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Merck
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S7547

Sigma-Aldrich

D-sorbitolo

≥98% (GC), BioXtra

Sinonimo/i:

D-glucitolo

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250 G
CHF 52.10
1 KG
CHF 174.00

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250 G
CHF 52.10
1 KG
CHF 174.00

About This Item

Formula empirica (notazione di Hill):
C6H14O6
Numero CAS:
Peso molecolare:
182.17
Beilstein:
1721899
Numero CE:
Numero MDL:
Codice UNSPSC:
12352201
ID PubChem:
NACRES:
NA.25

CHF 52.10


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Densità del vapore

<1 (vs air)

Tensione di vapore

<0.1 mmHg ( 25 °C)

Nome Commerciale

BioXtra

Saggio

≥98% (GC)

Stato

powder or chunks

Impurezze

<0.001% Phosphorus (P)
<0.1% Insoluble matter

Residuo alla calcinazione

<0.1%

Colore

white

Intervallo di pH utile

5.0-7.0 (25 °C, 182 g/L)

Punto di fusione

98-100 °C (lit.)

Solubilità

H2O: 1 M, clear, colorless (room temperature)

Anioni in tracce

chloride (Cl-): <0.005%
sulfate (SO42-): <0.01%

Cationi in tracce

Al: <0.0005%
Ca: <0.0005%
Cu: <0.0005%
Fe: <0.0005%
K: <0.005%
Mg: <0.0005%
NH4+: <0.05%
Na: <0.005%
Pb: <0.001%
Zn: <0.0005%

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

May be used for washing spheroplasts[1] and in isoelectric focusing to minimize endoosmotic flow in agarose gels.[2] May be used to induce osmotic stress.

Azioni biochim/fisiol

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, or dietary supplement. D-Sorbitol has also been found in cosmetics, paper, and pharmaceuticals. Naturally, D-sorbitol occurs widely in plants via photosynthesis, ranging from algae to higher order fruits of the family Rosaceae.

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

11 - Combustible Solids

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, type N95 (US)


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Supelco

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D-(+)-trealosio suitable for microbiology, &#8805;99.0%, composed of two &#945;-glucose units that is used as a protectant, stabilizer and to support proper folding

Millipore

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D-(+)-trealosio

Isoelectric focusing.
D E Garfin
Methods in enzymology, 182, 459-477 (1990-01-01)
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
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
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
Beau Op de Beeck et al.
ChemSusChem, 6(1), 199-208 (2013-01-12)
The catalytic valorization of cellulose is currently subject of intense research. Isosorbide is among the most interesting products that can be formed from cellulose as it is a potential platform molecule and can be used for the synthesis of a

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