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453196

Sigma-Aldrich

D-Glucose-1,6-13C2

≥99 atom % 13C, ≥99% (CP)

Sinônimo(s):

Labeled Glucose, Dextrose-1,6-13C2

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About This Item

Fórmula empírica (Notação de Hill):
13C2C4H12O6
Número CAS:
287100-67-8
Peso molecular:
182.14
Número MDL:
MFCD00144082
Código UNSPSC:
12352114
ID de substância PubChem:
24868768
NACRES:
NA.12

pureza isotópica

≥99 atom % 13C

Ensaio

≥99% (CP)

Formulário

powder

atividade óptica

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

pf

150-152 °C

alteração de massa

M+2

temperatura de armazenamento

room temp

cadeia de caracteres SMILES

O[13CH2][C@@H]1O[13CH2][C@@H](O)[C@H](O)[C@H]1O.O

InChI

1S/C6H12O6/c7-1-3(9)5(11)6(12)4(10)2-8/h1,3-6,8-12H,2H2/t3-,4+,5+,6+/m0/s1/i1+1,2+1

chave InChI

GZCGUPFRVQAUEE-OFAMVBKFSA-N

Embalagem

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.

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

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Certificados de análise (COA)

Lot/Batch Number
MBBD1284
MBBC6792
MBBC5780
MBBC4695
MBBC4328

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

Sigma-Aldrich

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

D-Glucose-13C6,1,2,3,4,5,6,6-d7 99 atom % 13C, 77 atom % D, 99% (CP)

608238

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

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

Sigma-Aldrich

552003

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

Sigma-Aldrich

660663

D-Glicose-13C6

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

Sigma-Aldrich

282650

D-Glucose-6,6-d2

L-Glutamine-13C5 98 atom % 13C, 95% (CP)

Sigma-Aldrich

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Cloreto de amônio-15N ≥98 atom % 15N, ≥99% (CP)

Sigma-Aldrich

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Cloreto de amônio-15N

Ralph J DeBerardinis et al.
Proceedings of the National Academy of Sciences of the United States of America, 104(49), 19345-19350 (2007-11-23)
Tumor cell proliferation requires rapid synthesis of macromolecules including lipids, proteins, and nucleotides. Many tumor cells exhibit rapid glucose consumption, with most of the glucose-derived carbon being secreted as lactate despite abundant oxygen availability (the Warburg effect). Here, we used
Tigran V Yuzbashev et al.
Biotechnology and bioengineering, 113(11), 2425-2432 (2016-05-18)
Bio-based succinic acid production can redirect industrial chemistry processes from using limited hydrocarbons to renewable carbohydrates. A fermentation process that does not require pH-titrating agents will be advantageous to the industry. Previously, a Yarrowia lipolytica strain that was defective for
Xuemei Tong et al.
Proceedings of the National Academy of Sciences of the United States of America, 106(51), 21660-21665 (2009-12-10)
Tumor cells are metabolically reprogrammed to fuel cell proliferation. Most transformed cells take up high levels of glucose and produce ATP through aerobic glycolysis. In cells exhibiting aerobic glycolysis, a significant fraction of glucose carbon is also directed into de

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