2,3-Dihydroxypropanal - Moligand™,≥90% , CAS No.56-82-6

CAS: 56-82-6 Cat. No.: D589509 Peso molecular: 90.08

GRADE & PURITY Moligand™, ≥90%

Synonyms

delta-(+)-Glyceraldehyde | HY-128748 | DL-Glyceraldehyde, >=90% (GC) | GLYCERALDEHYDE, (+/-)- | SB44379 | D-(+)-Glyceraldehyde; (R)-2,3-Dihydroxy-propanal | gliceraldehido | Glycerinaldehyd | NSC67934 | NSC-67934 | Q423211 | STL453543 | Propanal, 2,3-dihy

Storage

Store at 2-8°C,Protected from light,Argon charged

Shipped In

Wet ice

Descripción general

Product description：

Glyceraldehyde is a simple monosaccharide. According to the number of carbon atoms and the type of carbonyl group, glyceraldehyde is a triose. It is a colorless sweet compound. 

Application：

Dl-glyceraldehyde has been used for: 

As a modifier for preparing crystalline solutions 

As a substrate for measuring aldose reductase activity 

The specific activity of GAPDH (glyceraldehyde-3-phosphate dehydrogenase) was determined in the preparation of d/ L-glyceraldehyde raw materials

Explanation：

Dl-glyceraldehyde is the substrate of aldose reductase.  

Specifications

Sinónimos

delta-(+)-Glyceraldehyde | HY-128748 | DL-Glyceraldehyde, >=90% (GC) | GLYCERALDEHYDE, (+/-)- | SB44379 | D-(+)-Glyceraldehyde; (R)-2, 3-Dihydroxy-propanal | gliceraldehido | Glycerinaldehyd | NSC67934 | NSC-67934 | Q423211 | STL453543 | Propanal, 2, 3-dihy

Especificaciones y pureza

Moligand™, ≥90%

Mecanismos bioquímicos y fisiológicos

Glyceraldehyde is a potent crosslinking agent and is considered non-toxic. It is an intermediate in many metabolic pathways, such as the glycolysis and pentose phosphate pathways.

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C, Protected from light, Argon charged

Enviado en

Wet ice

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

Grado

Moligand™

Pureza

≥90%

Nombres e identificadores

• Sonrisas canónicas: C(C(C=O)O)O
• IUPAC Name: 2,3-dihydroxypropanal
• InChIKey: MNQZXJOMYWMBOU-UHFFFAOYSA-N
• INCHI: 1S/C3H6O3/c4-1-3(6)2-5/h1,3,5-6H,2H2
• Isómeros SMILES: C(C(C=O)O)O
• Peso molecular: 90.08
• Reaxy-Rn: 635844
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=635844&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: Monosaccharides
• Alternative Parents: Alpha-hydroxyaldehydes Secondary alcohols 1,2-diols Short-chain aldehydes Primary alcohols Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Monosaccharide - Alpha-hydroxyaldehyde - Secondary alcohol - 1,2-diol - 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 monosaccharides. These are compounds containing one carbohydrate unit not glycosidically linked to another such unit, and no set of two or more glycosidically linked carbohydrate units. Monosaccharides have the general formula CnH2nOn.
• External Descriptors: DL-glyceraldehyde

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

Objetivos asociados (humanos)

AKR1B1 Tclin Aldose reductase (1 Activities)

Discover Target: AKR1B1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

AKR1B1 Tclin Aldose reductase (1404 Activities)

Discover Target: AKR1B1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Objetivos asociados (no humanos)

Catharanthus roseus (29 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Light sensitive；Air sensitive
• Punto de fusión (°C): 145°C
• Peso molecular: 90.080 g/mol
• XLogP3: -1.600
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 90.0317 Da
• Monoisotopic Mass: 90.0317 Da
• Topological Polar Surface Area: 57.500 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 43.300
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• 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. Ruite Lai, Qidong Hou, Guanjie Yu, Chao Xie, Hengli Qian, Tianliang Xia, Xinyu Bai, Yao Tang, Mian Laiq Ur Rehman, Meiting Ju.  (2023)  Incorporation of tin into zirconium phosphate to boost efficient conversion of trioses to lactic acid.  CATALYSIS COMMUNICATIONS,      [PMID:] [10.1016/j.catcom.2023.106803]

2. Jinsheng Huang, Huiling Huang, Yiyao Wang, Bin Xu, Minzhao Lin, Shisong Han, Yuanyuan Yuan, Yong Wang, Xintao Shuai.  (2023)  Retinol-binding protein-hijacking nanopolyplex delivering siRNA to cytoplasm of hepatic stellate cell for liver fibrosis alleviation.  BIOMATERIALS,      [PMID:37167895] [10.1016/j.biomaterials.2023.122134]

3. Gui-Hua Wei, Ting Lu, Hai-Yan Liu, Jiao-Xuan Bai, Qian Wang, Guang-Yue Li, Ying-Hua Liang.  (2023)  Exploring the continuous cleavage-oxidation mechanism of the catalytic oxidation of cellulose to formic acid: A combined experimental and theoretical study.  FUEL,      [PMID:] [10.1016/j.fuel.2023.127667]

