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Tert-Butyl N-(2-Bromoethyl)Carbamate

    • Product Name Tert-Butyl N-(2-Bromoethyl)Carbamate
    • Alias Boc-2-bromoethylamine
    • Einecs 698-939-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    466142

    Chemical Name Tert-Butyl N-(2-Bromoethyl)Carbamate
    Synonyms Boc-2-bromoethylamine
    Molecular Formula C7H14BrNO2
    Molecular Weight 224.10 g/mol
    Cas Number 75629-57-1
    Appearance Colorless to pale yellow liquid
    Boiling Point 87°C at 2 mmHg
    Density 1.239 g/cm3
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles CC(C)(C)OC(=O)NCCBr

    As an accredited Tert-Butyl N-(2-Bromoethyl)Carbamate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of Tert-Butyl N-(2-Bromoethyl)carbamate, sealed with a PTFE-lined screw cap, labeled with safety information.
    Shipping Tert-Butyl N-(2-Bromoethyl)carbamate is shipped in tightly sealed containers to prevent moisture and contamination. It should be stored and transported at room temperature, away from sources of heat and light. Proper labeling and documentation are required, and the package must comply with all relevant chemical transport and hazardous material regulations.
    Storage Tert-Butyl N-(2-Bromoethyl)carbamate should be stored in a tightly sealed container, protected from moisture and direct sunlight. Keep it in a cool, dry, and well-ventilated area, preferably at 2–8 °C (refrigerated). Store away from incompatible materials such as strong acids, bases, and oxidizing agents. Ensure proper labeling and restrict access to authorized personnel only.
    Application of Tert-Butyl N-(2-Bromoethyl)Carbamate

    Applications of Tert-Butyl N-(2-Bromoethyl)Carbamate in Industrial Manufacturing

    As a direct manufacturer of Tert-Butyl N-(2-Bromoethyl)Carbamate, we supply this intermediate for use in advanced downstream processes across highly specialized chemical sectors. The applications below reflect its authentic industrial utility in regulated and technically demanding manufacturing environments.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Low-impurity Tert-Butyl N-(2-Bromoethyl)Carbamate performs a critical role as an alkylating intermediate in the multistep synthesis of select APIs, including β-lactam structure modifications for targeted oncology and neurological compounds. Manufacturers use this compound during the N-protection and bromoethylation steps, precisely controlling its addition to minimize byproducts and maximize yield uniformity batch after batch.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for API
    • USP/NF & European Pharmacopoeia monographs for intermediates and APIs
    • 21 CFR Part 210/211 (US FDA)
    • EDQM CEP procedures for intermediate sourcing traceability

    Typical usage ratio

    • Added at 1.2:1 to 2:1 molar ratio relative to core amine substrate, adjusted based on target conversion rate and impurity profile requirements

    Downstream process integration

    • Integrated at the protected amination or N-alkylation stage during API intermediate synthesis
    • Purification typically follows via chromatography or solvent extraction before final deprotection and crystallization

    Final product types

    • Protected amine-based pharmaceutical actives
    • Oncology and CNS drug intermediates
    • Generic and custom-synthesized APIs prepared for regulatory registration

    2. Peptide Synthesis and Modification

    Protections like tert-butyl carbamates are essential in solid-phase and solution-phase peptide manufacturing. Manufacturers employ Tert-Butyl N-(2-Bromoethyl)Carbamate as a selective N-terminal protection and functional linker for introducing bromoethyl moieties, which enables subsequent site-specific conjugation reactions with biologics or diagnostic labels.

    Industry compliance standards

    • EU GMP Annex 1 and 2 for peptide synthesis
    • ISO 13485 for peptide-based medical diagnostics
    • USP Peptide monographs (Section Peptides and Polypeptides)
    • FDA Part 211 for bulk drug peptide substances

    Typical usage ratio

    • Standard loading of 0.8–1.5 molar equivalents per amino acid residue, adjusted for resin substitution and sequence hydrophobicity

    Downstream process integration

    • Loaded onto protected amino acid serine during initial peptide chain assembly
    • Deprotection and bromoethyl functional group exposure occur after target chain completion, prior to payload conjugation or cyclization

    Final product types

    • Custom therapeutic peptides
    • Peptidomimetic drug candidates
    • Diagnostic peptide conjugates for immunoassays

    3. Agrochemical Intermediate Platforms

    The carbamate group, featuring a bromoethyl functionality, makes this material a vital intermediate for agrochemical manufacturers developing new-generation active compounds such as insect growth regulators and herbicide precursors. Process designers use the bromoethyl substitution pattern to achieve specific bioactivity and selective crop safety by incorporating it during the penultimate synthetic conversion, ensuring traceable impurity profiles for strict environmental registrations.

