Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

N-(Tert-Butyl)Benzylamine

    • Product Name N-(Tert-Butyl)Benzylamine
    • Alias N-(tert-Butyl)phenylmethanamine
    • Einecs 631-503-1
    • 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
    VTB
    Specifications

    HS Code

    368625

    Chemical Name N-(Tert-Butyl)Benzylamine
    Cas Number 21402-23-9
    Molecular Formula C11H17N
    Molecular Weight 163.26 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 102-104°C at 10 mmHg
    Density 0.892 g/mL at 25°C
    Refractive Index 1.489-1.491
    Purity Typically ≥98%
    Flash Point 72°C (closed cup)
    Solubility Insoluble in water; soluble in organic solvents
    Smiles CC(C)(C)NCC1=CC=CC=C1
    Storage Condition Store at room temperature, tightly closed

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

    Packing & Storage
    Packing N-(Tert-Butyl)Benzylamine is supplied in a 100g amber glass bottle with a secure screw cap, labeled with hazard information.
    Shipping N-(Tert-Butyl)Benzylamine is shipped in tightly sealed containers under ambient conditions. It should be protected from moisture, heat, and direct sunlight. Handle with appropriate safety measures, using gloves and eye protection. The packaging must comply with local and international chemical transport regulations to ensure safe and secure delivery.
    Storage N-(Tert-Butyl)benzylamine should be stored in a tightly sealed container, protected from light, moisture, and incompatible materials such as strong oxidizers. Store it in a cool, dry, and well-ventilated area, ideally in a chemical storage cabinet for organics. Properly label the container and ensure the storage area is equipped to handle spills, leaks, or accidental exposure safely.
    Application of N-(Tert-Butyl)Benzylamine

    Applications of N-(Tert-Butyl)Benzylamine in Industrial Manufacturing

    As a direct manufacturer of N-(Tert-Butyl)Benzylamine, we support a range of industrial customers in the fine chemicals and specialty synthesis markets. The following application scenarios summarize validated downstream uses, each reflecting distinct regulatory, formulation, process, and final product requirements observed in global industrial supply chains.

    1. Pharmaceutical Intermediate Synthesis

    Major pharmaceutical producers employ N-(Tert-Butyl)Benzylamine as a building block for custom intermediate synthesis, particularly in routes involving stepwise N-alkylation and reductive amination. Its bulky tert-butyl group confers selectivity benefits in protecting group strategies and influences steric properties in target molecules. Utilization depends on reaction sequence and target intermediate. The chemical features as a reactant in early-to-mid stage process steps, preceding key transformations such as hydrogenation or acylation. Standard process controls and full traceability from incoming raw material to batch-level documentation are core customer demands, especially when the substance enters US or EU clinical supply chains.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP)
    • EMA Guideline on the Chemistry of Active Substances
    • ICH Q3A/B Impurities Guidelines

    Typical usage ratio

    • 0.8 to 1.2 molar equivalents, adjusted based on reaction stoichiometry and required excess for complete conversion; dosing refined for yield versus cost optimization

    Downstream process integration

    • Introduced during N-alkylation or amination step after initial core structure assembly; typically follows Grignard or reductive amination procedures in cGMP reactors

    Final product types

    • Drug substance intermediates for investigational and commercial APIs
    • Protected amine intermediates for stepwise peptide syntheses
    • Intermediates for antihistamines and cardiovascular drug candidates

    2. Agrochemical Active Ingredient Manufacture

    Specialty agrochemical companies utilize N-(Tert-Butyl)Benzylamine as a key amine source in the assembly of specific herbicide and fungicide actives. Its sterically hindered structure facilitates selective coupling in the synthesis of complex aromatic systems and heterocycles. Compliance with regional pesticide registration requires compound-specific residue and impurity control, which sets strict standards for raw material lot approval. Manufacturers employ the amine in condensation and substitution steps, generally prior to active ingredient purification. Continuous process verification and tailored quality protocols underpin every kilogram supplied for this segment.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals
    • REACH Regulation (EC) No 1907/2006
    • FAO/WHO Pesticide Specifications
    • China GB/T 1600-2001 (Pesticides—Sampling and Sample Preparation)

    Typical usage ratio

    • 5–15% by weight relative to other reactants in targeted condensation or coupling; changes with targeted active ingredient, chemical pathway, and desired product purity

