Triphosgene
ALDRICH/330752 - reagent grade, 98%
Synonym: Bis(trichloromethyl) carbonate
CAS Number: 32315-10-9
Empirical Formula (Hill Notation): C3Cl6O3
Molecular Weight: 296.75
EC Number: 250-986-3
MDL Number: MFCD00062848
Linear Formula: Cl3COCOOCCl3
Product Type: Chemical
| assay | 98% |
| bp | 203-206 °C (lit.) |
| form | powder |
| functional group | carbonate |
| chloro | |
| grade | reagent grade |
| InChI | 1S/C3Cl6O3/c4-2(5,6)11-1( |
| InChI key | UCPYLLCMEDAXFR-UHFFFAOYSA |
| mp | 79-83 °C (lit.) |
| Quality Level | 200 ![]() |
| reaction suitability | reaction type: Coupling Reactions |
| SMILES string | ClC(Cl)(Cl)OC(=O)OC(Cl)(C |
| storage temp. | 2-8°C |
| Application: | Triphosgene can be employed as a reagent to prepare: • Thiocarbonates from thiols and alcohols by one-pot, three-component reaction. • Substituted azetidin-2-ones from acids and imines via ketene–imine cycloaddition reaction. • Methyl (S)-2-isocyanato-3-phenylpr • Acyl azides derivatives from various carboxylic acids and sodium azide. • Immunosuppressant agent cyclosporin by solid-phase peptide synthesis. • Allyl azides from allyl alcohols and sodium azide in one pot method. • Esterification coupling reagent di-2-thienyl carbonate, from 2(5H)-thiophenone. • 2-Chloronicotinaldehyde |
| General description: | Triphosgene [Bis(trichloromethyl)carb It is also commonly employed as a coupling agent in the synthesis of carbonyl compounds. |
| Packaging: | 5, 25, 100, 500 g in glass bottle |
| Symbol | ![]() GHS05,GHS06 |
| Signal word | Danger |
| Hazard statements | H314 - H330 |
| Precautionary statements | P260 - P271 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 |
| Hazard Codes | T+ |
| Risk Statements | 26-34 |
| Safety Statements | 36/37/39-45 |
| RIDADR | UN 2928 8(6.1) / PGII |
| WGK Germany | WGK 2 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Purity | 98% |
| bp | 203-206 °C (lit.) |
| mp | 79-83 °C (lit.) |
| Storage Temp. | 2-8°C |
| UNSPSC | 12352108 |



