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Dihydrocarvone

    • Product Name Dihydrocarvone
    • Alias DHC
    • Einecs 212-197-2
    • 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

    425452

    name Dihydrocarvone
    CAS_number 7749-10-8
    molecular_formula C10H16O
    molar_mass 152.23 g/mol
    appearance Colorless to pale yellow liquid
    odor Characteristic minty odor
    boiling_point 227-229 °C
    density 0.932 g/mL at 25 °C
    refractive_index 1.475-1.480
    solubility_in_water Insoluble
    storage_temperature Store at room temperature
    flash_point 93 °C
    SMILES CC1=CCCC(C(C)C1=O)C

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

    Packing & Storage
    Packing Dihydrocarvone is packaged in a sealed amber glass bottle, labeled clearly, containing 100 grams with hazard and safety information displayed.
    Shipping Dihydrocarvone is shipped in tightly sealed containers, compliant with international chemical transport regulations. It should be stored in a cool, dry, and well-ventilated area, away from incompatible substances. Proper labeling and documentation are required, and transportation must minimize exposure to heat, moisture, and direct sunlight to ensure safety and material integrity.
    Storage Dihydrocarvone should be stored in a tightly sealed container, away from light and moisture, in a cool, well-ventilated area. Keep it separate from oxidizing agents and sources of ignition. Store at room temperature and avoid exposure to heat. Proper labeling and secondary containment are recommended to prevent accidental spillage or contamination.
    Application of Dihydrocarvone

    Applications of Dihydrocarvone in Industrial Manufacturing

    Dihydrocarvone is a specialty monoterpenoid widely utilized across multiple industrial value chains for its unique chemical structure and reactivity. Our manufacturing process ensures tight batch control for downstream integration in regulated industries. The following sections outline specific, proven application fields and their technical and compliance considerations.

    1. Fine Fragrance Formulation

    Perfumery houses and aroma chemical suppliers utilize dihydrocarvone as a high-impact modifier to impart green, minty, and slightly woody olfactory notes in designer perfumes, colognes, and functional fragrances. Our technical grade supports precise formulation composition, integrating well with terpenoid and synthetic aroma materials in the compounding stage for niche and mass market blending.

    Industry compliance standards

    • International Fragrance Association (IFRA) Guidelines (latest amendment)
    • EU Regulation (EC) No 1223/2009 for cosmetic safety
    • ISO 9235: Aromatic natural raw materials - vocabulary
    • REACH (EC 1907/2006) registration for ingredient traceability

    Typical usage ratio

    • 0.01% – 0.25% content in finished fragrance concentrate, adjusted based on desired profile impact and threshold variability in target markets

    Downstream process integration

    • Metered dosing during top or heart note blending
    • Co-solubilization with other terpene derivatives before bulk compounding
    • Stability studies in ethanol/water matrices for long-term holding
    • Final QC using gas chromatography to confirm marker presence

    Final product types

    • Eau de parfum and eau de toilette concentrates
    • Personal care body sprays and deodorants
    • Household air fresheners and diffusers
    • Personalized fragrance kits and fine scent markers

    2. Food & Beverage Flavouring Ingredient

    Major food manufacturers and contract flavor houses integrate dihydrocarvone selectively as a minor component for minty, herbal, or green taste notes in hard and soft confectionery, chewing gum, and specialty beverages. The material is used under tightly regulated additive regimes, with full batch and traceability data, as part of declared natural or nature-identical flavoring systems. Our controlled purity profile supports global multi-jurisdictional flavor launches.

    Industry compliance standards

    • EU Regulation (EC) No 1334/2008: Flavourings and certain food ingredients with flavouring properties
    • FDA Title 21 CFR 172.515 (Flavouring Substances, GRAS List)
    • JECFA evaluations for monoterpenoid food ingredients
    • FSSC 22000 Food Safety Management System (for supply chain transparency)

    Typical usage ratio

    • 0.001% – 0.01% of total food mass, variable per regional regulatory maximum permitted levels and finished product matrix

    Downstream process integration

    • Dosed at pre-mix or post-cook stage for confectionery flavor maskers
    • Dissolved in carrier oils or propylene glycol during flavor compounding
    • Assayed by headspace GC/MS to ensure compliance with flavor load specs
    • Declarable as “natural flavoring” when sourced from renewable feedstock

    Final product types

    • Sugar-free chewing gum
    • Mental-lozenge flavored candies
    • Herbal tonic beverages and ready-to-drink teas
    • Minted chocolate or biscuit inclusions

    3. Agrochemical Intermediate Synthesis

    Leading crop-protection formulators and chemical process companies select dihydrocarvone as a strategic intermediate for the custom synthesis of pheromone analogs and biologically derived insect attractants. Its structural reactivity enables functional group interconversions under mild conditions, supporting the production of regulated biorational pesticides for integrated pest management solutions in orchard, vineyard, and greenhouse environments.

    Industry compliance standards

    • Good Manufacturing Practice (GMP) for Agrochemical Intermediates as per local regulatory authorities
    • OECD Principles for Industrial Chemicals and Pesticides
    • US EPA 40 CFR Part 158: Data Requirements for Pesticides
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products

    Typical usage ratio

    • 10% – 30% of total organic raw material charge in pheromone analog synthesis batches; adjusted based on reaction pathway selectivity and impurity tolerances

    Downstream process integration

    • Charged to esterification or hydrogenation reactors for functionalization
    • Coupled with other bio-derived compounds under catalyst activation
    • In-line compositional analysis using HPLC or NMR
    • Used as a precursor, not a final active, in technical concentrate formulations

    Final product types

    • Sex pheromone-based insect lures
    • Field-release dispensers for orchard pest control
    • Encapsulated attractant microcapsules
    • Agricultural monitoring trap baits

    4. Pharmaceutical Synthesis Building Block

    Specialty fine chemical producers and contract API manufacturers employ dihydrocarvone as a chiral source for stereoselective synthesis routes. Its bicyclic structure provides a basis for industrial-scale preparation of select intermediates for antitussives, anti-inflammatory candidates, and experimental neuroactive substances. We supply high-purity, GMP-compliant lots compatible with multistep synthesis and subsequent API purification.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and Ph. Eur. substance and impurity monographs (when applicable)
    • ISO 9001:2015 (Quality Management for chemical manufacturing)
    • FDA DMF registration (when required for US market submissions)

    Typical usage ratio

    • 20% – 70% molar equivalent as a main chiral scaffold, varying per synthetic step and optical purity requirement

    Downstream process integration

    • Charged to asymmetric hydrogenation or chiral resolution reactions
    • Serves as a precursor in acylation, halogenation, or reduction steps
    • Residuals monitored by enantiomeric excess (ee) analysis
    • Integrated into GMP-compliant batch records for traceability

    Final product types

    • Pharmaceutical intermediates for antitussives
    • Experimental CNS-active agent APIs (early candidate libraries)
    • Template molecules for patent-protected syntheses
    • Process R&D samples for scale-to-cGMP bridging

    5. Flavor and Aroma Encapsulation Matrix Component

    Encapsulation specialists in the food additives sector rely on dihydrocarvone as a functional compound in flavor encapsulation matrices, enabling controlled release and stability in heat-processed products. The molecule’s volatility and chemical compatibility allow targeted microencapsulation by spray drying or coacervation techniques, providing lasting aroma in consumer-ready powders and granules. Our supply meets required flavoring standards for food integration.

    Industry compliance standards

    • Codex Alimentarius General Standard for Food Additives (GSFA)
    • ISO 22000 Food Safety Management systems (ingredient sourcing)
    • FDA 21 CFR Part 170 (Food Additive Petitions for microencapsulated materials)
    • EFSA food flavoring regulations (EU food legislation)

    Typical usage ratio

    • 0.003% – 0.03% in encapsulated flavor premix; ratio set according to release profile requirements and masking effectiveness in finished products

    Downstream process integration

    • Dosed into emulsion or aqueous phase prior to spray-drying
    • Combined with gum Arabic, maltodextrin, or modified starch carriers
    • Heat-stability and release kinetics validated by accelerated shelf-life testing
    • Batch records align with allergen management and HACCP controls

    Final product types

    • Dry beverage and soup bases with mint or herbal notes
    • Powdered instant desserts
    • Encapsulated flavor granules for bakery
    • Dissolvable aroma tabs in beverage sticks

    6. Industrial Cleaning Agent Fragrance Modifier

    Formulators in the home and institutional cleaning chemicals sector select dihydrocarvone for its fresh, cooling sensory profile in floor care, hard surface, and wet wipe products. The material is solubilized into fragrance bases or detergent blends where it imparts lasting, non-residual scents even in alkaline or surfactant-rich systems. Manufacturers conduct compatibility and headspace tests to optimize user perception and regulatory alignment.

