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Cas:593-81-7
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inquiryAppearance: off white or light yellow crystalhygroscopicity Index Standard Analytic method Assay(Dry) % 98% HG2941-89(97)
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inquiryTrimethylamine hydrochloride Product Name: Trimethylamine hydrochloride Molecular Weight: 95.57 CAS NO: 593-81-7 EC NO: 209-810-0 Molecular Form
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inquiryTrimethylamine hydrochloride Basic information Product Name: Trimethylamine hydrochloride Synonyms: FEMA 3241;N, N-DIMETHYLMETHYLAMINE HCL;TRIMETHYLAMINE HYDROCHLORIDE;TRIMETHYLAMMONIUM
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inquiryProduct Description Product website: http://www.finerchem.com Product Name Trimethylamine hydrochloride CAS No. 593-81-7
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inquirytrimethylamine-N-oxide
N,N-dimethyl-formamide
1-chloro-2,4-dinitro-benzene
A
2,4-Dinitrophenol
B
trimethylamine hydrochloride
Conditions | Yield |
---|---|
for 24h; Ambient temperature; | A 97% B 98% |
trimethylamine-N-oxide
1-chloro-2,4-dinitro-benzene
A
2,4-Dinitrophenol
B
trimethylamine hydrochloride
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide for 24h; Ambient temperature; | A 97% B 98% |
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
With oxalic acid at 100 - 120℃; Eschweiler-Clarke methylation; | 84% |
Conditions | Yield |
---|---|
Stage #1: methanol With ammonium hydroxide; Ag/TiO2 at 25℃; for 10h; UV-irradiation; Stage #2: With hydrogenchloride In water | 80% |
N,N-dimethyl-formamide
trimethylamine hydrochloride
Conditions | Yield |
---|---|
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% |
cyclopropanesulfonyl-1-d chloride
isopropyl alcohol
trimethylamine
A
trimethylamine hydrochloride
B
propan-2-yl cyclopropanesulfonate
Conditions | Yield |
---|---|
In dichloromethane at 25℃; for 36h; | A n/a B 11.7% C 27.4% |
N,N-dimethoxyamine
trimethylamine
A
trimethylamine hydrochloride
B
tetramethlyammonium chloride
Conditions | Yield |
---|---|
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% |
1,1,1,3,3,3-hexamethyl-disilazane
A
Bis(trimethylsilyl)aminochlorodimethylaminoboran
B
trimethylamine hydrochloride
Conditions | Yield |
---|---|
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 |
toluene
methyl 3-chloropropionate
trimethylamine
A
trimethylamine hydrochloride
B
(2-methoxycarbonylethyl)trimethylammonium chloride
Conditions | Yield |
---|---|
at -5℃; |
methanol
methyl 3-chloropropionate
trimethylamine
A
trimethylamine hydrochloride
B
(2-methoxycarbonylethyl)trimethylammonium chloride
Conditions | Yield |
---|---|
at -5℃; |
diethyl ether
methyl 3-chloropropionate
trimethylamine
A
trimethylamine hydrochloride
B
(2-methoxycarbonylethyl)trimethylammonium chloride
Conditions | Yield |
---|---|
at -5℃; |
3-Chloropropionitrile
ethanol
trimethylamine
A
trimethylamine hydrochloride
B
acrylonitrile
piperidine
trimethyl-(3-oxo-3-phenyl-propenyl)-ammonium; chloride
A
1-phenyl-3-(piperidin-1-yl)prop-2-en-1-one
B
trimethylamine hydrochloride
Conditions | Yield |
---|---|
In acetonitrile at 25℃; Rate constant; |
piperidine
trans-β-(p-nitrophenylsulfinyl)vinyltrimethylammonium chloride
A
trimethylamine hydrochloride
Conditions | Yield |
---|---|
In N,N-dimethyl-formamide at 25℃; Rate constant; further solvent; |
piperidine
trans-β-(p-nitrophenylsulfonyl)-vinyltrimethylammonium chloride
A
β-piperidyl aminovinyl sulfone
B
trimethylamine hydrochloride
Conditions | Yield |
---|---|
In acetonitrile at 25℃; Rate constant; |
methanol
benzyltrimethylammonium chloride
A
trimethylamine hydrochloride
B
1,1'-(1,2-ethanediyl)bisbenzene
C
toluene
D
benzyl alcohol
Conditions | Yield |
---|---|
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. |
methanol
(3,5-dimethoxybenzyl)trimethylammonium chloride
A
1,3-dimethoxy-5-methylbenzene
B
1-methylmethoxy-3,5-dimethoxybenzene
C
N,N-dimethylammonium chloride
D
trimethylamine hydrochloride
Conditions | Yield |
---|---|
at 30℃; for 2h; Irradiation; | A 46 % Chromat. B 12 % Chromat. C 23 % Chromat. D 77 % Chromat. |
benzyltrimethylammonium chloride
A
N,N-dimethylammonium chloride
B
trimethylamine hydrochloride
C
1,1'-(1,2-ethanediyl)bisbenzene
D
toluene
E
benzyl alcohol
Conditions | Yield |
---|---|
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. |
benzyltrimethylammonium chloride
A
trimethylamine hydrochloride
B
1,1'-(1,2-ethanediyl)bisbenzene
C
toluene
D
benzyl alcohol
Conditions | Yield |
---|---|
With water at 30℃; for 2h; Irradiation; Further byproducts given; | A 77 % Chromat. B 10 % Chromat. C 27 % Chromat. D 45 % Chromat. |
vinylsulfonyl chloride
trimethylamine
A
