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593-81-7

Basic Information
CAS No.: 593-81-7
Name: Trimethylamine hydrochloride
Molecular Structure:
Molecular Structure of 593-81-7 (Trimethylamine hydrochloride)
Formula: C3H10ClN
Molecular Weight: 95.5712 [g/mol]
Synonyms: Methanamine,N,N-dimethyl-, hydrochloride (9CI);Trimethylamine, hydrochloride (8CI);Trimethylamine hydrochloric acid;Trimethylamine monohydrochloride;Trimethylammonium chloride;
EINECS: 209-810-0
Density: 0.692g/cm3
Melting Point: 283-284 °C (dec.)(lit.)
Boiling Point: 2.8oC at 760 mmHg
Flash Point:
Solubility: Soluble in water
Appearance: white to slightly cream crystalline powder
Hazard Symbols: IrritantXi
Risk Codes: 36/37/38
Safety: 26-36-37/39
Transport Information:
PSA: 3.24000
LogP: 0.97980
Synthetic route
1184-78-7

trimethylamine-N-oxide

68-12-2, 33513-42-7

N,N-dimethyl-formamide

97-00-7

1-chloro-2,4-dinitro-benzene

A

51-28-5

2,4-Dinitrophenol

B

593-81-7

trimethylamine hydrochloride

Conditions
ConditionsYield
for 24h; Ambient temperature;A 97%
B 98%
1184-78-7

trimethylamine-N-oxide

97-00-7

1-chloro-2,4-dinitro-benzene

A

51-28-5

2,4-Dinitrophenol

B

593-81-7

trimethylamine hydrochloride

Conditions
ConditionsYield
In N,N-dimethyl-formamide for 24h; Ambient temperature;A 97%
B 98%
4637-24-5

N,N-dimethyl-formamide dimethyl acetal

593-81-7

trimethylamine hydrochloride

Conditions
ConditionsYield
Stage #1: N,N-dimethyl-formamide dimethyl acetal With [1,4-bis(diphenylphosphino)butane](1,5-cyclooctadiene)rhodium(I) tetrafluoroborate; hydrogen In methanol at 25℃; under 30003 Torr; Autoclave;
Stage #2: With hydrogenchloride In methanol; water Reagent/catalyst;
96%
50-00-0

formaldehyd

124-40-3

dimethyl amine

593-81-7

trimethylamine hydrochloride

Conditions
ConditionsYield
With oxalic acid at 100 - 120℃; Eschweiler-Clarke methylation;84%
67-56-1

methanol

593-81-7

trimethylamine hydrochloride

Conditions
ConditionsYield
Stage #1: methanol With ammonium hydroxide; Ag/TiO2 at 25℃; for 10h; UV-irradiation;
Stage #2: With hydrogenchloride In water
80%
68-12-2, 33513-42-7

N,N-dimethyl-formamide

593-81-7

trimethylamine hydrochloride

Conditions
ConditionsYield
With hydrogenchloride; lithium borohydride; chloro-trimethyl-silane In tetrahydrofuran for 24h; Ambient temperature;72%
Stage #1: N,N-dimethyl-formamide With tris(bis(trimethylsilyl)amido)lanthanum(III); 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane In benzene at 25℃; for 1h; Inert atmosphere; Glovebox;
Stage #2: With hydrogenchloride In methanol at 0℃;
50%
Stage #1: N,N-dimethyl-formamide With tris((4,4-dimethyl-2-oxazolinyl)phenylborate) MgMe; 4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane
Stage #2: With hydrogenchloride
18%
146475-62-9

cyclopropanesulfonyl-1-d chloride

67-63-0

isopropyl alcohol

75-50-3

trimethylamine

A

593-81-7

trimethylamine hydrochloride

B

146475-51-6

propan-2-yl cyclopropanesulfonate

C

N,N-dimethylcyclopropanesulfonamide-1-d

Conditions
ConditionsYield
In dichloromethane at 25℃; for 36h;A n/a
B 11.7%
C 27.4%
88470-26-2

