L-(+)-Arabinose - Native , CAS No.5328-37-0

CAS: 5328-37-0 Cat. No.: L432840 Molecular Weight: 150.13 Beilstein Registry Number: 1723085 EC Number: 226-214-6

GRADE & PURITY Native

Synonyms

SCHEMBL43055 | (2R,3S,4S)-2,3,4,5-tetrahydroxypentanal | DL-Arabinose | O,O-Dimethyl S-(2-(ethylthio)ethyl) phosphorodithioate | AM83956 | B18R611M38 | L-ARABINOSE [WHO-DD] | PYMYPHUHKUWMLA-VAYJURFESA-N | DL-arabinose (ring open form) | DS-14408 | EN300-1

Storage

Room temperature,Argon charged,Desiccated,Cool

Shipped In

Normal

Overview

Other Notes

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Specifications

Synonyms

SCHEMBL43055 | (2R, 3S, 4S)-2, 3, 4, 5-tetrahydroxypentanal | DL-Arabinose | O, O-Dimethyl S-(2-(ethylthio)ethyl) phosphorodithioate | AM83956 | B18R611M38 | L-ARABINOSE [WHO-DD] | PYMYPHUHKUWMLA-VAYJURFESA-N | DL-arabinose (ring open form) | DS-14408 | EN300-1

Specifications & Purity

Native

Biochemical and Physiological Mechanisms

L-Arabinose is the naturally occurring isomer and is a constituent of plant polysaccharides. Most bacteria contain an inducible arabinose operon that codes for a series of enzymes and transporters that allows L-arabinose to be used as the sole carbon sou

Storage

Room temperature, Argon charged, Desiccated, Cool

Shipped In

Normal

Grade

Native

Names and Identifiers

• Canonical Smiles: C(C(C(C(C=O)O)O)O)O
• IUPAC Name: (2R,3S,4S)-2,3,4,5-tetrahydroxypentanal
• InChIKey: PYMYPHUHKUWMLA-VAYJURFESA-N
• INCHI: 1S/C5H10O5/c6-1-3(8)5(10)4(9)2-7/h1,3-5,7-10H,2H2/t3-,4-,5+/m0/s1
• Isomeric SMILES: C([C@@H]([C@@H]([C@H](C=O)O)O)O)O
• WGK Germany: 3
• Alternate CAS: 87-72-9
• Molecular Weight: 150.13
• Beilstein: 1723085
• Reaxy-Rn: 2325068
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2325068&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Class Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates
        • Level5 Monosaccharides
          • Level6 Pentoses

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Monosaccharides
• Direct Parent: Pentoses
• Alternative Parents: Beta-hydroxy aldehydes Alpha-hydroxyaldehydes Secondary alcohols Polyols Short-chain aldehydes Primary alcohols Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Pentose monosaccharide - Beta-hydroxy aldehyde - Alpha-hydroxyaldehyde - Secondary alcohol - Polyol - Organic oxide - Hydrocarbon derivative - Short-chain aldehyde - Primary alcohol - Carbonyl group - Aldehyde - Alcohol - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as pentoses. These are monosaccharides in which the carbohydrate moiety contains five carbon atoms.
• External Descriptors: aldehydo-arabinose - L-arabinose

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

Chemical and Physical Properties

• Solubility: DMSO: 40 mg/mL (266.44 mM), Need ultrasonic；H2O: 400 mg/mL (2664.36 mM), Need ultrasonic
• Sensitivity: Moisture sensitive
• Specific Rotation[α]: +102 to +106 deg(C=10, H2O)
• Melt Point(°C): 157-160°C
• Molecular Weight: 150.130 g/mol
• XLogP3: -2.300
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 4
• Exact Mass: 150.053 Da
• Monoisotopic Mass: 150.053 Da
• Topological Polar Surface Area: 98.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 104.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 3
• 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

References

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