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HCID 222301Erstellt: 27. Oktober 2026

Sulfur trioxide triethylamine complex

TriethylAmine Sulfur Trioxide · NSC 8168 · NSC 68185 · fur trioxide triethyL · Triethylammonium trioxide copolymer · N,N-Diethylethanamine sulfur trioxide · TRIETHYLAMINE-SULFUR TRIOXIDE COMPLEX · Sulfur trioxide-triethylamine complex

https://huagongshe.com/de/chemical/222301

Molekülstruktur von Sulfur trioxide triethylamine complex

Identifikatoren & physikalische Daten

CAS No.761-01-3
SummenformelC6H15NO3S
Durchschnittliche Molmasse181,26 g/mol
Monoisotopische Masse181,07726434 g/mol
SMILESCCN(CC)CC.O=S(=O)=O
InChIKeyYYHPEVZFVMVUNJ-UHFFFAOYSA-N
PubChem CID222301
EC No.629-333-5
DTXSIDDTXSID90278539

Chemische & physikalische Eigenschaften

Polarare Oberfläche (TPSA)55,5
H-Brücken-Donoren0
H-Brücken-Akzeptoren4
Frei drehbare Bindungen3
Schwere Atome11
Formalladung0
Komplexität87,5
Schmelzpunkt~85 °C
Lagerbedingungen2-8°C
LöslichkeitChloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
Aggregatzustandpowder to crystal
FarbeWhite to Light yellow to Light orange
BRN3993165
InChIInChI=1S/C6H15N.O3S/c1-4-7(5-2)6-31-4(2)3/h4-6H2,1-3H3
InChIKeyYYHPEVZFVMVUNJ-UHFFFAOYSA-N
SMILESS(=O)(=O)=O.N(CC)(CC)CC

Sicherheit & Vorschriften

GHS-EinstufungDangerH314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 40 reports by companies from 2 notifications to the ECHA C&L Inventory.
Hazard Classes and CategoriesSkin Corr. 1B (100%)
F3-10-21
Wassergefährdungsklasse (WGK)3
UN-TransportnummerUN 3261 8/PG 2
Zollcode29211990
R-Sätze (R)34
GefahrensymboleC
Sicherheitshinweise (S)26-36/37/39-45
Gefahrenklasse8
VerpackungsgruppeII

Anwendungen & Verwendung

Verwenden

Reactant for reagent for synthesis of:Anticoagulant and antiplatelet persulfated glycosides or flavonoids containing an oligopolysulfated moietyNarciclasine derivatives for use as anticancer agentsSulfate-conjugated methylprednisolone for use as a colon-specific prodrugTetrasaccharide substrates of heparanase by glycosylation of disaccharidesSynthetic heparin oligosaccharide microarrays for analysis of heparin-protein interactionsDexamethasone 21-sulfate sodium for use as a colon-specific prodrug