| Company Name: |
Energy Chemical Gold |
| Tel: |
400-0056266 |
| Email: |
marketing1@energy-chemical.com |
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| | Sulfur trioxide trimethylamine complex Basic information |
| Product Name: | Sulfur trioxide trimethylamine complex | | Synonyms: | SULFUR TRIOXIDE TRIMETHYLAMINEOMPLEX;TRIMETHYLAMINE SULFUR TRIOXIDE;TRLIMETHYLAMINE SULPHUR TRIOXIDE COMPLEX;Sulphur trioxide trimethyl amine complex 95%;Trimethylamine-sulphur trioxide complex;sulphur trioxide--trimethylamine (1:1);Methanamine, N,N-dimethyl-, compd. with sulfur trioxide (1:1);Sulfur trioxide campd. with trimethylamine | | CAS: | 3162-58-1 | | MF: | C3H9NO3S | | MW: | 139.17 | | EINECS: | 221-614-7 | | Product Categories: | | | Mol File: | 3162-58-1.mol |  |
| | Sulfur trioxide trimethylamine complex Chemical Properties |
| Melting point | 232 °C (dec.) (lit.) | | solubility | DMSO (Slightly), Methanol (Slightly) | | form | Powder | | color | White to off-white | | Water Solubility | Soluble in hot water and ethanol. Slightly soluble in dimethyl sulfoxide and methanol. Insoluble in water. | | Sensitive | Moisture Sensitive | | BRN | 3681759 | | InChI | InChI=1S/C3H9N.O3S/c2*1-4(2)3/h1-3H3; | | InChIKey | DXASQZJWWGZNSF-UHFFFAOYSA-N | | SMILES | N(C)(C)C.S(=O)(=O)=O |
| Hazard Codes | C | | Risk Statements | 34 | | Safety Statements | 26-36/37/39-45 | | RIDADR | UN 3261 8/PG 2 | | WGK Germany | 3 | | F | 3-9-21 | | Hazard Note | Corrosive/Moisture Sensitive | | HazardClass | 8 | | PackingGroup | II | | HS Code | 29211990 | | Storage Class | 11 - Combustible Solids |
| | Sulfur trioxide trimethylamine complex Usage And Synthesis |
| Chemical Properties | White powder. Soluble in hot water, ethanol; soluble with
difficulty in cold water and acetone; not dissociated
in benzene and chloroform solutions; distinctly different
from the isomeric adduct of trimethylamine
oxide and sulfur dioxide. | | Uses | Reactant for sulfation reactions involving:
- Synthesis of sulfate-conjugated resveratrol metabolites
- Chitooligosaccharides used for anti-HIV-1 activity
- Dodecyl thioglycopyranoside used as a surfactant for enantiomeric separation
- Glycosaminoglycans which facilitate activation of signaling pathways dependent on sulfation pattern
- Polysaccharides as heparan sulfate mimetics
Nucleophile for the synthesis of α-tosyloxy ketones | | Uses | Separation of isomers, soil sterilant, catalyst for
thermosetting resins. | | reaction suitability | reagent type: oxidant |
| | Sulfur trioxide trimethylamine complex Preparation Products And Raw materials |
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