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1-Pyrrolidinobutyronitrile

    • Product Name 1-Pyrrolidinobutyronitrile
    • Alias 4-Cyanobutyrolactam
    • Einecs 629-073-5
    • 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

    215714

    Cas Number 3470-98-2
    Molecular Formula C8H14N2
    Molecular Weight 138.21
    Iupac Name 1-pyrrolidin-1-ylbutanenitrile
    Appearance Colorless to pale yellow liquid
    Boiling Point 246-247 °C
    Density 0.96 g/cm3
    Refractive Index 1.456
    Flash Point 102 °C
    Solubility In Water Low
    Melting Point -14 °C
    Smiles C1CCN(C1)CCCC#N

    As an accredited 1-Pyrrolidinobutyronitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1-Pyrrolidinobutyronitrile is supplied in a 250 mL amber glass bottle with a secure screw cap and chemical hazard labeling.
    Shipping 1-Pyrrolidinobutyronitrile is shipped in tightly sealed, chemical-resistant containers under cool, dry conditions. Proper labeling with hazard information is required, and transportation must comply with local and international regulations for nitriles. Avoid exposure to heat and incompatible substances. Ensure containers are protected from physical damage during transit.
    Storage 1-Pyrrolidinobutyronitrile should be stored in a cool, dry, and well-ventilated place, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Keep the container tightly closed and clearly labeled. Avoid moisture and direct sunlight. Store in an appropriate chemical storage cabinet, following all relevant safety regulations and guidelines.
    Application of 1-Pyrrolidinobutyronitrile

    Applications of 1-Pyrrolidinobutyronitrile in Industrial Manufacturing

    As a specialized manufacturer supplying high-purity 1-pyrrolidinobutyronitrile to the global market, we support multiple high-value sectors that require consistent quality, batch traceability, and direct process integration. This section highlights major real-world downstream applications, detailing industry standards, practical formulation ratios, process points, and end product forms—all reflecting verified industrial use.

    1. Pharmaceutical Intermediate for CNS-Active Agents

    Many pharmaceutical producers utilize this compound as a key intermediate in the synthesis of active pharmaceutical ingredients, particularly in the CNS (central nervous system) therapeutic category. It participates in the construction of complex heterocyclic structures through alkylation and nitrile functional group transformations, contributing to critical molecular scaffolds required by leading drug formulations. Rigorous compliance with international pharmacopoeial specifications and current GMP guidelines is essential at this manufacturing linkage.

    Industry compliance standards

    • USP-NF (United States Pharmacopeia–National Formulary) for intermediates
    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EDQM CEP for European API manufacturers (where in use)
    • FDA 21 CFR Part 211 for process controls

    Typical usage ratio

    • Batch input ranges from 1.8% to 7% (w/w), adjusted per target API synthetic route and yield optimization patterns

    Downstream process integration

    • Charged as an intermediate in multi-stage batch reactors for nucleophilic substitution or reductive amination, generally after initial base skeleton assembly but before final API purification

    Final product types

    • Finished APIs for CNS drugs such as anticonvulsants and antidepressants
    • Pharmaceutical intermediates supplied for contract synthesis
    • Custom medicinal chemistry scaffolds for research compounds

    2. Agrochemical Synthesis (Herbicide & Pesticide Acting Agents)

    This raw material is a core nitrile building block for downstream agrochemical producers working on novel herbicide and insecticide compounds. Its molecular structure enables modification by hydrolysis or ring-closure reactions, producing target actives with enhanced selectivity or stability on crops. Compliance with the full chain of agricultural chemical manufacturing regulations underpins all usage scenarios in this domain.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001 QMS for agrochemical production
    • REACH (EC No. 1907/2006) and CLP (EC No. 1272/2008) for registration and labeling in the EU
    • National Ministry of Agriculture regulations, e.g., EPA (USA) 40 CFR Part 180

    Typical usage ratio

    • Included at 2%–12% (w/w) in technical concentrate formulations, depending on desired reaction conversion and crop application rates

    Downstream process integration

    • Introduced during active ingredient synthesis, via controlled addition in high-pressure reactors, prior to acid or base hydrolysis, followed by purification to technical grade

    Final product types

    • Technical grade herbicides containing substituted pyrrolidine frameworks
    • Key intermediates for class II and class III insecticides
    • Custom agrochemical blends for crop-specific applications

    3. Custom Synthesis for Fine Chemicals and Specialty Organics

    Producers in the fine chemicals sector employ this compound as a precursor for specialty nitriles and nitrogen-containing heterocycles. Its reliable reactivity profile enables controlled cyclization, functionalization, or incorporation as a chained building block during contract R&D and small-batch pilot runs. Documentation of purity and batch consistency is mandatory to comply with specialty chemical standards, especially when downstream products enter regulated markets.

    Industry compliance standards

    • ISO 9001 for design and batch manufacturing of fine chemicals
    • Chemical Hazard Classification under UN GHS
    • REACH Annex VII-IX for registration dossiers
    • Internal QMS and traceability systems per buyer audit

    Typical usage ratio

    • Input concentrations from 5% up to 30% (w/w) for lab-scale custom synthesis and solvent-controlled scale-ups

    Downstream process integration

    • Fed into jacketed glass or stainless steel reactors during ring extension, cyclization, or reduction reactions, followed by in-process QC sampling at each conversion stage

    Final product types

    • Niche heterocyclic compounds used as reference standards
    • Fine organic intermediates for specialty dyes and catalysts
    • Advanced research reagents supplied to academic and industrial R&D labs

    4. Intermediate for Performance Polymer Additives

    Specialty polymer manufacturers rely on this compound for the synthesis of monomers and chain-modifying agents, especially where improved nitrogen-content or functional group specificity is targeted in engineered materials. Quality requirements align with the needs of sectors producing plastics for electrical, medical or high-performance mechanical components, requiring tight impurity controls and documentation through the entire workflow.

    Industry compliance standards

    • ISO 14001 for environmental management in polymer production
    • RoHS 2015/863/EU for restricted substance content
    • UL Yellow Card standards for electrical polymer grades
    • Customer-agreed technical specifications and validated material certificates

    Typical usage ratio

    • Generally 0.5%–3% (w/w) relative to the polymerization mass, with dosage modified for targeted mechanical or dielectric properties

    Downstream process integration

    • Injected via metered dosing units into continuous or batch reactors during pre-polymer, copolymer, or masterbatch additive synthesis

    Final product types

    • Monomer-modified resins for electrical insulation applications
    • Polymer additives for automotive and appliance-grade plastics
    • Specialty films and coatings requiring enhanced functional groups
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