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3-Bromo-2,2-Dimethyl-1-Propanol

    • Product Name 3-Bromo-2,2-Dimethyl-1-Propanol
    • Alias 3-Bromo-neopentyl alcohol
    • Einecs 250-457-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    778598

    Chemical Name 3-Bromo-2,2-Dimethyl-1-Propanol
    Cas Number 30120-57-1
    Molecular Formula C5H11BrO
    Molecular Weight 167.05
    Appearance Colorless to pale yellow liquid
    Boiling Point 73-76°C at 18 mmHg
    Density 1.300 g/mL at 25°C
    Melting Point -13°C
    Refractive Index 1.458-1.460
    Flash Point 93°C
    Solubility Soluble in water and organic solvents
    Purity Typically ≥ 98%
    Synonyms 1-Propanol, 3-bromo-2,2-dimethyl-
    Storage Conditions Store below 30°C, tightly closed

    As an accredited 3-Bromo-2,2-Dimethyl-1-Propanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a secure screw cap, labeled “3-Bromo-2,2-Dimethyl-1-Propanol,” includes hazard warnings.
    Shipping **Shipping Description:** 3-Bromo-2,2-Dimethyl-1-Propanol is shipped in tightly sealed containers, under cool, dry conditions. It is classified as a hazardous material and requires appropriate labeling and documentation. Handle with care, following all relevant regulations to ensure safety during transportation. Protect from heat, ignition sources, and avoid rough handling to prevent leaks or spills.
    Storage Store 3-Bromo-2,2-dimethyl-1-propanol in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, oxidizing agents, acids, and strong bases. Use appropriate personal protective equipment when handling. Clearly label the storage container and ensure compatibility with other stored chemicals to prevent hazardous reactions.
    Application of 3-Bromo-2,2-Dimethyl-1-Propanol

    Applications of 3-Bromo-2,2-Dimethyl-1-Propanol in Industrial Manufacturing

    3-Bromo-2,2-dimethyl-1-propanol serves as a specialized intermediate in several high-value chemical sectors. We manufacture this compound for downstream partners who require stringent consistency, purity, and tailored chemical profiles. Below, we outline the primary industrial application scenarios with detailed integration methods, compliance highlights, process roles, and finished product types.

    1. Pharmaceutical Intermediates for Active Ingredient Synthesis

    Many pharmaceutical manufacturers utilize this compound in the synthesis of APIs, particularly in the preparation of quaternary ammonium derivatives, antihistamines, and certain CNS agents. Customers adjust the use level according to the complexity of subsequent reactions and desired yield, often relying on this raw material for the introduction of bromoalkyl groups to complex molecules. Our technical teams support qualification runs and product audits, ensuring impurity profiles meet strict pharmacopeial requirements before scale-up.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide
    • United States Pharmacopeia (USP) General Chapter <823>
    • European Pharmacopoeia (Ph. Eur.) Residual Solvents Limits
    • FDA cGMP 21 CFR Parts 210/211

    Typical usage ratio

    • 0.2–0.5 molar equivalents versus key active precursor; labs scale up by stoichiometry and impurity allowance
    • Adjustments depend on protection/deprotection yields in multi-step syntheses

    Downstream process integration

    • Used as an alkylating or bromo-functionalizing agent following initial substrate protection
    • Reactant in the step prior to forming target API scaffold, handled in sealed reactors with in-line GC monitoring
    • Subject to full traceability through batch records and in-process QC testing

    Final product types

    • Prescription antihistamines with bromoalkyl side chains
    • Mood stabilizer API intermediates used in CNS medications
    • Veterinary injectable agents
    • Specialty hospital-use APIs

    2. Agrochemical Intermediate Manufacturing

    Major agrochemical groups specify this material for the synthesis of selective herbicide intermediates and insecticidal compounds. Its reactive bromine enables direct substitution onto aromatic systems and facilitates the creation of tailored alkylated side chains. Factories require batch certificates, impurity statements, and full trace documentation as these intermediates feed into regulated pesticidal actives.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications
    • REACH (EC) No 1907/2006 for substance registration
    • ISO 9001:2015 Quality Management
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • 0.8–1.2 molar equivalents against primary aromatic or heterocyclic substrate
    • Levels depend on process yield and target impurity profile for export registration

    Downstream process integration

    • Dosed as a feedstock for bromination and Grignard-type couplings
    • Added to anhydrous systems under nitrogen protection to avoid hydrolysis
    • All process steps monitored for by-product formation using HPLC

    Final product types

    • Precursor to sulfonylurea-based herbicides
    • Building block for pheromone-mimic insecticides
    • Active components in pre-emergent weed control agents
    • Intermediate for fungicide side-chain modification

    3. Specialty Polymer Modification Agents

    Research and commercial polymer producers use our material to introduce functional bromoalkyl groups into pre-polymers or polyols. These modifications enhance compatibility with flame retardant systems or improve crosslinking density in polyurethane foams. Customers select grades with specific impurity controls, aiming for precise molecular weight distribution and stability during curing. Laboratory support confirms reactivity profiles in pilot batches before full process adoption.

