L-(-)-Arabitol - Moligand™, ≥99% , CAS No.7643-75-6

CAS: 7643-75-6 Cat. No.: A115319 Peso molecular: 152.15 Beilstein Registry Number: 1720521 Número EC: 231-582-6

GRADE & PURITY Moligand™, ≥99%

Synonyms

A0518 | HEBKCHPVOIAQTA-IMJSIDKUSA-N | MFCD00064290 | s6045 | A-8280 | C66BD5E8-5966-4CB8-8AD1-4DBC52950BBD | N-(9-FLUORENYLMETHYLOXYCARBONYL)-8-AMINO-OCTANOIC ACID | 1,2,3,4,5-Pentahydroxypentane | WURCS=2.0/1,1,0/[h221h]/1/ | A827622 | (2S,4S)-Pentane-1,

Storage

Room temperature,Argon charged

Shipped In

Normal

Descripción general

L-Arabinitol is a potential biomarker for the comsuption of the food products such as sweet potato, deerberry, moth bean, and is also associated with Alzheimer's disease and ribose-5-phosphate isomerase deficiency.

Specifications

Sinónimos

A0518 | HEBKCHPVOIAQTA-IMJSIDKUSA-N | MFCD00064290 | s6045 | A-8280 | C66BD5E8-5966-4CB8-8AD1-4DBC52950BBD | N-(9-FLUORENYLMETHYLOXYCARBONYL)-8-AMINO-OCTANOIC ACID | 1, 2, 3, 4, 5-Pentahydroxypentane | WURCS=2.0/1, 1, 0/[h221h]/1/ | A827622 | (2S, 4S)-Pentane-1,

Especificaciones y pureza

Moligand™, ≥99%

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged

Enviado en

Normal

Grado

Moligand™

Pureza

≥99%

Nombres e identificadores

• Pubchem Sid: 488189741
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488189741
• Sonrisas canónicas: C(C(C(C(CO)O)O)O)O
• IUPAC Name: (2S,4S)-pentane-1,2,3,4,5-pentol
• InChIKey: HEBKCHPVOIAQTA-IMJSIDKUSA-N
• INCHI: 1S/C5H12O5/c6-1-3(8)5(10)4(9)2-7/h3-10H,1-2H2/t3-,4-/m0/s1
• Isómeros SMILES: C([C@@H](C([C@H](CO)O)O)O)O
• WGK Alemania: 3
• Peso molecular: 152.15
• Beilstein: 1720521
• Reaxy-Rn: 1902256
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1902256&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Clase Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Sugar alcohols
• Alternative Parents: Monosaccharides Secondary alcohols Polyols Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Sugar alcohol - Monosaccharide - Secondary alcohol - Polyol - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as sugar alcohols. These are hydrogenated forms of carbohydrate in which the carbonyl group (aldehyde or ketone, reducing sugar) has been reduced to a primary or secondary hydroxyl group.
• External Descriptors: arabinitol

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

• Solubilidad: Soluble in water
• Sensibilidad: Moisture sensitive.
• Rotación específica [α]: -12 ° (C=5, 8% Sodium borate)
• Punto de fusión (°C): 101-104°C
• Peso molecular: 152.150 g/mol
• XLogP3: -2.500
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 152.068 Da
• Monoisotopic Mass: 152.068 Da
• Topological Polar Surface Area: 101.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 76.100
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• 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. Wenjie Li, Shenghui Hao, Hengyang Li, Qi An, Lina Yang, Bing Guo, Zijing Xue, Yongli Liu, Long Guo, Yuguang Zheng, Dan Zhang.  (2023)  Exploring Antioxidant and α-Glucosidase Inhibitory Activities in Mulberry Leaves (Morus alba L.) across Growth Stages: A Comprehensive Metabolomic Analysis with Chemometrics.  MOLECULES,  29  (1): (171).  [PMID:38202754] [10.3390/molecules29010171]

2. Xue-Feng Shao, Chao Wang, Yong-Jian Yang, Biao Feng, Zi-Qin Zhu, Wu-Jun Wang, Yi Zeng, Li-Wu Fan.  (2018)  Screening of sugar alcohols and their binary eutectic mixtures as phase change materials for low-to-medium temperature latent heat storage. (Ⅰ): Non-isothermal melting and crystallization behaviors.  ENERGY,      [PMID:] [10.1016/j.energy.2018.07.081]

3. Feng Sha, Yucong Zheng, Jiao Chen, Kequan Chen, Fei Cao, Ming Yan, Pingkai Ouyang.  (2018)  D-Tagatose manufacture through bio-oxidation of galactitol derived from waste xylose mother liquor.  GREEN CHEMISTRY,  20  (10): (2382-2391).  [PMID:] [10.1039/C8GC00091C]

4. Rui Jia, Keyan Sun, Rongchun Li, Youyou Zhang, Wenxia Wang, Heng Yin, Dawei Fang, Quan Shi, Zhicheng Tan.  (2017)  Heat capacities of some sugar alcohols as phase change materials for thermal energy storage applications.  JOURNAL OF CHEMICAL THERMODYNAMICS,      [PMID:] [10.1016/j.jct.2017.08.004]