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(1R)-(-)-Camphorquinone

    • Product Name (1R)-(-)-Camphorquinone
    • Alias CQ
    • Einecs 241-678-0
    • 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
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    Specifications

    HS Code

    664658

    Chemical Name (1R)-(-)-Camphorquinone
    Cas Number 527-17-3
    Molecular Formula C10H14O2
    Molar Mass 166.22 g/mol
    Appearance Yellow crystalline solid
    Melting Point 198-201 °C
    Boiling Point 305 °C
    Density 1.22 g/cm3
    Optical Rotation -46° (c=1, ethanol)
    Solubility Slightly soluble in water, soluble in organic solvents
    Inchi InChI=1S/C10H14O2/c1-6-3-7(11)5-8(6)10(12)9(2,4)6/h3,6,8H,4-5H2,1-2H3/t6-,8+/m1/s1
    Pubchem Cid 68206

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

    Packing & Storage
    Packing A 25g amber glass bottle with a screw cap, labeled “(1R)-(-)-Camphorquinone”, chemical structure, hazard symbols, and supplier details.
    Shipping (1R)-(-)-Camphorquinone is shipped in tightly sealed, light-resistant containers to maintain stability and prevent degradation. The chemical is transported according to standard regulations for non-hazardous organic compounds, with packages clearly labeled. It should be kept away from heat, moisture, and direct sunlight during transit to ensure product integrity.
    Storage (1R)-(-)-Camphorquinone should be stored in a tightly sealed container, protected from light, moisture, and air, as it is sensitive to these conditions. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. For optimal stability, refrigeration (2–8°C) is recommended, and the container should be clearly labeled and kept out of direct sunlight.
    Application of (1R)-(-)-Camphorquinone

    Applications of (1R)-(-)-Camphorquinone in Industrial Manufacturing

    As a direct manufacturer of (1R)-(-)-Camphorquinone, we support various high-value industrial production chains where this compound operates as a critical photoinitiator. Below are selected mature downstream application scenarios based on validated market demand, regulatory compliance, and production process integration.

    1. Dental Light-Curing Resin Materials

    Leading dental product manufacturers specify (1R)-(-)-Camphorquinone as the primary photoinitiator in light-activated restorative resins, flowable composites, and dental adhesives. By precisely responding to blue light wavelengths, it catalyzes the polymerization of acrylate monomers, delivering strong, rapid curing under clinical conditions. Quality control protocols focus on minimizing residual monomer and ensuring consistent cure depth across varied clinical scenarios, from bulk-fill composites to specialized orthodontic adhesives.

    Industry compliance standards

    • ISO 4049: Dentistry – Polymer-based restorative materials
    • ISO 20795-2: Dentistry – Base polymers – Denture relining and tissue conditioning materials
    • EU Regulation (EU) 2017/745 on medical devices (MDR)
    • FDA 21 CFR 872.3690 for dental resin devices

    Typical usage ratio

    • 0.15% – 1.0% by weight in dental resin formulations; levels are refined based on resin opacity, desired polymerization speed, and photoactivation source intensity

    Downstream process integration

    • Added during the bulk blending stage with other monomers and fillers, dissolved before packaging to ensure uniform photoinitiator distribution for predictable in-situ curing at the point of use

    Final product types

    • Light-curable dental restorative composites
    • Root canal sealers
    • Light-cured bonding agents
    • Fissure sealant materials

    2. Industrial UV-Curing Adhesives and Sealants

    In industrial assembly environments, (1R)-(-)-Camphorquinone enables rapid-setting acrylate and methacrylate adhesives where visible-light initiated curing outperforms traditional heat-curing or dual-cure chemistries. Downstream manufacturers adjust the photoinitiator content for clear, pigmented, or filled adhesive systems to maintain bond strength and minimize tack-free time in automated lines, notably in electronics device encapsulation and micro-assembly applications.

