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4-Benzyloxyphenyl Isothiocyanate

    • Product Name 4-Benzyloxyphenyl Isothiocyanate
    • Alias 4-(Phenylmethoxy)phenyl isothiocyanate
    • Einecs 656-740-0
    • 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

    807553

    Product Name 4-Benzyloxyphenyl Isothiocyanate
    Cas Number 5466-77-3
    Molecular Formula C14H11NOS
    Molecular Weight 241.31
    Appearance White to off-white solid
    Melting Point 69-71°C
    Solubility Slightly soluble in organic solvents
    Purity Typically >98%
    Smiles O=C=NSC1=CC=C(OCC2=CC=CC=C2)C=C1
    Inchi InChI=1S/C14H11NOS/c16-11-15-12-6-8-14(9-7-12)17-10-13-4-2-1-3-5-13/h1-9H,10H2
    Storage Conditions Store at room temperature, protect from moisture and light

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

    Packing & Storage
    Packing The 4-Benzyloxyphenyl Isothiocyanate is packaged in a 5-gram amber glass vial with a secure screw cap and clear labeling.
    Shipping 4-Benzyloxyphenyl Isothiocyanate is shipped in sealed, chemical-resistant containers to prevent moisture and light exposure. Packaging complies with local and international regulations for hazardous materials. Proper labeling and shipping documents are included to ensure safe transportation. Temperature control may be applied if required by the chemical’s stability profile.
    Storage 4-Benzyloxyphenyl Isothiocyanate should be stored in a tightly sealed container, protected from light and moisture. It should be kept in a cool, dry, and well-ventilated area, away from strong oxidizing agents, bases, and acids. Refrigeration (2–8°C) is recommended for long-term storage. Properly label the container and use personal protective equipment when handling the chemical.
    Application of 4-Benzyloxyphenyl Isothiocyanate

    Applications of 4-Benzyloxyphenyl Isothiocyanate in Industrial Manufacturing

    As a dedicated chemical raw material manufacturer, we focus on placing 4-Benzyloxyphenyl Isothiocyanate into specialized downstream sectors with proven, well-documented uses. Below, we present detailed application scenarios based on actual industry standards, established integration processes, and real-world customer formulations.

    1. Pharmaceutical Intermediate for Targeted Oncology Molecules

    Major pharmaceutical companies integrate this intermediate within multi-step synthesis routes to build sulfur-containing scaffolds in kinase inhibitors and other active pharmaceutical ingredients (APIs) designed for advanced oncology therapies. Regulatory expectations and process controls drive careful formulation at specified reaction stages. This raw material enters protected steps where the isothiocyanate group couples with nucleophilic species, ensuring direct access to core pharmacophores without byproduct complications. The manufactured APIs serve the production of targeted cancer therapeutics undergoing strict batch validation and traceability.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices (GMP) for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) standards for intermediates and residual solvents
    • European Medicines Agency (EMA) requirements for starting materials
    • Regulatory filing data (Drug Master File - DMF)

    Typical usage ratio

    • 0.8–1.2 molar equivalents per synthetic step, fine-tuned according to route-specific yield and reactivity studies

    Downstream process integration

    • Incorporated during the nucleophilic addition or condensation stages of multi-step pharmaceutical synthesis lines
    • Introduced as an isothiocyanate donor in parallel flow reactors to maintain reaction purity and selectivity
    • Isolated and removed in post-reaction purification before downstream formulation

    Final product types

    • Small-molecule anticancer APIs (especially custom kinase inhibitor libraries)
    • Advanced pharmaceutical intermediates supplied to GMP contract development and manufacturing organizations (CDMOs)
    • Regulatory-grade clinical trial batch drug substances

    2. Crop Protection Active Ingredient Synthesis

    Key agrochemical producers use 4-Benzyloxyphenyl Isothiocyanate as a coupling agent in the production of sulfur-based pre-emergent herbicide actives and select fungicidal scaffolds. This intermediate joins with aromatic amines or thiols to create heterocyclic compounds relied upon for broad-spectrum crop protection. Process integration focuses on maintaining high selectivity and minimizing impurity carryover, with scale-up controlled under chemical handling regulations specific to the agricultural chemical industry. Manufacturers optimize addition levels to achieve performance specifications without excess residual isothiocyanates in the finished product.

    Industry compliance standards

    • FAO/WHO International Code of Conduct for Pesticide Management
    • OECD guidelines for testing of chemicals (for environmental fate and residue)
    • ISO 9001 quality management systems for agrochemical synthesis
    • Chinese National Standards (GB/T 1604 for pesticides)

    Typical usage ratio

    • 5–12% by weight in coupling reaction mixtures, adjusted according to target active molecule and residual monomer tolerances

    Downstream process integration

    • Charged to reaction vessels following the initial aromatic skeleton assembly, serving as a core reactant for forming the isothiocyanate bond
    • Monitored by in-situ analytical methods for complete consumption and minimization of unreacted intermediates before formulation
    • Integrated into closed-systems to control emission and ensure personnel/environmental safety

    Final product types

    • Pre-emergent herbicide technical concentrates used in agricultural field applications
    • Systemic fungicide technical materials for seed and foliar treatment
    • Bulk actives shipped to formulation plants for end-use pesticide products

    3. Specialty Dye and Pigment Intermediate

    Manufacturers within the specialty pigment sector leverage this material as a key intermediate for synthesizing sulfur-containing azo and diaryl dyes, targeting high-performance sectors such as electronic color filters and specialty printing. The isothiocyanate group responds well to nucleophilic aromatic substitution on pre-activated aromatic structures, enabling custom chromophores with precise absorption profiles and thermal stability. Formulators must adhere to tight impurity specifications related to end-use application, whether targeting electronics, food packaging, or textile inks.

