Poly(propylene oxide), triamine terminated
Product Information
Molecular Formula
C2H5C[CH2[OCH2CH(CH3)]nNH2]3
Molecular Weight
average Mn 440
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
1-[2,2-Bis(2-methylpropoxymethyl)butoxy]propan-2-amine
IUPAC Name
1-[2,2-bis(2-methylpropoxymethyl)butoxy]propan-2-amine
SMILES
CCC(COCC(C)C)(COCC(C)C)COCC(C)N
InChI
InChI=1S/C17H37NO3/c1-7-17(11-19-8-14(2)3,12-20-9-15(4)5)13-21-10-16(6)18/h14-16H,7-13,18H2,1-6H3
InChI Key
SRYMBUMLIMKZJO-UHFFFAOYSA-N
Boiling Point
158 °C/17 mmHg(lit.)
Flash Point
235.4 °F
Purity
95%
Density
0.981 g/mL at 25 °C (lit.)
Appearance
powder
Application
Epoxy hardener; Modified aliphatic amine hardener blend.
Storage
2-8°C
Refractive Index
n20/D 1.461 (lit.)
Vapor Pressure
1.2 [mmHg]
Safety Information
Hazards
H302 + H312 - H318 - H411
Precautionary Statement
P280 - P280 - P301 + P312 + P330 - P305 + P351 + P338 + P310
Computed Properties
XLogP3
2.9
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
4
Rotatable Bond Count
13
Exact Mass
303.27734404 g/mol
Monoisotopic Mass
303.27734404 g/mol
Topological Polar Surface Area
53.7Ų
Heavy Atom Count
21
Formal Charge
0
Complexity
230
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
1
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes
