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Merck
CN

W252409

Glucose pentaacetate

≥99%

Synonym(s):

α-D(+)-Glucose pentaacetate, 1,2,3,4,6-Penta-O-acetyl-α-D-glucopyranose

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About This Item

Empirical Formula (Hill Notation):
C16H22O11
CAS Number:
604-68-2
Molecular Weight:
390.34
PubChem Substance ID:
24900987
UNSPSC Code:
12164502
Council of Europe no.:
2524c
FEMA Number:
2524
EC Number:
210-073-2
MDL number:
MFCD00064071
Beilstein/REAXYS Number:
98852
Grade:
Kosher
Biological source:
synthetic

Key Documents

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biological source

synthetic

Quality Level

300, 400

grade

Kosher

assay

≥99%

optical activity

[α]20/D +98°, c = 1 in chloroform

mp

109-111 °C (lit.)

application(s)

flavors and fragrances

SMILES string

CC(=O)OC[C@H]1O[C@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O

InChI

1S/C16H22O11/c1-7(17)22-6-12-13(23-8(2)18)14(24-9(3)19)15(25-10(4)20)16(27-12)26-11(5)21/h12-16H,6H2,1-5H3/t12-,13-,14+,15-,16+/m1/s1

InChI key

LPTITAGPBXDDGR-LJIZCISZSA-N

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H317

Hazard Classifications

Skin Sens. 1A

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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Certificates of Analysis (COA)

Lot/Batch Number
S39349
11209BN
10910KS
10511AN
09217AW

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Jinqiang Zhang et al.
Nanotechnology, 30(3), 035401-035401 (2018-11-18)
WS2 nanotubes with carbon coatings in a core-shell structure (i.e. WS2@C) are synthesized through a facile method based on the Lewis acid-activated thioglycosylation chemistry. The obtained WS2@C shows a conformal coverage of conductive amorphous carbon on the surface of WS2
Tanya McDonald et al.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 40(3), 678-691 (2019-03-21)
Triheptanoin is anticonvulsant in several seizure models. Here, we investigated changes in glucose metabolism by triheptanoin interictally in the chronic stage of the pilocarpine mouse epilepsy model. After injection of [U-13C6]-glucose (i.p.), enrichments of 13C in intermediates of glycolysis and
Shigeru Tamogami et al.
Plant physiology and biochemistry : PPB, 109, 166-170 (2016-10-04)
To investigate the biotransformation pathway of airborne geraniol by Achyranthes bidentata (A. bidentata), deuterium labeled geraniol was applied with or without methyl jasmonate (MeJA), and the biosynthesized metabolites were analyzed. In A. bidentata leaves, geraniol was conjugated with glucose. The conjugate was
W J Malaisse et al.
Archives of biochemistry and biophysics, 381(1), 61-66 (2000-10-06)
Hepatocytes from fed rats were incubated for 120 min in the presence of alpha-D-[1,2-13C]glucose pentaacetate (1.7 mM), both D-[1,2-13C]glucose (1.7 mM) and acetate (8.5 mM), alpha-D-glucose penta[2-13C]acetate (1.7 mM), or D-[1,2-13C]glucose (8.3 mM). The amounts of 13C-enriched L-lactate and D-glucose
H Jijakli et al.
Endocrine, 10(3), 219-224 (1999-09-14)
The metabolism of alpha-D-glucose pentaacetate and its positive insulinotropic action in isolated rat pancreatic islets are both unexpectedly resistant to D-mannoheptulose, as judged from experiments conducted over 90-120 min incubation. In the present study, the possible effects of the heptose
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