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inquiryProduct Name 1,4,7,10,13-Pentaazatridecane CAS 112-57-2 MF C8H23N5 MW 189.3 EINECS 203-986-2 Appearance: colourless to l
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A substitute for perfluorooctanoic acid, mainly used as a surfactant, dispersant, additive, etc Appearance:White solid or Colorless liquid Purity:99.3 % We will ship the goods in a timely manner as required We can provide relevant documents acc
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inquirySuperior quality, moderate price & quick delivery. Appearance:colourless or light yellow liquid Storage:Stored in cool, dry and ventilation place; Away from fire and heat Package:25kg/drum, or as per your request. Application:Used as Pharmaceu
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inquiryHangzhou Fanda Chemical Co.,Ltd (FandaChem) , a China-based chemical company, specialize in exporting 1,4,7,10,13-Pentaazatridecane (TEPA; Tetraethylenepentamine) CAS:112-57-2, Please contact us by email freely. We are leading exporter in Ch
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inquiryhigh purity lowest priceAppearance:solid or liquid Storage:in sealed air resistant place Package:drum and bag Application:for pharma use Transportation:by sea or air Port:Beijing or Guangzhou
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Trustworthy manufacturer tetraethylenepentamine Cas 112-57-2 with top purity Application:Trustworthy manufacturer tetraethylenepentamine Cas 112-57-2 with top purity
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inquirybulk?production Application:Pharmaceutical intermediates
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inquiry1,4,7,10,13-Pentaazatridecane Basic information Product Name: 1,4,7,10,13-Pentaazatridecane
Cas:112-57-2
Min.Order:10 Gram
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inquirySpecifications Tetraethylene pentamine CAS: 112-57-2 UN:2320 CN:82505 Yellow or brownish yellow viscous liquid. Tetraethylene pentamine CP Specification Item
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Min.Order:1 Kilogram
Negotiable
Type:Lab/Research institutions
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inquiry1,2-dichloro-ethane
A
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
B
ethylenediamine
Conditions | Yield |
---|---|
With ammonia |
1,5-diamino-3-azapentane
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
With ammonia; water; 1,2-dichloro-ethane unter Druck; |
ethyleneimine
triethylentetramine
A
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
B
tris(2-aminoethyl)-N,N,N'-ethyldiamine
Conditions | Yield |
---|---|
With hydrogenchloride In water at 25℃; Kinetics; Thermodynamic data; acid-catalyzed ring opening reactions at various temperature, Ea, ΔH are given; | |
With hydrogenchloride In water at 55℃; | A 64.5 % Chromat. B 35.5 % Chromat. |
With hydrogenchloride In water at 35℃; | A 61.4 % Chromat. B 38.6 % Chromat. |
1-<2-<(2-aminoethyl)amino>ethyl>aziridine
ethylenediamine
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
With hydrogen cation In water at 40 - 60℃; Rate constant; Thermodynamic data; Ea, ΔH; | |
With hydrogen cation In water |
{COFeC8H23N5}(2+)
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
In water in acidic medium; | |
In water in acidic medium; |
diethylenetriaminediacetonitrile
A
1-<2-(2-aminoethyl)aminoethyl>piperazine
B
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
With hydrogen; Cr-doped Raney cobalt In tetrahydrofuran at 120℃; under 75007.5 Torr; for 3h; Product distribution / selectivity; Autoclave; |
1,2-dichloro-ethane
A
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
B
ethylenediamine
C
1,5-diamino-3-azapentane
D
triethylentetramine
Conditions | Yield |
---|---|
Stage #1: 1,2-dichloro-ethane With ammonia Stage #2: With sodium hydroxide Product distribution / selectivity; | |
With ammonium hydroxide at 140℃; under 105011 Torr; |
1,2-dichloro-ethane
A
piperazine
B
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
C
ethylenediamine
D
1,5-diamino-3-azapentane
E
triethylentetramine
Conditions | Yield |
