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2,4-Difluorophenyl Isothiocyanate

    • Product Name 2,4-Difluorophenyl Isothiocyanate
    • Alias DFPIC
    • Einecs 211-934-1
    • 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

    615991

    Productname 2,4-Difluorophenyl Isothiocyanate
    Casnumber 2746-96-9
    Molecularformula C7H3F2NS
    Molecularweight 171.17 g/mol
    Appearance Colorless to pale yellow liquid
    Boilingpoint 90-92 °C at 20 mmHg
    Density 1.308 g/cm³
    Refractiveindex 1.588
    Solubility Soluble in organic solvents (e.g., dichloromethane, ethanol)
    Purity Typically ≥ 98%
    Smiles C1=CC(=C(C=C1F)N=C=S)F
    Inchi InChI=1S/C7H3F2NS/c8-5-1-2-7(10-4-11)6(9)3-5/h1-3H

    As an accredited 2,4-Difluorophenyl Isothiocyanate 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 5 grams of 2,4-Difluorophenyl Isothiocyanate; tightly sealed with a screw cap and hazard label.
    Shipping 2,4-Difluorophenyl Isothiocyanate is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. It should be packaged according to hazardous material regulations, with appropriate labeling and documentation. The chemical must be transported at ambient temperature, away from incompatible substances, and handled by trained personnel using recommended safety procedures.
    Storage 2,4-Difluorophenyl Isothiocyanate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep away from moisture, acids, and incompatible materials. Store under inert atmosphere if possible. Proper labeling and secondary containment are recommended to prevent accidental exposure or leaks.
    Application of 2,4-Difluorophenyl Isothiocyanate

    Applications of 2,4-Difluorophenyl Isothiocyanate in Industrial Manufacturing

    2,4-Difluorophenyl Isothiocyanate serves as a specialized chemical intermediate widely adopted by manufacturers operating in advanced materials, pharmaceutical synthesis, and fine chemical production. Our facility supplies this raw material with stringent specifications, supporting stringent downstream quality and regulatory requirements. Below, we outline practical industrial scenarios, formulation parameters, integration points, and corresponding compliance considerations for this product.

    1. Pharmaceutical Intermediate for API Synthesis

    Major pharmaceutical companies utilize this raw material as a key building block during the synthesis of complex active pharmaceutical ingredients, particularly for targeted therapies and fluorinated compounds. Its bifunctional reactivity enables the installation of isothiocyanate and difluorophenyl moieties, which downstream chemists exploit in stepwise API construction. Cross-contamination risk management and exact stoichiometry control are critical in this scenario to assure final quality and meet regulatory requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU Guidelines for Good Manufacturing Practice (EudraLex Volume 4)
    • United States Pharmacopeia (USP) general chapters on API synthesis
    • Chinese Pharmacopoeia API requirements (latest edition)

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to amine or nucleophile coupling partners, adjusted for desired product yield and step efficiency

    Downstream process integration

    • Charged into multi-step API synthesis after key precursor purification, typically during the late-stage assembly of heterocyclic or aromatic frameworks

    Final product types

    • Active pharmaceutical ingredients (APIs), e.g., fluorinated kinase inhibitors, antimicrobial agents, cancer therapies
    • Regulatory filing reference materials

    2. Agrochemical Intermediate for Herbicide Production

    Large-scale agrochemical synthesis operations use 2,4-Difluorophenyl Isothiocyanate to construct active cores for a class of selective post-emergent herbicides. The electron-deficient difluorophenyl group enhances activity against target plants and improves metabolic stability. Manufacturers typically introduce the intermediate in a condensation or cyclization step under controlled temperature and pH, affecting downstream toxicology and product consistency.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management for Agrochemical Manufacturing
    • OECD Guidelines for the Testing of Chemicals (Section 1: Test No. 105 - Water Solubility, etc.)

