88559
2,2′-硫二乙醇
≥99.0% (GC)
别名:
2,2′-硫代双乙醇, 双(2-羟乙基)硫醚, 硫代二甘醇, 硫代双乙醇标准液 CRM
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关于此项目
线性分子式:
S(CH2CH2OH)2
化学文摘社编号:
分子量:
122.19
EC Number:
203-874-3
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
1236325
MDL number:
assay
≥99.0% (GC)
refractive index
n20/D 1.521, n20/D 1.5215 (lit.)
bp
164-166 °C/20 mmHg (lit.)
mp
−16 °C (lit.)
density
1.221 g/mL at 25 °C (lit.)
SMILES string
OCCSCCO
InChI
1S/C4H10O2S/c5-1-3-7-4-2-6/h5-6H,1-4H2
InChI key
YODZTKMDCQEPHD-UHFFFAOYSA-N
Application
Thiodiglycol (2,2′-Thiodiethanol, TDE) is used as a solvent and as a refractive index modifying component of mounting media for microscopy. Thiodiglycol may also be used as a charge modifier for procedures such as electrospray ionization mass spectrometry. Thiodiglycol is used as a reference material in the evaluation of the degradation of sulfur mustard gas by bacteria.
Other Notes
This product has been replaced by 166782-ALDRICH | 2,2′-Thiodiethanol ≥99%
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Warning
hcodes
pcodes
Hazard Classifications
Eye Irrit. 2
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
监管及禁止进口产品
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Julien Besnard et al.
Journal of experimental botany, 69(21), 5221-5232 (2018-10-13)
Phloem-derived amino acids are the major source of nitrogen supplied to developing seeds. Amino acid transfer from the maternal to the filial tissue requires at least one cellular export step from the maternal tissue prior to the import into the
Chromatography of amino acids on sulfonated polystyrene resins.
S MOORE et al.
The Journal of biological chemistry, 192(2), 663-681 (1951-10-01)
Karolin K Kroening et al.
Analytical and bioanalytical chemistry, 393(8), 1949-1956 (2009-02-14)
Sulfur mustard (HD), bis(2-chloroethyl)sulfide, is one of a class of mustard agents which are chemical warfare agents. The main chemical warfare hydrolysis degradation products of sulfur mustards are: thiodiglycol, bis(2-hydroxyethylthio)methane, 1,2-bis(2-hydroxyethylthio)ethane, 1,3-bis(2-hydroxyethylthio)propane, and 1,4-bis(2-hydroxyethylthio)butane. The aim of this study is