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297046

D-Glucose-1-13C

99 atom % 13C

Synonym(s):

Labeled Glucose, Dextrose-1-13C

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About This Item

Empirical Formula (Hill Notation):
13CC5H12O6
CAS Number:
40762-22-9
Molecular Weight:
181.15
UNSPSC Code:
12352005
NACRES:
NA.12
PubChem Substance ID:
24857895
MDL number:
MFCD00037545
Beilstein/REAXYS Number:
2263682
Isotopic purity:
99 atom % 13C
Assay:
99% (CP)
Mass shift:
M+1
Form:
powder
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isotopic purity

99 atom % 13C

Quality Level

200

assay

99% (CP)

form

powder

optical activity

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

technique(s)

bio NMR: suitable

mp

150-152 °C (lit.)

mass shift

M+1

storage temp.

room temp

SMILES string

OC[C@H]1O[13CH](O)[C@H](O)[C@@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/i6+1

InChI key

WQZGKKKJIJFFOK-USBRANDWSA-N

Application

D-Glucose-1-13C can be used:
  • To predict the primary reaction mechanism in pyrolysis of glucose.
  • To study C−C bond cleavage mechanism in the conversion of labeled glucose into alkanediols using Ni−MgO−ZnO catalyst.
  • In tracer enrichment determination in blood plasma using high-resolution mass spectrometry.

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.

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Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MBBF1637
MBBF1387
MBBF0459
MBBD9769
MBBD8960

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Articles

Glycolysis via the Embden-Meyerhof-Parnas Glycolytic Pathway

Review the 10 steps of glycolysis in the Embden-Meyerhof-Parnas glycolytic pathway. Easily compare reaction stages and buy the enzymes for your life science research.

Isotopic Labeling for NMR Spectroscopy of Biological Solids

Isotopic Labeling for NMR Spectroscopy of Biological Solids;

Determination of the Isotopic Enrichment of 13C-and 2H-Labeled Tracers of Glucose Using High-Resolution Mass Spectrometry: Application to Dual-and Triple-Tracer Studies.
Trotzmuller M, et al.
Analytical Chemistry, 89(22), 12252-12260 (2017)
Catalytic conversion of glucose into alkanediols over nickel-based catalysts: a mechanism study.
Tan Z, et al.
Royal Society of Chemistry Advances, 6(67), 62747-62753 (2016)
M Fleur Sernee et al.
Cell host & microbe, 26(3), 385-399 (2019-09-13)
Parasitic protists belonging to the genus Leishmania synthesize the non-canonical carbohydrate reserve, mannogen, which is composed of β-1,2-mannan oligosaccharides. Here, we identify a class of dual-activity mannosyltransferase/phosphorylases (MTPs) that catalyze both the sugar nucleotide-dependent biosynthesis and phosphorolytic turnover of mannogen. Structural
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Global Trade Item Number

SKUGTIN
297046-10G04061826656792
297046-1G04061826656808
297046-250MG04061826656815