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HS Code |
356755 |
| Product Name | 3-Chloro-Benzo[B]Thiophene-2-Carboxylic Acid Hydrazide |
| Molecular Formula | C9H7ClN2OS |
| Molecular Weight | 226.68 g/mol |
| Appearance | Off-white to pale yellow solid |
| Melting Point | Approximately 180-200°C (may vary by source) |
| Solubility | Slightly soluble in water; more soluble in organic solvents like DMSO |
| Purity | Typically ≥ 95% |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Smiles | C1=CC2=C(C(=C1)Cl)SC(=C2)C(=O)NN |
| Boiling Point | Decomposes before boiling |
| Synonyms | 3-Chlorobenzo[b]thiophene-2-carbohydrazide |
| Inchi | InChI=1S/C9H7ClN2OS/c10-7-3-1-2-6-5(7)4-14-8(6)9(13)12-11/h1-4H,11H2,(H,12,13) |
As an accredited 3-Chloro-Benzo[B]Thiophene-2-Carboxylic Acid Hydrazide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed in a 25g amber glass bottle, labeled with the chemical name, purity, hazard warnings, and batch number for laboratory use. |
| Shipping | The chemical **3-Chloro-Benzo[B]Thiophene-2-Carboxylic Acid Hydrazide** is shipped in tightly sealed containers, stored in a cool, dry location away from incompatible substances. It is packaged according to regulatory guidelines, with appropriate hazard labeling and documentation, ensuring safe handling and transport to prevent moisture, light, or contaminant exposure during transit. |
| Storage | Store 3-Chloro-Benzo[B]thiophene-2-carboxylic acid hydrazide in a tightly sealed container at room temperature, ideally between 2–8°C. Protect from direct sunlight, moisture, and sources of ignition. Store in a cool, dry, and well-ventilated area away from incompatible substances such as strong acids and oxidizers. Ensure containers are clearly labeled and access is limited to authorized personnel. |
Applications of 3-Chloro-Benzo[B]Thiophene-2-Carboxylic Acid Hydrazide in Industrial ManufacturingAs a specialized manufacturer of chemical intermediates, we supply 3-Chloro-Benzo[B]Thiophene-2-Carboxylic Acid Hydrazide to a select range of advanced downstream industries. Its unique aromatic structure, reactivity, and halogen functionality make it a critical building block in complex organic synthesis. The following application scenarios reflect our extensive technical engagement with genuine production customers worldwide. 1. Active Pharmaceutical Ingredient (API) Synthesis: Heterocyclic Drug ScaffoldsPharmaceutical companies use our material as a core fragment in the synthesis of heterocyclic APIs, notably for second-generation benzothiophene-based therapeutics. In these routes, it acts as a hydrazide building block for condensation with aldehydes or ketones during the assembly of drug candidates for oncology, metabolic, and CNS disorders. Downstream chemists adjust its incorporation based on target molecule design and route development studies, requiring reliable impurity control and batch reproducibility. Industry compliance standards
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2. Agrochemical Intermediate: Synthesis of Systemic FungicidesLeading agrochemical formulators employ our hydrazide compound in the construction of thiophene-based fungicidal actives. It serves as a functionalized precursor for the core ring system in systemic agents, inserted through acylation or hydrazone coupling stages. Strict control of purity and halogen content is essential to meet product stewardship commitments and ensure consistent bioactivity in field applications. Industry compliance standards
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3. Organic Electronic Materials: Synthesis of Functional Thiophene MonomersManufacturers in the organic semiconductor sector rely on this compound for its utility as a halogenated monomer source. It participates in Suzuki–Miyaura or Stille-type couplings to assemble π-conjugated systems for optoelectronic devices. The halogen and hydrazide functionalities allow precise tuning of electronic properties and facilitate cross-coupling during polymer backbone formation, essential for the fabrication of OLEDs and thin-film transistors. Industry compliance standards
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4. Specialty Dye and Pigment Manufacturing: Heterocyclic Colorant SynthesisDye and pigment producers exploit our hydrazide for the targeted synthesis of thiophene-based azo and hydrazone pigments. Its electron-rich aromatic system and reactivity support high-intensity shade development for specialty textile and plastic applications. Downstream colorant synthesis incorporates this intermediate in diazotization or coupling steps, demanding tight process control for shade reproducibility. Industry compliance standards
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Every successful synthesis project relies on the quality and consistency of the starting materials. As a chemical manufacturer with hands-on experience producing heterocyclic compounds, I have seen the demands that medicinal chemistry, agrochemical development, and specialty synthesis place on raw materials. 3-Chloro-Benzo[B]Thiophene-2-Carboxylic Acid Hydrazide (sometimes abbreviated as 3-Cl-BTCA Hydrazide) stands out as one of those specialized intermediates that often get ignored in traditional catalogs, but plays an essential behind-the-scenes role in synthesis flows.
