D-(+)-Xylose - Moligand™, ≥99% , CAS No.58-86-6

CAS: 58-86-6 Cat. No.: X101012 Fórmula: C5H10O5 Peso molecular: 150.13 Beilstein Registry Number: 1562108 Número CE: 200-400-7 PubChem CID: 644160
Disponível para encomenda
GRAU & PUREZA Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥99%
Synonyms
CHEBI:15936 | XYLOSE [WHO-DD] | X-7910 | XYLOSE [HSDB] | HY-N0537 | D-xylo-pentose | Q27077130 | ( inverted exclamation markA)-Xylos | X-7950 | CCG-231055 | XYLOSE [MI] | C74347 | W-202083 | D-Xylose,(S) | Xylose, D- | DL-Xylose | XYLOSE [VANDF] | (+-)-Xy
Storage
Room temperature,Argon charged,Desiccated
Shipped In
Normal
★
Tamanho
Alemanha (EU)
USA*
Preço
Qtd
25g
X101012-25g
—
2 Em stock
12,06€
100g
X101012-100g
—
3 Em stock
30,28€
500g
X101012-500g
1 Em stock
2 Em stock
95,36€
Enter a quantity for the sizes you want to add.
🧪
Por que este grau

Moligand™, ≥99% Moligand™ para fluxos de trabalho cromatográficos e analíticos sensíveis que exigem interferência mínima da linha de base.

🌡

Armazenamento e envio

Room temperature,Argon charged,Desiccated Envio Normal. Consulte o COA específico do lote para obter as especificações exatas.

📋

Documentos de qualidade

SDS, COA, ficha técnica e folha de especificações disponíveis para download. COA específico do lote acessível por meio de pesquisa por número de lote.

📚

Comprovação documental

Citado em 43 publicações revisadas por pares nas áreas de cromatografia, síntese orgânica e reações de acoplamento cruzado.

Visão geral

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.

Especificações

Sinónimos
CHEBI:15936 | XYLOSE [WHO-DD] | X-7910 | XYLOSE [HSDB] | HY-N0537 | D-xylo-pentose | Q27077130 | ( inverted exclamation markA)-Xylos | X-7950 | CCG-231055 | XYLOSE [MI] | C74347 | W-202083 | D-Xylose,(S) | Xylose, D- | DL-Xylose | XYLOSE [VANDF] | (+-)-Xy
Especificações e pureza
Moligand™, ≥99%
Condições de armazenamento de armazenamento
Room temperature,Argon charged,Desiccated
Enviado em
Normal
Grau
Moligand™
Pureza
≥99%
Nomes e identificadores
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/508810435
SMILES isoméricas
C([C@H]([C@@H]([C@H](C=O)O)O)O)O
WGK Alemanha
2
PubChem CID
644160
Peso molecular
150.13
Beilstein
1562108

Documentação

📋 Ficha de dados de segurança (FDS)

Documento abrangente sobre perigos, manuseamento, armazenamento e conformidade regulamentar.

<<<<<<< HEAD Baixar SDS → ======= Baixar SDS → >>>>>>> release248-p3

✅ Certificado de análise (COA)

Dados de qualidade específicos do lote. Introduza o número de lote para obter o COA exato.

Consultar COA →

📊 Ficha técnica

Resumo de referência rápida das especificações e aplicações do produto.

Ver ficha técnica →

🔬 Folha de especificações

Atributos de qualidade completos e critérios de aceitação para este grau.

Ver folha de especificações →

Dados avançados

Alvos associados (não 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 ação
Certificados(CoA,COO,BSE/TSE e Mapa de Análise)
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.

43 results found

Lot NumberCertificate TypeDataItem
I2621204I2621204Certificate of AnalysisSep 30, 2026 X101012
I2621203I2621203Certificate of AnalysisSep 30, 2026 X101012
I2621181I2621181Certificate of AnalysisSep 28, 2026 X101012
E2611105E2611105Certificate of AnalysisMay 22, 2026 X101012
E2609141E2609141Certificate of AnalysisMay 20, 2026 X101012
E2611079E2611079Certificate of AnalysisMay 19, 2026 X101012
E2611117E2611117Certificate of AnalysisMay 18, 2026 X101012
F2214756F2214756Certificate of AnalysisMar 18, 2026 X101012
K2528354K2528354Certificate of AnalysisNov 18, 2025 X101012
E2613042E2613042Certificate of AnalysisNov 18, 2025 X101012
D2613083D2613083Certificate of AnalysisNov 18, 2025 X101012
K2528347K2528347Certificate of AnalysisNov 18, 2025 X101012
K2528330K2528330Certificate of AnalysisNov 18, 2025 X101012
E2509370E2509370Certificate of AnalysisApr 25, 2025 X101012
E2509371E2509371Certificate of AnalysisApr 25, 2025 X101012
E2509372E2509372Certificate of AnalysisApr 25, 2025 X101012
E2509373E2509373Certificate of AnalysisApr 25, 2025 X101012
J2509101J2509101Certificate of AnalysisApr 25, 2025 X101012
K2505051K2505051Certificate of AnalysisApr 25, 2025 X101012
G2409322G2409322Certificate of AnalysisJul 03, 2024 X101012
G2409318G2409318Certificate of AnalysisJul 03, 2024 X101012
G2409319G2409319Certificate of AnalysisJul 03, 2024 X101012
G2409320G2409320Certificate of AnalysisJul 03, 2024 X101012
G2409321G2409321Certificate of AnalysisJul 03, 2024 X101012
E2507511E2507511Certificate of AnalysisJun 26, 2024 X101012
E2507510E2507510Certificate of AnalysisJun 26, 2024 X101012
A2506180A2506180Certificate of AnalysisJun 26, 2024 X101012
A2403235A2403235Certificate of AnalysisDec 20, 2023 X101012
A2403236A2403236Certificate of AnalysisDec 20, 2023 X101012
A2403234A2403234Certificate of AnalysisDec 20, 2023 X101012
E2325757E2325757Certificate of AnalysisMay 06, 2023 X101012
E2325567E2325567Certificate of AnalysisMay 06, 2023 X101012
E2325518E2325518Certificate of AnalysisMay 06, 2023 X101012
E2325516E2325516Certificate of AnalysisMay 06, 2023 X101012
L2304065L2304065Certificate of AnalysisMay 06, 2023 X101012
F2214569F2214569Certificate of AnalysisMay 30, 2022 X101012
F2214557F2214557Certificate of AnalysisMay 30, 2022 X101012
D2328045D2328045Certificate of AnalysisMay 30, 2022 X101012
B2218585B2218585Certificate of AnalysisFeb 24, 2022 X101012
B2218575B2218575Certificate of AnalysisFeb 24, 2022 X101012
B2218574B2218574Certificate of AnalysisFeb 24, 2022 X101012
B2218467B2218467Certificate of AnalysisFeb 24, 2022 X101012
I2228179I2228179Certificate of AnalysisFeb 09, 2022 X101012
Propriedades químicas e físicas
SolubilidadeSoluble in 1M Water: 20℃
SensibilidadeHygroscopic
Rotação específica [α]20 ° (C=10, H2O)
Ponto de fusão (°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
FAQs e artigos
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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
Carbohydrate Oxidases: Catalytic Mechanisms and Bioanalytical Applications
Citations of This Product
Calculadoras de soluções
Revisões

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