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4-Amino-4'-Nitrodiphenyl Sulfide

    • Product Name 4-Amino-4'-Nitrodiphenyl Sulfide
    • Alias 4-Nitro-4'-aminodiphenyl sulfide
    • Einecs 221-001-9
    • 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
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    Specifications

    HS Code

    575726

    Product Name 4-Amino-4'-Nitrodiphenyl Sulfide
    Chemical Formula C12H10N2O2S
    Molecular Weight 246.29 g/mol
    Cas Number 19379-44-9
    Appearance Yellow to brown solid
    Melting Point 131-134°C
    Solubility Slightly soluble in organic solvents
    Purity Typically >98%
    Synonyms 4-Amino-4'-Nitrophenyl Sulfide
    Structure Diphenyl sulfide with amino and nitro substituents at para positions
    Smiles Nc1ccc(SC2=CC=C(C=C2)[N+](=O)[O-])cc1
    Inchi Key KRNNNQSLFLHIKE-UHFFFAOYSA-N
    Storage Temperature Store at room temperature

    As an accredited 4-Amino-4'-Nitrodiphenyl Sulfide 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 4-Amino-4'-Nitrodiphenyl Sulfide, tightly sealed, labeled with hazard symbols and product details.
    Shipping 4-Amino-4'-Nitrodiphenyl Sulfide is shipped in tightly sealed containers to prevent moisture and contamination. It is classified as a hazardous material, requiring proper labeling and documentation. The packaging follows chemical safety regulations, and transport is typically by ground or air freight, adhering to all international and local hazardous material guidelines.
    Storage 4-Amino-4'-Nitrodiphenyl Sulfide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Keep it away from direct sunlight, moisture, and heat sources. Ensure proper labeling and secure storage to prevent accidental release or contact. Use secondary containment if necessary to avoid spills.
    Application of 4-Amino-4'-Nitrodiphenyl Sulfide

    Applications of 4-Amino-4'-Nitrodiphenyl Sulfide in Industrial Manufacturing

    4-Amino-4'-Nitrodiphenyl Sulfide serves as a specialty intermediate with targeted use in high-value chemical manufacturing chains. Our plant-grade material supports advanced downstream synthesis in fields that demand consistent purity and controlled reactivity. Below, we highlight key industrial application areas, together with practical dosing ranges, process roles, industry standards, and real-world end products.

    1. Sulfur-Containing Azo Dye Synthesis

    Dye manufacturers apply this chemical as a diazo component for producing high-performance sulfur-containing azo dyes, valued for their brightness, fastness, and unique color shades. It supports colorant production for technical textiles, industrial coatings, and plastics pigmentation. Producers emphasize batch scheduling to synchronize amine sulfidation and diazotization stages, maintain quality via HPLC and TLC, and validate color fastness through accelerated aging tests.

    Industry compliance standards

    • Oeko-Tex Standard 100 for textile safety certification
    • REACH hazardous substance regulations (EC 1907/2006)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • ISO 9001 Quality Management System

    Typical usage ratio

    • 0.8–1.3 molar equivalents relative to the corresponding diazonium reactant, adjusted by targeted dye shade and reaction route

    Downstream process integration

    • Enters initial coupling sequence following in-situ diazotization or amination step
    • Requires slow addition under controlled pH (5.5–6.5) and temperature (0–5°C) to minimize side products
    • Post-coupling, proceeds through filtration and multi-stage washing to achieve target chroma and purity

    Final product types

    • Sulfur-bridged azo disperse dyes for polyester dyeing
    • Water-soluble direct dyes with high tinctorial strength
    • Acid dye blends for polyamide and wool textiles
    • Technical pigments for plastics and coatings

    2. Advanced Rubber Vulcanization Accelerator Synthesis

    Multipurpose rubber plants use this compound as a precursor in the synthesis of specialized sulfur-bridged accelerators. These accelerators ensure precise vulcanization kinetics, uniform cross-linking, and control of physical properties such as resilience, heat aging, and abrasion resistance. Chemists optimize feed ratios and reaction parameters to meet performance and safety specifications relevant to tire and industrial rubber goods.

    Industry compliance standards

    • ASTM D4671 Standard Classification for Rubber Chemicals
    • ISO 9001 and IATF 16949 (for automotive rubber components)
    • EU Directive 2000/53/EC (End-of-Life Vehicles Directive, relevant for rubber parts in vehicles)

    Typical usage ratio

    • 0.2–0.6% of total accelerator precursor mass in the masterbatch; batch chemists adjust based on the required vulcanization rate and end mechanical properties

    Downstream process integration

    • Integrated into multi-stage synthesis of sulfenamide and thiocarbamate accelerators via nucleophilic substitution followed by sulfidation
    • Downstream purification typically through solvent extraction and crystallization to meet color and composition specs

    Final product types

    • High-performance vulcanization accelerators (e.g., MBTS, TBBS derivatives)
    • Polymer-bound masterbatch for tire tread
    • Resilient elastomer compounds for conveyor belts and seals

    3. Synthesis of Specialty Ligands for Metal Complex Catalysts

    Catalysis developers employ this material for the stepwise creation of chelating ligands engineered for organometallic complexes. Its bifunctional amino and nitro groups facilitate selective anchoring on aromatic rings, creating active sites for catalyzing hydrogenation, coupling, and polymerization reactions. Synthesis architects maintain stringent impurity profiles and trace metal limits through chromatographic QC and controlled reaction atmosphere.

