Vinyl Propionate (stabilized with MEHQ) - ≥98%(GC) , CAS No.105-38-4

CAS: 105-38-4 Cat. No.: V162937 Peso molecular: 100.12 Número EC: 203-293-5 PubChem CID: 7750

GRADE & PURITY ≥98%(GC)

Synonyms

FT-0631583 | InChI=1/C5H8O2/c1-3-5(6)7-4-2/h4H,2-3H2,1H | Vinyl Propionate (stabilized with MEHQ) | EINECS 203-293-5 | BRN 1741731 | NSC 5275 | DTXSID9051537 | UNII-2437OJ3190 | Vinylester kyseliny propionove | Propionic acid, vinyl ester | SCHEMBL15133 |

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Sinónimos

FT-0631583 | InChI=1/C5H8O2/c1-3-5(6)7-4-2/h4H, 2-3H2, 1H | Vinyl Propionate (stabilized with MEHQ) | EINECS 203-293-5 | BRN 1741731 | NSC 5275 | DTXSID9051537 | UNII-2437OJ3190 | Vinylester kyseliny propionove | Propionic acid, vinyl ester | SCHEMBL15133 |

Especificaciones y pureza

≥98%(GC)

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥98%(GC)

Nombres e identificadores

• Pubchem Sid: 504751443
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504751443
• Sonrisas canónicas: CCC(=O)OC=C
• IUPAC Name: ethenyl propanoate
• InChIKey: UIWXSTHGICQLQT-UHFFFAOYSA-N
• INCHI: 1S/C5H8O2/c1-3-5(6)7-4-2/h4H,2-3H2,1H3
• Isómeros SMILES: CCC(=O)OC=C
• RTECS: UF8575000
• PubChem CID: 7750
• Peso molecular: 100.12
• Reaxy-Rn: 1741731

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives
        • Level5 Carboxylic acid esters
          • Level6 Enol esters

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Carboxylic acid esters
• Direct Parent: Enol esters
• Alternative Parents: Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Enol ester - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as enol esters. These are ester derivatives of enols. They have the general formula RC=COC(=O)R' where R, R' = H or organyl group.
• 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

Propiedades químicas y físicas

• Solubilidad: Solubility in water: Practically insoluble
• Sensibilidad: Light sensitive
• Índice de refracción: 1.40
• Punto de inflamación (°F): 8°C(lit.)
• Punto de inflamación (°C): 8°C(lit.)
• Punto de ebullición (°C): 95℃
• Punto de fusión (°C): -80℃
• Peso molecular: 100.120 g/mol
• XLogP3: 1.100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 100.052 Da
• Monoisotopic Mass: 100.052 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 76.100
• 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

Referencias

1. Wei Chen, Huihui Wang, Wu Lan, Aiping Zhang, Chuanfu Liu.  (2022)  Fabrication of sugarcane bagasse ester-based porous nanofiber membrane by electrospinning for efficient oil-water separation.  INDUSTRIAL CROPS AND PRODUCTS,      [PMID:] [10.1016/j.indcrop.2022.115480]

2. Zhangjie Luo, Yiying Li, Xingyu Liu, Qiang Chen, Chunmei Ding, Jie Zheng, Hong Chen, Jianshu Li.  (2026)  Transforming a general design strategy into elastomer-crosslinked hybrid hydrogels with co-constructed hydrophobic–hydrophilic networks for electronic skin.  Materials Today,      [PMID:] [10.1016/j.mattod.2026.103196]