Methacrylamide

Product Information

Molecular Formula:
C4H7NO
Molecular Weight:
85.10
Description
Methacrylamide (CAS# 79-39-0) is a useful research chemical compound.
Synonyms
2-methyl-2-propenamide; 2-methylprop-2-enamide
IUPAC Name
2-methylprop-2-enamide
Canonical SMILES
CC(=C)C(=O)N
InChI
InChI=1S/C4H7NO/c1-3(2)4(5)6/h1H2,2H3,(H2,5,6)
InChI Key
FQPSGWSUVKBHSU-UHFFFAOYSA-N
Boiling Point
215 °C
Melting Point
108 °C
Flash Point
215°C
Purity
> 98.0 % (GC) (T)
Density
1.115 g/cm3
Appearance
White to almost white powder to crystal
Application
A congener of acrylamide; Used in the chemical, leather processing, paper-pulp-board, polymers, textile processing, and paints-lacquers-varnishes industries; Used as an adhesive, binding agent, corrosion inhibitor, and intermediate.
Storage
Store below +30 °C.
Refractive Index
1.3992 (estimate)
LogP
0.74810
Vapor Pressure
0.1 [mmHg]

Safety Information

Hazards
H302:
Harmful if swallowed.
Precautionary Statement
P260, P261, P264, P270, P271, P280, P301+P312, P304+P340, P305+P351+P338, P309+P311, P312, P314, P330, P337+P313, P403+P233, P405, and P501
Signal Word
Warning

Computed Properties

XLogP3
0.1
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
1
Exact Mass
85.052763847 g/mol
Monoisotopic Mass
85.052763847 g/mol
Topological Polar Surface Area
43.1Ų
Heavy Atom Count
6
Formal Charge
0
Complexity
85.5
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
EP-2960300-A1 Photo-curable coating composition and coated article 2014-06-23
EP-2955219-A1 Water soluble pouch comprising an embossed area 2014-06-12
US-2015360837-A1 Water soluble pouch comprising an embossed area 2014-06-12
WO-2015189762-A2 Organic resin laminate 2014-06-12
WO-2015191796-A1 Water soluble pouch comprising an embossed area 2014-06-12
US-2015376439-A1 Coating composition for a food or beverage can 2014-05-30
US-2015343274-A1 Multi-layered golf balls made with a thiol-ene composition 2014-05-29
EP-2942208-A1 Method for producing a decorated wall or floor panel 2014-05-09
WO-2015169647-A1 Method for producing a decorated wall or floor panel 2014-05-09
US-2015309210-A1 Hydrophilized carbosiloxane vinylic monomers 2014-04-25

Literatures

PMID Publication Date Title Journal
22589068 2012-12-01 Characterization of methacrylated type-I collagen as a dynamic, photoactive hydrogel Biointerphases
22928921 2012-10-08 Biohybrid glycopolymer capable of ionotropic gelation Biomacromolecules
22144174 2012-10-01 Isolation and characterization of an acrylamide-degrading yeast Rhodotorula sp. strain MBH23 KCTC 11960BP Journal of basic microbiology
22673816 2012-07-20 Preparation and characterization of molecularly imprinted polymer for di(2-ethylhexyl) phthalate: application to sample clean-up prior to gas chromatographic determination Journal of chromatography. A
22402576 2012-06-15 Ionic comonomer effect of poly(N-isopropylacrylamide) copolymer containing D-π-A type pyran-based fluorescent dye Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
22525873 2012-06-01 Removal of potentially genotoxic acetamide and arylsulfonate impurities from crude drugs by molecular imprinting Journal of chromatography. A
22700335 2012-06-01 Purification of synthetic oligonucleotides via catching by polymerization Current protocols in nucleic acid chemistry
21978326 2012-05-01 Development of a pH-responsive imprinted polymer for diclofenac and study of its binding properties in organic and aqueous media Drug development and industrial pharmacy
22447582 2012-05-01 Synthesis and characterization of antibacterial dental monomers and composites Journal of biomedical materials research. Part B, Applied biomaterials
22265786 2012-04-01 The mechanical properties and cytotoxicity of cell-laden double-network hydrogels based on photocrosslinkable gelatin and gellan gum biomacromolecules Biomaterials
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

Related Products

Online Inquiry
  • Verification code
USA
  • International:
  • US & Canada (Toll free):
  • Email:
  • Fax:
UK
  • Email:
Copyright © 2024 BOC Sciences. All rights reserved.
Inquiry Basket