D-(+)-Xylose - Moligand™, ≥98% , CAS No.58-86-6

CAS: 58-86-6 Cat. No.: X101009 Fórmula: C5H10O5 Peso molecular: 150.13 Beilstein Registry Number: 1562108 Número EC: 200-400-7 PubChem CID: 644160
Disponible para pedir
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
Xylose | (+)-Xylose | Wood sugar | D-(+)-Xylose
Storage
Room temperature,Argon charged,Desiccated
Shipped In
Normal
★
Size
USA
Alemania (EU)*
Price
Qty
25g
X101009-25g
3 Disponible
—
9,90US$
100g
X101009-100g
1 Disponible
—

15,90US$

29,90US$
Guardar 14,00 US$ (46.82%)
500g
X101009-500g
Disponible ≥10
1 Disponible

53,90US$

89,90US$
Guardar 36,00 US$ (40.04%)
Enter a quantity for the sizes you want to add.
🧪
Why this grade

Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature,Argon charged,Desiccated Ships Normal 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 43 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

D-(+)-Xylose is classified as a monosaccharide of the aldopentose type, which means that it contains five carbon atoms and includes a formyl functional group.
An aldopentose monosaccharide.

Specifications

Sinónimos
Xylose | (+)-Xylose | Wood sugar | D-(+)-Xylose
Especificaciones y pureza
Moligand™, ≥98%
Mecanismos bioquímicos y fisiológicos
A method for estimating the amount of xylose in urine after oral administration can be used to diagnose carbohydrate absorption and non-pancreatic Molecular Absorption Disorders. Xylose plays an important role in the bioconversion of plant biomass into fu
Condiciones de almacenamiento de almacenamiento
Room temperature,Argon charged,Desiccated
Enviado en
Normal
Grado
Moligand™
Pureza
≥98%
Nombres e identificadores
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508810437
Isómeros SMILES
C([C@H]([C@@H]([C@H](C=O)O)O)O)O
WGK Alemania
2
PubChem CID
644160
Peso molecular
150.13
Beilstein
1562108

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

Objetivos asociados (no humanos)
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

