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Merck
CN

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:
Molecular Weight:
488.66
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
231-472-8
Beilstein/REAXYS Number:
2312625
MDL number:
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Product Name

Pentaerythritol tetrakis(3-mercaptopropionate), >95%

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

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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.

pictograms

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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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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
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
Dailyn Guzmán et al.
Polymers, 12(2) (2020-02-09)
The pure trifunctional glycidyl monomer from phloroglucinol (3EPO-Ph) was synthesized and used as feedstock in the preparation of novel bio-based thermosets by thiol-epoxy curing. The monomer was crosslinked with different commercially available thiols: tetrafunctional thiol (PETMP), trifunctional thiol (TTMP) and
Yetunde Adewunmi et al.
Applied and environmental microbiology, 86(4) (2019-12-08)
Plant-derived aldehydes are constituents of essential oils that possess broad-spectrum antimicrobial activity and kill microorganisms without promoting resistance. In our previous study, we incorporated p-anisaldehyde from star anise into a polymer network called proantimicrobial networks via degradable acetals (PANDAs) and

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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