Our production approach has always anchored itself in reproducibility; after dozens of individual campaigns and kilogram-scale runs, I have come to appreciate the subtle challenges faced in the synthesis of this hydrazide derivative. This is not a low-cost, bulk commodity—it’s a fine organic intermediate, often used by process chemists pursuing new APIs or complex functionalized materials. Customers approaching us frequently share frustrations about batch-to-batch variance and inconsistent purity grades from resellers. There’s no substitute for the direct control a true producer maintains over critical steps: proper chlorination of the benzo[b]thiophene backbone, careful carboxylation, and then hydrazinolysis under anhydrous conditions. Each stage demands careful calibration of parameters—temperature, reagent equivalents, solvent choices—to achieve a hydrazide that does not carry through colored impurities or unwanted isomers.
Over the years, product specifications have evolved. Early customers would sometimes request broad purity ranges, but project outcomes forced us to refine these targets much tighter. The standard material we prepare for sale delivers a minimum purity of 98% (HPLC), with water and ash content held to strict upper limits. We do not offer watered-down technical grades. After consulting with researchers and formulation engineers in pharmaceutical R&D, we understood that even minor byproducts often introduce uncertainty or trap purification resources. This is why each batch receives full documentation including chromatograms, melting point, and route-of-synthesis information—unfiltered and directly available, never “massaged” to fit stock templates.
Physically, this hydrazide presents as a free-flowing pale crystalline powder, but bulk customers occasionally request it granulated or micronized. Our in-house team adjusts drying and grinding procedures for each order, based on transparent discussions about end use. Particle size makes a difference, especially for labs scaling up screening or trying to avoid static aggregation during transfer. We take all handling factors into account since we have witnessed process lines grind to a halt because some distant supplier cut corners on material finishing. Vacuum drying, inert atmosphere packing, and triple-layered polyethylene liners all came directly from customer feedback after real-world frustrations.
Chemists working with thiophene scaffolds often run into a brick wall searching for versatile connection points. The 3-chloro substitution pattern on the benzo[b]thiophene ring provides an avenue for further selective transformation unavailable with non-chlorinated analogs. The carboxylic acid hydrazide function sits ready for directional modification—cyclization, condensation, or as a direct partner in constructing pyrazoles, triazoles, and other fused ring systems. We have participated in several collaborative scales with medicinal teams pursuing kinase inhibitor leads, where the behavior of trace amounts of hydrazide byproducts made the difference between multi-gram breakthrough and dead-end synthesis.
This compound’s role isn’t limited to pharmaceuticals. One of the lessons picked up after a decade of manufacturing heterocycles: electronics, dyes, photographic chemicals, and new agrochemical candidates all leverage tailored intermediates like this. With our in-house pilot lines, we have trialed gram-to-kilogram modifications to the hydrazide unit, offering unique handles for downstream acylation or aza-coupling steps. Some institutions have even built custom derivatives on our substrate, pushing their programs from bench to kilogram scale before submitting preclinical packages.
Customers looking for benzo[b]thiophene derivatives quickly face a maze of similar-sounding names: various chloro isomers, non-chlorinated siblings, carboxylic acids, esters, and hydrazide forms all circulate on the market. Over the years, we have handled the full suite and can speak to why each form fits different applications. The presence of the 3-chloro group shifts reactivity and significantly changes the course of downstream substitution. For some cyclizations, this particular hydrazide enables a clean one-step building of new rings that fail with the unsubstituted cousin. Anyone who has tried to swap in the 2-chloro or 5-chloro versions quickly learns that the position of substitution is everything—the 3-chloro layout gives electronic and steric effects that can drive reaction yields or alter byproduct profiles.
