I1006
1,2-O-Isopropylidene-α-D-glucofuranose
≥98% (TLC)
Synonym(s):
Monoacetone glucose
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About This Item
Empirical Formula (Hill Notation):
C9H16O6
CAS Number:
Molecular Weight:
220.22
EC Number:
242-420-9
UNSPSC Code:
12352103
PubChem Substance ID:
Beilstein/REAXYS Number:
82670
MDL number:
InChI
1S/C9H16O6/c1-9(2)14-7-5(12)6(4(11)3-10)13-8(7)15-9/h4-8,10-12H,3H2,1-2H3/t4-,5+,6-,7-,8-/m1/s1
InChI key
BGGCXQKYCBBHAH-OZRXBMAMSA-N
SMILES string
CC1(C)O[C@H]2O[C@H]([C@H](O)CO)[C@H](O)[C@H]2O1
assay
≥98% (TLC)
storage temp.
−20°C
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Fermentation of 1,2-O-iso-propylidene-D-glucofuranose ("monoacetone glucose") by anaerobic bacteria.
S H Cmelik
Zentralblatt fur Bakteriologie. 1. Abt. Originale. A: Medizinische Mikrobiologie, Infektionskrankheiten und Parasitologie, 247(4), 495-501 (1980-01-01)
Various species of Clostridium, Bacteroides, Propionibacterium and Eubacterium were incubated in a 1% solution of 1,2-O-iso-propylidene-D-glucofuranose in a peptone-yeast-extract (PY) medium according to the VPI-technique. The volatile and non volatile acids were investigated by gas-liquid chromatography. All microorganisms showed a
Aifric O'Sullivan et al.
Molecular nutrition & food research, 55(7), 1018-1025 (2011-04-27)
Research reports suggest that vitamin D affects glucose and insulin metabolism; however, the exact mechanisms are unclear. ²H NMR analysis of monoacetone glucose (MAG) after tracer administration provides a non-invasive method of profiling hepatic glucose metabolism. This study examined the
G N Richards et al.
Carbohydrate research, 219, 91-99 (1991-10-14)
Methyl alpha,beta-D-glucofuranoside (1) and 1,2-O-isopropylidene-alpha-D-glucofuranose (2) have been polymerized thermally, using 0.1% phosphoric acid as catalyst. The resulting alcohol-insoluble polymers were analyzed by gel-permeation chromatography and methylation analysis. The two starting materials gave polymers that were very similar in molecular-weight
Eunsook S Jin et al.
Analytical biochemistry, 327(2), 149-155 (2004-03-31)
A triple-tracer method was developed to provide absolute fluxes contributing to endogenous glucose production and hepatic tricarboxylic acid (TCA) cycle fluxes in 24-h-fasted rats by (2)H and (13)C nuclear magnetic resonance (NMR) analysis of a single glucose derivative. A primed
Eunsook S Jin et al.
American journal of physiology. Endocrinology and metabolism, 288(4), E654-E662 (2004-11-25)
The metabolic mechanism of hepatic glucose overproduction was investigated in 3,3'-5-triiodo-l-thyronine (T3)-treated rats and Zucker diabetic fatty (ZDF) rats (fa/fa) after a 24-h fast. 2H2O and [U-13C3]propionate were administered intraperitoneally, and [3,4-13C2]glucose was administered as a primed infusion for 90
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