Deuterated chloroform

From Wikipedia, the free encyclopedia
  (Redirected from Deuterochloroform)
Jump to: navigation, search
Deuterated chloroform
Stereo, skeletal formula of deuterated chloroform Spacefill model of deuterated chloroform
CAS number 865-49-6 YesY
PubChem 71583
ChemSpider 64654 YesY
EC number 212-742-4
UN number 1888
Beilstein Reference 1697633
Jmol-3D images Image 1
Molecular formula CDCl3
Molar mass 120.384 g mol-1
Density 1.500 g cm-3
Melting point −64 °C (−83 °F; 209 K)
Boiling point 61 °C (142 °F; 334 K)
EU classification Harmful Xn
R-phrases R22, R38, R40, R48/20/22
S-phrases S36/37
NFPA 704
Flammability code 0: Will not burn. E.g., water Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
Related compounds
Related compounds Chloroform

Deuterated dichloromethane

Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
 YesY (verify) (what is: YesY/N?)
Infobox references

Deuterated chloroform (CDCl3), is an isotopologue of chloroform (CHCl3) in which the hydrogen atom ("H") is replaced with a deuterium (heavy hydrogen) isotope ("D"). Deuterated chloroform is a common solvent used in NMR spectroscopy of organic molecules.[1] In proton NMR spectroscopy, the deuterium does not exhibit a large interfering peak, whereas protium (regular hydrogen) shows a large peak in the spectrum. In carbon-13 NMR, the sole carbon deuterated chloroform shows a triplet at a chemical shift of 77 ppm with the three peaks being about equal size.[1]