A8509
Lithium acetoacetate
≥90% (HPLC)
Synonym(s):
Acetoacetic acid lithium salt
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About This Item
Linear Formula:
CH3COCH2COOLi
CAS Number:
Molecular Weight:
108.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
5774841
Product Name
Lithium acetoacetate, ≥90% (HPLC)
InChI
1S/C4H6O3.Li/c1-3(5)2-4(6)7;/h2H2,1H3,(H,6,7);/q;+1/p-1
SMILES string
[Li+].CC(=O)CC([O-])=O
InChI key
UTLRZTUJSMCBHB-UHFFFAOYSA-M
assay
≥90% (HPLC)
form
powder
storage temp.
−20°C
Quality Level
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Application
Lithium acetoacetate can be used as an acetoacetate standard for the measurement of acetoacetate in biological samples. It can also be used for the preparation of sodium acetoacetate.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Cristian Palmiere et al.
Legal medicine (Tokyo, Japan), 14(1), 17-20 (2011-12-20)
Isopropyl alcohol (IPA) is widely used as an industrial solvent and cleaning fluid. After ingestion or absorption, IPA is converted into acetone by alcohol dehydrogenase. However, in ketosis, acetone can be reduced to IPA. The aim of this study was
Preparation of crystalline lithium acetoacetate.
Hall LM
Analytical Biochemistry, 3(1), 75-80 (1962)
Bei Han et al.
Applied microbiology and biotechnology, 91(3), 565-576 (2011-05-03)
Development of a butanologenic strain with high selectivity for butanol production is often proposed as a possible route for improving the economics of biobutanol production by solventogenic Clostridium species. The acetoacetate decarboxylase (aadc) gene encoding acetoacetate decarboxylase (AADC), which catalyzes
Douglas Ganini et al.
Free radical biology & medicine, 51(3), 733-743 (2011-05-26)
Acetoacetate (AA) and 2-methylacetoacetate (MAA) are accumulated in metabolic disorders such as diabetes and isoleucinemia. Here we examine the mechanism of AA and MAA aerobic oxidation initiated by myoglobin (Mb)/H(2)O(2). We propose a chemiluminescent route involving a dioxetanone intermediate whose
Mathieu Coincon et al.
The Journal of biological chemistry, 287(43), 36208-36221 (2012-08-22)
Crystal structures of divalent metal-dependent pyruvate aldolase, HpaI, in complex with substrate and cleavage products were determined to 1.8-2.0 Å resolution. The enzyme·substrate complex with 4-hydroxy-2-ketoheptane-1,7-dioate indicates that water molecule W2 bound to the divalent metal ion initiates C3-C4 bond
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