---|---|
With ammonium hydroxide In water at 120℃; under 90009 Torr; Concentration; |
1,2-dichloro-ethane
A
piperazine
B
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
C
1,5-diamino-3-azapentane
D
triethylentetramine
Conditions | Yield |
---|---|
With ammonium hydroxide; ethylenediamine In water at 100℃; under 18751.9 Torr; |
ethanolamine
A
piperazine
B
1-(2-hydroxyethyl)piperazine
C
aminoethylpiperazine
D
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
E
ethylenediamine
F
1,5-diamino-3-azapentane
G
triethylentetramine
Conditions | Yield |
---|---|
With ammonia; hydrogen In water at 92℃; under 26463 Torr; Temperature; |
ethylenediamine
2,2'-iminobis[ethanol]
A
2-[2-(2-aminoethylamino)ethylamino]ethanol
B
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
With imidazolidone at 270℃; for 5h; Inert atmosphere; |
1,2-dichloro-ethane
A
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
B
ethylenediamine
Conditions | Yield |
---|---|
With ammonia |
1,5-diamino-3-azapentane
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
With ammonia; water; 1,2-dichloro-ethane unter Druck; |
ethyleneimine
triethylentetramine
A
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
B
tris(2-aminoethyl)-N,N,N'-ethyldiamine
Conditions | Yield |
---|---|
With hydrogenchloride In water at 25℃; Kinetics; Thermodynamic data; acid-catalyzed ring opening reactions at various temperature, Ea, ΔH are given; | |
With hydrogenchloride In water at 55℃; | A 64.5 % Chromat. B 35.5 % Chromat. |
With hydrogenchloride In water at 35℃; | A 61.4 % Chromat. B 38.6 % Chromat. |
1-<2-<(2-aminoethyl)amino>ethyl>aziridine
ethylenediamine
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
With hydrogen cation In water at 40 - 60℃; Rate constant; Thermodynamic data; Ea, ΔH; | |
With hydrogen cation In water |
{COFeC8H23N5}(2+)
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
In water in acidic medium; | |
In water in acidic medium; |
diethylenetriaminediacetonitrile
A
1-<2-(2-aminoethyl)aminoethyl>piperazine
B
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
With hydrogen; Cr-doped Raney cobalt In tetrahydrofuran at 120℃; under 75007.5 Torr; for 3h; Product distribution / selectivity; Autoclave; |
1,2-dichloro-ethane
A
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
B
ethylenediamine
C
1,5-diamino-3-azapentane
D
triethylentetramine
Conditions | Yield |
---|---|
Stage #1: 1,2-dichloro-ethane With ammonia Stage #2: With sodium hydroxide Product distribution / selectivity; | |
With ammonium hydroxide at 140℃; under 105011 Torr; |
1,2-dichloro-ethane
A
piperazine
B
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
C
ethylenediamine
D
1,5-diamino-3-azapentane
E
triethylentetramine
Conditions | Yield |
---|---|
With ammonium hydroxide In water at 120℃; under 90009 Torr; Concentration; |
1,2-dichloro-ethane
A
piperazine
B
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
C
1,5-diamino-3-azapentane
D
triethylentetramine
Conditions | Yield |
---|---|
With ammonium hydroxide; ethylenediamine In water at 100℃; under 18751.9 Torr; |
ethanolamine
A
piperazine
B
1-(2-hydroxyethyl)piperazine
C
aminoethylpiperazine
D
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
E
ethylenediamine
F
1,5-diamino-3-azapentane
G
triethylentetramine
Conditions | Yield |
---|---|
With ammonia; hydrogen In water at 92℃; under 26463 Torr; Temperature; |
ethylenediamine
2,2'-iminobis[ethanol]
A
2-[2-(2-aminoethylamino)ethylamino]ethanol
B
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
With imidazolidone at 270℃; for 5h; Inert atmosphere; |
2-oxo-imidazolidine-1-ethanol
2-aminoethylimidazolidone
1,5-diamino-3-azapentane
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
Stage #1: 2-oxo-imidazolidine-1-ethanol; 2-aminoethylimidazolidone; 3-azapentane-1,5-diamine at 270℃; under 3375.34 - 10501.1 Torr; for 9h; Autoclave; Inert atmosphere; Stage #2: With water; sodium hydroxide at 200℃; under 2550.26 Torr; for 4h; Autoclave; Inert atmosphere; |
2-oxo-imidazolidine-1-ethanol
1,5-diamino-3-azapentane
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
at 270℃; under 2475.25 - 7125.71 Torr; for 6h; Autoclave; Inert atmosphere; |