N,N-dimethoxyamine

75-50-3

trimethylamine

A

593-81-7

trimethylamine hydrochloride

B

75-57-0

tetramethlyammonium chloride

Conditions
ConditionsYield
With tert-butylhypochlorite In diethyl ether 1) -78 deg C, 0.5 h, 2) -8 deg C, 24 h;A 15.7%
B 22.8%

Cl2B-N(CH3)2*N(CH3)3

999-97-3

1,1,1,3,3,3-hexamethyl-disilazane

A

32882-72-7

Bis(trimethylsilyl)aminochlorodimethylaminoboran

B

593-81-7

trimethylamine hydrochloride

Conditions
ConditionsYield
In benzene stirring for 1 week in dry benzene; sepn. of trimethylamine hydrochloride and benzene;A 16%
B n/a
In benzene stirring for 1 week in dry benzene; sepn. of trimethylamine hydrochloride and benzene;A 16%
B n/a
108-88-3

toluene

6001-87-2

methyl 3-chloropropionate

75-50-3

trimethylamine

A

593-81-7

trimethylamine hydrochloride

B

16332-33-5

(2-methoxycarbonylethyl)trimethylammonium chloride

Conditions
ConditionsYield
at -5℃;
67-56-1

methanol

6001-87-2

methyl 3-chloropropionate

75-50-3

trimethylamine

A

593-81-7

trimethylamine hydrochloride

B

16332-33-5

(2-methoxycarbonylethyl)trimethylammonium chloride

Conditions
ConditionsYield
at -5℃;
60-29-7

diethyl ether

6001-87-2

methyl 3-chloropropionate

75-50-3

trimethylamine

A

593-81-7

trimethylamine hydrochloride

B

16332-33-5

(2-methoxycarbonylethyl)trimethylammonium chloride

Conditions
ConditionsYield
at -5℃;
542-76-7

3-Chloropropionitrile

64-17-5

ethanol

75-50-3

trimethylamine

A

593-81-7

trimethylamine hydrochloride

B

107-13-1

acrylonitrile

110-89-4

piperidine

120225-40-3

trimethyl-(3-oxo-3-phenyl-propenyl)-ammonium; chloride

A

4452-12-4

1-phenyl-3-(piperidin-1-yl)prop-2-en-1-one

B

593-81-7

trimethylamine hydrochloride

Conditions
ConditionsYield
In acetonitrile at 25℃; Rate constant;
110-89-4

piperidine

120225-39-0

trans-β-(p-nitrophenylsulfinyl)vinyltrimethylammonium chloride

A

593-81-7

trimethylamine hydrochloride

B

p-nitrophenyl β-piperidylaminovinyl sulfoxide

Conditions
ConditionsYield
In N,N-dimethyl-formamide at 25℃; Rate constant; further solvent;
110-89-4

piperidine

110065-18-4

trans-β-(p-nitrophenylsulfonyl)-vinyltrimethylammonium chloride

A

107415-63-4

β-piperidyl aminovinyl sulfone

B

593-81-7

trimethylamine hydrochloride

Conditions
ConditionsYield
In acetonitrile at 25℃; Rate constant;
67-56-1

methanol

56-93-9

benzyltrimethylammonium chloride

A

593-81-7

trimethylamine hydrochloride

B

103-29-7

1,1'-(1,2-ethanediyl)bisbenzene

C

108-88-3

toluene

D

100-51-6

benzyl alcohol

Conditions
ConditionsYield
at 30℃; for 2h; Irradiation; Further byproducts given;A 77 % Chromat.
B 32 % Chromat.
C 27 % Chromat.
D 45 % Chromat.
With water at 30℃; for 2h; Irradiation; Further byproducts given;A 77 % Chromat.
B 10 % Chromat.
C 27 % Chromat.
D 45 % Chromat.
at 30℃; for 2h; Irradiation; Further byproducts given;A 77 % Chromat.
B 10 % Chromat.
C 27 % Chromat.
D 45 % Chromat.
67-56-1

