Choline O-Sulfate
Grundinformationen
- CAS
4858-96-2- Standard-SMILES
C[N+](C)(C)CCOS(=O)(=O)[O-]- InChIKey
WXCQAWGXWVRCGP-UHFFFAOYSA-N- Summenformel
- C5H13NO4S
- Durchschnittliche Molmasse
- 183,23 g/mol
- Monoisotopische Masse
- 183,05652907
Überblick
Choline sulfate is an ammonium betaine that is the conjugate base of choline hydrogen sulfate, obtained by deprotonation of the sulfate OH group. It is a member of choline sulfates and an ammonium betaine. It is a conjugate base of a choline hydrogen sulfate.
Namen und Bezeichner
- Bevorzugter Name
- Choline O-Sulfate
- IUPAC
- 2-(trimethylazaniumyl)ethyl sulfate
- Englischer Name
- Choline sulphate
- Summenformel
- C5H13NO4S
- Molmasse
- 183.22
Namen und Synonyme
choline sulfate4858-96-2Choline O-sulfate2-(trimethylammonio)ethyl sulfateNSC-462429Q5XI11K27CHEBI:16822DTXSID70274271Ethanaminium, N,N,N-trimethyl-2-(sulfooxy)-, inner saltRefChem:125759DTXCID002257512-(trimethylazaniumyl)ethyl sulfate
Weitere Namen anzeigen
CHOLINE O-SULFATE D13Sulfate(inner salt)-Choline
choline sulfate betainecholine sulphateCholine-O-sulfatecholine O-sulphateCholinesulfuric acid.Choline O-sulfate -SCHEMBL339063UNII-9Q5XI11K27
Datenbank-Bezeichner
- CAS
4858-96-2- PubChem CID
- 485
- DTXSID
DTXSID70274271- ChEBI
CHEBI:16822- UNII
- 9Q5XI11K27
- Nikkaji
- J814.134G
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- -0,9
- Polarare Oberfläche (TPSA)
- 74,8 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 4
- Frei drehbare Bindungen
- 3
- Schwere Atome
- 11
- Formalladung
- 0
- Komplexität
- 184
Physikochemische Eigenschaften
- Löslichkeit
- Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
- Aggregatzustand
- Cryst.
Chemie und Industrie
Pharmakologische Informationen
MeSH Pharmacological Classification
Endogenous factors or drugs that increase the transport and metabolism of LIPIDS including the synthesis of LIPOPROTEINS by the LIVER and their uptake by extrahepatic tissues.
Drugs used to specifically facilitate learning or memory, particularly to prevent the cognitive deficits associated with dementias. These drugs act by a variety of mechanisms.
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