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97336

Sigma-Aldrich

D-Sorbitol

liquid, tested according to Ph. Eur.

Synonym(s):

Sorbitolum liquidum non cristallisabile, D-Glucitol

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About This Item

Empirical Formula (Hill Notation):
C6H14O6
CAS Number:
50-70-4
Molecular Weight:
182.17
Beilstein:
1721899
EC Number:
200-061-5
MDL number:
MFCD00004708
UNSPSC Code:
12352201
PubChem Substance ID:
329770356
NACRES:
NA.21
Pricing and availability is not currently available.

Agency

USP/NF
tested according to Ph. Eur.

Quality Level

100

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)

SMILES string

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

InChI key

FBPFZTCFMRRESA-JGWLITMVSA-N

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Show Differences

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This Item
S1876S7547S6021
D-Sorbitol liquid, tested according to Ph. Eur.

97336

D-Sorbitol

D-Sorbitol &#8805;98% (GC)

S1876

D-Sorbitol

D-Sorbitol &#8805;98% (GC), BioXtra

S7547

D-Sorbitol

D-Sorbitol &#8805;98% (GC), for molecular biology

S6021

D-Sorbitol

Quality Level

100

Quality Level

300

Quality Level

200

Quality Level

200

solubility

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

solubility

water: 200 mg/mL, clear, colorless

solubility

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

solubility

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

form

liquid

form

powder or crystals

form

powder or chunks

form

powder or crystals

impurities

28-32% water

impurities

-

impurities

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

impurities

-

color

white

color

white

color

white

color

white

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 Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCM5412
BCCM1306
BCCL7069
BCCL3093
BCCK9604

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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
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
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
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
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