R4377
L-(+)-Ribose
≥98% (GC)
Synonym(s):
Aldehydo-L-ribose
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1 G
$345.80
About This Item
Empirical Formula (Hill Notation):
C5H10O5
CAS Number:
Molecular Weight:
150.13
Beilstein/REAXYS Number:
1723084
MDL number:
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.25
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Quality Level
assay
≥98% (GC)
form
powder
color
white to colorless
mp
81-82 °C (lit.)
storage temp.
2-8°C
SMILES string
OC[C@@H]1OC(O)[C@@H](O)[C@H]1O
InChI
1S/C5H10O5/c6-1-2-3(7)4(8)5(9)10-2/h2-9H,1H2/t2-,3-,4-,5?/m0/s1
InChI key
HMFHBZSHGGEWLO-OWMBCFKOSA-N
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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
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Shahid Mahmood et al.
Enzyme and microbial technology, 135, 109510-109510 (2020-03-10)
An enzyme, l-ribose isomerase (l-RI), mostly catalyzes the isomerization of l-ribose and l-ribulose. These so-called rare sugars are essential for the treatment of cancer and other viral diseases. In the present study, l-ribose isomerase produced from a bacterium, Mycetocola miduiensis
Jeremie J Crawford et al.
Electrophoresis, 37(15-16), 2217-2225 (2016-06-09)
Single enzyme molecule assays on E. coli β-galactosidase were performed using a capillary electrophoresis-based method. Three types of assays were performed. The catalytic rate of 20 individual molecules was assayed in duplicate in the presence of 50 μM substrate. The
Wen-Chi Tseng et al.
Journal of biotechnology, 259, 168-174 (2017-07-29)
A putative l-ribose isomerase (EC 5.3.1.B3, l-RI) gene of Actinotalea fermentans ATCC 43279 was chemically synthesized, subcloned into pET-21b vector, and then overexpressed in Escherichia coli. After 0.5mM IPTG induction at 20°C for 20h, the recombinant l-RI was highly expressed
Xin-Xia Xue et al.
Bioresource technology, 268, 292-299 (2018-08-08)
In this study, organic acid could be used as co-catalyst for assisting solid acid SO42-/SnO2-argil to convert hemicellulose-derived D-xylose into furfural. The relationship between pKa of organic acid and turnover frequency (TOF) of co-catalysis with organic acid plus SO42-/SnO2-argil was
Sirinan Shompoosang et al.
Journal of bioscience and bioengineering, 121(1), 1-6 (2015-06-03)
We biosynthesized 6-deoxy-L-talose, 6-deoxy-L-sorbose, 6-deoxy-L-gulose, and 6-deoxy-L-idose, which rarely exist in nature, from L-fucose by coupling and sequential enzymatic reactions. The first product, 6-deoxy-L-talose, was directly produced from L-fucose by the coupling reactions of immobilized D-arabinose isomerase and immobilized L-rhamnose
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