Cas no 5883-17-0 (N-Ethylacrylamide)

N-Ethylacrylamide is a versatile acrylamide derivative with the molecular formula C?H?NO. It is a reactive monomer commonly used in polymer synthesis, particularly in the production of polyacrylamides and hydrogels. The ethyl substitution enhances solubility in organic solvents while retaining the reactivity of the acrylamide group, making it suitable for radical polymerization applications. Its crosslinking properties are valuable in creating tailored polymeric networks for biomedical, adhesive, and coatings industries. N-Ethylacrylamide exhibits good thermal stability and compatibility with other monomers, enabling precise control over polymer properties. Proper handling is required due to its potential skin and respiratory sensitization.
N-Ethylacrylamide structure
N-Ethylacrylamide structure
Product Name:N-Ethylacrylamide
CAS No:5883-17-0
MF:C5H9NO
MW:99.1310613155365
MDL:MFCD00048514
CID:85475
PubChem ID:329767143
Update Time:2025-09-28

N-Ethylacrylamide Chemical and Physical Properties

Names and Identifiers

    • N-Ethylacrylamide
    • N-ethyl-2-Propenamide
    • N-ethylprop-2-enamide
    • Acrylsaeure-aethylamid
    • N-Aethyl-acrylamid
    • poly(N-ethylacrylamide)
    • EN300-6477121
    • AB9195
    • A8303
    • MFCD00048514
    • MFCD03458133
    • AS-56872
    • N-Ethylacrylamide, contains MEHQ as inhibitor, 99% (HPLC)
    • N-ETHYL ACRYLAMIDE
    • 2-Propenamide, N-ethyl-
    • AMY36703
    • FT-0695176
    • AKOS009808478
    • 5883-17-0
    • BB 0261739
    • 25215-59-2
    • SWPMNMYLORDLJE-UHFFFAOYSA-N
    • CS-W013719
    • DTXSID10430697
    • DB-072522
    • MDL: MFCD00048514
    • Inchi: 1S/C5H9NO/c1-3-5(7)6-4-2/h3H,1,4H2,2H3,(H,6,7)
    • InChI Key: SWPMNMYLORDLJE-UHFFFAOYSA-N
    • SMILES: O=C(C=C)NCC

Computed Properties

  • Exact Mass: 99.06840
  • Monoisotopic Mass: 99.068
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 7
  • Rotatable Bond Count: 3
  • Complexity: 78.1
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 29.1A^2
  • XLogP3: 0.5

Experimental Properties

  • Density: 0.93235?at 25?°C
  • Boiling Point: 219.8℃ at 760 mmHg
  • Flash Point: Degrees Fahrenheit:>230°F
    Degrees Celsius:>110°C
  • Refractive Index: n20/D 1.4700
  • PSA: 29.10000
  • LogP: 0.69940

N-Ethylacrylamide Security Information

  • Symbol: GHS07
  • Signal Word:Warning
  • Hazard Statement: H302
  • Warning Statement: P301+P312+P330
  • Hazardous Material transportation number:NONH for all modes of transport
  • WGK Germany:3
  • Hazard Category Code: 22-52
  • Safety Instruction: S26; S36
  • Hazardous Material Identification: Xn
  • Risk Phrases:R20/21/22; R36/37/38
  • HazardClass:IRRITANT
  • Storage Condition:2-8°C

N-Ethylacrylamide Pricemore >>

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N-Ethylacrylamide Suppliers

Amadis Chemical Company Limited
Gold Member
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(CAS:5883-17-0)N-Ethylacrylamide
Order Number:A8303
Stock Status:in Stock
Quantity:5g/25g
Purity:99%
Pricing Information Last Updated:Monday, 2 September 2024 15:16
Price ($):271.0/614.0

N-Ethylacrylamide Related Literature

Additional information on N-Ethylacrylamide

Introduction to N-Ethylacrylamide (CAS No. 5883-17-0)

N-Ethylacrylamide, chemically known by its CAS number 5883-17-0, is a significant compound in the field of chemical and pharmaceutical research. This amide derivative of acrylic acid has garnered considerable attention due to its versatile applications and potential in various scientific domains. The compound's unique structural properties make it a valuable intermediate in the synthesis of polymers, pharmaceuticals, and specialty chemicals.

The molecular structure of N-Ethylacrylamide consists of an acrylate group attached to an ethylamine moiety, which contributes to its reactivity and functionality. This configuration allows it to participate in a wide range of chemical reactions, including polymerization, condensation, and cross-linking processes. These reactions are fundamental in the development of advanced materials and biodegradable polymers, which are increasingly important in sustainable chemistry.

In recent years, N-Ethylacrylamide has been extensively studied for its role in the development of novel drug delivery systems. Researchers have explored its potential as a monomer in the creation of hydrogels, which are hydrophilic polymers capable of absorbing and releasing water. These hydrogels have promising applications in biomedical engineering, particularly in drug encapsulation and controlled release formulations. The ability of N-Ethylacrylamide to form stable gels under physiological conditions makes it an attractive candidate for such applications.

Moreover, the compound has shown promise in the field of nanotechnology. Its ability to undergo polymerization under controlled conditions allows for the synthesis of nanoparticles with specific sizes and shapes. These nanoparticles can be functionalized for targeted drug delivery, enhancing therapeutic efficacy while minimizing side effects. The versatility of N-Ethylacrylamide in forming stable and functional nanoparticles underscores its importance in advanced medical applications.

The pharmaceutical industry has also been keen on exploring the therapeutic potential of derivatives of N-Ethylacrylamide. By modifying its molecular structure, scientists have synthesized analogs that exhibit anti-inflammatory, analgesic, and even anticancer properties. These derivatives are being tested in preclinical studies to evaluate their safety and efficacy. The results from these studies are promising and suggest that further development could lead to new treatments for various diseases.

From an industrial perspective, N-Ethylacrylamide plays a crucial role in the production of specialty chemicals. Its use as a monomer in polymer synthesis has led to the development of high-performance materials used in coatings, adhesives, and composites. These materials exhibit enhanced durability and chemical resistance, making them suitable for demanding applications in industries such as aerospace and automotive manufacturing.

The environmental impact of using N-Ethylacrylamide has also been a focus of research. Studies have investigated its biodegradability and potential ecological effects. The compound's ability to break down into less harmful substances under certain conditions suggests that it can be used responsibly without posing significant environmental risks. This aspect is particularly important as industries strive to adopt more sustainable practices.

In conclusion, N-Ethylacrylamide (CAS No. 5883-17-0) is a multifunctional compound with broad applications across multiple scientific fields. Its role in polymer chemistry, drug delivery systems, nanotechnology, and industrial manufacturing highlights its importance as a versatile intermediate. As research continues to uncover new possibilities for this compound, its significance is expected to grow further, driving innovation and progress in various sectors.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:5883-17-0)N-Ethylacrylamide
A8303
Purity:99%/99%
Quantity:5g/25g
Price ($):271.0/614.0
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