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Safety Information

R4377

Sigma-Aldrich

L-(+)-Ribose

≥98% (GC)

Synonym(s):

Aldehydo-L-ribose

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About This Item

Empirical Formula (Hill Notation):
C5H10O5
CAS Number:
24259-59-4
Molecular Weight:
150.13
Beilstein:
1723084
MDL number:
MFCD00167010
UNSPSC Code:
12352201
PubChem Substance ID:
24899368
NACRES:
NA.25

Quality Level

200

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

R4377-VAR:
R4377-50MG:
R4377-5G:
R4377-1G:
R4377-250MG:
R4377-BULK:

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’.

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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
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
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
Rostyslav Antonyuk et al.
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie, 57(3), 985-994 (2016-12-22)
A method of lectin purification from carp roe (CCRA) was elaborated, which includes affinity chromatography on cross-linked ovomucoid and copolymers of polyvinyl alcohol and blood group-specific substances. That allowed obtaining lectin with electrophoretic purity and yielding of ˜ 42 mg÷kg
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