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309532

Sigma-Aldrich

Sorbitol F solution

70 wt. % in H2O, Contains mainly D-sorbitol with lesser amounts of other hydrogenated oligosaccharides

Sinonimo/i:

D-Sorbitol

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About This Item

Formula empirica (notazione di Hill):
C6H10O6
Numero CAS:
50-70-4
Peso molecolare:
178.14
Numero MDL:
MFCD00004708
Codice UNSPSC:
12352201
ID PubChem:
57648495
NACRES:
NA.21

Livello qualitativo

200

Forma fisica

viscous liquid

Concentrazione

70 wt. % in H2O

Colore

colorless

Indice di rifrazione

n20/D 1.46

Densità

1.28 g/mL at 25 °C

Stringa SMILE

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

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
FBPFZTCFMRRESA-JGWLITMVSA-N

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Applicazioni


  • The Improved Properties of Carboxymethyl Bacterial Cellulose Films with Thickening and Plasticizing.: Research demonstrates the effectiveness of sorbitol F solution in improving the mechanical and barrier properties of carboxymethyl bacterial cellulose films. This is crucial for developing advanced biodegradable packaging materials that meet environmental and performance criteria (Sun Z et al., 2022).

  • Elaboration of hemicellulose-based films: Impact of the extraction process from spruce wood on the film properties.: Investigates the use of sorbitol F solution in the production of hemicellulose-based films, emphasizing its effectiveness in influencing film properties such as flexibility, water resistance, and biodegradability, key for sustainable packaging solutions (Chadni M et al., 2020).

Altre note

To gain a comprehensive understanding of our extensive range of Sugar alcohols for your research, we encourage you to visit our Carbohydrates Category page.

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Anna Boccaccio et al.
Cellular and molecular life sciences : CMLS, 71(21), 4275-4283 (2014-04-29)
Two-pore channel proteins (TPC) encode intracellular ion channels in both animals and plants. In mammalian cells, the two isoforms (TPC1 and TPC2) localize to the endo-lysosomal compartment, whereas the plant TPC1 protein is targeted to the membrane surrounding the large
Arie Gruzman et al.
Journal of medicinal chemistry, 51(24), 8096-8108 (2008-12-04)
Type 2 diabetes mellitus has reached epidemic proportions; therefore, the search for novel antihyperglycemic drugs is intense. We have discovered that D-xylose increases the rate of glucose transport in a non-insulin-dependent manner in rat and human myotubes in vitro. Due
Youngkook Kwon et al.
ChemSusChem, 6(3), 455-462 (2013-01-25)
This Full Paper addresses the electrocatalytic hydrogenation of glucose to sorbitol or 2-deoxysorbitol on solid metal electrodes in neutral media. Combining voltammetry and online product analysis with high-performance liquid chromatography (HPLC), provides both qualitative and quantitative information regarding the reaction
J M van Griensven et al.
Clinical pharmacology and therapeutics, 58(6), 631-640 (1995-12-01)
To examine the effect of diabetes mellitus on the pharmacokinetics of tolrestat and to investigate its effect on red blood cell sorbitol levels according to a new pharmacodynamic model for this class of drugs. Single and multiple doses of tolrestat
G Molino et al.
The Journal of laboratory and clinical medicine, 131(5), 393-405 (1998-05-30)
D-Sorbitol (SOR) is safe, is easy to measure, and has an exceptionally high extraction ratio in the normal liver of 0.93+/-0.05 (mean+/-SD). Together with the general interest in hepatic hemodynamics, these facts motivated us to review the usefulness of this
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