607533
2-Ketobutyric acid-4-13C,3,3,4,4,4-d5 sodium salt hydrate
48-70 atom % D (13CD3), 97 atom % D (CD2), 99 atom % 13C, 98% (CP)
Synonym(s):
α-Keto-butyric acid-4-13C,3,3,4,4,4-d5 sodium, α-Ketobutyric acid-4-13C,3,3,4,4,4-d5 sodium salt, 2-Oxobutanoic acid-4-13C.3,3,4,4,5-d5 sodium salt, Sodium α-ketobutyrate-4-13C,3,3,4,4,4-d5
About This Item
Recommended Products
isotopic purity
99 atom % 13C
48-70 atom % D (13CD3)
97 atom % D (CD2)
Quality Level
assay
98% (CP)
form
solid
technique(s)
bio NMR: suitable
mp
210 °C (dec.) (lit.)
mass shift
M+6
SMILES string
O.[Na+].[2H][13C]([2H])([2H])C([2H])([2H])C(=O)C([O-])=O
InChI
1S/C4H6O3.Na.H2O/c1-2-3(5)4(6)7;;/h2H2,1H3,(H,6,7);;1H2/q;+1;/p-1/i1+1D3,2D2;;
InChI key
PVLJVKQSCAHPPR-RWBNLZSCSA-M
Packaging
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Certificates of Analysis (COA)
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Articles
Presenting an article about the selective protonation of methyl groups in highly deuterated proteins. In which the structural NMR studies of small proteins, a maximum number of proton chemical shifts are usually assigned and NOEs connecting large numbers of sites are subsequently quantified in terms of distance restraints that are then used to obtain an ensemble of structures.
We presents an informational article concerning biomolecular NMR and the use of Isotope Labeling Methods for Protein Dynamics Studies.
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