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
Stage #1: U1TEPA With water at 235 - 270℃; under 22502.3 Torr; for 5h; Inert atmosphere; Stage #2: With water; sodium hydroxide at 220℃; for 2.5h; Concentration; Temperature; Inert atmosphere; |
C
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
at 220 - 280℃; under 2.25023 - 12.7513 Torr; for 10h; |
Conditions | Yield |
---|---|
at 220 - 280℃; under 2.25023 - 12.7513 Torr; for 10h; |
ethyl trifluoroacetate,
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
N,N'-(((azanediylbis(ethane-2,1-diyl))bis(azanediyl))bis(ethane-2,1-diyl))bis(2,2,2-trifluoroacetamide)
Conditions | Yield |
---|---|
In methanol at -78 - 20℃; for 25h; | 100% |
In dichloromethane at 0 - 20℃; for 1.5h; | |
In dichloromethane at 0 - 20℃; for 3.5h; Inert atmosphere; |
guanidine hydrochloride
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
tridecanoic acid
Conditions | Yield |
---|---|
Stage #1: N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine; tridecanoic acid With toluene-4-sulfonic acid at 155℃; for 2.75h; Stage #2: guanidine hydrochloride at 152 - 176℃; for 5h; | 98.5% |
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Stearoyl chloride
Conditions | Yield |
---|---|
With triethylamine In acetone for 3h; Ambient temperature; | 98% |
2-acetyldimedone
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
1,13-bis[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl]-tetraethylenepentamine
Conditions | Yield |
---|---|
With molecular sieve In ethanol at 20℃; for 24h; | 98% |
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
2-hydroxy-3-(2-(2-methoxyethoxy)ethoxy)benzaldehyde
NH(CH2CH2NHCH2CH2NCHC6H3(OH)OCH2CH2OCH2CH2OCH3)2
Conditions | Yield |
---|---|
In methanol for 2h; Heating; | 96% |
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
2-Hydroxy-3-{2-[2-(2-{2-[2-(2-hydroxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-benzaldehyde
NH(CH2CH2NHCH2CH2NCHC6H3(OH)OCH2(CH2OCH2)5CH2OH)2
Conditions | Yield |
---|---|
In methanol for 2h; Heating; | 96% |
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
[Ni(tetraethylpentamine)][ReCl6]
Conditions | Yield |
---|---|
In methanol a soln. of Ni-salt and pentamine in methanol was added dropwise to the hot (50°C) soln. of (N(C4H9)4)2ReCl6 in methanol, the mixt. was slowly heated up to 50°C for about 0.5 h; filtered, washed with methanol and diethyl ether; elem. anal.; | 96% |
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
2-Hydroxy-3-[2-(2-{2-[2-(2-methoxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-benzaldehyde
NH(CH2CH2NHCH2CH2NCHC6H3(OH)OCH2(CH2OCH2)4CH2OCH3)2
Conditions | Yield |
---|---|
In methanol for 2h; Heating; | 95% |
methanol
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
[Ni(tetraethylpentamine)][ReCl6]*CH3OH
Conditions | Yield |
---|---|
In methanol a soln. of Ni-salt and pentamine in methanol was added dropwise to the soln. of (N(C4H9)4)2ReCl6 in methanol, the mixt. was stirred at room temp.; filtered, washed with methanol and diethyl ether; elem. anal.; | 92% |
rhodamine B
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
N-(rhodamine B)lactam-tetraethylenepentamine
Conditions | Yield |
---|---|
In ethanol at 80℃; for 12h; Solvent; Temperature; | 90.8% |
In ethanol at 80℃; Inert atmosphere; | 87% |
at 80℃; Inert atmosphere; | 87% |
In ethanol for 12h; Reflux; | 72% |
Conditions | Yield |
---|---|
In ethanol for 12h; Reflux; | 90.8% |
4-amino-2-methoxy-1-methyl-5-nitroso-6-oxo-1,6-dihydropyrimidine
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
In methanol at 20℃; | 90% |
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
acrylonitrile
Conditions | Yield |
---|---|
In water for 24h; Heating; | 89% |
salicylaldehyde
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
C29H35N5O3
Conditions | Yield |
---|---|
In ethanol for 8h; Reflux; | 89% |
In ethanol |
p-acetoxycinnamoyl chloride
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
N1,N4,N7,N10,N13-penta(4-o-acetylcoumaroyl)tetraethylenepentamine
Conditions | Yield |
---|---|
With triethylamine In tetrahydrofuran at 20℃; | 87% |
