Products

Tert-Butyl Bromoacetate

    • Product Name: Tert-Butyl Bromoacetate
    • Alias: BrCH2CO2C(CH3)3
    • Einecs: 'EINECS 252-549-7'
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    206795

    Chemical Name Tert-Butyl Bromoacetate
    Molecular Formula C6H11BrO2
    Molar Mass 195.05 g/mol
    Cas Number 5292-43-3
    Appearance Colorless to pale yellow liquid
    Boiling Point 75-77 °C at 14 mmHg
    Density 1.29 g/mL at 25 °C
    Refractive Index 1.426-1.429
    Flash Point 74 °C (closed cup)
    Solubility In Water Insoluble

    As an accredited Tert-Butyl Bromoacetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 250g Tert-Butyl Bromoacetate is packaged in a white, sealed HDPE bottle with a red screw cap and hazard labels.
    Shipping Tert-Butyl Bromoacetate should be shipped in tightly sealed containers, away from heat, moisture, and incompatible substances. Use appropriate packaging materials to prevent leakage. It should be labeled as a hazardous material and transported in compliance with local, national, and international regulations for flammable and potentially harmful chemicals. Handle with care.
    Storage Tert-Butyl Bromoacetate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it separate from incompatible substances like strong oxidizers and bases. Store at room temperature, and avoid exposure to moisture, as it may hydrolyze. Always follow appropriate chemical safety protocols and use suitable labeling.
    Application of Tert-Butyl Bromoacetate

    Applications of Tert-Butyl Bromoacetate in Industrial Manufacturing

    As a direct producer of Tert-Butyl Bromoacetate, we support industrial partners with consistent quality and reliable supply for advanced synthesis processes across specialized chemical sectors. The following sections detail key downstream application domains, informed by real-world formulations and manufacturing methods adopted by leading industry actors, with attention to regulatory alignment, process integration, and specification requirements.

    1. Pharmaceutical API Synthesis

    Large-scale pharmaceutical production regularly deploys Tert-Butyl Bromoacetate as a strategic building block in the preparation of complex molecules, especially for products requiring tert-butyl ester protected intermediates. Its selective alkylating properties support the stepwise synthesis of β-amino acids, ACE inhibitors, and peptidomimetic drugs. The compound typically participates in nucleophilic substitution and esterification reactions central to multi-stage GMP processes, while strict adherence to pharmacopeial standards governs both precursor use and in-process residue limits. Production sites frequently adjust input ratio margins per reaction scale, with stringent in-process monitoring to comply with international regulatory protocols.

    Industry compliance standards

    • ICH Q7A (Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients)
    • USP/NF and Ph.Eur. for input and residual solvent levels
    • EU Regulation (EC) No 1907/2006 (REACH)
    • 21 CFR Part 211 (US cGMP for Finished Pharmaceuticals)

    Typical usage ratio

    • Typically 1.0–1.3 molar equivalents relative to nucleophilic substrates; calculated based on the exact stoichiometry of the target intermediate; adjusted to minimize impurities in multi-step workflows

    Downstream process integration

    • Introduced during protection and alkylation stages in multi-step synthetic routes within GMP-compliant reactor trains
    • Residual removal through controlled aqueous workup or chromatography post-reaction

    Final product types

    • Intermediate esters en route to active pharmaceutical ingredients (APIs)
    • β-Amino acid derivatives for peptide APIs
    • ACE inhibitor precursors (e.g., Enalapril intermediates)
    • Protected glycine derivatives for further deprotection and functionalization

    2. Agrochemical Intermediates Manufacture

    In agricultural chemical production, Tert-Butyl Bromoacetate serves as a critical intermediate for the synthesis of selective herbicides and fungicides, enabling controlled esterification and introduction of tert-butyl groups that improve compound stability. Typical formulation procedures use the compound in alkylating reactions with active methylene or amine-containing substrates. The material’s integration directly influences downstream conversion yields and product performance, subject to tight control under international agrochemical residue and registration standards.

