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Catalog Number:
29827
CAS Number:
10373-78-1
Camphorquinone
Purity:
≥ 99% (GC)
Synonym(s):
2,3-Bornanedione, (+/-)-Camphorquinone
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$29.34 /5G
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Product Information

Camphorquinone is a versatile compound widely recognized for its applications in the fields of dentistry and photopolymerization. This bicyclic diketone is particularly valued for its role as a photoinitiator in dental materials, enabling the curing of resins and composites when exposed to light. Its unique structure allows for efficient absorption of light, making it an ideal choice for applications requiring rapid polymerization. Additionally, camphorquinone is utilized in the formulation of various adhesives and coatings, enhancing their performance and durability.

Researchers and industry professionals appreciate camphorquinone for its low toxicity and excellent compatibility with other materials, which contributes to safer and more effective formulations. Its ability to initiate polymerization at room temperature further enhances its practicality, making it a preferred choice in many applications. Whether in dental practices or industrial settings, camphorquinone stands out for its efficiency and reliability, providing significant benefits in product performance and user safety.

Synonyms
2,3-Bornanedione, (+/-)-Camphorquinone
CAS Number
10373-78-1
Purity
≥ 99% (GC)
Molecular Formula
C10H14O2
Molecular Weight
166.22
MDL Number
MFCD00064160
PubChem ID
25208
Melting Point
198 - 204 °C
Appearance
Yellow crystalline powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
2,3-Bornanedione, (+/-)-Camphorquinone
CAS Number
10373-78-1
Purity
≥ 99% (GC)
Molecular Formula
C10H14O2
Molecular Weight
166.22
MDL Number
MFCD00064160
PubChem ID
25208
Melting Point
198 - 204 °C
Appearance
Yellow crystalline powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Camphorquinone is widely utilized in research focused on:

  • Dental Applications: It serves as a photoinitiator in dental materials, particularly in light-cured resins. Its efficiency in initiating polymerization under light exposure enhances the durability and strength of dental restorations.
  • Cosmetic Formulations: Commonly found in cosmetic products, it acts as a UV filter and stabilizer, helping to protect skin formulations from degradation due to light exposure, thus improving product longevity.
  • Photopolymerization Processes: In the field of 3D printing and additive manufacturing, it is used to initiate polymerization in resin-based systems, allowing for precise control over the curing process and enhancing the quality of printed objects.
  • Pharmaceutical Development: It plays a role in the synthesis of various pharmaceutical compounds, particularly in the development of drug delivery systems, where its photoinitiating properties can be leveraged to control the release of active ingredients.
  • Research in Material Science: Utilized in the development of advanced materials, camphorquinone is involved in creating photo-responsive polymers, which can change properties when exposed to light, opening avenues for innovative applications in smart materials.

Citations