    Industry compliance standards

    • Detergents Regulation (EC) No 648/2004
    • IFRA guidance for household product applications
    • AISE guidelines for safe formulation and labeling
    • Global Product Safety Data Sheet (SDS) requirements

    Typical usage ratio

    • 0.02% – 0.15% in total fragrance component (not exceeding 0.1% in ready-to-use cleaning products); adjusted per desired intensity and surface residue avoidance

    Downstream process integration

    • Blended with natural or synthetic fragrance oils before detergent compounding
    • Stability tested in high pH and surfactant-rich matrices
    • Homogeneity checked by analytical GC
    • Evaluated by in-use panel for off-note suppression

    Final product types

    • Liquid and powder floor cleaners
    • Disinfectant wipes with fresh aroma
    • All-purpose and kitchen surface sprays
    • Odor-neutralizing toilet bowl and bathroom cleaners
    Free Quote

    Competitive Dihydrocarvone prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Dihydrocarvone: Building on Real Manufacturing Experience

    Understanding Dihydrocarvone from the Manufacturer’s Perspective

    As someone directly involved in the production of dihydrocarvone, every day begins with a sensory memory of its fresh, minty aroma drifting through the facility. Here, the focus has always been on attention to detail, constantly monitoring batch outcomes to guarantee quality from kettle to final drum. The product’s distinct nature—rooted in its structure and reactivity—sets it apart from other mint derivatives and cyclic ketones that otherwise might seem similar from a distance. Unlike distributors or agents who only ever see the packaged final material, people on this side of the industry get to witness—and solve for—the technical challenges that each lot presents, whether scaling up a new purification step or troubleshooting unexpected changes in feedstock consistency.

    From Start to Finish: What Sets Our Dihydrocarvone Apart

    Making dihydrocarvone is not simply about combining reagents and waiting for yields. The essential backbone comes from carvone, sourced from mint oils. Over several years, our team has refined hydrogenation conditions to avoid excessive overreduction, preserve the desired stereochemistry, and strip away any harsh sulfur traces that can taint the odor and affect downstream use. One miscalculated variable, and the final product’s color, purity, or even solubility can veer off target. From this work, it is now possible to offer customers consistent batches that really do retain a clean, crystalline appearance and a pure, robust character. It makes a huge difference whether dihydrocarvone is going into fragrance formulation, fine synthesis, or even as a chiral starting material for agrochemical intermediates.

    Model and Specification Details Shaped by Application Needs

    Through repeated feedback from our fragrance customers and research partners, we’ve come to focus production on two principal forms: {–}-dihydrocarvone and {+}-dihydrocarvone. Each enantiomer carries its own sensory fingerprint and reactivity pattern. In practice, most of the perfumery demand settles on the {–}-variant, because it mimics natural minty-fresh tones without introducing the harshness of some overly synthetic analogs. Customers weighing the {+}-enantiomer typically have requirements rooted in asymmetric synthesis, where a specific chirality may unlock a new blockbuster intermediate for active pharmaceutical ingredient development.

    The active ingredient concentration in every batch consistently falls above 98 percent GC purity, with water content kept tight below 0.1 percent by Karl Fischer titration. Appearance and odor are both checked during every lot finalization; any off-notes or haze instantly trigger a root cause review. This approach grew out of seeing how even small inconsistencies could ruin a fragrance batch or impair yield downstream. Our engineers rigged multiple inline sensors between reactors and distillation columns to track every phase’s progress, avoiding issues that only show up after final packaging. Running some of the larger batch reactors requires close coordination from the hydrogenation operator, whose instincts for temperature ramp rates often spell the difference between high purity and product waste.

