As a leading manufacturer and supplier of chemicals in China, DayangChem not only supply popular chemicals, but also DayangChem's R&D center offer custom synthesis services. DayangChem can provide different quantities of custom synthesis ch
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inquiryTIANFUCHEM--2155-94-4--N,N-Dimethylallylamine factory price Our company was built in 2009 with an ISO certificate.In the past 10 years, we have grown up as a famous fine chemicals supplier in China And we had established stable business
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inquiryName: N, N-Dimethylallylamine( DMAA) CAS:2155-94-4 MF: C5H12N Purity: 99% Use:Intermediate for chemical synthesis can be used as pesticides; cationic quaternary ammonium salt monomer, pharmaceutical intermediates Appearance: Colorless Liquid Sto
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inquiryN,N-Dimethylallylamine CAS:2155-94-4 Qingdao Belugas Import and Export Co., Ltd. is a scientific and technological company integrating research and development, production and trade of chemical intermediates, specializing in high quality organic int
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inquiryHenan Wentao Chemical Product Co.,Ltd is Located in Zhengzhou High-tech Development Zone with import and export license, We passed ISO 9001:2008 as well, Henan Wentao has developed more than 1000 compounds, which are widely used in the fields of prod
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inquiryJ&H CHEM R&D center can offer custom synthesis according to the contract research and development services for the fine chemicals, pharmaceutical, biotechnique and some of the other chemicals. J&H CHEM has some Manufacturing base in Jia
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inquiryZibo Hangyu Biotechnology Development Co., Ltd is a leading manufacturer and supplier of chemicals in China. We develop produce and distribute high quality pharmaceuticals, intermediates, special chemicals and OLED intermediates and other fine chemi
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inquirySuperior quality moderate price & quick delivery Appearance:colourless to faintly yellow liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:1kg/bag, 1kg/drum or 25kg/drum or as per your request. Applicat
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inquiryProduct Details Grade: pharmaceutical grade Purity:99%+ ProductionCapacity: 1000 Kilogram/Month Scope of use: For scientific research only(The product must be used legally) Our Advantage 1. Best quality with competitive price. 2. Quick shipping,
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inquiryN,N-Dimethylallylamine Basic information Product Name: N,N-Dimethylallylamine Synonyms: 2-Propen-1-amine, N,N-dimethyl-;N,N-DiMethylallylaMine, 98% 5GR;N-Allyldimethylamine 1-Dimethylamino-2-propene;N,N-DIMETHYLALLYLAMINE FOR SYNTHESIS;Allylam
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inquiry1.Applied in food field.it can improve the immune system and prolong life. 2.Appliedin cosmetic field.it can improve the skin care. 3.Applied in pharmaceutical field.it can treat various dieases. 4.Our product quality assurance will make our customer
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inquiryLocated in Hangzhou National Hi-Tech Industrial Development Zone, zhongqichem is a technical company mainly focus on the Custom synthesis, manufacturing, sales of chemicals to various industries. Benefiting from the outstanding customer service an
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high quality Storage:Sealed, dry, microtherm , avoid light and smell. Package:According to the demand of customer Application:Organic synthesis Transportation:by air or by sea