methanol

26050-72-6

(3,5-dimethoxybenzyl)trimethylammonium chloride

A

4179-19-5

1,3-dimethoxy-5-methylbenzene

B

73569-69-4

1-methylmethoxy-3,5-dimethoxybenzene

C

506-59-2

N,N-dimethylammonium chloride

D

593-81-7

trimethylamine hydrochloride

Conditions
ConditionsYield
at 30℃; for 2h; Irradiation;A 46 % Chromat.
B 12 % Chromat.
C 23 % Chromat.
D 77 % Chromat.
56-93-9

benzyltrimethylammonium chloride

A

506-59-2

N,N-dimethylammonium chloride

B

593-81-7

trimethylamine hydrochloride

C

103-29-7

1,1'-(1,2-ethanediyl)bisbenzene

D

108-88-3

toluene

E

100-51-6

benzyl alcohol

Conditions
ConditionsYield
With water In water at 30℃; for 2h; Mechanism; Irradiation; 253.7 nm;A 23 % Chromat.
B 77 % Chromat.
C 10 % Chromat.
D 27 % Chromat.
E 45 % Chromat.
56-93-9

benzyltrimethylammonium chloride

A

593-81-7

trimethylamine hydrochloride

B

103-29-7

1,1'-(1,2-ethanediyl)bisbenzene

C

108-88-3

toluene

D

100-51-6

benzyl alcohol

Conditions
ConditionsYield
With water at 30℃; for 2h; Irradiation; Further byproducts given;A 77 % Chromat.
B 10 % Chromat.
C 27 % Chromat.
D 45 % Chromat.
6608-47-5

vinylsulfonyl chloride

75-50-3

trimethylamine

A

7465-57-8

2-(N,N,N-trimethylamino)ethanesulfonate

B

593-81-7

trimethylamine hydrochloride

C

58928-02-2

Ethenesulfonic acid; compound with trimethyl-amine

Conditions
ConditionsYield
With potassium chloride; water In 1,2-dimethoxyethane at 1℃; Rate constant; Product distribution;
98821-29-5

trans-1-propene-1-sulfonyl chloride

75-50-3

trimethylamine

A

593-81-7

trimethylamine hydrochloride

B

94129-00-7

C6H15NO3S

C

(E)-Propene-1-sulfonic acid; compound with trimethyl-amine

Conditions
ConditionsYield
With potassium chloride; water In 1,2-dimethoxyethane at 1℃; Rate constant; Product distribution;
50-00-0

formaldehyd

ammonium chloride

A

64-18-6

formic acid

B

124-38-9

carbon dioxide

C

506-59-2

N,N-dimethylammonium chloride

D

593-81-7

trimethylamine hydrochloride

7647-01-0

hydrogenchloride

64-17-5

ethanol

29124-44-5

hydroxymethyl-trimethyl-ammonium; chloride

593-81-7

trimethylamine hydrochloride

29124-44-5

hydroxymethyl-trimethyl-ammonium; chloride

593-81-7

trimethylamine hydrochloride

Conditions
ConditionsYield
at 25℃; Geschwindigkeit der Zersetzung in Abhaengigkeit vom pH;

ethoxycarbonyl-trimethyl-ammonium; chloride

593-81-7

trimethylamine hydrochloride

polyoxymethylene

polyoxymethylene

593-81-7

trimethylamine hydrochloride

Conditions
ConditionsYield
With ammonium chloride at 120 - 170℃; analog lassen sich andere Ammoniumsalze anwenden;
64-17-5

ethanol

138-24-9

phenyltrimethylammonium chloride

platinum black

platinum black

A

110-82-7

cyclohexane

B

593-81-7

trimethylamine hydrochloride

Conditions
ConditionsYield
at 20 - 25℃; under 1520 - 2280 Torr; Hydrogenation;

