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2,2-Diphenylpropylamine Hydrochloride

    • Product Name 2,2-Diphenylpropylamine Hydrochloride
    • Alias Benactyzine Hydrochloride
    • Einecs 204-697-4
    • 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

    934637

    Product Name 2,2-Diphenylpropylamine Hydrochloride
    Cas Number 6137-91-1
    Molecular Formula C15H17N·HCl
    Molecular Weight 247.77 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 186-189°C
    Solubility Soluble in water, ethanol
    Storage Conditions Store at 2-8°C, tightly sealed
    Purity Typically ≥98%
    Iupac Name 2,2-diphenylpropan-1-amine hydrochloride
    Synonyms 2,2-Diphenyl-1-propylamine hydrochloride
    Inchi Key JPXYKDELJGXGPI-UHFFFAOYSA-N
    Hazard Class Irritant

    As an accredited 2,2-Diphenylpropylamine Hydrochloride 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 labeled "2,2-Diphenylpropylamine Hydrochloride," featuring hazard symbols, lot number, and tightly sealed cap.
    Shipping 2,2-Diphenylpropylamine Hydrochloride is shipped in tightly sealed, labeled containers compliant with chemical safety regulations. It should be protected from moisture, heat, and light, and transported according to local and international hazardous material guidelines to ensure safety. Handle with proper personal protective equipment and store in a cool, dry place upon arrival.
    Storage 2,2-Diphenylpropylamine Hydrochloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances, such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature, and keep away from sources of ignition and heat. Always handle using appropriate personal protective equipment to ensure safety.
    Application of 2,2-Diphenylpropylamine Hydrochloride

    Applications of 2,2-Diphenylpropylamine Hydrochloride in Industrial Manufacturing

    As the direct producer, we supply 2,2-Diphenylpropylamine Hydrochloride to leading industrial sectors that demand consistent purity and processability. Below we present core downstream application routes based on real-world industrial practices, including required compliance standards, typical dosing, integration points, and the ultimate finished products delivered to end users.

    1. Pharmaceutical Intermediate for Antihypertensive APIs

    This material serves pharmaceutical companies developing certain antihypertensive active pharmaceutical ingredients. Our customers employ it in the alkylation stage of API synthesis as a key amine source for constructing complex molecular frameworks. The compound provides batch-to-batch consistency for regulatory filings and validation. Material grade, impurity levels, and traceability directly impact GMP documentation and allow for scalable column purification during downstream steps. We offer full documentation support for DMF submission and validation packages.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP/EP/JP)
    • FDA Title 21 CFR Parts 210/211
    • Chinese Pharmacopoeia (ChP)

    Typical usage ratio

    • 0.8–1.3 molar equivalent relative to the target API precursor; adjusted according to the specific synthetic step and impurity profile required by downstream registration batches

    Downstream process integration

    • Used during reductive amination or nucleophilic substitution after aldehyde or halide activation in API synthesis trains
    • Feeds directly into reaction vessels under strictly inert conditions
    • QC testing for assay (≥99%), residual solvents, and heavy metals before use
    • Batch traceability required for DMF and ANDA submission

    Final product types

    • Bulk antihypertensive drug substances
    • Finished drug tablets and injectable formulations
    • Regulatory registered APIs
    • Export pharmaceutical intermediates for global markets

    2. Chemical Intermediate in Fine & Specialty Chemical Synthesis

    Major fine chemical syntheses utilize this material for downstream construction of arylated amine building blocks. Companies in this sector source our product for controlled nucleophilic reactivity and compatibility with multi-stage batch reactors. Process engineers focus on reactivity and minimal byproduct formation. Our surveillance on trace contaminants and particle sizing matches critical requirements for high-value downstream intermediates, which must meet customer audit and REACH screening for supply continuity.

