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3-Methylbenzyl Cyanide

    • Product Name 3-Methylbenzyl Cyanide
    • Alias m-Tolylacetonitrile
    • Einecs 210-425-5
    • 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

    337333

    Chemical Name 3-Methylbenzyl Cyanide
    Synonyms m-Toluyl cyanide, 3-Methylphenylacetonitrile
    Molecular Formula C9H9N
    Molecular Weight 131.18 g/mol
    Cas Number 620-17-7
    Appearance Colorless to pale yellow liquid
    Boiling Point 248-250°C
    Melting Point -11°C
    Density 1.01 g/cm³
    Refractive Index 1.522
    Flash Point 112°C
    Solubility In Water Insoluble
    Odor Aromatic

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

    Packing & Storage
    Packing A 100g amber glass bottle, tightly sealed, labeled "3-Methylbenzyl Cyanide", with hazard symbols, lot number, and manufacturer details.
    Shipping **Shipping for 3-Methylbenzyl Cyanide**: 3-Methylbenzyl cyanide should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It must be transported in compliance with relevant regulations for toxic and flammable organic chemicals, typically under UN2811 (Toxic Solid, Organic, N.O.S.), with proper labeling and documentation to ensure safety.
    Storage 3-Methylbenzyl Cyanide should be stored in a cool, dry, well-ventilated area away from sources of ignition, strong oxidizers, acids, and bases. Keep the container tightly closed and clearly labeled. Store in a chemical-resistant, airtight container to prevent moisture absorption and inhalation risks. Ensure proper spill containment and access to safety equipment such as eyewash stations and fire extinguishers nearby.
    Application of 3-Methylbenzyl Cyanide

    Applications of 3-Methylbenzyl Cyanide in Industrial Manufacturing

    3-Methylbenzyl cyanide is an intermediate essential to several specialized chemical processes. Our manufacturing facilities supply this raw material with controlled quality to fit the needs of downstream sectors. Each application scenario described below outlines specific regulatory, formulation, and process integration details, reflecting direct industry experience and compliance requirements.

    1. Agrochemical Intermediate Synthesis

    Producers of advanced herbicides and fungicides use 3-methylbenzyl cyanide as a building block for the synthesis of selected phenylpyrrole and phenylacetamide derivatives. Regulatory compliance in this segment is strict, requiring traceable sourcing and batch-specific documentation throughout nitrile reduction or amide coupling processes. Integration occurs during the multi-step synthesis of active ingredients, where cyanide functionality is introduced at the early intermediate stage and subsequently modified to deliver targeted bioactivity. Adjustment of raw material input is based on the stoichiometry of the downstream coupling or reduction reaction and the purity specifications of the active agrochemical molecule. Final products include commercial-scale, trusted fungicides and selective herbicides for global crop protection markets.

    Industry compliance standards

    • EU Regulation 1107/2009 (Plant Protection Product Approval)
    • EPA FIFRA Registration Requirements (USA)
    • ISO 9001:2015 Quality Management during agrochemical manufacturing
    • REACH Registration & Safety Data Sheet (SDS) compliance for transport and handling

    Typical usage ratio

    • Batch addition at 0.8 – 1.2 equivalents relative to target active compound
    • Ratio adjusted based on process yield, purity of raw material, and downstream conversion step

    Downstream process integration

    • Added during initial or secondary intermediate synthesis under inert atmosphere
    • Subject to in-process monitoring (HPLC/GC) to meet residual cyanide thresholds before further coupling or reduction
    • Process vessels require corrosion-resistant design due to potential reactivity

    Final product types

    • Phenylpyrrole fungicides (e.g. fludioxonil intermediates)
    • Phenylacetamide herbicide intermediates
    • Specialty agrochemical custom molecules for contract synthesis partners

    2. Pharmaceutical Intermediate—Sartans and Antihypertensive APIs

    Several manufacturers of bulk pharmaceutical ingredients rely on 3-methylbenzyl cyanide as a precursor in the synthetic routes to angiotensin II receptor antagonists (sartans) and related antihypertensive compounds. The product enters the process either via catalytic hydrogenation or via subsequent Grignard or alkylation reactions. Precise weighing and batch traceability are enforced to maintain GMP compliance and minimization of residual impurities, particularly cyanide and related byproducts. Input ratios depend on the specific sartan variant; for example, certain intermediates require a 1:1 equivalent, while other syntheses adjust ratios to minimize side-reactions based on impurity profile. We support clients through validated analytical methods for cyanide residue analysis, allowing consistent qualification at the pharmaceutical manufacturing stage. The finished drug substances reach global regulated markets after solid form selection and stringent batch release testing.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (USA cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia Monograph 04/2018:2079
    • USP <467> Residual Solvents Testing

