Xanthosine Dihydrate - ≥99% , CAS No.5968-90-1

CAS: 5968-90-1 Cat. No.: X137287 Peso molecular: 320.26 Número EC: 205-679-9 PubChem CID: 18530347
Disponible para pedir
GRADE & PURITY ≥99%
Synonyms
Xanthosine, dihydrate | SCHEMBL5352232 | 9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purine-2,6-dione;dihydrate | 9-beta-D-Ribofuranosyl xanthine dihydrate | ZCCPXSQIUORWCO-LGVAUZIVSA-N | HY-W013803 | DTXSID40975081 | MFCD00149347
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
X137287-1g
3
49,90US$
5g
X137287-5g
1
169,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

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

🌡

Storage & shipping

Store at 2-8°C 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 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Xanthosine comprises xanthine ring. It is derived from a purine metabolite and is a caffeine biosynthesis intermediate.
Xanthosine plays a key role in purine metabolism.High levels of xanthosine excretion is observed in breast cancer.


Application:

Xanthosine dihydrate has been used as a test compound in one dimensional liquid chromatography analysis (1D-LC ).

Specifications

Sinónimos
Xanthosine, dihydrate | SCHEMBL5352232 | 9-[(2R, 3R, 4S, 5R)-3, 4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purine-2, 6-dione;dihydrate | 9-beta-D-Ribofuranosyl xanthine dihydrate | ZCCPXSQIUORWCO-LGVAUZIVSA-N | HY-W013803 | DTXSID40975081 | MFCD00149347
Especificaciones y pureza
≥99%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥99%
Nombres e identificadores
Pubchem Sid504768730
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504768730
Sonrisas canónicasC1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=O)NC2=O.O.O
IUPAC Name9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purine-2,6-dione;dihydrate
InChIKeyZCCPXSQIUORWCO-LGVAUZIVSA-N
INCHI1S/C10H12N4O6.2H2O/c15-1-3-5(16)6(17)9(20-3)14-2-11-4-7(14)12-10(19)13-8(4)18;;/h2-3,5-6,9,15-17H,1H2,(H2,12,13,18,19);2*1H2/t3-,5-,6-,9-;;/m1../s1
Isómeros SMILES C1=NC2=C(N1[C@H]3[C@@H]([C@@H]([C@H](O3)CO)O)O)NC(=O)NC2=O.O.O
PubChem CID 18530347
Peso molecular 320.26

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
SuperclassNucleosides, nucleotides, and analogues
ClasePurine nucleosides
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentPurine nucleosides
Alternative Parents Xanthines  Glycosylamines  6-oxopurines  Pentoses  Alkaloids and derivatives  Pyrimidones  N-substituted imidazoles  Vinylogous amides  Oxolanes  Heteroaromatic compounds  Ureas  Secondary alcohols  Lactams  Oxacyclic compounds  Azacyclic compounds  Hydrocarbon derivatives  Organic oxides  Organonitrogen compounds  Primary alcohols  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Purine nucleoside - Glycosyl compound - N-glycosyl compound - Xanthine - 6-oxopurine - Pentose monosaccharide - Purinone - Purine - Imidazopyrimidine - Alkaloid or derivatives - Pyrimidone - Monosaccharide - N-substituted imidazole - Pyrimidine - Oxolane - Vinylogous amide - Imidazole - Heteroaromatic compound - Azole - Lactam - Urea - Secondary alcohol - Organoheterocyclic compound - Azacycle - Oxacycle - Organonitrogen compound - Alcohol - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organooxygen compound - Primary alcohol - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





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.

11 results found

Lot NumberCertificate TypeFechaArticulo
F2601440Certificate of AnalysisMay 26, 2026 X137287
F2601441Certificate of AnalysisMay 26, 2026 X137287
E2627501Certificate of AnalysisMay 21, 2026 X137287
C2426388Certificate of AnalysisJan 19, 2026 X137287
F2520616Certificate of AnalysisJun 17, 2025 X137287
F2520617Certificate of AnalysisJun 17, 2025 X137287
K2419654Certificate of AnalysisOct 30, 2024 X137287
K2419655Certificate of AnalysisOct 30, 2024 X137287
I2109442Certificate of AnalysisJun 15, 2023 X137287
I2109441Certificate of AnalysisJun 15, 2023 X137287
F1516066Certificate of AnalysisJan 24, 2023 X137287

Show more ⌵

Propiedades químicas y físicas
Peso molecular320.260 g/mol
XLogP3
Hydrogen Bond Donor Count7
Hydrogen Bond Acceptor Count9
Rotatable Bond Count2
Exact Mass320.097 Da
Monoisotopic Mass320.097 Da
Topological Polar Surface Area148.000 Ų
Heavy Atom Count22
Formal Charge0
Complexity434.000
Isotope Atom Count0
Defined Atom Stereocenter Count4
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
Citations of This Product
Referencias
1. Yun Chen, Hui Chen, Ganggang Shi, Min Yang, Fuchun Zheng, Zhijie Zheng, Shuyao Zhang, Shilong Zhong.  (2019)  Ultra-performance liquid chromatography-tandem mass spectrometry quantitative profiling of tryptophan metabolites in human plasma and its application to clinical study.  JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES,      [PMID:31586884] [10.1016/j.jchromb.2019.121745]
2. Yangping Wen, Juan Chang, Lanjiao Xu, Xiaoning Liao, Ling Bai, Yingdong Lan, Mingfang Li.  (2017)  Simultaneous analysis of uric acid, xanthine and hypoxanthine using voltammetric sensor based on nanocomposite of palygorskite and nitrogen doped graphene.  JOURNAL OF ELECTROANALYTICAL CHEMISTRY,      [PMID:] [10.1016/j.jelechem.2017.09.053]
3. Yong-Hao Ma, Jingjing Yang, Bolin Li, Yao-Wen Jiang, Xiaolin Lu, Zhan Chen.  (2016)  Biodegradable and injectable polymer–liposome hydrogel: a promising cell carrier.  Polymer Chemistry,  (11): (2037-2044).  [PMID:] [10.1039/C5PY01773D]
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