achieved. Melting Point 75°C: 3,3'-Iminodipropionitrile with a melting point of 75°C is used in polymer research applications, where controlled phase transition behavior is required. Boiling Point 283°C: 3,3'-Iminodipropionitrile with a boiling point of 283°C is used in high-temperature reaction systems, where thermal stability ensures consistent processing. Low Water Content <0.5%: 3,3'-Iminodipropionitrile with water content below 0.5% is used in electronic chemical manufacturing, where moisture-sensitive processes demand minimal hydrolysis risk. Stability Temperature up to 150°C: 3,3'-Iminodipropionitrile with stability up to 150°C is used in specialty coating formulations, where it maintains structural integrity under curing conditions. Fine Particle Size <100 µm: 3,3'-Iminodipropionitrile with particle size below 100 µm is used in catalyst preparation, where superior dispersion efficiency is obtained. Colorless Liquid State: 3,3'-Iminodipropionitrile in colorless liquid form is used in laboratory analytical procedures, where optical clarity allows accurate spectroscopic analysis. |
Competitive 3,3'-Iminodipropionitrile 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 admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Chemistry labs and industry settings often encounter a range of specialized chemicals, but few spark as much discussion among technical staff and researchers as 3,3'-Iminodipropionitrile. Those who have handled this compound know it’s not just one more reagent on a shelf. With its structure, 3,3'-Iminodipropionitrile—often called IDPN—shows up in both academic studies and specific manufacturing processes, especially when there’s a need to explore neurotoxicity or synthesize distinct organic compounds.
This colorless, oily liquid stands out for more than its physical traits. Its molecular formula, C6H10N4, and CAS number 111-19-3 make it easy to trace in scientific literature. Experience in research settings reveals IDPN’s main calling: it serves as a potent model neurotoxicant in animal behavior studies, particularly concerning neurodegenerative conditions. It doesn’t wear the same face as common solvents or reagents. In rat and mouse studies, it triggers reproducible vestibular toxicity without widespread systemic effects, which makes it a favorite for neuroscientists needing a reliable way to assess balance and motor system damage. Over the years, these properties have put it at the center of work investigating the mechanisms behind movement disorders.
Unlike more familiar chemicals, such as acetonitrile or other dinitriles, 3,3'-Iminodipropionitrile has a reputation as a selective disruptor. Many researchers point out that while some nitrile compounds snatch headlines for their reactivity or toxicity, IDPN distinguishes itself by inducing very specific axonopathy, especially in the peripheral and central vestibular system. This unique action lets teams drill down on nerve injury and recovery, using it as a powerful tool to build models for drug testing and disease understanding. There’s genuine value here for anyone tired of ambiguous results from substances that cause broad cytotoxicity. That consistency is what makes it so valuable in labs.
On the supply side, this compound typically arrives in brown glass bottles with screw caps, often in 100-gram, 500-gram, or 1-kilogram options. Purity usually sits above 98%, which matters a lot in research, since contaminants skew behavioral or cellular results in subtle but frustrating ways. Some sources specify moisture content or chloride level, showing the attention to detail that chemical suppliers develop after hearing the feedback of researchers who lose weeks of experiments to poor material.
From my own work, it’s clear that storage conditions never get taken lightly. IDPN needs a tightly sealed container and a cool, dry spot, far from oxidizers or open flames. Technicians in both small and large set-ups keep IDPN away from busy walkways, since spills create safety headaches that can interrupt an entire lab’s routine. Temperature swings and humidity—the invisible enemies in many storerooms—change this chemical’s stability, so checking storage guidelines often becomes part of the daily routine for careful staff. I’ve seen the difference between good and poor storage firsthand: degraded or contaminated IDPN throws a wrench into weeks of animal studies, wastes materials, and sometimes puts compliance with ethical review boards at risk.
Many people hear about 3,3'-Iminodipropionitrile from toxicology studies, but it has a less publicized side as a synthetic intermediate. The nitrile groups provide a reactive handle for chemists, letting them produce amines or other derivatives through reduction or hydrolysis. In research, its best-known application remains the induction of vestibular syndrome in rodent models. These studies deliver reproducible, quantifiable behavioral changes that lay the groundwork for neuropharmacological research and help define dose-response relationships for candidate therapies.
Beyond the lab, a handful of industries tap into its chemical framework to make specialty chemicals that feed into larger production chains, although these markets are smaller and more segmented than the scientific research market. In terms of comparison, IDPN’s difference from other nitriles lies not only in its unique structure—with terminal nitrile groups flanking a secondary amine—but also in its selectively targeted biological effect. This is not the default reagent for general organic synthesis or a quick test of cell viability; it’s a specialist tool.
Behind every batch of published research using IDPN, there’s usually a long string of animal behavioral assessments, histological tissue analysis, and biochemical quantification. Researchers value the repeatability they get from this compound: once dosed, animals show predictable head tilt and circling behavior. For people working on inner ear disorders or screening drugs that protect against neurodegeneration, this is exactly the sort of targeted effect that makes life in the lab a bit more manageable. Being able to control variables lets you isolate what your new therapy is actually doing, instead of just managing chaos.
Many companies and laboratories have shelves lined with nitrile-bearing chemicals, each with its own quirks and hazards. Coming from an environment where strict protocols shape every move, I notice IDPN’s distinct impact. Other dinitriles, like succinonitrile or adiponitrile, are integral to polymer production or act as solvents. In contrast, 3,3'-Iminodipropionitrile holds a narrower but deeper value in mechanistic studies. It triggers axon degeneration in a pattern that sidelines broader cytotoxic agents; this focused activity means less collateral tissue damage, so researchers can pinpoint changes in neural tissue without struggling against the “noise” caused by dead or damaged cells from off-target toxicity. That’s a rare trait.
In terms of handling, its oily, low-volatility character stands in contrast to volatile organic solvents. The odor is pungent, so ventilation and personal protective gear aren’t optional. Chemical hygiene habits pick up quickly when IDPN hits the bench, not only to manage the risk but also to ensure compliance with increasingly watchful regulatory bodies. Lab staff need confidence that their personal protective equipment provides real defense because occupational health risks aren’t theoretical—they’re written up in safety reports and tracked in medical exams.
Based on conversations with colleagues and my own time in multi-institutional research projects, it’s common to compare experiences working with IDPN to those with other neurotoxins such as MPTP or 6-hydroxydopamine. Each brings its own set of strengths and frustrations. IDPN stands out for stability and selectivity. Researchers get consistent behavioral outcomes at predictable doses, with recovery rates and subacute effects documented in published work. The learned wisdom here is that if a project demands a chronic, nonlethal model of inner ear or motor neuron damage, turning to IDPN means fewer surprises and, ultimately, better science.
Some partner labs have struggled with supply chain issues sourcing high-purity IDPN, and there’s the ever-present risk of regulatory tightening. A surprising number of research groups only realize too late the importance of audit trails for high-concern chemicals. Trustworthy suppliers and diligent record-keeping save headaches down the line, especially as national and international guidelines tighten for toxic and specialty chemicals to prevent accidental or deliberate misuse. Even experienced lab managers can lose track of the status of older stocks, leading to compliance problems or wasted materials. Real diligence means updating inventories, checking container seals, and logging every transaction—mundane work, but far from optional.
Disposal remains a major concern. Being a potent neurotoxin, IDPN demands chemical waste handling protocols that outstrip typical solvent disposal. Regular training and near-paranoid attention to labeling and containment mean accidents stay rare. The key is always assuming something could go wrong. Everyone in the lab environment knows spills and accidents only take one slip—training makes a difference, but culture cements it. Teams become vigilant not out of fear, but out of shared experience: a misplaced bottle or misunderstood label can set back months of expensive work, or worse, risk real harm to people.
People in the field suggest several strategies for safe, effective IDPN use, most built around simplicity and routine. The best laboratories set up laminated SOPs near chemical storage. Teams do walk-throughs, checking ventilation and working spill kits before every study. Restricted access helps, with a logbook for who retrieves or returns each batch, even for the most trusted staff. Some groups have double-person sign-out procedures for all controlled chemicals, not just for regulatory peace of mind, but because it catches those “off” feelings—if a bottle feels warm, has crud on the outside, or seems lighter than expected, two pairs of eyes beat one every time.
Training stands up as the cornerstone. Every new staff member walks through hands-on demos before IDPN ever leaves the cupboard. Online modules reinforce the need for gloves, splash goggles, and catch trays on benches dealing with neurotoxins. When accidents do happen, the difference between a near-miss and a lasting problem often comes down to muscle memory—where's the eyewash, how fast can you close the storage safe, who knows the number for local waste collection?
