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About This Item
Linear Formula:
(HSCH2CH2CO2CH2)3CC2H5
CAS Number:
Molecular Weight:
398.56
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
251-336-1
MDL number:
Assay:
≥95.0%
Quality Level
assay
≥95.0%
refractive index
n20/D 1.518 (lit.)
bp
220 °C/0.3 mmHg (lit.)
density
1.21 g/mL at 25 °C (lit.)
functional group
ester, thiol
SMILES string
CCC(COC(=O)CCS)(COC(=O)CCS)COC(=O)CCS
InChI
1S/C15H26O6S3/c1-2-15(9-19-12(16)3-6-22,10-20-13(17)4-7-23)11-21-14(18)5-8-24/h22-24H,2-11H2,1H3
InChI key
IMQFZQVZKBIPCQ-UHFFFAOYSA-N
General description
Trimethylolpropane tris(3-mercaptopropionate) is reported as a multi-thiol crosslinking reagent.
Application
Trimethylolpropane tris(3-mercaptopropionate) may be used in the following studies:
- Preparation of hydrogels, via crosslinking inulin derivatives.
- Construction of porous hybrid monolithic materials.
- As monomer for the preparation of a new thiol-ene based polymeric fluorescence sensor, via photo initiated polymerization.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
204.8 °F - closed cup
flash_point_c
96 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Giovanna Pitarresi et al.
Macromolecular bioscience, 8(10), 891-902 (2008-06-26)
Inulin was chosen as a starting polymer for biocompatible, pH-sensitive and biodegradable hydrogels. Three INUDVSA-TT hydrogels were obtained by crosslinking inulin derivatives with trimethylolpropane tris(3-mercaptopropionate) under varying conditions. The resulting hydrogels were cell compatible, as demonstrated by MTS and trypan
Soner Cubuk et al.
Analytica chimica acta, 812, 215-221 (2014-02-05)
This study describes the preparation and the characterization of a new thiol-ene based polymeric fluorescence sensor by photo initiated polymerization of trimethylolpropane tris(3-mercaptopropionate), 2-hydroxyethylacrylate, and 2,4,6-triallyloxy-1,3,5-triazine which are used as monomers and also a photo initiator (2,2-dimethoxy-2-phenylacetophenone) for its usage
Alexandra N Tsoras et al.
Frontiers in immunology, 11, 1547-1547 (2020-08-28)
Peptide subunit vaccines increase safety by reducing the risk of off-target responses and improving the specificity of the induced adaptive immune response. The immunogenicity of most soluble peptides, however, is often insufficient to produce robust and lasting immunity. Many biomaterials
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 381489-100ML | 04061831961256 |
| 381489-500ML | 04061831961263 |