    End-Use Considerations Learned Along the Way

    Dihydrocarvone’s biggest claim to fame rests on its versatility—and not just because the textbooks say so. Customers in the daily consumer goods sector, especially those chasing innovation in oral care, aromatherapy, and even home care products, regularly press for untarnished, high-purity material. One inadvertent sulfur byproduct or high boil-point tail, and the clean, minty flavor everyone expects is lost, prompting flavorists to look elsewhere. Years ago, batches occasionally picked up slightly burnt or earthy undertones if the hydrogenation catalyst wasn’t clean. Addressing that, we invested in upgraded catalyst handling, including pre-leaching and tighter filtration rigs. One result from these interventions: finished dihydrocarvone batches that integrate seamlessly into toothpaste tubes or air fresheners without that sharp “chemical” aftertaste found in goods made from lower-grade suppliers.

    Outside flavors and fine aromas, synthetic chemists enjoy the pressure-free handling that comes with our standard packing in corrosion-resistant drums, a lesson learned after seeing leachables crop up from poly liners during prolonged storage. For research and scale-up programs, being able to get both enantiomers without struggling through crystallization separations or high-cost syntheses reduces bottlenecks during lead candidate generation.

    Comparing Dihydrocarvone with Other Terpene-Derived Ketones

    Some buyers entering the market for minty notes or chiral ketones come with the idea that menthone, carvone, and dihydrocarvone can be easily swapped. Hands-on chemistry quickly dispels that notion. Carvone’s double bond next to the ketone changes its reactivity and, crucially, its aroma, introducing a spicier overtone that rarely melds well as a background note in oral care. Menthone’s profile brings more cooling, less green—sometimes too “camphoraceous” for refined blends. Dihydrocarvone emerges as a bridge, combining persistent mint freshness with a gentle fruitiness and a more rounded, natural mouthfeel. In synthetic applications, carvone’s alpha,beta-unsaturated ketone motif limits reduction choices, and menthone, while simpler, comes with fewer handles for asymmetric transformation. Dihydrocarvone’s reduced double bond gives a better platform for downstream derivatizations, especially if someone’s targeting hydroxy- or amino-functionalizations with retained chirality.

    For industrial users focused on environmental or regulatory pressures, dihydrocarvone delivers a clean compliance edge. Most of the off-odors and byproducts common with lesser grades stem from hasty or incomplete reaction workups. In our facility, repeated refinements in solvent recycling and vacuum distillation slashed residual contaminants. Finished goods easily align with tight European and North American standards for trace solvent residues—a fact regularly verified by our internal compliance team cross-checking with customer audits.

    Adaptability for Partners: From Pilot Trials to Mature Launches

    Early stage partners, particularly in the flavor and fragrance domain, often want to experiment at smaller scale before ramping up. Recognizing how unpredictable pilot results can sometimes be, our logistics team put together custom sample pack sizes, from small kilogram jars to half-drum sets. These early-stage collaborations sometimes bring unexpected technical hurdles—one customer reported mid-project that a competitor’s dihydrocarvone batches left behind odd spikes on their GC-MS trace. By opening facility doors for in-depth joint troubleshooting, together we uncovered a subtle side-product from poorly washed catalyst. These findings, rarely visible to traders or purely commercial operations, reflect a deeper commitment to continuous technical feedback and refinement.

    Once a partner settles on dihydrocarvone as a staple ingredient, larger shipments start flowing. Here, decades of hard-earned field experience prove critical: our shipping practices protect dihydrocarvone from temperature spikes and oxygen ingress, using custom thermal insulation and nitrogen headspace transfers where needed on transoceanic shipments. Building this infrastructure originally took time and trial, rescuing several would-be spoiled batches with same-day on-site repackaging. Now, customers often remark on the consistency—even after travel through difficult climates.

