D-(+)-gliceraldehído - ≥80% , CAS No.453-17-8

CAS: 453-17-8 Cat. No.: D134978 Peso molecular: 90.08 Beilstein Registry Number: 1720474 Número EC: 207-217-1

GRADE & PURITY ≥80%

Synonyms

DTXSID70196464 | GLYCERALDEHYDE; (2R)-2,3-DIHYDROXYPROPANAL | DB02536 | NSC 91534 | 1-(4-bromo-phenyl)-pentan-1-one | L-Leucyl-L-alanine hydrate | (2R)-2,3-DIHYDROXYPROPANAL | 3GR | 41A680M0WB | D-2,3-dihydroxypropanal | AKOS016844136 | BDBM16443 | EINECS

Storage

Conservar a 2-8°C,cargado con argón

Shipped In

Hielo húmedo

Descripción general

El D-(+)-gliceraldehído es el enantiómero R del monosacárido triosa gliceraldehído. El gliceraldehído es la más simple de todas las aldosas comunes y es un compuesto intermedio en el metabolismo de los hidratos de carbono.
Un intermediario en el metabolismo de los hidratos de carbono

Specifications

Sinónimos

DTXSID70196464 | GLYCERALDEHYDE; (2R)-2, 3-DIHYDROXYPROPANAL | DB02536 | NSC 91534 | 1-(4-bromo-phenyl)-pentan-1-one | L-Leucyl-L-alanine hydrate | (2R)-2, 3-DIHYDROXYPROPANAL | 3GR | 41A680M0WB | D-2, 3-dihydroxypropanal | AKOS016844136 | BDBM16443 | EINECS

Especificaciones y pureza

≥80%

Condiciones de almacenamiento de almacenamiento

Conservar a 2-8°C, cargado con argón

Enviado en

Hielo húmedo

Pureza

≥80%

Nombres e identificadores

• Sonrisas canónicas: C(C(C=O)O)O
• IUPAC Name: (2R)-2,3-dihydroxypropanal
• InChIKey: MNQZXJOMYWMBOU-VKHMYHEASA-N
• INCHI: 1S/C3H6O3/c4-1-3(6)2-5/h1,3,5-6H,2H2/t3-/m0/s1
• Isómeros SMILES: C([C@H](C=O)O)O
• WGK Alemania: 3
• Peso molecular: 90.08
• Beilstein: 1720474
• 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: Aldoses

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

• Sensibilidad: air sensitive
• Punto de inflamación (°F): 235.4 °F
• Punto de inflamación (°C): 113 °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: 1
• 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. Muge Niu, Yucui Hou, Weize Wu, Shuhang Ren, Ru Yang.  (2018)  Successive C1–C2 bond cleavage: the mechanism of vanadium(V)-catalyzed aerobic oxidation of D-glucose to formic acid in aqueous solution.  PHYSICAL CHEMISTRY CHEMICAL PHYSICS,  20  (26): (17942-17951).  [PMID:29926044] [10.1039/C8CP02352B]