    Industry compliance standards

    • ISO 14001 Environmental Management for chemical plants
    • ASTM D4716 Polymer Modifiers Standards
    • GHS classification and labelling for transport and storage
    • RoHS compliance where electronic applications are concerned

    Typical usage ratio

    • 0.5–2.0 wt% of polyol blend for polyurethane; low addition for crosslink adjustments
    • Level tailored based on final mechanical and fire performance requirements

    Downstream process integration

    • Introduced post-polyol blending, just prior to catalyst addition in batch reactors
    • Dispensed via automated metering for reproducibility
    • In-line FTIR monitoring of crosslink progress

    Final product types

    • FR-rated flexible polyurethane foams
    • High-impact epoxy resin systems
    • Custom copolymer composites for engineering plastics
    • Adhesive and sealant modifying agents

    4. Fine Chemical Intermediates for Fragrance and Flavor Compounds

    Manufacturers in the fragrance and F&F additive sector apply this compound for constructing branched, functionally diverse molecules used in high-end essence formulations. The compound’s structure allows precise introduction of tertiary or quaternary carbon skeletons, which influence odor profile and volatility. Our production records track batch-to-batch consistency and meet customer audit demands for food-safety documentation. Pre-shipment, we provide impurity and residual solvent data to support downstream compliance filings.

    Industry compliance standards

    • IFRA (International Fragrance Association) Safety Standards
    • FCC Food Chemicals Codex purity requirements
    • ISO 9001 traceability for raw material sourcing
    • FDA 21 CFR 172.515 (Flavoring Substances)

    Typical usage ratio

    • Trace to 1.0 wt% of reaction mass for limited sequence synthesis
    • Adjusted according to the target aroma threshold and side chain introduction

    Downstream process integration

    • First introduced post-initial aldehyde condensation
    • Reacted under controlled temperature to minimize by-product esters
    • Intermediate captures verified by GC-MS prior to final hydrogenation or distillation

    Final product types

    • High purity musk essence intermediates
    • Alkyl-branched fragrance fixatives
    • Custom flavor modifiers in beverage bases
    • Trace fragrance elements for personal care applications
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    Certification & Compliance
    More Introduction

    3-Bromo-2,2-Dimethyl-1-Propanol: A Practical Workhorse for Modern Synthesis

    Manufacturing specialty chemicals demands a balance between product reliability, operational safety, and meeting the unique needs of each downstream industry we serve. Among the many molecules synthesized at scale in our facility, 3-Bromo-2,2-Dimethyl-1-Propanol continues to hold a steady place in our portfolio. Its straightforward structure and unassuming character don't do justice to the versatility it delivers in both lab and industrial environments. Pulling from decades of hands-on production and application feedback, let’s explore what sets this compound apart and how it benefits real-world synthesis.

    Model and Production Details

    3-Bromo-2,2-Dimethyl-1-Propanol, known by its molecular formula C5H11BrO, comes from a controlled batch bromination, where we’ve dialed in the reaction to maximize yield without the byproduct headaches that can haunt less deliberate approaches. The product leaves our reactors with a reliably high assay by GC, and each drum ships with our own material number tied directly to the production log—not a reseller’s invoice. The substance rolls off our line as a clear to pale yellow liquid, with density and refractive index falling within tight margins batch after batch.

    Over the years, scaling up taught us a few practical lessons. Freshly distilled product keeps moisture at bay, which makes all the difference for downstream reactions. The right solvent handling during packaging, and using moisture-absorbing liners, means you’ll open a drum to the same condition as when it left our warehouse. Consistent melting points and bromine content are the result of strict temperature profiles during synthesis and a filtration step that removes trace salts. For our customers, this translates to fewer surprises and more confidence in each run.

