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
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3993165
Assay:
≥95% sulfur basis
Form:
powder
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
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
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Effect of hexadimethrine bromide on the conversion of 4-14C-progesterone into aldosterone and corticosterone by rat adrenals.
A G Fazekas et al.
Steroids, 9(5), 499-506 (1967-05-01)
Deepika Vaidyanathan et al.
Glycobiology, 30(11), 847-858 (2020-04-19)
The chemoenzymatic synthesis of heparin, through a multienzyme process, represents a critical challenge in providing a safe and effective substitute for this animal-sourced anticoagulant drug. D-glucuronyl C5-epimerase (C5-epi) is an enzyme acting on a heparin precursor, N-sulfoheparosan, catalyzing the reversible
SULFATION PATHWAYS: Potential benefits of a sulfated resveratrol derivative for topical application.
Marta Correia-da-Silva et al.
Journal of molecular endocrinology, 61(2), M27-M39 (2018-03-29)
Resveratrol (RSV) is a polyphenolic compound with antioxidant, anti-inflammatory and anti-aging properties partly associated with sirtuin 1 (SIRT1)-activation in the skin. However, poor water solubility may limit RSV efficacy. This work aimed to clarify the interest of a new synthetic
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 84739-50G | 04061833555996 |
| 84739-10G | 04061833433218 |