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490717

Sigma-Aldrich

Sodium pyruvate-13C3

99 atom % 13C

Synonym(s):

Pyruvic acid-13C3 sodium salt

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About This Item

Linear Formula:
13CH313CO13CO2Na
CAS Number:
142014-11-7
Molecular Weight:
113.02
MDL number:
MFCD00084084
UNSPSC Code:
12352106
PubChem Substance ID:
24872594
NACRES:
NA.12

isotopic purity

99 atom % 13C

Quality Level

200

form

solid

technique(s)

mass spectrometry (MS): suitable

mp

>300 °C (lit.)

mass shift

M+3

storage temp.

2-8°C

SMILES string

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

InChI

1S/C3H4O3.Na/c1-2(4)3(5)6;/h1H3,(H,5,6);/q;+1/p-1/i1+1,2+1,3+1;

InChI key

DAEPDZWVDSPTHF-HCULJTSZSA-M

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Packaging

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H317,H319

Hazard Classifications

Eye Irrit. 2 - Skin Sens. 1B

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Izargi Vega-Mas et al.
Scientific reports, 9(1), 8925-8925 (2019-06-22)
Proper carbon (C) supply is essential for nitrogen (N) assimilation especially when plants are grown under ammonium (NH4+) nutrition. However, how C and N metabolic fluxes adapt to achieve so remains uncertain. In this work, roots of wheat (Triticum aestivum
Eran Mick et al.
eLife, 9 (2020-05-29)
Mitochondrial dysfunction is associated with activation of the integrated stress response (ISR) but the underlying triggers remain unclear. We systematically combined acute mitochondrial inhibitors with genetic tools for compartment-specific NADH oxidation to trace mechanisms linking different forms of mitochondrial dysfunction
Jordan M Wilkins et al.
Aging, 12(14), 15134-15156 (2020-07-09)
Multiple sclerosis (MS) is a central nervous system inflammatory demyelinating disease and the most common cause of non-traumatic disability in young adults. Despite progress in the treatment of the active relapsing disease, therapeutic options targeting irreversible progressive decline remain limited.

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