    Usage Across Industries

    The value of 3-Bromo-2,2-Dimethyl-1-Propanol lies not just in its reactivity, but in how it helps customers shorten the distance between starting materials and complex targets. Its primary applications land in the areas of pharma intermediates, agrochemical building blocks, and specialty resin modifiers. Many teams have told us that this compound slots in almost too conveniently for preparing brominated derivatives, especially where steric hindrance from the two methyl groups deters side reactions sometimes seen with simpler haloalcohols.

    We’ve seen its hydroxyl group open synthetic doors: it reacts smoothly with acid chlorides to furnish esters, and transforms under basic conditions to yield valuable epoxides. Carbamate or urea formation, often a stumbling block with more labile alcohols, proceeds cleanly under well-established conditions. The tertiary carbon resists unwanted rearrangements, even during prolonged heating—in fact, several customers switched to this molecule after facing decomposition issues with other secondary brominated alcohols in their route. That said, the bromine substituent stands out as a reliable leaving group during nucleophilic displacement. We regularly receive requests for custom derivatives—phosphonate substitutions, alkylations, benzylations—which all build off of this core competence.

    In the field of polymer research, we’ve observed another area of value. When incorporated into polyesters or polycarbonates, 3-Bromo-2,2-Dimethyl-1-Propanol imparts an unusual combination of rigidity and controlled reactivity. Our partners interested in flame-retardant materials rely on the bromine atom for both its reactivity in further transformations and its role as a built-in flame-suppressing element. With careful post-reaction purification, the main chain integration remains stable, avoiding discoloration or embrittlement that might otherwise appear with less robust monomers.

    Pharmaceutical process chemists, particularly those working under cGMP, appreciate the way our product comes triple-checked for trace impurities. We tailor each lot to accommodate strict compliance demands—addressing issues like residual solvents, trace heavy metals, and batch-to-batch uniformity, partly because we share the same regulatory scrutiny in our facility audits. Every year, clients return to us with new proposals in advanced synthesis, and the shared history of reliable supply builds a partnership rooted in real production needs, not just box-ticking.

    What Sets 3-Bromo-2,2-Dimethyl-1-Propanol Apart from Other Options

    With so many brominated alcohols on the market, choosing the right one can feel like trying to match puzzle pieces in the dark. From direct conversations with formulators and synthetic chemists, there are a few key differences that motivate the choice of this molecule over others:

    Selective Reactivity: Unlike primary brominated alcohols, 3-Bromo-2,2-Dimethyl-1-Propanol delivers a level of selectivity that cuts down on side reactions. The dual methyl shielding offers some steric protection, which reduces random elimination and substitution byproducts once the molecule is introduced into multi-step syntheses. Both our in-house and customer feedback have confirmed that the resulting intermediates show improved purity, meaning less time is spent on additional purification.

    Thermal Stability: Many brominated compounds show a tendency to decompose or discolor under heat or prolonged storage. We have stress-tested this compound through repeated heating and cooling cycles, observing no measurable degradation or significant color change, even at temperatures above routine handling. This gives users confidence during steps that require temperature ramps, whether in batch reactors or continuous flow systems.

    Lower Corrosivity in Handling: The alcohol group, balanced by its tertiary character, sits at a chemical sweet spot. We have compared this product directly with more reactive bromoalkanols—especially those prone to releasing free hydrobromic acid under ambient humidity. With our 3-Bromo-2,2-Dimethyl-1-Propanol, the rate of acid release drops significantly, sparing both process equipment and workers from unexpected corrosion or fume issues. This practical edge makes a noticeable difference in isolated plant environments where ventilation capacity or safety margins are stretched.

    Consistency and Contaminant Control: No chemist wants to run a series of reactions and discover a new spot on the LCMS for every incoming drum. Our plant’s analytical systems, which include GC, NMR, and ICP-OES, are maintained and attuned to catch even the smallest blips that might upset sensitive downstream workflows. Over hundreds of production batches, this has led to dramatically fewer recalls and customer returns—not through marketing bravado but by hard-won process auditing.

    Supply Chain and Sustainability Considerations

    Decisions around chemical supply are not made in a vacuum. End users demand a product that arrives on time, in optimal condition, and aligned with evolving expectations for responsible sourcing. Over the past several years, global logistics volatility and stricter safety legislation pushed us to rethink not only production, but also how we package, transport, and manage risk with every shipment. For 3-Bromo-2,2-Dimethyl-1-Propanol, this means using drums and jerrycans rated for chemical compatibility, and sealing every unit under nitrogen to suppress both vapor loss and atmospheric exposure.

