|
HS Code |
442467 |
| Chemical Name | 3-Iodophenylacetic Acid |
| Molecular Formula | C8H7IO2 |
| Molecular Weight | 262.05 g/mol |
| Cas Number | 625-95-6 |
| Appearance | White to off-white crystalline powder |
| Melting Point | 156-160°C |
| Solubility In Water | Slightly soluble |
| Smiles | C1=CC(=CC=C1CC(=O)O)I |
| Inchi | InChI=1S/C8H7IO2/c9-7-3-1-2-6(4-7)5-8(10)11/h1-4H,5H2,(H,10,11) |
| Density | 2.11 g/cm3 (estimated) |
| Storage Temperature | Store at 2-8°C |
As an accredited 3-Iodophenylacetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle labeled "3-Iodophenylacetic Acid," features hazard symbols, lot number, expiry date, and secure screw cap. |
| Shipping | **3-Iodophenylacetic Acid** is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is transported as a non-hazardous, solid chemical under ambient temperature. Packaging ensures safe handling and compliance with regulatory guidelines for chemical substances. Specialized labeling and documentation accompany each shipment to ensure identification and traceability. |
| Storage | 3-Iodophenylacetic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect it from moisture and direct sunlight. Ideally, store this chemical at room temperature, avoiding excessive heat. Ensure proper chemical labeling and follow all safety protocols and local regulations for storage. |
Applications of 3-Iodophenylacetic Acid in Industrial ManufacturingAs an experienced manufacturer of 3-Iodophenylacetic Acid, our focus remains on end-user production requirements across several high-value industrial sectors. The following sections outline verified downstream applications, detailing integration points, regulated compliance, practical formulation experience, and representative finished goods produced using this specialty intermediate. 1. Pharmaceutical Intermediate for Thyroid Hormone DerivativesThis compound plays a key role in the synthesis of advanced pharmaceutical intermediates, especially for developing organoiodine molecules related to thyroid hormone analogs and anti-thyroid drugs. Facilities depend on precise incorporation to build specialty scaffolds required for downstream active pharmaceutical ingredient (API) synthesis, which must adhere to stringent regulatory and batch consistency criteria. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Building Block for Peptide and Peptidomimetic SynthesisResearch-focused peptide synthesis facilities utilize this raw material to build specialized iodinated amino acid derivatives and peptidomimetic structures. It provides a controlled route for site-specific iodination or as a precursor in solid-phase and solution-phase peptide assembly, vital for producing modified therapeutic candidates and molecular probes. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Precursor for Agrochemical SynthesisMajor agrochemical manufacturers require this specialty acid in controlled settings for producing selective herbicide intermediates and fungicide actives. Its stable aryl-iodo structure allows downstream functionalization essential for delivering bioactive compounds with precise crop-protection profiles, meeting regulatory requirements across geographically diverse end markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Intermediate for Liquid Crystal Material ProductionManufacturers engaged in high-performance liquid crystal (LC) technology for electronics utilize this compound as a controlled precursor to synthesize specialty aryl-iodo mixtures, influencing electro-optical properties of advanced display technologies. Its functional group supports subsequent cross-coupling transformations, facilitating precise tuning of LC mixture characteristics under tight process controls. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3-Iodophenylacetic Acid 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!
In the last decade, 3-iodophenylacetic acid has secured a clear position within the fine chemicals landscape. Our production team recognizes both routine and advanced uses of this high-purity intermediate, which serves research labs and manufacturing facilities ranging from pharmaceuticals to agrochemicals. By focusing on process reproducibility, chemical stability, and customer feedback, we have refined every step that puts this product on the market.
3-iodophenylacetic acid begins its story not inside a catalog, but in our custom reactors. Each gram reflects years of handling iodine chemistry and aromatic substitution, respecting the sensitivities of the process and repeating each batch with unwavering attention. The white or off-white solid arrives typically in crystalline form, with melting ranges and purity set by analysis. Every production cycle brings a new set of eyes to quality, as this compound often forms the spine of more complex building blocks downstream.
