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Key Documents

83870

Sigma-Aldrich

D-Ribose 5-phosphate barium salt hexahydrate

≥99.0% (TLC)

Synonym(s):

R-5-P-Ba

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About This Item

Empirical Formula (Hill Notation):
C5H9BaO8P · 6H2O
CAS Number:
Molecular Weight:
473.51
Beilstein:
3781061
EC Number:
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25

Quality Level

Assay

≥99.0% (TLC)

form

powder

optical activity

[α]20/D +12±2°, c = 1% in 0.2 M HCl

storage temp.

2-8°C

SMILES string

[Ba++].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]O[H].[H]C(=O)[C@H](O)[C@H](O)[C@H](O)COP([O-])([O-])=O

InChI

1S/C5H11O8P.Ba.6H2O/c6-1-3(7)5(9)4(8)2-13-14(10,11)12;;;;;;;/h1,3-5,7-9H,2H2,(H2,10,11,12);;6*1H2/q;+2;;;;;;/p-2/t3-,4+,5-;;;;;;;/m0......./s1

InChI key

WUZJSCGFQURQNK-BJLVBTRRSA-L

Related Categories

Application

D-Ribose 5-phosphate is used as a substrate to identify, differentiate and characterize ribose-5-phosphate isomerase(s) and phosphopentomutase(s). Ribose 5-phosphate is used to study the processes and effects of glycation in vivo and in vitro.

Other Notes

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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Claudia Vanesa Piattoni et al.
Plant physiology, 156(3), 1337-1350 (2011-05-07)
Nonphosphorylating glyceraldehyde-3-phosphate dehydrogenase (np-Ga3PDHase) is a cytosolic unconventional glycolytic enzyme of plant cells regulated by phosphorylation in heterotrophic tissues. After interaction with 14-3-3 proteins, the phosphorylated enzyme becomes less active and more sensitive to regulation by adenylates and inorganic pyrophosphate.
Luke J Alderwick et al.
Glycobiology, 21(4), 410-425 (2010-11-04)
Mycobacterium tuberculosis arabinogalactan (AG) is an essential cell wall component. It provides a molecular framework serving to connect peptidoglycan to the outer mycolic acid layer. The biosynthesis of the arabinan domains of AG and lipoarabinomannan (LAM) occurs via a combination
Bianca Derrer et al.
FEBS letters, 584(19), 4169-4174 (2010-09-15)
Most organisms synthesise the B(6) vitamer pyridoxal 5-phosphate (PLP) via the glutamine amidotransferase PLP synthase, a large enzyme complex of 12 Pdx1 synthase subunits with up to 12 Pdx2 glutaminase subunits attached. Deletion analysis revealed that the C-terminus has four
L E Meshalkina et al.
Biochemistry. Biokhimiia, 76(9), 1061-1064 (2011-11-16)
The Michaelis constant values for substrates of transketolase from human tissues were determined over a wide range of substrate concentrations. It is shown that K(m) values determined by other authors are significantly overestimated and explained why this is so.
Maia M Cherney et al.
Journal of molecular biology, 413(4), 844-856 (2011-10-04)
Phosphoribosyl pyrophosphate (PRPP) synthetase catalyzes the transfer of the pyrophosphate group from ATP to ribose-5-phosphate (R5P) yielding PRPP and AMP. PRPP is an essential metabolite that plays a central role in cellular metabolism. The enzyme from a thermophilic archaeon Thermoplasma

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