Vinyl Butyrate - ≥98%(GC),Containing stabilizer MEHQ , CAS No.123-20-6

CAS: 123-20-6 Cat. No.: V162944 Peso molecular: 114.14 Beilstein Registry Number: 1744930 Número EC: 204-609-4 PubChem CID: 31247

GRADE & PURITY ≥98%(GC), Containing stabilizer MEHQ

Synonyms

Vinyl butyrate, >=99.0% (GC) | vinyl n-butyrate | Butanoic acid, etheyl ester | VINYLBUTYRATE | AKOS006223438 | AI3-24888 | J-004899 | FS-4033 | FT-0694075 | NSC 5280 | A805027 | SCHEMBL23026 | Butyric Acid Vinyl Ester | Butyric acid, vinyl ester | EINECS

Storage

Store at 2-8°C

Shipped In

Wet ice,FedEx DG Service

Descripción general

Vinyl butyrate causes the transesterification of natural flavonoid bergenin immobilized onto carboxylic acid functionalized controlled pore glass.
Vinyl butyrate was used as acyl donor in the synthesis of citronellyl esters (acetate, propionate, butyrate, caprate and laurate) using immobilized Candida antarctical ipase B.

Specifications

Sinónimos

Vinyl butyrate, >=99.0% (GC) | vinyl n-butyrate | Butanoic acid, etheyl ester | VINYLBUTYRATE | AKOS006223438 | AI3-24888 | J-004899 | FS-4033 | FT-0694075 | NSC 5280 | A805027 | SCHEMBL23026 | Butyric Acid Vinyl Ester | Butyric acid, vinyl ester | EINECS

Especificaciones y pureza

≥98%(GC), Containing stabilizer MEHQ

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice, FedEx DG Service

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: 504753437
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504753437
• Sonrisas canónicas: CCCC(=O)OC=C
• IUPAC Name: ethenyl butanoate
• InChIKey: MEGHWIAOTJPCHQ-UHFFFAOYSA-N
• INCHI: 1S/C6H10O2/c1-3-5-6(7)8-4-2/h4H,2-3,5H2,1H3
• Isómeros SMILES: CCCC(=O)OC=C
• WGK Alemania: 2
• RTECS: ET7000000
• PubChem CID: 31247
• Número ONU: 2838
• Grupo de embalaje: II
• Peso molecular: 114.14
• Beilstein: 1744930
• Reaxy-Rn: 1744933

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Fatty Acyls
      • Subclass Fatty acid esters

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Fatty Acyls
• Subclass: Fatty acid esters
• Intermediate Tree Nodes: Not available
• Direct Parent: Fatty acid esters
• Alternative Parents: Enol esters Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Fatty acid ester - Enol ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - 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 fatty acid esters. These are carboxylic ester derivatives of a fatty acid.
• 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: Slightly soluble in water, soluble in methanol
• Índice de refracción: 1.41
• Punto de inflamación (°F): 68 °F
• Punto de inflamación (°C): 20℃
• Punto de ebullición (°C): 116°C
• Peso molecular: 114.140 g/mol
• XLogP3: 1.400
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 114.068 Da
• Monoisotopic Mass: 114.068 Da
• Topological Polar Surface Area: 26.300 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 86.500
• 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. Yao Jian, Gui Lun, Yin Shaocheng.  (2021)  A novel esterase from a soil metagenomic library displaying a broad substrate range.  AMB Express,  11  (1): (1-10).  [PMID:33666762] [10.1186/s13568-021-01198-5]

3. Dami Li, Yaoyao Zhang, Xing Qiao, Shangde Sun.  (2025)  Effects of substitution sites and acyl chain length on antioxidant capacity and bioaccessibility of high-active resveratrol monoesters in vitro.  FOOD CHEMISTRY,      [PMID:40112713] [10.1016/j.foodchem.2025.143845]

4. Mengli Geng, Dandan Ma, Zhaojun Wang, Qiuming Chen, Maomao Zeng, Jie Chen, Benu Adhikari, Hongyang Pan, Zhiyong He.  (2026)  Enzymatically synthesized kaempferol fatty acid esters enhance glycolipid metabolism regulation and α-glucosidase inhibition.  FOOD RESEARCH INTERNATIONAL,      [PMID:] [10.1016/j.foodres.2026.118422]