Producing organoiodine chemicals like this one requires skill that crosses the boundaries of textbook synthesis. High-grade iodine and phenylacetic acid derivatives can be prone to degradation if procedures drift. Our technicians document every reaction run with raw data, retaining samples batch by batch, and passing product through rigorous purification. This process aims to control dust content, minimize unwanted by-products, and keep trace-metal levels within established thresholds.
Contamination, even at low levels, can disrupt downstream synthesis. Customers have shared stories of reactivity problems when material isn’t up to par. By routinely applying microanalytical and chromatographic checks, we guard product consistency. The test results are as much for us as for our clients; they signal that every bottle carries what the label promises.
On a standard order, purity by HPLC or GC often exceeds 98%. Particle size is neither too fine for dustiness nor too coarse for easy dissolution. Specifications do not just provide peace of mind, but real value: beginners and experts alike rely on the product’s performance in cross-coupling and aryl ether formation. Repeat orders, not advertising, form the backbone of our feedback.
In labs, 3-iodophenylacetic acid gives chemists access to the iodinated aromatic ring—a reactive site for Suzuki, Sonogashira, and Heck couplings. Its acetic acid tail adds new versatility, opening the door for peptide conjugation or custom ester formation. A skilled bench chemist can exploit the acid’s functional group for further elaboration or use the iodine for rapid palladium-catalyzed reactions. We appreciate that time and cost pressures in manufacturing mean every gram counts; consistent material simplifies every step from early development to commercial scale.
With a melting point near 166-170°C and solid physical stability under ambient storage, this product keeps well if sealed against humidity. End users who have come to us after working with unstable, low-grade lots from unknown sources report a difference: predictable melting, dissolution, and downstream reactivity directly connect to the handling conditions in our warehouse and packaging lines.
Some clients run pilot programs or kilo-lab work before launching full scale. Here, the reproducibility of reactions using our material helps teams plan more confidently. Waste streams and recrystallizations decrease when input quality rises, leading to lower environmental impact for the same yield. By keeping analytical backup data available, we help clients trace any rare issue straight back to the source without administrative runaround.
How does 3-iodophenylacetic acid set itself apart from fluoro, bromo, or unsubstituted phenylacetic acid derivatives? The iodine atom is more than a placeholder; it’s the gate to a broader field. Its size and reactivity simplify metal-catalyzed bond formation. In fact, reaction conditions can often be milder than with bromo- or chloro-analogues. Some chemists find yield and purity improvements when sticking with the iodo compound for key steps, even if raw material costs sit higher.
Another edge appears in analytical monitoring—iodine gives stronger signatures by mass spectrometry, which helps teams track transformations and detect trace impurities in complex matrices. Robust mass balance and less false identification mean better confidence in process validation.
This compound also differs from 4- or 2-iodophenylacetic isomers. Placement of the iodine at the 3-position leads to different regioselectivity, opening routes inaccessible with other isomeric intermediates. Peptide and prodrug chemists, for example, have used this distinction to unlock patentable active pharmaceutical ingredients.
Our daily work involves more than filling bottles. We coordinate between pilot labs, scale-up engineers, and shipping specialists to deliver material free from the regulatory or logistical delays that sometimes hobble specialized chemicals. Many global researchers depend on reliable access, so we maintain stocks in several production lots and ship according to hazard compliance.
Packaging strategy comes from experience handling dense organoiodine solids. Paper, plastic, and glass all play a role. We’ve found glass bottles with heat-sealed liners lock out moisture and air, extending product life over long transits. Labels include batch numbers tying directly to retained samples. Every packed unit undergoes another visual check before departure, minimizing breakage and confusion.
For scale-up requests, our team welcomes direct communication with client chemists and engineers. Having faced the frustrations of vague customer support, we keep lines open and focus on solving real-world technical challenges. Changes in regulatory status, unexpected shipping holds, or sudden demand spikes—these issues prompt action, not finger-pointing.
End-users in North America, Europe, and Asia rely on transparent customs handling and safety documentation. Our compliance group keeps up with global transport requirements for organoiodine compounds, regularly updating protocols to avoid shipment rejection or hold-ups. Safety data travels with every shipment, giving clients data for internal use and regulatory filings.
