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α-Asarone

    • Product Name α-Asarone
    • Alias 2,4,5-Trimethoxy-1-propenylbenzene
    • Einecs 205-634-3
    • 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
    Specifications

    HS Code

    188983

    Cas Number 2883-98-9
    Molecular Formula C12H16O3
    Molecular Weight 208.25
    Iupac Name 1,2,4-Trimethoxy-5-prop-1-en-1-ylbenzene
    Appearance Colorless to pale yellow liquid
    Boiling Point 296°C
    Melting Point 14-15°C
    Solubility In Water Insoluble
    Density 1.045 g/cm³
    Synonyms trans-Asarone; (E)-Asarone

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

    Packing & Storage
    Packing α-Asarone, 25g: Supplied in an amber glass bottle with a secure cap, labeled with safety, purity, and handling instructions.
    Shipping α-Asarone should be shipped in tightly sealed, properly labeled containers, protected from light, moisture, and excessive heat. It must comply with local, national, and international regulations for handling and transport of chemicals. Suitable packaging ensures no leaks or spills, and shipping documentation should specify its hazardous nature and safety precautions.
    Storage α-Asarone should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Store at room temperature, ideally between 15–25°C. Ensure the storage area is secure and clearly labeled to prevent unauthorized access or accidental exposure. Protect from moisture and keep away from sources of ignition.
    Application of α-Asarone

    Applications of α-Asarone in Industrial Manufacturing

    As the original manufacturer of α-Asarone, we have supported industrial partners across multiple sectors by ensuring stringent quality compliance and reliable supply. Our production capabilities enable integration of α-Asarone into specific downstream formulations where its chemical properties meet defined process and regulatory demands. Below, we outline practical application scenarios based on current industry best practices and global market usage.

    1. Pharmaceutical Intermediates for Neurological APIs

    α-Asarone serves as a specialized intermediate in the synthesis of neurological active pharmaceutical ingredients, particularly anticonvulsant drugs. Formulation chemists incorporate this compound during the targeted functionalization of molecular structures leading to clinical actives such as those used in the management of epilepsy. Its phenylpropanoid backbone and methoxy substitution provide key reactivity for precise steps during multi-stage organic synthesis and facilitate improved final product yield and purity under GMP-compliant conditions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals
    • Pharmacopoeia requirements: USP, EP for relevant actives
    • Local DMF (Drug Master File) submission where required

    Typical usage ratio

    • Commonly 2–5% by weight per batch in multi-step synthesis, with variations determined by targeted yield optimization and purity controls

    Downstream process integration

    • Introduced as a reactive intermediate during stepwise condensation, alkylation or protection/deprotection processes in pharmaceutical fine chemical production lines

    Final product types

    • Active pharmaceutical ingredients (APIs) for neurological therapy
    • Epilepsy and anti-convulsant finished dosage forms (tablets, capsules)
    • Research-grade reference standards for laboratory validation

    2. Traditional Herbal Preparation Standardization

    Industrial processors of botanical extracts utilize α-Asarone as a defined chemical marker and sometimes as an enrichment agent when standardizing herbal products derived from Acorus species or related plants. Standardization ensures batch-to-batch consistency, allowing regulatory compliance for phytotherapeutic and nutraceutical products manufactured on automated extraction and blending lines. QA labs target defined ratios, balancing regulatory residue maxima and regional phytochemical limits.

    Industry compliance standards

    • WHO Guidelines on Good Agricultural and Collection Practices (GACP) for medicinal plants
    • ISO 19610:2017 (Traditional Chinese Medicine – Analytical Methodology)
    • Chinese Pharmacopoeia, Indian Pharmacopoeia controls for herbal raw materials

    Typical usage ratio

    • Typically standardized to 0.1–1.0% total content in finished extract, depending on regulatory upper limits, source material variance, and phytochemical profiles

    Downstream process integration

    • Dispersed into bulk concentrate during aqueous or ethanolic extraction stages, monitored by HPLC/GC for precise titration before granulation or spray drying

    Final product types

    • Botanical extracts standardized for supply to supplement and traditional remedy markets
    • Phytotherapy tablets and capsules
    • Ready-to-mix sachets containing specified herbal actives

    3. Specialized Fragrance and Flavor Compound Blending

    Manufacturers of flavor and fragrance compositions select α-Asarone for its nuanced aromatic profile that imparts a sweet, spicy nuance characteristic of Acorus–based volatiles. Commercial blenders integrate this compound within complex formulations for premium perfumery bases, incense, and, in certain jurisdictions, flavoring agents, strictly in line with legislative limits. Ingredient handling protocols address thermal stability and olfactory performance required by high-volume automated compounding plants.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • EU Regulation (EC) No 1334/2008 for flavoring substances (subject to restriction in some countries)
    • US FEMA GRAS List (pending regulatory review, with limits)