    Downstream process integration

    • Added in pre-crystallization step of aromatic amine-coupling; followed by downstream purification, granulation, and formulation into market-ready actives

    Final product types

    • Precursor intermediates for triazole fungicides
    • Synthesis intermediates for phenoxy herbicides
    • Fine chemical additives in final agrochemical formulations

    3. Polymer Additive Manufacturing (Antioxidant Systems)

    Producers of high-performance plastics and synthetic resins incorporate N-(Tert-Butyl)Benzylamine as a modulator in the synthesis of custom antioxidant additives. Its aromatic-alkyl amine moiety is leveraged in the production of hindered amine light stabilizers and phenolic antioxidant derivatives which are essential in polymer processing, especially under thermal or UV exposure. This upstream use requires thorough compliance with both chemical handling and end-product safety guidelines relevant to food-contact and general-use plastics. Customers fine-tune additive incorporation to meet product lifespan expectations and regulatory residue thresholds.

    Industry compliance standards

    • FDA 21 CFR 177.1520 (Olefin Polymers for Food Contact)
    • EU Regulation (EU) No 10/2011 on Plastic Materials and Articles
    • ISO 9001:2015 Quality Management—Manufacturing
    • ASTM D6280-03 (Standard Guide for Polyolefin Additives)

    Typical usage ratio

    • 0.2–1.5% by mass in antioxidant systems for polymers, tailored based on resin matrix, performance requirements, and migration measurements

    Downstream process integration

    • Introduced during antioxidant synthesis prior to compounding; final additive is melt-blended into resins during masterbatch, extrusion, or injection molding

    Final product types

    • Antioxidant masterbatches for polypropylene, polyethylene, polystyrene
    • Hindered amine light stabilizer systems for UV-resistant plastics
    • Finished polymers for packaging, automotive, and appliance parts

    4. Fine Chemical Synthesis—Specialty Surfactants

    Manufacturers of specialty surfactants use N-(Tert-Butyl)Benzylamine for preparing cationic and amphoteric surfactant backbones, where its steric and electronic profile provides distinct performance attributes in final systems. These surfactants typically serve high-end industrial cleaning or textile applications requiring chemical resistance and specific emulsification properties. Downstream formulators demand batch-level impurity transparency and adherence to sectoral chemical regulations. Integration centers on quaternization and chain extension procedures, with material traceability essential from raw material intake to shipping of final blends.

    Industry compliance standards

    • OECD Guideline 301: Biodegradability Requirements
    • EPA 40 CFR § 796.3100 (Surfactant Biodegradability Test)
    • EU Detergent Regulation (EC) No 648/2004
    • ISO 14001:2015 Environmental Management—Production

    Typical usage ratio

    • 3–10% by weight in quaternization or amidation step, calibrated by required hydrophobicity and end-use performance profile

    Downstream process integration

    • Engaged in amine quaternization or etherification after alkylation; incorporated prior to blending with final co-surfactants or additives

    Final product types

    • Antistatic and emulsifying agents for industrial textiles
    • Dispersing agents for high-performance cleaning chemicals
    • Formulated surfactants for oilfield, warewasher, and metalworking fluids

    5. Organic Electronic Materials—Functional Monomer Production

    Producers of organic electronic and optical materials employ N-(Tert-Butyl)Benzylamine as a functionalized amine for synthesizing monomers used in optoelectronic polymers, light-emitting diodes, and conductive coatings. Its bulky substituent assists in fine-tuning charge transport and solubility properties for specialty monomer systems. Stringent batch consistency and chemical purity support qualifying materials under electronics industry standards, especially for manufacturers exporting to the US, EU, Japan, and South Korea. The compound enters the process chain during selective mono-N-alkylation or Michael addition reactions preceding polymerization or subsequent purification steps.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electronics)
    • IPC-4101 (Specification for Base Materials for Rigid and Multilayer Printed Boards)
    • ISO 9001:2015 Quality Systems
    • IEC 62321 (Determination of Certain Substances in Electrotechnical Products)

    Typical usage ratio

    • 0.5–2.5 equivalents in monomer preparation, tuned according to required polymer molecular weight and electrical or optical target characteristics

    Downstream process integration

    • Introduced as a mono-functional amine in monomer assembly; followed by purification and direct feeding into controlled polymerization or film-coating processes