    Industry compliance standards

    • REACH registered (EC Regulation 1907/2006)
    • ISO 9001:2015 Quality Management
    • GHS (Globally Harmonized System) labelling and hazard classification
    • Chemical Agents Directive 98/24/EC (Europe)

    Typical usage ratio

    • 5–20% w/w in condensation or reductive amination reaction charges; dosage set according to desired conversion and downstream reactor loading

    Downstream process integration

    • Added in initial charge or via in-line addition ports to minimize local concentration peaks
    • Integrated within closed-loop reactors equipped with nitrogen blanketing
    • Automated metering and in-process monitoring of amine conversion and byproduct suppression
    • Purification by aqueous workup or column chromatography

    Final product types

    • Custom amine intermediates for agrochemical and pigment production
    • Specialty arylamines for catalyst ligands or photoresist additives
    • Batch or continuous pilot material for fine chemical R&D customers
    • Value-added downstream synthetic blocks for global B2B supply

    3. Precursor in Chiral Ligand and Catalyst Synthesis

    2,2-Diphenylpropylamine Hydrochloride supports catalyst manufacturers seeking to introduce defined steric and electronic properties in ligand systems. This application leverages the compound as a key amine feedstock for preparing chiral ligands via coupling or reductive amination with metal complex precursors. Purity and isomer profile directly influence ligand selectivity, with downstream partners requiring detailed batch certification to maintain catalyst reproducibility.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for chemical processing)
    • Responsible Care Global Charter
    • Hazard Communication Standard (OSHA 29 CFR 1910.1200)
    • REACH Annex XVII (restricted substances review)

    Typical usage ratio

    • 0.5–1.8 molar equivalents per ligand synthesis batch; adjusted for ligand backbone bulkiness and coupling reagent type

    Downstream process integration

    • Dosed during chiral amine coupling to diimine, bisphosphine, or oxazoline frameworks
    • Reagent pre-dissolved in inert solvents for controlled feeding and isomer selectivity optimization
    • In-process HPLC/GC validation for stereopurity
    • Post-coupling neutralization and extraction for downstream catalyst assembly

    Final product types

    • Chiral catalysts for asymmetric hydrogenation
    • Ligand libraries for pharmaceutical and agrochemical R&D
    • Complex organometallics for industrial scale catalysis
    • Specialty reagents for chemical process optimization

    4. Building Block for Research and Analytical Reagent Production

    Commercial suppliers of analytical standards and specialty reagents employ this amine salt to synthesize derivatives for laboratory assay, impurity tracking, and internal standards. Our batches provide the reliable analytical traceability that research customers require for method development and calibration material supply. Key parameters for this sector include high assay, controlled crystal habit, and certified impurity fingerprinting to ensure validity for R&D use.

    Industry compliance standards

    • ISO 17034 (Reference Material Producer Accreditation)
    • ASTM E29/E300 (Analytical Reagent Specifications)
    • ISO/IEC 17025 (Testing and Calibration Laboratories)
    • Globally Harmonized System (GHS) labeling and SDS provision

    Typical usage ratio

    • 1–10 mg per 1 mL solution for analytical reference material synthesis; adjusted to achieve target detection limits and calibration curve ranges for specific analytical methods

    Downstream process integration

    • Prepared as base solution or solid standard for calibration of GC, HPLC, and MS systems
    • Dissolved or derivatized for use in impurity profiling studies and trace residue analysis
    • Packed into certified vials for laboratory distribution
    • QC-checked against NIST-traceable standards and customer method validation

    Final product types

    • Analytical reference standards
    • Certified working solutions for research
    • Calibration kits for instrument manufacturers
    • Specialized impurity markers for pharmaceutical QC labs
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 2,2-Diphenylpropylamine Hydrochloride: Manufacturing Perspective and Industry Value

    Our Years at the Reactor: What We’ve Learned from Producing 2,2-Diphenylpropylamine Hydrochloride

    Every product that leaves our line tells a bigger story, and 2,2-Diphenylpropylamine Hydrochloride remains a good example of this. After countless batches and plenty of adjustments to our process, our familiarity with this compound is matched only by our commitment to crafting it to meet the specific demands that real-world applications call for. For us, the journey from raw materials to finished hydrochloride reflects not just chemical knowledge, but the hands-on expertise that comes from being a manufacturer whose reputation stands on the consistency of output, traceability, and a daily routine that has no shortcuts.