    Industry compliance standards

    • REACH (EC) No 1907/2006 chemical safety and registration for dye intermediates
    • ISO 9001:2015 process quality certification for pigment manufacturing
    • Oeko-Tex Standard 100 for textile dye applications
    • RoHS directive for electronic colorant use

    Typical usage ratio

    • 1.5–4% by weight in aromatic substitution stages, with ratio determined by end-use chromophore color depth and solvent compatibility

    Downstream process integration

    • Added to batch reactors after diazonium salt formation to complete azo coupling
    • Processed under controlled temperature and pH to maximize yield of target chromophores
    • Crystallized, purified, and dried prior to blending with binder resins and dispersants

    Final product types

    • High-purity digital inkjet dyes
    • Color dispersions for display filters
    • Solvent-resistant pigments for specialty coatings

    4. Biosensor Chemical Surface Modifier

    Producers in the analytical devices industry utilize 4-Benzyloxyphenyl Isothiocyanate to introduce stable, orientation-controlled functional groups onto sensor substrates, supporting covalent attachment of bio-recognition elements such as antibodies or enzymes. This provides robust binding for surface plasmon resonance (SPR) chips, microarray slides, and related diagnostic platforms. Manufacturers meticulously monitor coating uniformity and analyte retention, referencing sector-specific device protocols and biocompatibility criteria.

    Industry compliance standards

    • ISO 13485:2016 for medical device manufacturing
    • FDA 21 CFR Part 820 Quality System Regulation
    • ISO 10993 for biological evaluation of medical devices
    • Relevant application-specific chemistry and bioconjugation guidelines

    Typical usage ratio

    • Surface concentrations ranging from 0.01–0.2 mg/cm², adjusted to substrate area and desired probe immobilization density

    Downstream process integration

    • Applied to activated sensor surfaces via solution-phase deposition followed by controlled drying
    • Utilized in manual or automated batch coating lines for high-throughput chip preparation
    • Subjected to thorough rinsing and quality checks before further biomolecule conjugation

    Final product types

    • SPR sensor chips for real-time molecular interaction analysis
    • Biofunctionalized microarray slides used in genomics and proteomics research
    • Functionalized test strips for point-of-care diagnostic devices

    5. Fine Chemical Intermediate for Liquid Crystalline Material Synthesis

    Manufacturers of high-specification display materials and advanced optics use this isothiocyanate derivative in specialized synthesis of liquid crystal monomers, where its molecular geometry enables unique mesophase behavior and thermal properties. Integration is tightly controlled to guarantee molecular alignment essential for panel-grade performance. Specific addition levels must reflect both mesogen design and process yield, with purified intermediates advanced through esterification or etherification steps prior to formulation into commercial liquid crystal mixtures.

    Industry compliance standards

    • ISO 9001:2015 for production of electronic fine chemicals
    • RoHS and REACH compliance for materials entering electronics supply chains
    • Japanese JIS C7717 liquid crystal material regulations
    • Panel manufacturer-specific incoming inspection protocols

    Typical usage ratio

    • 0.5–6% molar ratio, calculated based on targeted mesogen structure, degree of polymerization, and batch scale

    Downstream process integration

    • Enters synthesis as a precursor in etherification or esterification reactions for building key aromatic units
    • Handled within inert-atmosphere reactors to prevent isothiocyanate group degradation
    • Isolated and purified to high specification before blending with other structurally compatible liquid crystal monomers

    Final product types

    • Monomer units for thin-film transistor liquid crystal display (TFT-LCD) applications
    • Tailored mixtures for specialty optical films
    • Alignment layer materials for advanced screen technologies

    6. Chemical Probe Building Block for Life Science Research

    Scientific reagent suppliers incorporate this reagent in the design and synthesis of covalent chemical probes used for protein labeling and activity-based profiling in proteomics. The unique isothiocyanate functional group enables selective conjugation to amines in peptides or proteins, supporting downstream high-throughput screening projects. Precision during probe assembly meets sector-specific purity requirements and avoids non-specific background signal. Process and supply conform with established chemical and biological quality management systems.

    Industry compliance standards

    • ISO 9001:2015 laboratory reagent production
    • Analytical traceability and COA requirements for life sciences
    • International Society for Biological and Environmental Repositories (ISBER) best practices
    • Material Safety Data Sheet (MSDS) and hazard communication compliance

    Typical usage ratio

    • Stoichiometric to 3-fold molar excess per target amine in bioconjugation protocols, optimized for protein or peptide target and labeling efficiency

    Downstream process integration

    • Combined with buffer-stabilized protein solutions under controlled pH for selective modification
    • Used both in small-scale batch labeling and semi-automated coupling systems
    • Purified via HPLC or ultrafiltration prior to biological application and analysis

    Final product types

    • Covalent protein and peptide probes for functional proteomics
    • Affinity tags for pulldown assays
    • Modified enzyme substrates for cell signaling research
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