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97336

Sigma-Aldrich

D-sorbitol

liquid, tested according to Ph. Eur.

Synonyme(s) :

D-glucitol

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About This Item

Formule empirique (notation de Hill):
C6H14O6
Numéro CAS:
50-70-4
Poids moléculaire :
182.17
Numéro Beilstein :
1721899
Numéro CE :
200-061-5
Numéro MDL:
MFCD00004708
Code UNSPSC :
12352201
ID de substance PubChem :
329770356
Nomenclature NACRES :
NA.21

Agence

USP/NF
tested according to Ph. Eur.

Niveau de qualité

100

Densité de vapeur

<1 (vs air)

Pression de vapeur

<0.1 mmHg ( 25 °C)

Pureté

72-92%

Forme

liquid

Impuretés

28-32% water

Couleur

white

Plage de pH utile

5.0-7 (25 °C, 182 g/L)

Pf

98-100 °C (lit.)

Solubilité

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

Chaîne SMILES 

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

Clé InChI

FBPFZTCFMRRESA-JGWLITMVSA-N

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Catégories apparentées

Autres remarques

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

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)

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Certificats d'analyse (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&nbsp;400&nbsp;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&nbsp;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

Reddy Ranjith K Sama et al.
Journal of cellular physiology, 228(11), 2222-2231 (2013-04-30)
FUsed in Sarcoma/Translocated in LipoSarcoma (FUS/TLS or FUS) has been linked to several biological processes involving DNA and RNA processing, and has been associated with multiple diseases, including myxoid liposarcoma and amyotrophic lateral sclerosis (ALS). ALS-associated mutations cause FUS to
G Molino et al.
The Journal of laboratory and clinical medicine, 131(5), 393-405 (1998-05-30)
D-Sorbitol (SOR) is safe, is easy to measure, and has an exceptionally high extraction ratio in the normal liver of 0.93+/-0.05 (mean+/-SD). Together with the general interest in hepatic hemodynamics, these facts motivated us to review the usefulness of this
Shahram Attarian et al.
Orphanet journal of rare diseases, 9, 199-199 (2014-12-19)
Charcot-Marie-Tooth type 1A disease (CMT1A) is a rare orphan inherited neuropathy caused by an autosomal dominant duplication of a gene encoding for the structural myelin protein PMP22, which induces abnormal Schwann cell differentiation and dysmyelination, eventually leading to axonal suffering
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
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