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Methacrylamide - 98%, high purity , CAS No.79-39-0
Basic Description
Synonyms
AKOS000121166 | alpha-Methyl acrylic amide | EPA Pesticide Chemical Code 052901 | M0077 | Methacrylamide 2-Methylpropenamide | methyl acrylamide | Tox21_300001 | EINECS 201-202-3 | Methacrylic amide | 2-methylprop-2-enamide | Methacrylamide, purum, >=98.0
Specifications & Purity
≥98%
Shipped In
Normal
Product Description
Application
Methacrylamide is a reagent used in the production of polymers and copolymers. It is also used as a raw material in the production of chemicals for industrial and professional use such as textiles, leather, fur, bulk, large scale chemicals (including petroleum products), fine chemicals, formulation [mixing] of preparations and/or re-packaging (excluding alloys), building and construction work, electricity, steam, gas, water supply and sewage treatment.
Taxonomic Classification
Kingdom
Organic compounds
Superclass
Organic acids and derivatives
Class
Carboxylic acids and derivatives
Subclass
Carboxylic acid derivatives
Intermediate Tree Nodes
Carboxylic acid amides
Direct Parent
Primary carboxylic acid amides
Alternative Parents
Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework
Aliphatic acyclic compounds
Substituents
Primary carboxylic acid amide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
Description
This compound belongs to the class of organic compounds known as primary carboxylic acid amides. These are compounds comprising primary carboxylic acid amide functional group, with the general structure RC(=O)NH2.
External Descriptors
acrylamides
Data sources
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
Associated Targets(Human)
Mechanisms of Action
Mechanism of Action
Action Type
target ID
Target Name
Target Type
Target Organism
Binding Site Name
References
Names and Identifiers
Pubchem Sid
504751136
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504751136
IUPAC Name
2-methylprop-2-enamide
INCHI
InChI=1S/C4H7NO/c1-3(2)4(5)6/h1H2,2H3,(H2,5,6)
InChIKey
FQPSGWSUVKBHSU-UHFFFAOYSA-N
Smiles
CC(=C)C(=O)N
Isomeric SMILES
CC(=C)C(=O)N
WGK Germany
1
RTECS
UC6475000
Molecular Weight
85.1
Beilstein
605397
Reaxy-Rn
605397
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=605397&ln=
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
Chemical and Physical Properties
Solubility
Soluble in water (202g/L at 20°C)
Sensitivity
Moisture sensitive.
Boil Point(°C)
215 °C
Melt Point(°C)
106-110°C
Molecular Weight
85.100 g/mol
XLogP3
0.100
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
1
Rotatable Bond Count
1
Exact Mass
85.0528 Da
Monoisotopic Mass
85.0528 Da
Topological Polar Surface Area
43.100 Ų
Heavy Atom Count
6
Formal Charge
0
Complexity
85.500
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
The total count of all stereochemical bonds
0
Covalently-Bonded Unit Count
1
Citations of This Product
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