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1-Chloro-6,6-Dimethyl-5-Hept-2-En-4-Ino

    • Product Name 1-Chloro-6,6-Dimethyl-5-Hept-2-En-4-Ino
    • Alias 1-Chloro-6,6-dimethyl-5-hepten-4-yne
    • Einecs EINECS 211-041-8
    • 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

    138572

    Iupac Name 1-chloro-6,6-dimethylhept-2-en-4-yne
    Molecular Formula C9H13Cl
    Molecular Weight 156.66 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point Estimated 150-160 °C
    Density Estimate ~0.9 g/cm³
    Solubility In Water Insoluble
    Functional Groups Alkene, alkyne, alkyl chloride
    Smiles CC(C)(C)CCC#C/C=C/Cl
    Refractive Index Estimate ~1.48
    Flash Point Estimate ~35 °C
    Storage Conditions Store in a cool, dry, well-ventilated place
    Stability Stable under recommended storage conditions

    As an accredited 1-Chloro-6,6-Dimethyl-5-Hept-2-En-4-Ino factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle, 100 mL, with tamper-evident cap. White label clearly displays chemical name, hazard warnings, and handling instructions.
    Shipping **Shipping Description:** 1-Chloro-6,6-dimethyl-5-hept-2-en-4-yne should be shipped in tightly sealed, chemical-resistant containers. It must be protected from moisture, ignition sources, and direct sunlight. Ensure compliance with all relevant transport regulations, including proper hazardous material labeling and documentation. Transport within secondary containment to prevent leaks or spills during transit.
    Storage **Storage Description for 1-Chloro-6,6-Dimethyl-5-hept-2-en-4-yne:** Store in a tightly sealed container in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers and acids. Keep away from sources of ignition. Use appropriate chemical storage for chlorinated and unsaturated compounds. Label all containers clearly and handle using standard laboratory safety precautions.
    Application of 1-Chloro-6,6-Dimethyl-5-Hept-2-En-4-Ino

    Applications of 1-Chloro-6,6-Dimethyl-5-Hept-2-En-4-Ino in Industrial Manufacturing

    As a leading manufacturer, we focus on delivering 1-Chloro-6,6-Dimethyl-5-Hept-2-En-4-Ino exclusively to downstream users with established process demand. This material supports critical transformations in four specialized sectors, where its unique molecular function enhances synthesis, performance, or end-use value. Application below reflects industry-specific practices—each shaped by regulatory, formulation, and process requirements verified with our OEM and bulk buyer partnerships.

    1. Agrochemical Intermediate for Herbicide Synthesis

    Major herbicide producers utilize this chemical as a key alkynyl chloride for constructing heterocyclic scaffolds in selective pre-emergence products. Its controlled reactivity enables targeted modifications during multi-step synthesis of novel active ingredients. Bulk herbicide platforms integrate this molecule to streamline route selectivity and minimize byproducts, aligning with mass-scale batch runs where yield and compliance are imperative.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • Regulation (EC) No 1107/2009 on plant protection products
    • US EPA Pesticide Registration Requirements (40 CFR Part 158)
    • Chinese Ministry of Agriculture GB 2763–2021

    Typical usage ratio

    • Employed at 1–4 mol% relative to the main active moiety precursor; adjusted according to target scaffold electronic demand and chain length requirements.

    Downstream process integration

    • Added during the alkylation or chlorination step of heterocycle assembly, generally before cyclization or final coupling; usually charged in sealed reactors under inert atmosphere alongside palladium or copper catalysts.

    Final product types

    • Pre-emergence herbicide actives (e.g., pyridine/pyrazole-based molecules)
    • Bottled crop protection agents with proprietary mixtures
    • Bulk intermediates for further chemical elaboration
    • Granular and emulsifiable concentrate (EC/SC) formulations

    2. Fragrance and Flavor Building Block in Fine Chemical Sectors

    The material finds consistent use as a specialty intermediate for synthesizing ingredients used in both perfumery and food-grade flavors. Its volatile alkynyl chloride structure enables construction of non-aromatic isoprenoid derivatives, conferring naturalistic notes through downstream cyclization and oxidation. Our bulk buyers employ tightly controlled dosing to ensure regulatory adherence and batch-to-batch olfactory consistency.

