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BOC4-SPER-CO2H, also known as tetra-Boc-spermine-5-carboxylic acid, is a spermidine derivative characterized by the presence of four Boc (tert-butyloxycarbonyl) protecting groups and a carboxylic acid functional group. It plays a crucial role in the development of degradable multivalent cationic lipids and nucleic acid transfer reactions, making it a valuable compound in the field of gene delivery.

119798-08-2

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119798-08-2 Usage

Uses

Used in Gene Delivery:
BOC4-SPER-CO2H is used as a key intermediate in the synthesis of degradable multivalent cationic lipids with disulfide-bond spacers. These lipids are essential for the development of efficient gene delivery systems, as they enable the safe and targeted delivery of genetic material into cells.
Used in Nucleic Acid Transfer Reactions:
BOC4-SPER-CO2H is utilized as a spermidine derivative in nucleic acid transfer reactions, which are vital for the manipulation and analysis of nucleic acids, such as DNA and RNA. Its unique structure allows for the formation of stable complexes with nucleic acids, facilitating their transfer and subsequent applications in research and therapeutics.

Check Digit Verification of cas no

The CAS Registry Mumber 119798-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,7,9 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 119798-08:
(8*1)+(7*1)+(6*9)+(5*7)+(4*9)+(3*8)+(2*0)+(1*8)=172
172 % 10 = 2
So 119798-08-2 is a valid CAS Registry Number.

119798-08-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2,5-bis[(2-methylpropan-2-yl)oxycarbonyl-[3-[(2-methylpropan-2-yl)oxycarbonylamino]propyl]amino]pentanoic acid

1.2 Other means of identification

Product number -
Other names tetra-Boc-carboxy spermine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:119798-08-2 SDS

119798-08-2Relevant academic research and scientific papers

A columnar phase of dendritic lipid-based cationic liposome-DNA complexes for gene delivery: Hexagonally ordered cylindrical micelles embedded in a DNA honeycomb lattice

Ewert, Kai K.,Evans, Heather M.,Zidovska, Alexandra,Bouxsein, Nathan F.,Ahmad, Ayesha,Safinya, Cyrus R.

, p. 3998 - 4006 (2006)

Gene therapy holds great promise as a future approach to fighting disease and is explored in worldwide clinical trials. Cationic liposome (CL)-DNA complexes are a prevalent nonviral delivery vector, but their efficiency requires improvement and the unders

Precision templating with DNA of a virus-like particle with peptide nanostructures

Ruff, Yves,Moyer, Tyson,Newcomb, Christina J.,Demeler, Borries,Stupp, Samuel I.

, p. 6211 - 6219 (2013)

We report here the preparation of filamentous virus-like particles by the encapsulation of a linear or circular double-stranded DNA template with preassembled mushroom-shaped nanostructures having a positively charged domain. These nanostructures mimic the capsid proteins of natural filamentous viruses and are formed by self-assembly of coiled-coil peptides conjugated at opposite termini with cationic segments and poly(ethylene glycol) (PEG) chains. We found that a high molecular weight of PEG segments was critical for the formation of monodisperse and uniformly shaped filamentous complexes. It is proposed that electrostatic attachment of the nanostructures with sufficiently long PEG segments generates steric forces that increase the rigidity of the neutralized DNA template. This stiffening counterbalances the natural tendency of the DNA template to condense into toroids or buckle multiple times. The control achieved over both shape and dimensions of the particles offers a strategy to create one-dimensional supramolecular nanostructures of defined length containing nucleic acids.

A highly efficient approach for the synthesis of cationic lipid DOSPA

Li, Yanhong,Debs, Robert J.,Heath, Timothy D.

, p. 2284 - 2286 (2007/10/03)

A highly efficient strategy has been developed for the synthesis of the cationic lipid, N-[2-({2,5-bis[(3-aminopropyl)amino]-1-oxopentyl}amino)ethyl]-N, N-dimethyl-2,3-bis[(1-oxo-9-octadecenyl)oxy] salt with hydrogen chloride (DOSPA). It involves the linkage of a cationic head group and a hydrophobic moiety in the presence of the standard coupling reagents. Georg Thieme Verlag Stuttgart.

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