Glycine, N-(carboxymethyl)-N-(1-oxododecyl)-

Base Information

• Chemical Name: Glycine, N-(carboxymethyl)-N-(1-oxododecyl)-
• CAS No.: 3775-51-7
• Molecular Formula: C16H29NO5
• Molecular Weight: 315.41
• Hs Code.: 2922499990
• European Community (EC) Number: 223-226-3
• NSC Number: 78334
• UNII: SG3Y16F296
• DSSTox Substance ID: DTXSID7063186
• Nikkaji Number: J217.675K
• Wikidata: Q27289194
• Mol file: 3775-51-7.mol

Synonyms:3775-51-7;Lauroyliminodiacetic acid;Glycine, N-(carboxymethyl)-N-(1-oxododecyl)-;Acetic acid, (lauroylimino)di-;Acetyl carboxymethyl lauroyl glycine;2-[carboxymethyl(dodecanoyl)amino]acetic acid;Lauroyl iminodiacetic acid;N-Carboxymethyl-N-(1-oxododecyl)-glycine;UNII-SG3Y16F296;SG3Y16F296;EINECS 223-226-3;NSC 78334;NSC-78334;N-(Carboxymethyl)-N-(1-oxododecyl)glycine;SCHEMBL1115961;DTXSID7063186;NSC78334;AKOS024367227;N-Carboxymethyl-N-(1-oxododecyl)glycine;2-[N-(carboxymethyl)dodecanamido]acetic acid;2-(N-Carboxymethyl-N-dodecanoylamino)acetic acid;EN300-22879241;Q27289194;Z1262460842

Chemical Property of Glycine, N-(carboxymethyl)-N-(1-oxododecyl)-

Chemical Property:

• Vapor Pressure: 9.66E-12mmHg at 25°C
• Refractive Index: 1.492
• Boiling Point: 509.1 °C at 760 mmHg
• Flash Point: 261.7 °C
• PSA: 94.91000
• Density: 1.101 g/cm³
• LogP: 2.90510
• XLogP3: 4.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 14
• Exact Mass: 315.20457303
• Heavy Atom Count: 22
• Complexity: 327

Purity/Quality:

98%min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCC(=O)N(CC(=O)O)CC(=O)O

Technology Process of Glycine, N-(carboxymethyl)-N-(1-oxododecyl)-

There total 3 articles about Glycine, N-(carboxymethyl)-N-(1-oxododecyl)- 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: 70.0%

lauric acid (143-07-7) + iminodiacetic acid (142-73-4) → N-lauryl iminodiacetic acid (3775-51-7)

Guidance literature:

With sodium hydroxide; 1-hydroxy-pyrrolidine-2,5-dione; dicyclohexyl-carbodiimide; In tetrahydrofuran; for 12h;

Reference yield:

formaldehyd (50-00-0,30525-89-4,61233-19-0) + lauric acid amide (1120-16-7) + carbon monoxide (201230-82-2) → N-dodecanoylglycine (7596-88-5) + N-lauryl iminodiacetic acid (3775-51-7)

Guidance literature:

With water; hydrogen; dicobalt octacarbonyl; In ethyl acetate; at 80 - 110 ℃; for 1.5h;

Reference yield:

n-dodecanoyl chloride (112-16-3) + iminodiacetic acid (142-73-4) → N-lauryl iminodiacetic acid (3775-51-7)

Guidance literature:

With sodium hydroxide;

upstream raw materials:

n-dodecanoyl chloride

iminodiacetic acid

formaldehyd

lauric acid amide

Refernces

• 1、 Stern, R.,Reffet, D.,Hirschauer, A.,Commereuc, D.,Chauvin, Y.. "NEW SYNTHESIS OF N-ACYLIMINODIACETIC ACID BY CONDENSATION OF AMIDES WITH FORMALDEHYDE IN THE PRESENCE OF CARBON MONOXIDE CATALYZED BY DICOBALT OCTACARBONYL". . p. 1111 - 1113. Retrieved 2007/10/02.