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HS Code |
901311 |
| Chemical Name | 4-(Bromomethyl)-Benzoic Acid, 1,1-Dimethylethyl Ester |
| Molecular Formula | C13H15BrO2 |
| Molecular Weight | 283.16 g/mol |
| Cas Number | 141612-84-4 |
| Appearance | White to off-white solid |
| Purity | Typically >98% |
| Solubility | Soluble in common organic solvents (e.g., dichloromethane, ethanol) |
| Smiles | CC(C)(C)OC(=O)C1=CC=C(C=C1)CBr |
| Inchikey | RXBPUSYRCBGJRB-UHFFFAOYSA-N |
| Storage Temperature | 2-8°C |
As an accredited 4-(Bromomethyl)-Benzoic Acid, 1,1-Dimethylethyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle with a secure screw cap, labeled with product name, purity, hazard symbols, and manufacturer details. |
| Shipping | 4-(Bromomethyl)-Benzoic Acid, 1,1-Dimethylethyl Ester must be shipped in tightly sealed containers, protected from light and moisture. Classified as a hazardous material, it requires transport in compliance with relevant safety regulations, including proper labeling, cushioning, and secondary containment to prevent leaks. Shipping should be via certified carriers authorized to handle chemicals. |
| Storage | Store 4-(Bromomethyl)-Benzoic Acid, 1,1-Dimethylethyl Ester in a tightly sealed container, away from moisture and direct sunlight, at a temperature between 2–8 °C (refrigerator). Keep the chemical in a cool, well-ventilated, and dry area, separated from strong oxidizers and incompatible substances. Properly label the container and restrict access to trained personnel only. |
Applications of 4-(Bromomethyl)-Benzoic Acid, 1,1-Dimethylethyl Ester in Industrial Manufacturing4-(Bromomethyl)-Benzoic Acid, 1,1-Dimethylethyl Ester serves as a key intermediate across several advanced manufacturing fields. As a direct producer, we support clients demanding precise reactivity, strict purity controls, and batch consistency for multi-step syntheses. Below, we outline major downstream sectors and operational practices built around this specialty chemical. 1. Active Pharmaceutical Ingredient (API) Synthesis for Oncology DrugsPharmaceutical developers use this compound to introduce brominated aryl structures into complex APIs, particularly within anti-cancer agent frameworks like kinase inhibitors. Our material’s reproducible reactivity enables reliable nucleophilic substitution steps. It enters target molecule assembly at a key stage for side-chain installation, where trace impurities and particle sizing influence yield and purification efficiency. Industry compliance standards
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2. Advanced Organic Synthesis for Electronic MaterialsManufacturers of electronic-grade polymers integrate this specialty building block in the creation of liquid crystal monomers and hole-transport materials. The bromomethyl group facilitates Grignard couplings, Suzuki cross-couplings, and ester substitution steps, producing highly pure intermediates necessary for optoelectronic device performance. Quality control focuses on trace halogen and organometallic contamination. Industry compliance standards
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3. Agrochemical Intermediate for Selective Herbicide SynthesisLeading agrochemical formulators apply this raw material as a substrate for arylation reactions in the production of selective post-emergence herbicides. The bromomethyl group participates in key alkylation stages to create molecules exhibiting preferential weed control. Process safety and traceability receive heightened attention to meet regulatory checks on pesticide impurity profiles. Industry compliance standards
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4. Fragrance and Fine Chemical SynthesisProducers specializing in aroma chemicals use this benzoic acid ester derivative to construct aromatic backbones for high-value musk and floral note molecules. The compound’s controlled bromination enables site-specific substitutions, necessary for the development of proprietary fragrance ingredients. Stringent batch uniformity and aromatic purity levels remain essential for consistent olfactory profiles in finished blends. Industry compliance standards
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After years navigating the ever-evolving standards of fine organic synthesis, our facility puts considerable energy into developing 4-(Bromomethyl)-Benzoic Acid, 1,1-Dimethylethyl Ester. Bringing this compound from concept to scaled production never turns out simple. Through technical improvements and a deep familiarity with each batch as it comes off our lines, we see firsthand how the market for this ester now extends far beyond niche academic applications. It forms a solid backbone for the next generation of fine chemicals, thanks to how it connects with certain pharmaceutical and material science goals.
The core of this molecule stands on a benzene ring, substituted at the para-position by a bromomethyl group and esterified with tert-butyl on the carboxylic acid. While its IUPAC name can seem lengthy, the structure is both stable and versatile. We know this from our process development phase, spent adjusting and re-adjusting to get the optimal bromination without complicating byproducts. Only direct control of reaction conditions delivers material that meets the consistent purity targets our customers need for sensitive downstream syntheses.
Choosing the tert-butyl ester as a protecting group goes beyond theory — it shows its value every day in our reactors. For chemists running multi-step syntheses, the tert-butyl ester resists hydrolysis over a pragmatic range of temperatures and solvents. We learned early that using methyl esters or ethyl esters exposes customers to unwanted transesterification or cleavage by mild acid, especially in late steps. The tert-butyl group stands strong through many transformations, only cleaving off cleanly with acidolysis at the end. That reliability, which saves both time and raw materials, motivated us to focus our resources on perfecting this specification, even though it demands more thorough purification than simpler esters.
