N-Lauryldiethanolamine supplier

Name
N-LAURYLDIETHANOLAMINE
EINECS 216-277-8
CAS No. 1541-67-9
Article Data24
CAS DataBase
Density 0.927 g/cm³
Solubility
Melting Point 185-190℃
Formula C₁₆H₃₅NO₂
Boiling Point 401.115 °C at 760 mmHg
Molecular Weight 273.459
Flash Point 171.237 °C
Transport Information
Appearance colorless or light yellow liquid
Safety 26-36/37/39
Risk Codes 36/37/38
Molecular Structure
Hazard Symbols
Synonyms N,N-Bis(2-hydroxyethyl)laurylamine;N,N-Bis(hydroxyethyl)dodecanamine;N,N-Bis(hydroxyethyl)laurylamine;N,N-Di(hydroxyethyl)laurylamine;N-Dodecyldiethanolamine;N-Lauryldiethanolamine;NSC 525737;TB 128K;Ethanol,2,2'-(dodecylimino)di- (6CI,7CI,8CI);2,2'-(Dodecylimino)diethanol;2,2'-(Laurylimino)diethanol;Bis(2-hydroxyethyl)dodecylamine;Bis(2-hydroxyethyl)laurylamine;Bis(hydroxyethyl)dodecylamine;Bis(b-hydroxyethyl)laurylamine;Dodecylbis(2-hydroxyethyl)amine;Dodecylbis(hydroxyethyl)amine;Dodecyldiethanolamine;Elest EA;Lauryldiethanolamine;N,N-Bis(2-hydroxyethyl)dodecylamine;N,N-Bis(2-hydroxyethyl)lauramine;
PSA 43.70000
LogP 3.19390

Synthetic route

: 143-15-7
1-dodecylbromide

: 111-42-2
2,2'-iminobis[ethanol]

: 1541-67-9
N-lauryldiethanolamine

Conditions

Conditions	Yield
With potassium carbonate; potassium iodide In acetonitrile for 12h; Inert atmosphere; Reflux;	98%
Stage #1: 1-dodecylbromide; 2,2'-iminobis[ethanol] In ethanol at 60℃; for 24h; Stage #2: With sodium hydroxide In ethanol for 1h; Cooling;	73.1%
With potassium carbonate at 170℃; for 7h;	70%

: 16613-87-9
2-(N-dodecylamino)ethanol

HO(CH2)2-β-halide: HO(CH2)2-β-halide

: 1541-67-9
N-lauryldiethanolamine

Conditions

Conditions	Yield
	86.6%

: 67-56-1
methanol

: 50-00-0
formaldehyd

: 124-22-1
n-Dodecylamine

: 1541-67-9
N-lauryldiethanolamine

Conditions

Conditions	Yield
With tert.-butylhydroperoxide; titanium(III) chloride at 20℃; for 0.5h; Acidic aq. solution; Inert atmosphere;	18%

...Expand

: 75-21-8
oxirane

: 124-22-1
n-Dodecylamine

A: 16613-87-9
2-(N-dodecylamino)ethanol

B: 1541-67-9
N-lauryldiethanolamine

C: 99705-34-7
6-dodecyl-3-oxa-6-aza-octane-1,8-diol

Conditions

Conditions	Yield
Geschwindigkeit der Reaktion;

...Expand

: 75-21-8
oxirane

: 124-22-1
n-Dodecylamine

: 1541-67-9
N-lauryldiethanolamine

: 111-42-2
2,2'-iminobis[ethanol]

: 112-52-7
1-chlorododecane

: 1541-67-9
N-lauryldiethanolamine

Conditions

Conditions	Yield
With benzyl alcohol
In isopropyl alcohol at 140℃;

: 75-21-8
oxirane

: 3-Methyl-undecylamine

: 1541-67-9
N-lauryldiethanolamine

: 75-21-8
oxirane

: 124-22-1
n-Dodecylamine

potassium carbonate: potassium carbonate

A: 16613-87-9
2-(N-dodecylamino)ethanol

B: 1541-67-9
N-lauryldiethanolamine

C: 99705-34-7
6-dodecyl-3-oxa-6-aza-octane-1,8-diol

Conditions

Conditions	Yield
Geschwindigkeit der Reaktion;

...Expand

: 75-21-8
oxirane

: 124-22-1
n-Dodecylamine

potassium hydroxide: potassium hydroxide

A: 16613-87-9
2-(N-dodecylamino)ethanol

B: 1541-67-9
N-lauryldiethanolamine

C: 99705-34-7
6-dodecyl-3-oxa-6-aza-octane-1,8-diol

Conditions

Conditions	Yield
Geschwindigkeit der Reaktion;

