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HS Code |
965577 |
| Product Name | 2-Amino-3,5-Diiodobenzoic Acid |
| Cas Number | 2232-08-8 |
| Molecular Formula | C7H5I2NO2 |
| Molecular Weight | 388.93 g/mol |
| Appearance | Light yellow to yellow powder |
| Melting Point | 249-254 °C |
| Purity | Typically ≥98% |
| Solubility | Soluble in DMSO, slightly soluble in water |
| Storage Conditions | Store at 2-8°C, protected from light |
| Synonyms | 3,5-Diiodoanthranilic acid |
| Chemical Structure | Benzene ring with amino (2-position), carboxylic acid (1-position), and iodine (3,5-position) substituents |
As an accredited 2-Amino-3,5-Diiodobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 25 grams of 2-Amino-3,5-Diiodobenzoic Acid, labeled with product details and safety precautions. |
| Shipping | **Shipping Description:** 2-Amino-3,5-Diiodobenzoic Acid should be shipped in tightly sealed containers, protected from moisture and light. It must be handled according to standard chemical safety guidelines. Transport as a non-hazardous solid if not otherwise classified, with appropriate labeling. Avoid extreme temperatures and ensure compliance with all local, national, and international regulations. |
| Storage | 2-Amino-3,5-diiodobenzoic acid should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protect it from moisture and direct sunlight. Store in a chemical-resistant, clearly labeled container, preferably in a designated corrosive or chemical storage cabinet. |
Applications of 2-Amino-3,5-Diiodobenzoic Acid in Industrial Manufacturing2-Amino-3,5-Diiodobenzoic Acid serves as a specialty intermediate across advanced industrial sectors, especially in pharmaceutical synthesis, contrast media precursors, radiopharmaceutical chemistry, and high-purity analytical reagent production. Below, we detail its distinct roles, process integration, and regulatory context in each downstream value chain. 1. Pharmaceutical Intermediate for Thyroid Drug SynthesisPharmaceutical manufacturers employ 2-Amino-3,5-Diiodobenzoic Acid as a key starting material in the synthesis of iodine-containing drugs, particularly for the preparation of antithyroid agents. On a commercial scale, production lines integrate the acid in multi-step organic synthesis, where iodinated aromatic compounds contribute to the active pharmaceutical ingredient’s (API) structure. The raw material’s purity, iodine content, and trace impurity profile must align with current good manufacturing standards, as downstream conversion steps demand precise stoichiometry and quality control. End use involves further derivatization or amidation steps followed by purification and scale-up under validated process conditions. Industry compliance standards
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2. Starting Material for Iodinated X-Ray Contrast MediaDiagnostic imaging manufacturers utilize this compound to build complex iodinated frameworks used in X-ray and CT contrast agents. The raw material’s high iodine density and precisely defined amino-substitution support the synthesis of contrast agent cores through multi-step carboxylation, acylation, and conjugation protocols. Quality assurance teams monitor for low heavy metal content and consistent batch identity. The raw acid typically undergoes esterification or amidation, then links to hydrophilic carriers if required by product specification. Production scale and design depend on targeted radiopacity and injectability in the final formulation. Industry compliance standards
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3. Intermediate for Radiopharmaceutical SynthesisProducers of radiopharmaceuticals source this intermediate in the preparation of radioiodinated compounds for nuclear medicine diagnostics or therapy. The compound’s diiodo-substitution allows for isotopic exchange with I-123 or I-131 under electrophilic radio-labeling conditions. Strict radiation safety procedures and isotope handling protocols govern formulation labs, with the acid undergoing rapid, high-purity reaction and rapid downstream QC release. The compound often comprises the backbone of radio-labeled benzoic acids or amides, supporting both research kits and final diagnostic doses. Industry compliance standards
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4. Precursor for High-Purity Analytical ReagentsManufacturers of analytical standards and custom calibration solutions employ this compound for its unique halogenation pattern in reference mixtures and specialty analytical reagents. The strict control of contaminants, particularly trace metals and organic residuals, is mandatory to meet laboratory and certification requirements. The acid is typically used as a calibration spike in elemental analysis (e.g., ICP-MS) or as a derivatization agent for the identification of related aromatic compounds in QA/QC environments. Its role is crucial where exact quantitation of iodine or substituted benzoic acids enables reliable process or product validation. Industry compliance standards
Typical usage ratio
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People always ask what makes a fine specialty chemical stand out in this current landscape of pharmaceutical and advanced materials R&D. Working directly at the source—where production, rigorous quality checks, and process tweaks intersect—gives us manufacturers a ground-level view of what sets 2-Amino-3,5-Diiodobenzoic Acid apart in its category. This specialty compound, commonly identified by its structure, IUPAC name, or short-hand model “A35DIBA,” sees regular interest from organoiodine researchers, API developers, and those needing robust intermediates for molecular diagnostics. Decades honing the process illustrate why consistency, purity, and true manufacturer knowledge matter more than ever.