ethylsulfanylcarbonyl-trimethyl-ammonium; chloride

A

124-38-9

carbon dioxide

B

593-81-7

trimethylamine hydrochloride

C

75-08-1

ethanethiol

75-21-8

oxirane

593-81-7

trimethylamine hydrochloride

67-48-1

choline chloride

Conditions
ConditionsYield
With sodium hydroxide at 24.9℃; Thermodynamic data; ΔrH1;100%
With sodium hydroxide at 24.9℃;100%
593-81-7

trimethylamine hydrochloride

603-33-8

triphenylbismuthane

7787-60-2

bismuth(III) chloride

Conditions
ConditionsYield
byproducts: benzene; heating (CH3)3NHCl with triphenyl bismuth at 130°C (also in presence of ethanol);;100%
byproducts: benzene; heating (CH3)3NHCl with triphenyl bismuth at 130°C (also in presence of ethanol);;100%
105931-10-0

Hf(C5(CH3)5)2(CH2CH(CH3)CH2)

593-81-7

trimethylamine hydrochloride

156278-76-1

(Hf(C5(CH3)5)2(CH2CH(CH3)2))Cl

Conditions
ConditionsYield
In dichloromethane-d2 to Hf-compd. and (HNMe3)Cl CD2Cl2 is vacuum transferred at -78°C(N2); tube is allowed to warm to 23°C and to stand with occasional shaking for 4 h;100%
72708-53-3

tris(trimethylsilylmethyl)gallium

593-81-7

trimethylamine hydrochloride

A

75-76-3

tetramethylsilane

B

72709-13-8

Ga(3+)*2CH2Si(CH3)3(1-)*Cl(1-)*N(CH3)3=Ga(CH2Si(CH3)3)2Cl*N(CH3)3

Conditions
ConditionsYield
In benzene under N2 or Ar mixt. in stoich. quantity stirred at room temp. for 2 h; volatile components removed by vac. distn., crude product sublimed at 32°C; elem. anal.;A 100%
B 98.5%
16872-09-6

1,2-dicarba-closo-dodecaborane(12)

593-81-7

trimethylamine hydrochloride

B9H11C2(2-)*2(CH3)3NH(1+)=[(CH3)3NH]2[B9H11C2]

Conditions
ConditionsYield
With KOH In ethanol; water B compd. (34.7 mmol) added to EtOH soln. of KOH (104 mmol), refluxed for4 h (TLC control), evapd., dissolved (H2O), excess Me3NHCl added; ppt. filtered off, dried;100%
593-81-7

trimethylamine hydrochloride

616-38-6

carbonic acid dimethyl ester

75-57-0

tetramethlyammonium chloride

Conditions
ConditionsYield
With 1-ethyl-3-methylimidazolium bromide at 169.84℃; for 8h;99%
With 1-ethyl-3-methylimidazolium bromide at 169.84℃; for 8h;
81476-76-8

dimethyl η5-cyclopentadienyl η5-pentamethylcyclopentadienyl zirconium

593-81-7

trimethylamine hydrochloride

[Zr(η5-cyclopentadienyl)(η5-pentamethylcyclopentadienyl)(CH3)Cl]

Conditions
ConditionsYield
In tetrahydrofuran stirring 4 days at room temp., evapn.; extn. (toluene), filtration, evapn., purity: 95% (NMR), analytically pure material obtained by repeated recrystn. (toluene/hexanes), elem. anal.;99%
In tetrahydrofuran
249284-51-3

[U(N(CH2CH2NSiMe2But)2(CH2CH2NSiMeButCH2))]

