| EC Index Number | 204-800-2 |
|---|---|
| UNSPSC Code | 12352303 |
| Beilstein/REAXYS Number | 1710584 |
| MDL number | MFCD00009436 |
| SMILES string | CCCCOP(=O)(OCCCC)OCCCC |
| InChI | 1S/C12H27O4P/c1-4-7-10-14-17(13,15-11-8-5-2)16-12-9-6-3/h4-12H2,1-3H3 |
| InChI key | STCOOQWBFONSKY-UHFFFAOYSA-N |
| agency | Ph. Eur. |
| vapor density | 9.2 (vs air) |
| vapor pressure | 27 mmHg ( 178 °C) |
| product line | EMPROVE® EXPERT |
| form | liquid |
| autoignition temp. | 770 °F |
| Quality Level | 500 |
| refractive index | n20/D 1.424 (lit.) |
| bp | 180-183 °C/22 mmHg (lit.) |
| mp | −79 °C (lit.) |
| transition temp | flash point 146 °C |
| solubility | 6 g/L |
| density | 0.979 g/mL at 25 °C (lit.) |
| application(s) | liquid formulationpharma/biopharma processespharmaceutical |
| storage temp. | 15-25°C |
Answer:It is an organic phosphate ester used in solvent/detergent viral inactivation processing with a compatible detergent and validated conditions.
Answer:The EMPROVE EXPERT Ph Eur product is supplied in a 2.5 L glass bottle.
Answer:No. Viral inactivation requires a defined solvent/detergent formulation, qualified process parameters and process-specific validation; the reagent alone does not establish clearance.
Merck Tri-n-butyl Phosphate EMPROVE EXPERT is an organic phosphate ester used as a process chemical in biopharmaceutical manufacturing, particularly solvent/detergent treatment workflows. This product meets a Ph Eur grade designation and is supplied as 2.5 L in a glass bottle. Tri-n-butyl phosphate (TBP; CAS 126-73-8) is hydrophobic and must be handled as a chemical processing agent rather than an aqueous buffer component. In solvent/detergent viral inactivation processes, TBP is typically combined with a compatible detergent at defined concentrations and under validated contact conditions. The compound's identity and controlled manufacturing documentation help support raw-material qualification and process traceability. Selection must consider the process fluid, mixing efficiency, exposure time and downstream clearance of process additives. For manufacturing use, assess the safety data, compatibility and removal strategy alongside the established virus-inactivation validation protocol.
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