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2,2-Dichlorocyclopropane-1-Carboxamide

    • Product Name 2,2-Dichlorocyclopropane-1-Carboxamide
    • Alias CC12C(C1Cl)C2(C(=O)N)Cl
    • Einecs 251-858-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    298911

    Chemicalname 2,2-Dichlorocyclopropane-1-Carboxamide
    Molecularformula C4H5Cl2NO
    Molecularweight 154.00
    Casnumber 72919-30-9
    Iupacname 2,2-dichlorocyclopropane-1-carboxamide
    Appearance White to off-white solid
    Solubility Slightly soluble in water
    Smiles C1C(C1(C(=O)N)Cl)Cl
    Inchi InChI=1S/C4H5Cl2NO/c5-4(6)1-2(1)3(7)8/h1-2,4H,(H2,7,8)
    Synonyms 2,2-Dichlorocyclopropanecarboxamide

    As an accredited 2,2-Dichlorocyclopropane-1-Carboxamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 50 grams, sealed cap, labeled with chemical name, hazards, batch number, supplier details, and handling instructions.
    Shipping 2,2-Dichlorocyclopropane-1-Carboxamide ships in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It is stored and transported as a hazardous material, compliant with all relevant regulations. The package is clearly labeled with handling and hazard information, and includes necessary documentation for safe and legal transit.
    Storage 2,2-Dichlorocyclopropane-1-carboxamide should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight and incompatible materials such as strong oxidizers and acids. Avoid exposure to moisture and sources of ignition. Clearly label the storage container, and restrict access to trained personnel. Store at room temperature unless otherwise specified by the manufacturer.
    Application of 2,2-Dichlorocyclopropane-1-Carboxamide

    Applications of 2,2-Dichlorocyclopropane-1-Carboxamide in Industrial Manufacturing

    As an established manufacturer directly supplying 2,2-Dichlorocyclopropane-1-Carboxamide, we focus on real, technically supported downstream use cases. Below we outline verified applications across multiple industrial segments, emphasizing on-the-ground formulation practices, compliance standards, processing workflow, and finished product categories for each scenario where this intermediate provides essential performance and value.

    1. Agrochemical Synthesis: Intermediate for Insecticide Active Ingredient Manufacture

    This compound plays a key role as a synthetic intermediate in creating certain pyrethroid-type insecticides. Our material enters the process during the core cyclopropanation route, facilitating efficient halogenation steps and ensuring batch-to-batch reproducibility for high-value crop protection actives.

    Industry compliance standards

    • ISO 9001:2015 for chemical synthesis QC
    • FAO/WHO Specifications for Plant Protection Products (as applicable to end products)
    • REACH Annex VII for intermediate evaluation (EU market)
    • US EPA Toxic Substances Control Act (TSCA) Section 5 for new chemical intermediates

    Typical usage ratio

    • Integrated at 0.8-1.5 molar equivalents relative to cyclopropanation substrate; final addition rate may vary by process scale, retention is monitored by in-process GC analysis

    Downstream process integration

    • Charged post-initial cyclization and before acylation steps; reacted under controlled temperature (60-85°C) in glass-lined reactors; final conversion monitored before quenching and subsequent transformation

    Final product types

    • Pyrethroid technical concentrate
    • Emulsifiable concentrate formulations for crop protection
    • Wettable powders for field application
    • Larvicidal granules for public health programs

    2. Fine Chemical Custom Synthesis: Intermediate for Chiral Pharmaceutical Building Blocks

    Pharma sector clients use this compound for synthesis of advanced building blocks with cyclopropane rings, critical for manufacturing several chiral pharma actives and research molecules that demand stringent impurity control and traceable chain of custody.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <1078> Good Storage and Distribution Practices for Bulk Pharmaceutical Excipients
    • FDA cGMP regulations (21 CFR Part 211 for API intermediates)
    • ISO 14001:2015 (where environmental control is required in API production)

    Typical usage ratio

    • 0.5-2.3 molar equivalents depending on target enantiomer selectivity; routinely adjusted per stepwise yield and racemization avoidance in multi-stage synthesis

    Downstream process integration

    • Loaded after protective group installation, subjected to chiral resolution steps post-hydrogenation, with solvent switching as per proprietary process requirements

    Final product types

    • Non-commercial API intermediates (out-licensing, preclinical use)
    • Commercialized chiral building blocks for small-molecule drugs
    • Custom reference standards (analytical supply for QC labs)
    • Molecular probes for lead optimization programs

    3. Industrial Polymer Modification: Chain-Stop Reagent in Specialty Polyolefin Manufacturing

    Polymer producers utilize the cyclopropane moiety as a chain-terminating agent for certain specialty polyolefins, enabling precise control of molecular weight distribution and crystallinity in end-use plastic materials tailored for niche applications.

    Industry compliance standards

    • ISO 11357 (polymer DSC analysis compliance)
    • ASTM D3418 (melting/crystallization analysis standards)
    • REACH Registration for Polymer Additives (Europe)
    • RoHS 3 (2015/863/EU) certification for downstream finished goods

    Typical usage ratio

    • 0.03–0.10 wt% relative to total monomer feed; adjusted via online viscometry during semi-batch or continuous reactor operation

    Downstream process integration

    • Dosed at the final stage of polymerization prior to devolatilization; incorporated with tailored mixing to facilitate even termination across product batch

    Final product types

    • Specialty copolymer pellets for film extrusion
    • Block copolymers for industrial adhesives
    • Plastic modifiers for electrical insulation
    • Polyolefin masterbatches for rheology control

    4. Specialty Material Synthesis: Precursor for Advanced Organic Electronic Materials

    In the high-value sector of organic electronics, this compound acts as a critical building block in the synthesis of certain cyclopropane-bridged oligomers, used to tailor molecular architecture for improved charge mobility and thermal stability in finished electronic materials.

    Industry compliance standards

    • IEC 62899-201 for printed electronics material evaluation
    • ISO 9001:2015 production traceability
    • RoHS 2 (2011/65/EU) for electronic components containing new organics
    • UL 94 flammability classification (for end-use transparency and safety)

    Typical usage ratio

    • Introduced at 1.0–2.1 molar equivalents, based on targeted molecular geometry in oligomer backbone; fine-tuned according to desired optoelectronic characteristics

    Downstream process integration

    • Coupled with aromatic monomers during Suzuki or Heck cross-coupling; purified via repeated chromatography prior to thin-film deposition

    Final product types

    • Precursor resins for organic semiconductors
    • Functional polymer layers for OLED displays
    • Specialty molecular dopants for conductive inks
    • Sensitizer intermediates for photovoltaic cells
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