    Industry compliance standards

    • FAO/WHO JMPR (Joint Meeting on Pesticide Residues) technical specifications
    • OECD Good Laboratory Practice (GLP)
    • China GB 2763—Maximum Residue Limits for Pesticides
    • EU Regulation (EC) No 1107/2009 on plant protection products

    Typical usage ratio

    • Utilized at 0.8–1.5 molar equivalents, based on the reactivity of coupling partners and target selectivity; higher ratios for pilot synthesis, optimized lower ranges for scaled batch production

    Downstream process integration

    • Enters at initial alkylation stage in batch or continuous flow synthesis lines for agrochemical intermediates
    • Followed by hydrolysis, purification, or condensation steps depending on desired end molecule

    Final product types

    • Pyridine-based herbicide precursors
    • Fungicide intermediate esters
    • Active ester building blocks for crop protection chemical production

    3. Peptide and Amino Acid Derivative Production

    Biotech and pharmaceutical manufacturing sectors use Tert-Butyl Bromoacetate extensively for preparing orthogonally protected amino acid derivatives vital for solid-phase and solution-phase peptide synthesis. The tert-butyl group provides reversible protection for carboxylic acid functions, permitting precise chain elongation and subsequent selective deprotection. Input ratios, process temperature, and solvent conditions directly affect final yield and purity, required to satisfy international peptide manufacturing protocols and high-purity grade specifications.

    Industry compliance standards

    • ICH Q11: Development and Manufacture of Drug Substances
    • USP General Chapter <1047>, Peptide Synthesis
    • ISO 9001:2015 for quality management of chemical raw materials
    • EP monographs for protected amino acids

    Typical usage ratio

    • Applied at 1.1–1.2 equivalents versus amino acid substrates; excess minimized to simplify downstream purification

    Downstream process integration

    • Used during protection stages to form tert-butyl esters of amino acids prior to peptide coupling
    • Product transferred to solid-phase synthesis or solution-phase condensation steps

    Final product types

    • Orthogonally protected peptide building blocks
    • Custom N-protected amino acid derivatives for R&D and commercial peptide APIs
    • Functionalized intermediates for bioconjugation reagents

    4. Fine Chemical Synthesis for Specialty Materials

    Manufacturers in the fine chemicals sector depend on Tert-Butyl Bromoacetate to introduce bromoacetyl or tert-butyl ester functionalities in high-purity specialty compounds. The material plays a pivotal role in the synthesis of custom esters, chiral auxiliaries, and performance materials for electronic or coating applications, supporting controlled modifications within rigorously documented batch operations. Batch formulas and handling protocols obey prevailing safety and quality control systems established by sector-specific regulatory frameworks.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems)
    • REACH Annex XVII for hazardous substances use in manufacturing
    • Responsible Care® chemical management
    • Internal SOPs for specialty material synthesis in compliance with customer NDA/QC requirements

    Typical usage ratio

    • Typically 1.0–1.5 equivalents, dependent on the extent of functionalization and target material batch size; process yield and product specs determine exact input level

    Downstream process integration

    • Introduced at targeted functionalization step for chiral auxiliary or ester moiety installation
    • Integrated with solvent selection and purification protocols set by end-use application requirements

    Final product types

    • Specialty organic building blocks for electronic chemicals
    • Performance materials for functional coatings
    • Chiral auxiliaries for asymmetric synthesis

    5. Custom Synthesis and CRO/CMO Route Development

    Contract research and manufacturing organizations (CROs/CMOs) working on route scouting and non-GMP advanced intermediates include Tert-Butyl Bromoacetate in exploratory process development for new molecular entities and scale-up feasibility studies. Its reliable reactivity profile enables rapid structure-activity relationship screening across projects governed by client-specific quality protocols and early phase chemical registration requirements. Each route development project determines precise input ratios based on analytical follow-up and yield optimization.

    Industry compliance standards

    • ISO 9001:2015 for contract synthesis activities
    • OECD GLP (where analytical data used in regulatory submissions)
    • Non-GMP R&D batch documentation according to ICH Q7 reference
    • Confidentiality and intellectual property standards per client agreements

    Typical usage ratio

    • Input ratios range from 0.9–2.0 equivalents depending on target molecule, research batch size, and structure complexity; finalized via in-process data review

    Downstream process integration

    • Applicable to initial alkylation, protection, or acylation reactions during route validation
    • Laboratory and pilot-scale batch processes monitored for yield and impurity tracking using standard QC/analytical methods

    Final product types

    • Custom advanced intermediates
    • Protected acid or ester derivatives for further modification
    • Research chemicals for pharmaceutical pipeline and fine chemical evaluation
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    Certification & Compliance
    More Introduction

    Tert-Butyl Bromoacetate: Manufacturer’s Perspective on Reliable Building Blocks for Chemical Synthesis

    During years in the plant, chemists and production engineers gain respect for reagents that deliver consistent results batch after batch. Tert-butyl bromoacetate has earned its place among these reliable workhorses, and as a manufacturer, we give careful attention to every stage of its journey — from raw material sourcing, through synthesis, to packaging and storage, aiming to meet the exacting needs of researchers and industrial clients alike.