hydrogen iodide
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
In ethanol; water at 150℃; for 96h; | 87% |
3,5-dichloropyridine
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
With 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; sodium t-butanolate; bis(dibenzylideneacetone)-palladium(0) In 1,4-dioxane for 5h; Heating; | A 86% B 14% |
3,4,5-Trimethoxybenzoyl chloride
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
With potassium carbonate In water; ethyl acetate | 85% |
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
With potassium iodide In N,N-dimethyl-formamide at 90℃; for 72h; Autoclave; | 85% |
carbon disulfide
dimethyltin dichloride
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
tetraethylenepentamine bis(dithiocarbamate) dimethyltin(IV)
Conditions | Yield |
---|---|
With KOH In methanol addn. of CS2 to methanolic soln. of amine deriv. at 0°C, addn. ofmethanolic soln. of KOH, stirring for 3 h at 4°C, addn. of metha nolic soln. of tin compd., stirring for 3 h at room temp.; evapn., washing with methanol and diethyl ether, drying in vac. over P2O5, elem. anal.; | 81% |
phosphoric acid
water
zinc(II) acetate dihydrate
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
In water High Pressure; Zn(OAc)2*2H2O dispersed into H2O; H3PO4 slowly added; tetraethylenepentamine added dropwise with stirring; heated in autoclave at 393 K for 2 dsunder autogenous pressure; filtered; washed (H2O); dried at room temp.; elem. anal.; | 80% |
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
In ethanol at 20℃; for 24h; | 78% |
pyridine-2-carbaldehyde
water
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
In methanol polyamine (2 mmol) and 2-pyridinecarboxaldehyde (4 mmol) refluxed in MeOH, MeOH soln. of CuCl2*2H2O (2 mmol) added, mixt. refluxed for 1 h; concd., ppt. filtered off, washed (Et2O), dried (vac.), elem. anal.; | 78% |
ferrocenecarboxaldehyde
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
1,15-diferrocenyl-2,5,8,11,14-pentaazapentadecane
Conditions | Yield |
---|---|
Stage #1: ferrocenecarboxaldehyde; N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine In methanol at 70℃; for 24h; Inert atmosphere; Stage #2: With sodium tetrahydroborate In methanol at 0 - 20℃; for 12.5h; Inert atmosphere; | 77% |
With LiAlH4 In tetrahydrofuran; ethanol refluxing the aldehyde and the amine in EtOH for 3 h, evapn. to dryness,dissoln. (THF), addn. of LiAlH4, reflux under argon for 1 h, quenching with H2O; filtration, evapn. to dryness, addn. of basic H2O and CH2Cl2, drying (Na2SO4), chromy. (alumina; CH2Cl2, then CH2Cl2/MeOH); elem. anal.; | 70% |
carbon monoxide
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
Conditions | Yield |
---|---|
With sodium hydroxide; hydrogen iodide; iron(II) sulfate In water at room temp. under CO pressure of 3 atm for 6 d; washing with ethanol, then ether, drying in vacuum; | 76% |
With HI; FeSO4; NaOH In water at room temp. under CO pressure of 3 atm for 6 d; washing with ethanol, then ether, drying in vacuum; | 76% |
With sodium hydroxide; hydrogen iodide; iron(II) sulfate In water at room temp. under CO pressure of 3 atm for 3 d; washing with ethanol, then ether, drying in vacuum; | 57% |
With FeSO4; HI; NaOH In water at room temp. under CO pressure of 3 atm for 3 d; washing with ethanol, then ether, drying in vacuum; | 57% |
Conditions | Yield |
---|---|
In water High Pressure; mixt. of CoCl2*6H2O, SnCl4*5H2O, Se amine and water heated in sealed tube at 157°C for 1 d; washed with EtOH, dried in vac.; elem. anal.; | 75% |
Conditions | Yield |
---|---|
In water High Pressure; tetraethylenepentamine/H2O soln. heated at 180 °C for 7 d in container under autogenous pressure; filtration, washing (ethanol, diethyl ether), drying and stored under vac., elem. anal.; | 75% |
dimethyl 5,5'-(oxybis(methylene))bis(furan-2-carboxylate)
N-(2-aminoethyl)-N'-{2-[(2-aminoethyl)amino]ethyl}ethane-1,2-diamine
1,4,7-Trioxa-10,13,16,19,22-pentaazadifuro<2,1,5-a,x:2,1,5-f,g>cyclotetraeicosane-9,23-dione
Conditions | Yield |
---|---|
In ethanol for 20h; Heating; | 73.8% |
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