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310824

Sigma-Aldrich

D-Glucose-2-d1

98 atom % D, 99% (CP)

Synonym(e):

Deuterierte Glucose, Markierte Glucose, Dextrose-2-d1

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About This Item

Lineare Formel:
HOCH2[CHOH]3CDOHCHO
CAS-Nummer:
30737-83-8
Molekulargewicht:
181.16
MDL-Nummer:
MFCD00151501
UNSPSC-Code:
12352202
PubChem Substanz-ID:
24858818

Isotopenreinheit

98 atom % D

Assay

99% (CP)

Form

powder

Optische Aktivität

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

mp (Schmelzpunkt)

150-152 °C (lit.)

Massenverschiebung

M+1

SMILES String

[2H][C@](O)(C=O)[C@@H](O)[C@H](O)[C@H](O)CO

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/i3D

InChIKey

GZCGUPFRVQAUEE-FPCZXLAFSA-N

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Verpackung

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.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MBBC4927
MBBB9544V
MBBB7100V
027H3602
00904TX

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Journal of bacteriology, 190(21), 7079-7086 (2008-09-02)
The lysin motif (LysM) is a ubiquitous protein module that binds peptidoglycan and structurally related molecules. Here, we used single-molecule force spectroscopy (SMFS) to measure and localize individual LysM-peptidoglycan interactions on both model and cellular surfaces. LysM modules of the
José Antonio Picanço Diniz et al.
PloS one, 3(3), e1733-e1733 (2008-03-06)
In previous reports we proposed a new genus for Rhabdoviridae and described neurotropic preference and gross neuropathology in newborn albino Swiss mice after Curionopolis and Itacaiunas infections. In the present report a time-course study of experimental encephalitis induced by Itacaiunas
William Lee et al.
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Astrocytes play an important role in cell-cell signaling in the mammalian central nervous system. The ability of astrocytes to communicate with surrounding cells through gap-junctional coupling or signaling via the release of transmitters makes characterization of these cells difficult in
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Diabetes, 60(2), 496-506 (2011-01-29)
Peroxisome proliferator-activated receptor (PPAR)-α/γ dual agonists have been developed to alleviate metabolic disorders. However, several PPARα/γ dual agonists are accompanied with unwanted side effects, including body weight gain, edema, and tissue failure. This study investigated the effects of a novel
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