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Disodium Cocoyl Glutamate

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Identification
Molecular formula
C20H37N2O7Na2
CAS number
61789-40-0
IUPAC name
disodium;3-[2-carboxylatoethyl(dodecyl)amino]propanoate
State
State

At room temperature, Disodium Cocoyl Glutamate is a solid. It is commonly processed into powder form for use in formulations, where it is dissolved to create cleansing products.

Melting point (Celsius)
280.00
Melting point (Kelvin)
553.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
476.50g/mol
Molar mass
0.0000g/mol
Density
0.3200g/cm3
Appearence

Disodium Cocoyl Glutamate appears as a white to off-white solid powder. It is typically used in personal care products such as shampoos and body washes, where it acts as a mild surfactant with excellent foaming properties.

Comment on solubility

Solubility of Disodium 3-[2-carboxylatoethyl(dodecyl)amino]propanoate

Disodium 3-[2-carboxylatoethyl(dodecyl)amino]propanoate, commonly referred to as a surfactant compound due to its amphiphilic nature, showcases interesting solubility characteristics:

  • Aqueous Solubility: This compound is readily soluble in water, which is attributed to its dual functional groups. The carboxylate group enhances ionic interactions with water molecules.
  • Organic Solvent Solubility: It also demonstrates some degree of solubility in organic solvents, although it is significantly lower compared to its solubility in water.
  • pH Dependence: The solubility can be affected by the pH of the solution. At higher pH levels, the carboxylate group remains deprotonated, enhancing solubility.
  • Temperature Sensitivity: As with many surfactants, increasing temperature may further facilitate solubility in both water and organic solvents.

In summary, the solubility profile of this compound can be described as follows:

  1. The compound readily dissolves in water, making it useful in aqueous formulations.
  2. Increased pH levels enhance its solubility due to the ionic nature of the carboxylate group.
  3. Temperature increases can positively influence solubility in both polar and non-polar environments.

Understanding the solubility of disodium 3-[2-carboxylatoethyl(dodecyl)amino]propanoate is crucial for its applications in various fields, including pharmaceuticals and industrial formulations.

Interesting facts

Interesting Facts about Disodium 3-[2-Carboxylatoethyl(dodecyl)amino]propanoate

Disodium 3-[2-carboxylatoethyl(dodecyl)amino]propanoate is a fascinating compound with unique properties and wide-ranging applications. Below are some noteworthy facts:

  • Versatile Use: This compound is primarily utilized as a surfactant due to its amphiphilic nature, allowing it to interact with both water and oil molecules effectively.
  • Biochemical Relevance: The structure of this compound features a dodecyl group and a carboxylate functionality which are relevant in biological systems. These characteristics allow for interactions with cell membranes, making it a subject of interest in pharmaceutical formulations.
  • Eco-Friendly Options: With increasing environmental awareness, compounds like disodium 3-[2-carboxylatoethyl(dodecyl)amino]propanoate are becoming crucial in developing biodegradable surfactants, reducing environmental impact compared to conventional surfactants.
  • Research Applications: It has been extensively studied for its potential in drug delivery systems. The ability to stabilize active ingredients makes it attractive for pharmaceutical chemists looking to improve drug solubility and absorption.

Moreover, the synthesis of this compound often involves specific reactions that highlight important principles of organic and medicinal chemistry. As one research paper puts it, "The manipulation of functional groups in the synthesis provides insight into structure-activity relationships essential for improving drug design."
These attributes contribute to its significance in both academic research and industrial applications, making it a compound worthy of exploration and study in the field of chemistry.

Synonyms
3655-00-3
DISODIUM LAURIMINODIPROPIONATE
Deriphat 160
UNII-KAS63U0A87
KAS63U0A87
COLATERIC HFA
Sodium N-dodecyliminodipropionate
HSDB 2790
REWOTERIC AM-LP
MIRATAINE H 2C
beta-Alanine, N-(2-carboxyethyl)-N-dodecyl-, disodium salt
EINECS 222-899-0
Sodium N-lauryl-beta-iminodipropionate
Propionic acid, 3,3'-(dodecylimino)di-, disodium salt
N-Lauryl-beta-iminodipropionate sodium salt
Disodium 3,3'-(dodecylimino)bis(propionate)
Disodium beta,beta'-(laurylimino)dipropionate
DTXSID9063116
.beta.-Alanine, N-(2-carboxyethyl)-N-dodecyl-, disodium salt
Disodium N-lauryl-beta,beta'-iminodipropionate
Disodium N-lauryl-beta-iminodipropionate
DISODIUM LAURIMINODIPROPIONATE [HSDB]
DISODIUM 3,3'-(DODECYLIMINO)DIPROPIONATE
DISODIUM N-LAURYL-.BETA.-IMINODIPROPIONATE
N-(2-Carboxyethyl)-N-dodecyl-beta-alanine, disodium salt
beta-Alanine, N-(2-carboxyethyl)-N-dodecyl-, sodium salt (1:2)
.beta.-Alanine, N-(2-carboxyethyl)-N-dodecyl-, sodium salt (1:2)
N-(2-CARBOXYETHYL)-N-DODECYL-.BETA.-ALANINE, DISODIUM SALT
Sodium Ndodecyliminodipropionate
DTXCID0039194
Sodium Nlaurylbetaiminodipropionate
Disodium Nlaurylbetaiminodipropionate
NLaurylbetaiminodipropionate sodium salt
Disodium Nlaurylbeta,beta'iminodipropionate
Disodium 3,3'(dodecylimino)bis(propionate)
Disodium beta,beta'(laurylimino)dipropionate
DISODIUM LAURIMINODIPROPIONATE [INCI]
N(2Carboxyethyl)Ndodecylbetaalanine, disodium salt
betaAlanine, N(2carboxyethyl)Ndodecyl, disodium salt
Propionic acid, 3,3'(dodecylimino)di, disodium salt
222-899-0
disodium;3-[2-carboxylatoethyl(dodecyl)amino]propanoate
SCHEMBL337202
Disodium N-(2-carboxyethyl)-N-dodecyl-beta-alaninate
KSDGSKVLUHKDAL-UHFFFAOYSA-L
N-dodecyliminodipropionate disodium
DAA65500
Sodium3,3'-(dodecylazanediyl)dipropanoate
N-Dodecyl-B-iminodipropionic acid, disodium
Sodium 3,3'-(dodecylazanediyl)dipropanoate
Sodium 3,3'-(dodecylazanediyl)dipropionate
CS-0451700
N-(2-Carboxyethyl)-N-lauryl-.beta.-alanine
G77834
3,3'-(Dodecylimino)dipropionic acid,sodium salt
Q27282156