n-Dodecyl β-D-maltoside （DDM） - UltraBio™, Ultra pure, ≥98% , CAS No.69227-93-6

CAS: 69227-93-6 Cat. No.: N475300 Peso molecular: 510.62 Beilstein Registry Number: 55318 Número EC: 614-943-6

GRADE & PURITY UltraBio™, Ultra pure, ≥98%

Synonyms

n-Dodecyl-b-D-maltoside | MFCD00043012 | (2R,3R,4S,5S,6R)-2-((2R,3S,4R,5R,6R)-6-(dodecyloxy)-4,5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol | N-Dodecyl b-D-maltoside | DS-6568 | EN300-207344 |

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Descripción general

n-Dodecyl β-D-maltoside is a non-ionic surfactant belonging to the alkyl polyglucoside family.n-Dodecyl β-D-maltoside has been used in a study to assess the effect of detergents on the thermal behavior of elastin-like polypeptides (ELP). It has also been used in a study to investigate how membrane structures will respond to detergent solubilization from amino acid sequences.Non-ionic detergent for the stabilization and activation of enzymes and for membrane research.

Specifications

Sinónimos

n-Dodecyl-b-D-maltoside | MFCD00043012 | (2R, 3R, 4S, 5S, 6R)-2-((2R, 3S, 4R, 5R, 6R)-6-(dodecyloxy)-4, 5-dihydroxy-2-(hydroxymethyl)tetrahydro-2H-pyran-3-yloxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3, 4, 5-triol | N-Dodecyl b-D-maltoside | DS-6568 | EN300-207344 |

Especificaciones y pureza

UltraBio™, Ultra pure, ≥98%

Condiciones de almacenamiento de almacenamiento

Store at -20°C, Argon charged

Enviado en

Ice chest + Ice pads

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

Grado

Ultra pure, UltraBio™

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504756729
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504756729
• Sonrisas canónicas: CCCCCCCCCCCCOC1C(C(C(C(O1)CO)OC2C(C(C(C(O2)CO)O)O)O)O)O
• IUPAC Name: (2R,3R,4S,5S,6R)-2-[(2R,3S,4R,5R,6R)-6-dodecoxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
• InChIKey: NLEBIOOXCVAHBD-QKMCSOCLSA-N
• INCHI: 1S/C24H46O11/c1-2-3-4-5-6-7-8-9-10-11-12-32-23-21(31)19(29)22(16(14-26)34-23)35-24-20(30)18(28)17(27)15(13-25)33-24/h15-31H,2-14H2,1H3/t15-,16-,17-,18+,19-,20-,21-,22-,23-,24-/m1/s1
• Isómeros SMILES: CCCCCCCCCCCCO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O[C@@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)O)O
• WGK Alemania: 3
• Peso molecular: 510.62
• Beilstein: 55318
• Reaxy-Rn: 22092137
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=22092137&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Lipids and lipid-like molecules
    • Clase Fatty Acyls
      • Subclass Fatty acyl glycosides

• Kingdom: Organic compounds
• Superclass: Lipids and lipid-like molecules
• Clase: Fatty Acyls
• Subclass: Fatty acyl glycosides
• Intermediate Tree Nodes: Not available
• Direct Parent: Fatty acyl glycosides of mono- and disaccharides
• Alternative Parents: Alkyl glycosides O-glycosyl compounds Disaccharides Oxanes Secondary alcohols Polyols Oxacyclic compounds Acetals Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Fatty acyl glycoside of mono- or disaccharide - Alkyl glycoside - Disaccharide - Glycosyl compound - O-glycosyl compound - Oxane - Secondary alcohol - Acetal - Organoheterocyclic compound - Oxacycle - Polyol - Primary alcohol - Organooxygen compound - Hydrocarbon derivative - Organic oxygen compound - Alcohol - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as fatty acyl glycosides of mono- and disaccharides. These are compounds composed of a mono- or disaccharide moiety linked to one hydroxyl group of a fatty alcohol or of a phosphorylated alcohol (phosphoprenols), a hydroxy fatty acid or to one carboxyl group of a fatty acid (ester linkage) or to an amino alcohol.
• External Descriptors: disaccharide derivative - glycoside

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

Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Heat sensitive；Moisture sensitive
• Punto de fusión (°C): 224-226°C
• Peso molecular: 510.600 g/mol
• XLogP3: 1.400
• Hydrogen Bond Donor Count: 7
• Hydrogen Bond Acceptor Count: 11
• Rotatable Bond Count: 16
• Exact Mass: 510.304 Da
• Monoisotopic Mass: 510.304 Da
• Topological Polar Surface Area: 179.000 Ų
• Heavy Atom Count: 35
• Formal Charge: 0
• Complexity: 554.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 10
• 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

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