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HS Code |
235197 |
| Chemical Name | 5-Benzyloxyindole-2-Carboxylic Acid |
| Cas Number | 18856-29-4 |
| Molecular Formula | C16H13NO3 |
| Molecular Weight | 267.28 |
| Appearance | White to off-white solid |
| Melting Point | 206-210°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in DMSO, slightly soluble in methanol |
| Storage Temperature | 2-8°C |
| Inchi Key | WIVYMSWWNZMWAZ-UHFFFAOYSA-N |
| Smiles | C1=CC=C(C=C1)COC2=CC3=C(C=C2)N=CC(=O)O3 |
As an accredited 5-Benzyloxyindole-2-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 5g amber glass bottle with a tamper-evident cap and clear labeling indicating 5-Benzyloxyindole-2-Carboxylic Acid. |
| Shipping | 5-Benzyloxyindole-2-Carboxylic Acid is shipped in tightly sealed containers to protect against moisture and contamination. Packages are clearly labeled and handled under appropriate safety regulations for chemicals. Transport is conducted at ambient temperature, unless otherwise specified, in compliance with local, national, and international shipping guidelines for laboratory reagents. |
| Storage | Store 5-Benzyloxyindole-2-Carboxylic Acid in a tightly sealed container, protected from light and moisture, at room temperature (15–25°C) in a cool, dry, well-ventilated area. Keep away from incompatible materials such as strong acids, bases, and oxidizing agents. Ensure the storage area is appropriately labeled and complies with regulatory guidelines for chemical safety. |
Applications of 5-Benzyloxyindole-2-Carboxylic Acid in Industrial ManufacturingAs an original producer of 5-Benzyloxyindole-2-Carboxylic Acid, we support multiple downstream industries that rely on this advanced indole derivative for specialized intermediate synthesis. Our focus is on real-world manufacturing applications where strict regulatory, process, and performance requirements demand consistency in material quality and traceability at every production step. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisPharmaceutical manufacturers utilize this compound in the multi-step synthesis of advanced indole-based APIs. The raw material acts as an essential building block in the formation of heterocyclic cores for antineoplastic and anti-inflammatory drug classes. Downstream chemists integrate our molecule at a critical point in process routes, enabling high-yield coupling and late-stage derivatization while maintaining control over enantiopurity and trace contaminants. Industry compliance standards
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2. Fine Chemical Synthesis for Agrochemical ActivesFine chemical formulators deploy this ingredient in synthetic routes leading to novel crop protection agents. Its indole scaffold serves as the foundation for constructing bioactive carboxamides or indole-based herbicide precursors. This compound sees frequent use in pilot and commercial scale production cycles, where reproducibility and impurity control affect both process validation and environmental discharge compliance. Industry compliance standards
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3. Specialty Dyes and Pigments ManufacturingThe advanced aromatic structure of this molecule enables its use in the synthesis of high-purity indole-based colorants for specialty dye houses. As a core intermediate, it participates in targeted substitutions, forming high-stability chromophores for electronics, inks, and technical textile applications. Attention to byproduct removal and consistency during batch processing is critical in this sector. Industry compliance standards
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4. R&D and Reference Standard Supply for Analytical LaboratoriesQualified laboratory reagent manufacturers and analytical contract labs apply this compound as a reference intermediate for chromatographic and structural studies. Its structure supports critical validation work in pharmaceutical impurity profiling, biotechnology lead screening, and academic research into indole-based compound libraries. Industry compliance standards
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Labs and manufacturing teams who routinely work with specialty indole derivatives recognize the hurdles in balancing purity, availability, and stability. Over the years, 5-Benzyloxyindole-2-Carboxylic Acid has become a regular request from both pharmaceutical developers and research chemists. From where we stand on the factory floor, every batch is more than a string of numbers or an item on a spec sheet. We feel the push from our customers for tighter controls and greater lot-to-lot dependability—beyond anything offered by generic resellers.
Our product, characterized by the classic benzyloxy substitution at the 5-position and the carboxylic group at the 2-position on the indole ring, appears as an off-white to almost white powder. This material often reaches markets with a purity not dropping below 98% by HPLC, as confirmed in our own QC laboratories. The primary application occupies a narrow field: intermediate use in the synthesis of small-molecule drugs, particularly in programs exploring kinase inhibitors, serotonin analogues, and experimental anti-tumor agents. Academic laboratories, too, prefer this compound when running pathway-specific labeling or when building structure-activity relationships for new indole-core pharmaceuticals.
What distinguishes our manufacturing approach is the refusal to cut corners in upstream processing. We rely on controlled benzyloxy protection chemistry rather than broad, catch-all synthetic steps. Choosing to avoid trace metal catalysts in final stages comes directly from listening to feedback about downstream purification headaches and bioassay interference. Some competitors lean on short cycles, trading off reagent cost for residual impurity, but we’ve stuck with a slower route to maintain the cleanest possible product.
