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MilliporeSigma

W379301

D-(−)-Ribose

≥98%

Synonym(s):

Dextro-ribose

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100 G

$41.20

1 EACH

$58.00

1 KG

$596.00

$41.20

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About This Item

Empirical Formula (Hill Notation):
C5H10O5
CAS Number:
50-69-1
Molecular Weight:
150.13
NACRES:
NA.21
PubChem Substance ID:
24901881
UNSPSC Code:
12352201
FEMA Number:
3793
EC Number:
200-059-4
MDL number:
MFCD00135453
Beilstein/REAXYS Number:
1723081
Organoleptic:
odorless
Biological source:
synthetic
Food allergen:
no known allergens

Key Documents

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Product Name

D-(−)-Ribose, ≥98%

InChI key

PYMYPHUHKUWMLA-LMVFSUKVSA-N

InChI

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

SMILES string

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

biological source

synthetic

reg. compliance

FDA 21 CFR 117

assay

≥98%

optical activity

[α]21/D −19.7°, c = 4 in H2O

mp

88-92 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

organoleptic

odorless

Quality Level

300

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This Item
W379312R9629PHR2101
D-(−)-Ribose ≥98%

Sigma-Aldrich

W379301

D-(−)-Ribose

Sigma-Aldrich

Sigma-Aldrich

W379312

D-Ribose

D-(−)-Ribose BioReagent, suitable for cell culture

Sigma-Aldrich

R9629

D-(−)-Ribose

Ribose Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR2101

Ribose

organoleptic

odorless

organoleptic

odorless

organoleptic

-

organoleptic

-

biological source

synthetic

biological source

corn

biological source

microbial

biological source

-

food allergen

no known allergens

food allergen

no known allergens

food allergen

-

food allergen

-

documentation

see Safety & Documentation for available documents

documentation

-

documentation

-

documentation

-

assay

≥98%

assay

-

assay

≥99% (GC)

assay

-

optical activity

[α]21/D −19.7°, c = 4 in H2O

optical activity

-

optical activity

-

optical activity

-

Application

  • Protective effect of thymoquinone on glycation of human myoglobin induced by d-ribose.: This study investigates the protective effects of thymoquinone against d-ribose-induced glycation in human myoglobin, highlighting potential therapeutic applications in preventing protein glycation (Liu et al., 2023).

Disclaimer

For R&D or non-EU Food use. Not for retail sale.

General description

D-(−)-Ribose has been in an in vitro study of the effect of non-enzymatic ribation in modifying bone collagen leading to bone fragility.[1]

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
SHBR2614
SHBS1315
SHBP0617
SHBL9545
SHBL2109

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D-ribose and deoxy-D-ribose induce apoptosis in human quiescent peripheral blood mononuclear cells.
Barbieri D, et al.
Biochemical and Biophysical Research Communications, 201(3), 1109-1116 (1994)
Alice Pavlowsky et al.
Current biology : CB, 28(11), 1783-1793 (2018-05-22)
Memory consolidation is a crucial step for long-term memory (LTM) storage. However, we still lack a clear picture of how memory consolidation is regulated at the neuronal circuit level. Here, we took advantage of the well-described anatomy of the Drosophila
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
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
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®
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