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Details

Stereochemistry ACHIRAL
Molecular Formula C9H16O2
Molecular Weight 156.2221
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HEXYL ACRYLATE

SMILES

CCCCCCOC(=O)C=C

InChI

InChIKey=LNMQRPPRQDGUDR-UHFFFAOYSA-N
InChI=1S/C9H16O2/c1-3-5-6-7-8-11-9(10)4-2/h4H,2-3,5-8H2,1H3

HIDE SMILES / InChI

Molecular Formula C9H16O2
Molecular Weight 156.2221
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
The potential dermal irritating effect of residual (meth)acrylic monomers in pressure sensitive adhesive tapes.
2010
Prediction of the reduced glutathione (GSH) reactivity of dental methacrylate monomers using NMR spectra - Relationship between toxicity and GSH reactivity.
2009-11
Hydrophobically modified oligoethylenimines as highly efficient transfection agents for siRNA delivery.
2009-11
On the nature of ionic liquids and their effects on lipases that catalyze ester synthesis.
2009-03-25
CEC separation of peptides using a poly(hexyl acrylate-co-1,4-butanediol diacrylate-co-[2-(acryloyloxy)ethyl]trimethyl ammonium chloride) monolithic column.
2008-09
Determination of trace levels of benzodiazepine in urine using capillary electrochromatography-time of flight mass spectrometry.
2008-05
Online preconcentration using monoliths in electrochromatography capillary format and microchips.
2007-11
Alkyl chain length effects on copolymerization kinetics of a monoacrylate with hexanediol diacrylate.
2007-10-27
Electrochromatography in poly(dimethyl)siloxane microchips using organic monolithic stationary phases.
2007-06
Chemoselective alkylation of N-alkylaminooxy-containing peptides.
2006-08-03
Development of acrylate-based monolithic stationary phases for electrochromatographic separations.
2005-11
Non-particulate (continuous bed or monolithic) acrylate-based capillary columns for reversed-phase liquid chromatography and electrochromatography.
2005-04-15
Tools for fluorescent molecularly imprinted polymers.
2005-01-15
Antimicrobial activity of p-hydroxyphenyl acrylate derivatives.
2004-12-15
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:58:53 GMT 2025
Edited
by admin
on Mon Mar 31 19:58:53 GMT 2025
Record UNII
X0670P452A
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AGEFLEX N-HA
Preferred Name English
HEXYL ACRYLATE
Systematic Name English
ACRYLIC ACID, HEXYL ESTER
Common Name English
HEXYL 2-PROPENOATE
Systematic Name English
2-PROPENOIC ACID, HEXYL ESTER [HSDB]
Common Name English
NSC-11786
Code English
N-HEXYL ACRYLATE
Common Name English
Code System Code Type Description
HSDB
5463
Created by admin on Mon Mar 31 19:58:53 GMT 2025 , Edited by admin on Mon Mar 31 19:58:53 GMT 2025
PRIMARY
EPA CompTox
DTXSID5022194
Created by admin on Mon Mar 31 19:58:53 GMT 2025 , Edited by admin on Mon Mar 31 19:58:53 GMT 2025
PRIMARY
FDA UNII
X0670P452A
Created by admin on Mon Mar 31 19:58:53 GMT 2025 , Edited by admin on Mon Mar 31 19:58:53 GMT 2025
PRIMARY
NSC
11786
Created by admin on Mon Mar 31 19:58:53 GMT 2025 , Edited by admin on Mon Mar 31 19:58:53 GMT 2025
PRIMARY
ECHA (EC/EINECS)
219-698-5
Created by admin on Mon Mar 31 19:58:53 GMT 2025 , Edited by admin on Mon Mar 31 19:58:53 GMT 2025
PRIMARY
CAS
2499-95-8
Created by admin on Mon Mar 31 19:58:53 GMT 2025 , Edited by admin on Mon Mar 31 19:58:53 GMT 2025
PRIMARY
PUBCHEM
17259
Created by admin on Mon Mar 31 19:58:53 GMT 2025 , Edited by admin on Mon Mar 31 19:58:53 GMT 2025
PRIMARY