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2-Methyl-5-Nitro-1H-Indole-3-Carbaldehyde

    • Product Name 2-Methyl-5-Nitro-1H-Indole-3-Carbaldehyde
    • Alias 2-Methyl-5-Nitroindole-3-Carbaldehyde
    • Einecs 630-593-0
    • 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

    679112

    Product Name 2-Methyl-5-Nitro-1H-Indole-3-Carbaldehyde
    Cas Number NA
    Molecular Formula C10H8N2O3
    Molecular Weight 204.18 g/mol
    Appearance Light yellow to brown solid
    Purity Typically ≥98%
    Solubility Soluble in DMSO, DMF, partially soluble in ethanol
    Storage Conditions Store at 2-8°C, protected from light
    Iupac Name 2-Methyl-5-nitro-1H-indole-3-carbaldehyde
    Smiles CC1=CC2=C(C=C(C=C2[NH]1)N(=O)=O)C=O
    Inchi InChI=1S/C10H8N2O3/c1-6-4-8-7(5-13)2-3-9(12(14)15)10(8)11-6/h2-5,11H,1H3
    Synonyms 2-Methyl-5-nitroindole-3-carbaldehyde

    As an accredited 2-Methyl-5-Nitro-1H-Indole-3-Carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with screw cap, labeled with chemical name, warnings, and batch details. Net quantity: 25 grams.
    Shipping **Shipping Description:** 2-Methyl-5-Nitro-1H-Indole-3-Carbaldehyde is shipped in tightly sealed containers, protected from light and moisture. It is transported as a laboratory chemical, compliant with relevant safety regulations. Ensure compatibility with other substances; handle as a potentially harmful solid. Consult MSDS for hazard, storage, and emergency guidelines before shipping or receiving.
    Storage **2-Methyl-5-Nitro-1H-Indole-3-Carbaldehyde** should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances such as strong oxidizers. Keep the storage area cool, dry, and well-ventilated. Store at room temperature or as indicated on the manufacturer’s label. Use appropriate labeling, and ensure access is restricted to trained personnel following standard laboratory safety protocols.
    Application of 2-Methyl-5-Nitro-1H-Indole-3-Carbaldehyde

    Applications of 2-Methyl-5-Nitro-1H-Indole-3-Carbaldehyde in Industrial Manufacturing

    As an experienced producer of advanced indole derivatives, we deliver 2-Methyl-5-Nitro-1H-Indole-3-Carbaldehyde that consistently meets the stringent requirements of global specialty chemicals sectors. The following application scenarios reflect real-world, scaled deployment of this intermediate in regulated downstream manufacturing. In each industrial sector below, we highlight major compliance regimes, typical plant formulation ratios, integration points in process design, and representative finished products.

    1. Pharmaceutical Intermediate for API Synthesis

    Several innovative pharmaceutical companies employ this carbaldehyde as a functionalized building block for small-molecule API synthesis, particularly in the production of heterocyclic therapeutic agents for oncology and CNS indications. Its electron-deficient indole scaffold allows chemists to tailor synthetic routes for challenging bond constructions. Downstream usage typically adheres to strict compliance protocols and is subject to full traceability in the API manufacturing chain.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Guidelines (EudraLex Vol 4)
    • 21 CFR Parts 210/211 (FDA)
    • Pharmacopeia monographs (USP, EP, JP, depending on API registration)

    Typical usage ratio

    • Applied at 0.1–0.7 molar equivalents relative to the target core scaffold, based on desired API yield and process step
    • Process chemists tailor charge amounts according to substrate reactivity and batch scale

    Downstream process integration

    • Introduced during the key condensation or cyclization stages of multi-step synthesis, following initial heterocycle functionalization
    • Often isolated or quenched before downstream purification and subsequent coupling reactions

    Final product types

    • Indole-based small-molecule APIs for targeted cancer therapies
    • Central nervous system active molecules (antidepressants, anxiolytics, anticonvulsants)
    • Advanced pharma intermediates for continued derivatization

    2. Agrochemical Raw Material in Fungicide Synthesis

    Leading crop protection formulators use this compound as an essential precursor in the multi-step synthesis of novel indole-derived fungicidal agents. Its precise electronic properties enable selective transformations, improving fungicide molecule stability and spectrum. Manufacturers must meet strict global regulatory standards, especially for products intended for multicountry crop application.

