N-(2-Hydroxyethyl)acrylamide (stabilized with MEHQ)

Product Information

Molecular Formula:
C5H9NO2
Molecular Weight:
115.13
Description
N-(2-Hydroxyethyl)acrylamide (stabilized with MEHQ) is a vital compound used in the biomedical industry. It plays a significant role as a monomer in the synthesis of hydrogels for drug delivery systems, tissue engineering, and controlled release applications. This product exhibits stability due to the addition of MEHQ, ensuring quality and reliability.
Synonyms
N-(2-Hydroxyethyl)acrylamide; N-(2-hydroxyethyl)prop-2-enamide; N-Hydroxyethyl acrylamide; 2-Propenamide, N-(2-hydroxyethyl)-; N-(2-HYDROXYETHYL)ACRYLAMIDE (STABILIZED WITH MEHQ); N-Hydroxyethyl acrylamide(heaa),98%; HEAA; n-hydroxyethylacrylamide; N-2-hydroxyethylacrylamide; (2-hydroxyethyl)acrylamide; N-(2-Hydroxyethyl)acrylamide, (stabilized with MEHQ); N-(2-HYDROXYETHYL)ACRYLAMIDE(STABILIZED WITH MHQ); N-Hydroxyethyl acrylamide, contains 1,000 ppm monomethyl ether hydroquinone as stabilizer, 97%
IUPAC Name
N-(2-hydroxyethyl)prop-2-enamide
Canonical SMILES
C=CC(=O)NCCO
InChI
InChI=1S/C5H9NO2/c1-2-5(8)6-3-4-7/h2,7H,1,3-4H2,(H,6,8)
InChI Key
UUORTJUPDJJXST-UHFFFAOYSA-N
Boiling Point
129-130 °C
Flash Point
110 °C
Purity
>98.0%(GC)(T)
Density
1.111 g/mL at 25 °C
Appearance
Colorless to Light yellow to Light orange clear liquid
Storage
0-10℃
Refractive Index
n20/D 1.505

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P264:
Wash thoroughly after handling.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352:
IF ON SKIN:
Wash with plenty of soap and water.
P332+P313:
If skin irritation occurs:
Get medical advice/attention.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P362+P364:
Take off contaminated clothing. [As modified by IV ATP].
And wash it before reuse. [Added by IV ATP].

Computed Properties

XLogP3
-0.6
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
2
Rotatable Bond Count
3
Exact Mass
115.063328530 g/mol
Monoisotopic Mass
115.063328530 g/mol
Topological Polar Surface Area
49.3Ų
Heavy Atom Count
8
Formal Charge
0
Complexity
90.4
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-114195961-A Rigid nanoparticle modified polyacrylamide 2022-02-21
CN-114085391-A High-sensitivity flexible pressure sensing material in pure water and application thereof 2022-01-20
CN-114106749-A Low-viscosity thermosetting particle board starch adhesive and preparation method thereof 2021-12-24
CN-114149527-A Method for realizing controllable free radical polymerization in air atmosphere and application thereof 2021-12-10
CN-114014998-A Method for synthesizing copolymer by using soybean seed coat peroxidase catalysis 2021-12-02
CN-113979661-A Preparation method of nano calcium silicate suspension with high stability and good early strength effect 2021-11-30
CN-114133688-A Modified water-based organic siloxane-acrylate hybrid resin and preparation and application thereof 2021-11-29
CN-114014971-A Preparation method and application of acrylic-based hydrogel antifouling material without volatile organic compounds 2021-11-25
CN-113896844-A Carboxylic styrene-butadiene latex for carpet and preparation method thereof 2021-11-19
CN-113880467-A Modified circulating fluidized bed fly ash-based cementing material and preparation method thereof 2021-11-18

Literatures

PMID Publication Date Title Journal
22920409 2012-11-15 Preparation and characterization of composites built of poly(N-benzophenoyl methacrylamide-co-N-hydroxyethyl acrylamide) cores and silica raspberry-like shells with dual orthogonal functionality Journal of colloid and interface science
22385343 2012-04-09 Gel formation driven by tunable hydrophobic domain: design of acrylamide macromonomer with oligo hydrophobic segment Biomacromolecules
21972885 2011-11-14 Synthesis and characterization of poly(N-hydroxyethylacrylamide) for long-term antifouling ability Biomacromolecules
21314109 2011-03-14 Bioinspired imprinted PHEMA-hydrogels for ocular delivery of carbonic anhydrase inhibitor drugs Biomacromolecules
12069238 2002-06-01 High-throughput, high-sensitivity genetic mutation detection by tandem single-strand conformation polymorphism/heteroduplex analysis capillary array electrophoresis Analytical chemistry
12191509 2002-06-01 Chemically synthesized solid phase oligosaccharide probes for carbohydrate-binding receptors. Interactions of the E-, L- and P-selectins with sialyl-Le(x) and O-sulphated forms linked to biotin or to polyacrylamide Journal of immunological methods
12116153 2002-05-01 Poly-N-hydroxyethylacrylamide (polyDuramide): a novel, hydrophilic, self-coating polymer matrix for DNA sequencing by capillary electrophoresis Electrophoresis
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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