55201
DL-α-Hydroxy-β,β-dimethyl-γ-butyrolactone
purum, ≥97.0% (T)
Synonym(s):
β,β-Dimethyl-α-hydroxy-γ-butyrolactone, DL-Pantolactone, Dihydro-3-hydroxy-4,4-dimethyl-2(3H)-furanone
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About This Item
Recommended Products
grade
purum
Quality Level
Assay
≥97.0% (T)
form
solid
mp
74-78 °C (lit.)
solubility
H2O: 1 g/10 mL, clear, colorless to almost colorless
SMILES string
CC1(C)COC(=O)C1O
InChI
1S/C6H10O3/c1-6(2)3-9-5(8)4(6)7/h4,7H,3H2,1-2H3
InChI key
SERHXTVXHNVDKA-UHFFFAOYSA-N
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Related Categories
Application
DL-α-Hydroxy-β,β-dimethyl-γ-butyrolactone (DL-pantolactone) may be used in the preparation of 3,5-dinitrobenzoyl-DL-pantolactone.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 1
Flash Point(F)
251.6 °F - open cup
Flash Point(C)
122 °C - open cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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The Bacterial Degradation of Pantothenic Acid. III. Enzymatic Formation of Aldopantoic Acid*.
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Journal of the American Chemical Society, 125(51), 15696-15697 (2003-12-18)
Dilute solutions of (R)-(-)-pantolactone in CCl4 were studied by polarimetry in conjunction with theoretical calculations of [alpha]D. Our data demonstrate that the self-association of a chiral solute results in a change in [alpha]D that can be accounted for by the
Journal of agricultural and food chemistry, 54(16), 5823-5830 (2006-08-03)
D-Pantonohydrolase has attracted increasing attention as a biocatalyst for stereospecific production of D-pantoic acid. The Fusarium moniliforme D-pantonohydrolase was selected for directed evolution through error-prone Polymerase Chain Reaction (PCR) combined with DNA shuffling for improved activity and pH stability using
Nature, 373(6516), 683-685 (1995-02-23)
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