Ethyl Lauroyl Arginate Hydrochloride - ≥96% , CAS No.60372-77-2

CAS: 60372-77-2 Cat. No.: E304112 Molecular Weight: 421.02 EC Number: 434-630-6 PubChem CID: 25229630

GRADE & PURITY ≥96%

Synonyms

CUBZMGWLVMQKNE-LMOVPXPDSA-N | Q27293951 | SCHEMBL1038333 | BS-17290 | N2-(1-Oxododecyl)-L-arginine Ethyl Ester Hydrochloride | AKOS030528864 | XPD6ZY79TB | LAURAMIDE ARGININE ETHYL ESTER (LAE) | AS-13076 | Ethyl-N2-dodecanoyl-L-argininate hydrochloride |

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Specifications

Synonyms

CUBZMGWLVMQKNE-LMOVPXPDSA-N | Q27293951 | SCHEMBL1038333 | BS-17290 | N2-(1-Oxododecyl)-L-arginine Ethyl Ester Hydrochloride | AKOS030528864 | XPD6ZY79TB | LAURAMIDE ARGININE ETHYL ESTER (LAE) | AS-13076 | Ethyl-N2-dodecanoyl-L-argininate hydrochloride |

Specifications & Purity

≥96%

Storage

Store at -20°C, Argon charged

Shipped In

Ice chest + Ice pads

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥96%

Names and Identifiers

• Pubchem Sid: 504770029
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504770029
• Canonical Smiles: CCCCCCCCCCCC(=O)NC(CCCN=C(N)N)C(=O)OCC.Cl
• IUPAC Name: ethyl (2S)-5-(diaminomethylideneamino)-2-(dodecanoylamino)pentanoate;hydrochloride
• InChIKey: CUBZMGWLVMQKNE-LMOVPXPDSA-N
• INCHI: 1S/C20H40N4O3.ClH/c1-3-5-6-7-8-9-10-11-12-15-18(25)24-17(19(26)27-4-2)14-13-16-23-20(21)22;/h17H,3-16H2,1-2H3,(H,24,25)(H4,21,22,23);1H/t17-;/m0./s1
• Isomeric SMILES: CCCCCCCCCCCC(=O)N[C@@H](CCCN=C(N)N)C(=O)OCC.Cl
• PubChem CID: 25229630
• Molecular Weight: 421.02

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Amino acids, peptides, and analogues
        • Level5 Amino acids and derivatives
          • Level6 Alpha amino acids and derivatives
            • Level7 N-acyl-alpha amino acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Amino acids, peptides, and analogues
• Intermediate Tree Nodes: Amino acids and derivatives - Alpha amino acids and derivatives
• Direct Parent: N-acyl-alpha amino acids and derivatives
• Alternative Parents: Alpha amino acid esters Fatty acid esters N-acyl amines Secondary carboxylic acid amides Guanidines Carboxylic acid esters Propargyl-type 1,3-dipolar organic compounds Monocarboxylic acids and derivatives Carboximidamides Organic oxides Hydrochlorides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alpha-amino acid ester - N-acyl-alpha amino acid or derivatives - Fatty acid ester - Fatty amide - Fatty acyl - N-acyl-amine - Carboxamide group - Carboxylic acid ester - Guanidine - Secondary carboxylic acid amide - Organic 1,3-dipolar compound - Monocarboxylic acid or derivatives - Propargyl-type 1,3-dipolar organic compound - Carboximidamide - Organic nitrogen compound - Hydrochloride - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as n-acyl-alpha amino acids and derivatives. These are compounds containing an alpha amino acid (or a derivative thereof) which bears an acyl group at its terminal nitrogen atom.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemical and Physical Properties

• Solubility: DMSO (Slightly), Methanol (Slightly)
• Sensitivity: Moisture sensitive
• Melt Point(°C): 57-61°C
• Molecular Weight: 421.000 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 18
• Exact Mass: 420.287 Da
• Monoisotopic Mass: 420.287 Da
• Topological Polar Surface Area: 120.000 Ų
• Heavy Atom Count: 28
• Formal Charge: 0
• Complexity: 423.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3

References

1. Shupeng Su, Xinyi Yin, Wenyu Du, Liying Han, Qiu Wu, Hongyan Zhang.  (2023)  Novel concentrated O/W emulsion co-stabilized by like-charged chitosan nanoparticle and ethyl lauroyl arginate (LAE) surfactant at very low dosages.  LWT-FOOD SCIENCE AND TECHNOLOGY,      [PMID:] [10.1016/j.lwt.2023.115692]

2. Xianchang Liang, Wenjing Wang, Mingyuan Tang, Yuanyuan Kang, Mingjun Cui, Haichao Zhao.  (2025)  Preparation, characterization and antibacterial activities of bio-based schiff base Copper Complex intercalated montmorillonite.  APPLIED CLAY SCIENCE,      [PMID:] [10.1016/j.clay.2025.107809]

3. Junhua Lu, Wenyu Du, Mengjiao Wang, Liying Han, Hongyan Zhang, Shupeng Su.  (2025)  Facile preparation of high internal phase emulsion co-stabilized by like-charged chitosan nanoparticle and cationic surfactant at very low dosages.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:41072687] [10.1016/j.ijbiomac.2025.148175]

4. Chengyi Sun, Zhijie Zhu, Wen He, Zhaoxian He, Yuqing Hu, Xianfeng Du.  (2025)  Fabrication of antimicrobial high internal phase Pickering emulsions stabilized by starch nanoparticles-ethyl lauroyl arginate hydrochloride complexes for banana preservation.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:41352503] [10.1016/j.ijbiomac.2025.149486]

5. Zhen Ren, Zimou Feng, Huaxing Liang, Zhiyang Zhu, Yi Yang, Xinglin Lu.  (2026)  In Situ Surfactant-Assisted Assembly for Efficient Removal of PFAS by Low-Pressure Ultrafiltration Membrane Process.  ENVIRONMENTAL SCIENCE & TECHNOLOGY,      [PMID:41489990] [10.1021/acs.est.5c13478]