    Industry compliance standards

    • ISO 9001:2015 for agrochemical manufacturing quality management
    • FAO/WHO Maximum Residue Limit (MRL) assessment for international registration
    • REACH (EC 1907/2006) chemical safety, exposure, and traceability control
    • China National Standard GB 2763 for pesticide residue limits

    Typical usage ratio

    • Applied at 0.75–1.5 equivalents versus key heteroaromatic starting material, adjusted based on targeted conversion rates and desired byproduct control

    Downstream process integration

    • Introduced during final alkylation prior to purification and crystallization of the active agrochemical base
    • Impurity purging via aqueous workup and vacuum stripping to maintain registration grade

    Final product types

    • Insect growth regulators with advanced crop selectivity
    • Precursor molecules for broad-spectrum herbicide synthesis
    • Specialty crop protection active ingredients

    4. Specialty Monomer and Polymer Modifier Synthesis

    Specialty polymer manufacturers use Tert-Butyl N-(2-Bromoethyl)Carbamate to introduce protected amine functional groups for chain extension and crosslinking in advanced performance polymers. Its bromoethyl motif enables precise nucleophilic substitution, supporting elastomeric modification and block copolymer upgrades for applications demanding high-performance materials in electronics or specialty coatings.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemicals
    • RoHS 2011/65/EU and REACH SVHC screening for electronic and coating components
    • ASTM D4066 for polyamide and specialty polymer modifiers
    • UL 94 flame rating certification for electronics polymers

    Typical usage ratio

    • Used at 0.5–2.0% by weight of the total monomer feedstock, depending on the required density of functional groups and compatibility with the host polymer

    Downstream process integration

    • Dosed during pre-polymerization or as a post-polymer modification agent in solvent or melt-phase processes
    • Functional group deprotection and crosslinking occur in situ during thermal curing or chemical activation

    Final product types

    • Custom elastomers for electrical insulation
    • Functionalized block copolymers for adhesives or coatings
    • Polyamide and polyimide intermediates for high-temperature engineering plastics

    5. Fine Chemical and Intermediate Custom Synthesis

    Contract manufacturers and in-house fine chemical teams leverage the reactive bromoethyl-carbamate group for constructing building blocks in advanced intermediate routes, particularly for lab-scale or low-volume specialty molecules. Its selective reactivity profile enables stepwise elaboration of highly functionalized intermediates for further custom modification, reducing the need for protective group interchange and minimizing side-product formation.

    Industry compliance standards

    • ISO 9001:2015 for fine chemical production
    • Custom client QMS/QC protocols for intermediate validation
    • REACH compliance for transport, labeling, and safety documentation
    • GHS/OSHA Hazard Communication for workplace safety

    Typical usage ratio

    • 1.0–1.3 molar equivalents relative to target nucleophile, optimized on pilot scale for maximum intermediate yield and process economy

    Downstream process integration

    • Introduced as an alkylating agent in the core synthetic stage, with isolation of the protected intermediate ahead of downstream elaboration
    • Solvent-based process designed for rapid workup and filtration of byproducts

    Final product types

    • Pharmaceutical building blocks and advanced intermediates
    • Functional reagents for specialty laboratory syntheses
    • Custom intermediates for material science R&D
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    Certification & Compliance
    More Introduction

    Tert-Butyl N-(2-Bromoethyl)Carbamate: A Closer Look at a Core Organic Building Block

    Origin, Expertise, and Real-World Application

    Working on the manufacturing floor, it's easy to spot which reagents help chemists overcome bottlenecks in synthesis. Tert-Butyl N-(2-Bromoethyl)carbamate, often referred to by its chemists as Boc-2-bromoethylamine, belongs to that rare breed of products bridging research bench and industrial scale-up with the same reliability. Our team produces this compound for clients who demand consistent reactivity and precise batch-to-batch quality for scale-sensitive projects, whether developing bioactive pharmaceuticals, peptides, or specialty materials.

    Big projects in drug discovery rarely move in a straight line. When we produce Boc-2-bromoethylamine, we’re offering more than a chemical; we’re putting decades of hands-on synthesis and quality control into each bottle. Chemists need to know what they’re working with—the reactivity, the typical byproducts, and how it stands up to a little real-world adversity, such as humidity during handling or the need for high purity at every step. Through thousands of batches, meetings with process engineers, and listening to troubleshooting frustrations, we’ve tailored our workflow to put out product that stands up to that scrutiny.

    What Sets Tert-Butyl N-(2-Bromoethyl)Carbamate Apart

    Structurally, this compound carries a Boc-protected amine, making it a go-to intermediate for anyone developing amine-containing molecules without risking unwanted side reactions. The 2-bromoethyl group carries high reactivity for nucleophilic substitution. This difference makes it ideal when chemists want to install a protected ethylamine unit but need granular control over coupling points in complex synthetic sequences. We’ve seen this compound used in the functionalization of polymers, in preparing peptide side chains, and in building heterocyclic cores where other alkyl bromides simply do not deliver the selective activation or stability.

