D-Sorbitol - ≥98% , CAS No.50-70-4

CAS: 50-70-4 Cat. No.: S140157 Fórmula: C₆H₁₄O₆ Peso molecular: 182.18 Beilstein Registry Number: 1721899 Número EC: 200-061-5

GRADE & PURITY ≥98%

Synonyms

LACTITOL MONOHYDRATE IMPURITY E [EP IMPURITY] | Sorbitol FP | Sorbitab | MALTITOL IMPURITY A [EP IMPURITY] | Sorbitol 3% in plastic container | D-Sorbitol | SORBITOL [MART.] | Sorbitur | Cholaxine | Sorbex Rp | Sorbilax | sorbitol | SORBITOL (II) | SORBIT

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

It can be used to wash spheroplasts and minimize the internal permeation flow in agarose gel in isoelectric focusing. Can be used to induce osmotic stress.

Specifications

Sinónimos

LACTITOL MONOHYDRATE IMPURITY E [EP IMPURITY] | Sorbitol FP | Sorbitab | MALTITOL IMPURITY A [EP IMPURITY] | Sorbitol 3% in plastic container | D-Sorbitol | SORBITOL [MART.] | Sorbitur | Cholaxine | Sorbex Rp | Sorbilax | sorbitol | SORBITOL (II) | SORBIT

Especificaciones y pureza

≥98%

Mecanismos bioquímicos y fisiológicos

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,

Condiciones de almacenamiento de almacenamiento

Argon charged,Room temperature

Enviado en

Normal

Nota

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Pureza

≥98%

Nombres e identificadores

Pubchem Sid

508810432

Sonrisas canónicas

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

Isómeros SMILES

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

WGK Alemania

2

CAS alternativo

98201-93-5；68425-17-2；1259528-21-6

Peso molecular

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
    • Clase Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Clase: 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
• Descripción: 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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F2 Tclin Thrombin (11687 Activities)

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AR Tclin Androgen Receptor (11781 Activities)

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GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)

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MAOA Tclin Monoamine oxidase A (11911 Activities)

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DRD1 Tclin Dopamine D1 receptor (9720 Activities)

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SLC6A2 Tclin Norepinephrine transporter (10102 Activities)

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ADORA1 Tclin Adenosine A1 receptor (17603 Activities)

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SLC6A4 Tclin Serotonin transporter (12625 Activities)

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ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)

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OPRM1 Tclin Mu opioid receptor (19785 Activities)

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DRD3 Tclin Dopamine D3 receptor (14368 Activities)

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SLC6A3 Tclin Dopamine transporter (10535 Activities)

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KCNH2 Tclin HERG (29587 Activities)

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TBXA2R Tclin Thromboxane A2 receptor (5717 Activities)

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PDE4A Tclin Phosphodiesterase 4A (1943 Activities)

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HRH3 Tclin Histamine H3 receptor (10389 Activities)

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ACR Tchem Acrosin (277 Activities)

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Homo sapiens (32628 Activities)

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FEN1 Tchem Flap endonuclease 1 (12055 Activities)

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APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase (38016 Activities)

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ABCB11 Tchem Bile salt export pump (2311 Activities)

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GMNN Tbio Geminin (128009 Activities)

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CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)

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Hdac6 Histone deacetylase 6 (222 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

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Mecanismos de acción

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive
• Índice de refracción: 1.3477
• Rotación específica [α]: 106° (C=0.4,Acidified (NH4)6Mo7O24)
• Punto de ebullición (°C): 200 °C/0.002 mmHg
• Punto de fusión (°C): 110 °C
• Peso molecular: 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