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3,4,5-Trimethoxyphenyl Isothiocyanate

    • Product Name 3,4,5-Trimethoxyphenyl Isothiocyanate
    • Alias TMPITC
    • Einecs 642-245-1
    • 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

    459188

    Chemical Name 3,4,5-Trimethoxyphenyl Isothiocyanate
    Cas Number 3611-39-6
    Molecular Formula C10H11NO3S
    Molecular Weight 225.27 g/mol
    Appearance Yellow to brown solid
    Melting Point 100-103°C
    Solubility Soluble in organic solvents such as DMSO and ethanol
    Purity Typically >98%
    Smiles COc1cc(OC)c(N=C=S)c(OC)c1
    Inchi InChI=1S/C10H11NO3S/c1-12-7-4-8(13-2)10(11-6-15)9(5-7)14-3/h4-5H,1-3H3
    Storage Temperature 2-8°C

    As an accredited 3,4,5-Trimethoxyphenyl Isothiocyanate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 5-gram amber glass bottle, securely sealed, labeled with “3,4,5-Trimethoxyphenyl Isothiocyanate, C10H11NO3S,” and safety information.
    Shipping **Shipping Description:** 3,4,5-Trimethoxyphenyl Isothiocyanate is shipped in tightly sealed containers, protected from light and moisture. The package is clearly labeled, compliant with relevant chemical transport regulations. It is transported as a hazardous substance, requiring appropriate handling, UN-approved packaging, and documentation to ensure safety during transit, storage, and delivery.
    Storage 3,4,5-Trimethoxyphenyl Isothiocyanate should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong acids and bases. Keep the container tightly closed and protected from light and moisture. Use appropriate chemical-resistant containers to prevent leaks and contamination. Store in accordance with relevant chemical and safety regulations.
    Application of 3,4,5-Trimethoxyphenyl Isothiocyanate

    Applications of 3,4,5-Trimethoxyphenyl Isothiocyanate in Industrial Manufacturing

    As a specialized manufacturer of 3,4,5-Trimethoxyphenyl Isothiocyanate, we supply this intermediate to a focused segment of global industries where it supports controlled synthesis, stringent regulatory conditions, and advanced downstream formulations. Below we detail several real-world sectors where customers integrate this compound, together with essential technical specifications relevant to compliance, process utilization, typical ratios, and end-use production.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Kinase Inhibitors

    Major pharmaceutical synthesis operations utilize 3,4,5-Trimethoxyphenyl Isothiocyanate as a building block in targeted kinase inhibitor APIs, where its methoxylated aromatic ring enhances selectivity and reactivity for thioamide and thiazole moieties. Process chemists often employ it in late-stage functionalization of complex molecules under cGMP batch protocols, ensuring precise isothiocyanate incorporation through highly monitored steps for oncology and inflammation therapy compounds.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients)
    • European Pharmacopoeia (Ph. Eur.) and United States Pharmacopoeia (USP) monographs for APIs
    • 21 CFR Part 210/211 (US cGMP for Drugs)
    • REACH registration (EU) and K-REACH for chemical intermediates

    Typical usage ratio

    • 0.08–0.16 molar equivalents relative to second-stage substrate, fine-tuned to molar yield and process scale; reaction optimization data supports minor over-stoichiometric dosing in pilot lots.

    Downstream process integration

    • Integrated during heterocyclic ring formation or post-condensation conversions in mid- to late synthetic stepflows; introduced under nitrogen at 0–5°C with inert solvent (DMF, DMSO, or acetonitrile), followed by controlled workup and isolation.

    Final product types

    • Small-molecule kinase inhibitors for clinical and commercial oncology drugs
    • NCEs (new chemical entities) containing thioamide motifs
    • Thiazole- and thiourea-bearing pharmaceutical actives

    2. Advanced Agrochemical Synthesis: Sulfonylurea and Thiourea Herbicide Precursors

    Agrochemical manufacturers deploy the compound to form sulfur-containing moieties in the synthesis of high-selectivity herbicidal actives. Its well-defined reactivity with aminophenol intermediates and granular handle on product specificity mitigate side-chain impurities, supporting scalable batch and continuous flow protocols under multinational crop protection regulatory review.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • China Ministry of Agriculture Pesticide Registration Standards
    • ISO 9001:2015 Quality Management for Agrochemicals
    • OECD Guidelines on Herbicide Residue and Toxicology Testing

    Typical usage ratio

    • 0.12–0.24 equivalents relative to aromatic amines for thiourea formation; precise ratio governed by target molecule and pilot process adjustment for yield and purity.

    Downstream process integration

    • Fed at controlled rates in thiourea and sulfonylurea bond-forming reactions, typically within closed reactors with temperature- and pH-control modules to ensure batch consistency; subjected to aqueous or solvent extraction workflows prior to downstream formulation.

    Final product types

    • Sulfonylurea herbicides for cereal and rice applications
    • Custom thiourea crop protection actives
    • Low-volatile pre-mixed herbicidal concentrates

    3. Fine Chemical Intermediates for Organic Synthesis Labs and Process Development

    Leading fine chemical producers, as well as pharmaceutical R&D labs, use this compound as a selective isothiocyanate donor for routine and development-stage synthesis of heterocyclic scaffolds. Its specificity allows formation of highly functionalized isothiocyanates and carbothioamides under strictly monitored scale-up and kilo-lab batches, ensuring researchers and pilot plants can maintain traceability and reference-standard purity.

    Industry compliance standards

    • ISO 17034:2016 Reference Material Producer Requirements
    • OECD GLP for Chemicals and Pharmaceuticals
    • USP General Chapter <793> (Preparations for Laboratory Use)
    • CLP Regulation (EC) No. 1272/2008 Classification and Labeling

    Typical usage ratio

    • 0.10–0.15 equivalents per reactive site for reference material preparation; adapted depending on purity requirements and downstream solubility characteristics.

    Downstream process integration

    • Added during scaffold construction or in final derivatization stages; handled under fume hoods, weighed in gloveboxes or isolators for micro- and small-scale batch operations, enabling consistent reference synthesis standards.

    Final product types

    • Custom organic reference compounds for pharmaceutical R&D
    • Isothiocyanate-functionalized intermediates for chemical libraries
    • Validated laboratory standards for spectral and analytical use

    4. Dye and Pigment Intermediates in Specialty Colorant Manufacturing

    Specialty dye companies integrate this isothiocyanate into proprietary pigment formulations designed for advanced performance textiles and inks. Its reactivity profile provides superior linkage to aromatic amino-based chromophores, supporting colorfast, light-resistant final products across high-value coatings and labeling applications in demanding regulatory environments.

    Industry compliance standards

    • EN 71-3 (Safety of Toys – Migration of Certain Elements) for textile dyes
    • Oeko-Tex Standard 100 for textile processing
    • REACH Annex XVII (EU) — Substances of Very High Concern (SVHC) compliance
    • ISO 2846-1 (Pigments and Extenders for Printing Inks)

    Typical usage ratio

    • 0.06–0.11 mass percent in pre-condensation pigment paste, with formulation balance linked to target chromatic and stability profiles in the downstream matrix.

    Downstream process integration

    • Introduced during pigment or dye precursor synthesis, typically in closed kettles equipped for vacuum control and counter-current solvent removal, after initial aromatic condensation reactions are completed.

    Final product types

    • High-performance textile dyes for sportswear and uniforms
    • Light- and water-resistant ink pigments for industrial labeling
    • Specialty pigment dispersions for technical coatings and finishes
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