n-Octyl methacrylate

Product Information

Molecular Formula:
H3C(CH2)7OCOC(CH3)=CH2
Molecular Weight:
198.3
Description
OMA is hydrophobic methacrylate monomer.
Synonyms
Octyl methacrylate; octyl 2-methylprop-2-enoate; 2-Propenoic acid, 2-methyl-, octyl ester; Octyl 2-methyl-2-propenoate; Octyl 2-methylacrylate; Octyl 2-methylacrylate #; N-Octyl methacrylate,99+%; Methacrylic acid, octyl ester
IUPAC Name
octyl 2-methylprop-2-enoate
Canonical SMILES
CCCCCCCCOC(=O)C(=C)C
InChI
InChI=1S/C12H22O2/c1-4-5-6-7-8-9-10-14-12(13)11(2)3/h2,4-10H2,1,3H3
InChI Key
NZIDBRBFGPQCRY-UHFFFAOYSA-N
Boiling Point
105°C 0,3mm
Flash Point
82°C
Purity
99+%
Density
0,89 g/cm3
Solubility
less than 0.1 mg/mL at 64 °F
Storage
Store at 4 degrees celsius
Refractive Index
1.4370 (20℃)

Safety Information

Hazards
Combustible
, Unknown

Computed Properties

XLogP3
5
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
9
Exact Mass
198.161979940 g/mol
Monoisotopic Mass
198.161979940 g/mol
Topological Polar Surface Area
26.3Ų
Heavy Atom Count
14
Formal Charge
0
Complexity
173
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-113980189-A Polyester acrylic acid weather-resistant pressure-sensitive adhesive and preparation method thereof 2021-12-17
CN-114149750-A Adhesive, heat-curable adhesive tape, and preparation method and use method thereof 2021-12-14
CN-114133886-A Automobile paint surface protective film 2021-12-07
CN-114133688-A Modified water-based organic siloxane-acrylate hybrid resin and preparation and application thereof 2021-11-29
CN-114044881-A Phosphate modified waterborne epoxy ester resin and antirust primer and preparation method thereof 2021-11-26
KR-20210154114-A A assurance view sheet for the traffic lane 2021-11-26
CN-114163567-A Method for synthesizing dye-doped organic-inorganic composite latex by double in-situ emulsion copolymerization 2021-11-18
CN-114032054-A VOC-free aqueous polyurethane adhesive for medicine packaging and preparation method thereof 2021-11-12
CN-114031998-A Heat-resistant waterborne polyurethane coating and preparation method thereof 2021-11-10
CN-114057430-A Preparation method of water-based ceramic slurry for coating and battery diaphragm 2021-11-08

Literatures

PMID Publication Date Title Journal
19762947 2009-10-14 Self-assembly of poly(o-methoxyaniline) hollow nanospheres from a polymeric acid solution Nanotechnology
18552855 2008-07-01 Functional immobilization of signaling proteins enables control of stem cell fate Nature methods
17511997 2007-09-01 Side-chain effect on Langmuir and Langmuir-Blodgett film properties of poly(N-alkylmethacrylamide)-coated magnetic nanoparticle Journal of colloid and interface science
17477931 2007-06-22 Preparation of stir bars for sorptive extraction based on monolithic material Journal of chromatography. A
17509254 2007-05-01 Basal cell and squamous cell skin cancers Journal of the National Comprehensive Cancer Network : JNCCN
16970449 2006-09-21 Formation of silver nanoparticles in deoxyribonucleic acid-poly(o-methoxyaniline) hybrid: a novel nano-biocomposite The journal of physical chemistry. B
15679155 2005-01-14 Octyl-type monolithic columns of 530 microm i.d. for capillary liquid chromatography Journal of chromatography. A
14967529 2004-07-01 Synthesis and characterization of acrylic terpolymers with RGD peptides for biomedical applications Biomaterials
14566809 2003-11-01 Fibronectin anchorage to polymer substrates controls the initial phase of endothelial cell adhesion Journal of biomedical materials research. Part A
11562241 2001-09-26 Different surface-restructuring behaviors of poly(methacrylate)s detected by SFG in water Journal of the American Chemical Society
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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