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605409

Sigma-Aldrich

D-Glucose-3-13C

99 atom % 13C, 99% (CP)

Sinonimo/i:

Labeled Glucose, Dextrose-3-13C

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About This Item

Formula empirica (notazione di Hill):
13CC5H12O6
Numero CAS:
287100-64-5
Peso molecolare:
181.15
Numero MDL:
MFCD08459778
Codice UNSPSC:
12352005
ID PubChem:
329759056
NACRES:
NA.12

Purezza isotopica

99 atom % 13C

Livello qualitativo

200

Saggio

99% (CP)

Stato

powder

Attività ottica

[α]25/D +52.0°, c = 2 in H2O (trace NH4OH)

Punto di fusione

150-152 °C (lit.)

Spostamento di massa

M+1

Stringa SMILE

OC[C@H]1OC(O)[C@H](O)[13C@@H](O)[C@@H]1O

InChI

1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6?/m1/s1/i4+1
WQZGKKKJIJFFOK-UTTRQBQKSA-N

Categorie correlate

Confezionamento

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.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

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Certificati d'analisi (COA)

Lot/Batch Number
MBBC1358
MBBC0698
MBBC0650
TA1634V
TA1274V

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D-Glucose-13C6,1,2,3,4,5,6,6-d7 97 atom % D, 99 atom % 13C

Sigma-Aldrich

552151

D-Glucose-13C6,1,2,3,4,5,6,6-d7

D-Glucose-1,2,3-13C3 99 atom % 13C, 99% (CP)

Sigma-Aldrich

720127

D-Glucose-1,2,3-13C3

D-Fructose-13C6 99 atom % 13C, 99% (CP)

Sigma-Aldrich

587621

D-Fructose-13C6

D-glucosio-13C6 endotoxin tested, 99 atom % 13C

Sigma-Aldrich

660663

D-glucosio-13C6

D-Glucose-6,6-d2 ≥98 atom % D, ≥99% (CP)

Sigma-Aldrich

282650

D-Glucose-6,6-d2

D-Glucose-1,2,3,4,5,6,6-d7 97 atom % D

Sigma-Aldrich

552003

D-Glucose-1,2,3,4,5,6,6-d7

D-(+)-Glucosio ≥99.5% (GC)

Sigma-Aldrich

G8270

D-(+)-Glucosio

Chaevien S Clendinen et al.
Analytical chemistry, 87(11), 5698-5706 (2015-05-02)
The many advantages of (13)C NMR are often overshadowed by its intrinsically low sensitivity. Given that carbon makes up the backbone of most biologically relevant molecules, (13)C NMR offers a straightforward measurement of these compounds. Two-dimensional (13)C-(13)C correlation experiments like
Shilpa Nargund et al.
Biotechnology progress, 31(5), 1179-1186 (2015-06-23)
(13)C-metabolic flux analysis was used to understand copper deficiency-related restructuring of energy metabolism, which leads to excessive lactate production in recombinant protein-producing CHO cells. Stationary-phase labeling experiments with U-(13)C glucose were conducted on CHO cells grown under high and limiting
Oren Yishai et al.
ACS synthetic biology, 6(9), 1722-1731 (2017-05-31)
Decoupling biorefineries from land use and agriculture is a major challenge. As formate can be produced from various sources, e.g., electrochemical reduction of CO
Masao Goto et al.
Molecules (Basel, Switzerland), 20(10), 19014-19026 (2015-10-23)
Procyanidins, which are flavonoids that are found in a variety of plant species, reduce or prevent immune disorders, such as allergy and autoimmune diseases, through an unknown mechanism. In the present study, we investigated the effects of procyanidins on the
Sandhya G Rani et al.
Biochimica et biophysica acta, 1844(9), 1718-1728 (2014-07-02)
S100A13 is involved in several key biological functions like angiogenesis, tumor formation and cell apoptosis. It is a homodimeric protein that belongs to the S100 protein family. S100A13 is co-expressed with acidic fibroblast growth factor (FGF1) and interleukin-1α which are
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