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Ethyl 1,3-Dithiane-2-Carboxylate

    • Product Name Ethyl 1,3-Dithiane-2-Carboxylate
    • Alias NSC63833
    • Einecs 'EINECS 434-140-7'
    • 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

    291286

    Chemical Name Ethyl 1,3-Dithiane-2-Carboxylate
    Cas Number 87107-34-6
    Molecular Formula C7H12O2S2
    Molecular Weight 192.30 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 108-110°C at 14 mmHg
    Density 1.259 g/cm³
    Refractive Index 1.545
    Solubility Slightly soluble in water; soluble in organic solvents
    Melting Point -4°C
    Purity Typically ≥ 97%
    Smiles CCOC(=O)C1SCCSC1

    As an accredited Ethyl 1,3-Dithiane-2-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Ethyl 1,3-Dithiane-2-Carboxylate, 25 g: Supplied in a sealed amber glass bottle with tamper-evident cap, labeled with safety and chemical information.
    Shipping Ethyl 1,3-Dithiane-2-Carboxylate is shipped in tightly sealed containers, protected from moisture and light. It should be packed in accordance with chemical safety regulations, labeled properly, and handled using appropriate protective measures. During transit, it must be kept upright and stored in a cool, dry environment away from incompatible substances.
    Storage **Ethyl 1,3-dithiane-2-carboxylate** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, moisture, and incompatible substances such as oxidizing agents. Protect from light and heat. Proper labeling and secure storage are crucial to prevent accidental exposure and ensure chemical stability. Use appropriate safety measures when handling.
    Application of Ethyl 1,3-Dithiane-2-Carboxylate

    Applications of Ethyl 1,3-Dithiane-2-Carboxylate in Industrial Manufacturing

    As a dedicated manufacturer of Ethyl 1,3-Dithiane-2-Carboxylate, we support advanced intermediates production for diversified chemical industries. Below, find detailed application insights for well-established downstream sectors, including compliance frameworks, standard feed ratios, process roles, and actual end-product examples, all reflecting real manufacturing operations.

    1. Active Pharmaceutical Ingredient Synthesis

    Our material functions as a key intermediate in the multi-step synthesis of thiazole and pyrimidine analogues, especially those used for anti-inflammatory and antimicrobial pharmaceutical agents. Process chemists leverage its protective dithiane moiety for controlled functional group transformations in complex molecular scaffolds. Stringent adherence to pharma GMPs is essential at all stages, with analytical verification of intermediate purity before further conversion.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II guidelines
    • USP General Chapters — particularly requirements for residual solvents and related impurities
    • FDA 21 CFR 211

    Typical usage ratio

    • 10–25% of total reactant feed for the target API intermediate, adjusted based on batch scale and route efficiency

    Downstream process integration

    • Introduced during the carbonyl protection/deprotection step of API intermediate synthesis for heterocyclic core assembly
    • Subject to controlled addition under anhydrous conditions
    • Intermediate processed via chromatographic purification before final transformation to active molecule

    Final product types

    • NSAID precursor intermediates
    • Antibacterial heterocycle scaffolds
    • API building blocks for custom synthesis houses
    • Registered pharmaceutical substances (post further synthesis)

    2. Agrochemical Intermediate Production

    Within the agrochemical sector, producers use this compound for the preparation of sulfur-containing building blocks in fungicide and insecticide active ingredients. Its unique dithiane structure enables selective functionalization, streamlining route steps in crop protection substance R&D and scale-up. Project control involves strict traceability and the avoidance of residual solvent carryover in compliance with leading agrochemical acceptability guidelines, especially for European markets.

    Industry compliance standards

    • FAO/WHO Technical Specifications for Pesticides
    • ISO 9001:2015 Quality Management System
    • REACH regulation ((EC) No 1907/2006) for registration and traceability in Europe
    • Directive 91/414/EEC (EU plant protection product approval)

    Typical usage ratio

    • 5–18% by weight within multi-step agrochemical intermediate syntheses; batch ratios are process-optimized during scale-up validation

    Downstream process integration

    • Fed into alkylation or acylation steps to assemble dithiolane or pyrimidine moieties
    • Reacts with protected aldehydes/ketones under controlled temperature
    • Followed by extraction and phase separation before further esterification or cyclization

    Final product types

    • Sulfur-containing fungicide intermediates
    • Pyrimidine-based herbicidal scaffolds
    • Process intermediates for next-generation crop protection agents
    • Technical-grade actives for downstream formulation

    3. Specialty Chemical Building Block for Organic Synthesis

    In advanced organic synthesis laboratories and fine chemical manufacturing, Ethyl 1,3-Dithiane-2-Carboxylate serves as a masked aldehyde source for C–C bond formation, Grignard additions, or convergent fragment coupling. Its application is key to protecting sensitive carbonyls during challenging transformations. In these settings, strict analytical monitoring and quality assurance measures ensure contaminant levels remain within R&D and pilot plant tolerances.

    Industry compliance standards

    • ISO 9001:2015 for quality control of fine chemical products
    • GMP protocols for intermediates when supplying to regulated downstream (pharma/agro) partners
    • Hazardous chemical management per OSHA (29 CFR 1910.1200) and CLP Regulation
    • Internal analytical validation SOPs (NMR, HPLC)

    Typical usage ratio

    • 12–30% molar equivalents relative to coupling partners, based on reaction pathway and scale

    Downstream process integration

    • Used for carbonyl protection prior to C-alkylation or functional group exchange reactions
    • Subjected to hydrolysis, reductive cleavage, or nucleophilic substitution as required
    • Incorporated in multi-step syntheses for complex molecule generation in lab or pilot facilities

    Final product types

    • Custom specialty chemicals for R&D
    • Protected intermediates for medicinal chemistry
    • Labelled (deuterated or 13C) standards for analytical supply
    • Complex heterocycle frameworks for material science applications

    4. Fragrance and Flavor Synthesis Intermediate

    For the fragrances and flavors sector, this compound enables the manufacture of sulfur-containing aroma precursors and masking agents. R&D departments value its ability to introduce or protect labile functionalities during the assembly of complex aroma molecules. All operations must align with food safety regulations, including specific migration limits and allergen traceability where applicable.

    Industry compliance standards

    • FEMA GRAS specifications
    • IFRA Code of Practice (for fragrances)
    • European Regulation (EC) No 1334/2008 on flavorings
    • ISO 22000 food safety management (for food-related ingredients)

    Typical usage ratio

    • 3–10% of total synthesis batch, ratio defined by target molecule requirements; minimized to meet residue limits in end-use

    Downstream process integration

    • Added in reductive transformations to stabilize labile aldehyde groups
    • Removed after transformation to recover free carbonyls as part of finalization
    • Intermediate purified to match organoleptic and purity specifications before final blending

    Final product types

    • Sulfur-note flavor/fragrance precursors
    • Complex aroma chemicals for perfumers’ bases
    • Masked aldehyde building blocks used in high-end fragrance formulations
    • Food-compatible intermediates for specialty seasoning ingredients
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