N,N-Dimethylallylamine (We a a few suppliers that can offer custom synthesis service of this product) We are specialized in custom synthesis, chemical/pharmaceutical/ pesticides outsourcing and contract research. We are commit
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inquiry1,we produce and sell good chemicals around the world.2,our success rate is about 95%. this means, if customer order is accepted, the probability that the customer will obtain the ordered substances, is 95%.3,our staff consists of highly qualified in
Ansciep Chemical is a professional enterprise manufacturing and distributing fine chemicals and speciality chemicals. We have been dedicated to heterocycle compounds and phenyl rings for tens of years. This is our mature product for export. Our quali
N,N-DimethylallylamineAppearance:white crystalline powder Storage:Store in dry, dark and ventilated place Package:25KG drum Application:intermediate Transportation:by air, by sea, by express
Best quality with low priceAppearance:colourless to faintly yellow liquid Storage:ln stock Package:25kg/Barrel Application:Chemicals Transportation:Express/Sea/Air Port:Shanghai
Trimeric sodium phosphate detergent auxiliary agent is a kind of excellent properties, is one of the biggest component of detergent consumption during the production, it has four aspects: 1, chelation of heavy metal ions, heavy metal ions in the wate
Good Quality Package:1kg/bag Application:Medical or chemical Transportation:Air/Train/Sea Port:Shenzhen
N,N-Dimethylpropargylamin
A
N,N-dimethylaminopropane
B
N,N-dimethyl-2-propen-1-amine
Conditions | Yield |
---|---|
With hydrogen; copper-palladium; silica gel In ethanol at 25℃; under 760 Torr; Kinetics; | A n/a B 100% |
Conditions | Yield |
---|---|
With hydrogen; copper-palladium; silica gel In ethanol at 25℃; under 760.051 Torr; | 100% |
With piperazine; hydrogen In ethanol at 80℃; under 4500.45 Torr; for 24h; | 99% |
With piperazine; hydrogen In ethanol at 100℃; under 4500.45 Torr; for 24h; Green chemistry; | |
With hydrogen In ethanol at 100℃; under 4500.45 Torr; for 24h; chemoselective reaction; | 96 %Chromat. |
A
N,N-dimethyl-2-propen-1-amine
Conditions | Yield |
---|---|
With potassium hydroxide In water at 90 - 92℃; for 1.5h; | A 8% B 71% |
Allyl-dimethylcarbamoylmethyl-dimethyl-ammonium; bromide
A
N,N-dimethyl-2-propen-1-amine
B
2-(dimethylamino)-N,N-dimethylacetamide
C
2-Dimethylamino-pent-4-enoic acid dimethylamide
Conditions | Yield |
---|---|
With potassium hydroxide In benzene at 65 - 70℃; for 1h; metallic sodium in DMSO was also used instead of potassium hydroxide; | A n/a B n/a C 70% |
Allyl-(1-methoxycarbonyl-ethyl)-dimethyl-ammonium; bromide
A
N,N-dimethyl-2-propen-1-amine
B
2-Dimethylamino-2-methyl-pent-4-enoic acid methyl ester
C
acrylic acid methyl ester
Conditions | Yield |
---|---|
With sodium methylate In diethyl ether at 30 - 35℃; Yield given; | A n/a B 69% C n/a |
With sodium methylate In diethyl ether at 30 - 35℃; Yields of byproduct given; | A n/a B 69% C n/a |
Conditions | Yield |
---|---|
In water 1) 30 min, 2) reflux, 30 min.; | 62.5% |
In water Ambient temperature; | 51% |
In benzene | 36% |
Conditions | Yield |
---|---|
With formic acid for 8h; Heating; | 58% |
Conditions | Yield |
---|---|
With formaldehyd In water at 100℃; for 12h; | 46% |
Conditions | Yield |
---|---|
copper(l) chloride In water | 30% |
B
N,N-dimethylaminomethylferrocene
C
propene
D
N,N-dimethyl-2-propen-1-amine
Conditions | Yield |
---|---|
With sodium In ammonia | A 30% B 26% C n/a D n/a |
With Na In ammonia NH3 (liquid); | A 30% B 26% C n/a D n/a |