    Typical usage ratio

    • Seldom exceeds 0.01–0.05% in concentrated aroma blends; adjust according to IFRA or regional maximum concentration guidelines

    Downstream process integration

    • Dosed via metered pump systems into molten or solvent-blended bases during batch blending or continuous mixing; volatile release controlled by temperature and agitation profile

    Final product types

    • Perfume accords for fine fragrance and oriental-type scents
    • High-end incense stick and cone formulations
    • Traditional flavor bases in specialty seasoning (subject to national approval)

    4. Quality Control Marker in Herbal Origin Authentication

    Downstream users across herbal supply chains employ α-Asarone as a standardized reference compound for raw material authentication, using its specific chromatographic signature to verify botanical origin and prevent adulteration or substitution. This industrial marker system forms part of integrated quality management for both exported botanicals and local processing, aligning with growing regulatory scrutiny on traceability and identity preservation.

    Industry compliance standards

    • ISO 17025 (General requirements for the competence of testing and calibration laboratories)
    • Chinese Pharmacopoeia monographs for Acorus and related plants
    • AOAC International Herbal Supplement Testing Guidelines

    Typical usage ratio

    • Implemented as a calibration standard in the low ppm range (0.001–0.005%), for analytical method validation and residue threshold establishment

    Downstream process integration

    • Added as a spiking agent in HPLC, GC-MS, or TLC-based authentication protocols during incoming raw material inspection or end-point QC analysis

    Final product types

    • Herbal supplement certificates of analysis (COA) packages
    • Traceable authenticated botanicals for export and regulated OTC use
    • Laboratory proficiency testing kits

    5. Biologically Active Research Reagents and Analytical Standards

    Research organizations and commercial laboratories require α-Asarone as a high-purity standard and reagent for pharmacological investigation, metabolomics, and structural elucidation studies. Our GMP-grade production enables supply of consistent reference materials for use in controlled bioassays, receptor-ligand interaction studies, and metabolite profiling involving acorus-type phytomolecules.

    Industry compliance standards

    • ISO 9001:2015 (Quality management systems for laboratory reagents)
    • OECD Principles of Good Laboratory Practice (GLP)
    • USP Reference Standards requirements for critical quality attributes

    Typical usage ratio

    • Prepared as an analytical standard at 0.1–10 µg/mL for calibration curves; higher concentrations tailored for targeted bioactivity assays

    Downstream process integration

    • Diluted immediately before use into assay protocols or as spike-in standards for LC-MS, GC-MS, or in vitro cell-based experiments according to validated SOPs

    Final product types

    • Analytical reference standards for commercial and academic labs
    • Pharmacological tool compounds
    • Profiling kits for metabolite identification

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    Certification & Compliance
    More Introduction

    α-Asarone: Focused Quality for Specialized Formulations

    The Making of a High-Purity Ingredient

    For decades, our team has specialized in the production of α-Asarone, a naturally derived compound extracted mainly from Acorus species. In our line of work, the consistency of raw materials lays the foundation for a reliable manufacturing process. We source from fields that have shown stable crop yields and compound content year on year. After sourcing, our purification steps use vacuum distillation and fine chromatography — methods refined through experience with plant-based ingredients that don’t always behave predictably. These efforts have produced batches with a typical α-Asarone assay above 99.0%, as established by validated GC and HPLC analysis. Impurities remain well below standard industry allowance, both in breadth and in concentration. Every lot receives fingerprinting to deter adulteration or confusion with β-Asarone, which requires close analytical attention due to regulatory and safety distinctions between isomers. Our process doesn’t succeed on automation alone; each kilo passes hands-on checks by our crew, who have learned to spot issues that machines miss.

    Why α-Asarone Matters in Practice

    We began scaling up α-Asarone in answer to rising demand from customers in pharmaceutical synthesis and food flavoring research. Synthetic utility distinguishes α-Asarone from less versatile plant fractions and other phenylpropenes. The methoxy substitution pattern gives this molecule both stability and controlled reactivity, making it an essential intermediate for androgen receptor modulators, specific anticonvulsants, and varieties of flavoring agents where precisely tuned impact is crucial. Commercial food scientists trust our α-Asarone for its performance in delicate matrices—trace concentrations can generate recognizable woody-spicy notes without off-aromas. One supplier swapping in β-Asarone-rich batches from elsewhere might see their formulations flagged, either by internal QA or outside regulators, as β-Asarone carries toxicity concerns and tighter restrictions in many regions. From experience, we know small errors here disrupt years of research downstream.

