Trimethylammoniumchlorid

Trimethylazanium;chloride

HCID 11649CAS 593-81-7

Grundinformationen

Standard-SMILES
C[NH+](C)C.[Cl-]
InChIKey
SZYJELPVAFJOGJ-UHFFFAOYSA-N
Summenformel
C3H10ClN
Durchschnittliche Molmasse
95,57 g/mol

Überblick

See also: Trimethylamine Hydrochloride (preferred).

Namen und Bezeichner

Bevorzugter Name
Trimethylazanium;chloride
IUPAC
trimethylazanium chloride
Lokaler Name
Trimethylammoniumchlorid
Englischer Name
Trimethylamine hydrochloride
Summenformel
C3H10ClN
Molmasse
95.57

Namen und Synonyme

trimethylazanium;chlorideUW38SRM77KNS00077221TRIMETHYLAMMONIUM CHLORIDETRIMETHYLAMINE HCLFEMA 3241Trimthylamine bydrochlorideN, N-DIMETHYLMETHYLAMINE HCLTrimethylamine monohydrochlorideTrimethylammonium monohydrochlorideMethanamine,N,N-dimethyl-,hydrochlorideHJ 1042-2019)
Weitere Namen anzeigen
TrimethylamineHcl99%

Datenbank-Bezeichner

CAS
593-81-7
PubChem CID
11649

Eigenschaften

Berechnete Struktureigenschaften

Polarare Oberfläche (TPSA)
4,4 Ų
H-Brücken-Donoren
1
H-Brücken-Akzeptoren
1
Frei drehbare Bindungen
0
Schwere Atome
5

Physikochemische Eigenschaften

Schmelzpunkt
283 · 283-284 °C (dec.)(lit.)
Siedepunkt
132.32 °C · 132.32°C (rough estimate)
Dichte
0.9337 · 0.9337 (rough estimate)
Dampfdruck
0 Pa · 0Pa at 25℃
Brechungsindex
1.4413 · 1.4413 (estimate)
storage temp.
30 °C · Store below +30°C.

Sicherheit und Regulatorisches

Sicherheitsdaten

F
3-10
wgk
1
tsca
TSCA listed
hs_code
29211190
RTECS-Nr.
YH2700000
risk_code
36/37/38-38-36

Chemie und Industrie

Anwendungen · 1 Eintrag

VerwendenTrimethylamine hydrochloride is used in the manufacture of quaternary ammonium compounds, as insect attractant. It is also used as a raw material for the synthesis of choline chloride and ion exchange resins. Additionally, It acts as a cationic starch reagent, phase transfer catalyst, oil field chemicals, warning agent for natural gas and flotation agent.

Darstellung · 1 Eintrag

synthetischeTrimethylamine hydrochloride can be synthesized through the reaction of trimethylamine (TMA) and hydrochloric acid (HCl). The synthesis reaction can be written as follows:C3H9N+ HCl → C3H10ClNThe following steps are involved in obtaining trimethylamine hydrochloride:Step 1: Evaporation of hydrochloric acid solution The hydrochloric acid solution is evaporated, first over a free flame, and later on a steam bath. This process results in concentration of the solution, which aids in the formation of trimethylamine hydrochloride crystals.Step 2: Crystal formation and filtration As the solution becomes more and more concentrated, the trimethylamine hydrochloride crystals begin to form. The crystals are filtered periodically to remove them from the solution.Step 3: Drying The filtered crystals are dried in an air bath for a few minutes, with a temperature range of 100-110°.Step 4: Storage The air-dried crystals are then stored in a tightly closed bottle.Step 5: Centrifugation (optional) If the trimethylamine hydrochloride crystals are centrifuged, the product is obtained pure and dry.Overall, four runs yield an average of 710 g of pure trimethylamine hydrochloride and 82 g of slightly yellow-tinted product. This yield is equivalent to 89% of the theoretical amount based on ammonium chloride. The slight yellow coloration results from the evaporation of the last traces of solution.DOI: 10.15227/orgsyn.001.0079

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Ergänzende Hinweise

DefinitionChEBI: Trimethylamine hydrochloride is a hydrochloride salt formed by reaction of equimolar amounts of trimethylamine and hydrogen chloride. It contains a trimethylammonium.

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