Cas no 13794-28-0 (Ethyl 2-Isocyanatopropionate (>90%))

Ethyl 2-Isocyanatopropionate (>90%) is a reactive isocyanate ester commonly employed in organic synthesis and polymer chemistry. Its high purity (>90%) ensures consistent performance in applications such as the preparation of urethane derivatives, peptide coupling, and functionalized polymer intermediates. The compound’s isocyanate group exhibits strong electrophilic reactivity, enabling efficient nucleophilic addition reactions with amines, alcohols, and other active hydrogen-containing compounds. Its ethyl ester moiety further enhances solubility in organic solvents, facilitating homogeneous reaction conditions. Suitable for controlled modifications in specialty chemical synthesis, Ethyl 2-Isocyanatopropionate is valued for its versatility and reliability in producing tailored molecular architectures. Proper handling under inert conditions is recommended due to its moisture sensitivity.
Ethyl 2-Isocyanatopropionate (>90%) structure
13794-28-0 structure
Product Name:Ethyl 2-Isocyanatopropionate (>90%)
CAS No:13794-28-0
MF:C6H9NO3
MW:143.140561819077
MDL:MFCD00078449
CID:87159
PubChem ID:550681
Update Time:2025-05-25

Ethyl 2-Isocyanatopropionate (>90%) Chemical and Physical Properties

Names and Identifiers

    • Ethyl 2-isocyanatopropionate
    • 2-Isocyanatopropionic acid ethyl ester
    • (1-ethoxycarbonyl)-ethylisocyanate
    • Ethyl N-(oxomethylene)alaninate
    • ethyl 2-isocyanatopropanoate
    • MFCD00078449
    • EN300-1458621
    • Propanoic acid, 2-isocyanato-, ethyl ester
    • Ethyl 2-isocyanatopropanoate #
    • DTXSID50338688
    • AKOS005171727
    • ethyl isocyanatopropionate
    • Ethyl 2-Isocyanatopropionate (>90%)
    • MS-20712
    • A927743
    • 2-isocyanato-propionic acid ethyl ester
    • FT-0625960
    • 13794-28-0
    • SCHEMBL571924
    • STK504618
    • BBL104422
    • ethyl N-(oxomethylidene)alaninate
    • MDL: MFCD00078449
    • Inchi: 1S/C6H9NO3/c1-3-10-6(9)5(2)7-4-8/h5H,3H2,1-2H3
    • InChI Key: PFIQRPNWLUAMOF-UHFFFAOYSA-N
    • SMILES: O(CC)C(C(C)N=C=O)=O
    • BRN: 1237510

Computed Properties

  • Exact Mass: 143.05800
  • Monoisotopic Mass: 143.058
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 4
  • Complexity: 160
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 1.9
  • Topological Polar Surface Area: 55.7A^2

Experimental Properties

  • Color/Form: Colorless pungent odor liquid
  • Density: 1.087(lit.)
  • Melting Point: No data available
  • Boiling Point: 68℃/3mm(lit.)
  • Flash Point: 92℃(197℉)(lit.)
  • Refractive Index: 1.4170
  • PSA: 55.73000
  • LogP: 0.27380
  • Sensitiveness: Moisture Sensitive
  • Solubility: Hydrolyzable
  • Vapor Pressure: 1.8±0.3 mmHg at 25°C

Ethyl 2-Isocyanatopropionate (>90%) Security Information

Ethyl 2-Isocyanatopropionate (>90%) Customs Data

  • HS CODE:2929109000
  • Customs Data:

    China Customs Code:

    2929109000

    Overview:

    2929109000. Other isocyanates. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2929109000. other isocyanates. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Ethyl 2-Isocyanatopropionate (>90%) Pricemore >>

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Additional information on Ethyl 2-Isocyanatopropionate (>90%)

Ethyl 2-Isocyanatopropionate: A Comprehensive Overview

Ethyl 2-isocyanatopropionate, also known by its CAS number 13794-28-0, is a versatile organic compound with significant applications in various industries. This compound, which exists in a purity of over 90%, is widely recognized for its role in the synthesis of polyurethanes and other high-performance materials. Its structure, featuring an isocyanate group attached to a propionate ester, makes it highly reactive and suitable for a range of chemical reactions.

The synthesis of ethyl 2-isocyanatopropionate involves the reaction of phosgene with the corresponding amine or alcohol, followed by purification to achieve the desired purity level. Its physical properties, such as its boiling point and density, are critical in determining its suitability for specific applications. Recent studies have highlighted its potential in the development of advanced coatings and adhesives, where its reactivity and compatibility with various substrates are highly valued.

In terms of applications, ethyl 2-isocyanatopropionate has found extensive use in the production of polyurethanes, which are widely used in the automotive, construction, and furniture industries. The compound's ability to form stable polymeric networks through step-growth polymerization has made it a cornerstone in the manufacturing of flexible foams, rigid insulation materials, and elastomers.

Recent research has also explored the use of ethyl 2-isocyanatopropionate in bio-based materials. By incorporating renewable resources into its synthesis, scientists aim to develop more sustainable alternatives to traditional petroleum-based products. This shift towards greener chemistry aligns with global efforts to reduce environmental impact and promote circular economy principles.

The compound's reactivity also makes it a valuable intermediate in the synthesis of other isocyanates and related compounds. For instance, it can be used as a precursor for the production of aliphatic isocyanates, which are essential in the manufacture of high-performance polymers and specialty chemicals.

In addition to its industrial applications, ethyl 2-isocyanatopropionate has shown promise in biomedical applications. Researchers have investigated its potential as a building block for drug delivery systems and biocompatible polymers. Its ability to form hydrogels with tunable properties has opened new avenues for tissue engineering and regenerative medicine.

The stability and shelf life of ethyl 2-isocyanatopropionate are critical considerations for its storage and transportation. Proper handling and storage conditions are necessary to maintain its quality and prevent degradation due to moisture or exposure to air. Industry standards recommend storing the compound in sealed containers under dry conditions to ensure optimal performance.

From an environmental perspective, the production and use of ethyl 2-isocyanatopropionate have raised concerns regarding emissions and waste management. However, advancements in catalytic processes and recycling technologies are addressing these challenges, paving the way for more sustainable production methods.

In conclusion, ethyl 2-isocyanatopropionate (CAS No. 13794-28-0) is a multifaceted compound with a wide range of applications across industries. Its chemical properties, reactivity, and versatility make it an indispensable component in modern material science and chemical manufacturing. As research continues to uncover new applications and improve production methods, this compound will likely remain at the forefront of chemical innovation.

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