593-81-7

trimethylamine hydrochloride

183054-80-0

U[N(CH2CH2NSi(CH3)2(C(CH3)3))3]Cl

Conditions
ConditionsYield
In not given99%
31422-93-2

8,8'-μ-methylcarboniodioxy-bis(1,2-dicarbollido)-3-cobalt(1-)ate

593-81-7

trimethylamine hydrochloride

trimethyl ammonium 8,8'-dihydroxy-bis(1,2-dicarbollido)-3-cobalt(1-)ate

Conditions
ConditionsYield
With HCl In ethanol; water byproducts: CH3COOH; concd. HCl was added to suspn. of Co complex in aq. EtOH at 80°C;mixt. was shaken within ca. 30 min; Me3N*HCl in H2O was added; cooled overnight; septd.; crystd. at 80°C from MeCN by slow addition of CHCl3; cooled overnight; elem. anal.;99%
16853-85-3

lithium aluminium tetrahydride

593-81-7

trimethylamine hydrochloride

75-50-3

trimethylamine

17211-58-4, 50981-97-0, 60934-33-0

bis(trimethylamine)alane

Conditions
ConditionsYield
In diethyl ether under N2 or Ar; LiAlH4 and Me3NHCl cooled to -78°C; Et2O added; stirred; warmed to room temp.; 1 h; solvent removed in vac.; NMe3 gas condensed; stirred for 20 min; sublimed at 50°C into flask at -78°C;98%

cesium carba-closo-dodecaborate

593-81-7

trimethylamine hydrochloride

CB11Cl12(1-)*C3H9N*H(1+)

Conditions
ConditionsYield
Stage #1: cesium carba-closo-dodecaborate With antimonypentachloride at 180℃; for 168h; Inert atmosphere;
Stage #2: trimethylamine hydrochloride In water-d2
98%
50-00-0

formaldehyd

C4H24B22N2(2-)*2Cs(1+)

593-81-7

trimethylamine hydrochloride

C5H25B22N2(1-)*C3H9N*H(1+)

Conditions
ConditionsYield
Stage #1: formaldehyd With hydrogenchloride In 1,4-dioxane for 0.333333h; Inert atmosphere;
Stage #2: C4H24B22N2(2-)*2Cs(1+) In 1,4-dioxane; ethyl acetate for 3h; Inert atmosphere;
Stage #3: trimethylamine hydrochloride In 1,4-dioxane; water; ethyl acetate Inert atmosphere;
98%

di-μ-chlorobis[chloro(N,N'-bis-(2,6-(diisopropyl)phenyl)imidazol-2-ylidene)palladium]

593-81-7

trimethylamine hydrochloride

C27H36Cl3N2Pd(1-)*C3H9N*H(1+)

Conditions
ConditionsYield
In chloroform at 50℃; for 15h;98%

1.2H4N2*C5H19B9NS(1-)*H(1+)

593-81-7

trimethylamine hydrochloride

C3H9N*C5H19B9NS(1-)*H(1+)

Conditions
ConditionsYield
In water97%

C4H24B22N2(2-)*2Cs(1+)

593-81-7

trimethylamine hydrochloride

C4H24B22N2(1-)*C3H9N*H(1+)

Conditions
ConditionsYield
In water Inert atmosphere;97%

C4H24B22N2(2-)*2Cs(1+)

593-81-7

trimethylamine hydrochloride

2C3H9N*C4H24B22N2(2-)*2H(1+)

Conditions
ConditionsYield
In water Solvent;97%
634196-69-3

1,2-diphenyl-3-fluoro-1,2-closo-dodecacarborane

593-81-7

trimethylamine hydrochloride

[HN(CH3)3][3-fluoro-7,8-diphenyl-7,8-nido-undecacarborane]

Conditions
ConditionsYield
With KOH; CO2 In ethanol N2, a soln. of B compd. refluxed with KOH for 72 h, treated wit CO2, volatiles removed (vac.), dissolved (H2O), a soln. of N compd. (excess) added; ppt. extrd. (CH2Cl2), dried (MgSO4), evapd., recrystd. (CH2Cl2); elem. anal.;96.1%

dipotassium 7-(2-carboxybenzoylaminoethyl)-7,8-dicarba-nido-undecaborate(10)

