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
Show more names
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
- Formal charge
- 0
- Complexity
- 8
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.
- solubility
- SOLUBLE
- form
- Crystalline Powder
- color
- White to slightly cream
- PH
- 5 · 5 (100g/l, H2O, 20℃)
- Water Solubility
- SOLUBLE
- Sensitive
- Hygroscopic
- Merck
- 14 · 14,9710
- BRN
- 3905063 · 3905063
- Stability
- Hygroscopic
- InChI
- 1S/C3H9N.ClH/c1-4(2)3;/h1-3H3;1H
- InChIKey
- SZYJELPVAFJOGJ-UHFFFAOYSA-N
- SMILES
- Cl[H].CN(C)C
- LogP
- -2.25 at · -2.25 at 25℃
- CAS DataBase Reference
- 593 · 593-81-7(CAS DataBase Reference)
- FDA UNII
- 38 SRM77K · UW38SRM77K
- NIST Chemistry Reference
- Methanamine,n,n-dimethyl-,hydrochloride(593-81-7)
- EPA Substance Registry System
- Trimethylamine hydrochloride (593-81-7)
- UNSPSC Code
- 85151701 · 85151701
- NACRES
- 24 · NA.24
- Symbol(GHS)
- 7 · GHS07
- Signal word
- Warning
- Hazard statements
- 315 · H315-H319
- Precautionary statements
- 264 · P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313
- PPE
- 95 · dust mask type N95 (US), Eyeshields, Gloves
- Hazard Codes
- Xi
- Risk Statements
- 36 · 36/37/38-38-36
- Safety Statements
- 26 · 26-36-37/39
- WGK Germany
- 1 · 1
- RTECS
- 2700000 · YH2700000
- F
- 3 · 3-10
- TSCA
- TSCA listed
- HS Code
- 29211190 · 29211190
- Storage Class
- 11 · 11 - Combustible Solids
- Hazard Classifications
- 2 Skin · Eye Irrit. 2Skin Irrit. 2
- Hazardous Substances Data
- 593 · 593-81-7(Hazardous Substances Data)
- Toxicity
- 50 orally · LD50 orally in Rabbit: 3090 mg/kg
- REACH Registrations
- Active
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
- Toxicity
- LD50 orally in Rabbit: 3090 mg/kg
- risk_code
- 36/37/38-38-36
- Signal word
- Warning
- Symbol(GHS)
- GHS07
- hazard_code
- Xi
- safety_code
- 26-36-37/39
- Storage Class
- 11 - Combustible Solids
- Hazard statements
- H315-H319
- REACH Registrations
- Active
- Hazard Classifications
- Eye Irrit. 2Skin Irrit. 2
- Precautionary statements
- P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313
- Hazardous Substances Data
- 593-81-7(Hazardous Substances Data)
Chemistry & industry
Applications
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
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
Upstream & downstream products
Upstream raw materials
Downstream products
Suppliers100 total
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
Compound notes
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