2-Deoxy-D-ribose - BioReagent, for Cell culture, Moligand™, 10wt. % in medium chain triglycerides (MCTG) , CAS No.533-67-5

CAS: 533-67-5 Cat. No.: D485294 Summenformel: C₅H₁₀O₄ Molekulargewicht: 134.13 Beilstein Registry Number: 1721978 EG-Nummer: 208-573-0

GRADE & PURITY BioReagent, Moligand™, for Cell culture, 10wt. % in medium chain triglycerides (MCTG)

Synonyms

2-Deoxy-D-ribose, 97% | CHEBI:28816 | NSC-772796 | ASJSAQIRZKANQN-CRCLSJGQSA-N | BBL012499 | 2-Deoxy-D-ribose | 2-Deoxy-D-ribose, >=99.0% (TLC) | AM20100306 | 4-01-00-04181 (Beilstein Handbook Reference) | aldehydo-2-deoxy-D-ribose | D-erythro-Pentose, 2-

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Synonyme

2-Deoxy-D-ribose, 97% | CHEBI:28816 | NSC-772796 | ASJSAQIRZKANQN-CRCLSJGQSA-N | BBL012499 | 2-Deoxy-D-ribose | 2-Deoxy-D-ribose, >=99.0% (TLC) | AM20100306 | 4-01-00-04181 (Beilstein Handbook Reference) | aldehydo-2-deoxy-D-ribose | D-erythro-Pentose, 2-

Spezifikationen & Reinheit

BioReagent, for Cell culture, Moligand™, 10wt. % in medium chain triglycerides (MCTG)

Storage

Store at 2-8°C

Verschickt in

Wet ice

Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.

Note

BioReagent, für die Zellkultur, Moligand™

Namen und Kennungen

Pubchem Sid

504763826

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504763826

Kanonisches Lächeln

C(C=O)C(C(CO)O)O

IUPAC Name

(3S,4R)-3,4,5-trihydroxypentanal

InChIKey

ASJSAQIRZKANQN-CRCLSJGQSA-N

INCHI

1S/C5H10O4/c6-2-1-4(8)5(9)3-7/h2,4-5,7-9H,1,3H2/t4-,5+/m0/s1

Isomere SMILES

C(C=O)[C@@H]([C@@H](CO)O)O

WGK Deutschland

3

RTECS

SB7230000

Molekulargewicht

134.13

Beilstein

1721978

Reaxy-Rn

1904591

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1904591&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Klasse Organooxygen compounds
      • Subclass Carbonyl compounds
        • Ebene5 Aldehydes
          • Ebene6 Beta-hydroxy aldehydes

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Klasse: Organooxygen compounds
• Subclass: Carbonyl compounds
• Intermediate Tree Nodes: Aldehydes
• Direct Parent: Beta-hydroxy aldehydes
• Alternative Parents: Alpha-hydrogen aldehydes Secondary alcohols Polyols Short-chain aldehydes Primary alcohols Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Beta-hydroxy aldehyde - Alpha-hydrogen aldehyde - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Short-chain aldehyde - Primary alcohol - Alcohol - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as beta-hydroxy aldehydes. These are organic compounds containing an aldehyde substituted with a hydroxy group on the second carbon atom.
• External Descriptors: deoxypentose

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

Chemische und physikalische Eigenschaften

• Löslichkeit: water: 100mg/mL, clear to slightly hazy, colorless to light yellow
• Spezifische Drehung [α]: -56 ° (C=1, H2O)
• Schmelzpunkt (°C): 91°C
• Molekulargewicht: 134.130 g/mol
• XLogP3: -2.300
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 4
• Exact Mass: 134.058 Da
• Monoisotopic Mass: 134.058 Da
• Topological Polar Surface Area: 77.800 Ų
• Heavy Atom Count: 9
• Formal Charge: 0
• Complexity: 83.000
• 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