formic acid
allyl-trimethyl-ammonium; hydroxide
A
N,N-dimethyl-2-propen-1-amine
B
Methyl formate
C
3-formyloxy-propene
D
trimethylamine
Conditions | Yield |
---|---|
at 190 - 200℃; |
allyl trimethylammonium bromide
ethanolamine
A
N,N-dimethyl-2-propen-1-amine
B
trimethylamine
Conditions | Yield |
---|---|
at 154℃; Rate constant; |
Conditions | Yield |
---|---|
With ethanol at 150℃; |
Conditions | Yield |
---|---|
With sodium hydroxide | |
Stage #1: dimethyl amine; 3-chloroprop-1-ene In water at 20 - 30℃; Autoclave; Stage #2: With sodium hydroxide In water for 0.333333h; pH=11 - 13; pH-value; Autoclave; |
N-benzyl-N,N-dimethylprop-2-en-1-ylammonium bromide
N,N-dimethyl-2-propen-1-amine
Conditions | Yield |
---|---|
With sodium hydroxide; thiophenol |
N,N-dimethyl-2-propen-1-amine
Conditions | Yield |
---|---|
With potassium hydroxide |
3-(dimethylamino)-1-propyl acetate
A
N,N-dimethyl-2-propen-1-amine
B
acetic acid methyl ester
C
N,N'-dimethyl-1-propenylamine
D
acetic acid
E
dimethyl amine
F
prop-1-yne
Conditions | Yield |
---|---|
at 347.1℃; Mechanism; Kinetics; other temperatures, various pressures, effect of propene inhibitors; Ea, log A; |
Allyl-but-2-inyl-dimethyl-ammonium
A
3-buten-1-yne
B
N,N-dimethyl-2-propen-1-amine
Conditions | Yield |
---|---|
With potassium hydroxide; tert-butylamine at 50℃; Yield given; |
N,N-dimethyl-2-propen-1-amine
Conditions | Yield |
---|---|
bei der Destillation; |
A
N,N-dimethyl-2-propen-1-amine
Conditions | Yield |
---|---|
With potassium hydroxide durch Destillation; |
A
N,N-dimethyl-2-propen-1-amine
B
bisisopropenyl ether
C
dimethyl amine
hexa-N-methyl-N,N'-propanediyl-di-ammonium; dihydroxyide
A
N,N-dimethyl-2-propen-1-amine
B
4-methylpent-4-en-2-one
C
trimethylamine
Conditions | Yield |
---|---|
bei der Destillation; |
3-dimethylamino-2-methyl-N-isopropylpropanamide
3-chloroprop-1-ene
A
N,N-dimethyl-2-propen-1-amine
B
N-isopropylmethacrylamide
Conditions | Yield |
---|---|
In water |
hexadecyl allyl carbonate
diethylamine
A
N,N-dimethyl-2-propen-1-amine
B
1-Hexadecanol
Conditions | Yield |
---|---|
With tri(3-sulfonatophenyl)phosphine trisodium salt; palladium diacetate; pyrographite In n-heptane; water at 20℃; Tsuji-Trost reaction; Inert atmosphere; |
allyl 1-decyl carbonate
diethylamine
A
N,N-dimethyl-2-propen-1-amine
B
1-Decanol
Conditions | Yield |
---|---|
With tri(3-sulfonatophenyl)phosphine trisodium salt; palladium diacetate; pyrographite In n-heptane; water at 20℃; Tsuji-Trost reaction; Inert atmosphere; |
diethylamine
allyl butyl carbonate
A
N,N-dimethyl-2-propen-1-amine
B
butan-1-ol
Conditions | Yield |
---|---|
With tri(3-sulfonatophenyl)phosphine trisodium salt; palladium diacetate; pyrographite In n-heptane; water at 20℃; Tsuji-Trost reaction; Inert atmosphere; |
Conditions | Yield |
---|---|
With tri(3-sulfonatophenyl)phosphine trisodium salt; palladium diacetate; pyrographite In n-heptane; water at 20℃; Tsuji-Trost reaction; Inert atmosphere; |
Conditions | Yield |
---|---|
With tri(3-sulfonatophenyl)phosphine trisodium salt; palladium diacetate; pyrographite In n-heptane; water at 20℃; Tsuji-Trost reaction; Inert atmosphere; |
Conditions | Yield |
---|---|
With hydrogen; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; Rh(acac)2(CO)2 In tetrahydrofuran at 70℃; under 15001.2 Torr; for 68h; | 100% |
N,N-dimethyl-2-propen-1-amine
(E)-1-N,N-dimethylamino-1-propene
Conditions | Yield |
---|---|
With hydridocarbonylbis(triphenylphosphine)rhodium(I) In benzene-d6 at 60℃; for 2h; Inert atmosphere; | 99% |
+ In tetrahydrofuran at 17℃; for 23h; Yield given; | |
With trans-bisdinitrogenbis(1,2-diphenylphosphinoethane)molybdenum(0) In toluene for 2h; Heating; | 100 % Chromat. |
