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Sigma-Aldrich

Di(trimethylolpropane)

97%

Synonym(s):

2,2′-Oxybis(methylene)bis(2-ethyl-1,3-propanediol)

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About This Item

Linear Formula:
O[CH2C(C2H5)(CH2OH)2]2
CAS Number:
23235-61-2
Molecular Weight:
250.33
Beilstein/REAXYS Number:
1860782
EC Number:
245-509-0
MDL number:
MFCD00192117
UNSPSC Code:
12162002
PubChem Substance ID:
24866062
NACRES:
NA.23

assay

97%

bp

215 °C/4 mmHg (lit.)

mp

108-111 °C (lit.)

SMILES string

CCC(CO)(CO)COCC(CC)(CO)CO

InChI

1S/C12H26O5/c1-3-11(5-13,6-14)9-17-10-12(4-2,7-15)8-16/h13-16H,3-10H2,1-2H3

InChI key

WMYINDVYGQKYMI-UHFFFAOYSA-N

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General description

Di(trimethylolpropane) is a monomeric unit with primary hydroxyl groups, that can be used as a tetrafunctional core molecule.

Application

Di(trimethylolpropane) can be used for the synthesis of lipase catalyzed hyperbranched polymers. It can also be used in the formation of biodegradable polymers for drug delivery applications.

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Rheological properties of concentrated solutions of aliphatic hyperbranched polyesters
Vukovic J, et al.
Macromolecular Chemistry and Physics, 208(21), 2321-2330 (2007)
Synthesis, characterization and in vitro degradation of 3D-microstructured poly (varepsilon-caprolactone) resins
Theiler S, et al.
Polym. Chem., 1(8), 1215-1225 (2010)
Biodegradable cross-linked poly (trimethylene carbonate) networks for implant applications: Synthesis and properties
Yang L, et al.
Polymer, 54(11), 2668-2675 (2013)
Ankur S Kulshrestha et al.
Biomacromolecules, 8(6), 1794-1801 (2007-05-05)
Lipase-catalyzed terpolymerizations were performed with the monomers trimethylolpropane (B3), 1,8-octanediol (B2), and adipic acid (A2). Polymerizations were performed in bulk, at 70 degrees C, for 42 h, using immobilized lipase B from Candida antartica (Novozyme-435) as a catalyst. To determine

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