Listening to chemists working on the bench or the synthesis line shapes our ongoing improvement. A few years back, a customer struggling to filter their product asked us to investigate the cause. After sample swaps and technical calls, we found that a subtle change in our crystallization step affected particle morphology. This feedback loop led us to tweak temperature ramp rates and filtration aids—reducing byproduct entrapment and shortening customers’ process times.
Some requests focus on custom cut-sizes or extra drying for formulations sensitive to water traces. By investing in flexible milling and drying facilities, we can supply 3-iodophenylacetic acid tailored for slurry charging, direct dissolution, or solid blending without cross-contamination. Relationships with formulation teams in pharma and agrochem sectors keep standards high, and solutions practical.
Regular client audits add another check on our claims. Walking technical teams through workflow, sampling, and analytical steps keeps both sides on the same page and pushes each batch to higher levels of consistency. Open records and readily available QC data replace vague assurances every time.
High-value intermediates demand responsibility from both producer and user. By limiting exposure to airborne particles, providing sealed packaging, and offering clear handling procedures, we aim to protect users from unnecessary risk. Industrial partners frequently ask about storage stability—through testing, we know that controlling moisture, temperature, and light keeps this compound in optimal condition for months to years, with minimal degradation.
Waste handling remains a point of focus. Our synthesis avoids halogenated solvent waste where possible, and we provide technical guidance to clients on optimal waste management and minimization. By working across the value chain, we hope our careful approach flows downstream to final product handlers and technicians.
Training materials and support are developed hand-in-hand with environmental health experts. This support rests not just on documentation, but real-time answers to technical questions. Safety should progress on more than paper.
Researchers in discovery chemistry look for flexibility: 3-iodophenylacetic acid provides this by standing at the crossroads of several transformations. We see it deployed in both traditional solution-phase chemistry and more recent flow techniques. The product’s solubility in standard organic solvents means it bridges legacy and modern workup systems without elaborate modifications.
Interest in this intermediate grows with the expansion of medicinal chemistry, where custom derivatives and patentable structures require robust, predictable starting materials. Project teams position 3-iodophenylacetic acid as a launchpad for new drug candidates, drawing on the iodine’s unique reactivity and the acetic acid’s functional handle for downstream transformation.
Agrochemical and material science clients also turn to this compound for making specialty herbicides, pesticides, or optoelectronic additives. Their process goals vary, but the demand for batch-to-batch reproducibility crosses every sector. We listen closely, adapting our quality controls and documentation to fit unique validation, registration, or regulatory filings.
Manufacturing organoiodine compounds presents environmental responsibilities. By maximizing reaction yields, reclaiming solvents, and cutting energy use, we build sustainability into everyday practice. Iodine recovery processes, controlled emissions, and careful water management make the difference between waste and resource efficiency.
Our team studies new synthetic routes to lower overall input requirements, and incorporates green chemistry concepts wherever possible. Feedback from forward-thinking partners has led us to invest in safer raw materials and alternative crystallization solvents. These small shifts accumulate over time, reducing waste and energy costs for clients and producers alike.
By supporting client audits and transparency in sourcing, we offer credible assurance—promoting long-term business over transactional gains. Clients reporting improved EHS records after switching to more reliable sources motivate ongoing investments.
No short cuts exist in quality. Decades of technical work remind us: from the moment raw iodine and phenylacetic acid come in, each decision—temperature control, mixing, purification—binds product quality tightly to the people behind each step. Clients notice the difference: returns and complaints drop, but more importantly, collaborations grow deeper.
We have learned that rigid specifications only capture part of quality. Listening to downstream users, anticipating the quirks of new synthetic pathways, and sharing troubleshooting data form the full circle. Through this, every kilogram influences not only a single reaction, but the final success of entire research programs and manufacturing campaigns.
3-iodophenylacetic acid holds an important niche in the expanding universe of synthetic intermediates. Projects across several industries depend on reliability—purity, performance, and honest technical advice. Our ongoing work combines chemistry know-how, listening to feedback, and adapting to evolving client needs.
As research and market demands change, we continue to invest in training, equipment, and analytical support so every bottle of 3-iodophenylacetic acid reaches the highest standard possible. With transparent supply, continual improvement, and respect for the craft of chemistry, we look forward to supporting the next wave of innovation.