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Thermo Scientific Chemicals
Methyl pyruvate, 98%
CAS: 600-22-6 | C4H6O3 | 102.089 g/mol
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化學識別
CAS600-22-6
IUPAC Namemethyl 2-oxopropanoate
Molecular FormulaC4H6O3
InChI KeyCWKLZLBVOJRSOM-UHFFFAOYSA-N
SMILESCOC(=O)C(C)=O
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規格
規格表
規格表Identification (FTIR)Conforms
FormLiquid
Refractive Index1.4020-1.4060 @ 20?C
Appearance (Color)Clear colorless to pale yellow to pale orange
Assay (GC)≥97.5%
Methyl Pyruvate acts as a potent secretagogue used in the study of stimulus-secretion coupling. Also used in the preparation of quinoxalines as dual phoosphodiesterase 2/10 (PDE2/10) inhibitors. It increases free calcium ion concentration in the cytosol of pancreatic cells. It is used in the preparation of dimethyl 2,3-dimethylenebutanedioate.
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
Methyl Pyruvate acts as a potent secretagogue used in the study of stimulus-secretion coupling. Also used in the preparation of quinoxalines as dual phoosphodiesterase 2/10 (PDE2/10) inhibitors. It increases free calcium ion concentration in the cytosol of pancreatic cells. It is used in the preparation of dimethyl 2,3-dimethylenebutanedioate.
Solubility
Soluble in chloroform, methanol, ether, alcohol. Slightly soluble in water.
Notes
Store away from oxidizing agent, heat.
Methyl Pyruvate acts as a potent secretagogue used in the study of stimulus-secretion coupling. Also used in the preparation of quinoxalines as dual phoosphodiesterase 2/10 (PDE2/10) inhibitors. It increases free calcium ion concentration in the cytosol of pancreatic cells. It is used in the preparation of dimethyl 2,3-dimethylenebutanedioate.
Solubility
Soluble in chloroform, methanol, ether, alcohol. Slightly soluble in water.
Notes
Store away from oxidizing agent, heat.
RUO – Research Use Only
General References:
- G. Bond, P.A. Meheux; A. Ibbotson; P.B. Wells. Origin of enhanced rate in the platinum-catalysed enantioselective hydrogenation of methyl pyruvate. Catalysis Today. 1991, 10 (3), 371-378.
- I.M. Sutherland; A. Ibbotson; R.B. Moyes; P.B. Wells. Enantioselective hydrogenation I. Surface conditions during methyl pyruvate hydrogenation catalyzed by cinchonidine-modified platinum/silica (EUROPT-1). Journal of Catalysis. 1990, 125 (1), 77-88.