D-Xylulose - ≥98%(HPLC), 0.5M in Water , CAS No.551-84-8

CAS: 551-84-8 Cat. No.: S134209 Formula: C₅H₁₀O₅ Peso molecolare: 150.13

GRADE & PURITY ≥98%(HPLC), 0.5M in Water

Synonyms

ZAQJHHRNXZUBTE-WUJLRWPWSA-N | AKOS027320628 | D-xylulose | HY-W010256 | xylulose | CHEBI:17140 | Threo-2-pentulose(9ci) | rel-(3S,4R)-1,3,4,5-Tetrahydroxypentan-2-one | THREO-2-PENTULOSE, DL- | XYLOKETOSE | threo-2-Pentulose | DL-Threo-2-Pentulose | D-thr

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Panoramica

D-xylulose is a precursor of the pentiol D-arabitol.

Specifications

Sinonimi

ZAQJHHRNXZUBTE-WUJLRWPWSA-N | AKOS027320628 | D-xylulose | HY-W010256 | xylulose | CHEBI:17140 | Threo-2-pentulose(9ci) | rel-(3S,4R)-1,3,4,5-Tetrahydroxypentan-2-one | THREO-2-PENTULOSE, DL- | XYLOKETOSE | threo-2-Pentulose | DL-Threo-2-Pentulose | D-thr

Specifiche e purezza

≥98%(HPLC), 0.5M in Water

Meccanismi biochimici e fisiologici

D-xylulose is a monosaccharide, converted from xylitol in the glucuronate pathway.

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥98%(HPLC)

Nomi e identificatori

• Pubchem Sid: 528764025
• Sorrisi canonici: C(C(C(C(=O)CO)O)O)O
• IUPAC Name: (3S,4R)-1,3,4,5-tetrahydroxypentan-2-one
• InChIKey: ZAQJHHRNXZUBTE-WUJLRWPWSA-N
• INCHI: 1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h3,5-8,10H,1-2H2/t3-,5+/m1/s1
• Isomeri SMILES: C([C@H]([C@@H](C(=O)CO)O)O)O
• Peso molecolare: 150.13
• Reaxy-Rn: 2041242
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2041242&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Monosaccharides
• Direct Parent: Pentoses
• Alternative Parents: Beta-hydroxy ketones Acyloins Alpha-hydroxy ketones Secondary alcohols Polyols Primary alcohols Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Pentose monosaccharide - Beta-hydroxy ketone - Acyloin - Alpha-hydroxy ketone - Secondary alcohol - Ketone - Polyol - Organic oxide - Hydrocarbon derivative - Primary alcohol - Carbonyl group - Alcohol - Aliphatic acyclic compound
• Descrizione: 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: xylulose

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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Peso molecolare: 150.130 g/mol
• XLogP3: -2.600
• 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: 113.000
• 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

Riferimenti

1. Hengtao Tang, Zhi Chen, Yu Shao, Xin Ju, Liangzhi Li.  (2022)  Development of an enzymatic cascade to systematically utilize lignocellulosic monosaccharide.  JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE,  103  (4): (1974-1980).  [PMID:36448581] [10.1002/jsfa.12364]

2. Hengtao Tang, Zheng Zhou, Zhi Chen, Xin Ju, Liangzhi Li.  (2022)  Development of a sugar isomerase cascade to convert D-xylose to rare sugars.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2022.112672]

3. Muhammad Sajid, Muhammad Rizwan Dilshad, Muhammad Saif Ur Rehman, Dehua Liu, Xuebing Zhao.  (2021)  Catalytic Conversion of Xylose to Furfural by p-Toluenesulfonic Acid (pTSA) and Chlorides: Process Optimization and Kinetic Modeling.  MOLECULES,  26  (8): (2208).  [PMID:33921241] [10.3390/molecules26082208]

4. Yuan Zhao, Hao Xu, Kaifeng Lu, Yang Qu, Lingjun Zhu, Shurong Wang.  (2019)  Dehydration of xylose to furfural in butanone catalyzed by Brønsted-Lewis acidic ionic liquids.  Energy Science & Engineering,  7  (5): (2237-2246).  [PMID:] [10.1002/ese3.444]

5. Si Long, Zhi Chen, Xin Ju, Liangzhi Li.  (2025)  Application of microbial glucose isomerases in a cascade to convert xylose to rare sugars.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2025.114862]

6. Yuqiu Wu, Fanjin Meng, Jiaolong Fu, Yuyang Zhou, Huan Fan, Xin Ju, Liangzhi Li.  (2024)  PDA/SiO2 microspheres immobilize dual enzymes to increase temperature tolerance and catalyze the production of D-ribulose and D-xylulose from D-xylose.  Molecular Catalysis,      [PMID:] [10.1016/j.mcat.2024.113900]

7. Zou Zhufan, Yu Zhenjie, Guan Weixiang, Liu Yanfang, Yao Yumin, Han Yang, Li Guangyi, Wang Aiqin, Cong Yu, Liang Xinmiao, Zhang Tao, Li Ning.  (2024)  Selective production of methylindan and tetralin with xylose or hemicellulose.  Nature Communications,  15  (1): (1-12).  [PMID:38697973] [10.1038/s41467-024-48101-x]

8. Wei Zong, Zijing Liu, Haiyan Lan, Jianwei Yang, Yuxuan Xia, Zhongsheng Xu, Li Mai, Jie Wang, Yixi Bao.  (2025)  Structural characterization of a pectin polysaccharide from Phyllanthus emblica fruits and their antitumor effect via macrophage polarization in the cold immune microenvironment.  CARBOHYDRATE POLYMERS,      [PMID:40973298] [10.1016/j.carbpol.2025.124287]

9. Louis Patrick Conway, Fang Fang Liu, Qian Li, Josef Voglmeir.  (2017)  The Shewanella woodyi galactokinase pool phosphorylates glucose at the 6-position.  CARBOHYDRATE RESEARCH,      [PMID:29169041] [10.1016/j.carres.2017.10.018]

10. Zhanjun Li, Yunwei Liu, Mingru Kong, Yibin Xu, Kunlun Wang, Ke Ma, Qingfen Zhang.  (2025)  Production of furfural from regenerated hemicellulose via solid acid catalysis, ultrasonic pretreatment and microwave irradiation.  TALANTA,      [PMID:40318491] [10.1016/j.talanta.2025.128214]

11. Haihui Ren, Wen Xiao, Jiameng Han, Qiaorong Liu, Zunjian Zhang, Yuan Tian.  (2025)  An innovative method for simultaneous separation and determination of monosaccharide and sugar alcohol isomers associated with glycometabolism in beagle plasma using gas chromatography-mass spectrometry.  ANALYTICA CHIMICA ACTA,      [PMID:40670002] [10.1016/j.aca.2025.344326]

12. Wang Zhao, Jiansong Chen, Haishun Du, Zhiqiang Pang, Weiqi Wei, Xuejun Pan.  (2026)  Efficient conversion of biomass-derived xylose into furfural over boron phosphate solid acid in LiBr⋅3H2O/DCM biphasic system.  CARBOHYDRATE RESEARCH,      [PMID:41518913] [10.1016/j.carres.2026.109812]

13. Yuqi Peng, Si Long, Yuqing Zhong, JiaJia Chen, Zhi Chen, Xin Ju, Liangzhi Li.  (2026)  Exploration of glucose isomerases in enzymatic cascades converting glucose and xylose synergistically.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:41865939] [10.1016/j.ijbiomac.2026.151545]