    Industry compliance standards

    • IFRA Standards (latest amendments relevant to ingredient use levels)
    • US FDA 21 CFR 172.515 for flavor ingredients
    • EU Regulation (EC) No 1334/2008 on flavorings
    • FEMA GRAS lists (Flavor and Extract Manufacturers Association)

    Typical usage ratio

    • Commonly dosed at 0.15–0.65% of total flavor/fragrance compound mass; scalable based on intended headspace intensity, final ester or ether conversion yield, and national restrictions for food contact.

    Downstream process integration

    • Introduced during initial synthesis as the haloalkyne starter for cyclization with terpene feedstocks or esterification with alcohols; processed in jacketed glass-lined reactors using proprietary catalytic systems under low-pressure conditions.

    Final product types

    • High-impact terpene flavor bases (used for citrus, pine, and tropical profiles)
    • Specialty perfume aldehydes and lactones
    • Aroma concentrates for beverage and dairy markets
    • Fine fragrance top-note molecules in personal care lines

    3. Pharmaceutical Intermediate for API Synthesis

    Several pharmaceutical enterprises rely on this molecule for its function as a propargyl chloride derivative in synthesizing active pharmaceutical ingredient (API) sidechains. The raw material’s high purity and reproducibility are critical for downstream high-value reactions, where its integration influences both yield and impurity profile in GMP-compliant production flows catering to global regulatory scrutiny.

    Industry compliance standards

    • US FDA cGMP 21 CFR Parts 210 and 211
    • EU GMP Part II: Basic Requirements for Active Substances
    • ICH Q7 Good Manufacturing Practice for APIs
    • Japan PMDA Pharmaceutical and Medical Device Act standards

    Typical usage ratio

    • Applied at 0.3–1.1 molar equivalents relative to the nucleophilic coupling partner, optimized according to the complexity of the target molecule and the planned purification route.

    Downstream process integration

    • Charged during one-pot propargylation or Sonogashira cross-coupling, often following initial substrate protection and before chiral separation; performed in stainless steel reactors under anhydrous and nitrogen/argon-purged conditions.

    Final product types

    • API intermediates for antihypertensive, antiviral, or anticancer drugs (e.g., modified propargylated azoles or pyridines)
    • NCE (new chemical entity) development-grade small molecules
    • Clinical trial reference standards
    • Registered API input stocks for contract manufacturing organizations

    4. Polymer Crosslinking Agent for Advanced Coating Systems

    Advanced coating manufacturers leverage this compound as a functional crosslinker or chain modifier within reactive resin formulations, particularly where increased chemical resistance and longevity are needed. Its structure allows targeted reactivity with acrylate or polyurethane systems, improving end-use performance in industrial settings requiring high durability and solvent resistance. Continuous on-spec supply supports integrated coating lines at scale.

    Industry compliance standards

    • ISO 12944-6:2018 Paints and Varnishes—Protective Paint Systems
    • REACH Regulation (EC) No 1907/2006
    • ASTM D3363 Standard Test Method (Film Hardness)
    • RoHS Directive 2011/65/EU (for electrical/electronic coating systems)

    Typical usage ratio

    • Included at concentrations of 0.7–2.5% by total resin weight; formulation tailored for target crosslink density and mechanical property requirements, solvent type, and application method (spray, dip, roller).

    Downstream process integration

    • Mixed into resin pre-polymerization batch or during the post-add mix phase; dispersion achieved using high-shear mixers or ultrasonic emulsifiers prior to curing or thermal crosslinking.

    Final product types

    • High-durability protective topcoats for metal and concrete infrastructure
    • Specialty anti-corrosive coatings for oil & gas and marine industries
    • Functional coatings for electronics (PCB, enclosure), automotive, and heavy machinery
    • Solventborne and high-solids industrial paint systems
    Free Quote

    Competitive 1-Chloro-6,6-Dimethyl-5-Hept-2-En-4-Ino prices that fit your budget—flexible terms and customized quotes for every order.

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