carbonylhydridetris(triphenylphosphine)rhodium(I) In benzene-d6 at 60℃; for 2h; | 100 % Spectr. |
With [(+)-2,2'-bis(diphenylphosphino)-1,1'-binaphthyl]-(η4-1,5-cyclooctadiene)rhodium(I) perchlorate In tetrahydrofuran at 40℃; for 23h; Inert atmosphere; | n/a |
Conditions | Yield |
---|---|
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex In tetrahydrofuran at 60℃; Inert atmosphere; Sealed tube; | 99% |
N,N-dimethyl-2-propen-1-amine
Triethoxysilane
N,N-dimethyl-3-(triethoxysilyl)-1-propylamine
Conditions | Yield |
---|---|
With platinum-containing olefin organic polymer catalyst at 20℃; for 24h; | 98% |
With (TFAPDI)Co(2-ethylhexanoate)2 In neat (no solvent) at 23℃; for 1h; | 74% |
dicobalt octacarbonyl | |
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex at 80℃; for 20h; Schlenk technique; Inert atmosphere; regioselective reaction; | 94.8 %Spectr. |
With C28H34CoN3O4(1+)*C5H7O2(1-) In tetrahydrofuran at 50℃; for 6h; Sealed tube; |
N,N-dimethyl-2-propen-1-amine
(3aS,6R,7aR)-1-(bromoacetyl)-8,8-dimethylhexahydro-3a,6-methano-2,1-benzothiazole 2,2-dioxide
Conditions | Yield |
---|---|
In tetrahydrofuran at 20℃; for 6h; | 98% |
N,N-dimethyl-2-propen-1-amine
N,N-dimethyl allylamine-borane
Conditions | Yield |
---|---|
In diethyl ether (inert atm.); stirring (1 h, 0°C); MeOH addn., stirring (30 min, room temp.), solvent removal (vac.), trituration (petroleum ether), evpn. (vac.); | 98% |
Conditions | Yield |
---|---|
With C25H30N2NiO In acetonitrile at 25℃; for 1h; | 98% |
With C25H31N2NiO In acetonitrile at 20℃; for 1h; | 98% |
With N-(1-[2,2′-bipyridin-6-yl]ethylidene)-2,4,6-trimethylbenzenamine iron(II) bromide; sodium triethylborohydride In toluene at 20℃; for 24h; Catalytic behavior; Reagent/catalyst; Schlenk technique; Inert atmosphere; | 94% |
dimethylphosphane
N,N-dimethyl-2-propen-1-amine
A
3-(N,N-dimethylamino)-1-(dimethylphosphino)propane
B
1,3-bis(dimethylphosphino)propane
Conditions | Yield |
---|---|
With 2,2'-azobis(isobutyronitrile) In diethyl ether at -20℃; for 24h; Product distribution; Mechanism; Irradiation; reactions under var. conditions; | A 97% B n/a |
With 2,2'-azobis(isobutyronitrile) In diethyl ether at -20℃; for 24h; Irradiation; | A 97% B n/a |
2-chloro-4,6-dimethoxy-1 ,3,5-triazine
N,N-dimethyl-2-propen-1-amine
2-(dimethylamino)-4,6-dimethoxy-1,3,5-triazine
Conditions | Yield |
---|---|
In toluene Reflux; | 97% |
N,N-dimethyl-2-propen-1-amine
methyl iodide
N,N,N-trimethylallylammonium iodide
Conditions | Yield |
---|---|
In diethyl ether at 20℃; for 3h; Inert atmosphere; | 97% |
N,N-dimethyl-2-propen-1-amine
4,4,5,5-tetramethyl-[1,3,2]-dioxaboralane
C11H24BNO2
Conditions | Yield |
---|---|
With C28H30CoNP In benzene-d6 at 20℃; for 0.5h; Inert atmosphere; | 97% |
With [(2,6-(2,4,6-Me3-C6H2-NdCMe)2C5H3N)Fe(N2)]2(μ2-N2) In neat (no solvent) at 25℃; Reagent/catalyst; Inert atmosphere; | |
With (MesPDI)CoMe In neat (no solvent) at 23℃; for 0.25h; Schlenk technique; Inert atmosphere; Glovebox; |
N,N-dimethyl-2-propen-1-amine
3-chloroprop-1-ene
dimethyldiallylammonium chloride
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-2-propen-1-amine; 3-chloroprop-1-ene at 30 - 55℃; for 4.5h; Stage #2: With sodium hydroxide pH=11; Temperature; pH-value; | 97% |
Conditions | Yield |
---|---|
In diethyl ether at 0 - 20℃; for 2.25h; Schlenk technique; Inert atmosphere; | 97% |
diazoacetic acid ethyl ester
N,N-dimethyl-2-propen-1-amine
2-(N,N-dimethylamino)-4-pentenoic acid ethyl ester
Conditions | Yield |
---|---|
With 5,10,15,20-tetrakis(pentafluorophenyl)-21H,23H-porphyrin iron(III) chloride In dichloromethane at 20℃; for 0.0166667h; | 96% |
