55201
DL-泛酰内酯
purum, ≥97.0% (T)
别名:
β,β-二甲基-α-羟基-γ-丁内酯, DL-泛解酸内酯, 二氢-3-羟基-4,4-二甲基-2(3H)-呋喃酮
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关于此项目
经验公式（希尔记法）:
C6H10O3
化学文摘社编号:
分子量:
130.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-210-7
Beilstein/REAXYS Number:
80958
MDL number:
Assay:
≥97.0% (T)
Form:
solid
InChI key
SERHXTVXHNVDKA-UHFFFAOYSA-N
InChI
1S/C6H10O3/c1-6(2)3-9-5(8)4(6)7/h4,7H,3H2,1-2H3
SMILES string
CC1(C)COC(=O)C1O
grade
purum
assay
≥97.0% (T)
form
solid
mp
74-78 °C (lit.)
solubility
H2O: 1 g/10 mL, clear, colorless to almost colorless
functional group
ester, hydroxyl
Quality Level
Application
DL-α-羟基-β,β-二甲基-γ-丁内酯（DL-泛内酯）可用于制备 3,5-二硝基苯甲酰基-DL-泛内酯。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 1
flash_point_f
251.6 °F - open cup
flash_point_c
122 °C - open cup
ppe
Eyeshields, Gloves, type N95 (US)
The Bacterial Degradation of Pantothenic Acid. III. Enzymatic Formation of Aldopantoic Acid*.
Goodhue CT and Snell EE.
Biochemistry, 5(2), 403-408 (1966)
Separation and determination of the enantiomers of pantolactone by gas-liquid chromatography.
A Takasu et al.
Journal of chromatography, 389(1), 251-255 (1987-02-27)
Bing Chen et al.
Applied biochemistry and biotechnology, 162(3), 744-756 (2009-10-31)
The levo-lactonase gene of Fusarium proliferatum ECU2002 (EC3.1.1.25) was cloned and expressed in Escherichia coli JM109 (DE3) for biocatalytic resolution of industrially important chiral lactones, including DL-pantoyl lactone which was a key precursor to calcium D-pantothenate. By increasing the biomass
Keiji Sakamoto et al.
Journal of biotechnology, 118(1), 99-106 (2005-06-07)
We developed an enzymatic resolution system for DL-pantoyl lactone that uses immobilized mycelia of Fusarium oxysporum, which produce a lactone-hydrolyzing enzyme (lactonase). The lactonase catalyzes the stereospecific hydrolysis of D-pantoyl lactone. One hundred eighty repeated batch reactions (total reaction time
Pelayo Camps et al.
The Journal of organic chemistry, 73(17), 6657-6665 (2008-07-30)
A series of novel N,O-psiconucleosides has been prepared in both enantiomeric forms by resolution of an advanced racemic synthetic intermediate using (R)-N-phenylpantolactam as a chiral resolution agent. The absolute configuration of all of these compounds has been unequivocally established by
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