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Merck

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:
Peso molecular:
181.25
Beilstein/REAXYS Number:
3993165
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22

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

Related product

Referencia del producto
Descripción
Precios

pictograms

Corrosion

signalword

Danger

hcodes

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


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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)
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
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
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
E.E. Gilbert
Chemical Reviews, 62, 549-549 (1962)

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