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Details

Stereochemistry ABSOLUTE
Molecular Formula C17H29NO5.2Na
Molecular Weight 373.3954
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DISODIUM LAUROYL GLUTAMATE

SMILES

[Na+].[Na+].CCCCCCCCCCCC(=O)N[C@@H](CCC([O-])=O)C([O-])=O

InChI

InChIKey=HWUINYGRRJTXGE-UTLKBRERSA-L
InChI=1S/C17H31NO5.2Na/c1-2-3-4-5-6-7-8-9-10-11-15(19)18-14(17(22)23)12-13-16(20)21;;/h14H,2-13H2,1H3,(H,18,19)(H,20,21)(H,22,23);;/q;2*+1/p-2/t14-;;/m0../s1

HIDE SMILES / InChI

Molecular Formula Na
Molecular Weight 22.98976928
Charge 1
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C17H29NO5
Molecular Weight 327.4159
Charge -2
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

LAUROYL GLUTAMIC ACID is a small molecule organic gelator used to increase the solubility of poorly soluble compounds.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Inactive ingredient
BRIGHTENING DYNAMICS TRAVELING KIT JAFRA

Approved Use

Helps prevent sunburn. If used as directed, with other sun protection measures (see directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Launch Date

2014
PubMed

PubMed

TitleDatePubMed
Drug solubilization effect of lauroyl-L-glutamate.
2012-01
Real-time observation of fiber network formation in molecular organogel: supersaturation-dependent microstructure and its related rheological property.
2006-04-13
Architecture of a biocompatible supramolecular material by supersaturation-driven fabrication of its fiber network.
2005-12-29
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:06:54 GMT 2025
Edited
by admin
on Mon Mar 31 19:06:54 GMT 2025
Record UNII
O99ROV57IA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DISODIUM LAUROYL GLUTAMATE
INCI  
INCI  
Official Name English
AMISOFT LS 22
Preferred Name English
DISODIUM LAUROYL-L-GLUTAMATE
Common Name English
N-LAUROYL-L-GLUTAMIC ACID DISODIUM SALT
Common Name English
AMISOFT LS-22
Brand Name English
L-GLUTAMIC ACID, N-(1-OXODODECYL)-, DISODIUM SALT
Common Name English
L-GLUTAMIC ACID, N-(1-OXODODECYL)-, SODIUM SALT (1:2)
Common Name English
N-LAUROYLGLUTAMIC ACID DISODIUM SALT
Common Name English
Code System Code Type Description
RXCUI
1928076
Created by admin on Mon Mar 31 19:06:54 GMT 2025 , Edited by admin on Mon Mar 31 19:06:54 GMT 2025
PRIMARY
DAILYMED
O99ROV57IA
Created by admin on Mon Mar 31 19:06:54 GMT 2025 , Edited by admin on Mon Mar 31 19:06:54 GMT 2025
PRIMARY
CAS
50622-20-3
Created by admin on Mon Mar 31 19:06:54 GMT 2025 , Edited by admin on Mon Mar 31 19:06:54 GMT 2025
PRIMARY
FDA UNII
O99ROV57IA
Created by admin on Mon Mar 31 19:06:54 GMT 2025 , Edited by admin on Mon Mar 31 19:06:54 GMT 2025
PRIMARY
PUBCHEM
11337766
Created by admin on Mon Mar 31 19:06:54 GMT 2025 , Edited by admin on Mon Mar 31 19:06:54 GMT 2025
PRIMARY
EPA CompTox
DTXSID7074824
Created by admin on Mon Mar 31 19:06:54 GMT 2025 , Edited by admin on Mon Mar 31 19:06:54 GMT 2025
PRIMARY