In addition, the para-bromomethyl group provides an entry point to aromatic substitution, coupling, and cross-linking reactions. During scale-up, we focus on controlling the position and the sheer evenness of the bromination — any ortho content or dibrominated byproducts reduce yield and complicate isolation. The result is a starting material better suited for tailored linkers, protecting groups, or even active pharmaceutical ingredient intermediates, rather than generic bulk chemicals meant for less sensitive applications.
No two lots are exactly the same, despite the routine appearance of white solids flowing from the dryer. Temperature control during the bromination step, solvent recycling, and timed quenching differentiate batches that breeze through customer quality control from those that raise questions. The challenges surface most clearly when a customer requires the ester in kilogram quantities, with strict impurity profiles for use in new drug manufacturing. Getting the last traces of inorganic salts and overbrominated material out of the product pushes us to refine our methodology, which passes through multiple filtration and crystallization steps before the quality assurance team signs off.
The industry rewards suppliers who go beyond crude specification matching. For this ester, thin-layer chromatography and proton NMR provide the transparency customers require. Each time our quality control chemists spot a discrepancy, we trace it back through our logs and batch data, often revealing opportunities for minor tweaks in the bromination or esterification phases. Hearing from clients that our material gives cleaner reactions without extra purification validates this iterative process.
We speak regularly with research teams that evaluate new linkers, polymers, and active intermediates. During their method scouting, standard benzoic acid esters often fall short due to reactivity issues or uncooperative deprotection. Our 4-(Bromomethyl)-Benzoic Acid, 1,1-Dimethylethyl Ester fills the space for a stable, yet easily unmasked, carboxyl group, paired with a handle for robust substitution chemistry.
One long-term customer shared their procedure for constructing custom resins used in peptide synthesis. Early experiments with methyl esters broke down under the base conditions involved in loading and washing steps. Substituting with this tert-butyl ester conserved their functional group, allowed for clean linker attachment, and ensured a gentle deprotection sequence at the conclusion of synthesis. It solved several bottlenecks without introducing new ones. Direct communication with users like this drives our R&D team to keep improving isolation and packaging for easy handling in gloveboxes and scale-up reactors.
This same molecule enters medicinal chemistry programs hunting for new boron or sulfur-containing drugs. The ability of the bromomethyl group to undergo straightforward nucleophilic substitution opens avenues for attaching bioactive fragments or fluorescent probes. For those running automated synthesizers, high purity minimizes clogging, residue build-up, and inconsistent yields between runs. These details rarely make headlines but affect the bottom line and speed at which new drugs reach clinical evaluation.
Some might ask about the practicality of using such a refined intermediate over simpler, lower-cost options. From our experience, the biggest point of differentiation comes from reliability and downstream reactivity.
Other esters, such as methyl ors, bring the risk of untimely hydrolysis during standard organic work-ups. The byproducts can be tricky to remove, especially after several synthetic cycles. The tert-butyl ester persists safely through conditions that challenge less robust alternatives, often making a difference in scaled or automated processes. For brominated benzoic acids without the tert-butyl group, handling characteristics change dramatically. They tend toward unwanted polymerization or decomposition, especially under warehouse storage conditions with fluctuating humidity or exposure to light.
Product consistency also separates our material from samples sourced through trade intermediaries or smaller resellers. Trace metal content from non-dedicated glassware or poorly controlled bromine additions can derail even simple arylation reactions, adding unpredictable costs to synthesis development efforts. Our operation isolates raw material handling, bromination, and esterification in modular suites, ensuring each batch matches documentation every time. In-house analytics means we don’t wait for third-party verification, cutting delays and boosting reliability for our pharmaceutical and materials science clients.
We operate from a philosophy rooted in direct responsibility, built up through years of both successes and troubleshooting. Overseeing the whole value chain lets us respond quickly when specifications shift or clients provide feedback. In contrast to traders or distributors, our manufacturing engineers and process chemists share a common set of goals: optimize yields, reduce cycle times, protect operator safety, and maintain the rigorous documentation demanded by global regulatory bodies.
We routinely re-invest in plant improvements, rather than waiting for outside guidance. If a customer begins seeing higher trace halogen content, we tweak our washing protocols and improve filter design, not just audit paperwork. During scale-up, the impact of each operator’s judgment call becomes even clearer. Every time we introduce a new piece of analytical equipment — be it for chromatography, mass spectrometry, or melting point assessment — it is not just for show. That added transparency pays off during audits by giving a clear, traceable path from raw material to final shipment.
Over our decades making substituted aromatic esters, we have watched research cycles shorten and product lifecycles speed up. Analytical breakthroughs mean it’s no longer enough to deliver something “close enough.” Clients want detailed spectra, impurity profiling, storage condition studies, and shelf-life data. We redesign packaging, re-test dated lots, and gather long-term stability data in tandem with customers. This kind of operational partnership goes beyond simple supply — it creates a feedback loop that drives real innovation.
