L-(-)-Xylose - Moligand™, 10mM in DMSO , CAS No.609-06-3

CAS: 609-06-3 Cat. No.: L425042 Peso molecular: 150.13 Beilstein Registry Number: 1723080 Número EC: 210-174-1

GRADE & PURITY Moligand™, 10mM in DMSO

Synonyms

L(+)-Xylose | X0021 | HY-78139 | EINECS 210-174-1 | Q27082478 | L-Xyl | L-xylo-pentose | (+)-2-Bromopropanoic acid | NSC 26213 | AC-30677 | L-(-)-XYLOSE | L(-)-Xylose | (2S,3R,4S)-2,3,4,5-tetrahydroxypentanal | A4JW0V2MYA | UNII-A4JW0V2MYA | DTXSID5088334

Storage

Store at -80°C

Shipped In

Dry ice packs + Cold packs

Descripción general

L-(-)-Xylose is one of 2 isoforms of xylose. Xylose is a sugar originally isolated from wood. Xylose is classified as a monosaccharide of the aldopentose type, which means that it contains five carbon atoms and includes a formyl functional group.

Specifications

Sinónimos

L(+)-Xylose | X0021 | HY-78139 | EINECS 210-174-1 | Q27082478 | L-Xyl | L-xylo-pentose | (+)-2-Bromopropanoic acid | NSC 26213 | AC-30677 | L-(-)-XYLOSE | L(-)-Xylose | (2S, 3R, 4S)-2, 3, 4, 5-tetrahydroxypentanal | A4JW0V2MYA | UNII-A4JW0V2MYA | DTXSID5088334

Especificaciones y pureza

Moligand™, 10mM in DMSO

Condiciones de almacenamiento de almacenamiento

Store at -80°C

Enviado en

Dry ice packs + Cold packs

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Grado

Moligand™

Nombres e identificadores

• Sonrisas canónicas: C(C(C(C(C=O)O)O)O)O
• IUPAC Name: (2S,3R,4S)-2,3,4,5-tetrahydroxypentanal
• InChIKey: PYMYPHUHKUWMLA-WISUUJSJSA-N
• INCHI: 1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h1,3-5,7-10H,2H2/t3-,4+,5+/m1/s1
• Isómeros SMILES: C([C@@H]([C@H]([C@@H](C=O)O)O)O)O
• WGK Alemania: 3
• Peso molecular: 150.13
• Beilstein: 1723080
• Reaxy-Rn: 2325068
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2325068&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Monosaccharides
          • Level6 Pentoses

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Monosaccharides
• Direct Parent: Pentoses
• Alternative Parents: Beta-hydroxy aldehydes Alpha-hydroxyaldehydes Secondary alcohols Polyols Short-chain aldehydes Primary alcohols Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic 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
• Descripción: This 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: L-xylose

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive
• Rotación específica [α]: -20 ° (C=10, H2O)
• Punto de fusión (°C): 150°C
• Peso molecular: 150.130 g/mol
• XLogP3: -2.300
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 150.053 Da
• Monoisotopic Mass: 150.053 Da
• Topological Polar Surface Area: 98.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 104.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 3
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Yongchun Huang, Jie Bai, Jinman Shui, Zhanhai Su, Chengzhu Cao, Haiyan Wang, Qiong Wu, Shoude Zhang.  (2025)  Simultaneous determination of the monosaccharide types and their absolute configurations in polysaccharides based on UPLC-MS/MS.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39788268] [10.1016/j.ijbiomac.2025.139647]

2. Hongpeng Zhang, Jie Wang, Jielin Huang, Haonan Duan, Li Dong, Suojiang Zhang.  (2025)  Surface and spatial engineering of ZnAl hollow multi-shelled structures for photothermal synergistic catalysis of glycerol carbonate synthesis.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2025.126197]

3. Jie Bai, Yongchun Huang, Yuling Zhao, Lirong Zhang, Fuli Zhu, Yixizhuoma, Yuxin Weng, Shoude Zhang.  (2026)  Determination of the monosaccharide types and absolute configurations in polysaccharides with (S)-(-)-1-phenylethylamine based on UPLC-MS/MS.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:41638272] [10.1016/j.ijbiomac.2026.150674]