Bis(2-Hydroxyethyl) terephthalate
| _terephthalate.svg.png) | |
| Names | |
|---|---|
| Preferred IUPAC name Bis(2-hydroxyethyl) benzene-1,4-dicarboxylate[1] | |
| Other names Bis(2-hydroxyethyl) terephthalate | |
| Identifiers | |
| 3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.012.270 | 
| PubChem CID | |
| UNII | |
| CompTox Dashboard (EPA) | |
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| Properties | |
| C12H14O6 | |
| Molar mass | 254.238 g·mol−1 | 
| Appearance | White powder | 
| Density | 1.3 (±0.1) g/cm3 | 
| Melting point | 106 °C | 
| 0.593 g/L[2] | |
| Hazards | |
| Flash point | 172.0 (±19.4) °C | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Bis(2-Hydroxyethyl) terephthalate (BHET) is an organic compound; it is the ester of ethylene glycol and terephthalic acid. Together with 2-hydroxyethyl terephthalic acid, bis(2-Hydroxyethyl) terephthalate is an intermediate in the production of poly(ethylene terephthalate). It is the product of the glycolysis reaction of PET with Ethylene glycol.[3]
References
- ^ IUPAC Chemical Nomenclature and Structure Representation Division (2013). "P-65.1.1.2.1". In Favre, Henri A.; Powell, Warren H. (eds.). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. IUPAC–RSC. ISBN 978-0-85404-182-4.
- ^ Yuan, Peiquan; Liu, Baoshu; Li, Qiuju; Sun, Hua (2022). "Solubility Determination and Correlation for Bis(2-hydroxyethyl) Terephthalate (BHET) in Four Binary Solvents from 283.15 to 323.15 K". Journal of Chemical & Engineering Data. 67 (9): 2693–2705. doi:10.1021/acs.jced.2c00194.
- ^ "Polyethylene terephthalate is an often-recycled plastic, but industry is still seeking major improvements". Chemical & Engineering News. Retrieved 2025-03-15.
