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389374

Sigma-Aldrich

D-Glucose-13C6

≥99 atom % 13C, ≥99% (CP)

Sinónimos:
D-Glucose-ul-13C, Labeled Glucose, Dextrose-13C6
Empirical Formula (Hill Notation):
13C6H12O6
Número de CAS:
Peso molecular:
186.11
Número MDL:
ID de la sustancia en PubChem:

Nivel de calidad

200

pureza isotópica

≥99 atom % 13C

ensayo

≥99% (CP)

formulario

powder

actividad óptica

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

technique(s)

bio NMR: suitable
protein expression: suitable
protein purification: suitable

mp

150-152 °C (lit.)

cambio de masa

M+6

SMILES string

O[13CH2][13C@H]1O[13C@H](O)[13C@H](O)[13C@@H](O)[13C@@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/i1+1,2+1,3+1,4+1,5+1,6+1

InChI key

WQZGKKKJIJFFOK-NYKRWLDMSA-N

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Categorías relacionadas

Aplicación

D-Glucose-13C6 has been used:
  • for de novo fatty acid (FA) synthesis
  • as a component in tracing media for the analysis of stable isotope tracer
  • in minimal media for recombinant protein production
  • for cell suspension

Envase

1, 2, 3, 10, 25 g in glass bottle
100, 250 mg in glass bottle
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.

Acciones bioquímicas o fisiológicas

D-Glucose-13C6 functions as a tracer and helps to access glucose kinetics in vivo.

Código de clase de almacenamiento

13 - Non Combustible Solids

WGK

WGK 3

Punto de inflamabilidad F

Not applicable

Punto de inflamabilidad C

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)

Certificado de Análisis

Certificado de origen

Frank Malz et al.
Carbohydrate research, 342(1), 65-70 (2006-12-06)
Double Quantum (DQ) NMR, which utilizes the magnetic dipole interaction between the (13)C atoms, was used for the complete assignment of the (13)C NMR resonances to the corresponding carbon ring positions for the monoclinic and triclinic allomorphs of methyl 4'-O-methyl-beta-D-cellobioside-(13)C(12)(1-(13)C(12))
Proceedings: Teratogenic actions of C13-glucose on the early development of the mouse embryo.
H Spielman et al.
Naunyn-Schmiedeberg's archives of pharmacology, 287 Suppl, R86-R86 (1975-01-01)
Y Oda et al.
Biochemistry, 33(17), 5275-5284 (1994-05-03)
All of the individual carboxyl groups (the side-chain carboxyl groups of Asp and Glu, and the C-terminal alpha-carboxyl group) in Escherichia coli ribonuclease HI, which is an enzyme that cleaves the RNA strand of a RNA/DNA hybrid, were pH-titrated, and
Zoran Dinev et al.
Carbohydrate research, 341(10), 1743-1747 (2006-04-11)
A simple gram-scale synthesis of uridine diphospho(13C6)glucose is presented from D-(13C6)glucose. The critical step uses a 1H-tetrazole-catalyzed coupling of 2,3,4,6-tetra-O-acetyl-alpha-D-glucopyranosyl-1-phosphate and UMP-morpholidate. The uridine diphospho(13C6)glucose was used in the structural identification of (1-->3)-beta-D-glucan from Lolium multiflorum.
Metabolic profiling reveals a coordinated response of isolated lamb's (Valerianella locusta, L.) lettuce cells to sugar starvation and low oxygen stress
Victor BMM, et al.
Postharvest biology and technology, 126, 23-33 (2017)

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