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delta-Valerolactone, 98%, may contain polymer, Thermo Scientific Chemicals
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Catalog number L04794.14
also known as L04794-14
Price (USD)/ Each
45.65
Online exclusive
50.80 Save 5.15 (10%)
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Quantity:
25 g
Price (USD)/ Each
45.65
Online exclusive
50.80 Save 5.15 (10%)
delta-Valerolactone, 98%, may contain polymer, Thermo Scientific Chemicals
Catalog numberL04794.14
Price (USD)/ Each
45.65
Online exclusive
50.80 Save 5.15 (10%)
-
Chemical Identifiers
CAS542-28-9
IUPAC Nameoxan-2-one
Molecular FormulaC5H8O2
InChI KeyOZJPLYNZGCXSJM-UHFFFAOYSA-N
SMILESO=C1CCCCO1
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Specifications
Specification Sheet
Specification SheetFormLiquid
Assay (GC)≥97.5%
CommentProduct may contain variable amounts of polymerized product. Depolymerisation is possible by distillation.
Identification (FTIR)Conforms
Refractive Index1.4560-1.4600 @ 20°C
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δ-Valerolactone is employed as a chemical intermediate in the synthesis of polymers. It is also used to synthesize the copolyesters by lipase-catalyzed ring opening polymerization.
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
δ-Valerolactone is employed as a chemical intermediate in the synthesis of polymers. It is also used to synthesize the copolyesters by lipase-catalyzed ring opening polymerization.
Solubility
Miscible with water.
Notes
Store in a tightly closed container. Avoid breathing dust, vapor, mist, or gas.
δ-Valerolactone is employed as a chemical intermediate in the synthesis of polymers. It is also used to synthesize the copolyesters by lipase-catalyzed ring opening polymerization.
Solubility
Miscible with water.
Notes
Store in a tightly closed container. Avoid breathing dust, vapor, mist, or gas.
RUO – Research Use Only
General References:
- Rajashekhar, B.; Chakraborty, D. Co(II) and Mn(II) catalyzed bulk ring-opening polymerization of cyclic esters. Polym. Bull. 2014, 71 (9), 2185-2203.
- Suess, B.; Brockhoff, A.; Meyerhof, W.; Hofmann, T. Structures, orosensory activity, and T1R1/T1R3 receptor activation of amides generated by lactone aminolysis using food-related processing conditions. Eur Food Res. Technol. 2013, 237 (1), 57-70.