    Regulatory and Safety Considerations Tied to Real-World Production

    Handling, packaging, and logistical documentation for dihydrocarvone must always consider evolving regulatory and safety mandates. Staying ahead of new limits on residual solvents or potential impurities, plant personnel work closely with internal analytical chemists to upgrade detection routines. GC-MS, GPC, and even organoleptic test panels run as part of regular batch sign-offs, especially for food-grade inquiries. Any time a new regulatory requirement surfaces—whether from the EU, US, or an emerging Asian partner—the technical team updates test regimens, not out of obligation but out of pride. There’s no shortcut here: once, after a regulatory shift on minor-imurity thresholds, we reworked our hydrogenation sequence, sacrificing yield temporarily to reset compliance margins and eliminate customer risk.

    Material handling protocols matter just as much as batch recipe. Newer operators enter the plant for training and learn, firsthand, how to keep dihydrocarvone safe by maintaining tight drum seals, checking for vacuum integrity, and segregating incompatible materials. Real incidents, like a forklift ruptured container some years back, underlined the point that process learning never stands still in chemical manufacturing.

    Supporting a Dynamic Market Shift

    The dihydrocarvone market, like the broader specialty chemical sector, does not sit still. External factors—crop yield shifts for raw mint oil, changing consumer taste trends, and global supply chain hiccups—all feed into ongoing manufacturing strategies. Experienced staff developed hybrid raw material purchase programs, balancing forward contracts for mint oil with spot buys from vetted partners. Times when poor weather reduced mint harvest impacted prices and threatened continuity; building in extra supply buffers and preapproved backup sources for standard precursors allowed us to keep core customers supplied, even as other suppliers flagged “force majeure.” Outages at peer plants, and moments of product scarcity, elevated the importance of mature manufacturing that can flex output but never compromise on analytical quality.

    Changing regulatory and customer sustainability expectations led the process R&D team to invest in greener hydrogenation options. Piloting newer catalysts and solvent recapture equipment cut overall waste streams. These process improvements, drawn from both day-to-day production headaches and longer-term market trends, keep our dihydrocarvone competitive not just on the cost front, but on reliability and sustainability, both increasingly strong selection drivers for key accounts in Europe and North America.

    Challenges and Solutions Born from Direct Production

    Maintaining a tight product specification over hundreds of batches, in an environment with fluctuating raw material purity and ongoing process tweaks, brings its own set of complications. At times, seasonal shifts in mint oil isomer content forced adjustments to hydrogenation aggressiveness. On one occasion, reactor fouling from a new grade of issued catalyst led to lower conversions and risked a key delivery. By instigating round-the-clock operator check-ins and pulling weekly deeper analytics on intermediate samples, persistent issues were caught before material hit final drums. Direct, hands-on experience in these regard trumps any simulation or off-the-shelf SOP.

    Occasional feedback from an innovation-focused flavor house prompted a deep dive into low-level impurity build-up, spurring additional wash cycles post distillation. Only through real collaboration with end formulators did it become clear how minor “off” notes in early blends—often undetectable in QC but readily apparent to experienced flavorists—could be tracked back to handling and storage, not just process variables.

    Summary of Real-World Advantages

    The value customers realize from our dihydrocarvone comes down to three pillars learned from direct production: reliable purity that translates into predictable blending and flavor release, flexible supply that keeps innovation cycles moving even in uncertain market climates, and a robust safety and compliance program that confidently meets regulatory shifts. Whether entering a new consumer product segment, taking on a custom synthesis route, or simply seeking a worry-free, mint-derived building block, the cumulative expertise in our dihydrocarvone manufacturing strategy continues to deliver solutions rooted in careful process refinement and product stewardship.

    Future Directions and Ongoing Improvements

    Continuous improvement will always define the manufacturing journey for dihydrocarvone. Industry partners are already asking for new blends, customized concentrations, and tighter specifications to fit niche applications—demands easily understood when working at the heart of production, not far removed from the raw material, but close enough to the finished good to see its end-user value. Our technical team, in partnership with raw material suppliers and formulation labs, evaluates new process catalysts, explores circular solvent recovery options, and runs pilot studies for upcoming regulations or trace impurity headwinds.

    Much of the manufacturing know-how embedded in every batch reflects countless hours of fine-tuning, close calls, and productive collaboration with innovation-minded customers. Whether it’s understanding the chemistry, responding to regulatory shifts, or matching the nuanced preferences of flavorists and perfumers, making dihydrocarvone remains a dynamic, learned craft—shaped by both hard science and hands-on experience at scale.