Reproducibility matters more than ever. During scale-up, we saw firsthand how moisture control impacts final purity, so we invested in atmospheric dryers dedicated solely to our indole line. Additives or anti-caking agents, commonly used by middlemen to meet cosmetic standards, are absent in our lots; our line foremen check for flowability as part of daily operations without these artificial aids. Customers sourcing elsewhere sometimes complain of persistent specks or variable melting points. In regular client communications, they mention our powder remains consistent over repeated orders, which we attribute to never blending returns from previous batches back into new stock.
Most requests come from early-stage R&D outfits pursuing novel chemical spaces. In these settings, researchers often need just a few dozen grams, but they demand a material identical to their pilot-scale needs. Our doors are open for scale-ups. Over multiple years, firms have contracted us for single-kilo orders, gathering data during process validation for eventual regulatory submissions. The in-house QC data package, tailored for each lot, follows every shipment, as documentation and chain-of-custody questions surface frequently in compliance audits. All this comes from our background delivering not just to local universities, but to global veterinary, agricultural, and oncology research consortiums.
You might hear stories about alternate sources that liquidate warehouse overstock or blend left-over lots to drive prices down. We don’t find those strategies sustainable. On our shop floor, we see the outcome: one mismatched impurity profile, and a long-term client is lost. Our own technical team acts not just as suppliers, but as partners in troubleshooting, happy to clarify minor differences in lot history, residue limits, or analytics for every inquiry.
We often debate in production meetings—would it be easier to bump output by blending off-grade material, or to sell acceptably close material at a discount through a partner channel? We always land on quality as the only reasonable choice. Even slight drifts in melting point signal a shift in synthetic byproduct profile, and we’ve pulled entire lots back for rework when such issues crop up. If you’ve spent weeks on an in vitro screen, only to find variability linked to starting materials, that frustration lingers.
Users aiming for medicinal chemistry or pilot-scale preclinical work see little value in bargain materials with unknown handling. To them, it’s not just a question of “does this meet minimum specification?” but “can I trust this material batch for batch?” Our position near the start of the supply chain puts us in unique contact with these worries. The responsibility weighs on us daily, as traceability and reliability seem to grow tighter with each regulatory cycle.
On a structural level, 5-Benzyloxyindole-2-Carboxylic Acid offers a distinctive platform for derivatization. While several indole-2-carboxylic acids exist, the benzyloxy group at the 5-position opens up further options for ether cleavage, leading to various hydroxyindoles needed downstream. The benzyl protection group provides stability throughout more aggressive synthetic steps. Chemists working in peptide-like or heterocyclic scaffolds recognize this trait, as the benzyl group survives during harsher processing, and can be selectively removed at later stages with catalytic hydrogenation or other established deprotection strategies.
By contrast, plain indole-2-carboxylic acid lacks this modifiable handle, limiting late-stage functionalization. Similarly, using other protecting groups, like methoxy or alkoxy derivatives, affects not only the electron density at the 5-position, but also alters hydrogen-bonding character and downstream deprotection profiles. Over years of supplying this and related compounds, we’ve advised scores of development groups on the benefits of this precise benzyloxy protection, both in terms of synthetic flexibility and consistent yields in multistep sequences. Observations from customer pilot campaigns reinforce that fewer byproducts appear in oxidation-sensitive transformations when sticking to this structural motif.
Technicians and researchers on our feedback panels share practical concerns about storage and handling. Unlike some analogs prone to rapid oxidation or photodecomposition, our 5-Benzyloxyindole-2-Carboxylic Acid demonstrates stability under dry, room-temperature conditions for several months. Storage in amber glass further extends shelf life, as minor discoloration can start to show after prolonged exposure to sunlight—an issue first identified by a partner lab several years ago, spurring our switch to opaque packaging.
On the bench, the powder flows with enough ease for weighing—fine enough to minimize clumping, yet avoiding the static charge problems sometimes encountered with higher substituted indoles. Filtration steps are rarely delayed by particulate impurities, since our upstream isolation process specifically separates mother liquors to maximize crystal uniformity without introducing dust-forming excipients.
Solvent compatibility questions arise, especially from teams running parallel syntheses. In direct user reports, dissolving in common polar aprotic solvents, such as DMF, DMSO, or NMP, proceeds quickly at room temperature, so typical loading operations move faster. During one batch release, several users alerted us to a slight endotherm below 200°C, prompting a further examination of polymorph tendencies by our in-house crystallographers. The review identified a preferred crystal form, now standard across our production runs, which has reduced batch rework requests in the past twelve months.
