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Merck

97336

D-Sorbitol

liquid, tested according to Ph. Eur.

Synonym(s):

Sorbitolum liquidum non cristallisabile, D-Glucitol

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1 KG

PLN 262.00

PLN 262.00


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About This Item

Empirical Formula (Hill Notation):
C6H14O6
CAS Number:
Molecular Weight:
182.17
UNSPSC Code:
12352201
NACRES:
NA.21
PubChem Substance ID:
EC Number:
200-061-5
Beilstein/REAXYS Number:
1721899
MDL number:

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Product Name

D-Sorbitol, liquid, tested according to Ph. Eur.

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

agency

USP/NF
tested according to Ph. Eur.

vapor density

<1 (vs air)

vapor pressure

<0.1 mmHg ( 25 °C)

assay

72-92%

form

liquid

impurities

28-32% water

color

white

useful pH range

5.0-7 (25 °C, 182 g/L)

mp

98-100 °C (lit.)

solubility

water: soluble 182 g/L at 20 °C (68 °F)

Quality Level

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This Item
S3889S6021240850
assay

72-92%

assay

≥98% (GC)

assay

≥98% (GC)

assay

99% (GC)

solubility

water: soluble 182 g/L at 20 °C (68 °F)

solubility

water: soluble 182 g/L at 20 °C (68 °F)

solubility

water: soluble 182g/l at 20 °C (68 °F)

solubility

water: soluble 182 g/L at 20 °C (68 °F )

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

200

form

liquid

form

powder

form

powder or crystals

form

powder

useful pH range

5.0-7 (25 °C, 182 g/L)

useful pH range

5.0-7.0 (25 °C, 182 g/L)

useful pH range

5.0-7 (25 °C, 182 g/L)

useful pH range

5.0-7.0 (25 °C, 182 g/L)

impurities

28-32% water

impurities

-

impurities

-

impurities

-

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.

Storage Class

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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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
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
Rajesh Chandramohanadas et al.
The Journal of infectious diseases, 210(10), 1616-1626 (2014-05-28)
Malaria causes nearly 1 million deaths annually. Recent emergence of multidrug resistance highlights the need to develop novel therapeutic interventions against human malaria. Given the involvement of sugar binding plasmodial proteins in host invasion, we set out to identify such
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

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