Grundinformationen
- Standard-SMILES
CCN(CC)CC.O=S(=O)=O- InChIKey
YYHPEVZFVMVUNJ-UHFFFAOYSA-N- Summenformel
- C6H15NO3S
- Durchschnittliche Molmasse
- 181,26 g/mol
- Monoisotopische Masse
- 181,07726434
Namen und Bezeichner
- Bevorzugter Name
- Sulfur trioxide triethylamine complex
- IUPAC
- N,N-diethylethanamine;sulfur trioxide
- Englischer Name
- Sulfur trioxide-triethylamine complex
- Summenformel
- C6H15N.O3S
- Molmasse
- 181.25
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
761-01-3- PubChem CID
- 222301
- DTXSID
DTXSID90278539- EC Number
- 629-333-5
Eigenschaften
Berechnete Struktureigenschaften
- Polarare Oberfläche (TPSA)
- 55,5 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 4
- Frei drehbare Bindungen
- 3
- Schwere Atome
- 11
- Formalladung
- 0
- Komplexität
- 87,5
Physikochemische Eigenschaften
- Schmelzpunkt
- 85 °C · ~85 °C
- storage temp.
- 2 · 2-8°C
- Löslichkeit
- Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
- Aggregatzustand
- powder to crystal
- Farbe
- White to Light yellow to Light orange
- BRN
- 3993165 · 3993165
- InChI
- InChI=1S/C6H15N.O3S/c1-4-7(5-2)6-3;1-4(2)3/h4-6H2,1-3H3;
- InChIKey
- YYHPEVZFVMVUNJ-UHFFFAOYSA-N
- SMILES
- S(=O)(=O)=O.N(CC)(CC)CC
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H314 (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.
Gefahrenhinweise
Sicherheitsdaten
- F
- 3-10-21
- wgk
- 3
- ridadr
- UN 3261 8/PG 2
- hs_code
- 29211990
- risk_code
- 34
- hazard_code
- C
- safety_code
- 26-36/37/39-45
- hazard_class
- 8
- packing_group
- II
Chemie und Industrie
Anwendungen
VerwendenReactant 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
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