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Merck

381462

Pentaerythritol tetrakis(3-mercaptopropionate)

>95%

Synonym(s):

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

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About This Item

Linear Formula:
(HSCH2CH2COOCH2)4C
CAS Number:
7575-23-7
Molecular Weight:
488.66
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
24863819
EC Number:
231-472-8
Beilstein/REAXYS Number:
2312625
MDL number:
MFCD00022104

Key Documents

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InChI key

JOBBTVPTPXRUBP-UHFFFAOYSA-N

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

SMILES string

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

assay

>95%

refractive index

n20/D 1.531 (lit.)

bp

275 °C/1 mmHg (lit.)

density

1.28 g/mL at 25 °C (lit.)

Quality Level

200

Related Categories

Application

The Progress in Development of Dental Restorative Materials
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.

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

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

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ5756
MKCW6544
MKCT8642
MKCS5006
MKCR6717

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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
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
N A Traugutt et al.
Soft matter, 13(39), 7013-7025 (2017-09-21)
This study presents the first direct comparison of the influence of liquid-crystal order during synthesis on the thermo-mechanical behaviors of main-chain liquid-crystal elastomers (LCEs) in thiol-acrylate networks. Six polydomain nematic elastomer (PNE) chemistries were compared directly by synthesizing with the
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
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Articles

The Progress in Development of Dental Restorative Materials

Composite materials based on methacrylate monomers are used to provide aesthetic and functional restoration of dental tissue. Polymerization chemistries are being developed to improve the reliability of these materials.

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