    On the production floor, purity targets matter. Persistent trace impurities—residual solvents, overalkylated species, or decomposed carbamates—are caught before product ever leaves our site. In our experience, working up to 99%+ purity with careful distillation and crystallization steps avoids problems down the road, whether the endpoint is a six-step peptide coupling or a single impactful alkylation.

    Balancing Reactivity, Selectivity, and Safety

    Boc-2-bromoethylamine’s popularity comes down to how controllably it reacts. In research labs, it takes only a small deviation in temperature or moisture to throw off the critical balance between reactivity and selectivity. Over the years, we have refined our packing and storage protocols. Our batches come stabilized against atmospheric moisture yet remain free-flowing and easily portioned in either small-scale or kilo quantities. Our QC technicians apply both HPLC and NMR screening for every lot, since overlooked degradation or overreaction during synthesis can cost weeks of effort for our customers.

    Sourcing directly from a manufacturer who deals with the full spectrum from laboratory synthesis to pilot plant scale means chemists get insight into the quirks of handling, storage, and scaling. We've seen labs frustrated by off-odors, slow dissolution, or surface discoloration from lesser-quality sources—issues that trace back to poor purification or rushed packaging. By working with our clients, we continuously re-evaluate process parameters, helping both them and our own team anticipate and avoid waste, contamination, and inconsistent reaction yields.

    Comparison: Going Beyond Generic Alkylation Reagents

    Feedback from both academic and industrial partners highlights the practical advantages over related alkylating agents. Unprotected 2-bromoethylamine, a similar molecule, offers little control: its unshielded amine can favor unwanted side-reactions, especially during sensitive coupling reactions where selectivity is at a premium. As a manufacturer, we regularly run comparative quality checks in our own pilot reactions—tracking yield, product profile, and presence of side-products. Boc-2-bromoethylamine stands out in these trials by allowing precise introduction of the protected amine with only minimal deprotection steps downstream.

    Compared to longer-chain bromoaminocarboxylates or unprotected bromoamines, our product minimizes product loss during purification and storage. Our technical team regularly receives requests for advice on solvent systems and recommended deprotection protocols; over several thousand pilot projects, the data continues to back up the robust, uncomplicated behavior of Boc-protected bromoethylamines.

    Integrating into Synthesis Pathways

    From a chemical engineering perspective, a reliable supply of Boc-2-bromoethylamine is the difference between scaling a process smoothly and running into headaches with failed reactions or inconsistent lots. Our batch records stretch back years. They track both subtle seasonal shifts and process tweaks, all supported by analytical archives so researchers can trace outcomes if new impurity peaks show up later in their synthetic sequence.

    Pharmaceutical synthesis benefits directly from this backbone. Medicinal chemists choose our batches for amine alkylation steps where regulatory filings demand records of origin and traceability. We collaborate with clients to optimize routes for new molecular entities, especially where introducing a protected ethylamine is required at late stages. The reactivity profile allows for controlled coupling, smooth purification, and seamless downstream deprotection, which is crucial in multi-step synthesis.

    Our clients often report successful use in early research, scale-up, and even pilot plant runs. The batch-to-batch consistency ensures reproducibility in both biological screening and final product release. We support these goals with COA documentation and retain samples for years, so each batch’s analytical fingerprints are accessible if legacy reruns or regulatory clarifications arise years after the original material has been through the lab.

    Real-World Challenges: From Concept to Commercial Product

    Scaling up the production of Boc-2-bromoethylamine doesn’t always go as planned in larger processes. The volatility of brominated intermediates presents unique challenges, such as controlling vapor loss and managing safety during distillation. Our team’s operational experience pays off in these areas—equipment selection, flow control, and in-line monitoring keep process deviations minimal. Any upstream irregularity can jeopardize an entire campaign, so we maintain direct oversight from raw material release through final packaging.

    Product purity and stability are not just lines on a specification sheet; they are the distilled result of hundreds of process optimizations, often made in response to a single out-of-spec batch. Our internal feedback loops—operator logs, shift reports, and end-user feedback—prevent issues from recurring on future runs. We’ve turned lessons learned in handling sensitive intermediates into updated SOPs and, if necessary, plant modifications. These experiences help avoid oversized process corrections—each change is driven by real statistical process data, not guesswork or vendor templates.

    Sustainability, Waste Minimization, and Compliance

    Sustainability is fundamental now more than ever. In our facilities, waste streams—both aqueous and organic—present the largest compliance risk for brominated intermediates. Our team takes responsibility for solvent selection, washout, and recovery to minimize the overall environmental impact. We don’t just follow regulations; we host in-house audits of emissions, capture, and process vent treatment and retrain our process team as part of an active improvement cycle.

