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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)-

Glycine-13C2-15N

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Chemical Name: Glycine-13C2-15N
CAS Number: 211057-02-2
Product Number: AG00C1PM(AGN-PC-0QXONQ)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
78.045g/mol
XLogP3:
-3.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
78.036g/mol
Monoisotopic Mass:
78.036g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
5
Formal Charge:
0
Complexity:
42.9
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:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Glycine-13C2-15N, a uniquely labeled form of glycine, serves as a valuable tool in chemical synthesis due to its isotopic composition. By incorporating stable isotopes of carbon-13 and nitrogen-15, this compound enables precise tracking and elucidation of reaction pathways in complex chemical processes. The incorporation of Glycine-13C2-15N as a substrate or starting material in organic synthesis allows for the differentiation of isotopically labeled products from their unlabeled counterparts. This capability is particularly advantageous in the fields of pharmaceutical research, biochemical studies, and environmental monitoring. Researchers utilize Glycine-13C2-15N for metabolic tracing, structural elucidation, and as a reference standard in analytical chemistry. Its application in isotope dilution mass spectrometry facilitates accurate quantification of analytes and aids in the understanding of metabolic pathways. Additionally, Glycine-13C2-15N plays a crucial role in studying protein dynamics, protein folding, and protein-protein interactions by enabling the production of isotopically labeled proteins for NMR spectroscopy. With its versatility and significance in various research areas, Glycine-13C2-15N stands as a fundamental tool for advancing chemical synthesis methodologies and gaining insights into complex chemical systems.