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R1757

Sigma-Aldrich

D-(−)-Ribose

98%

Sinonimo/i:

D-Ribose

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About This Item

Formula empirica (notazione di Hill):
C5H10O5
Numero CAS:
50-69-1
Peso molecolare:
150.13
Beilstein:
1723081
Numero CE:
200-059-4
Numero MDL:
MFCD00135453
Codice UNSPSC:
12352201
ID PubChem:
24899349
NACRES:
NA.22

Saggio

98%

Attività ottica

[α]20/D −19.7°, c = 4 in H2O

Punto di fusione

88-92 °C (lit.)

Stringa SMILE

OC[C@@H](O)[C@@H](O)[C@@H](O)C([H])=O

InChI

1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h1,3-5,7-10H,2H2/t3-,4+,5-/m0/s1
PYMYPHUHKUWMLA-LMVFSUKVSA-N

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Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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Certificati d'analisi (COA)

Lot/Batch Number
BCCD9952
BCCC6987
BCBW4071
BCBT8955
BCBT3887

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2-Deoxy-L-ribose ≥97.0% (TLC)

Sigma-Aldrich

75617

2-Deoxy-L-ribose

D-(+)-Ribonic γ-lactone 97%

Sigma-Aldrich

857297

D-(+)-Ribonic γ-lactone

Verbascose analytical standard

Supelco

56217

Verbascose

D-(−)-Arabinose suitable for microbiology, ≥99.0%

Millipore

10850

D-(−)-Arabinose

D-(−)-Lyxose 99%

Sigma-Aldrich

220477

D-(−)-Lyxose

D-Ribose 5-phosphate disodium salt hydrate ≥98% (TLC), powder

Sigma-Aldrich

R7750

D-Ribose 5-phosphate disodium salt hydrate

Thomas L Willett et al.
Bone, 52(2), 611-622 (2012-11-28)
Non-enzymatic glycation (NEG) and advanced glycation endproducts (AGEs) may contribute to bone fragility in various diseases, ageing, and other conditions by modifying bone collagen and causing degraded mechanical properties. In this study, we sought to further understand how collagen modification
Lusani Norah Vhangani et al.
Food chemistry, 137(1-4), 92-98 (2012-12-04)
Maillard reaction products (MRPs) were prepared from aqueous ribose-lysine (RL) and fructose-lysine (FL) model systems at pH 9, heated at 60, 80 and 120 °C for 15, 60 and 120 min. Browning intensity (BI) and pH reduction were monitored throughout
Raman K Sharma et al.
Bioorganic & medicinal chemistry, 20(23), 6821-6830 (2012-10-27)
A series of peracetylated O-aryl α,β-d-ribofuranosides have been synthesized and an efficient biocatalytic methodology has been developed for the separation of their anomers which was otherwise almost impossible by column chromatographic or other techniques. The incubation of 2,3,5-tri-O-acetyl-1-O-aryl-α,β-d-ribofuranoside with Lipozyme®
Carine Baraguey et al.
Organic & biomolecular chemistry, 11(16), 2638-2647 (2013-03-05)
The pivaloyloxymethyl (PivOM) group is a biolabile 2'-O-ribose protection that is under development in a prodrug-based approach for siRNA applications. Besides an expected cellular uptake, nucleic acid sequences carrying PivOM showed also increased nuclease resistance and, in most cases, an
Anders Virtanen et al.
Critical reviews in biochemistry and molecular biology, 48(2), 192-209 (2013-03-19)
Deadenylation of eukaryotic mRNA is a mechanism critical for mRNA function by influencing mRNA turnover and efficiency of protein synthesis. Here, we review poly(A)-specific ribonuclease (PARN), which is one of the biochemically best characterized deadenylases. PARN is unique among the
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Protocolli

HPLC Analysis of Monosaccharides Ribose, Xylitol, and Mannose on Chromolith® NH2

Separation of Ribose, United States Pharmacopeia (USP) Reference Standard; Xylitol, analytical standard; Mannose, United States Pharmacopeia (USP) Reference Standard

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