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Catalog Number:
39173
CAS Number:
2767-84-2
(1S)-(+)-Camphorquinone
Purity:
≥ 97% (GC)
Synonym(s):
(1S)-(+)-2,3-Bornanedione, (1S)-(+)-Bornanedione
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Product Information

(1S)-(+)-Camphorquinone is a versatile compound widely recognized for its applications in organic synthesis and photochemistry. This bicyclic diketone is particularly valued in the field of polymer chemistry, where it serves as a photoinitiator in UV-curable coatings and inks, enabling rapid curing processes that enhance production efficiency. Its unique structure allows for effective energy transfer, making it an essential component in the formulation of high-performance materials. Additionally, (1S)-(+)-Camphorquinone is utilized in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals, due to its ability to facilitate reactions such as Michael additions and Diels-Alder reactions.

Researchers and industry professionals appreciate (1S)-(+)-Camphorquinone for its stability and reactivity, which provide significant advantages over similar compounds. Its application in the development of advanced materials and its role in enhancing the efficiency of chemical reactions make it a valuable asset in laboratories and manufacturing settings. With its proven track record in diverse applications, (1S)-(+)-Camphorquinone continues to be a preferred choice for those seeking reliable and effective solutions in their chemical processes.

Synonyms
(1S)-(+)-2,3-Bornanedione, (1S)-(+)-Bornanedione
CAS Number
2767-84-2
Purity
≥ 97% (GC)
Molecular Formula
C10H14O2
Molecular Weight
166.22
MDL Number
MFCD00064159
PubChem ID
25208
Melting Point
198 - 202 °C
Appearance
White to yellow crystalline powder
Optical Rotation
[α]20D = 95 - 103 ° (C = 1 in Toluene)
Conditions
Store at RT
General Information
Synonyms
(1S)-(+)-2,3-Bornanedione, (1S)-(+)-Bornanedione
CAS Number
2767-84-2
Purity
≥ 97% (GC)
Molecular Formula
C10H14O2
Molecular Weight
166.22
MDL Number
MFCD00064159
PubChem ID
25208
Melting Point
198 - 202 °C
Appearance
White to yellow crystalline powder
Optical Rotation
[α]20D = 95 - 103 ° (C = 1 in Toluene)
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(1S)-(+)-Camphorquinone is widely utilized in research focused on:

  • Photoinitiators in Polymer Chemistry: This compound serves as an effective photoinitiator in UV-curable coatings and inks, enhancing the curing process and improving the durability of the final products.
  • Organic Synthesis: It is employed in various organic synthesis reactions, particularly in the formation of complex molecules, making it a valuable tool for chemists in pharmaceuticals and agrochemicals.
  • Biological Research: Researchers use camphorquinone in studies related to oxidative stress and cell signaling, providing insights into cellular mechanisms and potential therapeutic targets.
  • Dental Applications: In dentistry, it is utilized in light-cured dental materials, improving the bonding and longevity of dental restorations, which is crucial for patient care.
  • Cosmetic Formulations: The compound is also found in cosmetic products for its antioxidant properties, helping to stabilize formulations and enhance skin benefits.

Citations