Substance
ID:327264
Names and Identifiers
IUPAC name
sulfonylideneoxidane; trimethylamine
IUPAC Traditional name
sulfur trioxide; trimethylamine
Synonyms
Trimethylamine sulfur trioxide complex硫磺三氧三甲胺联合体Sulfur trioxide trimethylamine complexNSC 9838三甲基铵三氧化硫共聚物
Registration numbers
EC Number
MDL Number
Beilstein Number
CAS Number
PubChem SID
Properties
Safety Information
GHS Pictograms
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
RID/ADR
UN 3261 8/PG 2
UN Number
3261
Safety Statements
26-36/37/39-45
Hazard Class
8
GHS Hazard statements
H314
Packing Group
2
GHS Signal Word
Danger
European Hazard Symbols
Corrosive (C)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
Risk Statements
34
GHS Precautionary statements
P280-P305+P351+P338-P310
MSDS Link
German water hazard class
3
Product Information
Linear Formula
(CH3)3N · SO3
Physical Property
Melting Point
232 °C (dec.)(lit.)
Molecule Details
Packaging
5, 100, 500 g in glass bottle
Application
Reactant for sulfation reactions involving:
• Synthesis of sulfate-conjugated resveratrol metabolites1
• Chitooligosaccharides used for anti-HIV-1 activity2
• Dodecyl thioglycopyranoside used as a surfactant for enantiomeric separation3
• Glycosaminoglycans which facilitate activation of signaling pathways dependent on sulfation pattern4
• Polysaccharides as heparan sulfate mimetics5Nucleophile for the synthesis of α-tosyloxy ketones6
5, 100, 500 g in glass bottle
Application
Reactant for sulfation reactions involving:
• Synthesis of sulfate-conjugated resveratrol metabolites1
• Chitooligosaccharides used for anti-HIV-1 activity2
• Dodecyl thioglycopyranoside used as a surfactant for enantiomeric separation3
• Glycosaminoglycans which facilitate activation of signaling pathways dependent on sulfation pattern4
• Polysaccharides as heparan sulfate mimetics5Nucleophile for the synthesis of α-tosyloxy ketones6
Molecular Spectra
No Data Available
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References
No Data Available
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