465151
Bis(2-hydroxyethyl) terephthalate
Sinônimo(s):
Bis(β-hydroxyethyl) terephthalate, Bis(2-hydroxyethyl) terephthalate, Bis(ethylene glycol) terephthalate, Bis(hydroxyethyl) terephthalate, Terephthalic acid diethylene glycol ester
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About This Item
Fórmula linear:
C6H4-1,4-(CO2CH2CH2OH)2
Número CAS:
Peso molecular:
254.24
Número CE:
Número MDL:
Código UNSPSC:
12162002
ID de substância PubChem:
NACRES:
NA.23
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Formulário
solid
Nível de qualidade
pf
106-109 °C (lit.)
cadeia de caracteres SMILES
OCCOC(=O)c1ccc(cc1)C(=O)OCCO
InChI
1S/C12H14O6/c13-5-7-17-11(15)9-1-2-10(4-3-9)12(16)18-8-6-14/h1-4,13-14H,5-8H2
chave InChI
QPKOBORKPHRBPS-UHFFFAOYSA-N
Categorias relacionadas
Descrição geral
Bis(2-hydroxyethyl) terephthalate belongs to the class of monomers known as diols or glycols. It is widely used to synthesize unsaturated polyester resins, polyethylene terephthalate (PET), and new biocompatible polymer systems. BHET can also be used as a plasticizer in polyester resins and rigid or flexible polyurethanes. Additionally, BHET and its derivatives have also been investigated for their potential use in biomedical applications, including drug delivery and tissue engineering, due to their excellent biocompatibility and mechanical properties.
Aplicação
Bis(2-hydroxyethyl) terephthalate canbe used as a monomer to prepare biodegradable aromatic-aliphatic copolyestersfor sustainable flexible packaging applications. The incorporation of BHET as abuilding block offers a promising approach to enhancing the properties ofbiodegradable plastics and promoting sustainable packaging solutions.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
Eyeshields, Gloves, type N95 (US)
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Yanbo Zhang et al.
International journal of biological macromolecules, 166, 251-258 (2020-10-31)
Hydrothermal degradation was used to pretreat terylene with an aim of noticeably improving the yield of fermentable monomers: terephthalic acid (TPA), mono (2- hydroxyethyl) terephthalic acid (MHET), bis-hydroxyethyl terephthalate (BHET), and ethylene glycol (EG). After 0.5 h of reaction time at
Martin Eckardt et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 36(12), 1882-1894 (2019-09-04)
Linear and cyclic oligomers are unavoidable non-intentionally added substances (NIAS) present in food contact materials made from common polyesters such as polyethylene terephthalate (PET), polybutylene terephthalate (PBT) and polyester coatings. Although polyester oligomers can migrate into fats in significant amounts
Uschara Thumarat et al.
Journal of bioscience and bioengineering, 120(5), 491-497 (2015-04-26)
This study described the genetic map of tandem genes (est1 and est119) encoding cutinase-type polyesterases in Thermobifida alba AHK119 and comparison of wild type and mutant enzymes of Est1 and Est119. Two genes were independently and constitutively expressed. The activity
Makoto Furukawa et al.
ChemSusChem, 11(23), 4018-4025 (2018-10-07)
Enzymatic degradation of poly(ethylene terephthalate) (PET) is promising because this process is safer than conventional industrial approaches. Recently, a cationic PET hydrolase (PETase) was identified from Ideonella sakaiensis. Pre-incubation of a low-crystallinity PET film with anionic surfactants prior to initiating
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 465151-100G | 4061832356877 |
| 465151-500G | 4061832356891 |
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