76152-19-7

Basic information

• Product Name: N^α-tert-butyloxycarbonyl-β-benzylester dodecyl-L-aspartamide
• Synonyms: N^α-tert-butyloxycarbonyl-β-benzylester dodecyl-L-aspartamide
• CAS NO: 76152-19-7
• Molecular Weight: 490.684
• Mol File: 76152-19-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N^α-tert-butyloxycarbonyl-β-benzylester dodecyl-L-aspartamide(CAS DataBase Reference)
• NIST Chemistry Reference: N^α-tert-butyloxycarbonyl-β-benzylester dodecyl-L-aspartamide(76152-19-7)
• EPA Substance Registry System: N^α-tert-butyloxycarbonyl-β-benzylester dodecyl-L-aspartamide(76152-19-7)

Safety Data

• Hazardous Substances Data: 76152-19-7(Hazardous Substances Data)

Upstream product

• 124-22-1 n-Dodecylamine 
• 7536-58-5 BOC-L-aspartic acid 4-benzyl ester 

Downstream Products

• 78222-59-0 N^α_asp-α_his-(6-bromohexanoyl)-N^im-tosyl-L-histidyl>-N-dodecyl-O-benzyl-L-aspartamide 
• 78222-56-7 N^α-(tert-butoxycarbonyl)-N^im-tosyl-L-histidyl-N-dodecyl-O-benzyl-L-aspartamide 
• 78222-57-8 (S)-3-{(S)-2-Amino-3-[1-(toluene-4-sulfonyl)-1H-imidazol-4-yl]-propionylamino}-N-dodecyl-succinamic acid benzyl ester 
• 159945-17-2 N^α-dodecanoyl-β-benzylester dodecyl-L-aspartamide 
• 76152-20-0 (S)-3-Amino-N-dodecyl-succinamic acid benzyl ester 
• 76152-21-1 (S)-3-Amino-N-dodecyl-succinamic acid benzyl ester; compound with trifluoro-acetic acid 

Relevant articles and documents

Vesicles and other supramolecular systems made from double-tailed synthetic glycolipids derived from galactosylated tris(hydroxymethyl)aminomethane

A series of double-tailed hydrocarbon glycolipids derived from tris(hydroxymethyl)aminomethane (Tris) have been prepared. These amphiphiles consist of three parts: a hydrophilic head derived from mono- or polygalactosylated Tris, a linking arm of peptidic

Aggregation Behaviour of Synthetic Peptide Surfactants

Single-chain surfactants with an amino-acid residue as part of a hydrophobic chain, SS'-bis-α-(6-trimethylammoniohexanoyl)-L-hemicysteinamide> bromide +C5CysC12)2>, N-dodecyl-Nα-(6-trimethylammoniohexanoyl)-S-benzyl-L-cysteinamide bromide +C5Cys(Bzl)C12>, and N-dodecyl-Nα-(6-trimethylammoniohexanoyl)-L-aspartamide bromide (N+C5AspC12) have been synthesized and the structures of the aggregates formed in aqueous media investigated.The peptide surfactants form tighter aggregates than ordinary micelles formed with octadecyltrimethylammonium chloride.The weight-average molecular weights of the aggregates in aqueous media were determined by the low angle laser light scattering technique: N+C5Cys(Bzl)C12, 7.04*1E6; (N+C5CysC12)2, 1.49*1E6; N+C5AspC12, 5.06*1E4.Consequently, N+C5AspC12 forms tight spherical micelles while (N+C5CysC12)2 and N+C5(Bzl)C12 constitute tight and large cylindrical micelles.This aggregation behaviour was also confirmed by elctronmicroscopy.The introduction of an amino-acid residue into the hydrophobic chain of a surfactant result in tightening of the aggregate structure in aqueous media, probably due to intermolecular hydrogen bonding among amino-acid moieties in the micelle.