61405

Methyl levulinate

≥98.0%

• Synonym(s): 4-Oxopentanoic acid methyl ester, 4-Oxovaleric acid methyl ester, Methyl β-acetylpropionate, Methyl 4-oxopentanoate, Methyl 4-oxovalerate, Methyl levulate
• Linear Formula: CH₃COCH₂CH₂COOCH₃
• CAS Number: 624-45-3
• Molecular Weight: 130.14
• Beilstein/REAXYS Number: 1754008
• EC Number: 210-846-4
• MDL number: MFCD00017499
• UNSPSC Code: 12352100
• PubChem Substance ID: 57651849
• NACRES: NA.22

Properties

• assay: ≥98.0%
• greener alternative product characteristics: Safer Solvents and Auxiliaries; Learn more about the Principles of Green Chemistry.
• sustainability: Greener Alternative Product
• refractive index: n20/D 1.422
• bp: 193-195 °C (lit.)
• density: 1.051 g/mL at 20 °C (lit.)
• functional group: ester; ketone
• greener alternative category: Aligned,
• SMILES string: COC(=O)CCC(C)=O
• InChI: 1S/C6H10O3/c1-5(7)3-4-6(8)9-2/h3-4H2,1-2H3
• Inchi Key: UAGJVSRUFNSIHR-UHFFFAOYSA-N

Description

General description

Methyl levulinate can be synthesized from glucose in the presence of a few drops of dilute sulfuric acid in methanol.[1]

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. This product is considered environmentally benign and has been enhanced for "Safer Solvents and Auxiliaries". Click here for more information.

Application

Methyl levulinate can undergo Meerwein–Ponndorf–Verley (MPV) reduction in the presence of lewis acid zeolite like Hf-beta to give 4-hydroxypentanoates.[2]

Safety Information

• Storage Class: 10 - Combustible liquids
• wgk_germany: WGK 3
• flash_point_f: 161.6 °F - closed cup
• flash_point_c: 72 °C - closed cup
• ppe: Eyeshields, Gloves, type ABEK (EN14387) respirator filter