    Product Fundamentals and Specifications

    Our facility produces tert-butyl bromoacetate to meet high purity requirements. The chemical formula, C6H11BrO2, puts it in the haloacetate ester category, where its tert-butyl ester group lends important stability advantages. In practical terms, we consistently reach assay levels above 98%, sometimes pushing even higher depending on lot and client parameters. Clear, colorless liquid is the physical form our clients most often request, often meeting the expected boiling point near 60–65°C at reduced pressure. The product ships without significant water content — moisture management is no small matter with halogenated esters, and the team in charge of storage works hard to limit possible hydrolysis or side reactions.

    Rigorous batch testing isn’t an afterthought in our production. Each container gets a specific lot number that can be traced straight back to the reaction vessel, the raw bromoacetic acid, the alcohol quality, and critical timepoints such as workup and distillation. Common GC and NMR spectra are taken to track side impurities, since common threats include di-tert-butyl ether and tert-butyl alcohol residues. Titration for acid value or halide content tells us immediately if deviating process pressure or temperature has impacted outcome. At scale, those small differences matter. End users — peptide chemists, small molecule researchers, and pharmaceutical API groups — often call to discuss how these analytical data points affect their results or overall yields.

    Why Tert-Butyl Bromoacetate Plays a Central Role in Synthesis

    Sitting in the heart of synthetic planning, tert-butyl bromoacetate enables attachments of protected acetic acid groups. The tert-butyl group stands out for offering a balance: it shields the acid during challenging transformations, then departs under mild acidic or tBu-specific conditions without damaging other functional groups. In peptide synthesis, this is crucial. For example, our partners in medicinal chemistry often protect glycine residues or serve as a key intermediate toward N-protected amino acids. Drug candidates that include piperazine, indole, or pyrrole skeletons see improved overall yields or simple workup when tert-butyl bromoacetate is the alkylating agent. The bromo substituent brings increased reactivity compared to chloro analogues, yet does not exhibit the volatility or high toxicity profile often encountered when using iodoacetic esters. Years of cumulative conversions bear out that tradeoff. End users frequently mention decreased side product formation, improved scalability, and cleaner resins for solid-phase protocols after switching to tert-butyl bromoacetate as the building block.

    Unlike methyl or ethyl bromoacetate, the tert-butyl variant’s unique steric profile influences selectivity in certain alkylations and minimizes unwanted overreactions. In our feedback records, industry clients note significant reductions in byproduct formation during O-alkylation, especially when working with polyhydroxyl or polyamine scaffolds. The bulky ester makes tert-butyl a go-to choice for applications that demand selectivity and planned deprotection. Skilled academic chemists and process developers continually push the boundaries of this reactivity, reporting new methods that expand on the foundation built by this stable but reactive molecule.

    Handling Practicalities That Affect Reliability

    Through countless production campaigns, a handful of supply chain points have taught us that small details drive reliability downstream. With tert-butyl bromoacetate, iodine-catalyzed side reactions must be watched for, so we source bromoacetic acid with strict rejection thresholds for residual halogens. Bath temperature control during esterification changes how much tert-butanol residue remains, which then impacts crystallinity if the reagent is concentrated for storage. Material exposed to light or high humidity can form HBr, leading to acidification; our operations crew stores product in light-blocked, inert-lined containers. Every so often, a client requests drum packaging rather than glass because of regulatory or transport needs, and we work to pre-vent polymer-plastic interactions that risk peroxide formation. Operating at scale uncovers a surprising range of challenges — small leaks, line residues, or cleaning solvents can alter product behavior, especially as production campaign sizes reach hundreds or thousands of kilograms. Our engineers revise piping, test sealants, and provide relevant data to clients who must meet Good Manufacturing Practice.