    Typical usage ratio

    • 5–15% by weight in concentrated intermediate blends, depending on the target active’s molecular ratio and crop safety data

    Downstream process integration

    • Introduced during post-synthetic modification of heteroaromatic seedlings, often in the penultimate step to impart herbicidal selectivity

    Final product types

    • Commercial herbicide active ingredients (technical grades)
    • Granular, emulsifiable concentrate, and suspension concentrate pesticide formulations

    3. Advanced Polymer Synthesis Modifier

    In specialty polymer and advanced materials R&D, the isothiocyanate functionality of this chemical enables covalent grafting onto backbone polymers, introducing fluorinated aromatic units for improved thermal and chemical stability. Research institutes and manufacturers of high-performance coatings incorporate this material into custom copolymerization reactions or post-polymer surface treatments to enhance end-product properties.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for polymer ingredient registration and use
    • ISO 9001:2015 for specialty chemical manufacturing QC
    • RoHS Directive EU 2011/65 for certain electronics polymer uses

    Typical usage ratio

    • Typically 0.5–5 wt% relative to the polymer backbone; formulators optimize ratio based on desired fluorine incorporation and final material properties

    Downstream process integration

    • Employed during solution or melt polymerization, or in a reactive extrusion process, with in-process monitoring to ensure uniform reagent dispersion

    Final product types

    • High-performance fluorinated polymers
    • Specialty coatings and films for electronics, aerospace, and anti-corrosive applications

    4. Diagnostic Reagent Synthesis in Life Science Manufacturing

    Manufacturers supplying the life sciences sector use this material for site-specific labeling and functionalization of peptides, antibodies, and other biomolecules destined for in-vitro diagnostics. The isothiocyanate group reacts with primary amine residues to form stable thiourea linkages, supporting the creation of custom enzyme conjugates and fluorescent probes. Batch QC must track residual levels and reaction completeness to verify compliance with analytical reagent safety.

    Industry compliance standards

    • ISO 13485:2016 for IVD reagent manufacturing
    • US FDA 21 CFR Part 820 for Quality System Regulation (Medical Devices and Diagnostics)
    • Good Laboratory Practice (GLP) for in-vitro reagent quality

    Typical usage ratio

    • 1.1–1.3 molar equivalents per available amine group on peptide or antibody targets; excess depends on degree of labeling and downstream purification protocol

    Downstream process integration

    • Reactant addition occurs during post-purification, generally before final formulation, with real-time UV/Vis monitoring to confirm labeling progress

    Final product types

    • Labeled oligonucleotide and peptide probes for clinical assays
    • Conjugated enzyme-linked immunosorbent assay (ELISA) reagents

    5. Building Block for Specialty Dye Manufacturing

    Specialty dye producers incorporate this chemical when synthesizing fluorinated aromatic dyes for use in high-fastness textile colorants and inkjet pigment formulations. The difluorophenyl isothiocyanate group enhances shade intensity and dye stability in demanding end-use environments. Controlled addition and downstream distillation steps prevent byproduct formation and impact final color purity.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile chemical safety
    • ISO 14001:2015 Environmental Management for dye manufacturing
    • ZDHC Manufacturing Restricted Substances List (MRSL) compliance

    Typical usage ratio

    • 3–8 mol% as a dye core intermediate; adjusted to match color strength specifications and application substrate

    Downstream process integration

    • Reactant addition occurs at the nucleophilic aromatic substitution step, preceding azo-coupling or metallization stage

    Final product types

    • Fluorinated textile dyes for synthetic fiber coloration
    • Pigment concentrates for inkjet printers and industrial ink systems

    6. Fine Chemical Synthesis for Research Reagents

    Producers of research-grade analytical reagents and building blocks select this compound to introduce difluorophenyl isothiocyanate moieties in small-molecule libraries and probe development projects. Laboratories prioritize purity assurance, traceability, and reproducibility where analytical standards or mechanistic probes demand rigorous qualification criteria.

    Industry compliance standards

    • ISO 17034:2016 for Reference Material Producers
    • ISO/IEC 17025 for Laboratory Testing and Calibration
    • Chemical Abstracts Service Registry requirements for research chemicals

    Typical usage ratio

    • Stoichiometric to slightly excess (1.0–1.2 equivalents) relative to substrate, enabling full conversion in small-batch syntheses

    Downstream process integration

    • Dosed under inert atmosphere at the functionalization stage; often followed by chromatography and analytical purity confirmation

    Final product types

    • Analytical standards for chromatography and mass spectrometry
    • Custom molecular probes and research diagnostics
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    Certification & Compliance
    More Introduction

    2,4-Difluorophenyl Isothiocyanate: Reliable Chemistry Built from Experience

    Industry Roots and Practical Value

    For three decades, we've been involved in manufacturing specialty fluorinated organics from the ground up. Our clear-sprayed reactors and tightly controlled distillation columns have run countless batches of 2,4-difluorophenyl isothiocyanate. We know this material through and through. Nobody working from a catalog or acting as a middleman can match the perspective that comes from loading every drum and running every analysis yourself. Years working with hands-on research chemists and scale-up engineers have taught us exactly what makes this compound important—and why attention to detail during synthesis matters as much as price or documentation.

