Pyridinium chlorochromate
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| Names | |||
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| IUPAC name
Pyridinium chlorochromate | |||
| Other names
PCC; Corey-Suggs reagent | |||
| Identifiers | |||
3D model (JSmol) |
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| ChEBI | |||
| ChemSpider | |||
| ECHA InfoCard | 100.043.253 | ||
| EC Number |
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PubChem CID |
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| UNII | |||
CompTox Dashboard (EPA) |
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| Properties | |||
| C5H6ClCrNO3 | |||
| Molar mass | 215.56 g/mol | ||
| Appearance | yellow-orange solid | ||
| Melting point | 205 °C (401 °F; 478 K) | ||
| Solubility in other solvents | soluble in acetone, acetonitrile, THF | ||
| Hazards | |||
| Occupational safety and health (OHS/OSH): | |||
Main hazards |
Toxic, oxidizer, carcinogenic, strong environmental pollutant | ||
| GHS labelling: | |||
| Danger | |||
| H272, H317, H350, H410 | |||
| P201, P221, P273, P280, P302+P352, P308+P313 | |||
| NFPA 704 (fire diamond) | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |||
Pyridinium chlorochromate (PCC) is a yellow-orange salt with the formula [C5H5NH]+[CrO3Cl]−. It is a reagent in organic synthesis used primarily for oxidation of alcohols to form carbonyls. A variety of related compounds are known with similar reactivity. PCC offers the advantage of the selective oxidation of alcohols to aldehydes or ketones, whereas many other reagents are less selective.