Our history manufacturing both unsubstituted indole-2-carboxylic acid and other benzyloxyindole variants gives us a close-up view on how small changes affect user outcomes. Substituted benzyloxyindoles with protective groups elsewhere on the ring usually present difficulties during late-stage hydrogenolysis, introducing unwanted side-reactions or incomplete cleavage ratios. Process chemists who returned to our benzyloxy product after trialing methoxy or pivaloxy groups cited sharper NMR spectra, simpler workup steps, and shorter silica gel chromatographs.
The flexibility offered by the benzyloxy protection at the 5-position means that function groups resist hydrolysis in alkaline conditions, allowing more robust reaction design in multi-step programs. Some partner facilities working at scale noted that running the same sequence with unsubstituted carboxylic acids led to loss of material through decarboxylation or ring cleavage, issues that have not surfaced with our product under comparable conditions. Over time, this consistency saves time and gives users peace of mind.
Handling experience has taught us that subtle differences in the work-up details really change downstream results. Our filtration techniques avoid introducing silica or inorganic impurities, and every finished kilogram undergoes multiple passes for detectable solvents by both GC and gravimetric methods. Direct customer conversations led us to report not just HPLC area percent, but also TLC profiles, melting range, water content, and residual solvents, making user documentation packs more robust for regulatory authorities.
Users working in regulated environments regularly request additional details on synthesis route, impurity profile, and storage advice. Our records, maintained batch by batch, reference synthetic genealogy and process amendments, creating a transparent path from raw material sourcing to finished inventory. Responding to one customer's suggestion, we extended our documentation archive to cover five years, supporting traceability efforts often cited by quality assurance teams at biopharma clients.
Long-term clients emphasize the value they find in open conversations with our production teams. Some have shared details about on-site troubleshooting, relying on our insights to adjust reaction conditions, now that they know each batch’s background. We offer personal access to both our operations and quality team, cutting through layers of generic email chains so questions reach those who actually produce the material. These partnerships, sometimes stretching a decade, have grown out of mutual trust built on repeated, reliable performance.
Supply demands shift. Regulatory environments tighten. New scientists join our clients’ teams every year with new ideas and eager questions. Our belief in chemical manufacturing rests on the idea that progress comes from honest exchanges about what works, what could work better, and how process limitations shape the possible outcomes downstream. If a formulation specialist needs to know about particle morphology, or an investigator faces solubility limits during a late-night run, those calls come straight to our support desks where the actual experts—those making the compound—hear the challenge first-hand.
Taking responsibility for the ecological impact of specialty chemicals has grown from being a regulatory checkbox to a genuine daily commitment. For 5-Benzyloxyindole-2-Carboxylic Acid, we’ve adjusted workflows to reduce halogenated solvent waste, and added value through closed-loop purification. After process changes last year prompted questions from regular buyers, we circulated lifecycle analysis data showing reductions in our energy expenditure per kilogram produced. Some operators in other sectors still default to high-load waste incineration, but tight in-plant monitoring and reprocessing have kept our actual landfill-bound waste minimal. Aided by monitoring sensors in both our reaction and workup areas, our internal audits show continuous progress as we trim down process water needs.
Handling safety is another core deliverable. As raw material hazards have shifted, our in-plant safety guidelines moved with them. Frontline workers, some with decades of tenure, bring concerns straight to our process engineering review each week. Actionable outcomes—like new PPE requirements for pilot plant staff during open transfers—emerge directly from these conversations. Frequent refresher sessions, simplified signage in local language, and staged order-of-addition training now stand as regular features based not on mandates, but experience.
Every kilogram leaving our site carries the marks of real feedback loops between production, quality, and our network of end users. This cooperative spirit helps drive modest but meaningful process enhancements: finer control of reaction pH, closer tracking of mother liquor composition, and nuanced tweaks in solid-liquid separation steps. When an analytics partner uncovered a rare glycine impurity at trace levels, we took note, rebuilt a segment of pre-purification, and since then have watched that contaminant disappear from our independent analyses. Examples like this tell the backstory to every improvement we implement, every technical note we add for our customers.
Working directly as a manufacturer means we adjust on the fly. Requests for ultra-low water or solvent levels in select batches led us to dedicate vessels exclusively to high-purity indole work, segregating cleaning systems to prevent cross-contamination with our larger commodity chemicals division. The extra time invested pays off in trust: our partners mention that their regulatory teams have less rework to justify when data sheets match real-world experience.
5-Benzyloxyindole-2-Carboxylic Acid is more than just a reagent or a line item in a catalog to us. From the careful sourcing of precursor indoles to the double-checked NMR and HPLC signatures, and from deep handling experience to continual tweaks prompted by user feedback, the product embodies more than a specification on a webpage. Our path forward stays rooted in serving industries, scientists, and technicians who count on dependable, consistent supply. Every order, large or small, draws on a decade’s worth of expertise on our factory floor, and every new challenge—technical, regulatory, environmental—receives our full attention as a matter of both pride and responsibility. Each batch that arrives in a laboratory carries a part of that commitment.