    Model, Identity, and Quality Control

    We produce 2,4-difluorophenyl isothiocyanate as a bench-verified, high-purity reagent, typically assigned our internal code DFPITC-824. Its CAS number is 30878-31-0; some folks in medicinal chemistry circles know it as the key partner in aryl thiourea frameworks. We manufacture it with a specification of at least 98% GC purity, and independent HPLC cross-checks. Every shipment leaves our plant accompanied by a full CoA stamped at our in-house lab, including water content by Karl Fischer and fluorine content by NMR for full transparency. Yield optimization efforts have focused both on minimizing dimer formation and on keeping traces of unconverted amine well below 0.2%.

    What Sets It Apart: Synthesis and Handling Insights

    Phenyl isothiocyanate analogues can look similar on paper, but once you start working at scale the differences show up quickly. 2,4-difluoro substitution brings kinetic reactivity toward nucleophiles that outpaces its 3,5-difluoro cousin—or unsubstituted phenyl isothiocyanate—by more than a factor of two in acylation-type reactions. Take peptide coupling: we’ve seen firsthand how 2,4-difluorophenyl isothiocyanate forms robust linkages to aliphatic amines in aqueous-organic conditions while most structural analogues lag behind or decompose. You’ll see tighter control over side product levels and fewer back-purification steps, even if pressure and temperature drift a bit.

    Unsubstituted and mono-fluorinated isothiocyanates often make promises but then gum up glassware with tar. Our 2,4-difluorinated grade flows clean, resists ambient moisture pick-up, and stores for more than 12 months at room temperature with almost no loss of reactivity. Trouble-shooting bulk batch output, we found that moisture sensitivity rose in singly fluorinated variants, which required special nitrogen packaging. With our material, even partial exposure to open air in the plant did not degrade the result, which means less rework and shipping delays.

    Application Experience: What Works and What Doesn’t

    Over the years, we’ve fielded calls from academic labs, pharma pilot plants, and startup biotech firms all searching for a reliable isothiocyanate for crosslinker synthesis, urea/thiourea formation in API development, or as a labeling intermediate. The feedback remains consistent: lower exotherm spikes, stronger selectivity for secondary amines, and cleaner removal of byproducts by flash chromatography. Our most experienced customers routinely order 25 kg lots long-term after finding that off-the-shelf grades don’t match our consistency from run to run.

    Some applications have surprised us. One materials science group used our 2,4-difluorophenyl isothiocyanate for surface modification of silica—reporting better immobilization efficiency than other isothiocyanates they’d tried. The reason relates to the electronic effects of the two fluorines, which alter both hydrophobicity and electron-donating properties on the isothiocyanate carbon. You might see the same principle in heterocycle formation or fluorescent tag synthesis, where trace moisture and side reactions spell trouble. We’ve even collaborated with an agrochemical group exploring novel ureas, which require minimal contamination to get regulatory acceptance; our material consistently helped them avoid technical setbacks later down the line.

    Production Realities and Problem-Solving Experience

    Lab-scale prep looks simple on paper, but scale-up exposes every weakness. Working at the plant scale, we’ve isolated how leftover chlorination reagents or poorly controlled temperature ramps cause trace byproducts that set off downstream complications. Our engineering tweaks—including multi-stage inline purification, specialized glass-lining, and active nitrogen blanketing—have cut process impurities in half. Environmental monitoring inside our production rooms confirms that critical control points have stayed tight for years, so customer rejections for contamination basically stopped. For sensitive end uses, we supply sealed bottles filled under inert gas, because an open-jar approach just ruins value for those seeking high assay reactivity.

    Shipping damage and packing failure threaten peroxides and sensitive organics. That experience drove us to invest in multilayer fluoropolymer liners, which resist both pinhole leaks and permeation under wide temperature swings during sea freight. We routinely ship to humid regions without cold chain headaches because of this packaging upgrade.

    Customer Feedback—And How We Use It

    Direct lines to our end users shape process improvements just as much as internal R&D. A few years back, several customers noticed batch-to-batch color drift, which we traced to a subtle variable in the crystallization solvent. By tweaking cooling curves and changing the final wash, we restored the bright white appearance users expect, without dropping yield.