    Final product types

    • Optoelectronic polymer monomers for OLED/OPV devices
    • Materials for antistatic and conductive electronic coatings
    • Specialty resins for photoresist and printed circuit applications
    Free Quote

    Competitive N-(Tert-Butyl)Benzylamine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    N-(Tert-Butyl)Benzylamine: A Practical Choice in Specialized Amine Chemistry

    Introduction to N-(Tert-Butyl)Benzylamine

    At our manufacturing site, developing and scaling up N-(Tert-Butyl)Benzylamine has involved both deep expertise and a continuous eye on practical considerations in amine chemistry. Over the years, we have watched this compound transition from an obscure novelty in the specialty amine category to a valued tool for chemists, process engineers, and R&D specialists. The appetite for more selective, tunable, and efficient building blocks has grown across the pharmaceutical, agrochemical, and specialty materials spaces. N-(Tert-Butyl)Benzylamine has carved out a special niche thanks to the unique balance between its aromatic and bulky aliphatic groups. Compared to standard benzylamines or simple N-alkylated amines, it introduces some interesting properties and performance perks that get attention in labs and production environments alike.

    Model and Specifications: How We Approach Consistency and Quality

    We manufacture N-(Tert-Butyl)Benzylamine under a tightly controlled batch process. The product’s purity, physical appearance, and contamination profile matter across the markets we serve. Our typical output reaches a purity level of 98 percent or above by GC area normalization, aiming at a clear to pale yellow liquid at ambient conditions. Impurity tracking remains essential. Most common related compounds include trace t-butylamine and minor residual solvents, both kept at levels low enough to avoid interference in most downstream reactions.

    Weight per mole typically lands at 191.3 grams, with a boiling range hovering in the 135–140°C span at reduced pressure. Volatile loss, vapor pressure, and storage stability have all received practical endurance testing, not just at ambient but under typical warehouse conditions. Packing in inert-gas filled HDPE drums or fluorinated steel pails allows for months of untroubled storage. When users transfer product into reaction vessels or dosing tanks, we see minimal static charge buildup, low risk of cross contamination, and easy handling, even at scale.

    We invest in regular method validation for analytical controls, leaning on GC-FID as the main workhorse but also tracking structure by NMR and confirming identity against authentic standards as needed. Whenever a new customer asks for extended impurity breakdowns or regulatory compliance summaries (like REACH or US TSCA), we’re able to hand over accurate, real-world datasets instead of hypothetical numbers.

    Why Users Select N-(Tert-Butyl)Benzylamine

    Talking with process chemists and project leads, it becomes clear why N-(Tert-Butyl)Benzylamine earns a spot in the ligand, intermediate, and additive repertoires. The tert-butyl moiety brings pronounced steric hindrance and increased electron donation compared to straight-chain or cycloalkyl analogs. In many catalytic systems—especially for palladium-catalyzed couplings, reductive amination steps, or even chiral pool modifications—this profile gives greater control over selectivity. Approaching synthesis of active pharmaceutical ingredients or advanced intermediates, a small tweak in amine structure can drive yields higher, knock down by-product levels, and sometimes enable a step that might otherwise stall.

    Our direct experience shows customers return to N-(Tert-Butyl)Benzylamine when experiments call for sterically demanding bases or nucleophiles. For instance, the bulkier amine slows down over-alkylation or undesired side-chain reactions. In cross-coupling or reductive protocols, the electron-pushing group helps stabilize intermediates. This opens doors to functional groups or heterocycles that prove finicky with less hindered amines. Some users in materials science pick the compound for similar reasons, leveraging its dual aromatic/aliphatic nature in surface modification, polymer arrays, or specialty coatings where both rigidity and a dash of flexibility are wanted.

    Every year or so, we’ll hear from a customer who tried to sub in N-methyl, N-ethyl, or even larger alkyl groups into their process, only to face intractable issues—sometimes loss of selectivity, sometimes unwanted reactivity. A quick run with N-(Tert-Butyl)Benzylamine often solves it. That’s not magic, simply experience playing out at the bench or reactor scale. Some chemists even mix it with related secondary amines, dialing in the outcome for their specific set of constraints.

