Trimethylamine

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Trimethylamine[1]
Skeletal formula of trimethylamine with all implicit hydrogens shown
Skeletal formula of trimethylamine with all implicit hydrogens shown
Ball and stick model of trimethylamine
Ball and stick model of trimethylamine
Spacefill model of trimethylamine
Spacefill model of trimethylamine
Names
Preferred IUPAC name
N,N-Dimethylmethanamine
Other names
(Trimethyl)amine (The name trimethylamine is deprecated.)[2]
Identifiers
3D model (JSmol)
956566
ChEBI
ChEMBL
ChemSpider
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EC Number
  • 200-875-0
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KEGG
RTECS number
  • PA0350000
UNII
UN number 1083
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  • InChI=1S/C3H9N/c1-4(2)3/h1-3H3 checkY
    Key: GETQZCLCWQTVFV-UHFFFAOYSA-N checkY
  • CN(C)C
Properties
C3H9N
Molar mass 59.112 g·mol−1
Appearance Colorless gas
Odor Fishy, ammoniacal
Density 670 kg m−3 (at 0 °C)
627.0 kg m−3 (at 25 °C)
Melting point −117.20 °C; −178.96 °F; 155.95 K
Boiling point 3 to 7 °C; 37 to 44 °F; 276 to 280 K
Miscible
log P 0.119
Vapor pressure 188.7 kPa (at 20 °C)[3]
95 μmol Pa−1 kg−1
Basicity (pKb) 4.19
0.612 D
Thermochemistry
−24.5 to −23.0 kJ mol−1
Hazards
GHS labelling:
GHS02: Flammable GHS05: Corrosive GHS07: Exclamation mark
Danger
H220, H315, H318, H332, H335
P210, P261, P280, P305+P351+P338
NFPA 704 (fire diamond)

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2
4
0
Flash point −7 °C (19 °F; 266 K)
190 °C (374 °F; 463 K)
Explosive limits 2–11.6%
Lethal dose or concentration (LD, LC):
500 mg kg−1 (oral, rat)
NIOSH (US health exposure limits):
PEL (Permissible)
 none[4]
REL (Recommended)
 TWA 10 ppm (24 mg/m3) ST 15 ppm (36 mg/m3)[4]
IDLH (Immediate danger)
 N.D.[4]
Related compounds
Related amines
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Trimethylamine (TMA) is an organic compound with the formula N(CH3)3. It is a trimethylated derivative of ammonia. TMA is widely used in industry.[5][6] At higher concentrations it has an ammonia-like odor, and can cause necrosis of mucous membranes on contact.[7] At lower concentrations, it has a "fishy" odor, the odor associated with rotting fish.

Physical and chemical properties

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TMA is a colorless, hygroscopic, and flammable tertiary amine. It is a gas at room temperature but is usually sold as a 40% solution in water. It is also sold in pressurized gas cylinders.

TMA protonates to give the trimethylammonium cation. Trimethylamine is a good nucleophile, and this reactivity underpins most of its applications. Trimethylamine is a Lewis base that forms adducts with a variety of Lewis acids.[8]

Production

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Industry and laboratory

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Trimethylamine is prepared by the reaction of ammonia and methanol employing a catalyst:[5]

3 CH3OH + NH3 → (CH3)3N + 3 H2O

This reaction coproduces the other methylamines, dimethylamine (CH3)2NH and methylamine CH3NH2.

Trimethylammonium chloride has been prepared by a reaction of ammonium chloride and paraformaldehyde:[9]

9 (CH2=O)n + 2n NH4Cl → 2n (CH3)3N•HCl + 3n H2O + 3n CO2

Biosynthesis

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Trimethylamine is produced by several[which?] routes in nature. Well studied are the degradation of choline and carnitine.[10]

Applications

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Trimethylamine is used in the synthesis of choline, tetramethylammonium hydroxide, plant growth regulators, herbicides, strongly basic anion exchange resins, dye leveling agents and a number of basic dyes.[5][6] Gas sensors to test for fish freshness detect trimethylamine.

Toxicity

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In humans, ingestion of certain plant and animal (e.g., red meat, egg yolk) food containing lecithin, choline, and L-carnitine provides certain gut microbiota with the substrate to synthesize TMA, which is then absorbed into the bloodstream.[11][12] High levels of trimethylamine in the body are associated with the development of trimethylaminuria, or fish odor syndrome, caused by a genetic defect in the enzyme which degrades TMA; or by taking large doses of supplements containing choline or L-carnitine.[11][12] TMA is metabolized by the liver to trimethylamine N-oxide (TMAO); TMAO is being investigated as a possible proatherogenic substance which may accelerate atherosclerosis in those eating foods with a high content of TMA precursors.[12] TMA also causes the odor of some human infections, bad breath, and bacterial vaginosis.

Trimethylamine is a full agonist of human TAAR5,[13][14][15] a trace amine-associated receptor that is expressed in the olfactory epithelium and functions as an olfactory receptor for tertiary amines.[15][16] One or more additional odorant receptors appear to be involved in trimethylamine olfaction in humans as well.[16]

Acute and chronic toxic effects of TMA were suggested in medical literature as early as the 19th century. TMA causes eye and skin irritation, and it is suggested to be a uremic toxin.[17] In patients, trimethylamine caused stomach ache, vomiting, diarrhoea, lacrimation, greying of the skin and agitation.[18] Apart from that, reproductive/developmental toxicity has been reported.[7] Some experimental studies suggested that TMA may be involved in etiology of cardiovascular diseases.[19][20]

Guidelines with exposure limit for workers are available e.g. the Recommendation from the Scientific Committee on Occupational Exposure Limits by the European Union Commission.[21]

Trimethylaminuria

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Main article: Trimethylaminuria

Trimethylaminuria is an autosomal recessive genetic disorder involving a defect in the function or expression of flavin-containing monooxygenase 3 (FMO3) which results in poor trimethylamine metabolism. Individuals with trimethylaminuria develop a characteristic fish odor—the smell of trimethylamine—in their sweat, urine, and breath after the consumption of choline-rich foods. A condition similar to trimethylaminuria has also been observed in a certain breed of Rhode Island Red chicken that produces eggs with a fishy smell, especially after eating food containing a high proportion of rapeseed.[22][23]

In the history of psychoanalysis

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The first dream of his own which Sigmund Freud tried to analyse in detail, when he was developing his theories about the interpretation of dreams, involved a patient of Freud's who had been given an injection of trimethylamine in the dream, with the chemical formula of the substance, written in bold letters on the bottle, jumping out at Freud.[24]

See also

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References

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  1. ^ Merck Index, 11th Edition, 9625.
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    Table 2: Microbial metabolites: their synthesis, mechanisms of action, and effects on health and disease
    Figure 1: Molecular mechanisms of action of indole and its metabolites on host physiology and disease
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  24. ^ Sigmund Freud, Standard Ed., 4:116-119.
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