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

CAS: 105-38-4 Cat. No.: V162937 Molecular Weight: 100.12 EC Number: 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

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 |

Specifications & Purity

≥98%(GC)

Storage

Store at 2-8°C

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥98%(GC)

Names and Identifiers

• Pubchem Sid: 504751443
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504751443
• Canonical Smiles: 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
• Isomeric SMILES: CCC(=O)OC=C
• RTECS: UF8575000
• PubChem CID: 7750
• Molecular Weight: 100.12
• Reaxy-Rn: 1741731

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: 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
• Description: 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

Chemical and Physical Properties

• Solubility: Solubility in water: Practically insoluble
• Sensitivity: Light sensitive
• Refractive Index: 1.40
• Flash Point(°F): 8°C(lit.)
• Flash Point(°C): 8°C(lit.)
• Boil Point(°C): 95℃
• Melt Point(°C): -80℃
• Molecular Weight: 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

References

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]