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Details

Stereochemistry ACHIRAL
Molecular Formula C22H42O2
Molecular Weight 338.5677
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of STEARYL METHACRYLATE

SMILES

CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C

InChI

InChIKey=HMZGPNHSPWNGEP-UHFFFAOYSA-N
InChI=1S/C22H42O2/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-24-22(23)21(2)3/h2,4-20H2,1,3H3

HIDE SMILES / InChI

Molecular Formula C22H42O2
Molecular Weight 338.5677
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Rapid analysis of trace levels of flavins by pressurized capillary electrochromatography-laser induced fluorescence detection with sulfonated N-octadecyl methacrylate monolith.
2010-12-15
Synthesis and solution rheology of poly[(stearyl methacrylate)-stat-([2-(methacryloyloxy)ethyl] trimethyl ammonium iodide)].
2010-11-15
Silica-based monolithic capillary columns-Effect of preparation temperature on separation efficiency.
2010-09-03
Preparation of a neutral porous monolith and its evaluation in pressurized capillary electrochromatography with neutral and charged solutes.
2010-05
[Development of a novel multi-functional adsorbent bearing with long-chain hydrophobic and anion exchange groups for the simple and rapid determination of residual acephate in vegetables].
2010
Selectivity comparisons of monolithic silica capillary columns modified with poly(octadecyl methacrylate) and octadecyl moieties for halogenated compounds in reversed-phase liquid chromatography.
2009-07-31
Different alkyl dimethacrylate mediated stearyl methacrylate monoliths for improving separation efficiency of typical alkylbenzenes and proteins.
2009-04-10
Architecture of hyperbranched polymers consisting of a stearyl methacrylate sequence via a living radical copolymerization.
2008-07-15
Architecture of brush-on-brush copolymers by photoinduced ATRP approach.
2008-06-01
Study of a monolithic silica capillary column coated with poly(octadecyl methacrylate) for the reversed-phase liquid chromatographic separation of some polar and non-polar compounds.
2007-12-14
Optimization of the porous structure and polarity of polymethacrylate-based monolithic capillary columns for the LC-MS separation of enzymatic digests.
2007-11
Preparation of polymethacrylate monolithic stationary phases having bonded octadecyl ligands and sulfonate groups: electrochromatographic characterization and application to the separation of polar solutes for pressurized capillary electrochromatography.
2007-10-26
Cross-linking-induced permanently perpendicular helix orientation in surface-grafted polyglutamate films.
2007-07-17
Preparation of high efficiency and highly retentive monolithic silica capillary columns for reversed-phase chromatography by chemical modification by polymerization of octadecyl methacrylate.
2007-07-13
[Pilot study of a cell membrane like biomimetic drug-eluting coronary stent].
2007-06
Preparation and characterization of long alkyl chain methacrylate-based monolithic column for capillary chromatography.
2007-02-23
Synthesis and purification of oxide nanoparticle dispersions by modified emulsion precipitation.
2005-06-07
Monitoring surface thermal transitions of ABA triblock copolymers with crystalline segments using phase contrast tapping mode atomic force microscopy.
2005-02-15
A novel crosslinkable polymer as drug-loaded coating for biomedical device.
2004-02
Capillary electrochromatography of peptides on microfabricated poly(dimethylsiloxane) chips modified by cerium(IV)-catalyzed polymerization.
2002-03-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:35:32 GMT 2025
Edited
by admin
on Mon Mar 31 18:35:32 GMT 2025
Record UNII
43A41KA91Q
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
STEARYL METHACRYLATE
Systematic Name English
N-OCTADECYL METHACRYLATE
Preferred Name English
Code System Code Type Description
ECHA (EC/EINECS)
251-013-5
Created by admin on Mon Mar 31 18:35:32 GMT 2025 , Edited by admin on Mon Mar 31 18:35:32 GMT 2025
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FDA UNII
43A41KA91Q
Created by admin on Mon Mar 31 18:35:32 GMT 2025 , Edited by admin on Mon Mar 31 18:35:32 GMT 2025
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CAS
32360-05-7
Created by admin on Mon Mar 31 18:35:32 GMT 2025 , Edited by admin on Mon Mar 31 18:35:32 GMT 2025
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PUBCHEM
122600
Created by admin on Mon Mar 31 18:35:32 GMT 2025 , Edited by admin on Mon Mar 31 18:35:32 GMT 2025
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EPA CompTox
DTXSID6027975
Created by admin on Mon Mar 31 18:35:32 GMT 2025 , Edited by admin on Mon Mar 31 18:35:32 GMT 2025
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