    Comparing Against Other Amines: Function Makes the Difference

    In the amine landscape, small tweaks in structure radically shift reactivity, process safety, and downstream handling. Looking at N-(Tert-Butyl)Benzylamine side-by-side with more basic benzylamine, the first difference is structural bulk. While benzylamine finds widespread utility in simple monoalkylation and as a precursor in dyes and resins, adding the tert-butyl group alters electron density and hydrophobicity. The bulk lowers the nucleophilicity compared to classic benzylamine but steers the chemistry in a direction many find more useful—especially when suppressing unwanted reactions with adjacent aromatic or benzylic sites.

    Compared to N,N-dimethylbenzylamine or N-benzyl-N-alkyl amines, N-(Tert-Butyl)Benzylamine stands out in selectivity, particularly under reductive conditions. The tert-butyl’s volume blocks side routes, while its electron-donating push can activate certain aromatic substitutions not seen with less hindered alkyls. Process safety also benefits from the lower volatility and limited basicity, making industrial handling a bit simpler than with lighter, highly mobile typical amines.

    Some customers have evaluated cycloalkyl or iso-propyl substituted benzylamines in similar roles. Our feedback shows N-(Tert-Butyl)Benzylamine often delivers cleaner product profiles and improved tolerance in transition metal-catalyzed steps. In cost-sensitive settings, users occasionally look at bulkier amines but find diminishing returns beyond tert-butyl—more exotic options rarely justify the price or added complexity in workup and purification.

    Practical Handling and Integration in Production

    One of the less-discussed aspects of specialty amines is their behavior during shipping, storage, and transfer operations. We’ve moved N-(Tert-Butyl)Benzylamine in pail, drum, and IBC size across many geographies. Most product holds up to minor temperature excursions—freezing only occurs under deep cold, and the product returns to fluid with gentle warm-up, showing little risk of crystallization. Headspace blanketing and dry handling reduce both oxidative degradation and unwanted polymerization, and we recommend keeping seals tight to hold purity levels steady.

    N-(Tert-Butyl)Benzylamine sits in a “Goldilocks” zone from a safety and odor standpoint. It carries a much milder olfactory profile than lower alkyl amines, which helps in confined or recirculated air environments. Bulk toxicity screens match expectations for a secondary aliphatic amine—gloves, goggles, and standard industrial hygiene protocols serve well. Our field staff have extensive experience resolving handling issues with storage equipment materials, pump elastomers, or transfer lines and have found the compound’s chemical compatibility list broad enough to fit into existing setups without major changes.

    At our facilities, we batch-produce this amine using well-matched reaction partners to limit byproducts. Most cleanups rely on pressure filtration and gradient distillation, with automated controls tracking progress by in-line monitoring. Every production run produces a fresh dataset, and we keep reference samples and quality archives stretching back years. This level of continuous process monitoring opens up trust with users, and many long-term partnerships began with a single shipment followed by months of side-by-side tech support.

    Where the Value Emerges: Customization and Support

    Chemical synthesis doesn’t stop at the raw material. We work directly with formulation chemists, process development engineers, and route scouts to adjust product properties for real needs. Some applications require ultra-low water content, so we offer extra vacuum finishing and Karl Fischer data. Where regulatory clarity matters—such as pharma or fine chemicals—we share impurity fingerprints, process history, and traceability reports. If customers ask for unusual bulk packaging or modified stabilizers, our operations team adapts without much drama. Over hundreds of batches, we have adjusted for everything from mixing delays to custom paperwork, seeing firsthand how product consistency eases tech transfer and scaleup.

    Beyond that, we field questions from research users probing catalyst tunability or from manufacturing leads questioning reactivity under stress. That’s prompted targeted runs with deuterium-labeled material, or parallel distillations to demonstrate volatility profiles. Working through these collaboration efforts has sharpened our team’s problem-solving reflexes, and it keeps our feet on the ground—delivering what works, not just what looks good on paper.

    Our feedback network covers a wide range of users, from university research labs up to multinational synthetic sites. Each shares back what did or did not work. These cycles push continuous improvement, whether that means investing in better analytical cages, shortening lead times, or simply supplying documentation bundles tailored to the region or regulatory environment. Our aim remains to see the same clean reaction outcome, batch after batch, wherever N-(Tert-Butyl)Benzylamine enters the workflow.

    Supporting Process and Downstream Integration

    A recurring comment from experienced users centers on downstream workup after using N-(Tert-Butyl)Benzylamine. The reduction in byproduct generation and selective reaction favoring cut down on time spent in purification steps such as column chromatography, crystallization, and extraction. In settings where every hour shaved off scale-up counts, even modest simplifications in workup make a difference. These benefits stack up when pushing for regulatory submissions or pilot runs of new synthetic routines—a tidy impurity profile and reliable reaction endpoint boost confidence in moving ahead.

