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Merck
CN

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

Key Documents

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Product Name

D-Glucose-1-13C, 99 atom % 13C

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

SMILES string

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

InChI key

WQZGKKKJIJFFOK-USBRANDWSA-N

isotopic purity

99 atom % 13C

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

Quality Level

200

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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.

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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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
Evaluation of primary reaction pathways in thin-film pyrolysis of glucose using 13C labeling and real-time monitoring.
Hutchinson CP and Lee YJ
ACS sustainable chemistry & engineering, 5(10), 8796-8803 (2017)
Ingjye Jiang et al.
Nucleic acids research, 39(20), 8992-9008 (2011-07-21)
Iron-inducible transcription of the ap65-1 gene in Trichomonas vaginalis involves at least three Myb-like transcriptional factors (tvMyb1, tvMyb2 and tvMyb3) that differentially bind to two closely spaced promoter sites, MRE-1/MRE-2r and MRE-2f. Here, we defined a fragment of tvMyb2 comprising
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