alpha-Angelicalactone, 98%
alpha-Angelicalactone, 98%
alpha-Angelicalactone, 98%
Thermo Scientific Chemicals

alpha-Angelicalactone, 98%

CAS: 591-12-8 | C5H6O2 | 98.10 g/mol
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5 g
25 g
100 g
Catalog number L07602.06
also known as L07602-06
Price (EUR)
27,50
Each
Quantity:
5 g
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Price (EUR)
27,50
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Chemical Identifiers
CAS591-12-8
IUPAC Name5-methyl-2,3-dihydrofuran-2-one
Molecular FormulaC5H6O2
InChI KeyQOTQFLOTGBBMEX-UHFFFAOYSA-N
SMILESCC1=CCC(=O)O1
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to yellow
Assay (GC)≥97.5%
Refractive Index1.4460-1.4500 @ 20?C
FormLiquid
Identification (FTIR)Conforms
alpha-Angelicalactone acts as acancer chemopreventive agent. It is used in the synthesis of glutathione and the activity of glutathione-S-transferase and UDP-glucunonosyltransferase detoxification enzymes in esophagus, stomach, intestine, and liver. It is used in oral care formulations to round out mint notes and in coffee flavors.

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
alpha-Angelicalactone acts as acancer chemopreventive agent. It is used in the synthesis of glutathione and the activity of glutathione-S-transferase and UDP-glucunonosyltransferase detoxification enzymes in esophagus, stomach, intestine, and liver. It is used in oral care formulations to round out mint notes and in coffee flavors.

Solubility
Soluble in water (5g/100mL) and alcohol.

Notes
Moisture-sensitive. Store under inert gas. Protect from moisture. Incompatible materials are Oxidizing agents.
RUO – Research Use Only

General References:

  1. Richard A. Amos; John A. Katzenellenbogen. An efficient synthesis of .gamma.-methylene-.gamma.-butyrolactone (.alpha.'-angelicalactone). Application to the synthesis of deoxyobtusilactone and deoxyisoobtusilactone.J. Org. Chem.1978, 43 (4), 560-564.