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279315

Sigma-Aldrich

Sodium acetate-2-13C

99 atom % 13C

Synonyme(s) :

Acetic-2-13C acid sodium salt

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About This Item

Formule linéaire :
13CH3CO2Na
Numéro CAS:
Poids moléculaire :
83.03
Numéro Beilstein :
4211334
Numéro MDL:
Code UNSPSC :
12142200
ID de substance PubChem :
Nomenclature NACRES :
NA.12

Pureté isotopique

99 atom % 13C

Niveau de qualité

Forme

solid

Technique(s)

bio NMR: suitable
protein expression: suitable

Pf

>300 °C (dec.) (lit.)

Changement de masse

M+1

Chaîne SMILES 

[Na+].[13CH3]C([O-])=O

InChI

1S/C2H4O2.Na/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1/i1+1;

Clé InChI

VMHLLURERBWHNL-YTBWXGASSA-M

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Description générale

Sodium acetate-2-13C is 13C isotopomer labeled precursor of sodium acetate.

Application

13C labeling in the methyl group has a significant effect on the Dynamic Nuclear Polarization of acetate. Sodium acetate-2-13C labeling can be used in structural studies analyzing the interactions between lipo oligosaccharide and host proteins. Incorporation of Sodium acetate-2-13C shows enriched 13C-NMR spectra indicating their biosynthesis of microbial products and novel polyketides. Hyperpolarized 13C-acetate MRI has been applied to examinations of both rodents and porcine models.

Conditionnement

This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Consulter la Bibliothèque de documents

Deborah M B Post et al.
Journal of endotoxin research, 12(2), 93-98 (2006-05-13)
The lipooligosaccharide (LOS) of a Neisseria meningitidis acetate auxotroph was metabolically labeled with either [2-13C]-sodium acetate or [1,2-13C2]-sodium acetate. In this study, we demonstrated that this label was efficiently incorporated into both the lipid A acyl moieties and the two
Peter Niedbalski et al.
The journal of physical chemistry. A, 121(17), 3227-3233 (2017-04-20)
Dynamic nuclear polarization (DNP) via the dissolution method has alleviated the insensitivity problem in liquid-state nuclear magnetic resonance (NMR) spectroscopy by amplifying the signals by several thousand-fold. This NMR signal amplification process emanates from the microwave-mediated transfer of high electron
Emmeli F R Mikkelsen et al.
Scientific reports, 7(1), 16002-16002 (2017-11-24)
11C-acetate is a positron emission tomography (PET) tracer of oxidative metabolism, whereas hyperpolarized 13C-acetate can be used in magnetic resonance imaging (MRI) for investigating specific metabolic processes. The aims of this study were to examine if the kinetic formalism of
Randy Lee Tyson et al.
Brain research, 992(1), 43-52 (2003-11-08)
[1-13C]Glucose, [2-13C]acetate and [3-13C]lactate were infused into male Sprague-Dawley rats (150-170 g) for periods of 3-100 min (n=4 per time) and neocortex extracts were analyzed using 13C-edited 1H magnetic resonance (MR) spectroscopy. The time dependence of the [4-13C]glutamine/[4-13C]glutamate labeling ratio
Fayrouz El Maddah et al.
Organic & biomolecular chemistry, 17(10), 2747-2752 (2019-02-21)
The marilones and marilines are a new family of polyketide metabolites recently isolated from the marine-derived fungus Stachylidium sp. 293K04. They are characterized by a phthalide and phthalimidine skeleton, respectively. From a series of feeding experiments using 13C-labeled precursors we

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