    Industry compliance standards

    • ISO 10993-5: Biological evaluation of medical devices – Cytotoxicity, where applicable to medical-grade adhesive products
    • REACH compliance for workplace safety and VOC limits
    • RoHS Directive (EU) 2011/65/EU for electronic products

    Typical usage ratio

    • 0.1% – 0.7% by weight; adjusted for depth of cure and degree of substrate transparency, with lower levels for low-viscosity systems and higher for opaque substrates

    Downstream process integration

    • Incorporated during the formulation of base adhesive resins with low-shear mixing under light-restrictive conditions, followed by automated packaging in UV-proof cartridges or syringes

    Final product types

    • Light-curing assembly adhesives
    • Electronics encapsulation gels
    • Precision device sealants
    • UV-curable mounting tapes

    3. 3D Printing Photopolymer Resins

    High-resolution stereolithography (SLA) and digital light processing (DLP) resin manufacturers leverage (1R)-(-)-Camphorquinone’s high quantum yield for visible light-initiated curing, especially for dental models, custom trays, and indirect bonding jigs. The controlled curing response under specific light sources optimizes build speed, interlayer adhesion, and final mechanical properties matched to end-use requirements. Formulation scientists select initiator levels based on print layer thickness and light penetration attributes.

    Industry compliance standards

    • ISO 13485: Quality management systems for medical device manufacturing (when producing dental models or guides intended for patient use)
    • ISO 10993 series for biocompatibility, as required
    • IEC 62366 for 3D printing equipment safety and usability (where applicable)
    • REACH Annex XVII for chemical safety

    Typical usage ratio

    • 0.2% – 0.9% by weight in 3D printing photopolymer formulations, variable based on photopolymer thickness and light intensity of the printer

    Downstream process integration

    • Dissolved in liquid photopolymer monomer blends during formulation, continuously mixed to limit photoinitiator sedimentation, then filtered and degassed before final vat packaging for SLA/DLP production

    Final product types

    • Dental 3D printing model resins
    • Light-curable temporary crown and bridge base resins
    • Soft tissue simulation materials
    • Indirect bonding jig resins

    4. Photocurable Coatings for Printed Circuit Boards (PCBs)

    PCB manufacturers specify (1R)-(-)-Camphorquinone in visible-light curable solder mask coatings and conformal coatings. Its absorption profile supports rapid surface curing, fine feature resolution, and controlled film hardness essential for automated high-speed production lines. Specialist coating formulators optimize the photoinitiator content to balance curing depth and prevent under-cured residues beneath dense traces or component shadows.

    Industry compliance standards

    • IPC-CC-830: Qualification and Performance of Electrical Insulating Compounds for Printed Wiring Assemblies
    • UL 94: Standard for Safety of Flammability of Plastic Materials
    • RoHS Directive (EU) 2011/65/EU for hazardous substance limits
    • ISO 9001:2015 (Quality Management Systems)

    Typical usage ratio

    • 0.08% – 0.3% by weight in coating systems; tuned for film thickness and desired curing rate under visible LED light sources

    Downstream process integration

    • Integrated into coating formulations during resin mixing; the mixture is then applied via screen or curtain coating before passing through controlled visible light tunnels for rapid curing and subsequent final curing or reflow processes

    Final product types

    • UV/visible-light cured solder mask coatings
    • Conformal coatings for moisture protection
    • Surface insulating coatings on rigid and flexible PCB substrates
    • Semi-transparent protective layers for microelectronics

    5. Ophthalmic Lens Resin Polymerization

    Specialized ophthalmic lens manufacturers employ (1R)-(-)-Camphorquinone as a photoinitiator in visible-light cured lens casting resins, supporting rapid shaping of high-index, impact-resistant lenses. Control of the initiator concentration is critical for avoiding yellowing while ensuring deep, uniform polymerization in molds for lenses used across corrective eyewear segments.

    Industry compliance standards

    • ISO 11979-5: Ophthalmic implants – Intraocular lenses – Part 5: Biocompatibility
    • ISO 8980-1: Ophthalmic optics – Uncut finished spectacle lenses – Specifications
    • FDA 21 CFR 886.1385 for eye lens products

    Typical usage ratio

    • 0.07% – 0.2% by weight in lens-grade resin syrups; formulation adjusted based on resin composition, target cure speed, and requirement to minimize post-cure coloration

    Downstream process integration

    • Added to monomer blends before mold filling, where controlled visible-light exposure in lens casting machines ensures full polymerization through lens thickness, followed by post-cure stabilization

    Final product types

    • Corrective spectacle lenses
    • Photochromic coated lenses
    • Ophthalmic device lenses for medical uses
    • Safety and protection visor inserts
    Free Quote

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