4. Yongfang Zhou, Thomas J.A. Slater, Xuanli Luo, Yi Shen.  (2022)  A versatile single-copper-atom electrocatalyst for biomass valorization.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2022.122218]

5. Xiaomei Ning, Xiaosong Zhou, Jin Luo, Liang Zhan.  (2021)  PtBi on carbon cloth as efficient flexible electrode for electro-oxidation of liquid fuels.  JOURNAL OF ELECTROANALYTICAL CHEMISTRY,      [PMID:] [10.1016/j.jelechem.2021.115958]

6. Haiyong Wang, Haosheng Xin, Chiliu Cai, Changhui Zhu, Zhongxun Xiu, Qiying Liu, Yujing Weng, Chenguang Wang, Xinghua Zhang, Shijun Liu, Zifang Peng, Longlong Ma.  (2020)  Selective C3-C4 Keto-Alcohol Production from Cellulose Hydrogenolysis over Ni-WOx/C Catalysts.  ACS Catalysis,      [PMID:] [10.1021/acscatal.0c02375]

7. Ting Lu, Yucui Hou, Weize Wu, Muge Niu, Wei Li, Shuhang Ren.  (2018)  Catalytic oxidation of cellulose to formic acid in V(V)-Fe(III)-H2SO4 aqueous solution with O2.  FUEL PROCESSING TECHNOLOGY,      [PMID:] [10.1016/j.fuproc.2018.02.001]

8. Xiaomei Ning, Yuhang Li, Hao Yu, Feng Peng, Hongjuan Wang, Yanhui Yang.  (2016)  Promoting role of bismuth and antimony on Pt catalysts for the selective oxidation of glycerol to dihydroxyacetone.  JOURNAL OF CATALYSIS,      [PMID:] [10.1016/j.jcat.2015.12.020]

9. Xiaomei Ning, Hao Yu, Feng Peng, Hongjuan Wang.  (2015)  Pt nanoparticles interacting with graphitic nitrogen of N-doped carbon nanotubes: Effect of electronic properties on activity for aerobic oxidation of glycerol and electro-oxidation of CO.  JOURNAL OF CATALYSIS,      [PMID:] [10.1016/j.jcat.2015.02.010]

10. Haichao Zhou, Jianglin Liu, Dalang Chen, Yanlin Qin, Tiejun Wang, Xueqing Qiu, Xuliang Lin.  (2025)  Boosting middle hydroxyl adsorption on lignin-derived carbon loaded MnO–Ni for glycerol conversion to dihydroxyacetone.  AICHE JOURNAL,      [PMID:] [10.1002/aic.70012]

11. Liu Yang, Shang Huishan, Zhang Bing, Yan Dongpeng, Xiang Xu.  (2024)  Surface fluorination of BiVO4 for the photoelectrochemical oxidation of glycerol to formic acid.  Nature Communications,  15  (1): (1-12).  [PMID:39289360] [10.1038/s41467-024-52161-4]

12. Tong Zhang, Haiyong Wang, Chenguang Wang, Qiying Liu.  (2025)  Catalytic hydrogenolysis of fructose to acetol over Ni/CeO2 catalysts.  INDUSTRIAL CROPS AND PRODUCTS,      [PMID:] [10.1016/j.indcrop.2025.122213]

13. Shuang Wei, Sheng Zhong, Chao Bao, Linbo Huang, Kexin Li, Ruirui Wang, Bin He, Ruirui Zhang, Ruixia Liu.  (2025)  Interfacial Electronic Modulation of Co3O4/CeO2 Heterojunction for Optimizing C–C Bond Cleavage and Intermediate Adsorption in Glycerol Oxidation to Glycolic Acid.  ACS Applied Materials & Interfaces,      [PMID:41128629] [10.1021/acsami.5c18111]

14. Zhenjun Liu, Tianpei Yang, Yi Shen.  (2025)  Enhancing the selectivity of glycerol electrooxidation toward C3 products through the synergistic effect of Au and Pt.  INTERNATIONAL JOURNAL OF HYDROGEN ENERGY,      [PMID:] [10.1016/j.ijhydene.2025.152668]

15. Jiafeng Niu, Xiaoyu Zhu, Huibing Chi, Bin Ma, Hao Zhu, Zhaoxin Lu, Ping Zhu, Fengxia Lu.  (2026)  Reshaping the Binding Pocket of Aldo–Keto Reductase for Enhanced Stereoselectivity and Activity.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,      [PMID:] [10.1021/acs.jafc.5c15071]

16. Chen-Xi Li, Qian Ren, Feng Peng, Ming-Fei Li.  (2026)  Lignin-tailored synergistic catalyst with cobalt single-atom and zinc clusters dual-site for conversion of hemicellulose to lactic acid.  BIORESOURCE TECHNOLOGY,      [PMID:] [10.1016/j.biortech.2026.134908]