    Throughout these steps, consistent feedback loops emerge. Academic groups with highly sensitive reactions tell us about impurity profiles never flagged on routine screening. Pharmaceutical pilot plants need stability studies extending over quarters, requiring us to test more than standard shelf-life. If specifications slip, we adjust — tightening reaction monitoring, optimizing distillation, and revising what is shipped. Trust is earned by facing these variables straight on, not by reading off certificates every batch. Engineers and chemists in the field often require real-time problem solving rather than off-the-shelf answers, especially as new projects build on familiar chemistry but in much more complex development programs.

    What Differentiates Tert-Butyl Bromoacetate from Similar Esters

    The tert-butyl ester stands apart from conventional methyl or ethyl bromoacetates in several tangible ways. Reaction pathways involving tert-butyl bromoacetate often reach higher overall yields because its larger group resists unwanted nucleophilic attacks. Traditional methyl and ethyl bromoacetates may react too readily, especially with strong nucleophiles, sometimes triggering overalkylation or rearrangement. For example, we observed in pilot runs that competing S-alkylation with sulfur-bearing amino acids proceeds much more controllably with tert-butyl than methyl. The resulting selectivity benefits flow directly into reaction workup and downstream purification, particularly in API synthesis for pharmaceutical clients who rely on high standards for both product purity and environmental performance.

    The tert-butyl group also brings deprotection advantages. Unlike methyl or ethyl esters, which require more forcing conditions to cleave, tert-butyl esters respond rapidly to mild, non-aqueous acid. This means expensive or sensitive intermediates survive longer, avoiding decomposition — a feature that underpins modern solid-phase and solution-phase peptide synthesis. The difference is not academic: real manufacturing cost savings and improved safety margins mount over hundreds or thousands of reactions. Those performing scale-up from lab to multi-ton volume quickly appreciate how handling, storage, and regulatory reporting all shift with a product less prone to accidental release or instability.

    Through several decades of fielded experience, we have also learned not to underestimate logistics. Unlike iodo- or fluoroacetates, bromoacetates present lower regulatory hurdles while maintaining effective reactivity. Our tert-butyl bromoacetate passes customs more smoothly, can be handled under broader guidelines in many regions, and end users report smoother workflows compared to working with lower-boiling alternatives like methyl bromoacetate. Every shipment reflects years of cumulative lessons — by collaborating with freight partners, monitoring route-specific temperature/humidity trends, and auditing the physical containers in which product is shipped.

    Applications: Scope and Breadth Across Industries

    Researchers in universities and industry apply tert-butyl bromoacetate as an alkylating agent in several contexts. In the pharmaceutical sector, it helps synthesize amino acid derivatives where label-free analytical tracking is essential — the tert-butyl group delivers clean mass spectrometric signals and can be removed gently, which helps reduce artifacts in final analysis. Fine chemical makers rely on its reactivity in preparing intermediates for agrochemicals, such as protected carboxylic acids and extended chain esters used in crop protection. Notably, resin manufacturers shifting to newer photopolymerizable materials cite tert-butyl bromoacetate as a preferred tool for capping agents, yielding improved batch consistency and shelf stability.

    The difference is more than theoretical. Contract manufacturing groups, especially those working with short timelines and broad portfolios, count on tert-butyl bromoacetate for rapid scale transitions. One week, an academic team may need a kilo for a new probe molecule; the next, a custom synthesis shop requests tonnage for an FDA-registered process. We maintain living logs of these requests, gathering technical notes from both successful and challenging projects. This collective experience means our production foremen draw on real data — which process variables matter for low vs high scale, which impurity signals flag an emerging problem, and which reaction quenching techniques avoid unnecessary side reactions. Through these touchpoints, new users can tap into a network of practical knowledge, reducing costly repetition of past mistakes.

    Safety and Environmental Realities

    Handling tert-butyl bromoacetate demands respect; as a manufacturer, our safety protocols go deep. Bromoacetates can cause irritation and toxicity if improperly managed. Worker training at our site centers on PPE, ventilation, spill response, and scrubbing systems for neutralizing off-gassed HBr. Every storage area gets regular audits for leakage, since even small losses can add risk and regulatory reporting obligations. Years of incident records confirm that most safety deviations stem from container damage, quick temperature spikes, or lack of training for new operators. To minimize these risks, production management routinely upgrades filling lines, reviews incident patterns, and adjusts SOPs based on both internal and global industry data.