    Regulatory compliance for brominated materials in pharmaceutical supply chains is complex. Our records don’t just check the boxes—each raw ingredient shipment, each blend, each release certificate is signed off by chemists and QA. Auditors walk our hallways, reviewing both the paper records and the physical material flow. Our goal has always been straightforward: chemists, not just paper-pushers, must stand behind every lot for its full lifecycle.

    Whenever a batch fails to meet internal acceptance criteria, it never leaves the plant. Downtime hurts, but a missed checkpoint is far more painful for those depending on our product. We keep full samples and analytical archives for years, and we remain accountable for each shipment.

    Quality Through Process Discipline

    Care in manufacturing begins long before the bottle lands in the researcher’s hand. We screen every incoming raw material, not simply by COA but by practical test runs in a scaled-down synthetic route. Only after passing stability and compatibility tests does a raw material go on to full-scale production. During synthesis, each step is monitored for conversion, side-reactions, and trace impurities—our in-process controls (IPCs) have evolved from years of hands-on experience and hard-won results, not from textbook protocols.

    Once the desired product dries and crystallizes, a dedicated QC team takes over. Analytical techniques such as HPLC, NMR, IR, and GC give us full coverage for both expected and emerging impurity profiles. We track not just the absolute purity, but solubility, morphology, and observed stability under common laboratory conditions.

    If process improvement is called for—perhaps due to a single subpar analytical result—a cross-functional group reviews not just the chemical operations, but also equipment performance and even batch documentation practices. No improvement holds unless it results in consistent, measurable gains on subsequent runs. Over time, this discipline reduces both batch variability and total waste, benefiting not just our customers, but the plant’s environmental footprint as well.

    Technical Support, Collaboration, and Shared Solutions

    Unlike intermediates that come from a faceless mass distributor, Boc-2-bromoethylamine has an entire support network behind it. Customers reach our technical staff directly—they speak with people who know how this material behaves in both the lab and full plant. These exchanges go beyond troubleshooting: together, we validate methods, refine work-ups, and share hyperspecific recommendations on solvent systems, deprotection timing, and handling nuances.

    In our experience, the best synthetic outcomes arise from open, ongoing technical dialog. When a process engineer calls with a sticky filtration or a new impurity band in the NMR, we don’t just send a replacement lot; we share our own bench data, typical product behaviors under variable humidity, and—if appropriate—updated workup advice. We try to treat collaborations as ongoing commitments, with personnel who follow up project by project, giving context to the lot history and application data.

    We get involved early when a new synthetic route is being developed. Often, our own chemists mimic initial steps at bench scale to anticipate and resolve process weaknesses before larger projects begin. Some of our longstanding partners have embedded our product advice into their own training protocols, feeding results and insights right back to our production and QA teams for continual refinement.

    Continuous Improvement and Foresight

    What started as small-scale support for academic research has now evolved into high-volume production for pharmaceutical and material science clients worldwide. With each shipment, we track post-delivery behavior: does the material store well through seasons, how does it handle in differing climates, does it dissolve cleanly under standard lab conditions? We keep feedback channels wide open, including direct shipment follow-up with users, to refine not just the product, but labeling, packaging, and logistical practices as supply chains evolve.

    Supply issues have become a recurring challenge for specialty reagents, especially for those that demand high purity and regulatory traceability. We hedge against this by retaining on-site stocks, qualifying alternate feedstocks, and keeping detailed analytics covering each batch, every supplier, and every process change. This foresight prevents shortages and keeps our chemists supplied through regulatory changes, regional disruptions, or unexpected surges in demand.

    Practical Impact of Specialist Chemical Manufacturing

    The difference between a laboratory chemical and a true industrial reagent comes down to long-term reliability. Generic products often show up with unreported byproducts, short shelf lives, or data sheets that don’t reflect the real on-the-bench experience. Working as a manufacturer, we've built in direct communication, quick reaction to deviations, and a persistent eye toward what actually helps chemists reach the next step in their work. This can’t be faked or templated—a robust, reliable, fit-for-scale reagent takes time, dedicated resources, and honest feedback.

    Through hard-won experience, technical dialog, and continuous process improvement, our team has shaped Boc-2-bromoethylamine into a tool that chemists actively choose, not settle for. Direct feedback from customers in medicinal chemistry, materials science, and polymer development keeps us pushing further—testing alternate packaging, analyzing new impurity trends, and working right next to those who use the product for ambitious new syntheses.

    This mutual development cycle shapes not just today's delivered batch, but the groundwork for tomorrow’s solutions. The dynamic, sometimes unpredictable world of organic synthesis keeps our plant moving, refining each detail so the next chemist receiving this product can focus not on a missed batch spec, but on pushing science forward.