    One large pharma company described how their R&D spent weeks revalidating HPLC methods every time they switched isothiocyanate suppliers. Since then, we’ve tightened our specification for related impurities to match their own analytics, which meant faster return to normal operations for them—and fewer headaches across a dozen similar buyers. This sort of real-time iterative improvement marks the difference between working with a volume manufacturer and a generic third-party trader, where frustrating delays often go unresolved.

    Sustainability Practices and Regulatory Landscape

    We have responded to growing pressure for greater transparency and greener chemistry. Step-wise solvent recycling, elimination of legacy chlorinated extraction solvents, and implementation of continuous-flow air scrubbing mean our facility routinely meets EU and North American emission limits. Routine audits cover worker safety around isothiocyanate exposure; all operators wear calibrated air-purifying respirators and monitored full-body protection. Our local water authority reviews our discharge treatments quarterly, and results have kept our plant running without serious permit delays or environmental incidents for over a decade.

    International end users require adherence to stricter import controls on aromatic isothiocyanates. We prepare full dossiers for customs or regulatory challenges, including detailed site of origin reports, impurity fingerprint data, and SDS documentation by batch year. We avoid licensing delays because our plant has built long-term reliability into every part of the operation. Our REACH pre-registration and compliance are confirmed by third-party consultants, so downstream legal or sourcing problems just don’t materialize.

    Differences from Commodity Organics

    There’s a real gulf between commodity phenyl isothiocyanates—often produced for agricultural feedstock at bargain-scale—and our specialty, bench-stable 2,4-difluorophenyl derivative. The best evidence comes from side-by-side reaction screening. Commodity lots might show visible oiling-out during evaporation, or give inconsistent chromatographic patterns. The high electronic activation by ortho- and para-fluorines in our product changes both lab behavior and shelf life. We guarantee moisture levels below 0.2% and routinely outperform litmus-test specifications set by institutional buyers. Our blending, packing, and QC teams are trained to reject anything showing even the faintest sign of yellowing—contrasted with the mixed-quality shipments too many labs have received from traders that lack in-house manufacturing.

    We’ve rescued clients from failed syntheses after poorly tracked cold-chain transport or fluctuating minimum order requirements from brokers. Credit for reliability goes to custom-built filtration setups assembled by our maintenance crew. It’s normal for third-party sellers to overlook the subtleties of small-scale filtration rates, but a scattered few milligrams of co-extracted phenol cost researchers weeks in lost experiments. By controlling every variable ourselves, we ship bottles where visual inspection matches spectral quality—no surprises, no “outlier” lots.

    Real-World Challenges and Our Solutions

    Problem-solving doesn’t stop after the material leaves our site. Some groups encountered unexpected clumping after lengthy storage. We investigated with parallel accelerated aging tests and switched anti-static handling to eliminate the issue. Others flagged packaging residue concerns on precision microbalance weighing. Here too, we rolled out a denser flask-washing protocol during filling, putting an end to cross-contamination worries. Rather than brushing off field reports, we integrate them into our next production cycle—with documented results.

    Storage and transport rarely generate headlines, but minor lapses ruin entire projects. Our isothiocyanate line faces regular quality demands from multinational buyers who track performance over many shipments. This level of feedback keeps our reliability higher than bulk dealers who lack both accountability and technical insight. All process information is traceable, from batch number to storage location; we maintain these records long after expiration to support user audits anytime supply chain transparency needs verification.

    Why Experienced Manufacturers Matter

    Fulfilling specialty chemical demand is more than a matter of shipping paperwork and matching CAS numbers. We scale up only after multiple pilot runs, confirming not just reactivity or purity, but also how the material stands up to real-world shipping, transfer, and use in customer hands. Decades of direct communication with users—the kind of practical, technical exchange missing from generic product listings—dramatically reduces project risk, especially for groups working under regulatory oversight or with sensitive IP. We’ve learned which types of drum liners break down under repeated opening, and which stoppers maintain tight seal integrity even after weeks of refrigerated storage.

    For buyers used to sifting through brokered, third-party traded material, the difference shows up in daily lab performance and big-picture reliability. Each bottle of 2,4-difluorophenyl isothiocyanate that leaves our site comes stamped with direct proof of quality, backed up by hands-on plant experience, so your project stays on track—from early discovery all the way through process optimization and into commercial validation.