Methyl pyruvate, 98%, Thermo Scientific Chemicals
Methyl pyruvate, 98%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Methyl pyruvate, 98%, Thermo Scientific Chemicals

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100 g
25 g
500 g
Catalog number A13966.22
also known as A13966-22
Price (USD)/ Each
94.65
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105.00 
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Quantity:
100 g
Request bulk or custom format
Price (USD)/ Each
94.65
Online exclusive
105.00 
Save 10.35 (10%)
Add to cart
Methyl pyruvate, 98%, Thermo Scientific Chemicals
Catalog numberA13966.22
Price (USD)/ Each
94.65
Online exclusive
105.00 
Save 10.35 (10%)
-
Add to cart
Chemical Identifiers
CAS600-22-6
IUPAC Namemethyl 2-oxopropanoate
Molecular FormulaC4H6O3
InChI KeyCWKLZLBVOJRSOM-UHFFFAOYSA-N
SMILESCOC(=O)C(C)=O
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SpecificationsSpecification SheetSpecification Sheet
FormLiquid
Refractive Index1.4020-1.4060 @ 20?C
Identification (FTIR)Conforms
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.
RUO – Research Use Only

General References:

  1. 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.
  2. 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.