(±)-Camphorquinone - ≥98%(GC), used for CQ-amines are used as a photo initiators for free radical polymerization.CQ was used as an initiator in the preparation of silver nanoparticle/silica/ polymer nanocomposites. Photopolymerization kinetics of dimethac

CAS: 10373-78-1 Cat. No.: C130002 Formula: C₁₀H₁₄O₂ Molecular Weight: 166.22 Beilstein Registry Number: 1909463 EC Number: 233-814-1

GRADE & PURITY ≥98%(GC)

Synonyms

BBL012870 | C1660 | (1R)-(-)-2,3-Bornanedione | 1,7,7-trimethylnorbornane-2,3-dione | FT-0624462 | dl-Camphoroquinone | DL-CAMPHORQUINONE | J-520412 | NSC-402031 | 1,7,7-trimethyl-bicyclo[2.2.1]heptane-2,3-dione | 1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-

Storage

Store at 2-8°C

Shipped In

Wet ice

Overview

Camphor quinone (CQ) can absorb UV radiation (due to π π * transition) and visible light in the range of 400-500nm (due to N, π * transition of α - dicarbonyl chromophore).

Specifications

Synonyms

BBL012870 | C1660 | (1R)-(-)-2,3-Bornanedione | 1,7,7-trimethylnorbornane-2,3-dione | FT-0624462 | dl-Camphoroquinone | DL-CAMPHORQUINONE | J-520412 | NSC-402031 | 1,7,7-trimethyl-bicyclo[2.2.1]heptane-2,3-dione | 1,7,7-Trimethylbicyclo[2.2.1]heptane-2,3-

Specifications & Purity

≥98%(GC)

Application

CQ-amines are used as a photo initiators for free radical polymerization.CQ was used as an initiator in the preparation of silver nanoparticle/silica/ polymer nanocomposites. Photopolymerization kinetics of dimethacrylates were studied using the CQ/amine

Storage

Store at 2-8°C

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥98%(GC)

Names and Identifiers

• Pubchem Sid: 488182956
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488182956
• Canonical Smiles: CC1(C2CCC1(C(=O)C2=O)C)C
• IUPAC Name: 1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione
• InChIKey: VNQXSTWCDUXYEZ-UHFFFAOYSA-N
• INCHI: 1S/C10H14O2/c1-9(2)6-4-5-10(9,3)8(12)7(6)11/h6H,4-5H2,1-3H3
• Isomeric SMILES: CC1(C2CCC1(C(=O)C2=O)C)C
• WGK Germany: 3
• Molecular Weight: 166.22
• Beilstein: 1909463
• Reaxy-Rn: 1909463
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1909463&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Class Prenol lipids
      • Subclass Monoterpenoids

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Class: Prenol lipids
• Subclass: Monoterpenoids
• Intermediate Tree Nodes: Not available
• Direct Parent: Bicyclic monoterpenoids
• Alternative Parents: Ketones Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic homopolycyclic compounds
• Substituents: Bicyclic monoterpenoid - Bornane monoterpenoid - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic homopolycyclic compound
• Description: This compound belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids containing exactly 2 rings, which are fused to each other.
• External Descriptors: Bicyclic monoterpenoids

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

ALB Tchem Serum albumin (2651 Activities)

Discover Target: ALB

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Soluble in ethanol, ethyl ether and benzene.
• Melt Point(°C): 198-202°C
• Molecular Weight: 166.220 g/mol
• XLogP3: 1.500
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 166.099 Da
• Monoisotopic Mass: 166.099 Da
• Topological Polar Surface Area: 34.100 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 278.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 2
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1