Esters or acids of benzo[b]thiophene provide some synthetic flexibility, but only the hydrazide group delivers direct access to condensation and heterocyclization steps essential for advanced pharmaceutical intermediates. In some cases, regulatory filing packages need exact tracing of synthetic intermediates; carrying the hydrazide motif right from the beginning, supported by chain-of-custody documents, helps customers avoid costly requalification later. Direct-from-manufacturer traceability isn’t just a buzzword—we maintain archived spectra, batch logs, and even raw material sample vials for five-plus years because large pharma clients demanded this level of support after running into lost-data headaches with less transparent suppliers.
One theme that comes up repeatedly in customer calls: “We’ve got a gram working, but we’re getting stuck at 500 grams.” Years back, we ran into the same scale-up pitfalls: sticky residues, oiling-out at the wrong temperature, unwanted solvent adducts that only show up above 100 grams. Our plant crew spent months troubleshooting crystallization windows and checking high-shear drying setups to beat caking. Many academic routes look flawless until you move past the flask and see everything collapse in a filter cake or during drying. Our current protocol follows direct workflow interaction—no step is signed off until plant and QC staff agree the batch flows from reactor through finish without surprises. Several competitors cut process validation steps to speed up orders; we learned from a costly rework batch that this shortcuts only stack up trouble down the road. There’s no substitute for real, on-the-floor experience, and current customers know exactly who’s handling their order, down to the operator.
The active involvement of our technical team often uncovers small tweaks that can save thousands in labor or solvent costs. A water addition rate here, or a pH adjustment there—those details don’t show up in generic protocols you see floating around online. One oncology startup came back after an initial test order, impressed that their pilot kilogram campaign matched our small-scale data sheet. Their own runs, mirroring our published workflow, reached comparable purity and handled downstream steps without a hitch. That’s a kind of real-world reproducibility that comes only from making the product at scale and refusing to cut corners, even when deadlines tighten.
Quality assurance for a specialty intermediate starts early. Each new batch begins with full traceability of starting materials—chlorinated benzo[b]thiophene, fresh hydrazine hydrate, all solvents—and testing for possible contaminants. The market remains flooded with resellers who lack batch-level insight: I’ve fielded too many requests from customers burned by lots containing elevated solvents or color bodies, blamed on “storage” issues. Because we manage the full lifecycle—procurement, reaction, drying, and final packing—we spot issues before release. Regular audits and deep dives into both spectral data and process logs keep our own team vigilant.
Every outgoing lot receives full HPLC, NMR, and elemental analysis. Our quality control team always runs side-by-side checks with both the in-house reference standard and, by request, customer-submitted check samples. If an anomaly turns up—even a few tenths of a percent—they track the batch history, review plant event logs, and, where necessary, reproduce the testing to confirm results. Experience taught us not to rely solely on a single method’s output. Parallel testing (orthogonal approaches) caught a solvent artifact missed by chromatographic assay in an early campaign—since then, two sets of eyes and two analytical tracks became SOP. This focus on rigor shields downstream users from surprises, especially on the high-value runs common in lead optimization or preclinical trial support.
One aspect too often overlooked by intermediaries and general traders concerns the needs of boots-on-the-ground chemists and engineers. Direct feedback streams have built our current process. Researchers do not waste time with generic pitches or catalogs bloated with unrelated chemicals. Most want clarity on reactivity, handling, assurance their sample matches the defined structure, and access to supply in scale if a hit emerges. Our technical staff spends plenty of time answering pointed formulation or modification questions—what solvent is best for re-dissolving, how to target your crystallization, why a recent run looks “off”. We see supporting these technical troubleshooting sessions not as a cost, but as an investment in customer trust. Customers return because they see change—process improvements and handling recommendations stem from their cases, not empty promises or pre-packaged “support.”