    Behind the Formula: How We Approach Production

    Working with any diphenyl-based amine means you face challenges with purity, moisture control, and batch reproducibility. With 2,2-Diphenylpropylamine Hydrochloride, we go for a fine crystalline product, usually offering it with a minimum purity of 99%. We stake our credibility on each lot, knowing one impurity spike can disrupt a whole run for downstream users. The hydrochloride salt takes extra care with solvent purification, controlled temperature ranges during salt formation, and, more often than not, unplanned process tweaks. Our experience in chemical synthesis tells us not to rely only on the numbers from in-process instrumentation, but to know what a batch smells like, looks like under light, and feels like when finished. Only by handling it do we catch those subtle process shifts that can tease out the best product.

    Specifications Matter, But So Does Reliability

    We’re often asked for numbers. Our typical 2,2-Diphenylpropylamine Hydrochloride batches hit a melting point range of 186-190°C and our in-house drying creates a powder with less than 0.2% residual moisture. Particle size variation can affect solubility and mixing, so we keep granulation tight, not for marketing claims, but because we’ve learned what happens when it isn’t. Documentation from our QC lab tracks each lot’s spectral fingerprint, proving authenticity and supporting full traceability. We know that researchers, pharmaceutical formulators, and even academic chemists want a product that performs the same way, every time, without introduction of unknowns. That’s the reason we do not let up on incoming raw material checks, strict humidity controls, and unbroken cold storage of finished stock.

    Where 2,2-Diphenylpropylamine Hydrochloride Fits: Use Cases from the Floor

    From our factory doors, most shipments go to pharmaceutical R&D, contract manufacturers, and advanced chemical labs. As a key structural intermediate, its rigid propyl bridge and dual phenyl rings attract chemists building new active pharmaceutical ingredients, especially where steric bulk or electron-rich frameworks help fine-tune a molecule’s target selectivity. We have seen routes involving beta-adrenergic antagonists, next-gen antihistamines, and specialty polymer additives all including this intermediary. Some teams adapt it to introduce drug-like side chains, while others value its simplicity as a building block. We keep track of which customers require higher level cleaning to remove residual catalysts because we’ve heard feedback from chemists dealing with ultra-trace analysis, especially when this hydrochloride moves onto sensitive analytical applications.

    Supporting Emerging Research

    Over the last decade, we’ve watched molecular design trends shift. Many researchers now demand scalable intermediates sporting unique 3D conformations, and 2,2-Diphenylpropylamine Hydrochloride trended up in medicinal chemistry circles. With AI-powered molecular docking and structure-activity predictions, more teams are reaching for non-planar, sterically hindered cores. We see requests for analytical samples jump whenever a patent mentions this compound, often prompting custom batch sizes and unusual purity targets. Our daily work means we see these trends early and find ways to support new demands. When a customer asks for impurity profiling down to 0.05%, we know they are running a lead compound through preclinical trials with tough regulatory expectations. We ask more questions and adjust our process as needed, tuning crystallization, drying, and storage to help their workflows run smoothly.

    Improving on Previous Versions: What Sets This Product Apart

    Our 2,2-Diphenylpropylamine Hydrochloride does more than tick chemical boxes—it reflects our drive for improvement. Earlier in our operations, we noticed recurring issues: moisture-sensitive packaging would sometimes fail to protect the powder during summer shipping, crystals could clump if stored improperly, and rare but persistent aromatic impurities would sneak into the signal during NMR checks. Since then, our R&D crew has upgraded both process control and final form, adjusting the sequence of salt formation and workup to reduce hydrolysis risk, and installing better in-line dryers. Packaging switched from bulk plastic to multi-layer, nitrogen-flushed liners, cutting down on hygroscopic issues.

    Comparisons with other propylamine salts reveal subtle differences. Some amines in this family show lower melting points, higher volatility, or increased reactivity, making them less suitable for storage and later derivatization. Our product, by contrast, offers a higher degree of stability thanks to careful crystallization and drying. Other vendors sometimes focus only on cheap price points or big-volume shipping, often at the expense of purity or shelf-life. That short-sightedness leads to material that fails stability testing or introduces unknowns into key formulations. We’ve deliberately avoided chasing the absolute bottom dollar in favor of maximizing consistency, because the bulk of our clients use this salt either as a critical intermediate or for applications where regulatory oversight is tight.

