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Details

Stereochemistry ACHIRAL
Molecular Formula C10H18O2
Molecular Weight 170.2487
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of HEXYL METHACRYLATE

SMILES

CCCCCCOC(=O)C(C)=C

InChI

InChIKey=LNCPIMCVTKXXOY-UHFFFAOYSA-N
InChI=1S/C10H18O2/c1-4-5-6-7-8-12-10(11)9(2)3/h2,4-8H2,1,3H3

HIDE SMILES / InChI

Molecular Formula C10H18O2
Molecular Weight 170.2487
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Design and characterization of PEGylated terpolymer biomaterials.
2010-09-15
Degradable, pH-sensitive, membrane-destabilizing, comb-like polymers for intracellular delivery of nucleic acids.
2010-09
Macroscopic frictional properties of poly(1-(2-methacryloyloxy)ethyl-3-butyl imidazolium bis(trifluoromethanesulfonyl)-imide) brush surfaces in an ionic liquid.
2010-04
Interaction of endothelial cells with methacrylic terpolymer biomaterials.
2010-02
In vitro drug release study of methacrylate polymer blend system: effect of polymer blend composition, drug loading and solubilizing surfactants on drug release.
2010-02
Phase Behavior of a Weakly Interacting Polystyrene and Poly(n-hexyl methacrylate) System: Evidence for the Coexistence of UCST and LCST.
2009-03-19
Preparation and characterization of hexyl methacrylate monolithic columns for CEC.
2008-09
Release of antimicrobial and antiviral drugs from methacrylate copolymer system: effect of copolymer molecular weight and drug loading on drug release.
2008-02
The effects of two monofunctional diluent monomers and two photoinitiator systems on the properties of UDMA-based composites.
2007-06
Preparation and characterization of methacrylate-based semi-micro monoliths for high-throughput bioanalysis.
2006-10
Poly(n-hexyl methacrylate) polymerization in three-component microemulsion stabilized by a cationic surfactant.
2006-04-15
Final report of the safety assessment of methacrylate ester monomers used in nail enhancement products.
2005
Synthesis and characterization of acrylic terpolymers with RGD peptides for biomedical applications.
2004-07
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:08:13 GMT 2025
Edited
by admin
on Mon Mar 31 19:08:13 GMT 2025
Record UNII
538B2Q3HSV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
N-HEXYL METHACRYLATE
HSDB  
Preferred Name English
HEXYL METHACRYLATE
Systematic Name English
N-HEXYL METHACRYLATE [HSDB]
Common Name English
NSC-24169
Code English
METHACRYLIC ACID, HEXYL ESTER
Common Name English
HEXYL 2-METHYL-2-PROPENOATE
Systematic Name English
2-PROPENOIC ACID, 2-METHYL-, HEXYL ESTER
Systematic Name English
Code System Code Type Description
FDA UNII
538B2Q3HSV
Created by admin on Mon Mar 31 19:08:13 GMT 2025 , Edited by admin on Mon Mar 31 19:08:13 GMT 2025
PRIMARY
EPA CompTox
DTXSID4025406
Created by admin on Mon Mar 31 19:08:13 GMT 2025 , Edited by admin on Mon Mar 31 19:08:13 GMT 2025
PRIMARY
NSC
24169
Created by admin on Mon Mar 31 19:08:13 GMT 2025 , Edited by admin on Mon Mar 31 19:08:13 GMT 2025
PRIMARY
PUBCHEM
8872
Created by admin on Mon Mar 31 19:08:13 GMT 2025 , Edited by admin on Mon Mar 31 19:08:13 GMT 2025
PRIMARY
CAS
142-09-6
Created by admin on Mon Mar 31 19:08:13 GMT 2025 , Edited by admin on Mon Mar 31 19:08:13 GMT 2025
PRIMARY
HSDB
5418
Created by admin on Mon Mar 31 19:08:13 GMT 2025 , Edited by admin on Mon Mar 31 19:08:13 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-521-9
Created by admin on Mon Mar 31 19:08:13 GMT 2025 , Edited by admin on Mon Mar 31 19:08:13 GMT 2025
PRIMARY