84739
Sulfur trioxide triethylamine complex
technical, ≥95% sulfur basis
Synonym(s):
NSC 68185, NSC 8168, Triethylamine sulfur trioxide complex
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About This Item
Linear Formula:
(CH3CH2)3N · SO3
CAS Number:
Molecular Weight:
181.25
Beilstein:
3993165
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22
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grade
technical
Quality Level
Assay
≥95% sulfur basis
form
powder
reaction suitability
reagent type: oxidant
mp
~85 °C
functional group
amine
storage temp.
2-8°C
SMILES string
O=S(=O)=O.CCN(CC)CC
InChI
1S/C6H15N.O3S/c1-4-7(5-2)6-3;1-4(2)3/h4-6H2,1-3H3;
InChI key
YYHPEVZFVMVUNJ-UHFFFAOYSA-N
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Application
Reactant for reagent for synthesis of:
- Anticoagulant and antiplatelet persulfated glycosides or flavonoids containing an oligopolysulfated moiety
- Narciclasine derivatives for use as anticancer agents
- Sulfate-conjugated methylprednisolone for use as a colon-specific prodrug
- Tetrasaccharide substrates of heparanase by glycosylation of disaccharides
- Synthetic heparin oligosaccharide microarrays for analysis of heparin-protein interactions
- Dexamethasone 21-sulfate sodium for use as a colon-specific prodrug
Other Notes
Reagent used for the sulfation of alcohols and other compounds
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Product No.
Description
Pricing
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Currently available anticoagulants for prevention and treatment of thrombosis have several limitations, thus, small organic scaffolds that can dissolve clots in vivo in a dose dependent manner with lesser side effects are highly desirable. Here we report the synthesis of
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E.E. Gilbert
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