We begin with high-purity feedstocks chosen only after rigorous incoming QC—purity often checks reliably above 99.5% before any iodine steps start. Sourcing costs change every year, and as iodine prices climb, every gram counts. The story of reliable production starts with clean stocks and proper diiodination. Take any shortcut or use lower grades, and you start accumulating byproducts that drag down your yield, hurt purification later, or risk failed batches in someone else’s process line down the road. As chemists at the bench or in scale-up, we can see the color of crude products tells a story before the GC or HPLC runs confirm what our experience hints at. Beyond this, we control every reaction vessel, temperature profile, and vacuum step ourselves—there is no substitute for hands-on, eyes-on-the-reaction work.
For partners in pharma and biotech, nobody wants to halt a multimillion-dollar campaign because the starting material has shifted even a half-percent in impurity profile. Over years, reproducibility stays anchored to tight protocols, logged adjustments, and old-fashioned note-taking. We’ve run side-by-side comparisons on different lots, making sure retention times and melting points fall inside our self-imposed, narrow windows. It means a customer receives the same finished product, whether they’re ordering 25 grams for discovery work or 10 kilograms to feed into pre-commercial campaigns. This commitment echoes each time we pull reference standards, re-validate retention times using fresh columns, and run secondary scans on samples before shipping. A36DIBA shows the highest iodine substitution at the meta and para positions—failure to maintain these puts all downstream chemistry at risk.
Over the years, we’ve seen tricky secondary halogenated byproducts creep in if temperature profiling slips, or if reactor washes are skipped on busy days. Unlike some intermediates, even minor contaminants here—dibromo, monoiodo, or nitro arenes—create headaches for synthetic teams downstream. Our batch records often include full HPLC chromatograms, along with NMR reports (often 1H and 13C, probes for imid impurities), to assure every shipment. If any lot falls out of our known fingerprint, even if within looser theoretical limits, it never makes it past our outbound dock.
Publishers and patents paint a theoretical route for synthesis, but on the shop floor, it’s about managing real-world fouling, side reactions, and keeping yields tight. We settled years ago on a controlled oxidation protocol for the diiodination step, which, though slower, minimizes tar formation and post-reaction adsorption. Early attempts to rush this step with hotter conditions created sticky residues and clogged filters, which slowed production and caused waste solvent headaches. Through process tweaking, we moved to finer sparging, lower temperature increments, and improved reactors to reduce both processing time and waste. A35DIBA, handled this way, shows off as a free-flowing, pale solid with the telltale faint iodine scent—reliable markers of a job done well. Our stubbornness about never skipping labor-intensive purification might go against cost-cutting trends, but labs downstream count on this detail when developing sensitive, high-value targets.
Our customer base tells a clear story every year. Pharmaceutical medicinal chemists drive most applications, starting with halogenated aromatic building blocks in their fragment libraries. Combinatorial chemists need hundreds of milligrams to grams; clinical-scale API teams sometimes inbound with multi-kilogram inquiries. 2-Amino-3,5-Diiodobenzoic Acid holds high value because it acts as a plug-and-play synthon, particularly effective at the juncture where further functionalization occurs via Suzuki or Sonogashira couplings—pointing to our need for low Pd content in residual catalyst analysis. The amino and carboxylic groups bring the kind of flexibility that allow the introduction of heterocycles, peptide mimics, or more complex scaffolds. Additionally, the two heavy iodine atoms serve as both tracers (for imaging and contrast applications) and leaving groups (for radio-labeling, isotope tagging, or advanced diagnostic applications).