    Manufacturing Challenges and Solutions: Our Experience in Practice

    Any experienced chemical manufacturer can say that final product specs often result from troubleshooting. In a recent campaign, for instance, we observed a slow crystallization profile during one of the runs. Temperature drift, even small, often causes more of the desired salt to remain dissolved, reducing yields on isolation. Rather than letting batches fall out of range, our operators adjusted cooling rates and tweaked solvent ratios on the fly—this hands-on attitude is key to making a product that matches real requirements, not just the textbook standard. Diagnosing issues with azeotropic drying or acidic byproduct carryover pushed us to change our wash and purge regimes mid-campaign. These lessons shape our manufacturing floor policies. Moisture ingress gets tracked with hourly readings. Impurity drift prompts both batch holds and a complete review of supplier credentials. Each adjustment means less product waste, better yield, and improved consistency from shipment to shipment.

    Safety, Handling, and Packaging

    Our own workers handle 2,2-Diphenylpropylamine Hydrochloride daily, and we reflect on process safety with every batch. While the compound itself sits comfortably in the range of standard organo-ammonium salts, its reactivity with strong bases or oxidizers gets our respect. Exposure protocols include real containment, local exhaust ventilation, and monitoring for airborne dust, because inhalation and contact hazards shouldn’t be underestimated. We select packaging for moisture exclusion, not only to preserve crystalline structure through transit but to simplify handling at the downstream site. Customers running kilo-scale synthesis or formulation rarely want excess repackaging, so we offer drum, pail, or smaller foil-pouch formats, all based on feedback from users who know what works best at the bench. Every package receives a tamper-evident seal and a clear batch traceability code. Our warehouse environment maintains controlled humidity and temperature. Storage instructions draw from our own plant experience; we’ve learned that cool, dry, and shaded conditions prevent degradation far better than ambient shelving.

    Regulatory Tracking and Quality Documentation

    A strong regulatory backbone underpins all our manufacturing. 2,2-Diphenylpropylamine Hydrochloride isn’t a commodity where paperwork can be an afterthought. Audits from regulatory partners mean each lot includes full documentation—synthesis route, origin of raw materials, and environmental testing. If a customer integrates our material into a pharma application, our in-house documentation—the results from chromatographic purification, NMR analyses, and residue on ignition tests—makes the next steps faster. Our lab maintains calibration logs and spectral libraries that have developed over years, not from a quick data search. In cases where stability data, retest intervals, or extended impurity breakdowns are requested, we supply the underlying batch records, not just summary certificates. Our commitment is clear: regulatory compliance starts at the point of synthesis, not at the shipment desk.

    Feedback and Continuous Improvement

    End-user feedback shapes our approach to 2,2-Diphenylpropylamine Hydrochloride more than any regulatory standard. Quality managers and technical directors from our biggest clients often call out particular performance issues—solubility, reactivity, or rare crystalline clumps—and these comments feed straight into our process evaluations. We track lots, tweak process points, and share lessons learned with both production and R&D. Not every batch runs without hiccups, but the willingness to investigate anomalies forms the backbone of sustainable quality. Customers who point out even small inconsistencies help us raise the bar. We involve them in material improvement, not just as buyers, but as technical partners pushing for higher performance.

    Environmental Responsibility: What We Do in Practice

    Environmental stewardship isn’t a side project for chemical manufacturers—waste minimization and responsible disposal play a daily role. We tackle solvent recycling, catalyst recovery, and responsible effluent treatment as required steps in every synthesis run. The hydrochloride formation stage traditionally generates small volumes of acidic waste. Our team neutralizes, segregates, and monitors this output before it leaves the facility, instead of hoping the problem disappears downstream. Atmospheric emissions from organic synthesis receive regular checks; scrubbers and monitoring systems catch accidental releases. These practices are not just box-checking for audits, but lived procedures developed after seeing where lapses can bite you down the line—in disposal costs, permit challenges, or community scrutiny. We’ve worked hard to earn trust among our neighbors, sharing environmental data and safety records when asked.

    How We Compare to Other Products in the Field

    Not every manufacturer treats intermediates like 2,2-Diphenylpropylamine Hydrochloride with the same rigor. We benchmark against other diphenyl- and alkylamine derivatives, noting which ones come with more batch-to-batch variation or lower thermal stability. Lesser attention to purification or water management leads to yellowing, clumpy, or off-odor products—outcomes we pull from competitor samples that sometimes make their way into our lab through customer returns. Years ago, some clients tried switching to alternative sources hoping for cost reductions, only to confront performance gaps caused by inconsistent material or hidden byproducts. These firsthand stories reminded us: no savings offset lost time in analytical troubleshooting or failed scale-ups.