    Ongoing regulatory shifts in brominated intermediates prompted changes to our material traceability and retention protocols. All shipment documentation includes the relevant transportation categorization, with batch numbers and COA (certificate of analysis) linked back to our master quality file. For international supply, we pre-arrange all required customs paperwork, which reduces hold-ups at port entry or destination warehousing. These steps help customers avoid costly delays, especially those coordinating tight production runs or just-in-time manufacturing.

    Sustainability sits high on our list, for both compliance and ethical reasons. We modernized our bromine recovery units so that batch waste is scrubbed efficiently, dramatically lowering environmental discharge. Our solvent recovery network ensures that process solvents return to the system with minimal contamination. Not only do these steps align with regulatory mandates, but they also cut operating expenses in the long run—a real win for cost-conscious supply partners.

    Lessons Learned from Field Applications

    Long before widespread adoption, every new chemical faces a trial by fire in the field. Over recent years, our team has been invited to support technical teams troubleshooting hurdles in their processes. In one case, a pharmaceutical partner encountered recurrent issues with side-product formation in the halogenation step of a key intermediate. After analyzing the issue on-site alongside their chemists, we provided our 3-Bromo-2,2-Dimethyl-1-Propanol, which immediately cut the impurity profile of the target step in half. They attributed this not only to the chemical’s inherent properties but also to our batch purity and low water content—real-world proof that upstream quality directly influences downstream success.

    Our own development team frequently runs pilot-scale syntheses when scaling up customer projects. We’ve found that optimizing the stoichiometry and solvent system makes a marked difference in yields with this compound. Even a small uptick in water content can steer reaction outcomes, so we designed a real-time Karl Fischer titration protocol around its handling. With fresh drums, we observed reproducible product yields, even across disparate reaction setups. These technical insights make their way into our customer training sessions, further reinforcing the bond of trust and shared technical knowledge.

    During a project with a specialty polymer house, the integration of 3-Bromo-2,2-Dimethyl-1-Propanol into a monomer blend introduced both performance and process benefits. The end polymer displayed an uptick in inherent fire resistance and avoided problematic cross-linking that plagued alternate systems relying on primary or benzylic alcohols. Such feedback from our partners guides continuous refinement in our own reactor conditions and purification protocols. We believe in co-developing solutions, so end-users see not only a chemical shipment but a relationship forged in technical collaboration.

    Addressing Limitations and Looking Forward

    No chemical answers every challenge. Over the years, we’ve listened to users who’ve bumped into limitations with 3-Bromo-2,2-Dimethyl-1-Propanol. Some customers find its relatively high boiling point poses challenges for removal from certain product mixtures where distillation is used for purification. Others highlight that in mass-transfer limited reactions, the bulky methyl groups require adjustment to temperature or agitation to maintain homogeneous conditions.

    Our response draws on collective experience, both in-house and from global users. We share best practice guidelines for solvent choices and agitation speeds—not as mere notes in the back of a catalog, but through webinars, workshops, and shared pilot runs. In one instance, shifting the reaction base and solvent polarity, plus adopting a staged reagent charging method, helped an agrochemical team lift their conversion rates. Field data from these improvements loops directly into our support literature and technical notes, and in some cases, sparks reconsideration of how we prepare and deliver the compound itself.

    Environmental and workplace health is another conversation we refuse to shy away from. Though 3-Bromo-2,2-Dimethyl-1-Propanol avoids the more stringent labeling reserved for certain bioaccumulative halogenated compounds, we still support safe-lab practices: glove selection, fume hood operation, and precise spill cleanup protocols. Our technical outreach covers these angles, and we invest in end-user training, not just for compliance but for worker peace of mind. Customers report fewer near-misses and improved comfort across plant personnel, which we attribute to a blend of reliable chemical character and proactive education.

    Conclusion: Real Chemical Value Built from Real Experience

    In the ever-shifting landscape of specialty chemicals manufacturing, technical validity must anchor trust—both within our own plant walls and in our partnerships with end-users. 3-Bromo-2,2-Dimethyl-1-Propanol stands out not by chasing novelty or marketing hyperbole, but by serving as a practical, durable, and surprisingly adaptable intermediate. Years of relentless optimization, supply chain investment, and engagement with those in the trenches have shaped both our product and our outlook. As chemistry challenges evolve, compounds like this will remain essential building blocks, supported by manufacturers willing to invest time, energy, and expertise in every drum they send out the door.