    Environmental controls drive a large part of our process design. Waste streams containing organobromine require careful neutralization; local environmental statutes do not permit dumping effluent or spent solvents with halide content above strict thresholds. We reclaim or destroy spent processing material by conversion to less hazardous forms, balancing both legal obligations and standards our clients expect. In-house R&D evaluates new reagents every year, seeking greener alternatives or lower-load protocols for long-term sustainability. Open communication with end users helps uncover new challenges — whether it’s a change in regional effluent standards, an unexpected persistence of bromide residue, or opportunities to recycle byproducts into secondary products. These efforts may not draw the brightest headlines, but they produce real, traceable improvements over time.

    Ongoing Dialogue with End Users

    In the manufacture and commercial supply of tert-butyl bromoacetate, insight rarely comes from written datasheets alone. Continuous two-way communication underpins real improvement. Technical specialists trading details of their reaction plans or impurity concerns lay out problems that standard product literature never anticipates. For example, a large client flagged minor elevated chloride levels from inlet water variation; another found that subtle changes in storage temperature affected color and stability in final dosed containers. Each of these lessons drives tighter process discipline and new testing standards on our side of the operation.

    Market shifts sometimes push synthetic planning in unexpected directions. A surge in demand for pet care pharmaceuticals, driven by new treatments containing amino acid-linked intermediates, led to sudden increases in large-scale tert-butyl bromoacetate requests. Smaller research teams often need very short turnarounds at pilot scale, accompanied by extra analytical data or small-batch stability notes that the larger contract manufacturers may not prioritize. In response, we implemented lot-specific quality notes, expanding on industry standards and collaborating directly with scientists to troubleshoot unusual product behaviors. For instance, late stage filtration or distillation tweaks sometimes make all the difference for a chromatography-dependent protocol — we feed these success stories back into our process improvement cycle, leading to new standard operating procedures.

    This ongoing dialogue enables more than incremental improvements. End users innovating with previously unreported reaction schemes feed findings directly to our R&D; in turn, we modify test protocols or trial packaging runs to see if wider benefit arises. Occasionally, new regulatory limits or changes in raw material sourcing alter the risk profile for a class of downstream reactions, prompting holistic reevaluation of our approach. Through it all, direct feedback — positive or negative — reinforces the connection between manufacturer and chemical end user. By investing in these relationships, we ensure the reliability, consistency, and quality that providers of tert-butyl bromoacetate need to solve real-world chemical challenges.

    Solutions to Common Challenges

    Bottlenecks do arise throughout the journey from raw material to laboratory or production floor, but each challenge met adds another layer of institutional knowledge the next batch benefits from. For moisture-sensitive applications, some clients request custom drying protocols and packaging under inert gas. We track data on reaction reproducibility, identifying seasonal or supplier-linked patterns that point to solutions — such as adjusting storage temperature or moving to lined drums for extended international transit. Where supply chain interruptions threaten continuity, our procurement teams hold multi-vendor agreements and backup inventory, all with traceable lot integrity so performance on the client side does not slip. Environmental and safety incidents are addressed not only by compliance, but by investment in training and equipment that barely existed in the industry a decade ago.

    Contamination worries, a common theme in production chemistry, drive daily action. Whether a batch arises from common glass-lined reactors or stainless facilities, we maintain cleaning schedules with full documentation, validating every new method first at pilot, then at manufacturing scale. In a competitive field, cutting corners on contamination control or traceability may look attractive in the short term, but real-world consequences often cost more in recalls, regulatory audits, or trust lost in the market than any saving justifies.

    The Manufacturer’s Commitment

    Tert-butyl bromoacetate, in the hands of experienced manufacturers and end users, acts as more than a chemical intermediate. Every batch reflects the collective experience of teams dedicated to delivering quality, transparency, and continuous learning. From initial synthesis route selection to responsible after-market feedback collection, we believe the best outcomes grow from honest assessment, adaptability, and respect for the users who turn these building blocks into finished science and life-saving products. This direct commitment to quality and communication ensures not just product reliability, but ongoing technical progress across the industries tert-butyl bromoacetate serves.

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