Pular para o conteúdo
Merck
Todas as fotos(2)

Documentos Principais

Visualizar Toda a Documentação

V900389

Sigma-Aldrich

D-(−)-Ribose

Vetec™, reagent grade, 99%

Sinônimo(s):

Aldehydo-D-ribose

Faça loginpara ver os preços organizacionais e de contrato
Todas as fotos(2)

About This Item

Fórmula empírica (Notação de Hill):
C5H10O5
Número CAS:
50-69-1
Peso molecular:
150.13
Beilstein:
1723081
Número CE:
200-059-4
Número MDL:
MFCD00135453
Código UNSPSC:
12352201
ID de substância PubChem:
329829799

grau

reagent grade

linha de produto

Vetec™

Ensaio

99%

Formulário

powder

pf

88-92 °C (lit.)

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

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

chave InChI

PYMYPHUHKUWMLA-LMVFSUKVSA-N

Procurando produtos similares? Visita Guia de comparação de produtos

Aplicação


  • Conditions and Mechanism of Formation of the Maillard Reaction Pigment, Furpenthiazinate, in a Model System and in Some Acid Hydrolyzates of Foods and its Biological Properties.: This article investigates the conditions and mechanisms under which ᴅ-(−)-Ribose participates in the Maillard reaction to form bioactive pigments like Furpenthiazinate. It details the implications for food chemistry and the nutritional properties of processed foods (Noda et al., 2024).

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.

Informações legais

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

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

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
WXBD6693V
WXBD3912V
WXBB0660V
WXBB0660

Não está vendo a versão correta?

Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

Pesquise por COA

Já possui este produto?

Encontre a documentação dos produtos que você adquiriu recentemente na biblioteca de documentos.

Visite a Biblioteca de Documentos

Os clientes também visualizaram

Slide 1 of 7

1 of 7

3,3′,5,5′-Tetrametilbenzidina ≥99%

Sigma-Aldrich

860336

3,3′,5,5′-Tetrametilbenzidina

Adenina ≥99%

Sigma-Aldrich

A8626

Adenina

Hypoxanthine ≥99.0%

Sigma-Aldrich

H9377

Hypoxanthine

Sodium butyrate 98%

Sigma-Aldrich

303410

Sodium butyrate

ProClin™ 300 ProClin™ preservative for use in IVD manufacturing, pkg of 400 mL, CMIT/MIT 3 %

Sigma-Aldrich

48914-U

ProClin™ 300

Adenosina 5′-difosfato bacterial, ≥95% (HPLC)

Sigma-Aldrich

A2754

Adenosina 5′-difosfato

D-(+)-Galactose ≥99% (HPLC)

Sigma-Aldrich

G0750

D-(+)-Galactose

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
Exibir todos os documentos relacionados

Nossa equipe de cientistas tem experiência em todas as áreas de pesquisa, incluindo Life Sciences, ciência de materiais, síntese química, cromatografia, química analítica e muitas outras.

Entre em contato com a assistência técnica