推荐产品
质量水平
方案
≥99% (GC)
表单
crystals
甜味
<0.6 × sucrose
颜色
white
溶解性
water: 50 mg/mL, clear, colorless
SMILES字符串
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-
InChI key
FBPFZTCFMRRESA-GUCUJZIJSA-N
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储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
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
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
Peter F Kador et al.
Journal of ocular pharmacology and therapeutics : the official journal of the Association for Ocular Pharmacology and Therapeutics, 25(4), 299-308 (2009-05-20)
The two most widely investigated animal models for diabetic retinopathy (DR) are the rat and dog. In dogs, aldose reductase (AR) is present only in retinal capillary pericytes and their destruction has been linked to polyol accumulation and resulting apoptosis.
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
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
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