Octadecyl acrylate

Product Information

Molecular Formula:
C21H40O2
Molecular Weight:
324.54
Description
Octadecyl acrylate (CAS# 4813-57-4) is a reagent used in the synthesis of comb-like polymers which are incorporated into waterborne latexes improving barrier properties.
Synonyms
octadecyl prop-2-enoate
IUPAC Name
octadecyl prop-2-enoate
Canonical SMILES
CCCCCCCCCCCCCCCCCCOC(=O)C=C
InChI
InChI=1S/C21H40O2/c1-3-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-23-21(22)4-2/h4H,2-3,5-20H2,1H3
InChI Key
FSAJWMJJORKPKS-UHFFFAOYSA-N
Boiling Point
402.85 ℃ (rough estimate)
Melting Point
32-34 ℃ (lit.)
Flash Point
>230 °F
Purity
> 97.0 % (GC)
Density
0.80 g/cm3
Appearance
White to light brown powder
Refractive Index
1.5344 (estimate)
LogP
6.97710

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
H335:
May cause respiratory irritation.
H411:
Toxic to aquatic life with long-lasting effects.
Precautionary Statement
P261, P264, P271, P272, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P333+P313, P337+P313, P362, P363, P391, P403+P233, P405, and P501
Signal Word
Warning

Computed Properties

XLogP3
9.4
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
19
Exact Mass
324.302830514 g/mol
Monoisotopic Mass
324.302830514 g/mol
Topological Polar Surface Area
26.3Ų
Heavy Atom Count
23
Formal Charge
0
Complexity
261
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114133783-A Polymer putty, putty coating, preparation method, putty coating and application 2021-12-30
CN-114164663-A High-performance durable polyurethane polyacrylate waterproof agent and preparation method thereof 2021-12-21
JP-2022040149-A Adhesive composition and laminated film using it 2021-12-21
CN-114163743-A Silicification-free rubber plug for syringe and preparation method thereof 2021-12-17
CN-113912893-A Colorful film and preparation method thereof 2021-12-15
CN-113912893-B Colorful film and preparation method thereof 2021-12-15
CN-114149750-A Adhesive, heat-curable adhesive tape, and preparation method and use method thereof 2021-12-14
CN-114045059-A Electrophoretic paint capable of preventing liquid and bacteria from adhering and application method thereof 2021-12-10
CN-114106235-A Method for realizing low-temperature solid state polymerization by regulating and controlling rotor phase temperature interval 2021-12-09
CN-114106244-A Fluorine-free waterproofing agent copolymer and preparation method thereof 2021-12-07

Literatures

PMID Publication Date Title Journal
23044125 2013-01-02 β-Cyclodextrin-based oil-absorbent microspheres: preparation and high oil absorbency Carbohydrate polymers
22826176 2012-11-01 Folate-conjugated thermo-responsive micelles for tumor targeting Journal of biomedical materials research. Part A
22699229 2012-07-01 Selectivity enhancement for the separation of tocopherols and steroids by integration of highly ordered weak interaction sites along the polymer main chain Analytical and bioanalytical chemistry
22204937 2012-04-06 Molecular-shape selective high-performance liquid chromatography: stabilization effect of polymer main chain by alternating copolymerization Journal of chromatography. A
22505922 2012-01-01 Micellar liquid chromatographic determination of carbaryl and 1-naphthol in water, soil, and vegetables International journal of analytical chemistry
21737085 2011-10-21 Acrylate ester-based monolithic columns for capillary electrochromatography separation of triacylglycerols in vegetable oils Journal of chromatography. A
21770163 2011-06-01 Thermo-responsive nanofiber mats fabricated by electrospinning of poly(N-isopropylacrylamide-co-stearyl acrylate) Journal of nanoscience and nanotechnology
21455910 2011-04-01 Controlling retention, selectivity and magnitude of EOF by segmented monolithic columns consisting of octadecyl and naphthyl monolithic segments--applications to RP-CEC of both neutral and charged solutes Electrophoresis
21462226 2011-04-01 Mixed ligand monolithic columns for reversed-phase capillary electrochromatography via hydrophobic and π interactions Electrophoresis
20715142 2010-10-01 Preparation of high-selective HPLC packing materials based on alternating copolymer-grafted silica Journal of separation science
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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