    Purity and Compliance—From Field Through Final Product

    We operate under the mandates of good manufacturing practices (GMP), as required by food, beverage, and pharma clients. Our documentation practices grew from years investing in batch-traceability software and hands-on record keeping. In plant-origin chemicals, pesticide and solvent residues can present major risks, so we’ve chosen to exceed minimum regulations for European and Asian markets. By prioritizing clean, primarily ethanol-based extraction before advanced purification, we avoid persistent off-flavors and mitigate risk of non-volatile contaminants. Testing for heavy metals, polyaromatic hydrocarbons, and residues happens every cycle, using ICP-MS and GC-MS platforms trusted by regulatory agencies. Not all suppliers run these checks routinely, but after dealing with contaminated lots in our industry’s past, we don’t take shortcuts. We cooperate regularly with outside reference labs, whose data corroborates our certificates of analysis. This extra layer of verification assures partners during their own product audits.

    Distinguishing α-Asarone from Other Similar Compounds

    We’ve faced repeated questions about the difference between α- and β-Asarone. In practice, our customers focus on α-Asarone due to its more favorable toxicological profile and its approval for use in a wider range of end products. β-Asarone, another component from Acorus, appears similar but differs in double-bond configuration. Regulatory agencies in Europe, North America, and parts of Asia set strict limits for β-Asarone in consumables, often below 1 ppm. α-Asarone does not share these limits, so batches with high α-to-β ratios pass more easily through pre-market checks. Customers looking to formulate into pharmaceuticals, dietary supplements, or food products rely on our high α/β selectivity. We provide certification for each shipment, following ongoing regulatory advisories to avoid border holds or product recalls. On occasion, even “pure” plant extracts from third parties have failed, due to overlooked β-Asarone content. We see this as a result of using crude purification, and our own experience has shown that finer separation delivers safer, more easily approved ingredients.

    Consistency in Large-scale Supply

    Scaling a niche phytochemical like α-Asarone brings real challenges. Harvest size, climate, and genetic drift in Acorus populations all influence the yield from year to year. We learned the hard way that single-origin supply chains risk price spikes and shortages if droughts or pests migrate through one region. To guarantee supply continuity, we work with a network of growers across different provinces, each subjected to identical quality standards. Our processing plant’s modular setup—multiple independently controlled reactors and chromatographic columns—lets us keep output steady even as raw material loads fluctuate. Teams regularly recalibrate equipment and update SOPs after each harvest round. Batch-to-batch logs stretch back over a decade, giving our partners a detailed record for compliance or recall tracking. Where unpredictable harvests threatened fulfillment in past years, our expanded relationship with farmers and diversified contracts now buffer both us and our clients from supply shocks. Chemical manufacturing lives or dies by predictable input and output; our direct oversight prevents unpleasant surprises.

    Usage Trends and Application Feedback

    Our customers come mostly from three fields: pharmaceutical development, specialty food and beverage, and academic research involving natural product synthesis. In the pharma sector, α-Asarone attracts attention for two reasons: synthetic handle and safety margin. Many research teams cite the methylenedioxyphenyl core as an entry point into CNS-active compounds with anticonvulsant or neuroprotective potential. Small volume contract manufacturers have scaled proprietary reactions starting with our α-Asarone batches, reporting both high chemical yields and fewer purification hurdles than when operating with lower-purity or isomer-contaminated stocks. Feedback also highlights reproducibility: a few milligrams variation between lots can affect research outcomes, and our tight batch tolerances cut wasted experiments.

    Flavor houses and beverage brands see α-Asarone’s value in moderate use levels, targeting niche recipes where a character spice note is in demand. We’ve worked with formulators who fine-tune aromatization in premium bitters or botanical gins, citing tight sensory control. Lower-quality or mixed-isomer materials have produced “off” or metallic notes in trials, sometimes resulting in expensive batch discards. Our technical support teams have visited client plants to assist with dissolution issues and formulation compatibility—many partners want sensory stability even after months on warehouse shelves. The most insightful suggestions often come straight from mixologists or product developers tinkering with new trends. These real-world insights get fed back into how we fine-tune our own purification parameters year by year.

    Academic labs are frequent customers too. We notice their orders peak during grant season, as institutions run comparative studies on structure-activity relationships or toxicity. Our transparent supply records make paperwork smoother for research compliance bodies, while assured traceability lets scientists focus on the experimental run, not chain-of-custody headaches. Well-designed academic studies sometimes identify by-products missed by older analytical controls; we welcome this feedback, seeing it as mutual quality improvement.

    Addressing Quality Control Issues in the Marketplace

    Over the years, many industry concerns have centered on batch integrity and accidental isomer substitution. Some foreign extracts reaching the market have shown inconsistent profiles due to mixed harvesting or incomplete purification. End users receiving these irregular lots describe erratic performance, unreliable scent, and, more critically, regulatory trouble tied to β-Asarone contamination. We’ve seen products recalled due to mislabeling or missed β content, leaving downstream brands exposed to legal risk and supply interruption. These recurring problems often result from over-reliance on bulk trading intermediaries who lack the in-house labs or field experience to detect subtle flaws before export.

