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Sulfur trioxide-trimethylamine complex, 95%

CAS: 3162-58-1 | C3H9NO3S | 139.17 g/mol

$75.19 - $637.27

Chemical Identifiers

CAS 3162-58-1
Molecular Formula C3H9NO3S
Molecular Weight (g/mol) 139.17
MDL Number MFCD00012421
InChI Key DXASQZJWWGZNSF-UHFFFAOYSA-N
Synonym sulfur trioxide trimethylamine complex, sulfur trioxide trimethylamine, sulfur trioxide-trimethylamine complex, sulphur trioxide trimethylamine 1:1, sulfur trioxide-trimethylamine, trimethylamine sulfur trioxide, sulfur trioxide; trimethylamine, 1n1&1&&so3 complex, trimethylamine, compd. with sulfur trioxide 1:1, trimethylamine, compound with sulphur trioxide
PubChem CID 222852
IUPAC Name N,N-dimethylmethanamine;sulfur trioxide
SMILES CN(C)C.O=S(=O)=O
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Products 3
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AAL0030214
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Thermo Scientific Chemicals
L0030214
25 g
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AAL0030222
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Thermo Scientific Chemicals
L0030222
100 g
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AAL0030236
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Thermo Scientific Chemicals
L0030236
500 g
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Description

Description

Sulfur trioxide-trimethylamine complex acts as a reagent for sulfonation and sulfamation reactions. It is used as a reactant for the synthesis of sulfate-conjugated resveratrol metabolites and chitooligosaccharides. It is used in association with dodecyl thioglycopyranoside, which acts as a surfactant for enantiomeric separation. Further, it acts as a nucleophile used for the preparation of alfa-tosyloxy ketones.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Sulfur trioxide-trimethylamine complex acts as a reagent for sulfonation and sulfamation reactions. It is used as a reactant for the synthesis of sulfate-conjugated resveratrol metabolites and chitooligosaccharides. It is used in association with dodecyl thioglycopyranoside, which acts as a surfactant for enantiomeric separation. Further, it acts as a nucleophile used for the preparation of alfa-tosyloxy ketones.

Solubility
Soluble in hot water and ethanol. Slightly soluble in dimethyl sulfoxide and methanol. Insoluble in water.

Notes
Moisture sensitive. Incompatible with strong oxidizing agents.
Specifications

Chemical Identifiers

3162-58-1
139.17
DXASQZJWWGZNSF-UHFFFAOYSA-N
222852
CN(C)C.O=S(=O)=O
C3H9NO3S
MFCD00012421
sulfur trioxide trimethylamine complex, sulfur trioxide trimethylamine, sulfur trioxide-trimethylamine complex, sulphur trioxide trimethylamine 1:1, sulfur trioxide-trimethylamine, trimethylamine sulfur trioxide, sulfur trioxide; trimethylamine, 1n1&1&&so3 complex, trimethylamine, compd. with sulfur trioxide 1:1, trimethylamine, compound with sulphur trioxide
N,N-dimethylmethanamine;sulfur trioxide

Specifications

3162-58-1
C3H9NO3S
MFCD00012421
UN3261
Moisture sensitive
Soluble in hot water and ethanol. Slightly soluble in dimethyl sulfoxide and methanol. Insoluble in water.
CN(C)C.O=S(=O)=O
139.17
139.17
Sulfur trioxide-trimethylamine complex
∽235°C (decomposition)
(CH3)3N:SO3
25 g
3681759
sulfur trioxide trimethylamine complex, sulfur trioxide trimethylamine, sulfur trioxide-trimethylamine complex, sulphur trioxide trimethylamine 1:1, sulfur trioxide-trimethylamine, trimethylamine sulfur trioxide, sulfur trioxide; trimethylamine, 1n1&1&&so3 complex, trimethylamine, compd. with sulfur trioxide 1:1, trimethylamine, compound with sulphur trioxide
DXASQZJWWGZNSF-UHFFFAOYSA-N
N,N-dimethylmethanamine;sulfur trioxide
222852
95%
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Safety and Handling

Safety and Handling

GHS H Statement
H314-H318
Causes severe skin burns and eye damage.
Causes serious eye damage.

P260-P264b-P270-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P501c

H302-H314

DOTInformation : Transport Hazard Class: 8; Packing Group: II; Proper Shipping Name: CORROSIVE SOLID, ACIDIC, ORGANIC, N.O.S.

EINECSNumber : 221-614-7

TSCA : No

Recommended Storage : Ambient temperatures

SDS
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RUO – Research Use Only