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Thermo Scientific Chemicals
2,3-Butanedione, 99%
CAS: 431-03-8 | C4H6O2 | 86.09 g/mol
化学物質識別子
CAS431-03-8
IUPAC Namebutane-2,3-dione
Molecular FormulaC4H6O2
InChI KeyQSJXEFYPDANLFS-UHFFFAOYSA-N
SMILESCC(=O)C(C)=O
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)Clear yellow
FormLiquid
Assay (GC)≥98.5%
Identification (FTIR)Conforms
Refractive Index1.3930-1.3980 @ 20?C
2,3-Butanedione is used to form triazine and pteridine ring systems by cyclocondensation with amines. It is also used to inactivate aminopeptidase-N and acts as a precursor to alpha-diones. It finds use in alcoholic beverages, foods, to modify arginyl residues in proteins and to give a buttery flavor to microwave popcorns.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2,3-Butanedione is used to form triazine and pteridine ring systems by cyclocondensation with amines. It is also used to inactivate aminopeptidase-N and acts as a precursor to alpha-diones. It finds use in alcoholic beverages, foods, to modify arginyl residues in proteins and to give a buttery flavor to microwave popcorns.
Solubility
Miscible with water.
Notes
Store in a cool place. Incompatible with acids, strong bases, metals, reducing agents and oxidizing agents.
2,3-Butanedione is used to form triazine and pteridine ring systems by cyclocondensation with amines. It is also used to inactivate aminopeptidase-N and acts as a precursor to alpha-diones. It finds use in alcoholic beverages, foods, to modify arginyl residues in proteins and to give a buttery flavor to microwave popcorns.
Solubility
Miscible with water.
Notes
Store in a cool place. Incompatible with acids, strong bases, metals, reducing agents and oxidizing agents.
RUO – Research Use Only
General References:
- Sensitizer for the photochemical epoxidation of alkenes: J. Am. Chem. Soc., 98, 4193 (1976).
- Like 1,2-Cyclohexanedione, A14401, has been used by Ley's group in combination with trimethyl orthoformate and camphorsulfonic acid for the protection of trans-1,2-diols as cyclic diacetals. The method is particularly applicable to the carbohydrate field: Synlett, 793 (1996); J. Chem. Soc., Perkin 1, 2023 (1997). See also 9,10-Phenanthrenequinone, A11762.
- El-Sayed, A. E.; Al-Fulaij, O. A.; Elaasar, A. A.; El-Defrawy, M. M.; El-Asmy, A. A. Spectroscopic characterization and biological activity of dihydrazone transition metal complexes: Crystal structure of 2, 3-butanedione bis (isonicotinylhydrazone). Spectrochim. Acta Mol. Biomol. Spectrosc. 2015, 135, 211-218.
- Mikhailov, O. V.; Chachkov, D. V. Molecular structures of asymmetric (555) macrotricyclic chelates formed in 3d metal ion-ethanedithioamide-hydrazinomethanethioamide-2, 3-butanedione quaternary systems. Russ. J. Inorg. Chem. 2015, 60 (2), 187-193.