593-81-7

trimethylamine hydrochloride

bis(trimethylammonium) 7-(2-carboxybenzoylaminoethyl)-7,8-dicarba-nido-undecaborate(10) monohydrate

Conditions
ConditionsYield
In not given cation metathesis react. of B compd. and Me3NHCl; recrystd. from water-EtOH: elem. anal.;96%
24034-98-8

1,2-(C6H5CH2)2-1,2-C2B10H10

593-81-7

trimethylamine hydrochloride

[Me3NH][7,8-(C6H5CH2)2-nido-7,8-C2B9H10]

Conditions
ConditionsYield
With KOH; HCl In methanol; water N2-atmosphere; stirring (0°C to room temp., 30 min), refluxing (overnight), evapn. H2O and HCl addn., pptn. on Me3NHCl addn.; filtering, washing (H2O), drying (vac.);96%

2-(2-trimethylsilylethynyl)-3,4-(o-carborano)-2,5-dihydrofuran

593-81-7

trimethylamine hydrochloride

2-ethynyl-3,4-(dodecahydro-nido-undecadicarbaborato)-2,5-dihydrofuran*trimethylammonium

Conditions
ConditionsYield
Stage #1: 2-(2-trimethylsilylethynyl)-3,4-(o-carborano)-2,5-dihydrofuran With sodium hydroxide In methanol for 1h; Reflux;
Stage #2: trimethylamine hydrochloride With hydrogenchloride In water
96%

potassium titanyl oxalate

10K(1+)*P2W17O61(10-)*99H2O = K10P2W17O61*99H2O

593-81-7

trimethylamine hydrochloride

TiOP2W17O61(8-)*8(CH3)3NH(1+) = ((CH3)3NH)8TiOP2W17O61

Conditions
ConditionsYield
In water a soln. of W-compound in NaOAc buffer (pH 5.25) was treated with Ti-compound at 65°C; stirred for 10 min; addn. of Me3NHCl at 25°C; precipitate washed (water), dried;;95%

(Me3NH)(1-H-CB9Cl9)

100-39-0

benzyl bromide

593-81-7

trimethylamine hydrochloride

(Me3NH)(1-C6H5CH2-CB9Cl9)

Conditions
ConditionsYield
With n-BuLi; NaOH In tetrahydrofuran; diethyl ether; water byproducts: Me3N; to THF soln. (Me3NH)(1-H-CB9Cl9) was slowly added n-BuLi in hexane at 0°C, mixt. was stirred at room temp. for 4 h and refluxed for 4 h,Me3N was removed, THF soln. PhCH2Br was added at 0°C, soln. was stirred for 4 h at room temp. and; refluxed overnight, solvent was removed, residue was treated with 5 % aq. NaOH, extd. with Et2O and treated with aq. Me3NHCl;95%
19610-39-0

1.2-dicarba-closo-dodecaborano-tetrahydrofurane

593-81-7

trimethylamine hydrochloride

[Me3NH][μ-7,8-CH2OCH2-7,8-C2B9H10]

Conditions
ConditionsYield
With KOH In ethanol (N2); KOH added to a soln. of B compd., refluxed overnight; solvent-removed, dissolved in H2O, pptd. ((CH3)3NHCl), filtered, washed (H2O), dried (vac.); elem. anal.;95%

C4H17B9NS(1-)*1.4H4N2*H(1+)

593-81-7

trimethylamine hydrochloride

C4H17B9NS(1-)*C3H9N*H(1+)

Conditions
ConditionsYield
In water95%
3344-70-5

1,12-dibromododecane

593-81-7

trimethylamine hydrochloride

1674-82-4

N,N,N,N',N',N'-hexamethyldodecane-1,12-diammonium dibromide

Conditions
ConditionsYield
With sodium hydroxide In methanol for 12h; Heating / reflux;94%
802892-30-4

