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148075 Aldrich

Camphor

96%

Synonym: (±)-Camphor, 1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one

  • CAS Number 76-22-2

  • Empirical Formula (Hill Notation) C10H16O

  • Molecular Weight 152.23

  •  Beilstein Registry Number 1907611

  •  EC Number 200-945-0

  •  MDL number MFCD00074738

  •  PubChem Substance ID 24848879

  • Popular Documents:  FTNMR (PDF)  

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Properties

Related Categories Artemisia vulgaris, Building Blocks, C10, Carbonyl Compounds, Cell Biology,
vapor density   5.2 (vs air)
vapor pressure   4 mmHg ( 70 °C)
InChI Key   DSSYKIVIOFKYAU-XCBNKYQSSA-N
assay   96%
autoignition temp.   870 °F
expl. lim.   3.5 %
bp   204 °C(lit.)
mp   175-177 °C(lit.)
solubility   ethanol: soluble1 g/L, clear, colorless

Description

Packaging

100, 500 g in poly bottle

Application

Camphor was used in the synthesis of single-walled nanotubes by chemical vapor deposition. It was used in two-phase based hollow fibre liquid-phase microextraction procedure for migration analysis of food packagings containing essential oils.

General description

Camphor is a novel carbon nanotube precursor.

Price and Availability

Safety & Documentation

Safety Information

Symbol 
Signal word 
Warning
Hazard statements 
Precautionary statements 
Target organs 
Lungs
RIDADR 
UN 2717 4.1 / PGIII
WGK Germany 
1
RTECS 
EX1225000
Flash Point(F) 
147.2 °F
Flash Point(C) 
64 °C
Protocols & Articles

Articles

Baeyer-Villiger Oxidation Reaction

The Baeyer–Villiger reaction involves the oxidation of ketones to esters by C-C bond cleavage of the carbonyl group and the introduction of an oxygen atom adjacent to it.1 This reaction can be accomp...
Keywords: Asymmetric synthesis, Catalysis, Oxidations

Peer-Reviewed Papers
15

References

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