Documentation isn’t just clerical overhead. Audits from internal safety teams and outside regulators look for clear, honest logs of what’s been ordered, stored, used, and disposed of. Over the years, a robust system keeps both researchers and the environment out of harm’s way. Containers get checked for leakage or discoloration during routine stock reviews, so any compromise is caught before a problem starts.
Purchasing IDPN from trustworthy suppliers matters too. Labs should favor vendors who provide detailed product analysis certificates, include storage recommendations, and update safety datasheets with every batch. It’s a lesson learned from painful mishaps: suppliers cutting corners on quality control might not show up with consequences on the first order, but these failures always surface eventually. Peer recommendations carry weight, as does engagement with supplier technical support. Being able to call and get clarification on purity, residual solvents, or packaging goes a long way when a research deadline looms and there’s no time for surprises.
Discussion of IDPN’s risks and compliance requirements always stirs debate in research communities. Changes in national and international chemical lists put the onus on handlers to demonstrate controls, especially when exporting or importing. Even university labs have seen projects stalled by shifting interpretations of chemical management guidelines. When asked about these challenges, many experienced researchers echo the same point: keeping documentation current and training fresh beats scrambling to catch up once a compliance question lands in your inbox. Sometimes there’s frustration at red tape, but nobody wants to face shut-down or penalties after an incident.
Ethical oversight never leaves the conversation. In animal research, IDPN sits in a narrow slice of permitted agents, justified only by strong scientific evidence that the induced model can’t be replicated by milder means. Review boards often request extra details—dose ranges, contingency plans, parallel controls—before signing off on protocols. Honest discussions within research teams before starting are the norm: Are there less hazardous alternatives? Is the model necessary at this scale? Labs that take the time to build consensus find smoother reviews and clearer communication with outside stakeholders. There’s no shame in revisiting assumptions or updating methods if better options appear down the road.
With decades of accumulated knowledge, some trends are emerging about IDPN’s future in research and development. Teams are exploring more refined dosing schedules to reduce animal burden, new methods to track neurodegeneration in real time, and adjacent fields like tissue culture where direct exposure can clarify cellular mechanisms. Analytical chemists are also stepping up efforts to fingerprint IDPN degradation products, tracking them through air and waste so accidental releases or contamination don’t slip through undetected.
The push for alternative models—mimicking effects with genetic manipulation, advanced imaging, or non-toxic analogs—keeps building as funding agencies and ethical oversight bodies press for lower animal use and reduced hazard. For now, IDPN’s role seems secure for highly controlled experiments, but pressure will likely mount for safer, even more targeted chemicals. Forward-thinking labs already treat current best practices as a floor, not a ceiling. Leaning into transparency about risks and sharing detailed protocols via open access channels further strengthens trust within the scientific community and with the public.
Researchers interested in scaling up beyond lab work face another layer of challenge. Industrial applications lean heavily on batch quality and traceability, since downstream products may enter supply chains subject to full regulatory scrutiny. Here, partnerships with chemical engineering teams and compliance consultants become vital. Automation and closed-system handling shrink opportunities for exposure. Where once technicians poured from bottles by hand, newer set-ups favor secured pumps and monitored tanks, all in pursuit of both productivity and zero-exposure goals.
Anyone entering the world of specialty chemicals soon learns that materials like 3,3'-Iminodipropionitrile demand much more than book learning. In practice, safe, reliable IDPN use grows out of a network of experts—mentor researchers, facility managers, and compliance officers—who pass down lessons shaped by mishaps and victories alike. Morning safety briefings, peer reviews of protocols, and quiet double-checks of inventory mark out the rhythms of a well-run lab, not just for ticking boxes, but to keep people protected and research on solid ground.
It’s easy to get lost in technical comparisons—chemical reactivity, selectivity, or animal model reliability—but on the ground, real success comes down to honest dialogue, preparedness, and shared responsibility. As regulations evolve and new technologies open doors, adapting routines while holding onto these core principles offers the best way forward. The story of IDPN isn’t just about its molecular structure or unique toxicity profile. Instead, it’s about the people behind the science—how they manage risk, learn from experience, and push the field ahead, one study at a time.