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Details

Stereochemistry ACHIRAL
Molecular Formula C14H18O7
Molecular Weight 298.2885
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PENTAERYTHRITYL TRIACRYLATE

SMILES

OCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C

InChI

InChIKey=HVVWZTWDBSEWIH-UHFFFAOYSA-N
InChI=1S/C14H18O7/c1-4-11(16)19-8-14(7-15,9-20-12(17)5-2)10-21-13(18)6-3/h4-6,15H,1-3,7-10H2

HIDE SMILES / InChI

Molecular Formula C14H18O7
Molecular Weight 298.2885
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Occupational methacrylate and acrylate allergy--cross-reactions and possible screening allergens.
2010-12
[Molecularly imprinted technique-flow injection-chemoluminescence system analysis detect phenol in water].
2010-11
Ultraviolet light crosslinking of poly(trimethylene carbonate) for elastomeric tissue engineering scaffolds.
2010-11
Holographically directed assembly of polymer nanocomposites.
2010-10-26
Biodegradable elastomeric networks: highly efficient cross-linking of poly(trimethylene carbonate) by gamma irradiation in the presence of pentaerythritol triacrylate.
2010-10-11
Novel concept microarray enabling PCR and multistep reactions through pipette-free aperture-to-aperture parallel transfer.
2010-10-06
A novel, neutral hydroxylated octadecyl acrylate monolith with fast electroosmotic flow velocity and its application to the separation of various solutes including peptides and proteins in the absence of electrostatic interactions.
2010-10
Sulfoalkylbetaine-based monolithic column with mixed-mode of hydrophilic interaction and strong anion-exchange stationary phase for capillary electrochromatography.
2010-09
Preparation and evaluation of a sulfoalkylbetaine-based zwitterionic monolithic column for CEC of polar analytes.
2009-08
Preparation and evaluation of a neutral methacrylate-based monolithic column for hydrophilic interaction stationary phase by pressurized capillary electrochromatography.
2009-05-22
Preparation of a mixed-mode hydrophilic interaction/anion-exchange polymeric monolithic stationary phase for capillary liquid chromatography of polar analytes.
2009-01-30
Methacrylate-based monolithic column with mixed-mode hydrophilic interaction/strong cation-exchange stationary phase for capillary liquid chromatography and pressure-assisted CEC.
2008-10
Integral geometry analysis of fluorescence micrographs for quantitative relative comparison of protein adsorption onto polymer surfaces.
2008-09-16
Controlling poly(beta-amino ester) network properties through macromer branching.
2008-03
New biomedical devices with selective peptide recognition properties. Part 1: Characterization and cytotoxicity of molecularly imprinted polymers.
2008-01-22
Hydroxyl functionalized thermosensitive microgels with quadratic crosslinking density distribution.
2007-09-01
Selective solid-phase extraction of trace cadmium(II) with an ionic imprinted polymer prepared from a dual-ligand monomer.
2007-06-12
Rapid and sensitive determination of the conversion of UV-cured acrylic ester resins by pyrolysis-gas chromatography in the presence of an organic alkali.
2007-05
Toxicology studies of pentaerythritol triacrylate (technical grade) (CAS No. 3524-68-3) in F344/N rats, B6C3F1 mice, and genetically modified (FVB Tg.AC hemizygous) mice (dermal studies).
2005-10
Synthesis of biodegradable cross-linked poly(beta-amino ester) for gene delivery and its modification, inducing enhanced transfection efficiency and stepwise degradation.
2005-09-22
An epidemic of occupational contact dermatitis from an acrylic glue.
2005-03
[Effect of synthesis conditions on the morphology and binding property of (-)-ephedrine imprinted polymers].
2005-01
Topical application of representative multifunctional acrylates produced proliferative and inflammatory lesions in F344/N rats and B6C3F1 mice, and squamous cell neoplasms in Tg.AC mice.
2005
Water-borne, in situ crosslinked biomaterials from phase-segregated precursors.
2003-03-01
Separation of ephedrine stereoisomers by molecularly imprinted polymers--influence of synthetic conditions and mobile phase compositions on the chromatographic performance.
2002-11
Allergic contact dermatitis from trimethylolpropane triacrylate and pentaerythritol triacrylate.
2002-10
Release of protein from highly cross-linked hydrogels of poly(ethylene glycol) diacrylate fabricated by UV polymerization.
2001-05
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:42:23 GMT 2025
Edited
by admin
on Mon Mar 31 21:42:23 GMT 2025
Record UNII
PJJ1161ULF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-PROPENOIC ACID, 1,1'-(2-(HYDROXYMETHYL)-2-(((1-OXO-2-PROPEN-1-YL)OXY)METHYL)-1,3-PROPANEDIYL) ESTER
Preferred Name English
PENTAERYTHRITYL TRIACRYLATE
INCI  
INCI  
Official Name English
2-PROPENOIC ACID, 2-(HYDROXYMETHYL)-2-(((1-OXO-2-PROPENYL)OXY)METHYL)-1,3-PROPANEDIYL ESTER
Systematic Name English
ACRYLIC ACID, TRIESTER WITH PENTAERYTHRITOL
Systematic Name English
PENTAERYTHRITOL TRIACRYLATE
Systematic Name English
Code System Code Type Description
CAS
3524-68-3
Created by admin on Mon Mar 31 21:42:23 GMT 2025 , Edited by admin on Mon Mar 31 21:42:23 GMT 2025
PRIMARY
FDA UNII
PJJ1161ULF
Created by admin on Mon Mar 31 21:42:23 GMT 2025 , Edited by admin on Mon Mar 31 21:42:23 GMT 2025
PRIMARY
PUBCHEM
19042
Created by admin on Mon Mar 31 21:42:23 GMT 2025 , Edited by admin on Mon Mar 31 21:42:23 GMT 2025
PRIMARY
EPA CompTox
DTXSID2025842
Created by admin on Mon Mar 31 21:42:23 GMT 2025 , Edited by admin on Mon Mar 31 21:42:23 GMT 2025
PRIMARY
ECHA (EC/EINECS)
222-540-8
Created by admin on Mon Mar 31 21:42:23 GMT 2025 , Edited by admin on Mon Mar 31 21:42:23 GMT 2025
PRIMARY