    Industry compliance standards

    • ISO 17025-accredited QC protocols for analytical traceability
    • ICH Q3D Elemental Impurity Guidelines (when intermediates are processed for pharmaceutical catalysts)
    • GMP Part II for fine chemical intermediates

    Typical usage ratio

    • 1.0 molar equivalent relative to central metal salt during ligand assembly; excess adjusted by solvent polarity, metal exchange yield, and target coordination geometry

    Downstream process integration

    • Introduced post-reduction (if nitro-to-amino conversion required), directly into ligand scaffold construction
    • Reaction staged under anhydrous and inert conditions (N2/Ar blanket) to prevent oxidation of functional moieties

    Final product types

    • Sulfur-containing organometallic catalyst complexes
    • Palladium and platinum ligands for advanced hydrogenation reactors
    • Base-metal catalysts for commodity polymer production

    4. Electron Donor Materials in Organic Semiconductor Research

    R&D laboratories and electronic material manufacturers select this molecule for use as a building block in constructing organic semiconductor layers. The electron-rich amino and withdrawing nitro substituents on a conjugated backbone enable precise electronic tuning, beneficial for organic field-effect transistors (OFETs) and photovoltaic applications. Process engineers adhere to hazardous chemical handling procedures and precise dosing to safeguard device reliability.

    Industry compliance standards

    • ISO 13485 (when integrated into medical diagnostic devices)
    • IEC 62321 guidelines for restricted substances in electronic materials
    • RoHS 3 Directive 2015/863/EU (Restriction of Hazardous Substances)

    Typical usage ratio

    • Typically 3–15% by weight of the organic electronic formulation; optimized in lab-scale prototyping based on film thickness and conductivity requirements

    Downstream process integration

    • Direct incorporation during solution casting or spin-coating for device active layers
    • Functional modifications (e.g., nitration, sulfonation) may precede blending, based on targeted electronic bandgap

    Final product types

    • Organic thin-film transistors for sensors
    • Active photoactive layers in flexible solar cells
    • Organic LEDs (OLEDs) and semiconductor testing substrates

    5. Intermediate for Agrochemical Active Ingredient Synthesis

    Crop protection manufacturers utilize this chemical as a key linkage moiety during the synthesis of complex organosulfur agrochemicals, notably those targeting soilborne pathogens and pests. Facility operators control dosing and contaminant profiles to minimize unwanted aniline/thiol byproducts that could impact downstream bioactivity. Regular batch validation secures product traceability for market entry.

    Industry compliance standards

    • FAO/WHO JMPR guidelines for pesticide specification and residue analysis
    • US EPA 40 CFR Part 180 Tolerance actions for pesticides
    • ISO 17034 Certified Reference Material procedures
    • GLP (Good Laboratory Practice) for pilot-scale evaluation

    Typical usage ratio

    • 0.5–1.2 molar equivalents depending on targeted pesticide backbone and crop use; formulation protocols adjust for active content and toxicity limits

    Downstream process integration

    • Introduced during the final or penultimate step of active ingredient assembly via aromatic nucleophilic substitution or acylation route
    • Followed by recrystallization and filtration to achieve approved purity profiles

    Final product types

    • Soil-applied fungicide active ingredients
    • Thioether-linked insecticidal actives
    • High-purity pesticide intermediates for further downstream derivatization

    6. Base Compound for High-Temperature Lubricant Additives

    Specialty lubricant formulators integrate this aromatic sulfide structure as a backbone for synthesizing antioxidant and anti-wear lubricant additives. Its thermal and chemical stability make it effective for automotive and industrial lubricants operating at elevated temperatures. Technical teams carry out stepwise alkylation, sulfonation, and formulation blending, verifying batch properties for performance and safety.

    Industry compliance standards

    • ASTM D6594 (High-Temperature Corrosion Testing)
    • API SN/CF for passenger car engine oils
    • SAE J300 (Viscosity Classification)
    • ISO 14001 Environmental Management (waste minimization)

    Typical usage ratio

    • 1.1–2.5% by weight in the additive concentrate; final content in finished lubricant depends on base oil composition and required oxidation resistance

    Downstream process integration

    • Added to reaction blend post-alkylation and prior to final distillation steps for additive concentrate manufacturing
    • QC teams confirm anti-oxidative functionality through differential scanning calorimetry (DSC) and tribometer testing

    Final product types

    • Engine oil antioxidants
    • High-load gear oil additives
    • Industrial hydraulic fluid protectants
    • High-temperature greases for heavy-duty equipment
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