492167
D-Glucose-12C6
99.5 atom % 12C
Synonym(s):
Dextrose-12C6
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About This Item
Empirical Formula (Hill Notation):
12C6H12O6
CAS Number:
Molecular Weight:
180.09
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
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description
13C-depleted
Quality Level
isotopic purity
99.5 atom % 12C
optical activity
[α]25/D +52.0°, c = 2 in H2O (trace NH4OH)
mp
150-152 °C (lit.)
mass shift
depleted
SMILES string
O[12CH2][12C@H]1O[12CH](O)[12C@H](O)[12C@@H](O)[12C@@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+0,2+0,3+0,4+0,5+0,6+0
InChI key
WQZGKKKJIJFFOK-DXVIFZLFSA-N
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Yi Xu et al.
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In this paper, the effects of cerium oxide nanoparticles (CeO2 NPs) on the group bacterial behaviors were elaborated. After 36-h cultivation, the biofilm biomass was enhanced by the sub-lethal concentrations of 0.5 and 2 mg/L CeO2 NP exposure. Meanwhile, the promoted
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The journal of physical chemistry. A, 124(4), 642-651 (2020-01-08)
Vacuum ultraviolet (VUV) electronic circular dichroism (ECD) spectra of d-glucose, α-d-glucopyranose, and β-d-glucopyranose were measured in aqueous solution down to 163 nm using a synchrotron radiation VUV-ECD spectrophotometer and theoretically analyzed using molecular dynamics (MD) simulations with explicit water molecules
Sara Groeneboer et al.
Rheumatology (Oxford, England), 50(7), 1226-1235 (2011-02-25)
To compare the ability of different cyclodextrin polysulphate (CDPS) derivatives to affect human articular cartilage cell metabolism in vitro. OA chondrocytes were cultured in alginate and exposed to 5 µg/ml of 2,3,6-tri-O-methyl-β-cyclodextrin (ME-CD), 2,3-di-O-methyl-6-sulphate-β-cyclodextrin (ME-CD-6-S), 2,6-di-O-methyl-3-sulphate-β-cyclodextrin (ME-CD-3-S), (2-carboxyethyl)-β-CDPS (CE-CDPS), (2-hydroxypropyl)-β-CDPS
Giovanni E Lombardo et al.
Molecular cancer therapeutics, 17(6), 1187-1195 (2018-03-23)
The high frequency of hTERT-promoting mutations and the increased expression of hTERT mRNA in anaplastic thyroid cancer (ATC) make TERT a suitable molecular target for the treatment of this lethal neoplasm. In this study, we encapsulated an anti-hTERT oligonucleotide in
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