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381489

Sigma-Aldrich

Trimethylolpropane tris(3-mercaptopropionate)

≥95.0%

Synonyme(s) :

1,1,1-Trimethylolpropane-tris(3-mercaptopropionate), 2,2-Bis(3-sulfanylpropanoyloxymethyl)butyl 3-sulfanylpropanoate, Trimethylolpropane tris(β-mercaptopropionate), Trimethylolpropane tris(3-mercaptopropanoate), Trimethylolpropane tris(3-mercaptopropropionate)

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About This Item

Formule linéaire :
(HSCH2CH2CO2CH2)3CC2H5
Numéro CAS:
Poids moléculaire :
398.56
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22

Niveau de qualité

Pureté

≥95.0%

Indice de réfraction

n20/D 1.518 (lit.)

Point d'ébullition

220 °C/0.3 mmHg (lit.)

Densité

1.21 g/mL at 25 °C (lit.)

Chaîne SMILES 

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

Clé InChI

IMQFZQVZKBIPCQ-UHFFFAOYSA-N

Description générale

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.

Pictogrammes

Exclamation mark

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

204.8 °F - closed cup

Point d'éclair (°C)

96 °C - closed cup

Équipement de protection individuelle

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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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
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
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
Hayden E Fowler et al.
Soft matter, 16(2), 330-336 (2019-11-09)
Programming the local orientation of liquid crystal elastomers (LCEs) is a differentiated approach to prepare monolithic material compositions with localized deformation. Our prior efforts prepared LCEs with surface-enforced spatial variations in orientation to localize deformation when the LCEs were subjected
K Lipponen et al.
The Analyst, 142(14), 2552-2557 (2017-06-16)
A micropillar array electrospray ionization (μPESI) platform fabricated from thiol-enes with 56 individual polyethylene glycol coated μPESI chips for bioanalytical mass spectrometry is introduced. Bioanalysis capability is shown by measurement of a protein, a protein digest and a cell lysate

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