Feedback gleaned from formulation teams using our ester in polymer scaffolds helps us tune particle size, flow properties, and free acid content. Each incremental improvement, grounded in feedback from practical use rather than theoretical conversation, strengthens the supply chain. Since our team controls both the chemistry and logistics, we address bottlenecks rapidly, whether they appear in shipping times or process modifications needed after new environmental regulations are put in place.
Anyone working hands-on with bromo compounds recognizes the need for robust process hazard analysis. Laboratory protocols rarely scale up seamlessly. We’ve seen how a small spike in reaction temperature or uneven bromine feed can escalate risk in untrained hands. The in-house safety team collaborates with process engineers to lay down containment boundaries, improve PPE protocols, and build custom venting for bromine handling. Only this degree of control ensures every batch leaving our facility meets both customer specification and workplace safety standards.
Waste management, especially for organobromine byproducts, gets thorough scrutiny. Our plant separates streams for halogenated and non-halogenated wastes, tracks each drum using digital logs, and works with regulated disposal partners. This reduces both legal risk and environmental impact, something we take seriously throughout every campaign. Regular plant audits and continuous staff training form a feedback loop — safety never takes a back seat to productivity.
With stricter regulatory frameworks emerging worldwide, fine chemical producers must ditch outdated methods that generate excess waste or rely on hazardous solvents. Our shift toward greener synthesis of 4-(Bromomethyl)-Benzoic Acid, 1,1-Dimethylethyl Ester reflects a commitment to long-term sustainability. Replacing older halogenation protocols with more selective reagents, stepping up solvent recovery, and integrating real-time monitoring have made a visible difference in process efficiency. The project took months to pay off but resulted in less waste and more predictable batch quality.
Regular engagement with academic researchers, sometimes through material donation or collaborative studies, keeps our R&D pipeline fresh. By understanding which structural features accelerate target compound assembly, we streamline our production without excessive yield sacrifice. From switchovers that minimize downtime to reusing mother liquor, each adjustment means less landfill volume and more consistent output for our clients.
Every batch run, analytic test, and customer feedback session provides actionable insight. By collecting and sharing detailed production logs, we build a bank of process knowledge. This helps reduce the learning curve for new technicians and gives the technical director data-driven arguments for the next investment.
Improved crystallization techniques sprang from a late-night QA session where a new impurity popped up in a kilogram-lot shipment. We gathered the team, compared historical process logs, and tracked the deviation to a slight change in cooling rate during precipitation. Correcting course cut the out-of-spec rate in half for the next month of production. These lessons learned — unglamorous but real — form the culture that’s required for chemical manufacturing in an era of growing regulation and customer scrutiny.
In the field of advanced aromatic esters, manufacturers face regular challenges in both raw material selection and finished product distribution. We source key inputs directly from traceable, vetted suppliers — not just the lowest bidders. Controlling each handoff from synthesis through packaging means a customer knows what they receive at every step. This contrasts sharply with traders patching together mixed-provenance lots with uncertain quality or delivery records.
For clients under GMP or ISO compliance, our transparent recordkeeping matters. Audit trails include batch numbers, handling logs, and condition ranges for every step. We also maintain historical control samples for comparison. These details matter most when customers pursue new product submissions or face regulatory site visits, creating a foundation of trust that supports productive long-term partnerships.
The growing complexity of medicinal chemistry, polymer science, and diagnostics keeps pushing the threshold for performance and quality. By continually refining our workflows and production controls, our team supports scientists as they expand the boundaries of what’s possible. Whether it’s adapting for new catalytic methods, offering custom impurity profiling, or taking on large-scale campaigns, we treat every project as an opportunity to raise the bar.
New opportunities arrive as clients expand into conjugated systems, specialty polymers, or patent-protected intermediates. Our readiness to customize both the purification approach and the packaging format allows us to support unique workflow needs — think high-throughput small-scale GMP runs or multi-tonne industrial campaigns. The lessons we gain from these collaborations feed back into technical upgrades on our own lines, ensuring we stay aligned with a rapidly changing industry landscape.
As manufacturers, we put faces and hands behind each shipment. Our technical team understands the subtleties of scale, the difference between a lab win and a full-plant success, and the need to keep learning from daily operations. Through decades of process improvements and near misses, our team has come to see that consistently high-quality 4-(Bromomethyl)-Benzoic Acid, 1,1-Dimethylethyl Ester can play a surprising number of roles in building value for customers. From stabilizing peptide linkers to launching new aryl modification protocols, it has become a staple for teams needing stable, reactive intermediates that measure up batch after batch.
The path from raw material to finished compound travels through precise chemistry, rigorous safety routines, and open communication up and down the supply chain. Whether shipped in small research bottles or large-scale drums, each package reflects the real-world experience of those who make it — from the engineer calibrating reactors to the chemist double-checking spectral purity. Meeting these challenges head on, learning from every run, and rapidly adapting to both client needs and industry changes allows us to keep supporting scientific and commercial progress, one molecule at a time.