Trimethylolpropane triglycidyl ether
Product Information
Molecular Formula
C15H26O6
Molecular Weight
302.36
Description
TMPTE is used in the synthesis of azidated trimethylolpropane triglycidyl ether for the preparation of polyether polyol based hyperbranched polyurethanes. It can be coated on polycarbonated chips for improving chemical resistance from different organic solvents. Cross-linking of TMPTE can be done with poly(4-venylphenol) (PVP) for the preparation of organic field effect transistors (OFETs).
Synonyms
2,2'-[[2-Ethyl-2-[(2-oxiranylmethoxy)methyl]-1,3-propanediyl]bis(oxymethylene)]bis[oxirane]; Butane, 1-(2,3-epoxypropoxy)-2,2-bis[(2,3-epoxypropoxy)methyl]-; Oxirane, 2,2'-[[2-ethyl-2-[(oxiranylmethoxy)methyl]-1,3-propanediyl]bis(oxymethylene)]bis-; 1,1,1-Trimethylolpropane triglycidyl ether; 2,2'-(((2-Ethyl-2-((oxiran-2-ylmethoxy)methyl)propane-1,3-diyl)bis(oxy))bis(methylene))bis(oxirane); ChemMod 48; Etriol triglycidyl ether; Triglycidyl trimethylolpropane ether
IUPAC Name
2-[2,2-bis(oxiran-2-ylmethoxymethyl)butoxymethyl]oxirane
SMILES
CCC(COCC1CO1)(COCC2CO2)COCC3CO3
InChI
InChI=1S/C15H26O6/c1-2-15(9-16-3-12-6-19-12,10-17-4-13-7-20-13)11-18-5-14-8-21-14/h12-14H,2-11H2,1H3
InChI Key
QECCQGLIYMMHCR-UHFFFAOYSA-N
Boiling Point
410.7±45.0°C at 760 mmHg
Flash Point
312.8 °F
Density
1.175±0.06 g/cm3
Appearance
powder
Storage
Store at 2-8°C
Grade
Tech Grade
Refractive Index
n20/D 1.477 (lit.)
Related CAS
153355-08-9 (Deleted CAS) 1149843-23-1 (Deleted CAS)
Computed Properties
XLogP3
-0.1
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
6
Rotatable Bond Count
13
Exact Mass
302.17293854 g/mol
Monoisotopic Mass
302.17293854 g/mol
Topological Polar Surface Area
65.3Ų
Heavy Atom Count
21
Formal Charge
0
Complexity
278
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
3
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| JP-3236461-U | Photosensitive resin composition for sandblasting | 2021-12-21 |
| CN-114032008-A | Solvent-resistant conductive coating of single-walled nanotube and preparation method thereof | 2021-12-20 |
| CN-114057993-A | Amido amine epoxy curing agent and preparation method and application thereof | 2021-12-20 |
| CN-114149566-A | Imidazoline epoxy curing agent and application thereof | 2021-12-20 |
| JP-2022031343-A | Photo-curing nail dressing | 2021-12-13 |
| CN-113912824-A | Modified epoxy acrylate prepolymer, photo-thermal dual-curing conductive adhesive and preparation method thereof | 2021-11-29 |
| CN-113956832-A | Double-component PU (polyurethane) structural adhesive and preparation method thereof | 2021-11-29 |
| CN-114031769-A | Quaternary ammonium salt leveling agent, preparation method thereof, electroplating solution containing quaternary ammonium salt leveling agent and electroplating method | 2021-11-29 |
| KR-20210154114-A | A assurance view sheet for the traffic lane | 2021-11-26 |
| CN-113861928-A | UV (ultraviolet) anti-static adhesive and preparation method of anti-static adhesive | 2021-11-23 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 16524435 | 2006-03-01 | Concomitant contact allergy to the resins, reactive diluents and hardener of a bisphenol A/F-based epoxy resin in subway construction workers | Contact dermatitis |