    In our plant, we avoid such pitfalls with a full-spectrum approach. Each harvest batch gets GC, HPLC, and, in some cases, NMR verification before and after purification. Veteran chemists check lots not just for numbers on a printout, but by matching profile data and physical evaluation. We conduct random spot-checks of containers to catch any transport damage or storage mishaps that could alter chemical composition. Documentation stays attached to every drum, from processing through shipment. All these steps grew out of past troubleshooting, where we learned that investing resources up front prevents delays, sunk costs, and disputes later. Customers who have switched from lower-priced but inconsistently sourced α-Asarone report fewer quality holds, smoother audits, and reduced waste.

    Environmental Responsibility in Production

    As consumer expectation and regulations evolve, we’ve integrated more stringent environmental controls into our processes. Several years back, solvent recycling at the plant was limited to cost-driven motivations—today, we employ closed-loop systems, reducing solvent losses to nearly negligible volumes per batch. This cuts both environmental impact and overhead. Wastewater is treated via multi-phase filtration and tested for chemical residues, ensuring outflow meets—often exceeds—regulatory baselines for industrial zones. We source biomass from agricultural partners who follow integrated pest management, cutting synthetic pesticide use to safeguard both product purity and soil long-term health. The routine checks we perform for agrochemical residues support these claims, building trust among eco-conscious clients. Our ongoing audits by third-party groups and open sharing of environmental data reflect a deepened commitment, not just a box on a compliance form.

    Supporting Partners with Data and Technical Knowledge

    Our long-term partnerships thrive on sharing technical know-how, not just selling an ingredient. Clients developing new formulations often ask for insight into α-Asarone’s thermal stability, solubility in new solvents, or compatibility with excipients. Over time, our technical team has built a resource base of application notes, stability data, and process optimization guidelines, updated with every significant formulation challenge faced by partners. Downstream audits—whether by food and pharma inspectors or enterprise risk teams—tend to pass quickly when supported by our traceability, validated analyses, and open documentation. Consulting on protocol design, including safe handling, formulation compatibility, and compliance with new labeling requirements, adds practical value for end users. Years of fielding questions from regulatory teams and plant chemists shape how we train new staff. Many of our collaborative projects with universities or research groups stem from our readiness to support proposals or share non-confidential technical data.

    Thinking Ahead: Meeting Evolving Market Standards

    The marketplace for natural and synthetic intermediates like α-Asarone continues to shift. Regulatory scrutiny has ratcheted higher; new pharmacopoeial guidelines sometimes change with little notice, and food ingredient blacklists expand as new research emerges. We stay alert to these developments by keeping close ties to both major clients and regulatory consultants across markets. Regular updates from food safety authorities, regional chemists’ associations, and customer QA teams drive our updates to specifications and documentation. Suppliers who lag behind, relying on stale methods or paperwork, can no longer keep up. Our own experience with market disruptions—a few years ago, one export route closed due to tightened contaminant rules—taught us to always have alternatives ready.

    Recycling and waste reduction goals will likely intensify, and end users are asking for more than certifications—they expect genuine proof of sustainability. We have responded by investing in scalable greener technologies and disclosing our sustainability metrics, even in regions where such detail is not yet mandated. Some partners have requested carbon footprint data as part of their supplier vetting; we have supplied lifecycle analyses and worked with them to phase out high-impact packaging materials. This sort of collaboration works both ways; some clients ship back drums for reconditioning and reuse, and we credits these returns in our replenishment contracts. It’s a model that cuts cost and environmental strain, made possible by close account management and transparent, cooperative relationships.

    Challenges and Future Steps

    Producing α-Asarone to top-standard purity, safety, and consistency remains demanding. Volatile weather, shifting pest populations, and even seed genetic drift can alter raw material profiles. Scaling technical support to meet the rising number of specialty customers keeps our R&D teams busy—each unique application can surface new technical or analytical puzzles. The global landscape for chemical regulation now demands real-time flexibility, as rules for one country or sector shift every year. Training and retaining analytical chemists, and equipping them with the best tools, draws significant ongoing investment.

    Continual process improvement, technical transparency, and active listening to our partners’ challenges have shaped our approach, from the farm to the final packaged drum. We know from years of feedback, troubleshooting, and shared wins and losses that specialty chemicals like α-Asarone will keep evolving in both application and scrutiny. The manufacturers who adapt, innovate, and maintain open lines of communication with both suppliers and clients will remain ahead—not just as vendors, but as reliable partners in development.