...Expand

: 75-21-8
oxirane

: 124-22-1
n-Dodecylamine

sodium carbonate: sodium carbonate

A: 16613-87-9
2-(N-dodecylamino)ethanol

B: 1541-67-9
N-lauryldiethanolamine

C: 99705-34-7
6-dodecyl-3-oxa-6-aza-octane-1,8-diol

Conditions

Conditions	Yield
Geschwindigkeit der Reaktion;

...Expand

: 75-21-8
oxirane

: 124-22-1
n-Dodecylamine

sodium hydroxide: sodium hydroxide

A: 16613-87-9
2-(N-dodecylamino)ethanol

B: 1541-67-9
N-lauryldiethanolamine

C: 99705-34-7
6-dodecyl-3-oxa-6-aza-octane-1,8-diol

Conditions

Conditions	Yield
Geschwindigkeit der Reaktion;

...Expand

: 75-21-8
oxirane

: 124-22-1
n-Dodecylamine

sodium: sodium

A: 16613-87-9
2-(N-dodecylamino)ethanol

B: 1541-67-9
N-lauryldiethanolamine

C: 99705-34-7
6-dodecyl-3-oxa-6-aza-octane-1,8-diol

Conditions

Conditions	Yield
Geschwindigkeit der Reaktion;

...Expand

: 112-53-8
1-dodecyl alcohol

P2O5: P2O5

: 1541-67-9
N-lauryldiethanolamine

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: zinc chloride, hydrogen chloride / 13 h / 140 °C 2: propan-2-ol / 140 °C View Scheme

: 51323-71-8
dodecyl mesylate

: 111-42-2
2,2'-iminobis[ethanol]

: 1541-67-9
N-lauryldiethanolamine

Conditions

Conditions	Yield
In ethanol Reflux;

: 1541-67-9
N-lauryldiethanolamine

: 60855-82-5
bis-(2-chloro-ethyl)-dodecyl-amine

Conditions

Conditions	Yield
With thionyl chloride In chloroform for 4h; Heating;	97%
With thionyl chloride In chloroform Heating;

: 1541-67-9
N-lauryldiethanolamine

: 74-88-4
methyl iodide

: N,N-bis(2-hydroxyethyl)-N-methyldodecan-1-aminium iodide

Conditions

Conditions	Yield
In methanol at 20℃; for 24h;	75%

: 96-21-9
1,3-dibromo-2-hydroxypropane

: 1541-67-9
N-lauryldiethanolamine

: C35H76N2O5(2+)*2Br(1-)

Conditions

Conditions	Yield
In ethanol at 90℃; for 72h;	28%

: 74-87-3
methylene chloride

: 1541-67-9
N-lauryldiethanolamine

: 22340-01-8
DEA-CDD

Conditions

Conditions	Yield
at 150℃;

: 1541-67-9
N-lauryldiethanolamine

: 3926-62-3
sodium monochloroacetic acid

: 10471-50-8
carboxymethyl-dodecyl-bis-(2-hydroxy-ethyl)-ammonium betaine

Conditions

Conditions	Yield
With water

: 1541-67-9
N-lauryldiethanolamine

: 1541-81-7
4-dodecyl-morpholine

Conditions

Conditions	Yield
With aluminum oxide

: 1541-67-9
N-lauryldiethanolamine

: 114225-35-3
2-{2-[dodecyl-(2-hydroxy-ethyl)-amino]-ethoxy}-ethanesulfonic acid ; sodium-salt

Conditions

Conditions	Yield
With sodium hydroxide anschliessend mit Natrium-<2-hydroxy-aethansulfonat> auf 210grad;

: 1541-67-9
N-lauryldiethanolamine

: 102-47-6
3,4-Dichlorophenylmethyl chloride

: (3,4-dichloro-benzyl)-dodecyl-bis-(2-hydroxy-ethyl)-ammonium; chloride

: 1541-67-9
N-lauryldiethanolamine

: 86-84-0
1-Naphthyl isocyanate

: dodecyl-bis-(2-[1]naphthylcarbamoyloxy-ethyl)-amine

: 1541-67-9
N-lauryldiethanolamine

: 107-07-3
2-chloro-ethanol

: 22642-51-9
dodecyl-tris-(2-hydroxy-ethyl)-ammonium; chloride

Conditions

Conditions	Yield
at 170℃;

: 1541-67-9
N-lauryldiethanolamine

: 2530-44-1
dodecyldiethanolamine oxide

Conditions

Conditions	Yield
With Cumene hydroperoxide; titanium(IV) isobutoxide In ethyl acetate
With dihydrogen peroxide In water at 75 - 85℃;
With dihydrogen peroxide In water

: 1541-67-9
N-lauryldiethanolamine

: N-Dodecyl-N-<β-hydroxy-ethyl>-2-amino-ethylphosphit

Conditions

Conditions	Yield
With phosphonic Acid at 150℃; under 10 - 15 Torr; for 18h;

