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Cumylamine

    • Product Name Cumylamine
    • Alias β-Phenylpropylamine
    • Einecs 202-218-1
    • 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

    614016

    IUPAC_name 2-phenylethan-1-amine
    Common_name Cumylamine
    Molecular_formula C8H11N
    Molar_mass 121.18 g/mol
    CAS_number 635-85-2
    Appearance Colorless to pale yellow liquid
    Boiling_point 215-217 °C
    Melting_point -61 °C
    Density 0.976 g/cm3
    Solubility_in_water Miscible
    Flash_point 92 °C
    Structural_formula C6H5CH2CH2NH2

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

    Packing & Storage
    Packing Cumylamine is packaged in a 100 g amber glass bottle with a secure cap, featuring hazard labels and a clear chemical identification.
    Shipping Cumylamine should be shipped in tightly sealed containers, protected from moisture and direct sunlight. It must comply with relevant transportation regulations, labeled as a chemical substance. Avoid exposure to extreme temperatures. Ensure proper packaging to prevent leaks or spills, and include safety data sheets. Handle only by trained personnel using appropriate protective equipment.
    Storage Cumylamine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from heat sources, open flames, and incompatible substances such as acids and oxidizers. Protect it from moisture and direct sunlight. Label containers clearly, and ensure safe storage in accordance with local regulations for handling amines and flammable compounds.
    Application of Cumylamine

    Applications of Cumylamine in Industrial Manufacturing

    As an established manufacturer of chemical raw materials, we supply Cumylamine to specialized clients across advanced industrial sectors. The following application scenarios highlight the real-world roles this material plays in downstream manufacturing, focusing on regulatory compliance, formulation, process integration, and finished product categories.

    1. Pharmaceutical Intermediate Synthesis

    Chemical manufacturers and contract synthesis facilities use Cumylamine as a key intermediate in the preparation of several active pharmaceutical ingredient (API) scaffolds, particularly for compounds featuring tertiary aromatic amines. Its high purity profile enables controlled N-alkylation and reductive amination steps, facilitating scalable multi-step syntheses under cGMP environments. Supply traceability and impurity control support downstream qualification and registration for regulated markets.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • Ph. Eur., USP, JP specifications for relevant APIs
    • US FDA 21 CFR Part 211
    • EU GMP Part II (APIs)

    Typical usage ratio

    • 20–60 mol% relative to API batch input, depending on molecular design and step conversion yield; optimized per registration batch data.

    Downstream process integration

    • Charged during the amination or N-alkylation stage; process flow varies depending on the synthesis route, often following aromatic substitution or reduction reactions.

    Final product types

    • Generic and custom APIs for CNS agents, antihistamines, antibacterial agents
    • NCE synthetic intermediates for drug discovery pipelines
    • Regulated fine chemical building blocks

    2. Agrochemical Active Ingredient Formulation

    Agrochemical formulators rely on Cumylamine in the synthesis of certain herbicide and fungicide actives, exploiting its unique aromatic backbone to achieve selective toxicity and target specificity. The compound enters manufacturing lines during precursor formation and further reacts to construct efficacy-determining active cores. Downstream, residue, and shelf-life profiling must comply with regional crop protection regulations, requiring traceable sourcing and impurity transparency.

    Industry compliance standards

    • FAO/WHO specification guidelines for pesticides
    • OECD GLP (Good Laboratory Practice)
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)
    • US EPA 40 CFR Part 158

    Typical usage ratio

    • 3–15% w/w in active core formation, adjusted according to target molecule yield and precursor conversion efficiency.

    Downstream process integration

    • Added during the initial amine coupling or condensation step; subsequent formulation by granulation, suspension, or emulsification for end-user application.

    Final product types

    • Selective herbicides for cereal crops
    • Fungicides for orchard and viticulture applications
    • Agro-intermediate stock for further synthetic transformation

    3. Specialty Polymer Modification

    Advanced polymer manufacturers employ Cumylamine as a functional modifier for engineering plastics and coatings where controlled introduction of pendant amine groups enhances end-use performance. The material reacts with activated monomers or as a post-polymerization additive, supporting custom plasticizer and compatibilizer grades for high-spec packaging and automotive interior parts. Material safety data and residual amine control must meet international standards for consumer-facing applications.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for Polymers)
    • EU REACH Regulation (EC) No 1907/2006
    • FDA 21 CFR 177.1520 (for plastic contact with food, if applicable)
    • RoHS Directive 2011/65/EU (for electronics applications)

    Typical usage ratio

    • 0.2–1.5% w/w in bulk polymerization or 0.5–2% as a post-polymerization surface modifier, proportion adjusted depending on target functionality and end-use.

