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线性分子式:
(CH3)3N · SO3
化学文摘社编号:
分子量:
139.17
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
EC Number:
221-614-7
Beilstein/REAXYS Number:
3681759
MDL number:
Form:
solid
InChI key
DXASQZJWWGZNSF-UHFFFAOYSA-N
InChI
1S/C3H9N.O3S/c2*1-4(2)3/h1-3H3;
SMILES string
CN(C)C.O=S(=O)=O
form
solid
reaction suitability
reagent type: oxidant
mp
232 °C (dec.) (lit.)
functional group
amine
Quality Level
Application
用作硫酸化反应的反应物:
α-甲苯氧基酮合成中的亲核试剂
- 硫酸结合型白藜芦醇代谢产物的合成
- 用于抗 HIV-1 活性的壳寡糖
- 十二烷基硫代吡喃糖苷,作为表面活性剂用于对映体分离
- 促进依赖于硫酸化模式的信号通路活化的糖胺聚糖
- 多糖,如硫酸类肝素
α-甲苯氧基酮合成中的亲核试剂
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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24S- and 27-hydroxycholesterol (24OHC and 27OHC) are potent regulators of different biochemical systems in vitro and are the major circulating oxysterols. A small fraction of these oxysterols has been reported to be sulphated but there are no detailed studies. We
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Macromolecular bioscience, 20(2), e1900403-e1900403 (2019-12-31)
Sulfated cellulose (CS) represents an interesting biopolymer due to bioactivity comparable to heparin. However, use of CS for making surface coatings or hydrogels requires the presence of reactive groups for covalent reactions. Here, an approach is presented to oxidize cellulose
Shuqian Hu et al.
Carbohydrate polymers, 236, 116052-116052 (2020-03-17)
In this study, a series water soluble sulfate polysaccharides (SPS) with different degrees of substitutions (DS = 0.02∼0.28) were prepared using a linear water-insoluble β-d-(1→3)-glucan. SPS-1, SPS-3 and SPS-7 with substitution degrees of 0.02, 0.06 and 0.25 were used as templates to
Mikael Pedersen et al.
Food additives & contaminants. Part A, Chemistry, analysis, control, exposure & risk assessment, 34(4), 482-488 (2017-01-21)
After administration of steroids to animals the steroids are partially metabolised in the liver and kidney to phase 2 metabolites, i.e., glucuronic acid or sulphate conjugates. During analysis these conjugated metabolites are normally deconjugated enzymatically with aryl sulphatase and glucuronidase
Jianhong Yang et al.
Biopolymers, 103(10), 539-549 (2015-04-11)
The 6-amino-6-deoxychitosan (NC) and their 2, 6-di-N-sulfonated derivatives were prepared via N-phthaloylation, tosylation, azidation, hydrazinolysis, reduction of azide groups and N-sulfonation, and their structures were systematically characterized by FT-IR, 2D HSQC NMR, XRD, gel permeation chromatography (GPC), and elemental analysis.
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