1-Me2NCH2CH2-1,2-C2B10H11

593-81-7

trimethylamine hydrochloride

7-Me2N(H)CH2CH2-7,8-C2B9H11

Conditions
ConditionsYield
With KOH In water (N2); addn. of methanol to a mixt. of boron compd. and KOH with stirringat 0°C, warming to room temp., stirring for 30 min, reflux overn ight, evapn., addn. of water, addn. of aq. ammonium salt; filtration, washing ppt. with water, n-hexane, drying in vac., recrystn.(ethanol); elem. anal.;94%

[Me3NH][1-H-CB11Cl11]

593-81-7

trimethylamine hydrochloride

75-03-6

ethyl iodide

Me3NH[EthylCB11Cl11]

Conditions
ConditionsYield
With tert-butoxide In tert-butyl alcohol a soln. of B-contg. compd. in tert-butanol was treated with KOBu(t) (3.5equivs.) for 30 min at 30°C; the volatiles were removed; the res idue was redissolved in tert-butanol and treated with EtI (7 equivs.) at30°C for 1 h; the volatiles were removed, the residue dissolved in H2O; addn. of concd. HCl (2 drops) and Me3NHCl (2.5 equivs.); mass- and (11)B NMR spectra studies;94%
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    593-81-7

    TIANFU-CHEM - Trimethylamine hydrochloride

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  • Casno:

    593-81-7

    High quality Trimethylamine Hydrochlorate supplier in China

    Min.Order: 1 Kilogram

    FOB Price:  USD $ 0.0-0.0/Kilogram

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  • High Quality Trimethylamine hydrochloride

  • Casno:

    593-81-7

    High Quality Trimethylamine hydrochloride

    Min.Order: 1 Gram

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  • High quality Trimethylamine hydrochloride

  • Casno:

    593-81-7

    High quality Trimethylamine hydrochloride

    Min.Order: 1 Kilogram

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Chemistry

Molecular structure of Trimethylamine hydrochloride (CAS NO.593-81-7) is:

Product Name: Trimethylamine hydrochloride
CAS Registry Number: 593-81-7
IUPAC Name: N,N-dimethylmethanamine hydrochloride
Molecular Weight: 95.5712 [g/mol]
Molecular Formula: C3H10ClN
H-Bond Donor: 1
H-Bond Acceptor: 1 
EINECS: 209-810-0
Melting Point: 283-284 °C (dec.)(lit.)
Storage temp.: 2-8°C
Water Solubility: Soluble
Sensitive: Hygroscopic
Enthalpy of Vaporization: 22.94 kJ/mol
Boiling Point: 2.8 °C at 760 mmHg
Vapour Pressure: 1720 mmHg at 25°C

Uses

 Trimethylamine hydrochloride (CAS NO.593-81-7) is used as a raw material of choline chloride, ion exchange resins, tetramethyl ammonium hydroxide, oil field chemicals, quaternary ammonium compounds, cationic starch reagents, phase transfer catalyst, pesticides as well as a warning agent for natural gas and flotation agent.

Toxicity Data With Reference

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intravenous 325mg/kg (325mg/kg)   Medicina et Pharmacologia Experimentalis. Vol. 16, Pg. 529, 1967.

Safety Profile

Hazard Codes: IrritantXi
Risk Statements: 36/37/38 
R36/37/38:Irritating to eyes, respiratory system and skin.
Safety Statements: 26-36-37/39 
S26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. 
S36:Wear suitable protective clothing. 
S37/39:Wear suitable gloves and eye/face protection.
WGK Germany: 1
RTECS: YH2700000
F: 3-10
HS Code: 29211190

Specification

 Trimethylamine hydrochloride , its cas register number is 593-81-7. It also can be called Trimethylammonium chloride ; Methanamine, N,N-dimethyl-, hydrochloride .It is a white to slightly cream crystalline powder.

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