D-Sorbitol - ≥98% , CAS No.50-70-4

CAS: 50-70-4 Cat. No.: S140157 Formule: C₆H₁₄O₆ Poids moléculaire: 182.18 Beilstein Registry Number: 1721899 Numéro CE: 200-061-5

GRADE & PURITY ≥98%

Synonyms

LACTITOL MONOHYDRATE IMPURITY E [EP IMPURITY] | Sorbitol FP | Sorbitab | MALTITOL IMPURITY A [EP IMPURITY] | Sorbitol 3% dans un récipient en plastique | D-Sorbitol | SORBITOL [MART.] | Sorbitur | Cholaxine | Sorbex Rp | Sorbilax | sorbitol | SORBITOL (II

Storage

Argon charged,Room temperature

Shipped In

Normal

Vue d’ensemble

Il peut être utilisé pour laver les sphéroplastes et minimiser le flux de perméation interne dans le gel d'agarose lors de la focalisation isoélectrique. Il peut être utilisé pour induire un stress osmotique.

Specifications

Synonymes

LACTITOL MONOHYDRATE IMPURITY E [EP IMPURITY] | Sorbitol FP | Sorbitab | MALTITOL IMPURITY A [EP IMPURITY] | Sorbitol 3% dans un récipient en plastique | D-Sorbitol | SORBITOL [MART.] | Sorbitur | Cholaxine | Sorbex Rp | Sorbilax | sorbitol | SORBITOL (II

Spécifications et pureté

≥98%

Mécanismes biochimiques et physiologiques

Le D-Sorbitol est un alcool de sucre couramment utilisé comme substitut du sucre. Il existe à l'état naturel et est également produit synthétiquement à partir du glucose. L'industrie alimentaire utilise le D-sorbitol comme additif sous forme d'édulcorant,

Conditions de stockage de stockage

Argon charged,Room temperature

Expédié en

Normal

Note

Dans la mesure du possible, les solutions doivent être préparées et utilisées le même jour. Toutefois, si vous devez préparer des solutions de base à l'avance, nous vous recommandons de les conserver sous forme d'aliquotes dans des flacons hermétiques à -20°C. Ces aliquotes sont généralement utilisables pendant un mois. En général, ces solutions peuvent être utilisées pendant un mois. Avant utilisation, et avant d'ouvrir le flacon, nous vous recommandons de laisser votre produit s'équilibrer à température ambiante pendant au moins 1 heure. Besoin de plus de conseils sur la solubilité, l'utilisation et la manipulation ? Veuillez consulter notre page de questions fréquemment posées (FAQ) pour plus de détails.

Pureté

≥98%

Noms et identifiants

Pubchem Sid

508810432

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

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Mécanismes d'action

Propriétés chimiques et physiques

• Sensibilité: Moisture sensitive
• 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