Trimethylazanium;chloride

HCID 11649

Basic information

CAS
593-81-7
Standard SMILES
C[NH+](C)C.[Cl-]
InChIKey
SZYJELPVAFJOGJ-UHFFFAOYSA-N
Molecular formula
C3H10ClN
Average molar mass
95.57 g/mol

Overview

See also: Trimethylamine Hydrochloride (preferred).

Names & identifiers

Preferred name
Trimethylazanium;chloride
IUPAC
trimethylazanium chloride
English name
Trimethylamine hydrochloride
Molecular formula
C3H10ClN
Molecular weight
95.57

Names & synonyms

trimethylazanium;chlorideUW38SRM77KNS00077221TRIMETHYLAMMONIUM CHLORIDETRIMETHYLAMINE HCLFEMA 3241Trimthylamine bydrochlorideN, N-DIMETHYLMETHYLAMINE HCLTrimethylamine monohydrochlorideTrimethylammonium monohydrochlorideMethanamine,N,N-dimethyl-,hydrochlorideHJ 1042-2019)
Show more names
TrimethylamineHcl99%

Database identifiers

CAS
593-81-7
PubChem CID
11649

Properties

Computed structural properties

Topological polar surface area
4.4 Ų
Hydrogen bond donors
1
Hydrogen bond acceptors
1
Rotatable bonds
0
Heavy atoms
5

Physicochemical properties

Melting point
283 · 283-284 °C (dec.)(lit.)
Boiling point
132.32 °C · 132.32°C (rough estimate)
Density
0.9337 · 0.9337 (rough estimate)
vapor pressure
0 Pa · 0Pa at 25℃
refractive index
1.4413 · 1.4413 (estimate)
storage temp.
30 °C · Store below +30°C.

Safety & regulation

Safety data

F
3-10
PPE
dust mask type N95 (US), Eyeshields, Gloves
wgk
1
tsca
TSCA listed
rtecs
YH2700000
hs_code
29211190

Chemistry & industry

Applications · 1 item

UsesTrimethylamine 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.

Preparation methods · 1 item

PreparationTrimethylamine 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

Suppliers100 total

国药集团化学试剂有限公司86-21-63210123 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
衢州润东化工有限公司0570-8789886 18892685668 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
爱斯特(成都)生物制药股份有限公司+86-28-85122536 85324413 · [email protected]

Additional notes

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

Related reactions

5 records

Compound notes

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