D-Sorbitol - UltraBio™, ≥99%(HPLC) , CAS No.50-70-4

CAS: 50-70-4 Cat. No.: D755727 Formule: C₆H₁₄O₆ Poids moléculaire: 182.18 Beilstein Registry Number: 1721899 Numéro CE: 200-061-5

GRADE & PURITY UltraBio™, ≥99%(HPLC)

Storage

Room temperature

Shipped In

Normal

Vue d’ensemble

May be used for washing spheroplasts and in isoelectric focusing to minimize endoosmotic flow in agarose gels. May be used to induce osmotic stress.

Sorbitol is a sugar alcohol and slowly metabolized sweetener. Sorbitol, a bacterial culture supplement, is used for the preparation of selective plating media to culture Sorbitol-fermenting bacteria including strains of Escherichia coli and Yersinia enterocolitica.

Specifications

Spécifications et pureté

UltraBio™, ≥99%(HPLC)

Mécanismes biochimiques et physiologiques

D-Sorbitol is a sugar alcohol that is commonly used as a sugar substitute. It occurs naturally and is also produced synthetically from glucose. The food industry uses D-sorbitol as an additive in the form of a sweetener, humectant, emulsifier, thickener,

Conditions de stockage de stockage

Room temperature

Expédié en

Normal

Grade

UltraBio™

Pureté

≥99%(HPLC)

Noms et identifiants

PH

5.0-7.0 (25 °C, 1 M in H 2 O)

Sourires canoniques

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

IUPAC Name

(2R,3R,4R,5S)-hexane-1,2,3,4,5,6-hexol

InChIKey

FBPFZTCFMRRESA-JGWLITMVSA-N

INCHI

1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/t3-,4+,5-,6-/m1/s1

Isomères SMILES

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

WGK Allemagne

2

CAS alternatif

98201-93-5；68425-17-2；1259528-21-6

Poids moléculaire

182.18

Beilstein

1721899

Reaxy-Rn

1721899

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1721899&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Sugar alcohols
• Alternative Parents: Monosaccharides Secondary alcohols Polyols Primary alcohols Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Sugar alcohol - Monosaccharide - Secondary alcohol - Polyol - Hydrocarbon derivative - Primary alcohol - Alcohol - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as sugar alcohols. These are hydrogenated forms of carbohydrate in which the carbonyl group (aldehyde or ketone, reducing sugar) has been reduced to a primary or secondary hydroxyl group.
• External Descriptors: glucitol

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

Propriétés chimiques et physiques

• Solubilité: H 2 O: 1 M at 20 °C, clear, colorless
• Indice de réfraction: 1.3477
• Rotation spécifique [α]: 106° (C=0.4,Acidified (NH4)6Mo7O24)
• Point d'ébullition (°C): 200 °C/0.002 mmHg
• Point de fusion (°C): 110 °C
• Poids moléculaire: 182.170 g/mol
• XLogP3: -3.100
• Hydrogen Bond Donor Count: 6
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 5
• Exact Mass: 182.079 Da
• Monoisotopic Mass: 182.079 Da
• Topological Polar Surface Area: 121.000 Ų
• Heavy Atom Count: 12
• Formal Charge: 0
• Complexity: 105.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 4
• 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