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描述
13C-depleted
质量水平
同位素纯度
99.5 atom % 12C
旋光性
[α]25/D +52.0°, c = 2 in H2O (trace NH4OH)
mp
150-152 °C (lit.)
质量偏移
depleted
SMILES字符串
O[12CH2][12C@H]1O[12CH](O)[12C@H](O)[12C@@H](O)[12C@@H]1O
InChI
1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6?/m1/s1/i1+0,2+0,3+0,4+0,5+0,6+0
InChI key
WQZGKKKJIJFFOK-DXVIFZLFSA-N
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
Jiali Tang et al.
Nature communications, 10(1), 4057-4057 (2019-09-08)
Simultaneous imaging and treatment of infections remains a major challenge, with most current approaches being effective against only one specific group of bacteria or not being useful for diagnosis. Here we develop multifunctional nanoagents that can potentially be used for
Joanna Potaś et al.
Materials (Basel, Switzerland), 14(1) (2020-12-31)
Polyelectrolyte complexes based on the electrostatic interactions between the polymers mixed are of increasing importance, therefore, the aim of this study was to develop hydrogels composed of anionic tragacanth gum and cationic chitosan with or without the addition of anionic
Koichi Matsuo et al.
The journal of physical chemistry. A, 124(4), 642-651 (2020-01-08)
Vacuum ultraviolet (VUV) electronic circular dichroism (ECD) spectra of d-glucose, α-d-glucopyranose, and β-d-glucopyranose were measured in aqueous solution down to 163 nm using a synchrotron radiation VUV-ECD spectrophotometer and theoretically analyzed using molecular dynamics (MD) simulations with explicit water molecules
Madhavan Chalat et al.
Molecular biology of the cell, 28(3), 452-462 (2016-12-10)
ATP8A2 is a P4-ATPase that flips phosphatidylserine and phosphatidylethanolamine across cell membranes. This generates membrane phospholipid asymmetry, a property important in many cellular processes, including vesicle trafficking. ATP8A2 deficiency causes severe neurodegenerative diseases. We investigated the role of the C-terminus
Sara Groeneboer et al.
Rheumatology (Oxford, England), 50(7), 1226-1235 (2011-02-25)
To compare the ability of different cyclodextrin polysulphate (CDPS) derivatives to affect human articular cartilage cell metabolism in vitro. OA chondrocytes were cultured in alginate and exposed to 5 µg/ml of 2,3,6-tri-O-methyl-β-cyclodextrin (ME-CD), 2,3-di-O-methyl-6-sulphate-β-cyclodextrin (ME-CD-6-S), 2,6-di-O-methyl-3-sulphate-β-cyclodextrin (ME-CD-3-S), (2-carboxyethyl)-β-CDPS (CE-CDPS), (2-hydroxypropyl)-β-CDPS
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