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Key Documents

381462

Sigma-Aldrich

Pentaerythritol tetrakis(3-mercaptopropionate)

>95%

Synonyme(s) :

Pentaerythritol (3-mercaptopropionate), Pentaerythritol terakis(3-mercaptopropionate), Pentaerythritol tetra(3-mercaptopropionate)

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About This Item

Formule linéaire :
(HSCH2CH2COOCH2)4C
Numéro CAS:
Poids moléculaire :
488.66
Numéro Beilstein :
2312625
Numéro CE :
Numéro MDL:
Code UNSPSC :
12162002
ID de substance PubChem :
Nomenclature NACRES :
NA.23

Niveau de qualité

Pureté

>95%

Indice de réfraction

n20/D 1.531 (lit.)

Point d'ébullition

275 °C/1 mmHg (lit.)

Densité

1.28 g/mL at 25 °C (lit.)

Chaîne SMILES 

SCCC(=O)OCC(COC(=O)CCS)(COC(=O)CCS)COC(=O)CCS

InChI

1S/C17H28O8S4/c18-13(1-5-26)22-9-17(10-23-14(19)2-6-27,11-24-15(20)3-7-28)12-25-16(21)4-8-29/h26-29H,1-12H2

Clé InChI

JOBBTVPTPXRUBP-UHFFFAOYSA-N

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Application

Pentaerythritol tetrakis(3-mercaptopropionate) can be used as a precursor to synthesize:
  • Polymeric degradable networks through thiol-ene click reactions with tri/tetra-acrylates.
  • Thiol-ene-methacrylate composites, which are applicable as dental restorative materials.
  • Network solid polymer electrolytes based on polydimethylsiloxane, for lithium-ion batteries.
It can also be used to functionalize poly(high internal phase emulsions) for removal of heavy metals from water.

Pictogrammes

Exclamation markEnvironment

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Manju Saraswathy et al.
Journal of the mechanical behavior of biomedical materials, 74, 296-303 (2017-06-27)
Significant efforts have been expended to mitigate plasticizer migration from crosslinked methacrylic and poly(vinyl chloride) polymer networks by synthesizing reactive plasticizers that can blend homogenously within the networks to reduce polymer property change, acute toxicity and downstream environmental effects of
Claudio Russo et al.
Polymers, 11(6) (2019-06-07)
Mechanical and rheological properties of novel dual-curing system based on sequential thiol-acrylate and thiol-epoxy reactions are studied with the aim of addressing the obtained materials to suitable advanced applications. The crosslinking process is studied by rheological analysis in order to
Gowtham Sathyanarayanan et al.
Analytical and bioanalytical chemistry, 410(25), 6677-6687 (2018-08-04)
We report the development and characterization of digital microfluidic (DMF) immobilized enzyme reactors (IMERs) for studying cytochrome P450 (CYP)-mediated drug metabolism on droplet scale. The on-chip IMERs consist of porous polymer (thiol-ene) monolith plugs prepared in situ by photopolymerization and
Hsih-Yin Tan et al.
PloS one, 13(5), e0197101-e0197101 (2018-05-11)
This paper presents the design and fabrication of a multi-layer and multi-chamber microchip system using thiol-ene 'click chemistry' aimed for drug transport studies across tissue barrier models. The fabrication process enables rapid prototyping of multi-layer microfluidic chips using different thiol-ene
Mei Chen et al.
ACS applied materials & interfaces, 9(27), 23246-23254 (2017-06-15)
A series of sticky superhydrophobicity surfaces with high water contact angle and high water adhesive force is facilely prepared via an all-solution-processed method based on polymerization-induced phase separation between liquid crystals (LCs) and epoxy resin, which produces layers of epoxy

Articles

With dentists placing nearly 100 million dental fillings into patients′ teeth annually in the U.S. alone, polymeric composite restoratives account for a very large share of the biomaterials market.

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