: 1541-67-9
N-lauryldiethanolamine

: 100-44-7
benzyl chloride

: 19379-90-9
N-benzyl-N-dodecyl-N,N-bis(beta-hydroxyethyl)ammonium chloride

: 1541-67-9
N-lauryldiethanolamine

: (R)-2-Amino-3-(2-{[2-((R)-2-amino-3-hydroxy-propylsulfanyl)-ethyl]-dodecyl-amino}-ethylsulfanyl)-propan-1-ol

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: 97 percent / SOCl2 / CHCl3 / 4 h / Heating 2: 65 percent / NaI, NaOH / ethanol / 4 h / 60 °C 3: 98 percent / SOCl2 / 5 h / 0 - 60 °C 4: 40 percent / NaBH4 / ethanol / a) RT, overnight, b) reflux, 4 h View Scheme

: 1541-67-9
N-lauryldiethanolamine

: 208519-27-1
(R)-2-Amino-3-(2-{[2-((R)-2-amino-2-carboxy-ethylsulfanyl)-ethyl]-dodecyl-amino}-ethylsulfanyl)-propionic acid

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 97 percent / SOCl2 / CHCl3 / 4 h / Heating 2: 65 percent / NaI, NaOH / ethanol / 4 h / 60 °C View Scheme

: 1541-67-9
N-lauryldiethanolamine

: (4R,14R)-9-dodecyl-4,14-dihydroxymethyl-6,12-dithia-3,9,15,18-tetraazabicyclo[15.3.1]heneicosa-1(18),17(19),20-triene-2,16-dione

Conditions

Conditions	Yield
Multi-step reaction with 5 steps 1: 97 percent / SOCl2 / CHCl3 / 4 h / Heating 2: 65 percent / NaI, NaOH / ethanol / 4 h / 60 °C 3: 98 percent / SOCl2 / 5 h / 0 - 60 °C 4: 1.) K2CO3 / 1.) CH2Cl2, 4 h, 2.) CH2Cl2 5: 36 percent / NaBH4 / ethanol / a) RT, overnight, b) reflux, 4 h View Scheme

N-Lauryldiethanolamine Specification

The N, N-Bis(2-hydroxyethyl)dodecylamine is an organic compound with the formula C₁₆H₃₅NO₂. The IUPAC name of this chemical is 2-[dodecyl(2-hydroxyethyl)amino]ethanol. With the CAS registry number 1541-67-9, it is also named as Bis(2-hydroxyethyl)dodecylamine.

Physical properties about N, N-Bis(2-hydroxyethyl)dodecylamine are: (1)ACD/LogP: 5.13 # of Rule of 5 Violations: 1; (2)#H bond acceptors: 3; (3)#H bond donors: 2; (4)#Freely Rotating Bonds: 17; (5)Polar Surface Area: 21.7 Å²; (6)Index of Refraction: 1.474; (7)Molar Refractivity: 82.96 cm³; (8)Molar Volume: 294.9 cm³; (9)Polarizability: 32.89×10^-24cm³; (10)Surface Tension: 37.1 dyne/cm; (11)Density: 0.927 g/cm³; (12)Flash Point: 171.2 °C; (13)Enthalpy of Vaporization: 75.37 kJ/mol; (14)Boiling Point: 401.1 °C at 760 mmHg; (15)Vapour Pressure: 4.21E-08 mmHg at 25°C.

Preparation: this chemical can be prepared by 1-bromo-dodecane and 2,2'-azanediyl-bis-ethanol. This reaction will need solvent propan-2-ol.

Uses of N, N-Bis(2-hydroxyethyl)dodecylamine: it can be used to produce bis-(2-chloro-ethyl)-dodecyl-amine by heating. It will need reagent SOCl₂ and solvent CHCl₃.

When you are using this chemical, please be cautious about it as the following:
This chemical is irritating to eyes, respiratory system and skin. When you are using it, wear suitable gloves and eye/face protection. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.

You can still convert the following datas into molecular structure:
(1)SMILES: OCCN(CCCCCCCCCCCC)CCO
(2)InChI: InChI=1/C16H35NO2/c1-2-3-4-5-6-7-8-9-10-11-12-17(13-15-18)14-16-19/h18-19H,2-16H2,1H3
(3)InChIKey: NKFNBVMJTSYZDV-UHFFFAOYAZ
(4)Std. InChI: InChI=1S/C16H35NO2/c1-2-3-4-5-6-7-8-9-10-11-12-17(13-15-18)14-16-19/h18-19H,2-16H2,1H3
(5)Std. InChIKey: NKFNBVMJTSYZDV-UHFFFAOYSA-N

Product Name

N-LAURYLDIETHANOLAMINE

Synthetic route

N-Lauryldiethanolamine Specification

Related Products

Hot Products