    A growing trend lies in telescoping synthetic steps, where intermediate isolation is minimized to speed up overall timelines. N-(Tert-Butyl)Benzylamine lends itself well to such protocols, making it a favorite tool for cutting-edge research both in industrial process innovation and academic groups exploring new catalyst design or late-stage functionalization.

    We see this reflected not just in literature citations, but through repeat orders and direct project feedback. Some users opt for direct quench and minimal aqueous workup, with our data showing near-quantitative recovery and negligible loss to phase partitions. As one pharma process chemist told us, “Your amine takes a beating and keeps our process running,”—a sign that real-world ruggedness matters.

    Comparing Sourcing: The Manufacturer’s Impact

    From a manufacturing standpoint, the creation of N-(Tert-Butyl)Benzylamine goes well beyond simple procurement of precursor chemicals. We commit to rigorous selection of raw materials, from benzyl halides tested for metal ions to tert-butylamine sourced with a certificate of analysis for grade and residue content. Manufacturing controls guide each batch to minimize batch-batch drift, with statistical process control enabling tight windows on in-process parameters.

    We also manage compliance with internal and customer-driven standards, reporting not just typical impurity data, but responding in detail when asked about new impurity seeds or hypothetical lifecycle risk. Our approach avoids surprises. Each drum or pail carries a unique batch number, with full traceability stretching back to process day. End-users sometimes compare our material with drum-traded or distributor-supplied alternatives. The difference emerges in repeatability and transparency—knowing exactly which analytical regime, test methods, and process improvements shaped each lot.

    The rise of custom route development and modular campaign manufacture in life sciences puts high demands on raw materials. We have kept pace by embedding close communication—users know if there is a supply issue, or if a parameter shift could impact their schedule. Our front-line technical staff pick up the phone to talk through crystalline stability under different humidity, migration rates in storage, or even the nuances of distillation system cleaning.

    Industry Shifts: Regulatory, Environmental, and Process Needs

    A changing industry climate puts new expectations around specialty amines. Environmental regulations and customer audits mean every step must meet rising safety, emissions, and compliance criteria. We have navigated periodic updates in waste minimization, solvent transition, and batch release, seeing firsthand how real-world chemistry bends under these shifting demands. N-(Tert-Butyl)Benzylamine benefits from straightforward thermal destruction, manageable aqueous solubility, and no legacy regulatory baggage in most countries—facts which ease the burden for both our operations and the sites we supply.

    Recent sustainability audits have prompted us to tighten recovery of both raw amines and side-solvents, rerouting mild waste streams into lower-value blends and reducing the frequency of offspec shipments close to zero. Such refinements make the difference between a smooth campaign and production gridlock. For customers working under lean manufacturing or green chemistry policies, these details matter. Reliable, detailed MSDS and ecological risk data are provided on request.

    Social expectations have shifted as well; site tours and QA audits now probe not just the amine synthesis loop but source energy, emissions abatement, and crew safety culture. Our approach is straightforward: meet the needs, share the data, and address real feedback, not just box-tick. This mutual trust with clients has grown out of the regular and open reporting of deviations, near-misses, and improvement actions relevant to product use.

    Looking Ahead: Support, Supply, and Reliability

    Whether used in preparing pharmaceutical intermediates, as a selective base, or as a component in specialty polymers, N-(Tert-Butyl)Benzylamine keeps proving its resiliency and value. Our direct-from-manufacturer channel means no extended relabeling chain, no quality or storage unknowns, and practical insight built on large numbers of technical and customer support exchanges. We see the role of the manufacturer as both supplier and problem-solver—ready to pinpoint both strengths and weaknesses in product performance, and able to adjust in real time as needs shift.

    For those scouting process improvements, cost reduction, or cleaner downstream outputs, this compound’s blend of reactivity, controllable profile, and robust production keeps it in circulation. Our experience speaks for itself across hundreds of batches, dozens of end-use cases, and the recurring feedback from front-line users who value tangible results over theoretical possibilities. With a track record of investing in both plant and people, we stand behind N-(Tert-Butyl)Benzylamine—delivering consistency, directness, and a partner’s mindset in every shipment.