2,2'-Sulfonyldiethanol
Suppliers
Names
[ CAS No. ]:
2580-77-0
[ Name ]:
2,2'-Sulfonyldiethanol
[Synonym ]:
EINECS 219-948-3
Ethanol,2'-sulfonyldi
bis-2-hydroxyethylsulfone
Diethanol sulfone
BHES 50
MFCD00002907
2,2′-Sulfonyldiethanol
2,2'-ETHYLIDENEBIS(4,6-DI-TERT-BUTYLPHENOL)
β-Hydroxyethyl sulfone
2,2'-sulfanediyldiethanol S,S-dioxide
2,2'-Sulphonylbis-ethanol
Bis(β-hydroxyethyl) sulfone
Ethanol, 2,2'-sulfonylbis-
Ethanol,2,2'-sulfonylbis
2,2'-Sulfonyldiethanol
Sulfonyldiethanol
Bis(2-hydroxyethyl) sulfone
Chemical & Physical Properties
[ Density]:
1.4±0.1 g/cm3
[ Boiling Point ]:
432.3±30.0 °C at 760 mmHg
[ Molecular Formula ]:
C4H10O4S
[ Molecular Weight ]:
154.185
[ Flash Point ]:
215.2±24.6 °C
[ Exact Mass ]:
154.029984
[ PSA ]:
82.98000
[ LogP ]:
-1.99
[ Vapour density ]:
5.5 (vs air)
[ Vapour Pressure ]:
0.0±2.3 mmHg at 25°C
[ Index of Refraction ]:
1.499
MSDS
Safety Information
[ Symbol ]:
GHS08
[ Signal Word ]:
Danger
[ Hazard Statements ]:
H334
[ Precautionary Statements ]:
P261-P342 + P311
[ Hazard Codes ]:
Xi
[ Risk Phrases ]:
43
[ Safety Phrases ]:
36/37
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2905590090
Precursor & DownStream
Precursor
DownStream
Customs
[ HS Code ]: 2905590090
[ Summary ]:
2905590090 other halogenated, sulphonated, nitrated or nitrosated derivatives of acyclic alcohols。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%
Articles
J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 845(1) , 114-20, (2007)
A sensitive method has been developed for the trace analysis of the sulphur mustard metabolite thiodiglycol (TDG) in urine, and its oxidation product thiodiglycol sulphoxide (TDGO) after reduction to ...
J. Anal. Toxicol. 32(1) , 10-6, (2008)
In July 2004, two individuals developed blisters after the destruction of a WWI-era munition. To determine the causative agent, urine samples were collected from both the highly blistered patient (pat...
Nucleic Acids Res. 32(2) , 623-631, (2004)
New linker phosphoramidite reagents containing a cleavable 3'-ester linkage are used for attaching the first nucleoside to the surface of a solid- phase support. Inexpensive, underivatized amino suppo...