carbonyl(5,10,15,20-tetraphenylporphyrinato)ruthenium(II) In toluene at 50℃; for 5h; | 87% |
hexarhodium hexadecacarbonyl at 60℃; | 82% |
With copper acetylacetonate In benzene at 60℃; for 22h; Inert atmosphere; | 35% |
carbonyl(5,10,15,20-tetraphenylporphyrinato)ruthenium(II) In dichloromethane at 20℃; for 24h; | 100 % Chromat. |
tetraallyltitanate
N,N-dimethyl-2-propen-1-amine
methylphenylsilane
{(CH3)2N(CH2)3Si(C6H5)(CH3)OTi(OC3H5)2O(CH2)3}2Si(CH3)C6H5
Conditions | Yield |
---|---|
dihydrogen hexachloroplatinate byproducts: propene; to a mixt. of titanate and silane (molar ratio 1:4) catalyst was added and heated to 100°C for 2.5 h; unreacted silane was removed at 50-80 °C and 1-2 Torr within 4 h; then titanosiloxane was reacted with excess amine at 50°C, 4 h;; unreacted amine was removed by heating in vac.; elem. anal.;; | 96% |
Conditions | Yield |
---|---|
With 2-chloro-4,6-dimethoxy-1 ,3,5-triazine In toluene Reflux; | 96% |
Conditions | Yield |
---|---|
With C25H30N2NiO In acetonitrile at 25℃; for 1h; | 96% |
With C25H31N2NiO In acetonitrile at 20℃; for 0.5h; | 96% |
trimethoxysilane
N,N-dimethyl-2-propen-1-amine
A
<3-(dimethylamino)propyl>trimethoxysilane
Conditions | Yield |
---|---|
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex; ammonium bicarbonate In toluene at 55℃; for 8h; Reagent/catalyst; | A 95.5% B 6.7% |
N,N-dimethyl-2-propen-1-amine
[N-(p-tolylsulfonyl)imino]phenyliodinane
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-2-propen-1-amine With 2C15H31BBr3N6(1-)*2Ag(1+) In dichloromethane for 0.0833333h; Inert atmosphere; Glovebox; Stage #2: [N-(p-tolylsulfonyl)imino]phenyliodinane In dichloromethane at 50℃; for 16h; Inert atmosphere; Glovebox; chemoselective reaction; | 95% |
N,N-dimethyl-2-propen-1-amine
1-diazo-2-heptadecanone
Conditions | Yield |
---|---|
chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium (II) In chloroform at 60℃; for 0.25h; | 94% |
N,N-dimethyl-2-propen-1-amine
Conditions | Yield |
---|---|
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex In toluene at 90℃; regioselective reaction; | 94% |
N,N-dimethyl-2-propen-1-amine
1-diazopentan-2-one
Conditions | Yield |
---|---|
chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium (II) In chloroform at 60℃; for 0.25h; | 93% |
N,N-dimethyl-2-propen-1-amine
1-diazo-2-tridecanone
Conditions | Yield |
---|---|
chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium (II) In chloroform at 60℃; for 0.25h; | 93% |
N,N-dimethyl-2-propen-1-amine
Conditions | Yield |
---|---|
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex In toluene at 90℃; regioselective reaction; | 93% |
N,N-dimethyl-2-propen-1-amine
Triethoxysilane
A
N,N-dimethyl-3-(triethoxysilyl)-1-propylamine
Conditions | Yield |
---|---|
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex; ammonium bicarbonate In toluene at 55℃; for 17h; Reagent/catalyst; | A 92.3% B 6.8% |
diazoacetone
N,N-dimethyl-2-propen-1-amine
3-dimethylamino-5-hexen-2-one
Conditions | Yield |
---|---|
chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium (II) In chloroform at 60℃; for 0.25h; | 92% |
N,N-dimethyl-2-propen-1-amine
1-diazo-3-methylbutan-2-one
Conditions | Yield |
---|---|
chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium (II) In chloroform at 60℃; for 0.25h; | 92% |
carbonyl(5,10,15,20-tetraphenylporphyrinato)ruthenium(II) In toluene at 50℃; for 5h; | 85% |
N,N-dimethyl-2-propen-1-amine
(dimethoxy)methylsilane
B
<3-(dimethylamino)propyl>dimethoxymethylsilane
Conditions | Yield |
---|---|
With platinum(0)-1,3-divinyl-1,1,3,3-tetramethyldisiloxane complex; ammonium bicarbonate In toluene at 45℃; for 12h; Reagent/catalyst; | A 8% B 91.4% |
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