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D-(+)-Arabitol - analytical standard, high purity , CAS No.488-82-4

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Item Number
A111947
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A111947-100mg
100mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$136.90
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Metabolite (5307)

Basic Description

Synonyms MFCD00070503 | Methyl decenoate | A827623 | D-(+)-Arabitol, >=99% | Lyxitol | ARABITE | SR-01000633502-1 | SR-01000633502-3 | (+)-ARABITOL | AS-11643 | D-lyxo-Pentitol | DTXCID2025979 | Oprea1_838482 | BOA443XF1X | D-Lyxitol | Isobutyl cis-2-methyl-2-bute
Specifications & Purity analytical standard
Shipped In Normal
Grade analytical standard

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic oxygen compounds
Class 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
Description 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

Associated Targets(Human)

SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Caenorhabditis elegans (1055 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name (2R,4R)-pentane-1,2,3,4,5-pentol
INCHI InChI=1S/C5H12O5/c6-1-3(8)5(10)4(9)2-7/h3-10H,1-2H2/t3-,4-/m1/s1
InChIKey HEBKCHPVOIAQTA-QWWZWVQMSA-N
Smiles C(C(C(C(CO)O)O)O)O
Isomeric SMILES C([C@H](C([C@@H](CO)O)O)O)O
WGK Germany 3
Molecular Weight 152.15
Beilstein 1720520
Reaxy-Rn 1902256
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1902256&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

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.

3 results found

Lot Number Certificate Type Date Item
G1608016 Certificate of Analysis Jun 16, 2025 A111947
I2104063 Certificate of Analysis Jun 07, 2023 A111947
J2211655 Certificate of Analysis Oct 14, 2022 A111947

Chemical and Physical Properties

Specific Rotation[α] 12° (C=5,Sodium borate(8%))
Melt Point(°C) 97-105°C
Molecular Weight 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

Citations of This Product

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). 
2. Xiaolan Li, Yufei Zhang, Hossain M. Zabed, Junhua Yun, Guoyan Zhang, Mei Zhao, Yuvaraj Ravikumar, Xianghui Qi.  (2023)  High-level production of d-arabitol by Zygosaccharomyces rouxii from glucose: Metabolic engineering and process optimization.  BIORESOURCE TECHNOLOGY,  367  (128251). 
3. Liangqing Zhang, Jiarong Qiu, Xing Tang, Yong Sun, Xianhai Zeng, Lu Lin.  (2021)  Efficient Synthesis of Sugar Alcohols over a Synergistic and Sustainable Catalyst.  CHINESE JOURNAL OF CHEMISTRY,  39  (9): (2467-2476). 
4. Gan Xiaorong, Zhao Huimin, Schirhagl Romana, Quan Xie.  (2019)  Non enzymatic fluorometric determination of glucose by using quenchable g-C3N4 quantum dots.  MICROCHIMICA ACTA,  186  (12): (1-10). 
5. 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,  160  (1078). 
6. 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). 
7. 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,  115  (233). 
8. 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,  295  (139647). 

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