D-(-)-Ribose - ≥99%(HPLC) , CAS No.50-69-1

CAS: 50-69-1 Cat. No.: R104821 Summenformel: C5H10O5 Molekulargewicht: 150.13 Beilstein Registry Number: 1723081 EG-Nummer: 200-059-4
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GRADE & PURITY ≥99%(HPLC)
Synonyms
AC7811 | D-(-)-Ribose, >=99.0% (sum of enantiomers, HPLC) | BCP9000577 | HY-W018772 | AKOS016842327 | SCHEMBL22679 | C5H10O5 | DTXSID101019160 | SUCRALFATE [ORANGE BOOK] | HY-109025A | PYMYPHUHKUWMLA-LMVFSUKVSA-N | Ribose, D- | MFCD06799032 | A828251 | d(
Storage
Store at 2-8°C,Argon charged,Desiccated
Shipped In
Wet ice
★
Size
Deutschland (EU)
USA*
Price
Qty
25g
R104821-25g
—
4 Auf Lager
14,66€
100g
R104821-100g
—
3 Auf Lager
39,83€
250g
R104821-250g
—
2 Auf Lager
86,69€
500g
R104821-500g
—
3 Auf Lager
138,75€
Enter a quantity for the sizes you want to add.
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Why this grade

≥99%(HPLC) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged,Desiccated Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 85 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyme
AC7811 | D-(-)-Ribose, >=99.0% (sum of enantiomers, HPLC) | BCP9000577 | HY-W018772 | AKOS016842327 | SCHEMBL22679 | C5H10O5 | DTXSID101019160 | SUCRALFATE [ORANGE BOOK] | HY-109025A | PYMYPHUHKUWMLA-LMVFSUKVSA-N | Ribose, D- | MFCD06799032 | A828251 | d(
Spezifikationen & Reinheit
≥99%(HPLC)
Biochemische und physiologische Mechanismen
Aldopentose monosaccharide that is phosphorylated into D-ribose 5-phosphate by ribokinase. [α]20/D −19.7°, c = 4 in H 2 O
Storage
Store at 2-8°C,Argon charged,Desiccated
Verschickt in
Wet ice
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Reinheit
≥99%(HPLC)
Namen und Kennungen
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508810417
Kanonisches Lächeln
C(C(C(C(C=O)O)O)O)O
IUPAC Name
(2R,3R,4R)-2,3,4,5-tetrahydroxypentanal
InChIKey
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
Isomere SMILES
C([C@H]([C@H]([C@H](C=O)O)O)O)O
WGK Deutschland
3
RTECS
VJ2275000
Molekulargewicht
150.13
Beilstein
1723081
Reaxy-Rn
2325068
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2325068&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
KlasseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Monosaccharides
Direct ParentPentoses
Alternative Parents Beta-hydroxy aldehydes  Alpha-hydroxyaldehydes  Secondary alcohols  Polyols  Short-chain aldehydes  Primary alcohols  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Pentose monosaccharide - Beta-hydroxy aldehyde - Alpha-hydroxyaldehyde - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Short-chain aldehyde - Primary alcohol - Carbonyl group - Aldehyde - Alcohol - Aliphatic acyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as pentoses. These are monosaccharides in which the carbohydrate moiety contains five carbon atoms.
External Descriptors D-ribose - aldehydo-ribose
3D-Struktur
Interaktives chemisches Strukturmodell





Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

18 results found

Lot NumberCertificate TypeDatumArtikel
G2629105Certificate of AnalysisAug 07, 2026 R104821
J2227650Certificate of AnalysisAug 04, 2026 R104821
J2227637Certificate of AnalysisAug 04, 2026 R104821
J2227630Certificate of AnalysisAug 04, 2026 R104821
J2227587Certificate of AnalysisAug 04, 2026 R104821
A2609469Certificate of AnalysisDec 19, 2025 R104821
A2609471Certificate of AnalysisDec 19, 2025 R104821
L2116442Certificate of AnalysisSep 17, 2025 R104821
G2609136Certificate of AnalysisSep 06, 2025 R104821
I2528465Certificate of AnalysisSep 06, 2025 R104821
F2125310Certificate of AnalysisApr 03, 2025 R104821
A2128082Certificate of AnalysisDec 19, 2024 R104821
F2424436Certificate of AnalysisJun 27, 2024 R104821
J1908153Certificate of AnalysisJul 07, 2023 R104821
H2408047Certificate of AnalysisSep 09, 2022 R104821
J2227620Certificate of AnalysisSep 09, 2022 R104821
D2528056Certificate of AnalysisSep 09, 2022 R104821
F2125313Certificate of AnalysisMay 19, 2021 R104821
Chemische und physikalische Eigenschaften
LöslichkeitSoluble in water. Insoluble in ether.
EmpfindlichkeitHygroscopic.
Spezifische Drehung [α]-21 ° (C=1, H2O)
Schmelzpunkt (°C)88-92°C
Molekulargewicht150.130 g/mol
XLogP3-2.300
Hydrogen Bond Donor Count4
Hydrogen Bond Acceptor Count5
Rotatable Bond Count4
Exact Mass150.053 Da
Monoisotopic Mass150.053 Da
Topological Polar Surface Area98.000 Ų
Heavy Atom Count10
Formal Charge0
Complexity104.000
Isotope Atom Count0
Defined Atom Stereocenter Count3
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQs und Artikel
An Introduction to Research-Grade Carbohydrates: Decoding the “Glycan Language” and a Product-Selection Guide (with Tables 1–3)
Physicochemical Properties of Diphenylamine, Analytical Applications, and a Review of Its DNA Colorimetric Reaction
Functional Systems of Nucleoside Metabolism-Related Enzymes in Drug Response and Disease Biology
Skin Anti-Aging Mechanisms of Carnosine and Decarboxy Carnosine: Active Carbonyl Scavenging, Oxidative-Stress Buffering, and Inhibition of Collagen Glycation Cross-Linking
How Does Collagen Tripeptide Act on the Skin: Stratum Corneum Delivery, Matrix Protection, and Regulation of Collagen Homeostasis
What Determines Collagen Function: From Triple-Helix Formation to Hierarchical Assembly, Crosslink Maturation, and Dynamic Remodeling
Glycosidic Bond Structure and Cleavage Mechanisms—Chemical and Enzymatic Cleavage of O-, N-, S-, and C-Glycosides
Citations of This Product
Lösungsrechner
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