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Merck
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84739

Sigma-Aldrich

Sulfur trioxide triethylamine complex

technical, ≥95% sulfur basis

Sinónimos:

NSC 68185, NSC 8168, Triethylamine sulfur trioxide complex

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About This Item

Fórmula lineal:
(CH3CH2)3N · SO3
Número de CAS:
761-01-3
Peso molecular:
181.25
Beilstein/REAXYS Number:
3993165
MDL number:
MFCD00043315
UNSPSC Code:
12352116
PubChem Substance ID:
57653022
NACRES:
NA.22

grade

technical

Quality Level

100

assay

≥95% sulfur basis

form

powder

reaction suitability

reagent type: oxidant

mp

~85 °C

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

related product

Referencia del producto
Descripción
Precios

911992

TBSAB, ≥95%

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Certificados de análisis (COA)

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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
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)
Cátia Vilas-Boas et al.
Marine drugs, 18(10) (2020-10-01)
Marine biofouling represents a global economic and ecological challenge and few eco-friendly antifouling agents are available. The aim of this work was to establish the proof of concept that a recently synthesized nature-inspired compound (gallic acid persulfate, GAP) can act
Tarek M Bedair et al.
Colloids and surfaces. B, Biointerfaces, 181, 174-184 (2019-05-28)
Drug-eluting stents (DESs) have been used for the treatment of cardiovascular diseases including stenosis. However, in-stent restenosis, thrombosis, and delayed re-endothelialization represent challenges for their clinical applications. Here, we demonstrate a novel work to overcome these limitations through surface modification
Irshad Ahmad et al.
International journal of biological macromolecules, 119, 360-368 (2018-07-17)
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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