7596-88-5

Basic information

• Product Name: N-Dodecanoylglycine
• Synonyms: N-Dodecanoylglycine
• CAS NO: 7596-88-5
• Molecular Formula: C₁₄H₂₇NO₃
• Molecular Weight: 257.36908
• Mol File: 7596-88-5.mol
• Article Data: 2

Chemical Properties

• Melting Point: 119 °C
• Boiling Point: 446.3°Cat760mmHg
• Flash Point: 223.7°C
• Appearance: /
• Density: 0.989g/cm³
• Vapor Pressure: 3.27E-09mmHg at 25°C
• Refractive Index: 1.466
• Storage Temp.: Refrigerator
• Solubility: DMSO (Sparingly, Heated), Methanol (Slightly, Heated)
• CAS DataBase Reference: N-Dodecanoylglycine(CAS DataBase Reference)
• NIST Chemistry Reference: N-Dodecanoylglycine(7596-88-5)
• EPA Substance Registry System: N-Dodecanoylglycine(7596-88-5)

Safety Data

• Hazardous Substances Data: 7596-88-5(Hazardous Substances Data)

Usage

Description

N-Dodecanoylglycine is a chemical compound that is derived from the combination of dodecanoic acid and glycine. It is known for its unique properties that make it suitable for various applications, particularly in the field of lubrication and material science.

Uses

Used in Lubricant Industry:
N-Dodecanoylglycine is used as an additive in HVI 350 mineral lubricating oil for enhancing its anti-wear and friction-reducing abilities. This application is crucial in ensuring the longevity and efficiency of machinery and equipment that rely on lubricants to reduce wear and tear, as well as to minimize energy consumption and operating costs.

InChI:InChI=1/C14H27NO3/c1-2-3-4-5-6-7-8-9-10-11-13(16)15-12-14(17)18/h2-12H2,1H3,(H,15,16)(H,17,18)

Upstream product

• 50-00-0 formaldehyd 
• 1120-16-7 lauric acid amide 
• 201230-82-2 carbon monoxide 
• 544-31-0 2-(palmitoylamino)ethanol 
• 111-57-9 N-stearoylethanolamine 
• 142-78-9 N-(2-hydroxyethyl)dodecanamide 
• 142-58-5 myristic monoethanolamide 
• 7112-02-9 N‐(2‐hydroxyethyl)octanamide 
• 7726-08-1 decanoic acid monoethanolamide 

Downstream Products

• 56-40-6 glycine 
• 123574-56-1 1-O-acetyl-2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-6-O-(2,2,2-trichloroethoxycarbonyl)-2-(2,2,2-trichloroethoxycarbonylamino)-D-glucopyranose 
• 140236-14-2 allyl 2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-6-O-(2,2,2-trichloroethoxycarbonyl)-2-(2,2,2-trichloroethoxycarbonylamino)-α-D-glucopyranoside 
• 133940-55-3 Dodecanoylamino-acetic acid (2R,3R,4R,5S,6R)-2-bromo-5-(diphenoxy-phosphoryloxy)-3-(2,2,2-trichloro-ethoxycarbonylamino)-6-(2,2,2-trichloro-ethoxycarbonyloxymethyl)-tetrahydro-pyran-4-yl ester 
• 145609-47-8 2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-6-O-(2,2,2-trichloroethoxycarbonyl)-2-(2,2,2-trichloroethoxycarbonylamino)-D-glucose 
• 123574-26-5 2-(diphenylphosphonooxy)ethyl 2-deoxy-3-O-(N-dodecanoylglycyl)-2-(N-dodecanoylglycylamino)-α-D-glucopyranoside 
• 123573-99-9 1,3-di(benzyloxycarbonyl)isopropyl 2-deoxy-3-O-(N-dodecanoylglycyl)-2-tetradecanoylamino-α-D-glucopyranoside 
• 140236-16-4 2-(diphenylphosphonooxy)ethyl 2-deoxy-4,6-O-isopropylidene-3-O-(N-dodecanoylglycyl)-2-tetradecanoylamino-α-D-glucopyranoside 
• 123573-81-9 2-(diphenylphosphonooxy)ethyl 2-deoxy-3-O-(N-dodecanoylglycyl)-2-tetradecanoylamino-α-D-glucopyranoside 
• 123598-20-9 2-(diphenylphosphonooxy)ethyl 2-deoxy-2-(N-dodecanoylglycylamino)-3-O-tetradecanoyl-α-D-glucopyranoside 
• 147720-79-4 1-O-acetyl-2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-2-tetradecanoylamino-6-O-(2,2,2-trichloroethoxycarbonyl)-α-D-glucopyranose 
• 147720-77-2 allyl 2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-2-tetradecanoylamino-6-O-(2,2,2-trichloroethoxycarbonyl)-α-D-glucopyranoside 
• 147720-68-1 2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-2-tetradecanoylamino-6-O-(2,2,2-trichloroethoxycarbonyl)-α-D-glucopyranosyl bromide 
• 147720-78-3 2-deoxy-4-O-diphenylphosphono-3-O-(N-dodecanoylglycyl)-2-tetradecanoylamino-6-O-(2,2,2-trichloroethoxycarbonyl)-α-D-glucopyranose 

Relevant articles and documents

Process for converting primary amidoalcohols to amidocarboxylic acids in high yield

The invention relates to an improved process for oxidizing a primary amidoalcohol to the corresponding amidocarboxylic acid in high yield.