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R-Methyl 3-hydroxybutyrate

    • Product Name R-Methyl 3-hydroxybutyrate
    • Alias Methyl (R)-3-hydroxybutyrate
    • Einecs 629-727-2
    • 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

    944395

    Chemical Name R-Methyl 3-hydroxybutyrate
    Cas Number 3976-69-0
    Molecular Formula C5H10O3
    Molecular Weight 118.13 g/mol
    Purity Typically ≥98%
    Appearance Colorless to pale yellow liquid
    Boiling Point 63-65°C at 5 mmHg
    Density 1.056 g/mL at 25°C
    Optical Rotation [α]D20 +20° to +25° (neat)
    Solubility Soluble in organic solvents; limited solubility in water

    As an accredited R-Methyl 3-hydroxybutyrate 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 with a secure screw cap, labeled “R-Methyl 3-hydroxybutyrate,” includes hazard symbols and handling instructions.
    Shipping R-Methyl 3-hydroxybutyrate is shipped in tightly sealed containers, protected from moisture and light. It should be transported in accordance with relevant chemical safety regulations, including labeling as a laboratory chemical. Packages are cushioned to prevent breakage and are accompanied by appropriate safety documentation and handling instructions during transit.
    Storage R-Methyl 3-hydroxybutyrate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect it from light and moisture. Keep the storage area equipped with appropriate spill containment and ensure proper labelling to prevent accidental misuse or exposure.
    Application of R-Methyl 3-hydroxybutyrate

    Applications of R-Methyl 3-hydroxybutyrate in Industrial Manufacturing

    R-Methyl 3-hydroxybutyrate serves as an essential intermediate and functional building block in multiple advanced chemical manufacturing sectors. Our factory supplies this material with high enantiomeric purity, which supports downstream customers in pharmaceutical synthesis, specialty polymer production, chiral chemical processes, electronic material fabrication, and flavor formulation. Below, we detail major real-world industrial applications, integration points, compliance details, and final product categories.

    1. API Intermediate for Chiral Drug Synthesis

    This material plays a critical role as a chiral pool intermediate for fermentation-based or asymmetric synthesis of active pharmaceutical ingredients (APIs). It enables the introduction of R-configuration centers in statins, β-lactam antibiotics, and antifungal agents. Leading pharmaceutical companies utilize it during scale-up due to its high stereochemical integrity and bio-based origin, assisting GMP compliance in both early and late-stage processes.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients)
    • USP–NF Monographs and General Chapters for API synthesis
    • European Pharmacopoeia (Ph. Eur.)
    • FDA 21 CFR Part 211 (CGMP for Finished Pharmaceuticals)

    Typical usage ratio

    • 10–40 mol% as precursor, depending on target API’s stereochemical requirements; formulators adjust equivalence for coupling efficiency and downstream resolution steps

    Downstream process integration

    • Enters N-alkylation, reductive amination, or lactonization stages in multi-step API synthesis pipelines
    • Used after initial fermentation or chemical resolution for coupling or ring-closing reactions
    • Introduced pre-crystallization to enhance purity of active stereoisomers

    Final product types

    • Cardiovascular APIs (e.g., statin-class drugs)
    • Antibiotic intermediates
    • Antifungal medication precursors
    • Chiral auxiliaries for contract pharmaceutical manufacturing

    2. Biodegradable Specialty Polymer Precursor

    Downstream polymer producers employ this compound as a key monomer for the synthesis of polyhydroxyalkanoates (PHAs), especially when aiming to modulate crystallinity and degradation rates in environmental packaging and medical-grade bioresorbable plastics. Its enantiopurity supports controlled copolymerization with methyl 3-hydroxybutyrate and lactide, resulting in consistent molecular weight distributions and tunable physical properties.