We also learn a great deal from non-pharma customers. Chemical engineers in pigment development programs need assurances about shade stability or compatibility with other aromatic building blocks. Agricultural researchers might require help adjusting input materials to meet new regulatory requirements or analytical targets. Our answer is transparency: the same sample data, the same batch history, and shipping preparations tailored to what research teams actually need. For many specialty projects, off-the-shelf and trader-sourced goods simply do not deliver—the gap between catalog description and hands-on documentation splits projects in two. We keep both the records and the test samples accessible for every single kilogram produced.
The academic and patent literature has confirmed the value of 3-chloro-substituted benzo[b]thiophenes as versatile synthetic tools. These systems provide anchor points for constructing antitumor, anti-inflammatory, and antimicrobial scaffolds, among other uses. Access to high-purity intermediates delivers better downstream selectivity and speeds up the transition from lab curiosity to actionable lead compound. Our direct production experience, paired with the published findings from medicinal chemistry groups, aligns behind this compound’s flexibility and reliability.
Market pressures sometimes push traders to offer “equivalents” or substitute compounds, usually driven by shelf availability rather than application fit. Experience shows these swaps rarely work smoothly. The wrong isomer or impurity can mean wasted purification and inconsistent bioactivity. Pilot project leaders who choose to partner with a manufacturer—one prepared to document both process and product history—report faster development times, lower batch rejection rates, and a smoother regulatory path. These outcomes reflect not marketing claims, but the documented results visible across the last decade of synthesis projects carried out with our support.
As a manufacturer, responsibility does not stop with shipping a drum or a box. Our factory puts substantial time into safe reaction handling, minimization of effluents, and ensuring operator safety during what can be tricky hydrazinolysis steps. We have invested in advanced scrubbing systems and closed reactor designs to capture any off-gassing or raw hydrazine traces. Years ago, a single adverse event on an open system led to a complete overhaul of our approach to staff training and environmental exposure; since then, we have logged a clean, incident-free safety record. Customers inheriting material from these improved facilities receive a product that has been prepared with genuine care for both team safety and local environmental compliance.
Packaging matters, especially for sensitive organics. The majority of 3-Chloro-Benzo[B]Thiophene-2-Carboxylic Acid Hydrazide orders travel in three-layer sealed liners within solid HDPE jars, then inside shock-resistant drums—a lesson we adopted after a high-value shipment once arrived at a customer’s site after a long ocean voyage, only to find minor humidity ingress had caked the material. Our current process ensures free-flow material upon delivery, even after weeks in customs or transit. Every drum receives both an external tamper seal and internal CO2/moisture soak test; buyers know exactly what to expect when opening the package, whether for gram-scale trials or full plant synthesis.
What keeps our team motivated is not only the current crop of pharmaceutical and specialty chemical programs but validation of this compound’s role in emerging R&D. The last several years brought a wave of inquiries from university technology transfer offices, startup incubators, and global biotech companies aiming to take next-generation benzo[b]thiophene templates from proof-of-concept to commercial scale. Our ability to scale supply, customize finishing, and document every step along the way is not an add-on but an expectation set by today’s demanding synthetic workflows. As project needs grow from bench through early pilot and then full GMP campaigns, our experience as real producers—not warehouse shufflers—pays forward in both assurance and reliability.
For customers concerned about future scale and regulatory pathways, we maintain both developmental and validation capacity for this intermediate. New projects draw on our archived production runs, cross-referencing analytical trends, and tracking any shifts due to regulatory or raw material shifts. We can accommodate new purification, drying, or even derivatization requests, aligned to the workflow of the researcher or process chemist, not to arbitrary “catalog” definitions.
Having handled and produced 3-Chloro-Benzo[B]Thiophene-2-Carboxylic Acid Hydrazide through many project cycles, our manufacturing experience is not composed of generic claims but evidence built batch by batch. Real manufacturing control means traceable origin, direct technical support, and flexibility in form tailored to specific synthetic targets. Consistent quality, clearly documented process history, and commitment to transparent communication set our approach apart from third-party brokered supply.
Our everyday operations reflect the feedback loop we have built with our end users: new practices, fresh quality targets, and honest handling support respond directly to what research and development teams need. Whether the requirement is a first gram or a multi-kilogram campaign, our work as actual producers delivers not just a chemical but the assurance and insight hard-won by making, testing, and delivering 3-Chloro-Benzo[B]Thiophene-2-Carboxylic Acid Hydrazide direct from the source.