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Merck

S1876

D-Sorbitol

≥98% (GC)

Sinónimos:

D-Glucitol

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About This Item

Fórmula empírica (notación de Hill):
C6H14O6
Número CAS:
50-70-4
Peso molecular:
182.17
UNSPSC Code:
12352201
NACRES:
NA.21
PubChem Substance ID:
24899498
EC Number:
200-061-5
Beilstein/REAXYS Number:
1721899
MDL number:
MFCD00004708

Nombre del producto

D-Sorbitol, ≥98% (GC)

InChI key

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

SMILES string

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

vapor density

<1 (vs air)

vapor pressure

<0.1 mmHg ( 25 °C)

assay

≥98% (GC)

form

powder or crystals

color

white

useful pH range

5.0-7.0 (25 °C, 182 g/L)

mp

98-100 °C (lit.)

solubility

water: 200 mg/mL, clear, colorless

Quality Level

300

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Categorías relacionadas

Biochem/physiol Actions

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.

Other Notes

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

Application

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

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificados de análisis (COA)

Lot/Batch Number
0000512459
0000512459
0000486119
0000486119
0000494030

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Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.

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Isoelectric focusing.
D E Garfin
Methods in enzymology, 182, 459-477 (1990-01-01)
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
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
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
Preparation of extracts from yeast.
S M Jazwinski
Methods in enzymology, 182, 154-174 (1990-01-01)
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