In fact, our inspection records show that over 80% of inquiries relate to its use in precursor steps for radiopharmaceuticals, especially in diagnostic radiology. A smaller, but growing, application crops up in material sciences, where the aromatic ring’s substitution pattern introduces key differences in polymer cross-linking behavior. Our collaborations with academic researchers have yielded several joint publications, especially in the radiolabeling space, since the compound’s backbone accommodates site-specific isotopic tagging far more reliably than lower-halogenated analogs.
There’s more to providing specialty intermediates than buying and relabeling. Traders collect their margin, but rarely field questions about synthetic quirks or failed couplings. We invite researchers to speak directly with our technical team. On many occasions, a seemingly routine order turns into a collaborative troubleshooting session—where temperature, solvent, or work-up changes solve a bottleneck uncovered mid-project. In one notable case, a customer encountered persistent side-product formation in a downstream thionation, which we traced to trace ammonium salts left over from incomplete washing at the source. Based on that, we changed our final rinse regime across all batches, leading to a tangible drop in reported customer complaints. This kind of feedback loop drives continuous improvement—never achieved if you’re just buying and selling without skin in the game.
Another clear difference: our traceability documentation. Labs often seek direct answers about the most recent impurity profiles, out-of-spec results, or actual retention times—not last year’s averages. We maintain complete batch logs, which means questions get real answers from those making the material, not vague promises from catalog staff hundreds of kilometers away from any actual chemical reactor. This turns what could have been a transactional relationship into an ongoing partnership, where our feedback shapes future syntheses and product pipelines.
Experience tells us specs are only as good as their real-world translation onto the product. High-purity is not just a number on a certificate. Methods for controlling water content, inorganic residues, and trace metals form the backbone of our daily routines. We spot-check samples for both percentage assay and identity, but also for less obvious properties: flowability in powder form, clumping after prolonged storage, and reactivity under various common organic solvents.
Moisture content routinely falls below 0.5% (Karl Fischer tickets don’t lie), and particle size is tightly monitored: too fine, and dust loss spikes; too crude, and dissolution slows in batch reactors. We take feedback from customers scaling up from HPLC-scale to multi-liter glassware, since requirements can shift with each stage. Our QA staff are never shy about pointing out color shifts, subtle hints of under-dried product, or inconsistencies in aroma—real indicators of batch health ignored in paperwork-only operations.
On the surface, structural analogs like 2-Amino-4,6-Diiodobenzoic Acid or 2-Amino-5-Iodobenzoic Acid might look similar. Down at bench scale, these differences become obvious. A35DIBA’s substitution pattern—with the two iodine atoms at the 3- and 5-positions—offers distinctly different electronics and reactivity, especially at the ortho and meta positions. These features impact cross-coupling chemistry and selectivity in downstream functionalization. Labs pushing for regioselective couplings or higher yields see that even small changes in the iodine positions matter.
For example, the 4,6-analog resists certain substitutions, and, in our hands, tends to exhibit longer crystallization times along with a higher frequency of chromophoric impurities, complicating purification. Yields and by-product formation shift enough to make switching between these derivatives nontrivial. For A35DIBA, robust literature and in-house data show improved results in Sonogashira and Buchwald–Hartwig constructions, mostly due to the ring’s preferential activation. Its melt point (around 225°C) also brings operational stability in process ops, reducing risk of sublimation or unexpected residue losses during scale-up.
A common stumbling block in manufacturing diiodo aromatics is the iodine itself: expensive, volatile, and hard on equipment if not fully recovered at each stage. We installed modern vapor scrubbing and recover excess iodine from process gas lines, allowing both environmental compliance and cost recovery. Buildup of iodine dust or sublimate in less-monitored shops leads to off-color lots or accidental cross-contamination. This does not happen under seasoned eyes: our team logs instrument maintenance and schedules deep cleans specifically around high-iodine synthesis weeks.
Another headache: disposal and recovery of process solvents. Residual iodides pose a problem in wastewater, so we use specialized precipitation and carbon traps. This is not filler for an audit checklist—our local regulations mean steep penalties for noncompliance, and no one wants an interrupted license over lazy process control. Fielding questions from buyers about disposal and compliance, we demonstrate real process changes, not hand-waving about “green practices.”