    Downstream process integration

    • Incorporated during copolymerization or reactive extrusion; may also be applied in surface functionalization by plasma or dipping process.

    Final product types

    • Antistatic and chemically resistant films
    • Specialty coatings for electronics and automotive parts
    • Functional masterbatches for engineering thermoplastics

    4. Organic Synthesis in Advanced Materials Research

    R&D organizations and material science labs utilize Cumylamine in the design and validation of novel organic frameworks for applications such as organic light-emitting diodes (OLEDs), specialty dyes, and advanced resin systems. The compound supports prototyping and pilot-scale studies by providing a reliable aromatic amine source for electrophilic substitution, condensation, and ring-closure reactions. Strict documentation and batch-level traceability are typically required for property correlation and patent support.

    Industry compliance standards

    • ISO 17025 for analytical traceability
    • Material safety data reporting per GHS (Globally Harmonized System)
    • CEN/TS 16611 (standard methods for chemical analysis in R&D)
    • Internal QA/QC procedures accredited to ISO 9001

    Typical usage ratio

    • Variable: 1–25 mol% relative to primary synthetic substrate. Optimization based on experimental design and functional group loading requirements.

    Downstream process integration

    • Deployed in precursor amination, electrophilic aromatic substitution, or as an amine source in resin pre-polymer formation; purity is critical for reproducible R&D outcomes.

    Final product types

    • OLED material prototypes
    • Experimental specialty dyes
    • Custom oligomers and crosslinking agents for composite materials

    5. Fragrance and Cosmetic Ingredient Synthesis

    Within the specialty aroma chemical production chain, Cumylamine serves as a building block in the synthesis of targeted fragrance intermediates, imparting distinct aromatic characteristics to functional additives. The ingredient enters multi-step organic syntheses, particularly during Mannich or reductive amination routes, with batch control essential for downstream safety and regulatory registrations in the personal care sector. All units must pass rigorous screening for residual amines and meet IFRA/PCPC guidelines for safe use.

    Industry compliance standards

    • International Fragrance Association (IFRA) Code of Practice
    • Cosmetic Ingredient Review (CIR) standards
    • CosIng (EU Cosmetic Ingredient Database)
    • ISO 22716 (Cosmetic GMP)

    Typical usage ratio

    • 0.5–2.0% w/w in intermediate stage, adjusted according to reaction pathway and required final purity.

    Downstream process integration

    • Introduced during aromachemical backbone assembly (Mannich, amination, or condensation reactions), followed by purification and blending prior to formulation into fragrance compositions.

    Final product types

    • Fragrance intermediates for fine perfumes
    • Functional cosmetic additives in creams and lotions
    • Personal care aroma blends
    Free Quote

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    Certification & Compliance
    More Introduction

    Cumylamine: Hands-on Experience from the Manufacturer’s Floor

    Introduction to Cumylamine in Our Production Environment

    Over the last few decades in the chemical industry, few organic amines have stood up to practical tests quite like Cumylamine. We produce Cumylamine with a careful balance of yield, purity, and process safety, relying on a team of experienced operators and chemical engineers who know the ins-and-outs of bench scaling and plant-scale operations. Our product has long served as a key intermediate across multiple synthesis routes, and its performance in end-user applications continues to drive our investment in quality raw materials, process reliability, and robust purification infrastructure. Cumylamine often goes underappreciated outside specialty chemistry circles, but those who have worked directly with this compound know its practical value.

    Overview of Cumylamine and Its Basic Properties

    Cumylamine, chemically referred to as 2-Phenyl-2-propylamine, features a benzene ring attached to a secondary carbon that carries an amino group. The molecule balances reactivity, solubility, and thermal stability in a way that few other amines match. In our facility, we manufacture Cumylamine to strict purity targets—mostly above 99%. We routinely check for residual benzyl precursors and any trace oxidation byproducts, since those can complicate downstream transformations. The crystalline form we supply flows cleanly and packs well for large-batch production. Even under varied humidity and temperature conditions, the product maintains appearance, scent, and, most importantly, chemical integrity.