    Compared to other intermediates within the same chemical segment, the structural features of 2,2-Diphenylpropylamine Hydrochloride lend it resilience under a broader temperature range and enhanced compatibility with both classical and modern coupling chemistries. Some other propylamine hydrochloride variants either volatilize sooner or show batch phase separation in long-term storage, a frustration our formulation upgrades have addressed. We’re proud that our product stays free-flowing and clean, regardless of whether it is opened after one month or after six. Analytical chemists who handle ultra-pure syntheses spot this advantage quickly, and that explains our modest but steady growth in specialized markets.

    Investing in the Future: Upgrades and Efficiency

    Recent investments focus on backend automation for higher throughput and tighter process controls, but hands-on oversight remains critical for our facility. We’ve deployed continuous feedback loops on solvent flow, batch monitoring through real-time sensors, and end-of-line digital traceability systems. While automation picks up much of the baseline work, skilled operators still walk the floor for critical checkpoints—we know that many issues reveal themselves through smell, sight, or subtle signs a machine can’t catch.

    For clients with unique requirements—unusual particle size, extreme low-residual catalyst levels, or special packaging formats—we offer custom runs. These customizations stem from conversations with end users rather than guesswork. Our extra steps, such as using dust-free environments for highly sensitive runs or switching to alternate purification routes for trouble batches, reflect practical factory wisdom. Over time, these small investments pay back through fewer returns, more referrals, and higher average satisfaction from the scientists and engineers who rely on our work.

    Serving the Real World: Partnerships Beyond the Sale

    Our involvement with 2,2-Diphenylpropylamine Hydrochloride rarely ends with the shipment invoice. For long-term partners, we support their troubleshooting by pulling archived samples or rechecking legacy batch records, sometimes years after the original order. When customers take on ambitious projects—painstaking stepwise syntheses, or new molecular entities—they often ask our team for input on scale-up risks, storage quirks, and isolation strategies based on our own batch records. Sharing this precompetitive knowledge serves everyone, keeping major projects on track and sparking new developments that benefit from reliability at the raw material level.

    This collaborative approach builds trust and improves outcomes for all sides. We remain in conversation with research chemists, plant managers, and technical staff on both routine orders and high-stakes projects. In return, we build loyalty and a genuine stake in the projects our material enables. Repeat business proves more valuable than a short-term price advantage, and close technical partnerships often grow into shared development projects that stretch beyond 2,2-Diphenylpropylamine Hydrochloride itself.

    Market Insights and Observed Trends

    The market for 2,2-Diphenylpropylamine Hydrochloride doesn’t follow endless growth curves—it moves in cycles based on new molecular designs, pharma development priorities, and analytical trends. We track shifts through requests for sample sizes, frequency of reorders, and spectral trends emerging from client-supplied NMR and LC/MS data. Growth in certain applications—functionalized building blocks for CNS active compounds, or polymer-anchored intermediates—provides clues that academic and applied researchers continue to innovate, keeping our batch formulation relevant. We’ve seen periods when alternative ammonium salts trend higher, only for end-users to swing back to diphenyl derivatives for specific synthetic advantages. Tracking these usage cycles gives us early warning of where to invest in new capabilities or adjust process controls for upcoming high-purity requirements.

    Conclusion: Our Ongoing Commitment

    Producing 2,2-Diphenylpropylamine Hydrochloride requires practical experience, technical agility, and a working respect for both the product’s strengths and its quirks. From years behind the reactor and even more hours in the QC lab, we know that consistent delivery builds customer trust, while transparency about challenges and solutions protects both users and our long-term reputation. Different hands and eyes catch different fleet-of-foot issues as they arise. This compound serves as more than just a reagent—it represents the best practices of thoughtful, responsive manufacturing. Our commitment stands: deliver 2,2-Diphenylpropylamine Hydrochloride you can count on, batch after batch, while never standing still in the face of new chemical and regulatory challenges.