N-éthylacrylamide - ≥98%, contient 150-400 ppm de MEHQ comme inhibiteur , CAS No.5883-17-0

CAS: 5883-17-0 Cat. No.: N136947 Formule: C₅H₉NO Poids moléculaire: 99.13 Numéro CE: 696-277-6

GRADE & PURITY ≥98%, contains 150-400 ppm MEHQ as inhibitor

Synonyms

A8303 | EN300-6477121 | N-ETHYL ACRYLAMIDE | AB9195 | N-ethylprop-2-enamide | N-ethylacrylamide | 2-Propenamide, N-ethyl- | AS-56872 | N-Ethylacrylamide, contains MEHQ as inhibitor, 99% (HPLC) | SWPMNMYLORDLJE-UHFFFAOYSA-N | MFCD00048514 | FT-0695176 | AK

Storage

A conserver entre 2 et 8°C

Shipped In

Glace humide

Vue d’ensemble

Déclaration d'application : monomère pour l'administration de médicaments ; polymères sensibles à la chaleur ; solutions avec des LCST spécifiques

Specifications

Synonymes

A8303 | EN300-6477121 | N-ETHYL ACRYLAMIDE | AB9195 | N-ethylprop-2-enamide | N-ethylacrylamide | 2-Propenamide, N-ethyl- | AS-56872 | N-Ethylacrylamide, contains MEHQ as inhibitor, 99% (HPLC) | SWPMNMYLORDLJE-UHFFFAOYSA-N | MFCD00048514 | FT-0695176 | AK

Spécifications et pureté

≥98%, contient 150-400 ppm de MEHQ comme inhibiteur

Conditions de stockage de stockage

A conserver entre 2 et 8°C

Expédié en

Glace humide

Pureté

≥98%

Noms et identifiants

Pubchem Sid

504764843

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504764843

Sourires canoniques

CCNC(=O)C=C

IUPAC Name

N-ethylprop-2-enamide

InChIKey

SWPMNMYLORDLJE-UHFFFAOYSA-N

INCHI

1S/C5H9NO/c1-3-5(7)6-4-2/h3H,1,4H2,2H3,(H,6,7)

Isomères SMILES

CCNC(=O)C=C

WGK Allemagne

3

Poids moléculaire

99.13

Reaxy-Rn

1743338

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1743338&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Acrylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Acrylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Acrylic acids and derivatives
• Alternative Parents: Secondary carboxylic acid amides Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acrylic acid or derivatives - Secondary carboxylic acid amide - Carboxamide group - 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 acrylic acids and derivatives. These are organic compounds containing acrylic acid CH2=CHCO2H or a derivative thereof.
• External Descriptors: Not available

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.

DOI: 10.1186/s13321-016-0174-y

Propriétés chimiques et physiques

• Point d'éclair (°F): >230 °F
• Point d'éclair (°C): >110 °C
• Poids moléculaire: 99.130 g/mol
• XLogP3: 0.500
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 99.0684 Da
• Monoisotopic Mass: 99.0684 Da
• Topological Polar Surface Area: 29.100 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 78.100
• 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