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R4377

Sigma-Aldrich

L-(+)-Ribose

≥98% (GC)

Sinônimo(s):

Aldehydo-L-ribose

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About This Item

Fórmula empírica (Notação de Hill):
C5H10O5
Número CAS:
24259-59-4
Peso molecular:
150.13
Beilstein:
1723084
Número MDL:
MFCD00167010
Código UNSPSC:
12352201
ID de substância PubChem:
24899368
NACRES:
NA.25

Ensaio

≥98% (GC)

forma

powder

cor

white to colorless

pf

81-82 °C (lit.)

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

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

chave InChI

HMFHBZSHGGEWLO-OWMBCFKOSA-N

Procurando produtos similares? Visita Guia de comparação de produtos

Outras notas

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

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificados de análise (COA)

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D-Ribulose solution ~1 M in H2O, ≥97.0% (HPLC)

Sigma-Aldrich

76512

D-Ribulose solution

L-(−)-Galactose ≥99% (HPLC)

Sigma-Aldrich

G7134

L-(−)-Galactose

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
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
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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