    Manufacturing Insights and Spec Control

    As a company that manages the full synthesis route, we control every step from reaction temperature to solvent drying. Our reactors handle both batch and semi-continuous runs; with Cumylamine, finding the right balance of residence time and agitation pays off in purity and consistency. Some customers have told us stories about inconsistent amines bought from traders who don’t interact with the production environment. We see firsthand the importance of monitoring the reaction kinetics, using in-line GC, and validating each batch by NMR. Setting limits well beyond the minimum ensures our Cumylamine performs in both bench-scale and commercial-scale settings.

    Common Uses: What We See in Downstream Applications

    Cumylamine’s greatest impact appears in pharmaceuticals and as a building block in specialty chemical synthesis. Many projects come to us looking for reliable arylamines for downstream coupling; Cumylamine proves particularly robust in reductive amination, Boc-protection reactions, and as a base for transition metal-catalyzed cross-couplings. In agrochemical development, customers appreciate the molecule’s reactivity, which supports regioselective modifications without excess byproduct. Over the years, we’ve supported multiple teams moving from lab scale to pilot scale, troubleshooting everything from incomplete conversion to filtration headaches. The common thread: a quality Cumylamine batch eases scale-up headaches.

    A frequent request we get involves Cumylamine’s use as an intermediate for custom ligands or in producing innovative therapeutic scaffolds. Our technical support team often helps synthesize rare analogues, adjusting process conditions to ensure customers don’t waste time with unknown contaminants. Academic groups call on us for reliable sourcing during grant-driven projects where consistency equals publication and funding outcomes. Having seen the compound perform under real-world lab and manufacturing pressures, we are quick to spot lot-to-lot issues that might otherwise escape attention.

    Comparisons with Related Products

    Many clients ask how Cumylamine differs from other alkyl or aryl amines. Experience tells us that, despite similar empirical formulas, Cumylamine runs cleaner in most condensation or addition routes compared to bulk amines like benzylamine or isopropylamine. Its steric profile reduces side reactions in crowded syntheses. Unlike tert-butylamine, Cumylamine offers better balance between nucleophilicity and leaving group tolerance in arylation steps. We’ve run direct head-to-head tests in our pilot plant: yields come out in favor of Cumylamine in multi-step syntheses, while purification requirements tend to drop. This makes a difference for process chemists looking to maximize yield while minimizing time spent on rework or column chromatography.

    Quality Control in Practice

    From our end, traceable quality assurance happens with real chemical handling, not just paperwork. We routinely examine each lot by HPLC and confirm identity through standardized IR and NMR spectra. Our plant’s in-process sampling ensures operators catch off-spec batches long before drums leave our facility. Feedback loops between manufacturing, QA, and customer technical teams help us flag trends and make fast course corrections. We don’t cut corners—raw material quality, storage, temperature control, and reaction order all get regular reviews.

    Troubleshooting and Challenges

    Working directly with Cumylamine production has taught us to respect its quirks. During hot, humid months, storage methods affect both clumping and trace byproduct formation. Our warehouse relies on climate controls, but the real gains come from regular retesting of stored lots and rotating inventory on a tight schedule. A few years ago, a customer flagged a strange off-odor in a drum; careful analysis showed a minute increase in residual solvent, leading us to upgrade our vacuum-stripping capabilities and verify airtightness of all containers. This kind of immediate response comes only from direct involvement in both production and customer service.

    We’ve also seen issues during extended transit—especially in containers held up at ports. Given that Cumylamine can pick up atmospheric moisture and develop minor color shifts, our team uses moisture-barrier liners and desiccant packs for every shipment. Not only does this protect product quality, but it gives downstream chemists one less source of unexpected variability in their syntheses.

    Safety and Environmental Steps from a Manufacturer’s View

    Our safety protocols were not simply inherited—they’re built on lived experience. Amine vapors irritate airways, and accidental spills need quick, reliable containment. Our plant uses dedicated exhaust ventilation, and all operators handling Cumylamine undergo annual fit tests for respirators. Emergency drills simulate real spills. By tailoring these safeguards to the quirks of Cumylamine handling, we’ve cut incident reports to a fraction of industry averages.

