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Catalog Number:
39177
CAS Number:
10334-26-6
(1R)-(-)-Camphorquinon
Purity:
≥ 98% (GC)
Synonym(s):
(1R)-(-)-2,3-Bornanedione
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Product Information

(1R)-(-)-Camphorquinone is a versatile compound widely utilized in various fields, particularly in organic synthesis and photochemistry. This bicyclic ketone is recognized for its unique ability to act as a photoinitiator, making it invaluable in the production of polymers and resins. Its strong UV absorption properties allow it to initiate polymerization processes effectively, which is crucial in industries such as coatings, adhesives, and dental materials. Additionally, (1R)-(-)-Camphorquinone serves as a key intermediate in the synthesis of complex organic molecules, enhancing its relevance in pharmaceutical research and development.

Researchers appreciate (1R)-(-)-Camphorquinone for its efficiency and effectiveness in various applications, including its role in the development of light-sensitive materials. Its unique structure not only contributes to its reactivity but also provides advantages over similar compounds, such as improved stability and a broader range of applications. This compound is essential for professionals seeking reliable and effective solutions in their chemical processes, making it a valuable addition to any laboratory or industrial setting.

Synonyms
(1R)-(-)-2,3-Bornanedione
CAS Number
10334-26-6
Purity
≥ 98% (GC)
Molecular Formula
C10H14O2
Molecular Weight
166.22
MDL Number
MFCD00082863
PubChem ID
25208
Melting Point
200 - 204 °C
Appearance
Light yellow to yellow crystalline powder
Optical Rotation
[α]20D = -95 to -105 ° (C = 1 in toluene)
Conditions
Store at RT
General Information
Synonyms
(1R)-(-)-2,3-Bornanedione
CAS Number
10334-26-6
Purity
≥ 98% (GC)
Molecular Formula
C10H14O2
Molecular Weight
166.22
MDL Number
MFCD00082863
PubChem ID
25208
Melting Point
200 - 204 °C
Appearance
Light yellow to yellow crystalline powder
Optical Rotation
[α]20D = -95 to -105 ° (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

(1R)-(-)-Camphorquinon is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, enabling the synthesis of complex molecules and facilitating the development of new pharmaceuticals.
  • Photochemistry: It is used in photochemical reactions, particularly in the study of light-induced processes, which can lead to advancements in solar energy applications and materials science.
  • Cosmetic Formulations: Due to its aromatic properties, it is incorporated into cosmetic products for fragrance and as a potential skin conditioning agent, enhancing product appeal.
  • Analytical Chemistry: This compound is employed as a standard in analytical methods, helping researchers accurately measure and analyze various substances in complex mixtures.
  • Biological Research: It plays a role in biological studies, particularly in understanding enzyme mechanisms and interactions, contributing to drug discovery and development.

Citations