DL-Glyceric Acid - 20% aqueous solution, about 2mol/L , CAS No.473-81-4

CAS: 473-81-4 Cat. No.: D278734 Peso molecular: 106.08

GRADE & PURITY 20% aqueous solution, about 2mol/L

Synonyms

GLYCERIC ACID, (D) | (+-)-Glyceric acid | STL268888 | 3E9B4D59-D526-4D1F-A6D8-566E4D962CA5 | GLYCERIC ACID [MI] | UNII-70KH64UX7G | 70KH64UX7G | beta-Hydroxylactic acid | DL-2,3-Dihydroxypropionic Acid | Glyceric Acid (20% in Water,ca.2 mol/L)

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Sinónimos

GLYCERIC ACID, (D) | (+-)-Glyceric acid | STL268888 | 3E9B4D59-D526-4D1F-A6D8-566E4D962CA5 | GLYCERIC ACID [MI] | UNII-70KH64UX7G | 70KH64UX7G | beta-Hydroxylactic acid | DL-2, 3-Dihydroxypropionic Acid | Glyceric Acid (20% in Water, ca.2 mol/L)

Especificaciones y pureza

20% aqueous solution, about 2mol/L

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

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

Nombres e identificadores

• Pubchem Sid: 488179546
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488179546
• Sonrisas canónicas: C(C(C(=O)O)O)O
• IUPAC Name: 2,3-dihydroxypropanoic acid
• InChIKey: RBNPOMFGQQGHHO-UHFFFAOYSA-N
• INCHI: 1S/C3H6O4/c4-1-2(5)3(6)7/h2,4-5H,1H2,(H,6,7)
• Isómeros SMILES: C(C(C(=O)O)O)O
• CAS alternativo: 600-19-1
• Peso molecular: 106.08
• Reaxy-Rn: 1721417
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1721417&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 acids and derivatives
• Alternative Parents: Beta hydroxy acids and derivatives Monosaccharides Alpha hydroxy acids and derivatives Secondary alcohols 1,2-diols Monocarboxylic acids and derivatives Carboxylic acids Primary alcohols Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Beta-hydroxy acid - Glyceric_acid - Sugar acid - Alpha-hydroxy acid - Hydroxy acid - Monosaccharide - 1,2-diol - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Alcohol - Carbonyl group - Organic oxide - Primary alcohol - Hydrocarbon derivative - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as sugar acids and derivatives. These are compounds containing a saccharide unit which bears a carboxylic acid group.
• External Descriptors: trionic acid

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

• Peso molecular: 106.080 g/mol
• XLogP3: -1.500
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 106.027 Da
• Monoisotopic Mass: 106.027 Da
• Topological Polar Surface Area: 77.800 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 69.300
• 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. Ye Wang, Ming Xu, Xi Wang, Ruixiang Ge, Yu-Quan Zhu, An-Zhen Li, Hua Zhou, Fengen Chen, Lirong Zheng, Haohong Duan.  (2023)  Unraveling the potential-dependent structure evolution in CuO for electrocatalytic biomass valorization.  Science Bulletin,      [PMID:37798176] [10.1016/j.scib.2023.09.033]

2. Xiaoyuan Liu, Yu Zou, Jiang Jiang.  (2023)  Selective aerobic photocatalytic glycerol oxidation on Au/TiO2 with borate additives.  APPLIED CATALYSIS A-GENERAL,      [PMID:] [10.1016/j.apcata.2023.119216]

3. 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]

4. Xiaoyuan Liu, Yu Zou, Jiang Jiang.  (2024)  Sunlight-driven selective oxidation of glycerol on formate oxidase mimicking AuPt/TiO2.  APPLIED CATALYSIS B-ENVIRONMENTAL,      [PMID:] [10.1016/j.apcatb.2024.123927]

5. 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]

6. Peng Sun, Ziyuan Wang, Xijier Chen, Yunze Luo, Jia Li, Jianguo Liu.  (2025)  Solar-Driven Faradaic Glycerol Upgrading in a Self-Sustained Current-Output Photoelectrochemical Device.  Solar RRL,      [PMID:] [10.1002/solr.202500765]

7. Zhang Yong, Qi Ying, Zhou Haiqing, Zhang Yan, Sun Jingying, Ma Wenqi, Hu Jiayi, Feng Ligang, Yu Fang.  (2026)  Built-in electric field engineering in Co2N0.67/CoP heterostructures for glycerol electrooxidation-assisted hydrogen production.  Nature Communications,      [PMID:] [10.1038/s41467-026-70731-6]