Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

76512

Sigma-Aldrich

D-Ribulose solution

~1 M in H2O, ≥97.0% (HPLC)

Synonym(s):

D-erythro-2-Ketopentose solution, D-erythro-2-Pentulose solution, D-Adonose solution, D-Arabinulose solution, D-Araboketose solution, D-Erythropentulose solution

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C5H10O5
CAS Number:
488-84-6
Molecular Weight:
150.13
MDL number:
MFCD00004704
UNSPSC Code:
12352204
PubChem Substance ID:
329767154
NACRES:
NA.32

Assay

≥97.0% (HPLC)

form

liquid

concentration

~1 M in H2O

color

colorless

storage temp.

2-8°C

SMILES string

OCC1(O)OC[C@@H](O)[C@H]1O

InChI

1S/C5H10O5/c6-2-5(9)4(8)3(7)1-10-5/h3-4,6-9H,1-2H2/t3-,4-,5?/m1/s1

InChI key

LQXVFWRQNMEDEE-ZZKAVYKESA-N

Biochem/physiol Actions

D-Ribulose is a metabolite in pentose and glucuronate interconversions. It plays a role in the D-arabitol production from U. fabae. Ribulose is a rare aldopentose that might show antitumoral and antiviral activities. It acts as a substrate for nicotinamide adenine dinucleotide phosphate (NADP+)-dependent D-arabitol dehydrogenase (ARD1p) enzyme and D-tagatose-3-epimerase from Rhodobacter sphaeroides. Its monophosphate D-ribulose 5-phosphate is an intermediate in the pentose phosphate pathway of glycolysis. D-Ribulose may be found in plants like algae, sugar beet leaves, and barley seed leaves.

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

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.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

L-(+)-Arabinose ≥99% (GC)

Sigma-Aldrich

A3256

L-(+)-Arabinose

Glycogen from oyster

Sigma-Aldrich

G8751

Glycogen from oyster

Tobias Link et al.
The Biochemical journal, 389(Pt 2), 289-295 (2005-03-31)
We have identified and characterized a novel NADP(+)-dependent D-arabitol dehydrogenase and the corresponding gene from the rust fungus Uromyces fabae, a biotrophic plant pathogen on broad bean (Vicia faba). The new enzyme was termed ARD1p (D-arabitol dehydrogenase 1). It recognizes
Muhammad Waheed Iqbal et al.
Enzyme and microbial technology, 131, 109427-109427 (2019-10-17)
d-Ribulose and l-fuculose are potentially valuable rare sugars useful for anticancer and antiviral drugs in the agriculture and medicine industries. These rare sugars are usually produced by chemical methods, which are generally expensive, complicated and do not meet the increasing
Chakkiath Paul Antony et al.
International journal of systematic and evolutionary microbiology, 62(Pt 7), 1613-1618 (2011-09-06)
A moderately haloalkaliphilic methylotrophic bacterium possessing the ribulose monophosphate pathway for carbon assimilation, designated MPL(T), was isolated from Lonar Lake sediment microcosms that were oxidizing methane for two weeks. The isolate utilized methanol and was an aerobic, Gram-negative, asporogenous, motile
Ye-Wang Zhang et al.
Applied microbiology and biotechnology, 87(6), 1993-1999 (2010-05-25)
Recombinant Escherichia coli harboring the L: -arabinose isomerase (BLAI) from Bacillus licheniformis was used as a biocatalyst to produce L: -ribulose in the presence of borate. Effects of substrate concentration, the borate to L: -arabinose ratio, pH, and temperature on
Ying Zhang et al.
PLoS computational biology, 7(12), e1002318-e1002318 (2012-01-05)
Function diversification in large protein families is a major mechanism driving expansion of cellular networks, providing organisms with new metabolic capabilities and thus adding to their evolutionary success. However, our understanding of the evolutionary mechanisms of functional diversity in such
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service