54 results found

Lot NumberCertificate TypeFechaArticulo
H2624430Certificate of AnalysisAug 14, 2026 X101009
H2624414Certificate of AnalysisAug 14, 2026 X101009
H2624413Certificate of AnalysisAug 14, 2026 X101009
H2624412Certificate of AnalysisAug 14, 2026 X101009
H2624411Certificate of AnalysisAug 14, 2026 X101009
H2615056Certificate of AnalysisFeb 11, 2026 X101009
C2603637Certificate of AnalysisFeb 11, 2026 X101009
C2603638Certificate of AnalysisFeb 11, 2026 X101009
C2603639Certificate of AnalysisFeb 11, 2026 X101009
C2603640Certificate of AnalysisFeb 11, 2026 X101009
C2603641Certificate of AnalysisFeb 11, 2026 X101009
H2506591Certificate of AnalysisJun 10, 2025 X101009
H2506594Certificate of AnalysisJun 10, 2025 X101009
H2506598Certificate of AnalysisJun 10, 2025 X101009
H2506599Certificate of AnalysisJun 10, 2025 X101009
L2416558Certificate of AnalysisDec 17, 2024 X101009
L2416564Certificate of AnalysisDec 17, 2024 X101009
L2426558Certificate of AnalysisDec 17, 2024 X101009
L2426559Certificate of AnalysisDec 17, 2024 X101009
L2426560Certificate of AnalysisDec 17, 2024 X101009
I2414421Certificate of AnalysisAug 26, 2024 X101009
I2414420Certificate of AnalysisAug 26, 2024 X101009
I2414419Certificate of AnalysisAug 26, 2024 X101009
I2414413Certificate of AnalysisAug 26, 2024 X101009
I2414412Certificate of AnalysisAug 26, 2024 X101009
G2426202Certificate of AnalysisJun 14, 2024 X101009
G2426203Certificate of AnalysisJun 14, 2024 X101009
G2426204Certificate of AnalysisJun 14, 2024 X101009
G2426205Certificate of AnalysisJun 14, 2024 X101009
F2420244Certificate of AnalysisJun 07, 2024 X101009
F2420245Certificate of AnalysisJun 07, 2024 X101009
F2420246Certificate of AnalysisJun 07, 2024 X101009
C2425611Certificate of AnalysisMar 11, 2024 X101009
C2425591Certificate of AnalysisMar 11, 2024 X101009
C2425590Certificate of AnalysisMar 11, 2024 X101009
C2425589Certificate of AnalysisMar 11, 2024 X101009
E2324647Certificate of AnalysisMay 04, 2023 X101009
E2324625Certificate of AnalysisMay 04, 2023 X101009
E2324632Certificate of AnalysisMay 04, 2023 X101009
E2324641Certificate of AnalysisMay 04, 2023 X101009
E2324644Certificate of AnalysisMay 04, 2023 X101009
B23211006Certificate of AnalysisNov 11, 2022 X101009
B2321994Certificate of AnalysisNov 11, 2022 X101009
B23211001Certificate of AnalysisNov 11, 2022 X101009
B23211000Certificate of AnalysisNov 11, 2022 X101009
L2209415Certificate of AnalysisNov 10, 2022 X101009
L2209416Certificate of AnalysisNov 10, 2022 X101009
L2209417Certificate of AnalysisNov 10, 2022 X101009
L2209913Certificate of AnalysisNov 10, 2022 X101009
I2212457Certificate of AnalysisAug 01, 2022 X101009
I2212456Certificate of AnalysisAug 01, 2022 X101009
I2212455Certificate of AnalysisAug 01, 2022 X101009
I2212454Certificate of AnalysisAug 01, 2022 X101009
I2212453Certificate of AnalysisAug 01, 2022 X101009
Propiedades químicas y físicas
SolubilidadSoluble in 1M Water: 20℃
SensibilidadHygroscopic
Rotación específica [α]20 ° (C=10, H2O)
Punto de fusión (°C)154-158°C
Peso molecular150.130 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
Preguntas frecuentes y artículos
An Introduction to Research-Grade Carbohydrates: Decoding the “Glycan Language” and a Product-Selection Guide (with Tables 1–3)
Isomerases: Overview and Recommended Application Technical Guide
Hemicellulases: A Review of Substrate Specificity, Catalytic Systems, and Research and Industrial Applications
Physicochemical Properties of Diphenylamine, Analytical Applications, and a Review of Its DNA Colorimetric Reaction
Pyran and the “Pyran Family” Research Selection Guide: Key Structural Points, a Classification Roadmap, and Experimental Selection Navigation
Formation of Nucleotide-Sugar Precursors and Regulatory Mechanisms in Plant Growth and Development
Synergy of Enzymes in Plant Cell Wall Hemicellulose Degradation: Xylanase, β-Xylosidase, and Debranching Enzymes
Comparison of Reducing Sugar Detection Methods: Selection of Fehling’s Reagent, Benedict’s Method, DNS Method, and HPLC
Moisturizing Mechanisms of Tremella fuciformis Polysaccharides: From Polysaccharide Structure and Hydration Rheology to Dynamic Film Formation on the Skin Surface
Skin Mechanism of Action of Pro-Xylane: From C-Xyloside Priming and CS/DS Chain Remodeling to the Dermal–Epidermal Junction
Sources, Host-Regulatory Mechanisms, and Tumor-Immune Effects of Gut Microbiota-Derived Metabolites
Effect of Glycosylation on the Hydrophilic–Lipophilic Partitioning and Solubility Behavior of Natural Products—Quercetin, Isoquercitrin, and Rutin as Examples
Glycosidic Bond Structure and Cleavage Mechanisms—Chemical and Enzymatic Cleavage of O-, N-, S-, and C-Glycosides
Citations of This Product
Calculadoras de soluciones
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