    Industry compliance standards

    • EN 13432 (Compostability Requirements for Packaging)
    • US FDA 21 CFR 177.1520 (Polymers Used in Food Contact Applications)
    • ISO 10993 (Biological Evaluation of Medical Devices)
    • ASTM D6400 (Compostable Plastics Specification)

    Typical usage ratio

    • 5–30 wt% as comonomer, adjusted based on desired film flexibility and end-use hydrolysis profile

    Downstream process integration

    • Feedstock for ring-opening polymerization or direct co-polymerization with lactide and glycolide
    • Added during solvent casting, melt extrusion, or injection molding stages for medical devices or packaging films
    • Batch reactor input for block copolymer synthesis in R&D and commercial production

    Final product types

    • Bioresorbable sutures and medical implants
    • Compostable packaging films
    • Drug delivery microspheres
    • Biodegradable mulch or agricultural films

    3. Chiral Building Block for Agrochemical Synthesis

    Industrial agrochemical manufacturers value the material for its chiral methyl substitute, which enables the downstream synthesis of herbicide safeners and certain enantiomerically pure insecticide intermediates. It fits modern sustainability demands thanks to its bio-based origin and processability within existing catalytic asymmetric synthesis modules. Selection of production batch mandates adherence to specific residue and traceability requirements set by agrochemical regulators worldwide.

    Industry compliance standards

    • REACH (EC No 1907/2006) Registration for chemical safety in Europe
    • US EPA 40 CFR part 158 (Agrochemical Data Requirements)
    • OECD Environmental, Health and Safety Guidelines
    • ISO 9001:2015 (Quality Management)

    Typical usage ratio

    • 15–25 mol% as chiral precursor adjusted based on final molecule functionalization and residue analysis thresholds

    Downstream process integration

    • Utilized during asymmetric hydrogenation, chiral epoxidation, or esterification steps in actives production
    • Added post-halogenation to introduce required optical purity before product purification
    • Enters multi-step synthesis for synthesizing protected intermediates in herbicide manufacturing

    Final product types

    • Safeners for crop protection formulations
    • Chiral herbicide intermediates
    • Active insecticidal compounds with high stereoselectivity
    • Precursor additives for fungicide blends

    4. Fine Chemical Intermediate for Electronic Materials

    Producers of high-value electronic chemicals use this compound as a fine chemical intermediate for synthesizing specialty aldehydes and esters with defined stereochemistry. These compounds act as functional group modifiers in liquid crystal display (LCD) alignment layers and organic electronic materials. The purity and narrow isomer distribution align it with precise requirements for electronic material reliability and batch repeatability.

    Industry compliance standards

    • SEMI C3 (Specifications for Chemicals in Microelectronics Manufacturing)
    • RoHS II Directive 2011/65/EU (Restriction of Hazardous Substances)
    • IPC-4101 (Specification for Base Materials for Printed Boards)
    • ISO 9001:2015 (Quality Management for electronic industry)

    Typical usage ratio

    • 1–10 mol%, optimized for performance in downstream coupling steps and film-forming efficiency in OLED and LCD manufacture

    Downstream process integration

    • Integrated into synthetic route for chiral aldehyde or ester intermediates
    • Introduced in controlled environment reactors before final purification for electronic grade standards
    • Blended in additive packages for alignment layer formulation in display manufacturing

    Final product types

    • High-resolution LCD alignment agents
    • OLED material intermediates
    • Photoresist additives
    • Liquid crystal modulator components

    5. High-Value Flavor & Fragrance Ingredient Synthesis

    Specialty fragrance and food flavoring producers leverage the material as a chiral modifier in lactone and ester synthesis, yielding natural-identical flavor compounds for beverage, confectionery, and fine fragrance markets. As a precursor with GRAS-compliant potential, it supports tailor-made flavor notes and stability for non-alcoholic and dairy-based applications, with processers routinely verifying lot traceability and sensory purity.

    Industry compliance standards

    • FAO/WHO JECFA (Food Additive Evaluations)
    • US FDA 21 CFR 172.515 (Synthetic Flavoring Substances and Adjuvants)
    • EU Regulation 1334/2008 (Flavourings and Source Materials)
    • ISO 22000:2018 (Food Safety Management)

    Typical usage ratio

    • 0.1–2.0 wt% in final flavor or aroma formulations, adjusted by organoleptic profile and IFRA maximum permitted levels

    Downstream process integration

    • Applied in catalytic esterification or lactonization to develop fruity, creamy, or buttery flavor notes
    • Enters controlled batch reactors for volatile compound synthesis in flavor houses
    • Introduced pre-blending for custom flavor compound formation by GC-MS-guided adjustment

    Final product types

    • Natural-identical flavor enchancers for beverages and dairy desserts
    • Fine fragrance intermediates
    • Ready-to-use compound flavors targeting the F&B market
    • Functional aroma boosters for confectionery
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