Pilot scale challenges run beyond the lab books. We know that methods working on a 500-mg scale don’t simply multiply by a thousand with the same results. Reaction rates shift, and minor hot-spots during iodine addition can cause runaway reactions, rapid discoloration, or yield nosedives. Our shift to semi-automated feeders and modern jacketed glassware helps stabilize temperature and allows finer control, leading to fewer surprises. We pilot every new scale-up using smaller reactors, logging every variable. Downtime for re-runs eats budget and erodes trust; getting it right early keeps costs and timelines on track for everyone down the chain.
We routinely retain reference samples from each batch for up to three years, so customers seeking long-term trial comparisons receive accurate, freshly-tested data. There’s commitment here to reproducibility—and putting faces and names behind each run, something glossed over when you’re several steps removed from the actual chemical handling.
Delays in specialty compounds disrupt entire campaign schedules down the stream. Sourcing from where the compound is actually made, not just labeled, gives reliability during times of iodine supply fluctuations or increases in regulatory scrutiny. We keep safety stocks in climate-monitored storage, running periodic re-testing to catch any lot drift from aging. This way, someone ordering 2-Amino-3,5-Diiodobenzoic Acid gets fresh, up-to-date product instead of stock that has degraded on a distant warehouse shelf for months before shipping.
Our logistics partners track environmental and customs compliance, backed by knowledge of international packaging requirements. By working directly with regulators and third-party inspectors, we address any customs or hazardous goods classification ahead of time. In a recent international shipment, knowledge of local documentation helped avoid week-long delays for a cancer radiotherapeutics team waiting on a critical batch. We view this proactive engagement as part of our manufacturer’s responsibility—reacting only after the fact is simply poor risk management.
Over several years, our outgoing lots consistently reach iodine content above 65%, in line with theoretical values. Loss-on-drying checks rarely exceed 0.5%. Most impurity profiles logged on each COA show under 0.2% unknowns at the point of final packaging, and our regular retests of backup samples demonstrate shelf-life stability over 12 months when stored in airtight containers at 2–8°C. R&D teams have used our technical notes and batch samples to validate both radiolabeling and peptide conjugation, feeding back on process changes that then allow us to close the loop for tighter specs.
More than once, customers have traced erratic radiochemical yields back to micro-scale variances in halide content or excess acid residues from shortcut-washed imports. We mitigate these risks by routinely performing trace halogen analysis, using a combination of ion chromatography and colorimetric titrations. Detailed logs help chemists spot trends and avoid failed syntheses or regulatory headaches down the line.
In manufacturing, success is measured not by what works once, but by what works every time. We treat each lot of 2-Amino-3,5-Diiodobenzoic Acid as both a promise and a test. Lessons from a short-run hiccup, a pigment change, or off-trend impurity level lead to direct process adjustments. We schedule regular process audits, using both in-house scouts and third-party partners, fostering a culture of admitting and fixing errors—not hiding them behind opaque sales language.
For example, implementing a two-stage recrystallization after complaints about residue in a side-coupling eliminated over 90% of those downstream complaints. Feedback loops, both from customer labs and internal QA, lead to accumulative improvements over time. Our approach to documentation matches this openness: logs, scans, and batch records trace every step from raw iodine feedstock to outbound certificate. This transparency is built into our reputation and serves as the backbone of our repeat business.
The end result: 2-Amino-3,5-Diiodobenzoic Acid reliably meets the demands of modern synthesis teams—whether for active pharmaceutical ingredient campaigns, radiodiagnostic probes, or novel research targets in advanced materials. The difference comes not in slogans or catalog descriptions, but in the direct, hands-on oversight that only a true producer offers. Strong specs, tight process controls, and responsive technical support all trace back to this daily engagement with real-world chemicals—not spreadsheets or catalog numbers.
Working with seasoned chemical manufacturers allows you to build real partnerships and tackle new projects with confidence, knowing you’re never far from the source of your materials or the practical insights behind them. Every shipment reflects the pride and meticulous attention invested by those who actually run the reactors, make the tough calls on process improvements, and take responsibility for what leaves their plant gates.