oxirane
1,5-diamino-3-azapentane
2-[2-(2-aminoethylamino)ethylamino]ethanol
Conditions | Yield |
---|---|
With water |
2-bromoethylamine hydrobromide
2-(2-Aminoethylamino)ethanol
2-[2-(2-aminoethylamino)ethylamino]ethanol
Conditions | Yield |
---|---|
With water |
1,5-diamino-3-azapentane
2-chloro-ethanol
2-[2-(2-aminoethylamino)ethylamino]ethanol
Conditions | Yield |
---|---|
In water | |
Stage #1: 3-azapentane-1,5-diamine; 2-chloro-ethanol In water for 8h; Reflux; Stage #2: With potassium carbonate In methanol for 0.5h; |
2-[2-(2-aminoethylamino)ethylamino]ethanol
Conditions | Yield |
---|---|
With tetrahydrofuran; lithium aluminium tetrahydride |
tetrahydrofuran
[2-(2-Amino-acetylamino)-acetylamino]-acetic acid ethyl ester
2-[2-(2-aminoethylamino)ethylamino]ethanol
Conditions | Yield |
---|---|
das Acetat reagiert; |
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; |
Conditions | Yield |
---|---|
With triethylamine In N,N-dimethyl-formamide at 20℃; for 24h; Inert atmosphere; | 60% |
2-[2-(2-aminoethylamino)ethylamino]ethanol
1,2-dioleoyl-sn-glycero-3-phosphocholine
Conditions | Yield |
---|---|
With Phospholipase D In ethyl acetate at 40℃; for 72h; Enzymatic reaction; | 3% |
2-[2-(2-aminoethylamino)ethylamino]ethanol
n-octyl chloroacetate
([2-(Bis-octyloxycarbonylmethyl-amino)-ethyl]-{2-[(2-hydroxy-ethyl)-octyloxycarbonylmethyl-amino]-ethyl}-amino)-acetic acid octyl ester
Conditions | Yield |
---|---|
With potassium carbonate |
2-[2-(2-aminoethylamino)ethylamino]ethanol
chloroacetic acid ethyl ester
([2-(Bis-ethoxycarbonylmethyl-amino)-ethyl]-{2-[ethoxycarbonylmethyl-(2-hydroxy-ethyl)-amino]-ethyl}-amino)-acetic acid ethyl ester
Conditions | Yield |
---|---|
With potassium carbonate |
2-[2-(2-aminoethylamino)ethylamino]ethanol
1,4,5,8-tetrahydroxy-2,3-dihydro-9,10-anthracenedione
Conditions | Yield |
---|---|
(i) Me2NCH2CH2NMe2, (ii) 2,3,5,6-tetrachloro-<1,4>benzoquinone, MeOCH2CH2OH; Multistep reaction; |
2-[2-(2-aminoethylamino)ethylamino]ethanol
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: triethylamine / N,N-dimethyl-formamide / 24 h / 20 °C / Inert atmosphere 2: dichloromethane / 24 h / 0 - 20 °C View Scheme |
2-[2-(2-aminoethylamino)ethylamino]ethanol
methyl 2,4,4,5,7,7,8,8,9,9,9-undecafluoro-2,5-bis(trifluoromethyl)-3,6-dioxanonanoate
Conditions | Yield |
---|---|
In dichloromethane for 10h; Cooling with ice; |
IUPAC Name: 2-[2-(2-Aminoethylamino)ethylamino]ethanol
Synonyms: 1,2-Ethanediamine, N-(2-aminoethyl)-N'-(2-hydroxyethyl)- ; Diethylenetriamine, N-(2-hydroxyethyl)- ; Ethanol, 2-((2-((2-aminoethyl)amino)ethyl)amino)- ; Ethanol, 2-[[2-[(2-aminoethyl)amino]ethyl]amino]- ; 2-(2-(2-Aminoethylamino)ethylamino)ethanol
CAS NO: 1965-29-3
Molecular Formula of N-(Hydroxyethyl)diethylenetriamine (CAS NO.1965-29-3) : C6H17N3O
Molecular Weight of N-(Hydroxyethyl)diethylenetriamine (CAS NO.1965-29-3) : 147.21868
Molecular Structure of N-(Hydroxyethyl)diethylenetriamine (CAS NO.1965-29-3) :
EINECS: 217-811-2
Mol File: 1965-29-3.mol
Index of Refraction: 1.487
Surface Tension: 41.9 dyne/cm
Density: 1.005 g/cm3
Flash Point: 129 °C
Enthalpy of Vaporization: 61.38 kJ/mol
Boiling Point: 289.7 °C at 760 mmHg
Vapour Pressure: 0.000238 mmHg at 25°C
N-(Hydroxyethyl)diethylenetriamine (CAS NO.1965-29-3) is used as intermediate in organic synthesis.
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | intraperitoneal | 320mg/kg (320mg/kg) | BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD GASTROINTESTINAL: PERITONITIS | AMA Archives of Industrial Health. Vol. 17, Pg. 129, 1958. |
rabbit | LD50 | skin | 2520uL/kg (2.52mL/kg) | AMA Archives of Industrial Hygiene and Occupational Medicine. Vol. 4, Pg. 119, 1951. | |
rat | LD50 | intraperitoneal | 146mg/kg (146mg/kg) | BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD BEHAVIORAL: EXCITEMENT | AMA Archives of Industrial Health. Vol. 17, Pg. 129, 1958. |
rat | LD50 | oral | 4630mg/kg (4630mg/kg) | BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD | AMA Archives of Industrial Health. Vol. 17, Pg. 129, 1958. |
Reported in EPA TSCA Inventory.
Poison by intraperitoneal route. Moderately toxic by skin contact. Mildly toxic by ingestion. A skin and severe eye irritant. When heated to decomposition it emits toxic fumes of NOx. See also AMINES.
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