2-(N,N,N-trimethylamino)ethanesulfonate
B
trimethylamine hydrochloride
C
Ethenesulfonic acid; compound with trimethyl-amine
Conditions | Yield |
---|---|
With potassium chloride; water In 1,2-dimethoxyethane at 1℃; Rate constant; Product distribution; |
trans-1-propene-1-sulfonyl chloride
trimethylamine
A
trimethylamine hydrochloride
B
C6H15NO3S
Conditions | Yield |
---|---|
With potassium chloride; water In 1,2-dimethoxyethane at 1℃; Rate constant; Product distribution; |
formaldehyd
A
formic acid
B
carbon dioxide
C
N,N-dimethylammonium chloride
D
trimethylamine hydrochloride
hydrogenchloride
ethanol
hydroxymethyl-trimethyl-ammonium; chloride
trimethylamine hydrochloride
water
hydroxymethyl-trimethyl-ammonium; chloride
trimethylamine hydrochloride
Conditions | Yield |
---|---|
at 25℃; Geschwindigkeit der Zersetzung in Abhaengigkeit vom pH; |
trimethylamine hydrochloride
Conditions | Yield |
---|---|
With ammonium chloride at 120 - 170℃; analog lassen sich andere Ammoniumsalze anwenden; |
ethanol
phenyltrimethylammonium chloride
A
cyclohexane
B
trimethylamine hydrochloride
Conditions | Yield |
---|---|
at 20 - 25℃; under 1520 - 2280 Torr; Hydrogenation; |
water
A
carbon dioxide
B
trimethylamine hydrochloride
C
ethanethiol
Conditions | Yield |
---|---|
With sodium hydroxide at 24.9℃; Thermodynamic data; ΔrH1; | 100% |
With sodium hydroxide at 24.9℃; | 100% |
Conditions | Yield |
---|---|
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% |
Hf(C5(CH3)5)2(CH2CH(CH3)CH2)
trimethylamine hydrochloride
(Hf(C5(CH3)5)2(CH2CH(CH3)2))Cl
Conditions | Yield |
---|---|
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% |
tris(trimethylsilylmethyl)gallium
trimethylamine hydrochloride
A
tetramethylsilane
B
Ga(3+)*2CH2Si(CH3)3(1-)*Cl(1-)*N(CH3)3=Ga(CH2Si(CH3)3)2Cl*N(CH3)3
Conditions | Yield |
---|---|
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% |
1,2-dicarba-closo-dodecaborane(12)
trimethylamine hydrochloride
Conditions | Yield |
---|---|
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% |
trimethylamine hydrochloride
carbonic acid dimethyl ester
tetramethlyammonium chloride
Conditions | Yield |
---|---|
With 1-ethyl-3-methylimidazolium bromide at 169.84℃; for 8h; | 99% |
With 1-ethyl-3-methylimidazolium bromide at 169.84℃; for 8h; |
dimethyl η5-cyclopentadienyl η5-pentamethylcyclopentadienyl zirconium
trimethylamine hydrochloride
Conditions | Yield |
---|---|
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 |
[U(N(CH2CH2NSiMe2But)2(CH2CH2NSiMeButCH2))]
trimethylamine hydrochloride
U[N(CH2CH2NSi(CH3)2(C(CH3)3))3]Cl
Conditions | Yield |
---|---|
In not given | 99% |
8,8'-μ-methylcarboniodioxy-bis(1,2-dicarbollido)-3-cobalt(1-)ate
water
trimethylamine hydrochloride
Conditions | Yield |
---|---|
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% |
lithium aluminium tetrahydride
trimethylamine hydrochloride
trimethylamine
bis(trimethylamine)alane
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
Stage #1: cesium carba-closo-dodecaborate With antimonypentachloride at 180℃; for 168h; Inert atmosphere; Stage #2: trimethylamine hydrochloride In water-d2 | 98% |
Conditions | Yield |
---|---|
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% |
trimethylamine hydrochloride
Conditions | Yield |
---|---|
In chloroform at 50℃; for 15h; | 98% |
Conditions | Yield |
---|---|
In water | 97% |
Conditions | Yield |
---|---|
In water Inert atmosphere; | 97% |
Conditions | Yield |
---|---|
In water Solvent; | 97% |
1,2-diphenyl-3-fluoro-1,2-closo-dodecacarborane
trimethylamine hydrochloride
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
In not given cation metathesis react. of B compd. and Me3NHCl; recrystd. from water-EtOH: elem. anal.; | 96% |
1,2-(C6H5CH2)2-1,2-C2B10H10
trimethylamine hydrochloride
Conditions | Yield |
---|---|
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% |
trimethylamine hydrochloride
Conditions | Yield |
---|---|
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% |
trimethylamine hydrochloride
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
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% |
1.2-dicarba-closo-dodecaborano-tetrahydrofurane
trimethylamine hydrochloride
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
In water | 95% |
1,12-dibromododecane
trimethylamine hydrochloride
N,N,N,N',N',N'-hexamethyldodecane-1,12-diammonium dibromide
Conditions | Yield |
---|---|
With sodium hydroxide In methanol for 12h; Heating / reflux; | 94% |
1-Me2NCH2CH2-1,2-C2B10H11
trimethylamine hydrochloride
Conditions | Yield |
---|---|
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% |
Conditions | Yield |
---|---|
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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