D0256
Dulcitol
≥99% (GC)
Sinónimos:
Dulcite, Galactitol
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Acerca de este artículo
Fórmula empírica (notación de Hill):
C6H14O6
Número CAS:
Peso molecular:
182.17
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
EC Number:
210-165-2
Beilstein/REAXYS Number:
1721903
MDL number:
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Permítanos ayudarleNombre del producto
Dulcitol, ≥99% (GC)
InChI key
FBPFZTCFMRRESA-GUCUJZIJSA-N
InChI
1S/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/t3-,4+,5+,6-
SMILES string
OC[C@@H](O)[C@H](O)[C@H](O)[C@@H](O)CO
assay
≥99% (GC)
form
crystals
sweetness
<0.6 × sucrose
color
white
solubility
water: 50 mg/mL, clear, colorless
Quality Level
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Application
Dulcitol (Galactitol), a sugar alcohol derived through reduction of galactose, is important in studies related to cataract formation, hepatosplenomegaly and mental retardation. It is used as a substrate to identify, differentiate and characterize galactitol dehydrogenase(s). Galactitol may be used as a reference compound in analytical procedures developed to analyze sugar alcohols in plants and food.
Biochem/physiol Actions
A sugar alcohol and slightly sweet tastant for human taste cells.
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.
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Lukas Müller et al.
Materials (Basel, Switzerland), 13(20) (2020-10-15)
Measuring thermo-physical properties of phase change materials (PCM) in a consistent and reliable manner is essential for system layout of thermal energy storages and correspondingly material selection. Only if basic properties are assessed in a comparable way a selection process
Joanne Hughes et al.
The Journal of pediatrics, 154(5), 721-726 (2009-02-03)
To determine the long-term outcome of dietary intervention in siblings from 14 Irish families with classical galactosemia (McKusick 230400), an autosomal recessive disorder of carbohydrate metabolism and galactose-1-phosphate uridyltransferase (GALT) deficiency. Outcomes in siblings on dietary galactose restriction were studied
H P Schwarz et al.
Clinical chemistry, 31(3), 420-422 (1985-03-01)
An oral dose of galactose, 1 g/kg of body weight, was administered to 24 children with the Duarte variant/classical galactosemia genetic compound (GtD/gt) and to 16 controls ranging in age from 0.3 to 10.7 years. Urine was then collected for
In vivo evidence of brain galactitol accumulation in an infant with galactosemia and encephalopathy.
G T Berry et al.
The Journal of pediatrics, 138(2), 260-262 (2001-02-15)
In a newborn infant with galactose-1-phosphate uridyltransferase deficiency and encephalopathy, brain magnetic resonance imaging revealed cytotoxic edema in white matter. Using in vivo proton magnetic resonance spectroscopy, we detected approximately 8 mmol galactitol per kilogram of brain tissue, an amount
Ignasi Barba et al.
Investigative ophthalmology & visual science, 51(9), 4416-4421 (2010-04-09)
To explore the metabolic profile of vitreous fluid of patients with proliferative diabetic retinopathy (PDR) using 1H-NMR-based metabonomic analysis. 1H-NMR spectra were acquired from vitreous samples obtained during vitrectomy from 22 patients with type 1 diabetes with PDR and from
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