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(R)-(-)-3-Chloro-1,2-Propanediol

    • Product Name (R)-(-)-3-Chloro-1,2-Propanediol
    • Alias (R)-(-)-3-Chloropropane-1,2-diol
    • Einecs 604-018-00-4
    • 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

    579212

    Name (R)-(-)-3-Chloro-1,2-Propanediol
    Cas Number 57090-45-6
    Molecular Formula C3H7ClO2
    Molecular Weight 110.54
    Appearance Colorless to pale yellow liquid
    Purity Typically ≥98%
    Boiling Point 213 °C
    Melting Point -35 °C
    Specific Rotation -42° to -46° (c=1, H2O)
    Density 1.346 g/cm3 at 20 °C
    Solubility In Water Miscible
    Storage Temperature 2-8 °C
    Smiles C([C@H](O)CO)Cl
    Inchi InChI=1S/C3H7ClO2/c4-1-3(6)2-5/h3,5-6H,1-2H2/t3-/m0/s1
    Refractive Index 1.468-1.472

    As an accredited (R)-(-)-3-Chloro-1,2-Propanediol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of (R)-(-)-3-Chloro-1,2-Propanediol, tightly sealed with a tamper-evident cap and labeled.
    Shipping (R)-(-)-3-Chloro-1,2-Propanediol is shipped in tightly sealed containers to prevent leaks and contamination. It is transported under cool, dry conditions, following all relevant hazardous material regulations. Appropriate labeling and documentation accompany the package to ensure safe handling and compliance with local, national, and international shipping standards.
    Storage (R)-(-)-3-Chloro-1,2-Propanediol should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light and moisture. Use appropriate chemical-resistant gloves and safety equipment when handling. Store in a dedicated corrosive-resistant cabinet if available.
    Application of (R)-(-)-3-Chloro-1,2-Propanediol

    Applications of (R)-(-)-3-Chloro-1,2-Propanediol in Industrial Manufacturing

    As a direct manufacturer of (R)-(-)-3-Chloro-1,2-Propanediol, we supply industrial customers engaged in chiral synthesis for pharmaceuticals, advanced agrochemical intermediates, fine specialty chemicals, and optically active material production. Below, we outline key downstream applications based on actual end uses, including specific industry requirements such as compliance standards, recommended formulation ranges, integration steps in production, and target finished product types.

    1. Chiral Intermediate for Active Pharmaceutical Ingredients (APIs)

    Our material serves as a crucial building block for synthesizing certain optically pure beta-blockers, antiviral agents, and statins that require strict enantiomeric purity. In these pharmaceutical syntheses, it introduces the (R)-configuration into complex drug molecules, forming core structures via nucleophilic substitution and epoxide ring-opening under controlled conditions. The raw material ensures the production of APIs meeting international pharmacopeial standards for chiral purity and trace impurity control, especially in GMP manufacturing environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide
    • US Pharmacopeia (USP) and European Pharmacopoeia (Ph. Eur.) for APIs
    • FDA 21 CFR Part 210/211 (for US-bound medicinal substances)
    • Chiral impurity limits as per specific API registration dosser requirements

    Typical usage ratio

    • 0.7–1.2 molar equivalents relative to target API core, adjusted according to route efficiency, usually optimized for maximum chiral induction

    Downstream process integration

    • Charged during the asymmetric synthesis or resolution stage, following initial substrate activation; usually dosed under inert atmosphere and at regulated temperatures to control stereoselectivity and minimize byproducts

    Final product types

    • Chiral β-blockers (e.g., Esmolol, Labetalol)
    • Statin intermediates (e.g., Atorvastatin chiral building blocks)
    • Antiviral intermediates with defined absolute configuration
    • Specialty optically active pharmaceutical precursors

    2. Precursor in Agrochemical Synthesis (Herbicide & Insecticide Intermediates)

    Industries manufacturing advanced agrochemicals utilize this chiral intermediate for the construction of heterocyclic rings and functionalized side chains with defined stereochemistry. It supports the production of highly selective herbicide and insecticide candidates, where the (R)-configuration yields improved biological activity and crop safety profiles compared to non-chiral alternatives. Regulatory and environmental compliance demand traceability through the synthesis route.

    Industry compliance standards

    • FAO/WHO specification for pesticide technical materials
    • ISO 9001:2015 for agrochemical quality systems
    • EU REACH Regulation (Registration, Evaluation, Authorisation and Restriction of Chemicals)
    • OECD Principles of Good Laboratory Practice (GLP) for study data

    Typical usage ratio

    • 5–12% w/w in multi-step reaction sequences, determined by the synthesis design and desired chiral content in the final intermediate; precise control required to avoid racemization

    Downstream process integration

    • Added in the construction of chiral amino alcohol structures or during halohydrin opening in heterocycle assembly, frequently under phase-transfer catalysis for enhanced enantioselectivity

    Final product types

    • Chiral herbicide intermediates (e.g., aryloxyphenoxypropionate herbicides)
    • Insecticide synthetic building blocks
    • Plant growth regulator intermediates

    3. Fine Chemical Synthesis for Epoxy Resin Hardener Components

    For specialty epoxy systems, this material is incorporated as a chiral diol precursor, enabling the production of high-performance curing agents with improved reactivity and mechanical strength. Its use allows the formulation of hardeners tailored for specific end-use properties in electronics and advanced composites, where fine-tuned chiral induction can impact crosslink density and network uniformity.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for fine chemical manufacture
    • RoHS (Restriction of Hazardous Substances) Directive for electronics applications
    • REACH SVHC compliance for downstream distribution in Europe

    Typical usage ratio

    • 1–8% w/w based on total reactive resin content, adjusted for formulation balance between flexibility and hardness of cured epoxy network

    Downstream process integration

    • Introduced post-epoxidation under controlled pH, followed by cure adjustment using additional amines or anhydrides; typically blended with other diols or coupling agents to target specific mechanical properties

    Final product types

    • Epoxy curing agents for electronic encapsulation
    • High-performance composite binders
    • Specialty adhesives for automotive and aerospace applications

    4. Stereospecific Intermediate in Optically Active Surfactant Manufacturing

    Formulators in surfactant production use this intermediate when engineering surfactants with defined (R)-configurations, important for specialty cleaning agents with targeted interaction or improved biodegradability. (R)-(-)-3-Chloro-1,2-Propanediol allows controlled introduction of chiral centers, enabling downstream esterification or etherification under mild conditions. These chiral surfactants are favored in applications such as pharmaceutical excipients, high-purity detergents, and emulsifiers for sensitive processes.

    Industry compliance standards

    • ISO 22716 (Cosmetic GMP for surfactant components)
    • US FDA 21 CFR 172.860 (for excipient use)
    • OECD guidelines for biodegradability testing
    • REACH Regulation Annex XVII (limitations in certain detergents)

    Typical usage ratio

    • 2–6% w/w as a precursor for the chiral hydrophilic segment, with adjustments made based on chain length requirements and target critical micelle concentration (CMC)

    Downstream process integration

    • Undergoes initial substitution or esterification before further assembly with long-chain fatty acids or alkoxylates; final surfactant configuration relies on precise process temperature and reagent feed control

    Final product types

    • Chiral surfactants for pharmaceutical and biotech processing
    • Specialty emulsifiers for cosmetic and personal care
    • High-purity detergents for electronic manufacturing
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