    Industry compliance standards

    • FAO/WHO Good Practices in the Manufacture and Quality Control of Pesticides
    • ISO 9001:2015 (Quality Management Systems in chemical plant operations)
    • REACH Regulation (EU) regarding substance registration and downstream use reporting
    • National pesticide registration guidelines (US EPA FIFRA, China ICAMA)

    Typical usage ratio

    • Commonly added at 3–6% w/w in the synthetic precursor blend
    • Adjusted within this range to modulate fungicide backbone substitution, based on target field spectrum

    Downstream process integration

    • Mixed with other specific indole and aldehyde reactants during condensation and halogenation steps in technical-grade active synthesis
    • Intermediate then progresses to formulation blending for finished crop protection agents

    Final product types

    • Systemic and contact indole-fungicides for cereals, rice, and specialty crops
    • Precursor for triazole-indole hybrid molecules targeting resistant phytopathogens
    • Formulated suspension concentrates and water-dispersible granules

    3. Dye Intermediate for Specialty Colorants

    Manufacturers in the fine dye industry employ 2-Methyl-5-Nitro-1H-Indole-3-Carbaldehyde to introduce chromophoric nitroindole functionality in the production of high-performance colorants. These specialty dyes, used extensively in both textile coloration and electronic display inks, rely on the accurate introduction of the carbaldehyde group for fastness and light stability. Consistent quality and documentation are required due to downstream exposure risks and export controls.

    Industry compliance standards

    • OEKO-TEX® STD 100 (Residual chemicals in finished dyes)
    • ZDHC MRSL (Chemical management in textile supply chain)
    • EU REACH Annex XVII (Restrictions on azo and nitro compounds)
    • ISO 9001 & 14001 (Quality and Environmental Management)

    Typical usage ratio

    • Between 2.5% and 7% of total batch mass, depending on target hue and subsequent reaction steps
    • Fine-tuned for molar balance in coupling or diazotization stages

    Downstream process integration

    • Directly charged into the condensation reactor with aromatic amines or coupling agents to form extended dye intermediates
    • Followed by further blending or sulfonation depending on the end-use sector (textile or inkjet)

    Final product types

    • Disperse dyes for polyester fibers
    • Sublimation inks for digital textile printing
    • Organic pigments for electronic display and imaging systems

    4. Building Block for OLED and Electronic Materials

    Producers of advanced materials for optoelectronics deploy this indole carbaldehyde in synthesizing specialized intermediates for organic light-emitting diode (OLED) emitters and charge transport layers. The nitro-methyl-indole core supports high electron mobility and photostability in device architectures. Traceability and purity are integral, governed by performance requirements and customer device qualification systems.

    Industry compliance standards

    • JEITA Standards for Electronic Materials
    • RoHS Directive 2011/65/EU (Restriction of hazardous substances)
    • ISO 9001:2015 for specialty electronic chemical production
    • Customer-specific device or display industry QC protocols

    Typical usage ratio

    • Ranges from 1.2% to 5% by weight in the active material precursor mixture
    • Adjusted based on layer thickness and molecular alignment requirements in device stack-up

    Downstream process integration

    • Feeds into the condensation or cross-coupling phase during oligomer or polymer synthesis for organic electronic layers
    • Resultant intermediates then used in vapor deposition or solution processing of device films

    Final product types

    • Emissive and transport layer molecules for OLED display panels
    • Active-layer precursors for organic photovoltaic (OPV) modules
    • Organic semiconductors for sensor arrays and flexible circuits

    5. Intermediate in Veterinary Drug Synthesis

    Manufacturers of veterinary pharmaceuticals include this advanced indole derivative as a critical intermediate for synthesizing new classes of indole-amide anti-infective agents. Its selective functional group reactivity enables controlled molecular modifications, which pharmacologists use for optimizing bioavailability and animal safety profiles. Veterinary API production must observe strict regulatory and pharmacopoeial supervision for batch release and documentation.

    Industry compliance standards

    • VICH GLs (Veterinary International Cooperation on Harmonisation guidelines)
    • Good Manufacturing Practice for Veterinary Medicinal Products (EU Directive 91/412/EEC)
    • Chinese Veterinary Pharmacopoeia or USP–Veterinary compendium where applicable
    • ISO 9001 Quality Management for pharmaceutical API plants

    Typical usage ratio

    • Specified at 0.12–0.45 moles per mole of primary amine substrate
    • Range depends on batch scale and target reaction selectivity for the specific veterinary API

    Downstream process integration

    • Dosed during acylation or alkylation route development of veterinary indole APIs
    • Subsequently purified via recrystallization ahead of downstream salt formation or complexation steps

    Final product types

    • Indole-based veterinary antibiotics
    • Oral tablet, injectable, and topical formulations for livestock and companion animals
    • Advanced raw material for further synthesis or formulation of antipathogenic agents
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