    Typical usage ratio

    • 1.0 – 1.3 equivalents relative to downstream coupling step, specified by medicinal route
    • Adjusted through pilot scale to match desired purity (≥99.5%) and yield

    Downstream process integration

    • Introduced after base-catalyzed cyanide alkylation or arylation
    • Pharmaceutical-grade closed systems with real-time QC sampling applied
    • Residue monitored for each batch to meet global drug master file requirements

    Final product types

    • Valsartan, Irbesartan, and related sartan intermediates
    • Other custom antihypertensive API starting materials
    • Pharmaceutical contract synthesis intermediates

    3. Fragrance Ingredient Intermediate

    Leading producers in the aroma chemicals sector incorporate 3-methylbenzyl cyanide primarily during the synthesis of specific nitrile-based fragrance notes. The compound enters transformation via catalytic reduction or hydrolysis, enabling further modifications to aldehyde or alcohol derivatives that underpin certain woody, green, or floral fragrance profiles. Regulatory regimes call for tight impurity controls and IFRA compliance on all input raw materials, particularly concerning residual solvent and side product levels in the final olfactory molecules. Usage ratios are tailored to the desired concentration of the cyanide-derived intermediate, with consideration for odor threshold and reactivity in subsequent reactions. The supply chain requires full batch documentation and allergen statement updates for each lot processed. Final outputs feed into compounders supplying the luxury and fine fragrance markets.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association)
    • REACH Annex XVII Restrictions for fragrance raw materials (EU)
    • Cosmetic Ingredient Review (CIR) guidelines for aroma compounds
    • ISO 9001:2015 QC and batch traceability

    Typical usage ratio

    • Ratio of 0.9 – 1.1 parts to target final aldehyde or alcohol intermediate
    • Tuned in pilot runs based on required purity and sensory analysis outcomes

    Downstream process integration

    • Fed into catalytic hydrogenation or hydrolysis units prior to distillation
    • Allergen profile and residual cyanide monitored through GC-MS during processing
    • Blending protocols incorporate in-line filtration to avoid carry-over contamination

    Final product types

    • Methyl-substituted benzyl alcohols for fragrance bases
    • Aldehyde aroma intermediates with specialty applications
    • Fine fragrance and personal care scent compositions

    4. Specialty Polymer Additive Production

    In advanced polymer manufacturing, companies use 3-methylbenzyl cyanide as a niche monomer precursor for specialty resins and crosslinkers, particularly in high-value adhesives and engineering plastics. Integration of the cyanide intermediate occurs through step-growth polymerizations or as a chemical modifier for functionalizing aromatic polyamides. Industry standards require documentation of purity, compliance to residual monomer content specifications, and adherence to regulatory controls on aromatic nitriles. Process operators adjust the monomer feed ratio according to molecular weight targets and desired mechanical properties. Our supply supports real-time specification adjustments and quality assurance protocols. The end-use products find application in electronics encapsulation, high-performance coatings, and advanced industrial adhesives demanding precise molecular structure control.

    Industry compliance standards

    • ISO 9001:2015 Certified Quality for additive supply
    • RoHS Directive (2011/65/EU) restriction for electronics and electrical polymers
    • ASTM D4066 for Polyamide Compound Standardization
    • REACH Annex XIV Authorization for monomer use

    Typical usage ratio

    • 0.5 – 2.0 wt% relative to primary monomer input for crosslinker applications
    • Adjusted based on polymer molecular weight target, viscosity, and performance benchmarks

    Downstream process integration

    • Charged during monomer premix or inline addition step
    • Quality checked for residual monomer and polymer chain length control
    • Batched under nitrogen atmosphere to prevent unwanted side reactions

    Final product types

    • Epoxy crosslinking additives
    • Specialty polyamide resins
    • Industrial adhesives for electronics and automotive applications
    • High-performance coatings with aromatic backbone
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