N-Lauryldiethanolamine

Base Information

• Chemical Name: N-Lauryldiethanolamine
• CAS No.: 1541-67-9
• Deprecated CAS: 173104-11-5,1079914-70-7
• Molecular Formula: C16H35NO2
• Molecular Weight: 273.459
• Hs Code.: 2922199090
• European Community (EC) Number: 216-277-8
• NSC Number: 525737
• UNII: EM71KK5P4A
• DSSTox Substance ID: DTXSID4042090
• Nikkaji Number: J206.767F
• Wikidata: Q27277241
• Metabolomics Workbench ID: 156949
• ChEMBL ID: CHEMBL3186559
• Mol file: 1541-67-9.mol

Synonyms:N-Lauryldiethanolamine;1541-67-9;Lauryldiethanolamine;N-Dodecyldiethanolamine;Ethanol, 2,2'-(dodecylimino)bis-;Dodecyldiethanolamine;2,2'-(Dodecylazanediyl)diethanol;Bis(hydroxyethyl)dodecylamine;2-[dodecyl(2-hydroxyethyl)amino]ethanol;2,2'-(Laurylimino)diethanol;n-Dodecylbis(hydroxyethyl)amine;Bis(2-hydroxyethyl)dodecylamine;Dodecylbis(2-hydroxyethyl)amine;N,N-Bis(2-hydroxyethyl)dodecylamine;2,2'-(DODECYLIMINO)DIETHANOL;N,N-Bis(hydroxyethyl)laurylamine;Ethanol, 2,2'-(dodecylimino)di-;N,N-Bis(2-hydroxyethyl)laurylamine;Bis(beta-hydroxyethyl)laurylamine;n-lauryl diethanolamine;UNII-EM71KK5P4A;NSC 525737;EM71KK5P4A;2,2'-(Dodecylimino)bisethanol;DTXSID4042090;Bis(.beta.-hydroxyethyl)laurylamine;EINECS 216-277-8;NSC-525737;AI3-16725;AI 3-16725;Erest EA;Ethanol,2,2'-(dodecylimino)bis-;NSC525737;ELEST EA;2-[dodecyl(2-hydroxyethyl)amino]ethan-1-ol;FENTACARE 1202;Dodecylbis(hydroxyethyl)amine;SCHEMBL43396;Ethanol,2'-(dodecylimino)di-;Ethanol,2'-(dodecylimino)bis-;N(CCO)(CCO)CCCCCCCCCCCC;CHEMBL3186559;DTXCID2022090;2,2-(Dodecylazanediyl)diethanol;C16H35NO2;Dodecyl bis(2-hydroxyethyl)amine;dodecyl-bis-(b-hydroxyethyl)amine;TB 128K;Bis(2-hydroxyethyl) Lauryl Amine;BAA54167;N-LAURYL DIETHANOLAMINE(JPN);Tox21_301529;MFCD00059002;AKOS009157613;N-LAURYL DIETHANOLAMINE [INCI];NCGC00255856-01;2,2'-(Dodecylazanediyl)bis(ethan-1-ol);2,2'-(DODECYLIMINO)BIS(ETHANOL);AS-60983;CAS-1541-67-9;CS-0447350;FT-0760772;L0020;N,N-Bis(2-hydroxyethyl)dodecylamine, AldrichCPR;A883747;J-009074;Q27277241

Chemical Property of N-Lauryldiethanolamine

Chemical Property:

• Appearance/Colour: colorless or light yellow liquid
• Vapor Pressure: 4.21E-08mmHg at 25°C
• Melting Point: 185-190℃
• Refractive Index: 1.4675 (589.3 nm 20℃)
• Boiling Point: 401.115 °C at 760 mmHg
• PKA: 14.41±0.10(Predicted)
• Flash Point: 171.237 °C
• PSA: 43.70000
• Density: 0.927 g/cm³
• LogP: 3.19390
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility.: Chloroform (Slightly), Methanol (Slightly)
• XLogP3: 4.5
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 15
• Exact Mass: 273.266779359
• Heavy Atom Count: 19
• Complexity: 159

Purity/Quality:

N-Lauryldiethanolamine ^*data from reagent suppliers

Safty Information:

• Statements: 36/37/38
• Safety Statements: 26-36/37/39

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCN(CCO)CCO
• Use Description: N-Lauryldiethanolamine, a specific chemical compound, serves diverse roles in various fields. In the realm of personal care and cosmetics, it acts as an emulsifier, surfactant, and conditioning agent in formulations such as shampoos, body washes, and creams, contributing to improved product texture and efficacy. In the agricultural sector, this compound finds application as an adjuvant in pesticide formulations, enhancing the spread and efficacy of agricultural chemicals on crops. Moreover, in the field of industrial chemistry, it can serve as a corrosion inhibitor in metalworking fluids, contributing to the protection of metal surfaces. Its applications in personal care, agriculture, and industrial chemistry highlight its significance in enhancing consumer products, supporting agriculture, and ensuring material longevity across these distinct domains.

Technology Process of N-Lauryldiethanolamine

There total 15 articles about N-Lauryldiethanolamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 98.0%

1-dodecylbromide (143-15-7) + 2,2'-iminobis[ethanol] (111-42-2) → N-lauryldiethanolamine (1541-67-9)

Guidance literature:

With potassium carbonate; potassium iodide; In acetonitrile; for 12h; Inert atmosphere; Reflux;

Reference yield: 86.6%

2-(N-dodecylamino)ethanol (16613-87-9) → N-lauryldiethanolamine (1541-67-9)

Guidance literature:

DOI:10.1007/BF00776798

Reference yield: 18.0%

methanol (67-56-1) + formaldehyd (50-00-0,30525-89-4,61233-19-0) + n-Dodecylamine (124-22-1) → N-lauryldiethanolamine (1541-67-9)

Guidance literature:

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

DOI:10.1021/ol802244n

upstream raw materials:

oxirane

n-Dodecylamine

1-dodecylbromide

2,2'-iminobis[ethanol]

Downstream raw materials:

DEA-CDD

dodecyldiethanolamine oxide

dodecylammonium chloride

N-benzyl-N-dodecyl-N,N-bis(beta-hydroxyethyl)ammonium chloride

Refernces

• 1、 Sun, Ya,Han, Fu,Zhou, Yawen,Xu, Baocai. "Synthesis and Properties of Quaternary Ammonium Gemini Surfactants with Hydroxyethyl at Head Groups". . p. 675 - 681. Retrieved 2019.
• 2、 Limanov,V.E. et al.. "-". . . Retrieved 1976.
• 3、 -. "Alkynyl quaternary ammonium salt multifunctional surfactants and preparation method thereof". Paragraph 0057-0063. . Retrieved 2017/05/02.