SULFUR TRIOXIDE TRIMETHYLAMINE COMPLEX

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Names

[ CAS No. ]:
3162-58-1

[ Name ]:
SULFUR TRIOXIDE TRIMETHYLAMINE COMPLEX

[Synonym ]:
SULFUR TRIOXIDE TRIMETHYLAMINEOMPLEX
TRIMETHYLAMINE SULFUR TRIOXIDE
SULFUR TRIOXIDE TRIMETHYLAMINE
Trimethylamine-sulphur trioxide complex
TRLIMETHYLAMINE SULPHUR TRIOXIDE COMPLEX
sulfur trioxide-trimethylamine complex
TRIMETHYLAMINE SULFUR TRIOXIDE COMPLEX
EINECS 221-614-7
Sulfur trioxide campd. with trimethylamine
MFCD00012421

Chemical & Physical Properties

[ Boiling Point ]:
2.8ºC at 760mmHg

[ Melting Point ]:
239ºC

[ Molecular Formula ]:
C3H9NO3S

[ Molecular Weight ]:
139.17300

[ Exact Mass ]:
139.03000

[ PSA ]:
86.54000

[ LogP ]:
0.46960

MSDS

Safety Information

[ Symbol ]:

GHS05

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H314

[ Precautionary Statements ]:
P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face particle respirator type N100 (US);Gloves;respirator cartridge type N100 (US);type P1 (EN143) respirator filter;type P3 (EN 143) respirator cartridges

[ Hazard Codes ]:
C: Corrosive;

[ Risk Phrases ]:
R34

[ Safety Phrases ]:
S26-S36/37/39-S45

[ RIDADR ]:
UN 3261 8/PG 2

[ Packaging Group ]:
II

Synthetic Route

Precursor & DownStream

Precursor

  • Trimethylamine
  • Sulfur trioxide

DownStream

Articles

Simultaneous quantification of cholesterol sulfate, androgen sulfates, and progestagen sulfates in human serum by LC-MS/MS.

J. Lipid Res. 56 , 1843-51, (2015)

Steroids are primarily present in human fluids in their sulfated forms. Profiling of these compounds is important from both diagnostic and physiological points of view. Here, we present a novel method...

Preparation and in vitro antioxidant activities of 6-amino-6-deoxychitosan and its sulfonated derivatives.

Biopolymers 103 , 539-49, (2015)

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 ...

Sulphatation does not appear to be a protective mechanism to prevent oxysterol accumulation in humans and mice.

PLoS ONE 8 , e68031, (2013)

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...


More Articles


Related Compounds

  • Sulphur trioxide-trimethylamine complex
  • N,N-Dimethylethylamine sulfur trioxide complex
  • pyridine-SO3 complex
  • SULFUR TRIOXIDE-TRIETHYLAMINE COMPLEX
  • sulfur trioxide
  • sulfur trioxide compound with trichlorostibane (1:1)
  • 1,1-Dimethylethyl (2S)-2-[[(1-methylpropyl)amino]carbonyl]-1-pyrrolidinecarboxylate
  • tert-butyl (S)-2-(ethyl(m-tolyl)carbamoyl)pyrrolidine-1-carboxylate
  • 4-methoxy-6-((tetrahydro-2H-pyran-4-yl)oxy)pyridin-3-amine
  • (S)-3-Iodo-7-methyl-6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one
  • 2,7-Diazaspiro[4.4]nonane-2-ethanol
  • 4,6-dichloro-N-(2-ethyl-4,5,6,7-tetrahydro-1,3-benzothiazol-7-yl)-N-methylpyridine-2-carboxamide
  • N-[2-(2,3-Dihydro-2-methyl-1H-indol-1-yl)-2-oxoethyl]-4-fluorobenzamide
  • 5-Methoxy-3'-(trifluoromethyl)biphenyl-2-carbaldehyde
  • N-(3,5-Dichlorophenyl)-2-[[[(1-methylethyl)amino]carbonyl]amino]acetamide
  • 4-Bromo-5-(bromomethyl)-2-chloro-3-(difluoromethyl)pyridine
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