165115
1,3-Acetonedicarboxylic acid
technical grade
Synonym(s):
3-Oxoglutaric acid
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About This Item
Linear Formula:
HOOCCH2COCH2COOH
CAS Number:
Molecular Weight:
146.10
Beilstein/REAXYS Number:
1447081
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
Recommended Products
grade
technical grade
assay
(Remarks on Titration H2SO4 <= 1.0%)
mp
133 °C (dec.) (lit.)
storage temp.
−20°C
SMILES string
OC(=O)CC(=O)CC(O)=O
InChI
1S/C5H6O5/c6-3(1-4(7)8)2-5(9)10/h1-2H2,(H,7,8)(H,9,10)
InChI key
OXTNCQMOKLOUAM-UHFFFAOYSA-N
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
392.0 °F - open cup
flash_point_c
200 °C - open cup
ppe
Eyeshields, Gloves, type N95 (US)
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V N Montesinos et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 15(2), 228-234 (2016-01-13)
Removal of Cr(VI) and citric acid (Cit) by heterogeneous photocatalytic Cr(VI) transformation under UV light over two commercial TiO2 samples (1 g L(-1)), Evonik P25 and Hombikat UV100, was studied at pH 2 and Cr(VI) concentrations between 0.2 and 3
Jian-Ping Huang et al.
Nature communications, 10(1), 4036-4036 (2019-09-08)
The skeleton of tropane alkaloids is derived from ornithine-derived N-methylpyrrolinium and two malonyl-CoA units. The enzymatic mechanism that connects N-methylpyrrolinium and malonyl-CoA units remains unknown. Here, we report the characterization of three pyrrolidine ketide synthases (PYKS), AaPYKS, DsPYKS, and AbPYKS
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