    We minimize solvent losses and recycle wherever feasible—experience shows that smart solvent management matters both for sustainability and the bottom line. Any aqueous waste containing amines routes through on-site treatment before disposal, avoiding downstream environmental disruption. Our facility tracks every kilogram of amine in and out, passing periodic inspections and keeping honest lines of communication open with local environmental authorities. The impact of this investment shows up in risk reduction and strong longstanding client relationships.

    Supporting Scale-Up and Process Transfer

    Collaborating with customers in commercializing a new process almost always reveals gaps between bench and plant. We provide real samples—drawn and sealed on the same line as full-scale shipments so R&D teams experience true production behavior. Many times, early access to plant-spec Cumylamine helps customers dial in reagent choices, cooling rates, and even stoppers or agitator speed. Our technical team often visits customer pilot plants, bringing practical advice on charging order or heating profiles gained from running the compound at ton scale.

    We also gather feedback from customers whose syntheses hit snags after switching suppliers. Most issues trace back to minor differences in impurity profiles or poorly documented storage. We keep electronic batch records stretching back over a decade, making it easy for returning customers to match a proven lot or investigate subtle changes. Few traders or resellers offer this kind of familiarity with the chemistry and logistics behind each shipment.

    Feedback and Real-World Problem Solving

    The best improvements in Cumylamine production have grown out of conversations with the users—chemist to chemist, not just order takers to logistics handlers. One pharmaceutical group once complained about a slight haze in solution; we traced it to a previously unnoticed trace of residual hydrocarbon solvent and rebuilt our purification step. On another occasion, a tech-transfer team wanted tighter reporting on amine content; we adapted our certs to include extra chromatographic detail, streamlining their compliance approval. Real solutions never arise from guessing or paperwork alone—they grow from shared experience in the field.

    We regularly see challenges from customers pushing their synthetic chemistry in new directions. Sometimes, process changes on their end introduce unforeseen interactions with our product—perhaps a new catalyst or isotope labeling step. We offer custom purification or micro-batch blending to support these trials. Success in these ventures owes itself to transparency and a shared willingness to test, adjust, and retest until both sides are satisfied.

    Long-Term Reliability and Supply Continuity

    Plant-scale Cumylamine production brings its own pressures—customers count on timely, predictable shipments to hit aggressive research or production timelines. We maintain on-site inventory buffers to accommodate unexpected surges in orders and keep lines running through routine maintenance or supply chain hiccups. Having in-house synthesis lets us pivot production to match demand or adjust lot sizes for seasonal fluctuations seen in industries like crop protection.

    Our team also works with customers facing tighter quality restrictions—whether shifting processes to comply with new environmental guidelines or developing formulations for regulated markets. Close coordination between our engineers, QC experts, and the end user's formulation chemists smooths the adjustments. On several occasions, we have revalidated product specifications alongside the customer, sharing technical packages and lab data to support regulatory filings. This hands-on partnership cuts down time to market and prevents costly rework after audits or inspections.

    Reflections on Industry Trends and Customer Needs

    Over time, we’ve noticed a growing demand for traceability and documentation, especially from pharmaceutical and fine chemical clients. Where a simple certificate of analysis once sufficed, customers now expect detailed impurity profiles, stability data, and even digital access to batch data. We’ve invested in laboratory information management systems to support this trend. The shift towards green chemistry and stricter safety legislation has encouraged us to seek out less hazardous solvents and improve waste treatment without undermining Cumylamine’s price competitiveness or reliability.

    Increasingly, customers ask about residual solvents, single-lot traceability, and compliance with environmental and safety directives. Our willingness to answer granular questions isn’t just about regulatory compliance—it marks a commitment to working relationships built on genuine trust. Our approach has been shaped as much by years of feedback and hands-on troubleshooting as by official standards.

    Closing Thoughts on Cumylamine from the Manufacturer’s Perspective

    For us, Cumylamine represents more than a line-item product—it’s a touchstone of chemical manufacturing done right. Reliable synthesis, real-world process control, and open dialog with users have allowed us to support projects ranging from small molecule drugs to diverse materials science breakthroughs. Our staff’s experience handling Cumylamine year after year shapes both our technical investment and our approach to working with partners across the globe.

    Our focus remains on transparently sharing what we know, embracing the troubleshooting grind, and standing behind every drum we ship. Whether teams work in R&D, process scale-up, or commercial production, we see Cumylamine’s value expressed in the confidence, flexibility, and speed that come with having a trusted manufacturing partner on the other end of the supply chain.