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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Propanoic-13C3 acid, 2-oxo-, sodium salt

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Chemical Name: Propanoic-13C3 acid, 2-oxo-, sodium salt
CAS Number: 142014-11-7
Product Number: AG001HKI(AGN-PC-0PRPMM)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Properties
MP:
>215°C (dec.)
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
113.021g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
113.008g/mol
Monoisotopic Mass:
113.008g/mol
Topological Polar Surface Area:
57.2A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
88.2
Isotope Atom Count:
3
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Sodium pyruvate-13C3 is a highly specialized compound that finds key applications in advanced chemical synthesis processes. By incorporating the stable isotope 13C into the structure of sodium pyruvate, this compound serves as a valuable tracer in metabolic studies and biochemical research. In chemical synthesis, Sodium pyruvate-13C3 plays a crucial role as a labeled precursor for the production of various organic molecules. The presence of 13C isotopes enables researchers to track the fate and transformation of sodium pyruvate in complex chemical reactions, facilitating the elucidation of reaction mechanisms and pathways. Additionally, Sodium pyruvate-13C3 can be utilized to synthesize isotopically labeled derivatives for use in nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry analysis. Its high purity and isotopic enrichment make it an indispensable tool for investigating metabolic processes, studying biochemical pathways, and advancing scientific understanding in diverse fields of chemistry.