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97336

Sigma-Aldrich

D-sorbitolo

liquid, tested according to Ph. Eur.

Sinonimo/i:

D-glucitolo

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About This Item

Formula empirica (notazione di Hill):
C6H14O6
Numero CAS:
50-70-4
Peso molecolare:
182.17
Beilstein:
1721899
Numero CE:
200-061-5
Numero MDL:
MFCD00004708
Codice UNSPSC:
12352201
ID PubChem:
329770356
NACRES:
NA.21

agenzia

USP/NF
tested according to Ph. Eur.

Livello qualitativo

100

Densità del vapore

<1 (vs air)

Tensione di vapore

<0.1 mmHg ( 25 °C)

Saggio

72-92%

Forma fisica

liquid

Impurezze

28-32% water

Colore

white

Intervallo di pH utile

5.0-7 (25 °C, 182 g/L)

Punto di fusione

98-100 °C (lit.)

Solubilità

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

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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Categorie correlate

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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Certificati d'analisi (COA)

Lot/Batch Number
BCCK1576
BCCK0728
BCCH8260
BCCH5741
BCCG5841

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D-sorbitolo European Pharmacopoeia (EP) Reference Standard

S1000000

D-sorbitolo

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

SAFC

1.11597

Parteck® SI 400 LEX (sorbitolo)

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

Sigma-Aldrich

S6021

D-sorbitolo

D-sorbitolo Pharmaceutical Secondary Standard; Certified Reference Material

Supelco

PHR1006

D-sorbitolo

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
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
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
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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