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97336

Sigma-Aldrich

D-Sorbitol

liquid, tested according to Ph. Eur.

Sinónimos:

D-Glucitol

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About This Item

Fórmula empírica (notación de Hill):
C6H14O6
Número de CAS:
50-70-4
Peso molecular:
182.17
Beilstein/REAXYS Number:
1721899
EC Number:
200-061-5
MDL number:
MFCD00004708
UNSPSC Code:
12352201
PubChem Substance ID:
329770356
NACRES:
NA.21

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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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_germany

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
BCCM1306
BCCL7069
BCCL3093
BCCK9604
BCCK1576

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D-Sorbitol European Pharmacopoeia (EP) Reference Standard

S1000000

D-Sorbitol

D-Sorbitol United States Pharmacopeia (USP) Reference Standard

USP

1617000

D-Sorbitol

Parteck&#174; SI 400 LEX (Sorbitol) EMPROVE&#174; EXPERT, Ph. Eur., BP, NF, JP

SAFC

1.11597

Parteck® SI 400 LEX (Sorbitol)

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

Sigma-Aldrich

S6021

D-Sorbitol

Parteck&#174; SI 400 (Sorbitol) EMPROVE&#174; ESSENTIAL, Ph. Eur., BP, NF, FCC, E 420, JSFA

SAFC

1.03140

Parteck® SI 400 (Sorbitol)

D-Sorbitol Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1006

D-Sorbitol

Arlene E Dent et al.
PloS one, 3(10), e3557-e3557 (2008-10-30)
Antibodies that impair Plasmodium falciparum merozoite invasion and intraerythrocytic development are one of several mechanisms that mediate naturally acquired immunity to malaria. Attempts to correlate anti-malaria antibodies with risk of infection and morbidity have yielded inconsistent results. Growth inhibition assays
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
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
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
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